☰

Nancy J. Cox - Publications

Affiliations: 
Genetic medicine Vanderbilt University Med Ctr, Nashville 
Tree Info Similar researchers PubMed Report error

95/500 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Pershad Y, Mack T, Poisner H, Jakubek YA, Stilp AM, Mitchell BD, Lewis JP, Boerwinkle E, Loos RJ, Chami N, Wang Z, Barnes K, Pankratz N, Fornage M, Redline S, ... ... Cox N, et al. Determinants of mosaic chromosomal alteration fitness. Medrxiv : the Preprint Server For Health Sciences. PMID 37905118 DOI: 10.1101/2023.10.20.23297280  0.382
2023 Mosley JD, Shelley JP, Dickson AL, Zanussi J, Daniel LL, Zheng NS, Bastarache L, Wei WQ, Shi M, Jarvik GP, Rosenthal EA, Khan A, Sherafati A, Kullo IJ, Walunas TL, ... ... Cox NJ, et al. Clinical consequences of a polygenic predisposition to benign lower white blood cell counts. Medrxiv : the Preprint Server For Health Sciences. PMID 37662324 DOI: 10.1101/2023.08.20.23294331  0.4
2023 Sun Q, Broadaway KA, Edmiston SN, Fajgenbaum K, Miller-Fleming T, Westerkam LL, Melendez-Gonzalez M, Bui H, Blum FR, Levitt B, Lin L, Hao H, Harris KM, Liu Z, Thomas NE, ... Cox NJ, et al. Genetic Variants Associated With Hidradenitis Suppurativa. Jama Dermatology. PMID 37494057 DOI: 10.1001/jamadermatol.2023.2217  0.305
2023 Gustavson DE, Coleman PL, Wang Y, Nitin R, Petty LE, Bush CT, Mosing MA, Wesseldijk LW, Ullén F, Below JE, Cox NJ, Gordon RL. Exploring the genetics of rhythmic perception and musical engagement in the Vanderbilt Online Musicality Study. Annals of the New York Academy of Sciences. PMID 36718543 DOI: 10.1111/nyas.14964  0.564
2022 Strayer N, Zhang S, Yao L, Vessels T, Bejan CA, Hsi RS, Shirey-Rice JK, Balko JM, Johnson DB, Phillips EJ, Bick A, Edwards TL, Velez Edwards DR, Pulley JM, Wells QS, ... ... Cox NJ, et al. Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs. Bioinformatics (Oxford, England). PMID 36472455 DOI: 10.1093/bioinformatics/btac780  0.339
2022 Bhattacharya A, Hirbo JB, Zhou D, Zhou W, Zheng J, Kanai M, Pasaniuc B, Gamazon ER, Cox NJ. Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies: Lessons from the Global Biobank Meta-analysis Initiative. Cell Genomics. 2. PMID 36341024 DOI: 10.1016/j.xgen.2022.100180  0.315
2022 Fernández-Rhodes L, Graff M, Buchanan VL, Justice AE, Highland HM, Guo X, Zhu W, Chen HH, Young KL, Adhikari K, Palmer ND, Below JE, Bradfield J, Pereira AC, Glover L, ... ... Cox NJ, et al. Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Hgg Advances. 4: 100149. PMID 36268164 DOI: 10.1016/j.xhgg.2022.100149  0.555
2022 Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Cox NJ, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084  0.337
2022 Fernández-Rhodes L, Graff M, Buchanan VL, Justice AE, Highland HM, Guo X, Zhu W, Chen HH, Young KL, Adhikari K, Palmer ND, Below JE, Bradfield J, Pereira AC, Glover L, ... ... Cox NJ, et al. Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Hgg Advances. 3: 100099. PMID 35399580 DOI: 10.1016/j.xhgg.2022.100099  0.586
2022 Wu P, Feng Q, Kerchberger VE, Nelson SD, Chen Q, Li B, Edwards TL, Cox NJ, Phillips EJ, Stein CM, Roden DM, Denny JC, Wei WQ. Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension. Nature Communications. 13: 46. PMID 35013250 DOI: 10.1038/s41467-021-27751-1  0.34
2021 Olson NC, Raffield LM, Moxley AH, Miller-Fleming TW, Auer PL, Franceschini N, Ngo D, Thornton TA, Lange EM, Li Y, Nickerson DA, Zakai NA, Gerszten RE, Cox NJ, Correa A, et al. Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Blacks. Circulation. Genomic and Precision Medicine. CIRCGEN121003421. PMID 34706549 DOI: 10.1161/CIRCGEN.121.003421  0.417
2021 Karas S, Etheridge AS, Nickerson DA, Cox NJ, Mohlke KL, Cecchin E, Toffoli G, Mathijssen RHJ, Forrest A, Bies RR, Innocenti F. Integration of DNA sequencing with population pharmacokinetics to improve the prediction of irinotecan exposure in cancer patients. British Journal of Cancer. PMID 34703007 DOI: 10.1038/s41416-021-01589-2  0.353
2021 Mikhaylova AV, McHugh CP, Polfus LM, Raffield LM, Boorgula MP, Blackwell TW, Brody JA, Broome J, Chami N, Chen MH, Conomos MP, Cox C, Curran JE, Daya M, Ekunwe L, ... ... Cox N, et al. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics. PMID 34582791 DOI: 10.1016/j.ajhg.2021.08.007  0.506
2021 Van Driest SL, Abul-Husn NS, Glessner JT, Bastarache L, Nirenberg S, Schildcrout JS, Eswarappa MS, Belbin GM, Shaffer CM, Mentch F, Connolly J, Shi M, Stein CM, Roden DM, Hakonarson H, ... Cox NJ, et al. Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients. Jama Internal Medicine. PMID 34180972 DOI: 10.1001/jamainternmed.2021.3108  0.362
2021 Zheng NS, Stone CA, Jiang L, Shaffer CM, Kerchberger VE, Chung CP, Feng Q, Cox NJ, Stein CM, Roden DM, Denny JC, Phillips EJ, Wei WQ. High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. Plos Genetics. 17: e1009593. PMID 34061827 DOI: 10.1371/journal.pgen.1009593  0.438
2021 Zheng NS, Stone CA, Jiang L, Shaffer CM, Kerchberger VE, Chung CP, Feng Q, Cox NJ, Stein CM, Roden DM, Denny JC, Phillips EJ, Wei WQ. High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. Plos Genetics. 17: e1009593. PMID 34061827 DOI: 10.1371/journal.pgen.1009593  0.438
2021 Althouse AD, Below JE, Claggett BL, Cox NJ, de Lemos JA, Deo RC, Duval S, Hachamovitch R, Kaul S, Keith SW, Secemsky E, Teixeira-Pinto A, Roger VL. Recommendations for Statistical Reporting in Cardiovascular Medicine: A Special Report From the American Heart Association. Circulation. CIRCULATIONAHA121055. PMID 34032474 DOI: 10.1161/CIRCULATIONAHA.121.055393  0.509
2021 Kawai VK, Shi M, Liu G, Feng Q, Wei W, Chung CP, Walunas TL, Gordon AS, Linneman JG, Hebbring SJ, Harley JB, Cox NJ, Roden DM, Stein CM, Mosley JD. Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis. Lupus. 9612033211014952. PMID 33977795 DOI: 10.1177/09612033211014952  0.38
2021 Kawai VK, Shi M, Liu G, Feng Q, Wei W, Chung CP, Walunas TL, Gordon AS, Linneman JG, Hebbring SJ, Harley JB, Cox NJ, Roden DM, Stein CM, Mosley JD. Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis. Lupus. 9612033211014952. PMID 33977795 DOI: 10.1177/09612033211014952  0.38
2021 Wu P, Nelson SD, Zhao J, Stone CA, Feng Q, Chen Q, Larson EA, Li B, Cox NJ, Stein CM, Phillips EJ, Roden DM, Denny JC, Wei WQ. DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions. Journal of the American Medical Informatics Association : Jamia. PMID 33712848 DOI: 10.1093/jamia/ocab019  0.318
2021 Wu P, Nelson SD, Zhao J, Stone CA, Feng Q, Chen Q, Larson EA, Li B, Cox NJ, Stein CM, Phillips EJ, Roden DM, Denny JC, Wei WQ. DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions. Journal of the American Medical Informatics Association : Jamia. PMID 33712848 DOI: 10.1093/jamia/ocab019  0.318
2020 Chen HH, Shaw DM, Petty LE, Graff M, Bohlender RJ, Polikowsky HG, Zhong X, Kim D, Buchanan VL, Preuss MH, Shuey MM, Loos RJF, Huff CD, Cox NJ, Bastarache JA, et al. Host genetic effects in pneumonia. American Journal of Human Genetics. PMID 33357513 DOI: 10.1016/j.ajhg.2020.12.010  0.584
2020 Zheng NS, Warner JL, Osterman TJ, Wells QS, Shu XO, Deppen SA, Karp SJ, Dwyer S, Feng Q, Cox NJ, Peterson JF, Michael Stein C, Roden DM, Johnson KB, Wei WQ. A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19. Journal of Biomedical Informatics. 103657. PMID 33309899 DOI: 10.1016/j.jbi.2020.103657  0.33
2020 Zheng NS, Warner JL, Osterman TJ, Wells QS, Shu XO, Deppen SA, Karp SJ, Dwyer S, Feng Q, Cox NJ, Peterson JF, Michael Stein C, Roden DM, Johnson KB, Wei WQ. A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19. Journal of Biomedical Informatics. 103657. PMID 33309899 DOI: 10.1016/j.jbi.2020.103657  0.33
2020 Zheng NS, Feng Q, Kerchberger VE, Zhao J, Edwards TL, Cox NJ, Stein CM, Roden DM, Denny JC, Wei WQ. PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records. Journal of the American Medical Informatics Association : Jamia. PMID 32974638 DOI: 10.1093/jamia/ocaa104  0.351
2020 Zheng NS, Feng Q, Kerchberger VE, Zhao J, Edwards TL, Cox NJ, Stein CM, Roden DM, Denny JC, Wei WQ. PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records. Journal of the American Medical Informatics Association : Jamia. PMID 32974638 DOI: 10.1093/jamia/ocaa104  0.351
2020 Walters CE, Nitin R, Margulis K, Boorom O, Gustavson DE, Bush CT, Davis LK, Below JE, Cox NJ, Camarata SM, Gordon RL. Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems. Journal of Speech, Language, and Hearing Research : Jslhr. 1-17. PMID 32791019 DOI: 10.1044/2020_Jslhr-19-00397  0.528
2020 Kawai VK, Shi M, Feng Q, Chung CP, Liu G, Cox NJ, Jarvik GP, Lee MTM, Hebbring SJ, Harley JB, Kaufman KM, Namjou B, Larson E, Gordon AS, Roden DM, et al. Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis - a phenome-wide association study and inverse-variance weighted meta-analysis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 32307929 DOI: 10.1002/Art.41291  0.397
2020 Kawai VK, Shi M, Feng Q, Chung CP, Liu G, Cox NJ, Jarvik GP, Lee MTM, Hebbring SJ, Harley JB, Kaufman KM, Namjou B, Larson E, Gordon AS, Roden DM, et al. Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis - a phenome-wide association study and inverse-variance weighted meta-analysis. Arthritis & Rheumatology (Hoboken, N.J.). PMID 32307929 DOI: 10.1002/Art.41291  0.397
2019 Flannick J, Mercader JM, Fuchsberger C, Udler MS, Mahajan A, Wessel J, Teslovich TM, Caulkins L, Koesterer R, Barajas-Olmos F, Blackwell TW, Boerwinkle E, Brody JA, Centeno-Cruz F, Chen L, ... ... Cox NJ, et al. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature. PMID 31118516 DOI: 10.1038/s41586-019-1231-2  0.324
2019 Flannick J, Mercader JM, Fuchsberger C, Udler MS, Mahajan A, Wessel J, Teslovich TM, Caulkins L, Koesterer R, Barajas-Olmos F, Blackwell TW, Boerwinkle E, Brody JA, Centeno-Cruz F, Chen L, ... ... Cox NJ, et al. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature. PMID 31118516 DOI: 10.1038/s41586-019-1231-2  0.324
2019 Unlu G, Gamazon ER, Qi X, Levic DS, Bastarache L, Denny JC, Roden DM, Mayzus I, Breyer M, Zhong X, Konkashbaev AI, Rzhetsky A, Knapik EW, Cox NJ. GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish. American Journal of Human Genetics. PMID 30827500 DOI: 10.1016/J.Ajhg.2019.01.017  0.392
2019 Unlu G, Gamazon ER, Qi X, Levic DS, Bastarache L, Denny JC, Roden DM, Mayzus I, Breyer M, Zhong X, Konkashbaev AI, Rzhetsky A, Knapik EW, Cox NJ. GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish. American Journal of Human Genetics. PMID 30827500 DOI: 10.1016/J.Ajhg.2019.01.017  0.392
2018 Feng Q, Wei WQ, Chung CP, Levinson RT, Sundermann AC, Mosley JD, Bastarache L, Ferguson JF, Cox NJ, Roden DM, Denny JC, Linton MF, Edwards DRV, Stein CM. Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records. Plos Medicine. 15: e1002642. PMID 30153257 DOI: 10.1371/Journal.Pmed.1002642  0.394
2018 Feng Q, Wei WQ, Chung CP, Levinson RT, Sundermann AC, Mosley JD, Bastarache L, Ferguson JF, Cox NJ, Roden DM, Denny JC, Linton MF, Edwards DRV, Stein CM. Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records. Plos Medicine. 15: e1002642. PMID 30153257 DOI: 10.1371/Journal.Pmed.1002642  0.394
2018 Wei WQ, Li X, Feng Q, Kubo M, Kullo IJ, Peissig PL, Karlson EW, Jarvik GP, Lee MTM, Shang N, Larson EA, Edwards T, Shaffer C, Mosley JD, Maeda S, ... ... Cox NJ, et al. Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. PMID 29703846 DOI: 10.1161/Circulationaha.117.031356  0.428
2018 Wei WQ, Li X, Feng Q, Kubo M, Kullo IJ, Peissig PL, Karlson EW, Jarvik GP, Lee MTM, Shang N, Larson EA, Edwards T, Shaffer C, Mosley JD, Maeda S, ... ... Cox NJ, et al. Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. PMID 29703846 DOI: 10.1161/Circulationaha.117.031356  0.428
2018 Cox NJ, Below JE. Critical Evaluation of Data Requires Rigorous but Broadly Based Statistical Inference. Circulation Research. 122: 1049-1051. PMID 29650629 DOI: 10.1161/CIRCRESAHA.118.312530  0.492
2018 Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, ... ... Cox NJ, et al. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science (New York, N.Y.). 359: 1233-1239. PMID 29590070 DOI: 10.1126/Science.Aal4043  0.465
2018 Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, ... ... Cox NJ, et al. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science (New York, N.Y.). 359: 1233-1239. PMID 29590070 DOI: 10.1126/Science.Aal4043  0.465
2018 Flannick J, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Cox NJ, et al. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 5: 180002. PMID 29360107 DOI: 10.1038/sdata.2018.2  0.557
2017 Jun G, Manning A, Almeida M, Zawistowski M, Wood AR, Teslovich TM, Fuchsberger C, Feng S, Cingolani P, Gaulton KJ, Dyer T, Blackwell TW, Chen H, Chines PS, Choi S, ... ... Cox NJ, et al. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America. PMID 29279374 DOI: 10.1073/Pnas.1705859115  0.633
2017 Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Cox NJ, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179  0.602
2017 Wei WQ, Bastarache LA, Carroll RJ, Marlo JE, Osterman TJ, Gamazon ER, Cox NJ, Roden DM, Denny JC. Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record. Plos One. 12: e0175508. PMID 28686612 DOI: 10.1371/Journal.Pone.0175508  0.373
2017 Wei WQ, Bastarache LA, Carroll RJ, Marlo JE, Osterman TJ, Gamazon ER, Cox NJ, Roden DM, Denny JC. Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record. Plos One. 12: e0175508. PMID 28686612 DOI: 10.1371/Journal.Pone.0175508  0.373
2017 Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Cox NJ, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329  0.593
2017 Manolio TA, Fowler DM, Starita LM, Haendel MA, MacArthur DG, Biesecker LG, Worthey E, Chisholm RL, Green ED, Jacob HJ, McLeod HL, Roden D, Rodriguez LL, Williams MS, Cooper GM, ... Cox NJ, et al. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 169: 6-12. PMID 28340351 DOI: 10.1016/J.Cell.2017.03.005  0.448
2017 Manolio TA, Fowler DM, Starita LM, Haendel MA, MacArthur DG, Biesecker LG, Worthey E, Chisholm RL, Green ED, Jacob HJ, McLeod HL, Roden D, Rodriguez LL, Williams MS, Cooper GM, ... Cox NJ, et al. Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research. Cell. 169: 6-12. PMID 28340351 DOI: 10.1016/J.Cell.2017.03.005  0.448
2017 Parra EJ, Mazurek A, Gignoux CR, Sockell A, Agostino M, Morris AP, Petty LE, Hanis CL, Cox NJ, Valladares-Salgado A, Below JE, Cruz M. Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal. Plos One. 12: e0172880. PMID 28245265 DOI: 10.1371/Journal.Pone.0172880  0.58
2016 Shekhar A, Lin X, Liu FY, Zhang J, Mo H, Bastarache L, Denny JC, Cox NJ, Delmar M, Roden DM, Fishman GI, Park DS. Transcription factor ETV1 is essential for rapid conduction in the heart. The Journal of Clinical Investigation. PMID 27775552 DOI: 10.1172/Jci87968  0.343
2016 Shekhar A, Lin X, Liu FY, Zhang J, Mo H, Bastarache L, Denny JC, Cox NJ, Delmar M, Roden DM, Fishman GI, Park DS. Transcription factor ETV1 is essential for rapid conduction in the heart. The Journal of Clinical Investigation. PMID 27775552 DOI: 10.1172/Jci87968  0.343
2016 Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Cox NJ, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642  0.628
2016 Hanis CL, Redline S, Cade BE, Bell GI, Cox NJ, Below JE, Brown EL, Aguilar D. Beyond type 2 diabetes, obesity and hypertension: an axis including sleep apnea, left ventricular hypertrophy, endothelial dysfunction, and aortic stiffness among Mexican Americans in Starr County, Texas. Cardiovascular Diabetology. 15: 86. PMID 27266869 DOI: 10.1186/S12933-016-0405-6  0.533
2016 Horikoshi M, Pasquali L, Wiltshire S, Huyghe JR, Mahajan A, Asimit JL, Ferreira T, Locke AE, Robertson NR, Wang X, Sim X, Fujita H, Hara K, Young R, Zhang W, ... ... Cox NJ, et al. Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. Human Molecular Genetics. PMID 26911676 DOI: 10.1093/Hmg/Ddw048  0.626
2016 Chhibber A, French CE, Yee SW, Gamazon ER, Theusch E, Qin X, Webb A, Papp AC, Wang A, Simmons CQ, Konkashbaev A, Chaudhry AS, Mitchel K, Stryke D, Ferrin TE, ... ... Cox NJ, et al. Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines. The Pharmacogenomics Journal. PMID 26856248 DOI: 10.1038/Tpj.2015.93  0.4
2016 Below JE, Parra EJ, Gamazon ER, Torres J, Krithika S, Candille S, Lu Y, Manichakul A, Peralta-Romero J, Duan Q, Li Y, Morris AP, Gottesman O, Bottinger E, Wang XQ, ... ... Cox NJ, et al. Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Scientific Reports. 6: 19429. PMID 26780889 DOI: 10.1038/Srep19429  0.569
2015 Zhang W, Gamazon ER, Zhang X, Konkashbaev A, Liu C, Szilágyi KL, Dolan ME, Cox NJ. SCAN database: facilitating integrative analyses of cytosine modification and expression QTL. Database : the Journal of Biological Databases and Curation. 2015. PMID 25818895 DOI: 10.1093/database/bav025  0.311
2015 Zhang W, Gamazon ER, Zhang X, Konkashbaev A, Liu C, Szilágyi KL, Dolan ME, Cox NJ. SCAN database: facilitating integrative analyses of cytosine modification and expression QTL. Database : the Journal of Biological Databases and Curation. 2015. PMID 25818895 DOI: 10.1093/database/bav025  0.311
2015 Mahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N, Im HK, Cingolani P, Flannick J, Fontanillas P, Fuchsberger C, Gaulton KJ, Teslovich TM, ... ... Cox NJ, et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Plos Genetics. 11: e1004876. PMID 25625282 DOI: 10.1371/Journal.Pgen.1004876  0.326
2015 Mahajan A, Sim X, Ng HJ, Manning A, Rivas MA, Highland HM, Locke AE, Grarup N, Im HK, Cingolani P, Flannick J, Fontanillas P, Fuchsberger C, Gaulton KJ, Teslovich TM, ... ... Cox NJ, et al. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Plos Genetics. 11: e1004876. PMID 25625282 DOI: 10.1371/Journal.Pgen.1004876  0.326
2015 Palmer ND, Goodarzi MO, Langefeld CD, Wang N, Guo X, Taylor KD, Fingerlin TE, Norris JM, Buchanan TA, Xiang AH, Haritunians T, Ziegler JT, Williams AH, Stefanovski D, Cui J, ... ... Cox NJ, et al. Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium. Diabetes. 64: 1853-66. PMID 25524916 DOI: 10.2337/Db14-0732  0.603
2014 Torres JM, Gamazon ER, Parra EJ, Below JE, Valladares-Salgado A, Wacher N, Cruz M, Hanis CL, Cox NJ. Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait. American Journal of Human Genetics. 95: 521-34. PMID 25439722 DOI: 10.1016/J.Ajhg.2014.10.001  0.59
2014 Mahajan A, Go MJ, Zhang W, Below JE, Gaulton KJ, Ferreira T, Horikoshi M, Johnson AD, Ng MC, Prokopenko I, ... ... Cox NJ, et al. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics. 46: 234-44. PMID 24509480 DOI: 10.1038/Ng.2897  0.651
2013 Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... Cox NJ, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864  0.304
2013 Gamazon ER, Huang RS, Cox NJ. SCAN: a systems biology approach to pharmacogenomic discovery. Methods in Molecular Biology (Clifton, N.J.). 1015: 213-24. PMID 23824859 DOI: 10.1007/978-1-62703-435-7_14  0.311
2013 Perera MA, Cavallari LH, Limdi NA, Gamazon ER, Konkashbaev A, Daneshjou R, Pluzhnikov A, Crawford DC, Wang J, Liu N, Tatonetti N, Bourgeois S, Takahashi H, Bradford Y, Burkley BM, ... ... Cox NJ, et al. Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study. Lancet. 382: 790-6. PMID 23755828 DOI: 10.1016/S0140-6736(13)60681-9  0.418
2013 Motsinger-Reif AA, Jorgenson E, Relling MV, Kroetz DL, Weinshilboum R, Cox NJ, Roden DM. Genome-wide association studies in pharmacogenomics: successes and lessons. Pharmacogenetics and Genomics. 23: 383-94. PMID 20639796 DOI: 10.1097/Fpc.0B013E32833D7B45  0.441
2012 Gamazon ER, Huang RS, Dolan ME, Cox NJ, Im HK. Integrative genomics: quantifying significance of phenotype-genotype relationships from multiple sources of high-throughput data. Frontiers in Genetics. 3: 202. PMID 23755062 DOI: 10.3389/fgene.2012.00202  0.301
2012 Guan W, Boehnke M, Pluzhnikov A, Cox NJ, Scott LJ. Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes. Genetic Epidemiology. 36: 820-8. PMID 22865662 DOI: 10.1002/Gepi.21668  0.366
2012 Grassi MA, Tikhomirov A, Ramalingam S, Lee KE, Hosseini SM, Klein BE, Klein R, Lussier YA, Cox NJ, Nicolae DL. Replication analysis for severe diabetic retinopathy. Investigative Ophthalmology & Visual Science. 53: 2377-81. PMID 22427569 DOI: 10.1167/Iovs.11-8068  0.306
2011 Testa JR, Cheung M, Pei J, Below JE, Tan Y, Sementino E, Cox NJ, Dogan AU, Pass HI, Trusa S, Hesdorffer M, Nasu M, Powers A, Rivera Z, Comertpay S, et al. Germline BAP1 mutations predispose to malignant mesothelioma. Nature Genetics. 43: 1022-5. PMID 21874000 DOI: 10.1038/Ng.912  0.52
2011 Wheeler HE, Gorsic LK, Welsh M, Stark AL, Gamazon ER, Cox NJ, Dolan ME. Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans. Plos One. 6: e21920. PMID 21755009 DOI: 10.1371/journal.pone.0021920  0.301
2011 Below JE, Gamazon ER, Morrison JV, Konkashbaev A, Pluzhnikov A, McKeigue PM, Parra EJ, Elbein SC, Hallman DM, Nicolae DL, Bell GI, Cruz M, Cox NJ, Hanis CL. Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Diabetologia. 54: 2047-55. PMID 21647700 DOI: 10.1007/S00125-011-2188-3  0.628
2011 Innocenti F, Cooper GM, Stanaway IB, Gamazon ER, Smith JD, Mirkov S, Ramirez J, Liu W, Lin YS, Moloney C, Aldred SF, Trinklein ND, Schuetz E, Nickerson DA, Thummel KE, ... ... Cox NJ, et al. Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue. Plos Genetics. 7: e1002078. PMID 21637794 DOI: 10.1371/Journal.Pgen.1002078  0.501
2011 Parra EJ, Below JE, Krithika S, Valladares A, Barta JL, Cox NJ, Hanis CL, Wacher N, Garcia-Mena J, Hu P, Shriver MD, Kumate J, McKeigue PM, Escobedo J, Cruz M. Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas Diabetologia. 54: 2038-2046. PMID 21573907 DOI: 10.1007/S00125-011-2172-Y  0.624
2011 Below JE, Cox NJ, Fukagawa NK, Hirvonen A, Testa JR. Factors that impact susceptibility to fiber-induced health effects. Journal of Toxicology and Environmental Health. Part B, Critical Reviews. 14: 246-66. PMID 21534090 DOI: 10.1080/10937404.2011.556052  0.534
2011 Grassi MA, Tikhomirov A, Ramalingam S, Below JE, Cox NJ, Nicolae DL. Genome-wide meta-analysis for severe diabetic retinopathy. Human Molecular Genetics. 20: 2472-81. PMID 21441570 DOI: 10.1093/hmg/ddr121  0.612
2011 Gamazon ER, Nicolae DL, Cox NJ. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci. Plos Genetics. 7: e1001292. PMID 21304891 DOI: 10.1371/journal.pgen.1001292  0.303
2011 Xicola RM, Below J, Doyle BJ, Garre P, Zhang W, Caldes T, Cox NJ, Llor X. Identification of a Chromosome 10 Region Potentially Implicated in Hereditary Non-Polyposis Colorectal Cancer Without Mismatch Repair Mutations Gastroenterology. 140. DOI: 10.1016/S0016-5085(11)60395-8  0.493
2010 Fajans SS, Bell GI, Paz VP, Below JE, Cox NJ, Martin C, Thomas IH, Chen M. Obesity and hyperinsulinemia in a family with pancreatic agenesis and MODY caused by the IPF1 mutation Pro63fsX60. Translational Research : the Journal of Laboratory and Clinical Medicine. 156: 7-14. PMID 20621032 DOI: 10.1016/J.Trsl.2010.03.003  0.559
2010 Pluzhnikov A, Below JE, Konkashbaev A, Tikhomirov A, Kistner-Griffin E, Roe CA, Nicolae DL, Cox NJ. Spoiling the whole bunch: quality control aimed at preserving the integrity of high-throughput genotyping. American Journal of Human Genetics. 87: 123-8. PMID 20598280 DOI: 10.1016/j.ajhg.2010.06.005  0.58
2010 Paterson AD, Waggott D, Boright AP, Hosseini SM, Shen E, Sylvestre MP, Wong I, Bharaj B, Cleary PA, Lachin JM, Below JE, Nicolae D, Cox NJ, Canty AJ, et al. A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Diabetes. 59: 539-49. PMID 19875614 DOI: 10.2337/Db09-0653  0.599
2009 Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, et al. Finding the missing heritability of complex diseases. Nature. 461: 747-53. PMID 19812666 DOI: 10.1038/Nature08494  0.303
2008 Kupfer S, Anderson JR, Below JE, Kittles R, Cox N, Ellis NA. T2051 Genetic Analysis of Base Excision Repair Genes in African-Americans and Caucasians with Colorectal Cancer Gastroenterology. 134: A-608-A-609. DOI: 10.1016/S0016-5085(08)62841-3  0.534
2007 Støy J, Edghill EL, Flanagan SE, Ye H, Paz VP, Pluzhnikov A, Below JE, Hayes MG, Cox NJ, Lipkind GM, Lipton RB, Greeley SA, Patch AM, Ellard S, Steiner DF, et al. Insulin gene mutations as a cause of permanent neonatal diabetes. Proceedings of the National Academy of Sciences of the United States of America. 104: 15040-4. PMID 17855560 DOI: 10.1073/Pnas.0707291104  0.542
2007 Hayes MG, Pluzhnikov A, Miyake K, Sun Y, Ng MC, Roe CA, Below JE, Nicolae RI, Konkashbaev A, Bell GI, Cox NJ, Hanis CL. Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. Diabetes. 56: 3033-44. PMID 17846124 DOI: 10.2337/Db07-0482  0.593
2005 Permutt MA, Wasson J, Cox N. Genetic epidemiology of diabetes. The Journal of Clinical Investigation. 115: 1431-9. PMID 15931378 DOI: 10.1172/JCI24758  0.313
2003 Cox NJ. Calpain 10 and genetics of type 2 diabetes. Current Diabetes Reports. 2: 186-90. PMID 12643138 DOI: 10.1007/S11892-002-0079-1  0.312
2002 Haddad L, Evans JC, Gharani N, Robertson C, Rush K, Wiltshire S, Frayling TM, Wilkin TJ, Demaine A, Millward A, Hattersley AT, Conway G, Cox NJ, Bell GI, Franks S, et al. Variation within the type 2 diabetes susceptibility gene calpain-10 and polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 2606-10. PMID 12050223 DOI: 10.1210/Jcem.87.6.8608  0.321
2002 Ehrmann DA, Schwarz PE, Hara M, Tang X, Horikawa Y, Imperial J, Bell GI, Cox NJ. Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 1669-73. PMID 11932299 DOI: 10.1210/Jcem.87.4.8385  0.301
2002 Fullerton SM, Bartoszewicz A, Ybazeta G, Horikawa Y, Bell GI, Kidd KK, Cox NJ, Hudson RR, Di Rienzo A. Geographic and haplotype structure of candidate type 2 diabetes susceptibility variants at the calpain-10 locus. American Journal of Human Genetics. 70: 1096-106. PMID 11891618 DOI: 10.1086/339930  0.31
2002 Cox NJ. Challenges in identifying genetic variation affecting susceptibility to type 2 diabetes: examples from studies of the calpain-10 gene. Human Molecular Genetics. 10: 2301-5. PMID 11673414 DOI: 10.1093/HMG/10.20.2301  0.305
2001 Evans JC, Frayling TM, Cassell PG, Saker PJ, Hitman GA, Walker M, Levy JC, O'Rahilly S, Rao PV, Bennett AJ, Jones EC, Menzel S, Prestwich P, Simecek N, Wishart M, ... ... Cox NJ, et al. Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. American Journal of Human Genetics. 69: 544-52. PMID 11481585 DOI: 10.1086/323315  0.301
1998 Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nature Genetics. 19: 292-6. PMID 9662408 DOI: 10.1038/985  0.302
1989 Cox NJ, Bell GI. Disease associations. Chance, artifact, or susceptibility genes? Diabetes. 38: 947-950. PMID 2568956 DOI: 10.2337/Diab.38.8.947  0.305
Low-probability matches (unlikely to be authored by this person)
2012 Chen LS, Hsu L, Gamazon ER, Cox NJ, Nicolae DL. An exponential combination procedure for set-based association tests in sequencing studies. American Journal of Human Genetics. 91: 977-86. PMID 23159251 DOI: 10.1016/j.ajhg.2012.09.017  0.299
2004 Cox NJ, Hayes MG, Roe CA, Tsuchiya T, Bell GI. Linkage of calpain 10 to type 2 diabetes: the biological rationale. Diabetes. 53: S19-25. PMID 14749261 DOI: 10.2337/Diabetes.53.2007.S19  0.298
2022 Zhou W, Kanai M, Wu KH, Rasheed H, Tsuo K, Hirbo JB, Wang Y, Bhattacharya A, Zhao H, Namba S, Surakka I, Wolford BN, Lo Faro V, Lopera-Maya EA, Läll K, ... ... Cox NJ, et al. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192. PMID 36777996 DOI: 10.1016/j.xgen.2022.100192  0.297
2023 Allaire P, He J, Mayer J, Moat L, Gerstenberger P, Wilhorn R, Strutz S, Kim DSL, Zeng C, Cox N, Shay JW, Denny J, Bastarache L, Hebbring S. Genetic and clinical determinants of telomere length. Hgg Advances. 4: 100201. PMID 37216007 DOI: 10.1016/j.xhgg.2023.100201  0.296
2013 Torres JM, Cox NJ, Philipson LH. Genome wide association studies for diabetes: perspective on results and challenges. Pediatric Diabetes. 14: 90-6. PMID 23350725 DOI: 10.1111/Pedi.12015  0.295
2021 Sun Q, Graff M, Rowland B, Wen J, Huang L, Miller-Fleming TW, Haessler J, Preuss MH, Chai JF, Lee MP, Avery CL, Cheng CY, Franceschini N, Sim X, Cox NJ, et al. Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Journal of Human Genetics. PMID 34376796 DOI: 10.1038/s10038-021-00968-0  0.295
2005 Iwasaki N, Horikawa Y, Tsuchiya T, Kitamura Y, Nakamura T, Tanizawa Y, Oka Y, Hara K, Kadowaki T, Awata T, Honda M, Yamashita K, Oda N, Yu L, Yamada N, ... ... Cox NJ, et al. Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population Journal of Human Genetics. 50: 92-98. PMID 15696376 DOI: 10.1007/S10038-004-0225-5  0.294
2015 Chen R, Wei Q, Zhan X, Zhong X, Sutcliffe JS, Cox NJ, Cook EH, Li C, Chen W, Li B. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis. Bioinformatics (Oxford, England). 31: 1452-9. PMID 25568282 DOI: 10.1093/Bioinformatics/Btu860  0.294
2015 Chen R, Wei Q, Zhan X, Zhong X, Sutcliffe JS, Cox NJ, Cook EH, Li C, Chen W, Li B. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis. Bioinformatics (Oxford, England). 31: 1452-9. PMID 25568282 DOI: 10.1093/Bioinformatics/Btu860  0.294
2017 Im HK, Barbeira A, Zheng J, Torres J, Dickinson S, Wheeler H, Bell G, Nicolae D, Cox N. Generating A Database of Phenotypic Consequences of Gene Regulation Across 40 Human Tissues European Neuropsychopharmacology. 27. DOI: 10.1016/J.Euroneuro.2016.09.466  0.293
2007 Bourgain C, Génin E, Cox N, Clerget-Darpoux F. Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases? European Journal of Human Genetics : Ejhg. 15: 260-3. PMID 17164797 DOI: 10.1038/sj.ejhg.5201753  0.292
1996 Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shephard JM, Williams SR, Risch N, Hinds D, Iwasaki N, ... ... Cox NJ, et al. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 Nature Genetics. 13: 161-166. PMID 8640221 DOI: 10.1038/Ng0696-161  0.29
2015 Gamazon ER, Wheeler HE, Shah KP, Mozaffari SV, Aquino-Michaels K, Carroll RJ, Eyler AE, Denny JC, Nicolae DL, Cox NJ, Im HK. A gene-based association method for mapping traits using reference transcriptome data. Nature Genetics. 47: 1091-8. PMID 26258848 DOI: 10.1038/Ng.3367  0.29
2015 Gamazon ER, Wheeler HE, Shah KP, Mozaffari SV, Aquino-Michaels K, Carroll RJ, Eyler AE, Denny JC, Nicolae DL, Cox NJ, Im HK. A gene-based association method for mapping traits using reference transcriptome data. Nature Genetics. 47: 1091-8. PMID 26258848 DOI: 10.1038/Ng.3367  0.29
2012 Mechanic LE, Chen HS, Amos CI, Chatterjee N, Cox NJ, Divi RL, Fan R, Harris EL, Jacobs K, Kraft P, Leal SM, McAllister K, Moore JH, Paltoo DN, Province MA, et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genetic Epidemiology. 36: 22-35. PMID 22147673 DOI: 10.1002/Gepi.20652  0.289
2024 Jiang L, Gangireddy S, Dickson AL, Kawai V, Cox NJ, Linton MF, Wei WQ, Stein CM, Feng Q. Characterizing genetic profiles for high triglyceride levels in U.S. patients of African ancestry. Medrxiv : the Preprint Server For Health Sciences. PMID 38559137 DOI: 10.1101/2024.03.11.24304107  0.289
2010 Fu YP, Hallman DM, Gonzalez VH, Klein BE, Klein R, Hayes MG, Cox NJ, Bell GI, Hanis CL. Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas. Journal of Ophthalmology. 2010. PMID 20871662 DOI: 10.1155/2010/861291  0.287
2010 Nicolae DL, Gamazon E, Zhang W, Duan S, Dolan ME, Cox NJ. Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS. Plos Genetics. 6: e1000888. PMID 20369019 DOI: 10.1371/journal.pgen.1000888  0.287
2013 Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Cox NJ, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69  0.287
2012 Lee Y, Gamazon ER, Rebman E, Lee Y, Lee S, Dolan ME, Cox NJ, Lussier YA. Variants affecting exon skipping contribute to complex traits. Plos Genetics. 8: e1002998. PMID 23133393 DOI: 10.1371/Journal.Pgen.1002998  0.286
2023 Davis A, Dickson AL, Daniel LL, Nepal P, Zanussi J, Miller-Fleming TW, Straub PS, Wei WQ, Liu G, Cox NJ, Hung AM, Feng Q, Stein CM, Chung CP. Association Between Genetically Predicted Expression of TPMT and Azathioprine Adverse Events. Research Square. PMID 36711487 DOI: 10.21203/rs.3.rs-2444787/v1  0.286
2017 Dolan ME, El Charif O, Wheeler HE, Gamazon ER, Ardeshir-Rouhani-Fard S, Monahan P, Feldman DR, Hamilton R, Vaughn DJ, Beard C, Fung C, Fossa SD, Hertz DL, Mushiroda T, Kubo M, ... ... Cox N, et al. Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 28611204 DOI: 10.1158/1078-0432.CCR-16-3224  0.285
2004 del Bosque-Plata L, Aguilar-Salinas CA, Tusié-Luna MT, Ramírez-Jiménez S, Rodríguez-Torres M, Aurón-Gómez M, Ramírez E, Velasco-Pérez ML, Ramírez-Silva A, Gómez-Pérez F, Hanis CL, Tsuchiya T, Yoshiuchi I, Cox NJ, Bell GI. Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population. Molecular Genetics and Metabolism. 81: 122-6. PMID 14741193 DOI: 10.1016/J.Ymgme.2003.10.005  0.283
2020 Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nature Medicine. 26: 98-109. PMID 31932796 DOI: 10.1038/S41591-019-0705-Y  0.283
2020 Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nature Medicine. 26: 98-109. PMID 31932796 DOI: 10.1038/S41591-019-0705-Y  0.283
1999 Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans Nature Genetics. 21: 213-215. PMID 9988276 DOI: 10.1038/6002  0.282
2000 Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PEH, Del Bosque-Plata L, Oda Y, Yoshiuchi I, Colilla S, Polonsky KS, et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus Nature Genetics. 26: 163-175. PMID 11017071 DOI: 10.1038/79876  0.279
2005 Clark VJ, Cox NJ, Hammond M, Hanis CL, Di Rienzo A. Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene. Human Genetics. 117: 258-66. PMID 15906097 DOI: 10.1007/S00439-005-1305-0  0.279
2009 Gamazon ER, Zhang W, Huang RS, Dolan ME, Cox NJ. A pharmacogene database enhanced by the 1000 Genomes Project. Pharmacogenetics and Genomics. 19: 829-32. PMID 19745786 DOI: 10.1097/FPC.0b013e3283317bac  0.279
2012 Davis LK, Gamazon ER, Kistner-Griffin E, Badner JA, Liu C, Cook EH, Sutcliffe JS, Cox NJ. Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci. Molecular Autism. 3: 3. PMID 22591576 DOI: 10.1186/2040-2392-3-3  0.278
2010 Gamazon ER, Huang RS, Cox NJ, Dolan ME. Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci. Proceedings of the National Academy of Sciences of the United States of America. 107: 9287-92. PMID 20442332 DOI: 10.1073/pnas.1001827107  0.278
2006 Yokoi N, Kanamori M, Horikawa Y, Takeda J, Sanke T, Furuta H, Nanjo K, Mori H, Kasuga M, Hara K, Kadowaki T, Tanizawa Y, Oka Y, Iwami Y, Ohgawara H, ... ... Cox NJ, et al. Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects. Diabetes. 55: 2379-86. PMID 16873704 DOI: 10.2337/db05-1203  0.278
2018 Zhao J, Cheng F, Jia P, Cox N, Denny JC, Zhao Z. An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies. Genome Medicine. 10: 7. PMID 29378629 DOI: 10.1186/S13073-018-0513-X  0.277
2017 Gamazon ER, Konkashbaev A, Derks EM, Cox NJ, Lee Y. Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping. Scientific Reports. 7: 5980. PMID 28729732 DOI: 10.1038/s41598-017-05744-9  0.276
2017 Gamazon ER, Konkashbaev A, Derks EM, Cox NJ, Lee Y. Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping. Scientific Reports. 7: 5980. PMID 28729732 DOI: 10.1038/s41598-017-05744-9  0.276
2018 Barbeira AN, Dickinson SP, Bonazzola R, Zheng J, Wheeler HE, Torres JM, Torstenson ES, Shah KP, Garcia T, Edwards TL, Stahl EA, Huckins LM, Nicolae DL, Cox NJ, et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nature Communications. 9: 1825. PMID 29739930 DOI: 10.1038/S41467-018-03621-1  0.274
2018 Barbeira AN, Dickinson SP, Bonazzola R, Zheng J, Wheeler HE, Torres JM, Torstenson ES, Shah KP, Garcia T, Edwards TL, Stahl EA, Huckins LM, Nicolae DL, Cox NJ, et al. Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. Nature Communications. 9: 1825. PMID 29739930 DOI: 10.1038/S41467-018-03621-1  0.274
2012 Pinto NR, Gamazon ER, Konkashbaev A, Im HK, Diskin S, London WB, Maris JM, Dolan ME, Cox NJ, Cohn SL. Relationship of divergent ancestral genetic variation on chromosome 6p22 and racial disparities in survival in neuroblastoma. Journal of Clinical Oncology. 30: 9516-9516. DOI: 10.1200/Jco.2012.30.15_Suppl.9516  0.271
2007 Huang RS, Duan S, Bleibel WK, Kistner EO, Zhang W, Clark TA, Chen TX, Schweitzer AC, Blume JE, Cox NJ, Dolan ME. A genome-wide approach to identify genetic variants that contribute to etoposide-induced cytotoxicity. Proceedings of the National Academy of Sciences of the United States of America. 104: 9758-63. PMID 17537913 DOI: 10.1073/Pnas.0703736104  0.271
2008 Estivill X, Cox NJ, Chanock SJ, Kwok PY, Scherer SW, Brookes AJ. SNPs meet CNVs in genome-wide association studies: HGV2007 meeting report Plos Genetics. 4. PMID 18437244 DOI: 10.1371/Journal.Pgen.1000068  0.27
2012 Elbein SC, Gamazon ER, Das SK, Rasouli N, Kern PA, Cox NJ. Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture? American Journal of Human Genetics. 91: 466-77. PMID 22958899 DOI: 10.1016/j.ajhg.2012.08.002  0.269
2010 Lee Y, Li J, Gamazon E, Chen JL, Tikhomirov A, Cox NJ, Lussier YA. Biomolecular Systems of Disease Buried Across Multiple GWAS Unveiled by Information Theory and Ontology. Amia Joint Summits On Translational Science Proceedings Amia Summit On Translational Science. 2010: 31-5. PMID 21347143  0.268
2012 Im HK, Gamazon ER, Nicolae DL, Cox NJ. On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy. American Journal of Human Genetics. 90: 591-8. PMID 22463877 DOI: 10.1016/j.ajhg.2012.02.008  0.268
2012 Scharf J, Yu D, Mathews C, Neale B, Stewart E, Fagerness J, Evans P, Gamazon E, Service S, Osiecki L, Illmann C, Cath D, King R, Dion Y, Sandor P, ... ... COX N, et al. Genome-Wide Association Study of Gilles de la Tourette Syndrome (IN10-1.002) Neurology. 78: IN10-1.002-IN10-1.00. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In10-1.002  0.268
2013 Lee SM, Karrison TG, Cox NJ, Im HK. Quantitative allelic test--a fast test for very large association studies. Genetic Epidemiology. 37: 831-9. PMID 24185610 DOI: 10.1002/gepi.21768  0.268
2017 Hulur I, Skol AD, Gamazon ER, Cox NJ, Onel K. Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. Plos One. 12: e0185730. PMID 28973033 DOI: 10.1371/Journal.Pone.0185730  0.268
2017 Hulur I, Skol AD, Gamazon ER, Cox NJ, Onel K. Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma. Plos One. 12: e0185730. PMID 28973033 DOI: 10.1371/Journal.Pone.0185730  0.268
2014 Pinto N, Gamazon ER, Antao N, Myers J, Stark AL, Konkashbaev A, Im HK, Diskin SJ, London WB, Ludeman SM, Maris JM, Cox NJ, Cohn SL, Dolan ME. Integrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patients. Clinical Pharmacology and Therapeutics. 95: 644-52. PMID 24549002 DOI: 10.1038/Clpt.2014.37  0.267
2011 Innocenti F, Cox NJ, Dolan ME. The use of genomic information to optimize cancer chemotherapy. Seminars in Oncology. 38: 186-95. PMID 21421109 DOI: 10.1053/j.seminoncol.2011.01.005  0.266
2019 Morley T, Bastarache L, Cox N, Ruderfer D. 11 Leveraging Phenotype Data To Identify Potential Carriers Of Deleterious Genetic Variants European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.152  0.266
2017 Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, ... ... Cox NJ, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010  0.265
2017 Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, ... ... Cox NJ, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010  0.265
2012 Torgerson DG, Capurso D, Ampleford EJ, Li X, Moore WC, Gignoux CR, Hu D, Eng C, Mathias RA, Busse WW, Castro M, Erzurum SC, Fitzpatrick AM, Gaston B, Israel E, ... ... Cox NJ, et al. Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects. The Journal of Allergy and Clinical Immunology. 130: 622-629.e9. PMID 22607992 DOI: 10.1016/J.Jaci.2012.03.045  0.265
2012 Yang JJ, Cheng C, Devidas M, Cao X, Campana D, Yang W, Fan Y, Neale G, Cox N, Scheet P, Borowitz MJ, Winick NJ, Martin PL, Bowman WP, Camitta B, et al. Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. Blood. 120: 4197-204. PMID 23007406 DOI: 10.1182/Blood-2012-07-440107  0.264
2005 Hayes MG, del Bosque-Plata L, Tsuchiya T, Hanis CL, Bell GI, Cox NJ. Patterns of linkage disequilibrium in the type 2 diabetes gene calpain-10. Diabetes. 54: 3573-6. PMID 16306378 DOI: 10.2337/Diabetes.54.12.3573  0.263
2021 Martucci VL, Richmond B, Davis LK, Blackwell TS, Cox NJ, Samuels D, Edwards DV, Aldrich MC. Fate or coincidence: Do COPD and major depression share genetic risk factors? Human Molecular Genetics. PMID 33704461 DOI: 10.1093/hmg/ddab068  0.263
2021 Martucci VL, Richmond B, Davis LK, Blackwell TS, Cox NJ, Samuels D, Edwards DV, Aldrich MC. Fate or coincidence: Do COPD and major depression share genetic risk factors? Human Molecular Genetics. PMID 33704461 DOI: 10.1093/hmg/ddab068  0.263
2008 Guan W, Pluzhnikov A, Cox NJ, Boehnke M. Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium. Human Heredity. 66: 35-49. PMID 18223311 DOI: 10.1159/000114164  0.263
2018 Gamazon ER, Segrè AV, van de Bunt M, Wen X, Xi HS, Hormozdiari F, Ongen H, Konkashbaev A, Derks EM, Aguet F, Quan J, Nicolae DL, Eskin E, Kellis M, ... ... Cox NJ, et al. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nature Genetics. PMID 29955180 DOI: 10.1038/S41588-018-0154-4  0.262
2018 Gamazon ER, Segrè AV, van de Bunt M, Wen X, Xi HS, Hormozdiari F, Ongen H, Konkashbaev A, Derks EM, Aguet F, Quan J, Nicolae DL, Eskin E, Kellis M, ... ... Cox NJ, et al. Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation. Nature Genetics. PMID 29955180 DOI: 10.1038/S41588-018-0154-4  0.262
2008 Onel K, Knight JA, Skol AD, Tennant TR, Banerjee M, Walgren R, Shao J, Allan JM, Beau MML, Larson RA, Graubert T, Cox NJ. A Genome-Wide Analysis to Identify Novel Susceptibility Loci for Therapy-Related Acute Myeloid Leukemia Blood. 112: 432-432. DOI: 10.1182/Blood.V112.11.432.432  0.262
1989 Cox NJ, Epstein PA, Spielman RS. Linkage studies on NIDDM and the insulin and insulin-receptor genes Diabetes. 38: 653-658. PMID 2565838 DOI: 10.2337/diab.38.5.653  0.262
2024 Lo Faro V, Bhattacharya A, Zhou W, Zhou D, Wang Y, Läll K, Kanai M, Lopera-Maya E, Straub P, Pawar P, Tao R, Zhong X, Namba S, Sanna S, Nolte IM, ... ... Cox NJ, et al. Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Cell Reports. Medicine. 5: 101430. PMID 38382466 DOI: 10.1016/j.xcrm.2024.101430  0.261
2013 Lonsdale J, Thomas J, Salvatore M, Phillips R, Lo E, Shad S, Hasz R, Walters G, Garcia F, Young N, Foster B, Moser M, Karasik E, Gillard B, Ramsey K, ... ... Cox NJ, et al. The Genotype-Tissue Expression (GTEx) project Nature Genetics. 45: 580-585. PMID 23715323 DOI: 10.1038/Ng.2653  0.261
2011 Patrinos GP, Innocenti F, Cox N, Fortina P. Genetic Analysis in Translational Medicine: The 2010 GOLDEN HELIX Symposium. Human Mutation. 32: 698-703. PMID 21438074 DOI: 10.1002/humu.21473  0.26
2008 Huang RS, Duan S, Kistner EO, Zhang W, Bleibel WK, Cox NJ, Dolan ME. Identification of genetic variants and gene expression relationships associated with pharmacogenes in humans. Pharmacogenetics and Genomics. 18: 545-9. PMID 18496134 DOI: 10.1097/Fpc.0B013E3282Fe1745  0.26
2020 Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, et al. A brief history of human disease genetics. Nature. 577: 179-189. PMID 31915397 DOI: 10.1038/S41586-019-1879-7  0.259
2020 Claussnitzer M, Cho JH, Collins R, Cox NJ, Dermitzakis ET, Hurles ME, Kathiresan S, Kenny EE, Lindgren CM, MacArthur DG, North KN, Plon SE, Rehm HL, Risch N, Rotimi CN, et al. A brief history of human disease genetics. Nature. 577: 179-189. PMID 31915397 DOI: 10.1038/S41586-019-1879-7  0.259
2014 MacArthur DG, Manolio TA, Dimmock DP, Rehm HL, Shendure J, Abecasis GR, Adams DR, Altman RB, Antonarakis SE, Ashley EA, Barrett JC, Biesecker LG, Conrad DF, Cooper GM, Cox NJ, et al. Guidelines for investigating causality of sequence variants in human disease. Nature. 508: 469-76. PMID 24759409 DOI: 10.1038/Nature13127  0.258
2013 Lee Y, Li H, Li J, Rebman E, Achour I, Regan KE, Gamazon ER, Chen JL, Yang XH, Cox NJ, Lussier YA. Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases. Journal of the American Medical Informatics Association : Jamia. 20: 619-29. PMID 23355459 DOI: 10.1136/Amiajnl-2012-001519  0.258
2014 Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, ... ... Cox NJ, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/Ana.24215  0.258
2014 Paschou P, Yu D, Gerber G, Evans P, Tsetsos F, Davis LK, Karagiannidis I, Chaponis J, Gamazon E, Mueller-Vahl K, Stuhrmann M, Schloegelhofer M, Stamenkovic M, Hebebrand J, Noethen M, ... ... Cox NJ, et al. Genetic association signal near NTN4 in Tourette syndrome. Annals of Neurology. 76: 310-5. PMID 25042818 DOI: 10.1002/Ana.24215  0.258
2016 Wheeler HE, Gamazon ER, Frisina R, Perez-Cervantes C, El Charif O, Mapes B, Fossa SD, Feldman D, Hamilton R, Vaughn DJ, Beard C, Fung C, Kollmannsberger C, Kim J, Mushiroda T, ... ... Cox N, et al. Variants in WFS1 and other Mendelian deafness genes are associated with cisplatin-associated ototoxicity. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 28039263 DOI: 10.1158/1078-0432.CCR-16-2809  0.256
2016 Wheeler HE, Gamazon ER, Frisina R, Perez-Cervantes C, El Charif O, Mapes B, Fossa SD, Feldman D, Hamilton R, Vaughn DJ, Beard C, Fung C, Kollmannsberger C, Kim J, Mushiroda T, ... ... Cox N, et al. Variants in WFS1 and other Mendelian deafness genes are associated with cisplatin-associated ototoxicity. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 28039263 DOI: 10.1158/1078-0432.CCR-16-2809  0.256
1995 Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Linkage studies in NIDDM with markers near the sulphonylurea receptor gene Diabetologia. 38: 1479-1481. PMID 8786023 DOI: 10.1007/Bf00400610  0.256
2012 Pinto N, Gamazon ER, Im HK, Konkashbaev A, Cox NJ, Dolan ME, Diskin SJ, London WB, Maris JM, Cohn SL. Abstract 2486: African ancestry is associated with high-risk disease and event-free survival in children with neuroblastoma Cancer Research. 72: 2486-2486. DOI: 10.1158/1538-7445.Am2012-2486  0.255
2013 Blair DR, Lyttle CS, Mortensen JM, Bearden CF, Jensen AB, Khiabanian H, Melamed R, Rabadan R, Bernstam EV, Brunak S, Jensen LJ, Nicolae D, Shah NH, Grossman RL, Cox NJ, et al. A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk. Cell. 155: 70-80. PMID 24074861 DOI: 10.1016/J.Cell.2013.08.030  0.255
2006 Tsuchiya T, Schwarz PE, Bosque-Plata LD, Geoffrey Hayes M, Dina C, Froguel P, Wayne Towers G, Fischer S, Temelkova-Kurktschiev T, Rietzsch H, Graessler J, Vcelák J, Palyzová D, Selisko T, Bendlová B, ... ... Cox NJ, et al. Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Molecular Genetics and Metabolism. 89: 174-84. PMID 16837224 DOI: 10.1016/J.Ymgme.2006.05.013  0.255
1997 Boehnke M, Cox NJ. Accurate Inference of Relationships in Sib-Pair Linkage Studies American Journal of Human Genetics. 61: 423-429. PMID 9311748 DOI: 10.1086/514862  0.253
2022 Zhou H, Arapoglou T, Li X, Li Z, Zheng X, Moore J, Asok A, Kumar S, Blue EE, Buyske S, Cox N, Felsenfeld A, Gerstein M, Kenny E, Li B, et al. FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Nucleic Acids Research. PMID 36350676 DOI: 10.1093/nar/gkac966  0.252
2013 Gamazon ER, Lamba JK, Pounds S, Stark AL, Wheeler HE, Cao X, Im HK, Mitra AK, Rubnitz JE, Ribeiro RC, Raimondi S, Campana D, Crews KR, Wong SS, Welsh M, ... ... Cox NJ, et al. Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients. Blood. 121: 4366-76. PMID 23538338 DOI: 10.1182/Blood-2012-10-464149  0.251
2016 Hillenmeyer S, Davis LK, Gamazon ER, Cook EH, Cox NJ, Altman RB. STAMS: STRING-Assisted Module Search for Genome Wide Association Studies and Application to Autism. Bioinformatics (Oxford, England). PMID 27542772 DOI: 10.1093/bioinformatics/btw530  0.25
2016 Hillenmeyer S, Davis LK, Gamazon ER, Cook EH, Cox NJ, Altman RB. STAMS: STRING-Assisted Module Search for Genome Wide Association Studies and Application to Autism. Bioinformatics (Oxford, England). PMID 27542772 DOI: 10.1093/bioinformatics/btw530  0.25
2023 Hirbo JB, Pasutto F, Gamazon ER, Evans P, Pawar P, Berner D, Sealock J, Tao R, Straub PS, Konkashbaev AI, Breyer MA, Schlötzer-Schrehardt U, Reis A, Brantley MA, Khor CC, ... ... Cox NJ, et al. Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome. Bmc Genomics. 24: 75. PMID 36797672 DOI: 10.1186/s12864-023-09179-7  0.25
2006 Pihlajamäki J, Salmenniemi U, Vänttinen M, Ruotsalainen E, Kuusisto J, Vauhkonen I, Kainulainen S, Ng MCY, Cox NJ, Bell GI, Laakso M. Common polymorphisms of calpain-10 are associated with abdominal obesity in subjects at high risk of type 2 diabetes. Diabetologia. 49: 1560-1566. PMID 16752174 DOI: 10.1007/S00125-006-0270-Z  0.248
2011 Pinto NR, Gamazon ER, Konkashbaev A, Cox NJ, Dolan ME, Diskin SJ, London WB, Devoto M, Maris JM, Cohn SL. Abstract A46: Genomic ancestry is associated with risk group and survival in children with neuroblastoma Cancer Epidemiology, Biomarkers & Prevention. 20. DOI: 10.1158/1055-9965.Disp-11-A46  0.247
2023 Toikumo S, Jennings MV, Pham B, Lee H, Mallard TT, Bianchi SB, Meredith JJ, Vilar-Rib L, Xu H, Hatoum AS, Johnson EC, Pazdernik V, Jinwala Z, Leger BS, Niarchou M, ... ... Cox NJ, et al. Multi-ancestry meta-analysis of tobacco use disorders based on electronic health record data prioritizes novel candidate risk genes and reveals associations with numerous health outcomes. Medrxiv : the Preprint Server For Health Sciences. PMID 37034728 DOI: 10.1101/2023.03.27.23287713  0.247
2019 Dennis J, Sealock J, Levinson RT, Farber-Eger E, Franco J, Fong S, Straub P, Hucks D, Song WL, Linton MF, Fontanillas P, Elson SL, Ruderfer D, Abdellaoui A, Sanchez-Roige S, ... ... Cox NJ, et al. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Molecular Psychiatry. PMID 31796895 DOI: 10.1038/S41380-019-0614-Y  0.247
2019 Dennis J, Sealock J, Levinson RT, Farber-Eger E, Franco J, Fong S, Straub P, Hucks D, Song WL, Linton MF, Fontanillas P, Elson SL, Ruderfer D, Abdellaoui A, Sanchez-Roige S, ... ... Cox NJ, et al. Genetic risk for major depressive disorder and loneliness in sex-specific associations with coronary artery disease. Molecular Psychiatry. PMID 31796895 DOI: 10.1038/S41380-019-0614-Y  0.247
2015 Maranville JC, Cox NJ. Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits. The Pharmacogenomics Journal. PMID 26149738 DOI: 10.1038/Tpj.2015.47  0.247
2010 Gamazon ER, Zhang W, Konkashbaev A, Duan S, Kistner EO, Nicolae DL, Dolan ME, Cox NJ. SCAN: SNP and copy number annotation. Bioinformatics (Oxford, England). 26: 259-62. PMID 19933162 DOI: 10.1093/Bioinformatics/Btp644  0.246
2009 Zhang W, Duan S, Bleibel WK, Wisel SA, Huang RS, Wu X, He L, Clark TA, Chen TX, Schweitzer AC, Blume JE, Dolan ME, Cox NJ. Identification of common genetic variants that account for transcript isoform variation between human populations. Human Genetics. 125: 81-93. PMID 19052777 DOI: 10.1007/s00439-008-0601-x  0.246
2010 Gamazon ER, Zhang W, Dolan ME, Cox NJ. Comprehensive survey of SNPs in the Affymetrix exon array using the 1000 Genomes dataset. Plos One. 5: e9366. PMID 20186275 DOI: 10.1371/journal.pone.0009366  0.245
2001 Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, Concannon P. Seven Regions of the Genome Show Evidence of Linkage to Type 1 Diabetes in a Consensus Analysis of 767 Multiplex Families American Journal of Human Genetics. 69: 820-830. PMID 11507694 DOI: 10.1086/323501  0.245
1995 Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs Diabetes. 44: 999-1001. PMID 7622007 DOI: 10.2337/Diab.44.8.999  0.244
2002 Pritchard JK, Cox NJ. The allelic architecture of human disease genes: common disease-common variant...or not? Human Molecular Genetics. 11: 2417-23. PMID 12351577 DOI: 10.1093/Hmg/11.20.2417  0.244
2021 Morley TJ, Han L, Castro VM, Morra J, Perlis RH, Cox NJ, Bastarache L, Ruderfer DM. Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing. Nature Medicine. PMID 34083811 DOI: 10.1038/s41591-021-01356-z  0.243
1998 Ober C, Cox NJ, Abney M, Di Rienzo A, Lander ES, Changyaleket B, Gidley H, Kurtz B, Lee J, Nance M, Pettersson A, Prescott J, Richardson A, Schlenker E, Summerhill E, et al. Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma. Human Molecular Genetics. 7: 1393-8. PMID 9700192 DOI: 10.1093/Hmg/7.9.1393  0.243
2014 Gamazon ER, Cox NJ, Davis LK. Structural architecture of SNP effects on complex traits. American Journal of Human Genetics. 95: 477-89. PMID 25307299 DOI: 10.1016/j.ajhg.2014.09.009  0.243
2014 Gamazon ER, Cox NJ, Davis LK. Structural architecture of SNP effects on complex traits. American Journal of Human Genetics. 95: 477-89. PMID 25307299 DOI: 10.1016/j.ajhg.2014.09.009  0.243
2013 Gamazon ER, Pinto N, Konkashbaev A, Im HK, Diskin SJ, London WB, Maris JM, Dolan ME, Cox NJ, Cohn SL. Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival. Journal of the National Cancer Institute. 105: 302-9. PMID 23243203 DOI: 10.1093/Jnci/Djs503  0.243
2020 Dumitrescu L, Mahoney ER, Mukherjee S, Lee ML, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski C, Hernandez Saucedo H, Widaman KF, Buckley R, Properzi M, ... ... Cox NJ, et al. Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Brain : a Journal of Neurology. 143: 2561-2575. PMID 32844198 DOI: 10.1093/Brain/Awaa209  0.241
2020 Dumitrescu L, Mahoney ER, Mukherjee S, Lee ML, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski C, Hernandez Saucedo H, Widaman KF, Buckley R, Properzi M, ... ... Cox NJ, et al. Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Brain : a Journal of Neurology. 143: 2561-2575. PMID 32844198 DOI: 10.1093/Brain/Awaa209  0.241
2008 Potash JB, Buervenich S, Cox NJ, Zandi PP, Akula N, Steele J, Rathe JA, Avramopoulos D, Detera-Wadleigh SD, Gershon ES, DePaulo JR, Feinberg AP, McMahon FJ. Gene-based SNP mapping of a psychotic bipolar affective disorder linkage region on 22q12.3: association with HMG2L1 and TOM1. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 59-67. PMID 17671966 DOI: 10.1002/Ajmg.B.30574  0.241
2023 Jia G, Li Y, Zhong X, Wang K, Pividori M, Alomairy R, Esposito A, Ltaief H, Terao C, Akiyama M, Matsuda K, Keyes DE, Im HK, Gojobori T, Kamatani Y, ... ... Cox NJ, et al. The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci. Nature Computational Science. 3: 403-417. PMID 38177845 DOI: 10.1038/s43588-023-00453-y  0.241
2007 Wittke-Thompson JK, Ambrose N, Yairi E, Roe C, Cook EH, Ober C, Cox NJ. Genetic studies of stuttering in a founder population. Journal of Fluency Disorders. 32: 33-50. PMID 17276504 DOI: 10.1016/J.Jfludis.2006.12.002  0.241
2005 Wittke-Thompson JK, Pluzhnikov A, Cox NJ. Rational inferences about departures from Hardy-Weinberg equilibrium. American Journal of Human Genetics. 76: 967-86. PMID 15834813 DOI: 10.1086/430507  0.24
1989 Xiang K, Cox NJ, Sanz N, Huang P, Karam JH, Bell GI. Insulin-receptor and apolipoprotein genes contribute to development of NIDDM in Chinese Americans. Diabetes. 38: 17-23. PMID 2562831 DOI: 10.2337/Diab.38.1.17  0.24
2023 Jakubek YA, Zhou Y, Stilp A, Bacon J, Wong JW, Ozcan Z, Arnett D, Barnes K, Bis JC, Boerwinkle E, Brody JA, Carson AP, Chasman DI, Chen J, Cho M, ... ... Cox N, et al. Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing. Nature Genetics. PMID 37904051 DOI: 10.1038/s41588-023-01553-1  0.24
2009 Knight JA, Skol AD, Shinde A, Hastings D, Walgren RA, Shao J, Tennant TR, Banerjee M, Allan JM, Le Beau MM, Larson RA, Graubert TA, Cox NJ, Onel K. Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility. Blood. 113: 5575-82. PMID 19299336 DOI: 10.1182/Blood-2008-10-183244  0.239
2011 Ziliak D, O'Donnell PH, Im HK, Gamazon ER, Chen P, Delaney S, Shukla S, Das S, Cox NJ, Vokes EE, Cohen EE, Dolan ME, Huang RS. Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers. Translational Research : the Journal of Laboratory and Clinical Medicine. 157: 265-72. PMID 21497773 DOI: 10.1016/j.trsl.2011.01.005  0.238
2021 Sun Y, Zhu J, Zhou D, Canchi S, Wu C, Cox NJ, Rissman RA, Gamazon ER, Wu L. A transcriptome-wide association study of Alzheimer's disease using prediction models of relevant tissues identifies novel candidate susceptibility genes. Genome Medicine. 13: 141. PMID 34470669 DOI: 10.1186/s13073-021-00959-y  0.238
2003 Tsalenko A, Ben-Dor A, Cox N, Yakhini Z. Methods for analysis and visualization of SNP genotype data for complex diseases. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 548-61. PMID 12603057 DOI: 10.1142/9789812776303_0051  0.235
2002 Elbein SC, Chu W, Ren Q, Hemphill C, Schay J, Cox NJ, Hanis CL, Hasstedt SJ. Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians. The Journal of Clinical Endocrinology and Metabolism. 87: 650-4. PMID 11836299 DOI: 10.1210/jcem.87.2.8210  0.235
2012 Urbanek M, Hayes MG, Lee H, Freathy RM, Lowe LP, Ackerman C, Jafari N, Dyer AR, Cox NJ, Dunger DB, Hattersley AT, Metzger BE, Lowe WL. The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy. Plos One. 7: e32958. PMID 22479352 DOI: 10.1371/journal.pone.0032958  0.235
2023 Sun Q, Rowland B, Wang W, Miller-Fleming TW, Cox N, Graff M, Faucon A, Shuey MM, Blue EE, Auer P, Li Y, Sankaran VG, Reiner AP, Raffield LM. Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19. Blood Cells, Molecules & Diseases. 103: 102782. PMID 37558590 DOI: 10.1016/j.bcmd.2023.102782  0.235
2019 Jia G, Li Y, Zhang H, Chattopadhyay I, Boeck Jensen A, Blair DR, Davis L, Robinson PN, Dahlén T, Brunak S, Benson M, Edgren G, Cox NJ, Gao X, Rzhetsky A. Estimating heritability and genetic correlations from large health datasets in the absence of genetic data. Nature Communications. 10: 5508. PMID 31796735 DOI: 10.1038/S41467-019-13455-0  0.234
2019 Jia G, Li Y, Zhang H, Chattopadhyay I, Boeck Jensen A, Blair DR, Davis L, Robinson PN, Dahlén T, Brunak S, Benson M, Edgren G, Cox NJ, Gao X, Rzhetsky A. Estimating heritability and genetic correlations from large health datasets in the absence of genetic data. Nature Communications. 10: 5508. PMID 31796735 DOI: 10.1038/S41467-019-13455-0  0.234
2019 Colbran LL, Gamazon ER, Zhou D, Evans P, Cox NJ, Capra JA. Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences. Nature Ecology & Evolution. PMID 31591491 DOI: 10.1038/S41559-019-0996-X  0.234
2019 Colbran LL, Gamazon ER, Zhou D, Evans P, Cox NJ, Capra JA. Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences. Nature Ecology & Evolution. PMID 31591491 DOI: 10.1038/S41559-019-0996-X  0.234
2020 Liu D, Zhou D, Sun Y, Zhu J, Ghoneim D, Wu C, Yao Q, Gamazon ER, Cox NJ, Wu L. A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk. Cancer Research. PMID 32907841 DOI: 10.1158/0008-5472.CAN-20-1353  0.234
2020 Liu D, Zhou D, Sun Y, Zhu J, Ghoneim D, Wu C, Yao Q, Gamazon ER, Cox NJ, Wu L. A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk. Cancer Research. PMID 32907841 DOI: 10.1158/0008-5472.CAN-20-1353  0.234
2020 Zhou D, Jiang Y, Zhong X, Cox NJ, Liu C, Gamazon ER. A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. Nature Genetics. PMID 33020666 DOI: 10.1038/s41588-020-0706-2  0.234
2020 Zhou D, Jiang Y, Zhong X, Cox NJ, Liu C, Gamazon ER. A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis. Nature Genetics. PMID 33020666 DOI: 10.1038/s41588-020-0706-2  0.234
2000 Horikawa Y, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Schwitzgebel V, German MS, Bell GI. β-Cell transcription factors and diabetes: No evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY Diabetes. 49: 1955-1957. PMID 11078465 DOI: 10.2337/Diabetes.49.11.1955  0.232
1996 Yamagata K, Takeda J, Menzel S, Chen X, Eng S, Lim LR, Concannon P, Hanis CL, Spielman RS, Cox NJ, Bell GI. Searching for NIDDM susceptibility genes: Studies of genes with triplet repeats expressed in skeletal muscle Diabetologia. 39: 725-730. PMID 8781769 DOI: 10.1007/Bf00418545  0.232
2013 Wheeler HE, Gamazon ER, Stark AL, O'Donnell PH, Gorsic LK, Huang RS, Cox NJ, Dolan ME. Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. The Pharmacogenomics Journal. 13: 35-43. PMID 21844884 DOI: 10.1038/tpj.2011.38  0.232
1991 Matsutani A, Koranyi L, Cox N, Permutt MA. Polymorphisms of GLUT2 and GLUT4 genes. Use in evaluation of genetic susceptibility to NIDDM in blacks. Diabetes. 39: 1534-42. PMID 1978828 DOI: 10.2337/diab.39.12.1534  0.231
2001 Mathias RA, Freidhoff LR, Blumenthal MN, Meyers DA, Lester L, King R, Xu JF, Solway J, Barnes KC, Pierce J, Stine OC, Togias A, Oetting W, Marshik PL, Hetmanski JB, ... ... Cox NJ, et al. Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families. Genetic Epidemiology. 20: 340-55. PMID 11255243 DOI: 10.1002/Gepi.5  0.231
2014 Wheeler HE, Aquino-Michaels K, Gamazon ER, Trubetskoy VV, Dolan ME, Huang RS, Cox NJ, Im HK. Poly-omic prediction of complex traits: OmicKriging. Genetic Epidemiology. 38: 402-15. PMID 24799323 DOI: 10.1002/gepi.21808  0.231
2014 Wheeler HE, Aquino-Michaels K, Gamazon ER, Trubetskoy VV, Dolan ME, Huang RS, Cox NJ, Im HK. Poly-omic prediction of complex traits: OmicKriging. Genetic Epidemiology. 38: 402-15. PMID 24799323 DOI: 10.1002/gepi.21808  0.231
2022 Partanen JJ, Häppölä P, Zhou W, Lehisto AA, Ainola M, Sutinen E, Allen RJ, Stockwell AD, Leavy OC, Oldham JM, Guillen-Guio B, Cox NJ, Hirbo JB, Schwartz DA, Fingerlin TE, et al. Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics. Cell Genomics. 2: 100181. PMID 36777997 DOI: 10.1016/j.xgen.2022.100181  0.23
2004 Cox NJ. Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED. Genetic Epidemiology. 1: 167-70. PMID 14964297 DOI: 10.1002/GEPI.1370010208  0.23
2008 Zhang W, Duan S, Kistner EO, Bleibel WK, Huang RS, Clark TA, Chen TX, Schweitzer AC, Blume JE, Cox NJ, Dolan ME. Evaluation of genetic variation contributing to differences in gene expression between populations. American Journal of Human Genetics. 82: 631-40. PMID 18313023 DOI: 10.1016/J.Ajhg.2007.12.015  0.23
2009 Huang RS, Chen P, Wisel S, Duan S, Zhang W, Cook EH, Das S, Cox NJ, Dolan ME. Population-specific GSTM1 copy number variation. Human Molecular Genetics. 18: 366-72. PMID 18948376 DOI: 10.1093/Hmg/Ddn345  0.229
1992 Cox NJ, Xiang K, Fajans SS, Bell GI. Mapping Diabetes-Susceptibility Genes: Lessons Learned From Search for DNA Marker for Maturity-Onset Diabetes of the Young Diabetes. 41: 401-407. PMID 1607066 DOI: 10.2337/Diab.41.4.401  0.228
2010 Huang RS, Johnatty SE, Gamazon E, Im HK, Ziliak D, Zhang W, Chen P, Beesley J, O'Donnell PH, Das S, Cox NJ, Vokes EE, deFazio A, Chenevix-Trench G, Cohen EEW, et al. Abstract 2761: Germline polymorphism discovered via a cell-based genome-wide approach predicts platinum response in ovarian and head and neck cancers Cancer Research. 70: 2761-2761. DOI: 10.1158/1538-7445.Am10-2761  0.227
2019 Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, ... ... Cox NJ, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/Appi.Ajp.2018.18070857  0.227
2019 Yu D, Sul JH, Tsetsos F, Nawaz MS, Huang AY, Zelaya I, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau G, ... ... Cox NJ, et al. Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. The American Journal of Psychiatry. 176: 217-227. PMID 30818990 DOI: 10.1176/Appi.Ajp.2018.18070857  0.227
2011 Gamazon ER, Huang RS, Dolan ME, Cox NJ. Copy number polymorphisms and anticancer pharmacogenomics. Genome Biology. 12: R46. PMID 21609475 DOI: 10.1186/gb-2011-12-5-r46  0.224
1990 Lutze M, Cox NJ, Smith VC, Pokorny J. Genetic studies of variation in Rayleigh and photometric matches in normal trichromats. Vision Research. 30: 149-62. PMID 2321360 DOI: 10.1016/0042-6989(90)90134-7  0.224
2007 Hoffmann K, Mattheisen M, Dahm S, Nürnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. Diabetologia. 50: 1418-22. PMID 17464498 DOI: 10.1007/s00125-007-0658-4  0.224
1996 Shoulders CC, Grantham TT, North JD, Gaspardone A, Tomai F, de Fazio A, Versaci F, Gioffre PA, Cox NJ. Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children. Human Genetics. 98: 557-66. PMID 8882875 DOI: 10.1007/s004390050259  0.224
2023 Coral DE, Fernandez-Tajes J, Tsereteli N, Pomares-Millan H, Fitipaldi H, Mutie PM, Atabaki-Pasdar N, Kalamajski S, Poveda A, Miller-Fleming TW, Zhong X, Giordano GN, Pearson ER, Cox NJ, Franks PW. A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes. Nature Metabolism. PMID 36703017 DOI: 10.1038/s42255-022-00731-5  0.223
1989 Cox NJ, Gogolin KJ, Horvath VJ, Barker DF, Wright E, Tran T, Skolnick MH, Boehm BO, Fehsel K, Bertrams J. Restriction fragment polymorphisms of the HLA-DR, HLA-DQ, and insulin gene regions in IDDM: the GAW5 data. Genetic Epidemiology. 6: 21-6. PMID 2567259 DOI: 10.1002/gepi.1370060106  0.223
2024 Sun Q, Rowland BT, Chen J, Mikhaylova AV, Avery C, Peters U, Lundin J, Matise T, Buyske S, Tao R, Mathias RA, Reiner AP, Auer PL, Cox NJ, Kooperberg C, et al. Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. Nature Communications. 15: 1016. PMID 38310129 DOI: 10.1038/s41467-024-45135-z  0.223
2011 Yang JJ, Cheng C, Devidas M, Cao X, Fan Y, Campana D, Yang W, Neale G, Cox NJ, Scheet P, Borowitz MJ, Winick NJ, Martin PL, Willman CL, Bowman WP, et al. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nature Genetics. 43: 237-41. PMID 21297632 DOI: 10.1038/Ng.763  0.223
2013 Hayes MG, Urbanek M, Hivert MF, Armstrong LL, Morrison J, Guo C, Lowe LP, Scheftner DA, Pluzhnikov A, Levine DM, McHugh CP, Ackerman CM, Bouchard L, Brisson D, Layden BT, ... ... Cox NJ, et al. Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. Diabetes. 62: 3282-91. PMID 23903356 DOI: 10.2337/Db12-1692  0.223
2016 Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, ... ... Cox NJ, et al. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Nature Communications. 7: 10635. PMID 26868379 DOI: 10.1038/Ncomms10635  0.222
2016 Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, ... ... Cox NJ, et al. A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology. Nature Communications. 7: 10635. PMID 26868379 DOI: 10.1038/Ncomms10635  0.222
2012 Wheeler HE, Maitland ML, Dolan ME, Cox NJ, Ratain MJ. Cancer pharmacogenomics: strategies and challenges. Nature Reviews. Genetics. 14: 23-34. PMID 23183705 DOI: 10.1038/nrg3352  0.221
2014 LaCroix B, Gamazon ER, Lenkala D, Im HK, Geeleher P, Ziliak D, Cox NJ, Huang RS. Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity. Bmc Genomics. 15: 292. PMID 24739237 DOI: 10.1186/1471-2164-15-292  0.221
2014 LaCroix B, Gamazon ER, Lenkala D, Im HK, Geeleher P, Ziliak D, Cox NJ, Huang RS. Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity. Bmc Genomics. 15: 292. PMID 24739237 DOI: 10.1186/1471-2164-15-292  0.221
1991 Bell GI, Xiang KS, Newman MV, Wu SH, Wright LG, Fajans SS, Spielman RS, Cox NJ. Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proceedings of the National Academy of Sciences of the United States of America. 88: 1484-8. PMID 1899928 DOI: 10.1073/PNAS.88.4.1484  0.219
2019 Wang Q, Chen R, Cheng F, Wei Q, Ji Y, Yang H, Zhong X, Tao R, Wen Z, Sutcliffe JS, Liu C, Cook EH, Cox NJ, Li B. A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data. Nature Neuroscience. PMID 30988527 DOI: 10.1038/S41593-019-0382-7  0.219
2019 Wang Q, Chen R, Cheng F, Wei Q, Ji Y, Yang H, Zhong X, Tao R, Wen Z, Sutcliffe JS, Liu C, Cook EH, Cox NJ, Li B. A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data. Nature Neuroscience. PMID 30988527 DOI: 10.1038/S41593-019-0382-7  0.219
2010 Shervais S, Kramer PL, Westaway SK, Cox NJ, Zwick M. Reconstructability analysis as a tool for identifying gene-gene interactions in studies of human diseases. Statistical Applications in Genetics and Molecular Biology. 9: Article18. PMID 20361857 DOI: 10.2202/1544-6115.1516  0.218
2023 Alagöz G, Eising E, Mekki Y, Bignardi G, Fontanillas P, Nivard MG, Luciano M, Cox NJ, Fisher SE, Gordon RL. The shared genetic architecture and evolution of human language and musical rhythm. Biorxiv : the Preprint Server For Biology. PMID 37961248 DOI: 10.1101/2023.11.01.564908  0.218
2010 Freathy RM, Hayes MG, Urbanek M, Lowe LP, Lee H, Ackerman C, Frayling TM, Cox NJ, Dunger DB, Dyer AR, Hattersley AT, Metzger BE, Lowe WL. Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from the International Association of Diabetes and Pregnancy Study Groups. Diabetes. 59: 2682-9. PMID 20682688 DOI: 10.2337/db10-0177  0.217
2012 Cox NJ, Gamazon ER, Wheeler HE, Dolan ME. Clinical translation of cell-based pharmacogenomic discovery. Clinical Pharmacology and Therapeutics. 92: 425-7. PMID 22910437 DOI: 10.1038/clpt.2012.115  0.217
2019 Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Cox NJ, et al. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 30911161 DOI: 10.1038/S41588-019-0364-4  0.216
2019 Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Cox NJ, et al. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 30911161 DOI: 10.1038/S41588-019-0364-4  0.216
2011 Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH. Parent-of-origin effects of the serotonin transporter gene associated with autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 139-44. PMID 21302342 DOI: 10.1002/Ajmg.B.31146  0.216
2012 Im HK, Gamazon ER, Stark AL, Huang RS, Cox NJ, Dolan ME. Mixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancer. Plos Genetics. 8: e1002525. PMID 22346769 DOI: 10.1371/journal.pgen.1002525  0.216
2013 Wheeler HE, Gamazon ER, Wing C, Njiaju UO, Njoku C, Baldwin RM, Owzar K, Jiang C, Watson D, Shterev I, Kubo M, Zembutsu H, Winer EP, Hudis CA, Shulman LN, ... ... Cox NJ, et al. Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 19: 491-9. PMID 23204130 DOI: 10.1158/1078-0432.Ccr-12-2618  0.215
2011 Huo D, Zheng Y, Ogundiran TO, Adebamowo C, Nathanson KL, Domchek SM, Rebbeck TR, John EM, Hennis A, Nemesure B, Wu S, Ambs S, Niu Q, Zhang J, Cox NJ, et al. Abstract LB-425: Replication of 18 susceptibility loci of breast cancer in women of African ancestry Cancer Research. 71. DOI: 10.1158/1538-7445.Am2011-Lb-425  0.215
2021 Vysotskiy M, Zhong X, Miller-Fleming TW, Zhou D, Cox NJ, Weiss LA. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Medicine. 13: 172. PMID 34715901 DOI: 10.1186/s13073-021-00972-1  0.215
2013 Chen F, Chen GK, Stram DO, Millikan RC, Ambrosone CB, John EM, Bernstein L, Zheng W, Palmer JR, Hu JJ, Rebbeck TR, Ziegler RG, Nyante S, Bandera EV, Ingles SA, ... ... Cox NJ, et al. A genome-wide association study of breast cancer in women of African ancestry. Human Genetics. 132: 39-48. PMID 22923054 DOI: 10.1007/S00439-012-1214-Y  0.215
2023 Wang Y, Namba S, Lopera E, Kerminen S, Tsuo K, Läll K, Kanai M, Zhou W, Wu KH, Favé MJ, Bhatta L, Awadalla P, Brumpton B, Deelen P, Hveem K, ... ... Cox NJ, et al. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts. Cell Genomics. 3: 100241. PMID 36777179 DOI: 10.1016/j.xgen.2022.100241  0.214
1996 Yairi E, Ambrose N, Cox N. Genetics of stuttering: a critical review. Journal of Speech and Hearing Research. 39: 771-84. PMID 8844557 DOI: 10.1044/Jshr.3904.771  0.214
2010 Chen SH, Pei D, Yang W, Cheng C, Jeha S, Cox NJ, Evans WE, Pui CH, Relling MV. Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity. Clinical Pharmacology and Therapeutics. 88: 191-6. PMID 20592726 DOI: 10.1038/Clpt.2010.94  0.214
2022 Eissman JM, Dumitrescu L, Mahoney ER, Smith AN, Mukherjee S, Lee ML, Scollard P, Choi SE, Bush WS, Engelman CD, Lu Q, Fardo DW, Trittschuh EH, Mez J, Kaczorowski CC, ... ... Cox NJ, et al. Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease. Brain : a Journal of Neurology. PMID 35552371 DOI: 10.1093/brain/awac177  0.214
2012 Owzar K, Li Z, Cox N, Jung SH. Power and sample size calculations for SNP association studies with censored time-to-event outcomes. Genetic Epidemiology. 36: 538-48. PMID 22685040 DOI: 10.1002/Gepi.21645  0.213
2012 Zheng Y, Ogundiran TO, Adebamowo C, Nathanson KL, Domchek SM, Rebbeck TR, Simon MS, John EM, Hennis A, Nemesure B, Wu S, Leske MC, Ambs S, Niu Q, Zhang J, ... Cox NJ, et al. Abstract 2606: Absence of association between common genetic polymorphisms in the TERT-CLPTM1L locus and breast cancer risk in women of African descent Cancer Research. 72: 2606-2606. DOI: 10.1158/1538-7445.Am2012-2606  0.213
2002 Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Molecular Psychiatry. 7: 278-88. PMID 11920155 DOI: 10.1038/Sj.Mp.4001033  0.213
2012 Wheeler HE, Gamazon ER, Njiaju UO, Wing C, Njoku C, Baldwin RM, Owzar K, Winer E, Hudis C, Shulman LN, Ratain MJ, Kroetz DL, Cox NJ, Dolan ME. Abstract 1881: Integration of cell line and Cancer and Leukemia Group B 40101 clinical trial genome-wide association analyses implicates multiple loci in paclitaxel-induced peripheral neuropathy Cancer Research. 72: 1881-1881. DOI: 10.1158/1538-7445.Am2012-1881  0.213
2005 Ng MCY, Miyake K, So WY, Poon EWM, Lam VKL, Li JKY, Cox NJ, Bell GI, Chan JCN. The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population Diabetologia. 48: 2018-2024. PMID 16132950 DOI: 10.1007/S00125-005-1914-0  0.212
2002 Cox NJ. Approaches to identifying genetic variation for complex phenotypes International Congress Series. 1246: 241-250. DOI: 10.1016/S0531-5131(02)01136-6  0.211
2005 Nicolae D, Cox NJ, Lester LA, Schneider D, Tan Z, Billstrand C, Kuldanek S, Donfack J, Kogut P, Patel NM, Goodenbour J, Howard T, Wolf R, Koppelman GH, White SR, et al. Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21. American Journal of Human Genetics. 76: 349-57. PMID 15611928 DOI: 10.1086/427763  0.211
2019 Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, ... ... Cox NJ, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/Brain/Awz206  0.21
2019 Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, ... ... Cox NJ, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/Brain/Awz206  0.21
2019 Gamazon ER, Zwinderman AH, Cox NJ, Denys D, Derks EM. Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits. Nature Genetics. PMID 31086352 DOI: 10.1038/S41588-019-0409-8  0.21
2019 Gamazon ER, Zwinderman AH, Cox NJ, Denys D, Derks EM. Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits. Nature Genetics. PMID 31086352 DOI: 10.1038/S41588-019-0409-8  0.21
2022 Dickson AL, Daniel LL, Jackson E, Zanussi J, Yang W, Plummer WD, Dupont WD, Wei WQ, Nepal P, Hung AM, Cox NJ, Van Driest SL, Feng Q, Yang JJ, Stein CM, et al. Race, Genotype, and Azathioprine Discontinuation : A Cohort Study. Annals of Internal Medicine. PMID 35724382 DOI: 10.7326/M21-4675  0.21
2008 Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH. Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1116-25. PMID 18361419 DOI: 10.1002/Ajmg.B.30733  0.21
2008 Duan S, Huang RS, Zhang W, Bleibel WK, Roe CA, Clark TA, Chen TX, Schweitzer AC, Blume JE, Cox NJ, Dolan ME. Genetic architecture of transcript-level variation in humans. American Journal of Human Genetics. 82: 1101-13. PMID 18439551 DOI: 10.1016/j.ajhg.2008.03.006  0.209
2009 Kawai T, Ng MC, Hayes MG, Yoshiuchi I, Tsuchiya T, Robertson H, Cox NJ, Polonsky KS, Bell GI, Ehrmann DA. Variation in the perilipin gene (PLIN) affects glucose and lipid metabolism in non-Hispanic white women with and without polycystic ovary syndrome. Diabetes Research and Clinical Practice. 86: 186-92. PMID 19782423 DOI: 10.1016/J.Diabres.2009.09.002  0.209
2014 Hart AB, Gamazon ER, Engelhardt BE, Sklar P, Kähler AK, Hultman CM, Sullivan PF, Neale BM, Faraone SV, de Wit H, Cox NJ, Palmer AA. Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder. Proceedings of the National Academy of Sciences of the United States of America. 111: 5968-73. PMID 24711425 DOI: 10.1073/Pnas.1318810111  0.208
2004 Chen YS, Akula N, Detera-Wadleigh SD, Schulze TG, Thomas J, Potash JB, DePaulo JR, McInnis MG, Cox NJ, McMahon FJ. Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33. Molecular Psychiatry. 9: 87-92; image 5. PMID 14699445 DOI: 10.1038/sj.mp.4001453  0.208
2014 Ahsan H, Halpern J, Kibriya MG, Pierce BL, Tong L, Gamazon E, McGuire V, Felberg A, Shi J, Jasmine F, Roy S, Brutus R, Argos M, Melkonian S, Chang-Claude J, ... ... Cox NJ, et al. A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 23: 658-69. PMID 24493630 DOI: 10.1158/1055-9965.Epi-13-0340  0.207
2019 Derks E, Gamazon E, Zwinderman A, Cox N, Denys D. MULTI-TISSUE TRANSCRIPTOME ANALYSIS REVEALS GENETIC MECHANISMS OF NEUROPSYCHIATRIC TRAITS European Neuropsychopharmacology. 29: S864. DOI: 10.1016/j.euroneuro.2017.08.149  0.207
2008 Duan S, Zhang W, Cox NJ, Dolan ME. FstSNP-HapMap3: a database of SNPs with high population differentiation for HapMap3. Bioinformation. 3: 139-41. PMID 19238253 DOI: 10.6026/97320630003139  0.206
2002 Sun L, Cox NJ, McPeek MS. A statistical method for identification of polymorphisms that explain a linkage result. American Journal of Human Genetics. 70: 399-411. PMID 11791210 DOI: 10.1086/338660  0.205
2013 Zheng Y, Ogundiran TO, Falusi AG, Nathanson KL, John EM, Hennis AJ, Ambs S, Domchek SM, Rebbeck TR, Simon MS, Nemesure B, Wu SY, Leske MC, Odetunde A, Niu Q, ... ... Cox NJ, et al. Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers. Carcinogenesis. 34: 1520-8. PMID 23475944 DOI: 10.1093/Carcin/Bgt090  0.205
2017 Wang K, Gaitsch H, Poon H, Cox NJ, Rzhetsky A. Classification of common human diseases derived from shared genetic and environmental determinants. Nature Genetics. PMID 28783162 DOI: 10.1038/ng.3931  0.205
2017 Wang K, Gaitsch H, Poon H, Cox NJ, Rzhetsky A. Classification of common human diseases derived from shared genetic and environmental determinants. Nature Genetics. PMID 28783162 DOI: 10.1038/ng.3931  0.205
2000 Ober C, Tsalenko A, Parry R, Cox NJ. A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. American Journal of Human Genetics. 67: 1154-62. PMID 11022011 DOI: 10.1016/S0002-9297(07)62946-2  0.204
2023 Jiang L, Liu G, Oeser A, Ihegword A, Dickson AL, Daniel LL, Hung AM, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Association between risk variants and progression from infection to sepsis. Medrxiv : the Preprint Server For Health Sciences. PMID 36747677 DOI: 10.1101/2023.01.27.23284540  0.204
1996 Gambino V, Menzel S, Trabb JB, Xiang KS, Lindner T, Louït A, Chen E, Mereu LE, Furuta H, Iwasaki N, Kawamura M, Omori Y, Rietzsch H, Schulze J, Schröder HE, ... ... Cox NJ, et al. An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes: Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM Diabetes. 45: 291-294. PMID 8593932 DOI: 10.2337/Diab.45.3.291  0.204
2001 Newman DL, Abney M, McPeek MS, Ober C, Cox NJ. The importance of genealogy in determining genetic associations with complex traits. American Journal of Human Genetics. 69: 1146-8. PMID 11590549 DOI: 10.1086/323659  0.203
1983 Cox NJ, Kidd KK. Can recovery from stuttering be considered a genetically milder subtype of stuttering? Behavior Genetics. 13: 129-139. PMID 6860250 DOI: 10.1007/Bf01065662  0.203
2001 Del Bosque-Plata L, Lin J, Horikawa Y, Schwarz PEH, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, German MS, Bell GI. Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects Diabetes. 50: 694-696. PMID 11246894 DOI: 10.2337/Diabetes.50.3.694  0.202
2021 Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, ... ... Cox NJ, ... ... Cox NJ, ... ... Cox NJ, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational Psychiatry. 11: 56. PMID 33462189 DOI: 10.1038/s41398-020-01082-z  0.202
2021 Tsetsos F, Yu D, Sul JH, Huang AY, Illmann C, Osiecki L, Darrow SM, Hirschtritt ME, Greenberg E, Muller-Vahl KR, Stuhrmann M, Dion Y, Rouleau GA, Aschauer H, Stamenkovic M, ... ... Cox NJ, ... ... Cox NJ, ... ... Cox NJ, et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Translational Psychiatry. 11: 56. PMID 33462189 DOI: 10.1038/s41398-020-01082-z  0.202
2018 Yang H, Chen R, Wang Q, Wei Q, Ji Y, Zheng G, Zhong X, Cox NJ, Li B. De Novo pattern discovery enables robust assessment of functional consequences of noncoding variants. Bioinformatics (Oxford, England). PMID 30256891 DOI: 10.1093/Bioinformatics/Bty826  0.202
2018 Yang H, Chen R, Wang Q, Wei Q, Ji Y, Zheng G, Zhong X, Cox NJ, Li B. De Novo pattern discovery enables robust assessment of functional consequences of noncoding variants. Bioinformatics (Oxford, England). PMID 30256891 DOI: 10.1093/Bioinformatics/Bty826  0.202
2012 Huo D, Zheng Y, Ogundiran TO, Adebamowo C, Nathanson KL, Domchek SM, Rebbeck TR, Simon MS, John EM, Hennis A, Nemesure B, Wu SY, Leske MC, Ambs S, Niu Q, ... ... Cox NJ, et al. Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry. Carcinogenesis. 33: 835-40. PMID 22357627 DOI: 10.1093/Carcin/Bgs093  0.201
2021 Gordon RL, Ravignani A, Hyland Bruno J, Robinson CM, Scartozzi A, Embalabala R, Niarchou M, Cox NJ, Creanza N. Linking the genomic signatures of human beat synchronization and learned song in birds. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 376: 20200329. PMID 34420388 DOI: 10.1098/rstb.2020.0329  0.201
2022 Liang Y, Pividori M, Manichaikul A, Palmer AA, Cox NJ, Wheeler HE, Im HK. Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries. Genome Biology. 23: 23. PMID 35027082 DOI: 10.1186/s13059-021-02591-w  0.2
1996 Yamagata K, Oda N, Kaisaki PJ, Menzel S, Furuta H, Vaxillaire M, Southam L, Cox RD, Lathrop GM, Boriraj VV, Chen X, Cox NJ, Oda Y, Yano H, Le Beau MM, et al. Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) Nature. 384: 455-458. PMID 8945470 DOI: 10.1038/384455A0  0.2
2000 Baier LJ, Permana PA, Yang X, Pratley RE, Hanson RL, Shen GQ, Mott D, Knowler WC, Cox NJ, Horikawa Y, Oda N, Bell GI, Bogardus C. A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. The Journal of Clinical Investigation. 106: R69-73. PMID 11018080 DOI: 10.1172/Jci10665  0.2
2008 Zhang W, Duan S, Kistner EO, Bleibel WK, Huang RS, Clark TA, Chen TX, Schweitzer AC, Blume JE, Cox NJ, Dolan ME. Evaluation of Genetic Variation Contributing to Differences in Gene Expression between Populations (DOI:10.1016/j.ajhg.2007.12.015) American Journal of Human Genetics. 82: 1223. DOI: 10.1016/J.Ajhg.2008.04.003  0.199
2011 Perera MA, Gamazon E, Cavallari LH, Patel SR, Poindexter S, Kittles RA, Nicolae D, Cox NJ. The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans. Clinical Pharmacology and Therapeutics. 89: 408-15. PMID 21270790 DOI: 10.1038/Clpt.2010.322  0.199
2018 Dumitrescu L, Deming Y, Lu Q, Beecham GW, Kunkle BW, Del-Aguila JL, Fernandez MV, Budde JP, Fagan AM, Jager PLD, Albert MS, Moghekar A, Riemenschneider M, Petersen RC, Barnes LL, ... ... Cox NJ, et al. P1-139: The Contribution Of Sex-Specific Associations In Genetic Studies Of Alzheimer'S Disease Pathology Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.142  0.199
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Cox NJ, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306  0.199
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... Cox NJ, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306  0.199
1997 Ambrose NG, Cox NJ, Yairi E. The genetic basis of persistence and recovery in stuttering. Journal of Speech, Language, and Hearing Research : Jslhr. 40: 567-80. PMID 9210115 DOI: 10.1044/Jslhr.4003.567  0.198
2007 Pauls D, Cath D, Heutink P, Grados M, Singer HS, Walkup JT, Illmann C, Scharf JM, Santangelo S, Stewart SE, Platko J, Pauls DL, Cox NJ, Robertson MM, Service S, et al. Genome scan for tourette disorder in affected-sibling-pair and multigenerational families American Journal of Human Genetics. 80: 265-272. PMID 17304708 DOI: 10.1086/511052  0.198
2002 Hanna GL, Veenstra-VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC, Leventhal BL, Cook EH. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. American Journal of Medical Genetics. 114: 541-52. PMID 12116192 DOI: 10.1002/Ajmg.10519  0.197
2010 Gamazon ER, Duan S, Zhang W, Huang RS, Kistner EO, Dolan ME, Cox NJ. PACdb: a database for cell-based pharmacogenomics. Pharmacogenetics and Genomics. 20: 269-73. PMID 20216476 DOI: 10.1097/Fpc.0B013E328337B8D6  0.196
2002 Ehrmann DA, Tang X, Yoshiuchi I, Cox NJ, Bell GI. Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 87: 4297-300. PMID 12213887 DOI: 10.1210/Jc.2002-020216  0.196
1999 Pannain S, Weiss RE, Jackson CE, Dian D, Beck JC, Sheffield VC, Cox N, Refetoff S. Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping. The Journal of Clinical Endocrinology and Metabolism. 84: 1061-71. PMID 10084596 DOI: 10.1210/Jcem.84.3.5541  0.195
1995 Menzel S, Yamagata K, Trabb JB, Nerup J, Permutt MA, Fajans SS, Menzel R, Iwasaki N, Omori Y, Cox NJ. Localization of MODY3 to a 5-cM region of human chromosome 12. Diabetes. 44: 1408-13. PMID 7589847  0.194
2016 Wheeler HE, Shah KP, Brenner J, Garcia T, Aquino-Michaels K, Cox NJ, Nicolae DL, Im HK. Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues. Plos Genetics. 12: e1006423. PMID 27835642 DOI: 10.1371/journal.pgen.1006423  0.194
2016 Wheeler HE, Shah KP, Brenner J, Garcia T, Aquino-Michaels K, Cox NJ, Nicolae DL, Im HK. Survey of the Heritability and Sparse Architecture of Gene Expression Traits across Human Tissues. Plos Genetics. 12: e1006423. PMID 27835642 DOI: 10.1371/journal.pgen.1006423  0.194
2005 Riaz N, Steinberg S, Ahmad J, Pluzhnikov A, Riazuddin S, Cox NJ, Drayna D. Genomewide significant linkage to stuttering on chromosome 12. American Journal of Human Genetics. 76: 647-51. PMID 15714404 DOI: 10.1086/429226  0.194
2020 Evans P, Cox NJ, Gamazon ER. The regulatory genome constrains protein sequence evolution: implications for the search for disease-associated genes. Peerj. 8: e9554. PMID 32765967 DOI: 10.7717/Peerj.9554  0.194
2020 Huckins LM, Chatzinakos C, Breen MS, Hartmann J, Klengel T, da Silva Almeida AC, Dobbyn A, Girdhar K, Hoffman GE, Klengel C, Logue MW, Lori A, Maihofer AX, Morrison FG, Nguyen HT, ... ... Cox N, et al. Analysis of Genetically Regulated Gene Expression Identifies a Prefrontal PTSD Gene, SNRNP35, Specific to Military Cohorts. Cell Reports. 31: 107716. PMID 32492425 DOI: 10.1016/J.Celrep.2020.107716  0.193
2001 Xu J, Meyers DA, Ober C, Blumenthal MN, Mellen B, Barnes KC, King RA, Lester LA, Howard TD, Solway J, Langefeld CD, Beaty TH, Rich SS, Bleecker ER, Cox NJ, et al. Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. American Journal of Human Genetics. 68: 1437-46. PMID 11349227 DOI: 10.1086/320589  0.192
2017 Cox NJ. Reaching for the next branch on the biobank tree of knowledge. Nature Genetics. 49: 1295-1296. PMID 28854181 DOI: 10.1038/ng.3946  0.192
2017 Cox NJ. Reaching for the next branch on the biobank tree of knowledge. Nature Genetics. 49: 1295-1296. PMID 28854181 DOI: 10.1038/ng.3946  0.192
1988 Cox NJ, Hodge SE, Marazita ML, Spence MA, Kidd KK. Some effects of selection strategies on linkage analysis Genetic Epidemiology. 5: 289-297. PMID 3049227 DOI: 10.1002/Gepi.1370050410  0.191
2008 French D, Yang W, Hamilton LH, Neale G, Fan Y, Downing JR, Cox NJ, Pui CH, Evans WE, Relling MV. Concordant gene expression in leukemia cells and normal leukocytes is associated with germline cis-SNPs. Plos One. 3: e2144. PMID 18478092 DOI: 10.1371/journal.pone.0002144  0.191
2012 Hou N, Zheng Y, Gamazon ER, Ogundiran TO, Adebamowo C, Nathanson KL, Domchek SM, Rebbeck TR, Simon MS, John EM, Hennis A, Nemesure B, Wu SY, Leske MC, Ambs S, ... ... Cox NJ, et al. Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 21: 552-6. PMID 22237986 DOI: 10.1158/1055-9965.Epi-11-0979  0.19
2001 Hara M, Wang X, Paz VP, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Bell GI. No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY. Diabetologia. 43: 1064-9. PMID 10990086 DOI: 10.1007/s001250051491  0.19
2002 Lynn S, Evans JC, White C, Frayling TM, Hattersley AT, Turnbull DM, Horikawa Y, Cox NJ, Bell GI, Walker M. Variation in the calpain-10 gene affects blood glucose levels in the British population. Diabetes. 51: 247-50. PMID 11756349 DOI: 10.2337/Diabetes.51.1.247  0.19
2009 Duan S, Huang RS, Zhang W, Mi S, Bleibel WK, Kistner EO, Cox NJ, Dolan ME. Expression and alternative splicing of folate pathway genes in HapMap lymphoblastoid cell lines. Pharmacogenomics. 10: 549-63. PMID 19374514 DOI: 10.2217/Pgs.09.8  0.19
2006 Nicolae DL, Wen X, Voight BF, Cox NJ. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. Plos Genetics. 2: e67. PMID 16680197 DOI: 10.1371/Journal.Pgen.0020067  0.189
2020 Anandi P, Dickson AL, Feng Q, Wei WQ, Dupont WD, Plummer D, Liu G, Octaria R, Barker KA, Kawai VK, Birdwell K, Cox NJ, Hung A, Stein CM, Chung CP. Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice. The Pharmacogenomics Journal. PMID 32054992 DOI: 10.1038/S41397-020-0163-4  0.189
2020 Anandi P, Dickson AL, Feng Q, Wei WQ, Dupont WD, Plummer D, Liu G, Octaria R, Barker KA, Kawai VK, Birdwell K, Cox NJ, Hung A, Stein CM, Chung CP. Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice. The Pharmacogenomics Journal. PMID 32054992 DOI: 10.1038/S41397-020-0163-4  0.189
2013 Ratain MJ, Cox NJ, Henderson TO. Challenges in interpreting the evidence for genetic predictors of ototoxicity. Clinical Pharmacology and Therapeutics. 94: 631-5. PMID 24241639 DOI: 10.1038/clpt.2013.178  0.189
1991 Mangklabruks A, Cox N, DeGroot LJ. Genetic factors in autoimmune thyroid disease analyzed by restriction fragment length polymorphisms of candidate genes Journal of Clinical Endocrinology and Metabolism. 73: 236-244. PMID 1677360 DOI: 10.1210/Jcem-73-2-236  0.188
2009 Perera MA, Thirumaran RK, Cox NJ, Hanauer S, Das S, Brimer-Cline C, Lamba V, Schuetz EG, Ratain MJ, Di Rienzo A. Prediction of CYP3A4 enzyme activity using haplotype tag SNPs in African Americans. The Pharmacogenomics Journal. 9: 49-60. PMID 18825162 DOI: 10.1038/tpj.2008.13  0.188
2011 Huang RS, Johnatty SE, Gamazon ER, Im HK, Ziliak D, Duan S, Zhang W, Kistner EO, Chen P, Beesley J, Mi S, O'Donnell PH, Fraiman YS, Das S, Cox NJ, et al. Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 17: 5490-500. PMID 21705454 DOI: 10.1158/1078-0432.Ccr-11-0724  0.188
2020 Zhong X, Yin Z, Jia G, Zhou D, Wei Q, Faucon A, Evans P, Gamazon ER, Li B, Tao R, Rzhetsky A, Bastarache L, Cox NJ. Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32296164 DOI: 10.1038/S41436-020-0786-5  0.188
2020 Zhong X, Yin Z, Jia G, Zhou D, Wei Q, Faucon A, Evans P, Gamazon ER, Li B, Tao R, Rzhetsky A, Bastarache L, Cox NJ. Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32296164 DOI: 10.1038/S41436-020-0786-5  0.188
2002 Rasmussen SK, Urhammer SA, Berglund L, Jensen JN, Hansen L, Echwald SM, Borch-Johnsen K, Horikawa Y, Mashima H, Lithell H, Cox NJ, Hansen T, Bell GI, Pedersen O. Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians. Diabetes. 51: 3561-7. PMID 12453914 DOI: 10.2337/Diabetes.51.12.3561  0.188
2023 Jiang L, Liu G, Oeser A, Ihegword A, Dickson AL, Daniel LL, Hung AM, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Association between risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study. Elife. 12. PMID 37882666 DOI: 10.7554/eLife.88538  0.187
1997 Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI. Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1) Nature. 384: 458-60. PMID 8945471 DOI: 10.1038/384458a0  0.187
2021 Dickson AL, Daniel LL, Zanussi J, Plummer WD, Wei WQ, Liu G, Reese T, Anandi P, Birdwell KA, Kawai V, Cox NJ, Dupont WD, Hung AM, Feng Q, Stein CM, et al. TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results. Clinical Pharmacology and Therapeutics. PMID 34582038 DOI: 10.1002/cpt.2428  0.186
2014 Smemo S, Tena JJ, Kim KH, Gamazon ER, Sakabe NJ, Gómez-Marín C, Aneas I, Credidio FL, Sobreira DR, Wasserman NF, Lee JH, Puviindran V, Tam D, Shen M, Son JE, ... ... Cox NJ, et al. Obesity-associated variants within FTO form long-range functional connections with IRX3. Nature. 507: 371-5. PMID 24646999 DOI: 10.1038/Nature13138  0.184
2021 Sun Y, Zhou D, Rahman MR, Zhu J, Ghoneim D, Cox NJ, Beach TG, Wu C, Gamazon ER, Wu L. A transcriptome-wide association study identifies novel blood-based gene biomarker candidates for Alzheimer's disease risk. Human Molecular Genetics. PMID 34387340 DOI: 10.1093/hmg/ddab229  0.184
2019 El Charif O, Mapes B, Trendowski MR, Wheeler HE, Wing C, Dinh PC, Frisina RD, Feldman DR, Hamilton R, Vaughn DJ, Fung C, Kollmannsberger C, Mushiroda T, Kubo M, Gamazon ER, ... Cox N, et al. Clinical and Genome-Wide Analysis of Cisplatin-Induced Tinnitus Implicates Novel Ototoxic Mechanisms. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 30952644 DOI: 10.1158/1078-0432.CCR-18-3179  0.182
2019 El Charif O, Mapes B, Trendowski MR, Wheeler HE, Wing C, Dinh PC, Frisina RD, Feldman DR, Hamilton R, Vaughn DJ, Fung C, Kollmannsberger C, Mushiroda T, Kubo M, Gamazon ER, ... Cox N, et al. Clinical and Genome-Wide Analysis of Cisplatin-Induced Tinnitus Implicates Novel Ototoxic Mechanisms. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 30952644 DOI: 10.1158/1078-0432.CCR-18-3179  0.182
2015 Davis LK, Lee SH, Gamazon ER, Im H, Yu D, Williams S, Sullivan PF, Mathews C, Knowles J, Scharf J, Wray N, Cox NJ. Characterizing an inverse axis between orthogonal sources of genetic risk Genetic Epidemiology. 39: 542-543. DOI: 10.1002/Gepi.21916  0.181
2008 Huo D, Kim HJ, Adebamowo CA, Ogundiran TO, Akang EE, Campbell O, Adenipekun A, Niu Q, Sveen L, Fackenthal JD, Fackenthal DL, Das S, Cox N, Di Rienzo A, Olopade OI. Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans. Breast Cancer Research and Treatment. 110: 367-76. PMID 17909964 DOI: 10.1007/S10549-007-9720-7  0.181
2022 Jiang L, Kerchberger VE, Shaffer C, Dickson AL, Ormseth MJ, Daniel LL, Leon BGC, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Genome-wide association analyses of common infections in a large practice-based biobank. Bmc Genomics. 23: 672. PMID 36167494 DOI: 10.1186/s12864-022-08888-9  0.181
2015 Gamazon ER, Wheeler HE, Shah KP, Mozaffari SV, Aquino-Michaels K, Carroll RJ, Eyler AE, Denny JC, Nicolae DL, Cox NJ, Im HK. A gene-based association method for mapping traits using reference transcriptome data Nature Genetics. 47: 1091-1098. DOI: 10.1038/ng.3367  0.179
1996 Gregory CY, Evans K, Wijesuriya SD, Kermani S, Jay MR, Plant C, Cox N, Bird AC, Bhattacharya SS. The Gene Responsible for Autosomal Dominant Doyne's Honeycomb Retinal Dystrophy (DHRD) Maps to Chromosome 2p16 Human Molecular Genetics. 5: 1055-1059. PMID 8817347 DOI: 10.1093/Hmg/5.7.1055  0.179
2019 Dennis J, Cox N, Zhong X. Variability In Expression Of Tmem163 In Brain Cortex Is Associated With Resilience To Multiple Brain Damage Phenotypes In A Biobank Population European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.08.105  0.178
2007 Carter KW, Pluzhnikov A, Timms AE, Miceli-Richard C, Bourgain C, Wordsworth BP, Jean-Pierre H, Cox NJ, Palmer LJ, Breban M, Reveille JD, Brown MA. Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis. Rheumatology (Oxford, England). 46: 763-71. PMID 17259653 DOI: 10.1093/Rheumatology/Kel443  0.178
2024 Jia G, Li Y, Zhong X, Wang K, Pividori M, Alomairy R, Esposito A, Ltaief H, Terao C, Akiyama M, Matsuda K, Keyes DE, Im HK, Gojobori T, Kamatani Y, ... ... Cox NJ, et al. Author Correction: The high-dimensional space of human diseases built from diagnosis records and mapped to genetic loci. Nature Computational Science. 3: 658. PMID 38214655 DOI: 10.1038/s43588-023-00488-1  0.178
2022 Daniel LL, Dickson AL, Zanussi JT, Miller-Fleming TW, Straub PS, Wei WQ, Plummer WD, Dupont WD, Liu G, Anandi P, Reese TS, Birdwell KA, Kawai VK, Hung AM, Cox NJ, et al. Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity. Clinical and Translational Science. PMID 35118815 DOI: 10.1111/cts.13243  0.177
2000 Ober C, Leavitt SA, Tsalenko A, Howard TD, Hoki DM, Daniel R, Newman DL, Wu X, Parry R, Lester LA, Solway J, Blumenthal M, King RA, Xu J, Meyers DA, ... ... Cox NJ, et al. Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations. American Journal of Human Genetics. 66: 517-26. PMID 10677312 DOI: 10.1086/302781  0.177
2014 Fang H, Liu X, Ramírez J, Choudhury N, Kubo M, Im HK, Konkashbaev A, Cox NJ, Ratain MJ, Nakamura Y, O'Donnell PH. Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. The Pharmacogenomics Journal. 14: 564-72. PMID 24980783 DOI: 10.1038/tpj.2014.27  0.177
2016 El Charif O, Wheeler HE, Mushiroda T, Kubo M, Gamazon ER, Feldman DR, Hamilton RJ, Vaughn DJ, Beard CJ, Fung C, Albany C, Johnson E, Fossa S, Cox N, Einhorn LH, et al. Genome-wide association study of cisplatin-induced peripheral neuropathy (CIPN) in testicular cancer survivors. Journal of Clinical Oncology. 34: 4543-4543. DOI: 10.1200/JCO.2016.34.15_SUPPL.4543  0.175
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Cox NJ, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022  0.175
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, ... ... Cox NJ, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022  0.175
2000 Colilla S, Rotimi C, Cooper R, Goldberg J, Cox N. Genetic inheritance of body mass index in African-American and African families. Genetic Epidemiology. 18: 360-76. PMID 10797595 DOI: 10.1002/(SICI)1098-2272(200004)18:4<360::AID-GEPI8>3.0.CO;2-H  0.175
1985 Goldin LR, Cox NJ, Pauls DL, Gershon ES, Kidd KK. The detection of major loci by segregation and linkage analysis: a simulation study. Genetic Epidemiology. 1: 285-96. PMID 6599402 DOI: 10.1002/Gepi.1370010307  0.174
2011 Huang RS, Gamazon ER, Ziliak D, Wen Y, Im HK, Zhang W, Wing C, Duan S, Bleibel WK, Cox NJ, Dolan ME. Population differences in microRNA expression and biological implications. Rna Biology. 8: 692-701. PMID 21691150 DOI: 10.4161/Rna.8.4.16029  0.173
2022 Chung CP, Karakoc G, Liu G, Gamboa JL, Mosley JD, Cox NJ, Stein CM, Kawai V. Ancestry, and leucopenia in patients with systemic lupus erythematosus. Lupus Science & Medicine. 9. PMID 36376015 DOI: 10.1136/lupus-2022-000790  0.173
2018 Deming Y, Dumitrescu L, Barnes LL, Thambisetty M, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Huentelman M, Crane PK, Resnick SM, Keene CD, ... ... Cox NJ, et al. Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathologica. PMID 29967939 DOI: 10.1007/s00401-018-1881-4  0.172
2018 Deming Y, Dumitrescu L, Barnes LL, Thambisetty M, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Huentelman M, Crane PK, Resnick SM, Keene CD, ... ... Cox NJ, et al. Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathologica. PMID 29967939 DOI: 10.1007/s00401-018-1881-4  0.172
2008 Duan S, Zhang W, Bleibel WK, Cox NJ, Dolan ME. SNPinProbe_1.0: a database for filtering out probes in the Affymetrix GeneChip human exon 1.0 ST array potentially affected by SNPs. Bioinformation. 2: 469-70. PMID 18841244 DOI: 10.6026/97320630002469  0.172
1998 Cook EH, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. American Journal of Human Genetics. 62: 1077-83. PMID 9545402 DOI: 10.1086/301832  0.172
2004 Ng MC, So WY, Cox NJ, Lam VK, Cockram CS, Critchley JA, Bell GI, Chan JC. Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Diabetes. 53: 1609-13. PMID 15161769 DOI: 10.2337/Diabetes.53.6.1609  0.172
2013 Urbanek M, Hayes MG, Armstrong LL, Morrison J, Lowe LP, Badon SE, Scheftner D, Pluzhnikov A, Levine D, Laurie CC, McHugh C, Ackerman CM, Mirel DB, Doheny KF, Guo C, ... ... Cox NJ, et al. The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study. Human Molecular Genetics. 22: 3583-96. PMID 23575227 DOI: 10.1093/Hmg/Ddt168  0.171
2016 Huo D, Feng Y, Haddad S, Zheng Y, Yao S, Han YJ, Ogundiran TO, Adebamowo C, Ojengbede O, Falusi AG, Zheng W, Blot W, Cai Q, Signorello L, John EM, ... ... Cox NJ, et al. Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. Human Molecular Genetics. 25: 4835-4846. PMID 28171663 DOI: 10.1093/Hmg/Ddw305  0.171
2016 Huo D, Feng Y, Haddad S, Zheng Y, Yao S, Han YJ, Ogundiran TO, Adebamowo C, Ojengbede O, Falusi AG, Zheng W, Blot W, Cai Q, Signorello L, John EM, ... ... Cox NJ, et al. Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. Human Molecular Genetics. 25: 4835-4846. PMID 28171663 DOI: 10.1093/Hmg/Ddw305  0.171
2014 Travis LB, Fossa SD, Sesso HD, Frisina RD, Herrmann DN, Beard CJ, Feldman DR, Pagliaro LC, Miller RC, Vaughn DJ, Einhorn LH, Cox NJ, Dolan ME. Chemotherapy-induced peripheral neurotoxicity and ototoxicity: new paradigms for translational genomics. Journal of the National Cancer Institute. 106. PMID 24623533 DOI: 10.1093/jnci/dju044  0.171
2016 Huo D, Feng Y, Haddad S, Zheng Y, Yao S, Han YJ, Ogundiran TO, Adebamowo C, Ojengbede O, Falusi AG, Zheng W, Blot W, Cai Q, Signorello L, John EM, ... ... Cox NJ, et al. Genome-wide Association Studies in Women of African Ancestry Identified 3q26.21 as a Novel Susceptibility Locus for Estrogen Receptor Negative Breast Cancer. Human Molecular Genetics. PMID 27594435 DOI: 10.1093/hmg/ddw305  0.171
2014 Zheng Y, Huo D, Ogundiran TO, Falusi AG, Ojengbede O, Adebamowo C, Blot WJ, Zheng W, Cai Q, Signorello LB, Nathanson KL, Domchek SM, Rebbeck TR, Simon MS, Hennis AJM, ... ... Cox NJ, et al. Abstract B11: Replication of previously identified breast cancer susceptibility loci in a breast cancer case-control study on women of African ancestry Cancer Epidemiology, Biomarkers & Prevention. 23. DOI: 10.1158/1538-7755.Disp13-B11  0.171
1993 Stoffel M, Xiang KS, Espinosa R, Cox NJ, Le Beau MM, Bell GI. cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young. Human Molecular Genetics. 2: 1-4. PMID 8490617 DOI: 10.1093/Hmg/2.1.1  0.17
1996 Iwasaki N, Kawamura M, Yamagata K, Cox NJ, Karibe S, Ohgawara H, Inagaki N, Seino S, Bell GI, Omori Y. Identification of microsatellite markers near the human genes encoding the β-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese Diabetes. 45: 267-269. PMID 8549873 DOI: 10.2337/Diab.45.2.267  0.17
2004 Cox NJ. Human genetics: an expression of interest. Nature. 430: 733-4. PMID 15306793 DOI: 10.1038/430733a  0.17
1985 Cox NJ, Suarez BK. Genetic analysis workshop III: Two‐point linkage analysis on pedigrees, nuclear families, and sibships Genetic Epidemiology. 2: 205-206. DOI: 10.1002/gepi.1370020215  0.17
1993 Ambrose NG, Yairi E, Cox N. Genetic aspects of early childhood stuttering. Journal of Speech and Hearing Research. 36: 701-6. PMID 8377483 DOI: 10.1044/Jshr.3604.701  0.169
1984 Cox NJ, Kramer PL, Kidd KK. Segregation analyses of stuttering. Genetic Epidemiology. 1: 245-53. PMID 6549563 DOI: 10.1002/Gepi.1370010304  0.168
2015 Evans PD, Mueller KL, Gamazon ER, Cox NJ, Tomblin JB. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Genes, Brain, and Behavior. 14: 387-97. PMID 25997078 DOI: 10.1111/Gbb.12223  0.168
2014 Wu K, Gamazon ER, Im HK, Geeleher P, White SR, Solway J, Clemmer GL, Weiss ST, Tantisira KG, Cox NJ, Ratain MJ, Huang RS. Genome-wide interrogation of longitudinal FEV1 in children with asthma. American Journal of Respiratory and Critical Care Medicine. 190: 619-27. PMID 25221879 DOI: 10.1164/Rccm.201403-0460Oc  0.168
2014 Wu K, Gamazon ER, Im HK, Geeleher P, White SR, Solway J, Clemmer GL, Weiss ST, Tantisira KG, Cox NJ, Ratain MJ, Huang RS. Genome-wide interrogation of longitudinal FEV1 in children with asthma. American Journal of Respiratory and Critical Care Medicine. 190: 619-27. PMID 25221879 DOI: 10.1164/Rccm.201403-0460Oc  0.168
2014 Grassi MA, Rao V, Winkler KP, Zhang W, Bogaard JD, Chen S, LaCroix B, Lenkala D, Rehman J, Malik AB, Cox NJ, Huang RS. Genetic variation is the major determinant of individual differences in leukocyte endothelial adhesion. Plos One. 9: e87883. PMID 24520339 DOI: 10.1371/Journal.Pone.0087883  0.167
2000 Hinokio Y, Horikawa Y, Furuta H, Cox NJ, Iwasaki N, Honda M, Ogata M, Iwamoto Y, Bell GI. β-cell transcription factors and diabetes: No evidence for diabetes- associated mutations in the hepatocyte nuclear factor-3β gene (HNF3B) in Japanese patients with maturity-onset diabetes of the young Diabetes. 49: 302-305. PMID 10868948 DOI: 10.2337/Diabetes.49.2.302  0.166
2015 O'Donnell PH, Trubetskoy V, Nurhussein-Patterson A, Hall JP, Huo D, Fleming GF, Ingle JN, Mayer IA, Morrow PKH, Storniolo AM, Forero-Torres A, Poznak CHV, Merkel DE, Rosner GL, Olopade OI, ... ... Cox N, et al. Clinical evaluation of germline polymorphisms (SNPs) associated with capecitabine (C) toxicity (tox) in metastatic breast cancer (MBC). Journal of Clinical Oncology. 33: 1049-1049. DOI: 10.1200/Jco.2015.33.15_Suppl.1049  0.166
2015 Trubetskoy V, Rodriguez A, Dave U, Campbell N, Crawford EL, Cook EH, Sutcliffe JS, Foster I, Madduri R, Cox NJ, Davis LK. Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes. Bioinformatics (Oxford, England). 31: 187-93. PMID 25270638 DOI: 10.1093/Bioinformatics/Btu591  0.166
2015 Trubetskoy V, Rodriguez A, Dave U, Campbell N, Crawford EL, Cook EH, Sutcliffe JS, Foster I, Madduri R, Cox NJ, Davis LK. Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes. Bioinformatics (Oxford, England). 31: 187-93. PMID 25270638 DOI: 10.1093/Bioinformatics/Btu591  0.166
2015 Maitland ML, Xu CF, Cheng YC, Kistner-Griffin E, Ryan KA, Karrison TG, Das S, Torgerson D, Gamazon ER, Thomeas V, Levine MR, Wilson PA, Bing N, Liu Y, Cardon LR, ... ... Cox NJ, et al. Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of Pazopanib. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 21: 365-72. PMID 25411163 DOI: 10.1158/1078-0432.Ccr-14-1683  0.165
2015 Maitland ML, Xu CF, Cheng YC, Kistner-Griffin E, Ryan KA, Karrison TG, Das S, Torgerson D, Gamazon ER, Thomeas V, Levine MR, Wilson PA, Bing N, Liu Y, Cardon LR, ... ... Cox NJ, et al. Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of Pazopanib. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 21: 365-72. PMID 25411163 DOI: 10.1158/1078-0432.Ccr-14-1683  0.165
1997 Kong A, Frigge M, Bell GI, Lander ES, Daly MJ, Cox NJ. Diabetes, dependence, asymptotics, selection and significance. Nature Genetics. 17: 148. PMID 9326932 DOI: 10.1038/Ng1097-148  0.165
2004 Schulze TG, Buervenich S, Badner JA, Steele CJ, Detera-Wadleigh SD, Dick D, Foroud T, Cox NJ, MacKinnon DF, Potash JB, Berrettini WH, Byerley W, Coryell W, DePaulo JR, Gershon ES, et al. Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees. Biological Psychiatry. 56: 18-23. PMID 15219468 DOI: 10.1016/J.Biopsych.2004.04.004  0.165
2014 Liu W, Ramírez J, Gamazon ER, Mirkov S, Chen P, Wu K, Sun C, Cox NJ, Cook E, Das S, Ratain MJ. Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver. Human Molecular Genetics. 23: 5558-69. PMID 24879639 DOI: 10.1093/hmg/ddu268  0.163
2014 Liu W, Ramírez J, Gamazon ER, Mirkov S, Chen P, Wu K, Sun C, Cox NJ, Cook E, Das S, Ratain MJ. Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver. Human Molecular Genetics. 23: 5558-69. PMID 24879639 DOI: 10.1093/hmg/ddu268  0.163
2006 Kurz T, Hoffjan S, Hayes MG, Schneider D, Nicolae R, Heinzmann A, Jerkic SP, Parry R, Cox NJ, Deichmann KA, Ober C. Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci. The Journal of Allergy and Clinical Immunology. 118: 396-402. PMID 16890764 DOI: 10.1016/j.jaci.2006.04.036  0.163
2003 Zhou YP, Sreenan S, Pan CY, Currie KP, Bindokas VP, Horikawa Y, Lee JP, Ostrega D, Ahmed N, Baldwin AC, Cox NJ, Fox AP, Miller RJ, Bell GI, Polonsky KS. A 48-hour exposure of pancreatic islets to calpain inhibitors impairs mitochondrial fuel metabolism and the exocytosis of insulin. Metabolism: Clinical and Experimental. 52: 528-34. PMID 12759879 DOI: 10.1053/Meta.2003.50091  0.163
2018 Choudhury N, Evans P, Ingle JN, Mayer IA, Morrow PKH, Storniolo AM, Forero-Torres A, Poznak CHV, Merkel DE, Dees EC, Fleming GF, Hahn OM, Hoffman PC, Olopade OI, Cox N, et al. Clinical evaluation of germline polymorphisms (SNPs) associated with disease response to capecitabine in metastatic breast cancer (MBC) (TBCRC 015). Journal of Clinical Oncology. 36: 1071-1071. DOI: 10.1200/Jco.2018.36.15_Suppl.1071  0.163
1996 Stoffel M, Le Beau MM, Espinosa R, Bohlander SF, Le Paslier D, Cohen D, Xiang KS, Cox NJ, Fajans SS, Bell GI. A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene. Proceedings of the National Academy of Sciences of the United States of America. 93: 3937-41. PMID 8632993 DOI: 10.1073/Pnas.93.9.3937  0.163
2004 Ng MC, So WY, Lam VK, Cockram CS, Bell GI, Cox NJ, Chan JC. Genome-wide scan for metabolic syndrome and related quantitative traits in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Diabetes. 53: 2676-83. PMID 15448100 DOI: 10.2337/Diabetes.53.10.2676  0.163
2003 Naoumova RP, Bonney SA, Eichenbaum-Voline S, Patel HN, Jones B, Jones EL, Amey J, Colilla S, Neuwirth CK, Allotey R, Seed M, Betteridge DJ, Galton DJ, Cox NJ, Bell GI, et al. Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 2070-7. PMID 14500288 DOI: 10.1161/01.Atv.0000095975.35247.9F  0.162
2002 Hara M, Alcoser SY, Qaadir A, Beiswenger KK, Cox NJ, Ehrmann DA. Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene. The Journal of Clinical Endocrinology and Metabolism. 87: 772-5. PMID 11836319 DOI: 10.1210/Jcem.87.2.8255  0.161
2008 Hoop JG, Roberts LW, Green Hammond KA, Cox NJ. Psychiatrists' attitudes regarding genetic testing and patient safeguards: a preliminary study. Genetic Testing. 12: 245-52. PMID 18452395 DOI: 10.1089/gte.2007.0097  0.16
1995 Tsaur ML, Menzel S, Lai FP, Espinosa R, Concannon P, Spielman RS, Hanis CL, Cox NJ, Le Beau MM, German MS. Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM. Diabetes. 44: 592-6. PMID 7729621 DOI: 10.2337/Diab.44.5.592  0.16
2013 Ratain MJ, Sun J, Nakamura Y, Cox NJ, Sahmoud T, Stephens P, Chen D, Miller VA, Ross JS, Yelensky R. Frequent LOH of CYP2D6 in ER+ breast cancer determined by next-generation sequencing (NGS). Journal of Clinical Oncology. 31: 534-534. DOI: 10.1200/JCO.2013.31.15_SUPPL.534  0.16
1997 Cook EH, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal BL. Evidence of linkage between the serotonin transporter and autistic disorder. Molecular Psychiatry. 2: 247-50. PMID 9152989 DOI: 10.1038/Sj.Mp.4000266  0.159
2011 Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH, Macdonald RL, Sutcliffe JS. Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism. Molecular Psychiatry. 16: 86-96. PMID 19935738 DOI: 10.1038/Mp.2009.118  0.158
2004 Abecasis G, Cox N, Daly MJ, Kruglyak L, Laird N, Markianos K, Patterson N. No bias in linkage analysis. American Journal of Human Genetics. 75: 722-3; author reply . PMID 15338460 DOI: 10.1086/424757  0.156
1988 Vinik AJ, Cox NJ, Xiang K, Fajans SS, Bell GI. Linkage studies of maturity onset diabetes of the young--R.W. pedigree. Diabetologia. 31: 778-778. PMID 3240841 DOI: 10.1007/Bf00274785  0.156
2004 Lindstrom SE, Cox NJ, Klimov A. Genetic analysis of human H2N2 and early H3N2 influenza viruses, 1957-1972: evidence for genetic divergence and multiple reassortment events. Virology. 328: 101-19. PMID 15380362 DOI: 10.1016/j.virol.2004.06.009  0.156
1995 Glaser B, Chiu KC, Liu L, Anker R, Nestorowicz A, Cox NJ, Landau H, Kaiser N, Thornton PS, Stanley CA. Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews. Human Molecular Genetics. 4: 879-86. PMID 7633448 DOI: 10.1093/HMG/4.5.879  0.155
2004 Blumenthal MN, Ober C, Beaty TH, Bleecker ER, Langefeld CD, King RA, Lester L, Cox N, Barnes K, Togias A, Mathias R, Meyers DA, Oetting W, Rich SS. Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA). Genes and Immunity. 5: 226-31. PMID 15029235 DOI: 10.1038/Sj.Gene.6364063  0.155
1989 Cox NJ, Spielman RS. The insulin gene and susceptibility to IDDM. Genetic Epidemiology. 6: 65-9. PMID 2567260 DOI: 10.1002/GEPI.1370060113  0.155
2021 Liu D, Zhu J, Zhou D, Nikas EG, Mitanis NT, Sun Y, Wu C, Mancuso N, Cox NJ, Wang L, Freedland SJ, Haiman CA, Gamazon ER, Nikas JB, Wu L. A transcriptome-wide association study identifies novel candidate susceptibility genes for prostate cancer risk. International Journal of Cancer. PMID 34520569 DOI: 10.1002/ijc.33808  0.155
2011 Huang RS, Gamazon ER, Ziliak D, Zhang W, Im HK, Wing C, Duan S, Bleibel WK, Cox NJ, Dolan ME. Abstract 4731: Population specific microRNA expression and biological implications Cancer Research. 71: 4731-4731. DOI: 10.1158/1538-7445.Am2011-4731  0.154
1995 Weiss RE, Sunthornthepvarakul T, Angkeow P, Marcus-Bagley D, Cox N, Alper CA, Refetoff S. Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred. The Journal of Clinical Endocrinology and Metabolism. 80: 116-21. PMID 7829599 DOI: 10.1210/Jcem.80.1.7829599  0.154
2001 Colilla S, Cox NJ, Ehrmann DA. Heritability of insulin secretion and insulin action in women with polycystic ovary syndrome and their first degree relatives. The Journal of Clinical Endocrinology and Metabolism. 86: 2027-31. PMID 11344202 DOI: 10.1210/JCEM.86.5.7518  0.154
2015 Kutny MA, Alonzo TA, Gamazon ER, Gerbing RB, Geraghty D, Lange B, Heerema NA, Sung L, Aplenc R, Franklin J, Raimondi SC, Hirsch BA, Konkashbaev A, Cox NJ, Onel K, et al. Ethnic variation of TET2 SNP rs2454206 and association with clinical outcome in childhood AML: a report from the Children's Oncology Group. Leukemia. PMID 26126966 DOI: 10.1038/Leu.2015.171  0.154
2016 Gamazon ER, Wheeler HE, Frisina RD, El Charif O, Mushiroda T, Kubo M, Ardeshir-Rouhani-Fard S, Feldman DR, Hamilton RJ, Vaughn DJ, Beard CJ, Fung C, Fossa SD, Einhorn LH, Cox N, et al. Variation in protein-coding sequence and the genetic basis of cisplatin-induced toxicities among testicular cancer survivors (TCS) in the Platinum Study. Journal of Clinical Oncology. 34: 1537-1537. DOI: 10.1200/JCO.2016.34.15_SUPPL.1537  0.153
2006 Suresh R, Ambrose N, Roe C, Pluzhnikov A, Wittke-Thompson JK, Ng MC, Wu X, Cook EH, Lundstrom C, Garsten M, Ezrati R, Yairi E, Cox NJ. New complexities in the genetics of stuttering: significant sex-specific linkage signals. American Journal of Human Genetics. 78: 554-63. PMID 16532387 DOI: 10.1086/501370  0.153
2006 Nicolae DL, Wu X, Miyake K, Cox NJ. GEL: a novel genotype calling algorithm using empirical likelihood. Bioinformatics (Oxford, England). 22: 1942-7. PMID 16809396 DOI: 10.1093/bioinformatics/btl341  0.153
2003 Colilla S, Nicolae D, Pluzhnikov A, Blumenthal MN, Beaty TH, Bleecker ER, Lange EM, Rich SS, Meyers DA, Ober C, Cox NJ. Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. The Journal of Allergy and Clinical Immunology. 111: 840-6. PMID 12704367 DOI: 10.1067/Mai.2003.170  0.152
2012 O'Donnell PH, Bush A, Spitz J, Danahey K, Saner D, Das S, Cox NJ, Ratain MJ. The 1200 patients project: creating a new medical model system for clinical implementation of pharmacogenomics. Clinical Pharmacology and Therapeutics. 92: 446-9. PMID 22929923 DOI: 10.1038/clpt.2012.117  0.152
2012 Gamazon ER, Ziliak D, Im HK, LaCroix B, Park DS, Cox NJ, Huang RS. Genetic architecture of microRNA expression: implications for the transcriptome and complex traits. American Journal of Human Genetics. 90: 1046-63. PMID 22658545 DOI: 10.1016/j.ajhg.2012.04.023  0.152
2003 Canizales-Quinteros S, Aguilar-Salinas CA, Reyes-Rodríguez E, Riba L, Rodríguez-Torres M, Ramírez-Jiménez S, Huertas-Vázquez A, Fragoso-Ontiveros V, Zentella-Dehesa A, Ventura-Gallegos JL, Vega-Hernández G, López-Estrada A, Aurón-Gómez M, Gómez-Pérez F, Rull J, ... Cox NJ, et al. Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia. Circulation Research. 92: 569-76. PMID 12609970 DOI: 10.1161/01.Res.0000064174.69165.66  0.151
2003 Iwasaki N, Cox NJ, Wang YQ, Schwarz PEH, Bell GI, Honda M, Imura M, Ogata M, Saito M, Kamatani N, Iwamoto Y. Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects Diabetes. 52: 209-213. PMID 12502515 DOI: 10.2337/Diabetes.52.1.209  0.15
1997 Ober C, Weitkamp LR, Cox N, Dytch H, Kostyu D, Elias S. HLA and mate choice in humans. American Journal of Human Genetics. 61: 497-504. PMID 9326314 DOI: 10.1086/515511  0.15
2000 Cox N, Cook E, Ambrose N, Yairi E, Rydmarker S, Lundström C, Garsten M, Hildesheimer M, Ezrati-Vinacour R. The Illinois-Sweden-Israel genetics of stuttering projects Journal of Fluency Disorders. 25: 179. DOI: 10.1016/S0094-730X(00)80199-0  0.149
2012 Zheng Y, Ogundiran TO, Adebamowo C, Nathanson KL, Domchek SM, Rebbeck TR, Simon MS, John EM, Hennis A, Nemesure B, Wu SY, Leske MC, Ambs S, Niu Q, Zhang J, ... Cox NJ, et al. Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry. Breast Cancer Research and Treatment. 132: 341-5. PMID 22134622 DOI: 10.1007/S10549-011-1890-7  0.148
2011 Gamazon ER, Im HK, O'Donnell PH, Ziliak D, Stark AL, Cox NJ, Dolan ME, Huang RS. Comprehensive evaluation of the contribution of X chromosome genes to platinum sensitivity. Molecular Cancer Therapeutics. 10: 472-80. PMID 21252287 DOI: 10.1158/1535-7163.MCT-10-0910  0.148
2003 Ksiazek TG, Erdman D, Goldsmith CS, Zaki SR, Peret T, Emery S, Tong S, Urbani C, Comer JA, Lim W, Rollin PE, Dowell SF, Ling AE, Humphrey CD, Shieh WJ, ... ... Cox N, et al. A novel coronavirus associated with severe acute respiratory syndrome. The New England Journal of Medicine. 348: 1953-66. PMID 12690092 DOI: 10.1056/NEJMoa030781  0.145
1988 Price RA, Cox NJ, Spielman RS, Van Loon JA, Maidak BL, Weinshilboum RM. Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity. Genetic Epidemiology. 5: 1-15. PMID 3162891 DOI: 10.1002/gepi.1370050102  0.144
2012 O'Donnell PH, Stark AL, Gamazon ER, Wheeler HE, McIlwee BE, Gorsic L, Im HK, Huang RS, Cox NJ, Dolan ME. Identification of novel germline polymorphisms governing capecitabine sensitivity. Cancer. 118: 4063-73. PMID 22864933 DOI: 10.1002/cncr.26737  0.144
2017 Morselli LL, Gamazon ER, Tasali E, Cox NJ, Van Cauter E, Davis LK. Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study. Diabetes. PMID 29084784 DOI: 10.2337/db16-1229  0.144
2017 Morselli LL, Gamazon ER, Tasali E, Cox NJ, Van Cauter E, Davis LK. Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study. Diabetes. PMID 29084784 DOI: 10.2337/db16-1229  0.144
2006 Dickel DE, Veenstra-VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH, Hanna GL. Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder. Archives of General Psychiatry. 63: 778-85. PMID 16818867 DOI: 10.1001/Archpsyc.63.7.778  0.143
2007 Zhang W, Bleibel WK, Roe CA, Cox NJ, Eileen Dolan M. Gender-specific differences in expression in human lymphoblastoid cell lines. Pharmacogenetics and Genomics. 17: 447-50. PMID 17502836 DOI: 10.1097/FPC.0b013e3280121ffe  0.143
1997 Kong A, Cox NJ. Allele-sharing models: LOD scores and accurate linkage tests. American Journal of Human Genetics. 61: 1179-88. PMID 9345087 DOI: 10.1086/301592  0.143
2019 Dennis J, Yengo-Kahn AM, Kirby P, Solomon GS, Cox NJ, Zuckerman SL. Diagnostic algorithms to study post-concussion syndrome using electronic health records: validating a method to capture an important patient population. Journal of Neurotrauma. PMID 30773988 DOI: 10.1089/neu.2018.5916  0.142
2019 Dennis J, Yengo-Kahn AM, Kirby P, Solomon GS, Cox NJ, Zuckerman SL. Diagnostic algorithms to study post-concussion syndrome using electronic health records: validating a method to capture an important patient population. Journal of Neurotrauma. PMID 30773988 DOI: 10.1089/neu.2018.5916  0.142
2023 Liu G, Jiang L, Kerchberger VE, Oeser A, Ihegword A, Dickson AL, Daniel LL, Shaffer C, Linton MF, Cox N, Chung CP, Wei WQ, Stein CM, Feng Q. The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach. Clinical and Translational Science. PMID 36645160 DOI: 10.1111/cts.13462  0.14
2008 Hoop JG, Roberts LW, Hammond KA, Cox NJ. Psychiatrists' attitudes, knowledge, and experience regarding genetics: a preliminary study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 439-49. PMID 18496226 DOI: 10.1097/GIM.0b013e318177014b  0.14
2014 Davis CT, Chen LM, Pappas C, Stevens J, Tumpey TM, Gubareva LV, Katz JM, Villanueva JM, Donis RO, Cox NJ. Use of highly pathogenic avian influenza A(H5N1) gain-of-function studies for molecular-based surveillance and pandemic preparedness. Mbio. 5. PMID 25505125 DOI: 10.1128/Mbio.02431-14  0.139
2014 Davis CT, Chen LM, Pappas C, Stevens J, Tumpey TM, Gubareva LV, Katz JM, Villanueva JM, Donis RO, Cox NJ. Use of highly pathogenic avian influenza A(H5N1) gain-of-function studies for molecular-based surveillance and pandemic preparedness. Mbio. 5. PMID 25505125 DOI: 10.1128/Mbio.02431-14  0.139
2017 Dennis J, Zuckerman S, Yengo-Kahn A, Cox N, Solomon G. 2456 Journal of Clinical and Translational Science. 1: 18-18. DOI: 10.1017/cts.2017.76  0.139
2022 Faucon A, Samaroo J, Ge T, Davis LK, Cox NJ, Tao R, Shuey MM. Improving the computation efficiency of polygenic risk score modeling: faster in Julia. Life Science Alliance. 5. PMID 35851544 DOI: 10.26508/lsa.202201382  0.135
2016 Geeleher P, Gamazon ER, Seoighe C, Cox NJ, Huang RS. Consistency in large pharmacogenomic studies. Nature. 540: E1-E2. PMID 27905415 DOI: 10.1038/nature19838  0.135
2016 Geeleher P, Gamazon ER, Seoighe C, Cox NJ, Huang RS. Consistency in large pharmacogenomic studies. Nature. 540: E1-E2. PMID 27905415 DOI: 10.1038/nature19838  0.135
2018 Gamazon ER, Trendowski MR, Wen Y, Wing C, Delaney SM, Huh W, Wong S, Cox NJ, Dolan ME. Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma. Scientific Reports. 8: 733. PMID 29335598 DOI: 10.1038/S41598-017-19004-3  0.134
2018 Gamazon ER, Trendowski MR, Wen Y, Wing C, Delaney SM, Huh W, Wong S, Cox NJ, Dolan ME. Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma. Scientific Reports. 8: 733. PMID 29335598 DOI: 10.1038/S41598-017-19004-3  0.134
1997 Marsh DG, Maestri NE, Freidhoff LR, Barnes KC, Togias A, Ehrlich E, Beaty T, Duffy D, Rosenthal R, Imani F, Dunston G, Furbert-Harris P, Malveaux F, Ober C, Cox NJ, et al. A genome-wide search for asthma susceptibility loci in ethnically diverse populations Nature Genetics. 15: 389-392. PMID 9090385 DOI: 10.1038/Ng0497-389  0.133
2023 Chung CP, Karakoc G, Dickson A, Liu G, Gamboa JL, Mosley JD, Cox NJ, Kawai VK. and the risk of adverse renal outcomes in patients of African ancestry with systemic lupus erythematosus. Lupus. 32: 763-770. PMID 37105192 DOI: 10.1177/09612033231172660  0.132
2017 Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism. Molecular Autism. 8: 14. PMID 28344757 DOI: 10.1186/S13229-017-0130-3  0.132
2017 Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism. Molecular Autism. 8: 14. PMID 28344757 DOI: 10.1186/S13229-017-0130-3  0.132
2022 Jia G, Zhong X, Im HK, Schoettler N, Pividori M, Hogarth DK, Sperling AI, White SR, Naureckas ET, Lyttle CS, Terao C, Kamatani Y, Akiyama M, Matsuda K, Kubo M, ... Cox NJ, et al. Discerning asthma endotypes through comorbidity mapping. Nature Communications. 13: 6712. PMID 36344522 DOI: 10.1038/s41467-022-33628-8  0.13
2006 Suarez BK, Duan J, Sanders AR, Hinrichs AL, Jin CH, Hou C, Buccola NG, Hale N, Weilbaecher AN, Nertney DA, Olincy A, Green S, Schaffer AW, Smith CJ, Hannah DE, ... ... Cox NJ, et al. Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample. American Journal of Human Genetics. 78: 315-33. PMID 16400611 DOI: 10.1086/500272  0.129
2019 Moore AM, Mahoney E, Dumitrescu L, De Jager PL, Koran MEI, Petyuk VA, Robinson RA, Ruderfer DM, Cox NJ, Schneider JA, Bennett DA, Jefferson AL, Hohman TJ. APOE ε4-specific associations of VEGF gene family expression with cognitive aging and Alzheimer's disease. Neurobiology of Aging. PMID 31791659 DOI: 10.1016/J.Neurobiolaging.2019.10.021  0.129
2019 Moore AM, Mahoney E, Dumitrescu L, De Jager PL, Koran MEI, Petyuk VA, Robinson RA, Ruderfer DM, Cox NJ, Schneider JA, Bennett DA, Jefferson AL, Hohman TJ. APOE ε4-specific associations of VEGF gene family expression with cognitive aging and Alzheimer's disease. Neurobiology of Aging. PMID 31791659 DOI: 10.1016/J.Neurobiolaging.2019.10.021  0.129
2010 Daviglus ML, Bell CC, Berrettini W, Bowen PE, Connolly ES, Cox NJ, Dunbar-Jacob JM, Granieri EC, Hunt G, McGarry K, Patel D, Potosky AL, Sanders-Bush E, Silberberg D, Trevisan M. NIH state-of-the-science conference statement: Preventing Alzheimer's disease and cognitive decline. Nih Consensus and State-of-the-Science Statements. 27: 1-30. PMID 20445638  0.127
2002 Colilla S, Tsalenko A, Pluznikov A, Cox NJ. Genome-wide approaches for identifying interacting susceptibility regions for asthma. Genetic Epidemiology. S266-71. PMID 11793680 DOI: 10.1002/gepi.2001.21.s1.s266  0.126
2022 Shahbazi M, Zhang X, Dinh PC, Sanchez VA, Trendowski MR, Shuey MM, Nguyen T, Feldman DR, Vaughn DJ, Fung C, Kollmannsberger C, Martin NE, Einhorn LH, Cox NJ, Frisina RD, et al. Comprehensive association analysis of speech recognition thresholds after cisplatin-based chemotherapy in survivors of adult-onset cancer. Cancer Medicine. PMID 36097363 DOI: 10.1002/cam4.5218  0.125
2019 Psotka M, Thomeas-McEwing V, Gamazon E, Hirota T, Friedman P, Konkashbaev A, Kubo M, Nakamura Y, Ratain M, Benza R, Cox N, Gomberg-Maitland M, Maitland M. Two Polymorphic Gene Loci Associated with Treprostinil Dose in Pulmonary Arterial Hypertension The Journal of Heart and Lung Transplantation. 38: S208. DOI: 10.1016/J.HEALUN.2019.01.505  0.125
2016 Hohman TJ, Dumitrescu L, Cox NJ, Jefferson AL. Genetic resilience to amyloid related cognitive decline. Brain Imaging and Behavior. PMID 27743375 DOI: 10.1007/S11682-016-9615-5  0.124
2016 Hohman TJ, Dumitrescu L, Cox NJ, Jefferson AL. Genetic resilience to amyloid related cognitive decline. Brain Imaging and Behavior. PMID 27743375 DOI: 10.1007/S11682-016-9615-5  0.124
2015 Ardlie KG, DeLuca DS, Segrè AV, Sullivan TJ, Young TR, Gelfand ET, Trowbridge CA, Maller JB, Tukiainen T, Lek M, Ward LD, Kheradpour P, Iriarte B, Meng Y, Palmer CD, ... ... Cox NJ, et al. The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans Science. 348: 648-660. DOI: 10.1126/science.1262110  0.123
2010 Wakschlag LS, Kistner EO, Pine DS, Biesecker G, Pickett KE, Skol AD, Dukic V, Blair RJ, Leventhal BL, Cox NJ, Burns JL, Kasza KE, Wright RJ, Cook EH. Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior. Molecular Psychiatry. 15: 928-37. PMID 19255579 DOI: 10.1038/Mp.2009.22  0.122
2006 Mehlmann M, Dawson ED, Townsend MB, Smagala JA, Moore CL, Smith CB, Cox NJ, Kuchta RD, Rowlen KL. Robust sequence selection method used to develop the FluChip diagnostic microarray for influenza virus. Journal of Clinical Microbiology. 44: 2857-62. PMID 16891503 DOI: 10.1128/Jcm.00135-06  0.122
2014 Geeleher P, Cox NJ, Huang RS. Clinical drug response can be predicted using baseline gene expression levels and in vitro drug sensitivity in cell lines. Genome Biology. 15: R47. PMID 24580837 DOI: 10.1186/gb-2014-15-3-r47  0.122
2013 Gamazon ER, Innocenti F, Wei R, Wang L, Zhang M, Mirkov S, Ramírez J, Huang RS, Cox NJ, Ratain MJ, Liu W. A genome-wide integrative study of microRNAs in human liver. Bmc Genomics. 14: 395. PMID 23758991 DOI: 10.1186/1471-2164-14-395  0.121
2021 Ross EJ, Gordon ER, Sothers H, Darji R, Baron O, Haithcock D, Prabhakarpandian B, Pant K, Myers RM, Cooper SJ, Cox NJ. Three dimensional modeling of biologically relevant fluid shear stress in human renal tubule cells mimics in vivo transcriptional profiles. Scientific Reports. 11: 14053. PMID 34234242 DOI: 10.1038/s41598-021-93570-5  0.121
2021 Visscher PM, Yengo L, Cox NJ, Wray NR. Discovery and implications of polygenicity of common diseases. Science (New York, N.Y.). 373: 1468-1473. PMID 34554790 DOI: 10.1126/science.abi8206  0.12
2024 Cox NJ. 2023 ASHG Leadership Award. American Journal of Human Genetics. 111: 429-432. PMID 38458166 DOI: 10.1016/j.ajhg.2024.02.003  0.12
2019 Smart CD, Shuey M, Elijovich F, Cox N, Madhur MS. Abstract P185: The Effect of Anti-Interleukin-17A Biologic Therapies on Cardiovascular Outcomes in Patients With Psoriasis Hypertension. 74. DOI: 10.1161/hyp.74.suppl_1.p185  0.12
2014 Rith S, Davis CT, Duong V, Sar B, Horm SV, Chin S, Ly S, Laurent D, Richner B, Oboho I, Jang Y, Davis W, Thor S, Balish A, Iuliano AD, ... ... Cox N, et al. Identification of molecular markers associated with alteration of receptor-binding specificity in a novel genotype of highly pathogenic avian influenza A(H5N1) viruses detected in Cambodia in 2013. Journal of Virology. 88: 13897-909. PMID 25210193 DOI: 10.1128/Jvi.01887-14  0.12
2015 Goetz MP, Sun JX, Suman VJ, Silva GO, Perou CM, Nakamura Y, Cox NJ, Stephens PJ, Miller VA, Ross JS, Chen D, Safgren SL, Kuffel MJ, Ames MM, Kalari KR, et al. Loss of heterozygosity at the CYP2D6 locus in breast cancer: implications for germline pharmacogenetic studies. Journal of the National Cancer Institute. 107. PMID 25490892 DOI: 10.1093/Jnci/Dju401  0.119
2015 Goetz MP, Sun JX, Suman VJ, Silva GO, Perou CM, Nakamura Y, Cox NJ, Stephens PJ, Miller VA, Ross JS, Chen D, Safgren SL, Kuffel MJ, Ames MM, Kalari KR, et al. Loss of heterozygosity at the CYP2D6 locus in breast cancer: implications for germline pharmacogenetic studies. Journal of the National Cancer Institute. 107. PMID 25490892 DOI: 10.1093/Jnci/Dju401  0.119
2011 Isakova-Sivak I, Chen LM, Matsuoka Y, Voeten JT, Kiseleva I, Heldens JG, den Bosch Hv, Klimov A, Rudenko L, Cox NJ, Donis RO. Genetic bases of the temperature-sensitive phenotype of a master donor virus used in live attenuated influenza vaccines: A/Leningrad/134/17/57 (H2N2). Virology. 412: 297-305. PMID 21315402 DOI: 10.1016/J.Virol.2011.01.004  0.119
2022 Rowland B, Sun Q, Wang W, Miller-Fleming T, Cox N, Graff M, Faucon A, Shuey MM, Blue EE, Auer P, Li Y, Sankaran VG, Reiner AP, Raffield LM. Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19. Medrxiv : the Preprint Server For Health Sciences. PMID 35262092 DOI: 10.1101/2022.02.28.22271562  0.119
2022 Akwo E, Pike MM, Ertuglu LA, Vartanian N, Farber-Eger E, Lipworth L, Perwad F, Siew E, Hung A, Bansal N, de Boer I, Kestenbaum B, Cox NJ, Ikizler TA, Wells Q, et al. Association of Genetically Predicted Fibroblast Growth Factor-23 with Heart Failure: A Mendelian Randomization Study. Clinical Journal of the American Society of Nephrology : Cjasn. 17: 1183-1193. PMID 35902130 DOI: 10.2215/CJN.00960122  0.118
2009 Garten RJ, Davis CT, Russell CA, Shu B, Lindstrom S, Balish A, Sessions WM, Xu X, Skepner E, Deyde V, Okomo-Adhiambo M, Gubareva L, Barnes J, Smith CB, Emery SL, ... ... Cox NJ, et al. Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans. Science (New York, N.Y.). 325: 197-201. PMID 19465683 DOI: 10.1126/Science.1176225  0.118
2015 Huan T, Rong J, Liu C, Zhang X, Tanriverdi K, Joehanes R, Chen BH, Murabito JM, Yao C, Courchesne P, Munson PJ, O'Donnell CJ, Cox N, Johnson AD, Larson MG, et al. Genome-wide identification of microRNA expression quantitative trait loci. Nature Communications. 6: 6601. PMID 25791433 DOI: 10.1038/Ncomms7601  0.117
2013 Trock SC, Burke SA, Cox NJ. Development of an influenza virologic risk assessment tool. Avian Diseases. 56: 1058-61. PMID 23402136 DOI: 10.1637/10204-041412-ResNote.1  0.117
2007 Hanna GL, Veenstra-Vanderweele J, Cox NJ, Van Etten M, Fischer DJ, Himle JA, Bivens NC, Wu X, Roe CA, Hennessy KA, Dickel DE, Leventhal BL, Cook EH. Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder. Biological Psychiatry. 62: 856-62. PMID 17544380 DOI: 10.1016/J.Biopsych.2007.01.008  0.116
2017 Mechanic LE, Lindström S, Daily KM, Sieberts SK, Amos CI, Chen HS, Cox NJ, Dathe M, Feuer EJ, Guertin MJ, Hoffman J, Liu Y, Moore JH, Myers CL, Ritchie MD, et al. Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology. Plos Genetics. 13: e1006945. PMID 28957327 DOI: 10.1371/Journal.Pgen.1006945  0.115
2017 Mechanic LE, Lindström S, Daily KM, Sieberts SK, Amos CI, Chen HS, Cox NJ, Dathe M, Feuer EJ, Guertin MJ, Hoffman J, Liu Y, Moore JH, Myers CL, Ritchie MD, et al. Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology. Plos Genetics. 13: e1006945. PMID 28957327 DOI: 10.1371/Journal.Pgen.1006945  0.115
2010 Balish AL, Davis CT, Saad MD, El-Sayed N, Esmat H, Tjaden JA, Earhart KC, Ahmed LE, Abd El-Halem M, Ali AH, Nassif SA, El-Ebiary EA, Taha M, Aly MM, Arafa A, ... ... Cox NJ, et al. Antigenic and genetic diversity of highly pathogenic avian influenza A (H5N1) viruses isolated in Egypt. Avian Diseases. 54: 329-34. PMID 20521654 DOI: 10.1637/8903-042909-Reg.1  0.115
2007 McDonald NJ, Smith CB, Cox NJ. Antigenic drift in the evolution of H1N1 influenza A viruses resulting from deletion of a single amino acid in the haemagglutinin gene. The Journal of General Virology. 88: 3209-13. PMID 18024888 DOI: 10.1099/vir.0.83184-0  0.115
1991 Mangklabruks A, Billerbeck AEC, Wajchenberg B, Knobel M, Cox NJ, Degroot LJ, Medeiros-Neto G. Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency Journal of Clinical Endocrinology and Metabolism. 72: 471-476. PMID 1671388 DOI: 10.1210/Jcem-72-2-471  0.115
2010 Stark AL, Zhang W, Zhou T, O'Donnell PH, Beiswanger CM, Huang RS, Cox NJ, Dolan ME. Population differences in the rate of proliferation of international HapMap cell lines. American Journal of Human Genetics. 87: 829-33. PMID 21109222 DOI: 10.1016/j.ajhg.2010.10.018  0.115
2021 Chowdhury F, Wang L, Al-Raqad M, Amor DJ, Baxová A, Bendová Š, Biamino E, Brusco A, Caluseriu O, Cox NJ, Froukh T, Gunay-Aygun M, Hančárová M, Haynes D, Heide S, et al. Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33824499 DOI: 10.1038/s41436-021-01129-6  0.114
2021 Chowdhury F, Wang L, Al-Raqad M, Amor DJ, Baxová A, Bendová Š, Biamino E, Brusco A, Caluseriu O, Cox NJ, Froukh T, Gunay-Aygun M, Hančárová M, Haynes D, Heide S, et al. Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33824499 DOI: 10.1038/s41436-021-01129-6  0.114
2014 Geeleher P, Cox N, Huang RS. pRRophetic: an R package for prediction of clinical chemotherapeutic response from tumor gene expression levels. Plos One. 9: e107468. PMID 25229481 DOI: 10.1371/journal.pone.0107468  0.112
1997 Lindner T, Gragnoli C, Schulze J, Rietzsch H, Petzold C, Schröder H, Cox NJ, Bell GI. The 31-cM Region of Chromosome 11 Including the Obesity Gene Tubby and ATP-Sensitive Potassium Channel Genes, SUR1 and Kir6.2, Does Not Contain a Major Susceptibility Locus for NIDDM in 127 Non-Hispanic White Affected Sibships Diabetes. 46: 1227-1229. PMID 9200660 DOI: 10.2337/Diab.46.7.1227  0.111
2006 Qin K, Ehrmann DA, Cox N, Refetoff S, Rosenfield RL. Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome. The Journal of Clinical Endocrinology and Metabolism. 91: 270-6. PMID 16263811 DOI: 10.1210/Jc.2005-2012  0.11
2019 Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Cox NJ, et al. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 31086353 DOI: 10.1038/S41588-019-0435-6  0.109
2019 Huckins LM, Dobbyn A, Ruderfer DM, Hoffman G, Wang W, Pardiñas AF, Rajagopal VM, Als TD, T Nguyen H, Girdhar K, Boocock J, Roussos P, Fromer M, Kramer R, Domenici E, ... ... Cox NJ, et al. Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. Nature Genetics. PMID 31086353 DOI: 10.1038/S41588-019-0435-6  0.109
2023 Schirle L, Samuels DC, Faucon A, Cox NJ, Bruehl S. Polygenic Contributions to Chronic Overlapping Pain Conditions in a Large Electronic Health Record Sample. The Journal of Pain. PMID 36736868 DOI: 10.1016/j.jpain.2023.01.018  0.109
Hide low-probability matches.