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Gail P. Jarvik - Publications

Affiliations: 
University of Washington, Seattle, Seattle, WA 
Area:
Public Health, Genetics
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Year Citation  Score
2021 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Jarvik GP, et al. The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 34887591 DOI: 10.1038/s41586-021-04064-3  0.312
2020 Namjou B, Stanaway IB, Lingren T, Mentch FD, Benoit B, Dikilitas O, Niu X, Shang N, Shoemaker AH, Carey DJ, Mirshahi T, Singh R, Nestor JG, Hakonarson H, Denny JC, ... ... Jarvik GP, et al. Evaluation of the MC4R gene across eMERGE network identifies many unreported obesity-associated variants. International Journal of Obesity (2005). PMID 32952152 DOI: 10.1038/S41366-020-00675-4  0.373
2020 Thomas M, Sakoda LC, Hoffmeister M, Rosenthal EA, Lee JK, van Duijnhoven FJB, Platz EA, Wu AH, Dampier CH, de la Chapelle A, Wolk A, Joshi AD, Burnett-Hartman A, Gsur A, Lindblom A, ... ... Jarvik GP, et al. Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk. American Journal of Human Genetics. PMID 32758450 DOI: 10.1016/J.Ajhg.2020.07.006  0.348
2020 Makhnoon S, Bowen DJ, Shirts BH, Fullerton SM, Meischke HW, Larson EB, Ralston JD, Leppig K, Crosslin DR, Veenstra D, Jarvik GP. Relationship between genetic knowledge and familial communication of CRC risk and intent to communicate CRCP genetic information: insights from FamilyTalk eMERGE III. Translational Behavioral Medicine. PMID 32579152 DOI: 10.1093/Tbm/Ibaa054  0.34
2020 Lynch JA, Sharp RR, Aufox SA, Bland ST, Blout C, Bowen DJ, Buchanan AH, Halverson C, Harr M, Hebbring SJ, Henrikson N, Hoell C, Holm IA, Jarvik G, Kullo IJ, et al. Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network. Journal of Personalized Medicine. 10. PMID 32413979 DOI: 10.3390/Jpm10020038  0.369
2020 Dikilitas O, Schaid DJ, Kosel ML, Carroll RJ, Chute CG, Denny JA, Fedotov A, Feng Q, Hakonarson H, Jarvik GP, Lee MTM, Pacheco JA, Rowley R, Sleiman PM, Stein CM, et al. Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups. American Journal of Human Genetics. 106: 707-716. PMID 32386537 DOI: 10.1016/J.Ajhg.2020.04.002  0.368
2020 Mosley JD, Levinson RT, Farber-Eger E, Edwards TL, Hellwege JN, Hung AM, Giri A, Shuey MM, Shaffer CM, Shi M, Brittain EL, Chung WK, Kullo IJ, Arruda-Olson AM, Jarvik GP, et al. The polygenic architecture of left ventricular mass mirrors the clinical epidemiology. Scientific Reports. 10: 7561. PMID 32372017 DOI: 10.1038/S41598-020-64525-Z  0.341
2020 Wiesner GL, Kulchak Rahm A, Appelbaum P, Aufox S, Bland ST, Blout CL, Christensen KD, Chung WK, Clayton EW, Green RC, Harr MH, Henrikson N, Hoell C, Holm IA, Jarvik GP, et al. Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network. Journal of Personalized Medicine. 10. PMID 32349224 DOI: 10.3390/Jpm10020030  0.333
2020 Zhang Y, Ho K, Keaton JM, Hartzel DN, Day F, Justice AE, Josyula NS, Pendergrass SA, Actkins K, Davis LK, Velez Edwards DR, Holohan B, Ramirez A, Stanaway IB, Crosslin DR, ... Jarvik GP, et al. A genome-wide association study of polycystic ovary syndrome identified from electronic health records. American Journal of Obstetrics and Gynecology. PMID 32289280 DOI: 10.1016/J.Ajog.2020.04.004  0.325
2019 Williams MS, Taylor CO, Walton NA, Goehringer SR, Aronson S, Freimuth RR, Rasmussen LV, Hall ES, Prows CA, Chung WK, Fedotov A, Nestor J, Weng C, Rowley RK, Wiesner GL, ... Jarvik GP, et al. Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network. Frontiers in Genetics. 10: 1059. PMID 31737042 DOI: 10.3389/Fgene.2019.01059  0.33
2019 Glessner JT, Li J, Desai A, Palmer M, Kim D, Lucas AM, Chang X, Connolly JJ, Almoguera B, Harley JB, Jarvik GP, Ritchie MD, Sleiman PMA, Roden DM, Crosslin D, et al. CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease. International Journal of Cardiology. PMID 31447229 DOI: 10.1016/J.Ijcard.2019.07.058  0.34
2019 Gordon AS, Rosenthal EA, Carrell DS, Amendola LM, Dorschner MO, Scrol A, Stanaway IB, DeVange S, Ralston JD, Zouk H, Rehm HL, Larson E, Crosslin DR, Leppig KA, Jarvik GP. Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting. American Journal of Human Genetics. PMID 31422818 DOI: 10.1016/J.Ajhg.2019.07.012  0.344
2019 Niu X, Amendola LM, Hart R, Bennette CS, Heagerty P, Horike-Pyne M, Trinidad SB, Rosenthal EA, Comstock B, Nefcy C, Hisama FM, Bennett RL, Grady WM, Gallego CJ, Tarczy-Hornoch P, ... ... Jarvik GP, et al. Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study. Contemporary Clinical Trials. 84: 105820. PMID 31400517 DOI: 10.1016/J.Cct.2019.105820  0.344
2019 Amendola LM, Hart MR, Bennett RL, Horike-Pyne M, Dorschner M, Shirts B, Jarvik GP. Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests. Journal of Genetic Counseling. PMID 31317629 DOI: 10.1002/Jgc4.1155  0.349
2019 Namjou B, Lingren T, Huang Y, Parameswaran S, Cobb BL, Stanaway IB, Connolly JJ, Mentch FD, Benoit B, Niu X, Wei WQ, Carroll RJ, Pacheco JA, Harley ITW, Divanovic S, ... ... Jarvik GP, et al. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Bmc Medicine. 17: 135. PMID 31311600 DOI: 10.1186/S12916-019-1364-Z  0.338
2019 Horowitz CR, Orlando LA, Slavotinek AM, Peterson J, Angelo F, Biesecker B, Bonham VL, Cameron LD, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, Hindorff LA, Jarvik GP, et al. The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research. American Journal of Human Genetics. PMID 31104772 DOI: 10.1016/J.Ajhg.2019.04.006  0.321
2019 Hellwege JN, Stallings S, Torstenson ES, Carroll R, Borthwick KM, Brilliant MH, Crosslin D, Gordon A, Hripcsak G, Jarvik GP, Linneman JG, Devi P, Peissig PL, Sleiman PAM, Hakonarson H, et al. Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network. Scientific Reports. 9: 6077. PMID 30988330 DOI: 10.1038/S41598-019-42427-Z  0.398
2019 Li M, Bennette CS, Amendola LM, Ragan Hart M, Heagerty P, Comstock B, Tarczy-Hornoch P, Fullerton SM, Regier DA, Burke W, Trinidad SB, Jarvik GP, Veenstra DL, Patrick DL. The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation. Journal of Genetic Counseling. 28: 477-490. PMID 30964586 DOI: 10.1007/S10897-018-0286-9  0.319
2019 Bombard Y, Brothers KB, Fitzgerald-Butt S, Garrison NA, Jamal L, James CA, Jarvik GP, McCormick JB, Nelson TN, Ormond KE, Rehm HL, Richer J, Souzeau E, Vassy JL, Wagner JK, et al. The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results. American Journal of Human Genetics. 104: 578-595. PMID 30951675 DOI: 10.1016/J.Ajhg.2019.02.025  0.38
2019 Chiang T, Liu X, Wu TJ, Hu J, Sedlazeck FJ, White S, Schaid D, Andrade M, Jarvik GP, Crosslin D, Stanaway I, Carrell DS, Connolly JJ, Hakonarson H, Groopman EE, et al. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30890783 DOI: 10.1038/S41436-019-0475-4  0.344
2019 Henrikson NB, Blasi PR, Fullerton SM, Grafton J, Leppig KA, Jarvik GP, Larson EB. "It would be so much easier": health system-led genetic risk notification-feasibility and acceptability of cascade screening in an integrated system. Journal of Community Genetics. PMID 30843145 DOI: 10.1007/S12687-019-00412-Z  0.322
2019 Justice AE, Karaderi T, Highland HM, Young KL, Graff M, Lu Y, Turcot V, Auer PL, Fine RS, Guo X, Schurmann C, Lempradl A, Marouli E, Mahajan A, Winkler TW, ... ... Jarvik GP, et al. Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nature Genetics. PMID 30778226 DOI: 10.1038/S41588-018-0334-2  0.32
2019 Safarova MS, Satterfield BA, Fan X, Austin EE, Ye Z, Bastarache L, Zheng N, Ritchie MD, Borthwick KM, Williams MS, Larson EB, Scrol A, Jarvik GP, Crosslin DR, Leppig K, et al. A phenome-wide association study to discover pleiotropic effects of , , and . Npj Genomic Medicine. 4: 3. PMID 30774981 DOI: 10.1038/S41525-019-0078-7  0.412
2019 Jorgenson E, Matharu N, Palmer MR, Yin J, Shan J, Hoffmann TJ, Thai KK, Zhou X, Hotaling JM, Jarvik GP, Ahituv N, Wessells H, Van Den Eeden SK. Reply to Liu et al.: Tissue specificity of gene expression and erectile dysfunction. Proceedings of the National Academy of Sciences of the United States of America. PMID 30755537 DOI: 10.1073/Pnas.1900162116  0.345
2018 Hall TO, Stanaway IB, Carrell DS, Carroll RJ, Denny JC, Hakonarson H, Larson EB, Mentch FD, Peissig PL, Pendergrass SA, Rosenthal EA, Jarvik GP, Crosslin DR. Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling. Genes and Immunity. PMID 30459343 DOI: 10.1038/S41435-018-0051-Y  0.348
2018 Rope AF, Kauffman TL, Himes P, Amendola LM, Punj S, Akkari Y, Potter A, Davis JV, Schneider JL, Reiss JA, Gilmore MJ, McMullen CK, Nickerson DA, Richards CS, Jarvik GP, et al. A case for expanding carrier testing to include actionable X-linked disorders. Clinical Case Reports. 6: 2092-2095. PMID 30455898 DOI: 10.1002/Ccr3.1806  0.322
2018 Stanaway IB, Hall TO, Rosenthal EA, Palmer M, Naranbhai V, Knevel R, Namjou-Khales B, Carroll RJ, Kiryluk K, Gordon AS, Linder J, Howell KM, Mapes BM, Lin FTJ, Joo YY, ... ... Jarvik GP, et al. The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype. Genetic Epidemiology. PMID 30298529 DOI: 10.1002/Gepi.22167  0.394
2018 Jorgenson E, Matharu N, Palmer MR, Yin J, Shan J, Hoffmann TJ, Thai KK, Zhou X, Hotaling JM, Jarvik GP, Ahituv N, Wessells H, Van Den Eeden SK. Genetic variation in the locus is associated with erectile dysfunction. Proceedings of the National Academy of Sciences of the United States of America. PMID 30297428 DOI: 10.1073/Pnas.1809872115  0.385
2018 Suri P, Palmer MR, Tsepilov YA, Freidin MB, Boer CG, Yau MS, Evans DS, Gelemanovic A, Bartz TM, Nethander M, Arbeeva L, Karssen L, Neogi T, Campbell A, Mellstrom D, ... ... Jarvik GP, et al. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain. Plos Genetics. 14: e1007601. PMID 30261039 DOI: 10.1371/Journal.Pgen.1007601  0.394
2018 Amendola LM, Berg JS, Horowitz CR, Angelo F, Bensen JT, Biesecker BB, Biesecker LG, Cooper GM, East K, Filipski K, Fullerton SM, Gelb BD, Goddard KAB, Hailu B, Hart R, ... ... Jarvik GP, et al. The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. American Journal of Human Genetics. 103: 319-327. PMID 30193136 DOI: 10.1016/J.Ajhg.2018.08.007  0.36
2018 Mosley JD, Feng Q, Wells QS, Van Driest SL, Shaffer CM, Edwards TL, Bastarache L, Wei WQ, Davis LK, McCarty CA, Thompson W, Chute CG, Jarvik GP, Gordon AS, Palmer MR, et al. A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Nature Communications. 9: 3522. PMID 30166544 DOI: 10.1038/S41467-018-05624-4  0.356
2018 Porter KM, Kauffman TL, Koenig BA, Lewis KL, Rehm HL, Richards CS, Strande NT, Tabor HK, Wolf SM, Yang Y, Amendola LM, Azzariti DR, Berg JS, Bergstrom K, Biesecker LG, ... ... Jarvik GP, et al. Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience. Molecular Genetics & Genomic Medicine. PMID 30133189 DOI: 10.1002/Mgg3.453  0.351
2018 Wang L, Pittman KJ, Barker JR, Salinas RE, Stanaway IB, Williams GD, Carroll RJ, Balmat T, Ingham A, Gopalakrishnan AM, Gibbs KD, Antonia AL, Heitman J, Lee SC, ... Jarvik GP, et al. An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease. Cell Host & Microbe. 24: 308-323.e6. PMID 30092202 DOI: 10.1016/J.Chom.2018.07.007  0.398
2018 Weymann D, Veenstra DL, Jarvik GP, Regier DA. Patient preferences for massively parallel sequencing genetic testing of colorectal cancer risk: a discrete choice experiment. European Journal of Human Genetics : Ejhg. PMID 29802320 DOI: 10.1038/S41431-018-0161-Z  0.339
2018 Punj S, Akkari Y, Huang J, Yang F, Creason A, Pak C, Potter A, Dorschner MO, Nickerson DA, Robertson PD, Jarvik GP, Amendola LM, Schleit J, Simpson DK, Rope AF, et al. Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory. American Journal of Human Genetics. PMID 29754767 DOI: 10.1016/J.Ajhg.2018.04.004  0.396
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, et al. Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. PMID 29703846 DOI: 10.1161/Circulationaha.117.031356  0.375
2018 Christensen KD, Bernhardt BA, Jarvik GP, Hindorff LA, Ou J, Biswas S, Powell BC, Grundmeier RW, Machini K, Karavite DJ, Pennington JW, Krantz ID, Berg JS, Goddard KAB. Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29388940 DOI: 10.1038/Gim.2017.243  0.377
2018 Fossey R, Kochan D, Winkler E, Pacyna JE, Olson J, Thibodeau S, Connolly JJ, Harr M, Behr MA, Prows CA, Cobb B, Myers MF, Leslie ND, Namjou-Khales B, Milo Rasouly H, ... ... Jarvik GP, et al. Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience. Journal of Personalized Medicine. 8. PMID 29301385 DOI: 10.3390/Jpm8010002  0.375
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Jarvik GP, et al. Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. 50: 26-41. PMID 29273807 DOI: 10.1038/S41588-017-0011-X  0.344
2017 Laurino MY, Truitt AR, Tenney L, Fisher D, Lindor NM, Veenstra D, Jarvik GP, Newcomb PA, Fullerton SM. Clinical verification of genetic results returned to research participants: findings from a Colon Cancer Family Registry. Molecular Genetics & Genomic Medicine. 5: 700-708. PMID 29178651 DOI: 10.1002/Mgg3.328  0.313
2017 Evans BJ, Jarvik GP. Impact of HIPAA's minimum necessary standard on genomic data sharing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28914268 DOI: 10.1038/Gim.2017.141  0.344
2017 Wolf SM, Amendola LM, Berg JS, Chung WK, Clayton EW, Green RC, Harris-Wai J, Henderson GE, Jarvik GP, Koenig BA, Lehmann LS, McGuire AL, O'Rourke P, Somkin C, Wilfond BS, et al. Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28858330 DOI: 10.1038/Gim.2017.137  0.311
2017 Holzinger ER, Verma SS, Moore CB, Hall M, De R, Gilbert-Diamond D, Lanktree MB, Pankratz N, Amuzu A, Burt A, Dale C, Dudek S, Furlong CE, Gaunt TR, Kim DS, ... ... Jarvik GP, et al. Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals. Biodata Mining. 10: 25. PMID 28770004 DOI: 10.1186/S13040-017-0145-5  0.312
2017 Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Jarvik GP, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916  0.363
2017 Mosley JD, Shoemaker MB, Wells QS, Darbar D, Shaffer CM, Edwards TL, Bastarache L, McCarty CA, Thompson W, Chute CG, Jarvik GP, Crosslin DR, Larson EB, Kullo IJ, Pacheco JA, et al. Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes. Circulation. Cardiovascular Genetics. 10. PMID 28416512 DOI: 10.1161/Circgenetics.116.001482  0.357
2017 Goodman JL, Amendola LM, Horike-Pyne M, Trinidad SB, Fullerton SM, Burke W, Jarvik GP. Discordance in selected designee for return of genomic findings in the event of participant death and estate executor. Molecular Genetics & Genomic Medicine. 5: 172-176. PMID 28361104 DOI: 10.1002/Mgg3.274  0.318
2017 Leppig KA, Thiese HA, Carrel D, Crosslin DR, Dorschner MO, Gordon AS, Hartzler A, Ralston J, Scrol A, Larson EB, Jarvik GP. Building a family network from genetic testing. Molecular Genetics & Genomic Medicine. 5: 122-129. PMID 28361098 DOI: 10.1002/Mgg3.259  0.358
2017 Sanderson SC, Brothers KB, Mercaldo ND, Clayton EW, Antommaria AH, Aufox SA, Brilliant MH, Campos D, Carrell DS, Connolly J, Conway P, Fullerton SM, Garrison NA, Horowitz CR, Jarvik GP, et al. Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US. American Journal of Human Genetics. PMID 28190457 DOI: 10.1016/J.Ajhg.2017.01.021  0.301
2017 Marouli E, Graff M, Medina-Gomez C, Lo KS, Wood AR, Kjaer TR, Fine RS, Lu Y, Schurmann C, Highland HM, Rüeger S, Thorleifsson G, Justice AE, Lamparter D, Stirrups KE, ... ... Jarvik GP, et al. Rare and low-frequency coding variants alter human adult height. Nature. PMID 28146470 DOI: 10.1038/Nature21039  0.368
2017 Patel RY, Shah N, Jackson AR, Ghosh R, Pawliczek P, Paithankar S, Baker A, Riehle K, Chen H, Milosavljevic S, Bizon C, Rynearson S, Nelson T, Jarvik GP, Rehm HL, et al. ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants. Genome Medicine. 9: 3. PMID 28081714 DOI: 10.1186/S13073-016-0391-Z  0.378
2017 Himes P, Kauffman TL, Muessig KR, Amendola LM, Berg JS, Dorschner MO, Gilmore M, Nickerson DA, Reiss JA, Richards CS, Rope AF, Simpson DK, Wilfond BS, Jarvik GP, Goddard KA. Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28079899 DOI: 10.1038/Gim.2016.198  0.349
2016 Kauffman TL, Wilfond BS, Jarvik GP, Leo MC, Lynch FL, Reiss JA, Sue Richards C, McMullen C, Nickerson D, Dorschner MO, Goddard KA. Design of a randomized controlled trial for genomic carrier screening in healthy patients seeking preconception genetic testing. Contemporary Clinical Trials. PMID 27940182 DOI: 10.1016/J.Cct.2016.12.007  0.364
2016 Smith ME, Sanderson SC, Brothers KB, Myers MF, McCormick J, Aufox S, Shrubsole MJ, Garrison NA, Mercaldo ND, Schildcrout JS, Clayton EW, Antommaria AH, Basford M, Brilliant M, Connolly JJ, ... ... Jarvik GP, et al. Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions. Bmc Medical Research Methodology. 16: 162. PMID 27881091 DOI: 10.1186/S12874-016-0263-7  0.313
2016 De R, Verma SS, Holzinger E, Hall M, Burt A, Carrell DS, Crosslin DR, Jarvik GP, Kuivaniemi H, Kullo IJ, Lange LA, Lanktree MB, Larson EB, North KE, Reiner AP, et al. Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts. Human Genetics. PMID 27848076 DOI: 10.1007/S00439-016-1738-7  0.356
2016 O'Daniel JM, McLaughlin HM, Amendola LM, Bale SJ, Berg JS, Bick D, Bowling KM, Chao EC, Chung WK, Conlin LK, Cooper GM, Das S, Deignan JL, Dorschner MO, Evans JP, ... ... Jarvik GP, et al. A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27811861 DOI: 10.1038/Gim.2016.152  0.33
2016 Mosley JD, Van Driest SL, Wells QS, Shaffer CM, Edwards TL, Bastarache L, McCarty CA, Thompson W, Chute CG, Jarvik GP, Crosslin DR, Larson EB, Kullo IJ, Pacheco JA, Peissig PL, et al. Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile using Historical Data. Circulation. Cardiovascular Genetics. PMID 27780847 DOI: 10.1161/Circgenetics.116.001530  0.335
2016 Jarvik GP, Evans JP. Mastering genomic terminology. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27657676 DOI: 10.1038/Gim.2016.139  0.309
2016 Tan N, Amendola LM, O'Daniel JM, Burt A, Horike-Pyne MJ, Boshe L, Henderson GE, Rini C, Roche MI, Hisama FM, Burke W, Wilfond B, Jarvik GP. Is "incidental finding" the best term?: a study of patients' preferences. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27490114 DOI: 10.1038/Gim.2016.96  0.322
2016 Amendola LM, Jarvik GP, Leo MC, McLaughlin HM, Akkari Y, Amaral MD, Berg JS, Biswas S, Bowling KM, Conlin LK, Cooper GM, Dorschner MO, Dulik MC, Ghazani AA, Ghosh R, et al. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. American Journal of Human Genetics. 99: 247. PMID 27392081 DOI: 10.1016/J.Ajhg.2016.06.001  0.303
2016 Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, et al. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics. 99: 246. PMID 27392080 DOI: 10.1016/J.Ajhg.2016.06.002  0.317
2016 Jarvik GP, Browning BL. Consideration of Cosegregation in the Pathogenicity Classification of Genomic Variants. American Journal of Human Genetics. 98: 1077-81. PMID 27236918 DOI: 10.1016/J.Ajhg.2016.04.003  0.371
2016 Rosenthal EA, Makaryan V, Burt AA, Crosslin DR, Kim DS, Smith JD, Nickerson DA, Reiner AP, Rich SS, Jackson RD, Ganesh SK, Polfus LM, Qi L, Dale DC, ... Jarvik GP, et al. Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project. Genetic Epidemiology. PMID 27229898 DOI: 10.1002/Gepi.21976  0.364
2016 Amendola LM, Jarvik GP, Leo MC, McLaughlin HM, Akkari Y, Amaral MD, Berg JS, Biswas S, Bowling KM, Conlin LK, Cooper GM, Dorschner MO, Dulik MC, Ghazani AA, Ghosh R, et al. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. American Journal of Human Genetics. PMID 27181684 DOI: 10.1016/J.Ajhg.2016.03.024  0.403
2016 Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, et al. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics. PMID 27181682 DOI: 10.1016/J.Ajhg.2016.04.011  0.37
2016 Simonti CN, Vernot B, Bastarache L, Bottinger E, Carrell DS, Chisholm RL, Crosslin DR, Hebbring SJ, Jarvik GP, Kullo IJ, Li R, Pathak J, Ritchie MD, Roden DM, Verma SS, et al. The phenotypic legacy of admixture between modern humans and Neandertals. Science (New York, N.Y.). 351: 737-41. PMID 26912863 DOI: 10.1126/Science.Aad2149  0.364
2016 Korngiebel DM, McMullen CK, Amendola LM, Berg JS, Davis JV, Gilmore MJ, Harding CO, Himes P, Jarvik GP, Kauffman TL, Kennedy KA, Simpson DK, Leo MC, Lynch FL, Quigley DI, et al. Generating a taxonomy for genetic conditions relevant to reproductive planning. American Journal of Medical Genetics. Part A. 170: 565-73. PMID 26889673 DOI: 10.1002/Ajmg.A.37513  0.358
2016 Bush WS, Crosslin DR, Obeng AO, Wallace J, Almoguera B, Basford MA, Bielinski SJ, Carrell DS, Connolly JJ, Crawford D, Doheny KF, Gallego CJ, Gordon AS, Keating B, Kirby J, ... ... Jarvik GP, et al. Genetic Variation among 82 Pharmacogenes: the PGRN-Seq data from the eMERGE Network. Clinical Pharmacology and Therapeutics. PMID 26857349 DOI: 10.1002/Cpt.350  0.393
2016 Leo MC, McMullen C, Wilfond BS, Lynch FL, Reiss JA, Gilmore MJ, Himes P, Kauffman TL, Davis JV, Jarvik GP, Berg JS, Harding C, Kennedy KA, Simpson DK, Quigley DI, et al. Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing. American Journal of Medical Genetics. Part A. PMID 26792268 DOI: 10.1002/Ajmg.A.37477  0.338
2016 Van Driest SL, Wells QS, Stallings S, Bush WS, Gordon A, Nickerson DA, Kim JH, Crosslin DR, Jarvik GP, Carrell DS, Ralston JD, Larson EB, Bielinski SJ, Olson JE, Ye Z, et al. Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records. Jama. 315: 47-57. PMID 26746457 DOI: 10.1001/Jama.2015.17701  0.373
2015 Gallego CJ, Perez ML, Burt A, Amendola LM, Shirts BH, Pritchard CC, Hisama FM, Bennett RL, Veenstra DL, Jarvik GP. Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome. Journal of Genetic Counseling. PMID 26637299 DOI: 10.1007/S10897-015-9902-0  0.345
2015 Cohen SA, Laurino M, Bowen DJ, Upton MP, Pritchard C, Hisama F, Jarvik G, Fichera A, Sjoding B, Bennett RL, Naylor L, Jacobson A, Burke W, Grady WM. Initiation of universal tumor screening for Lynch syndrome in colorectal cancer patients as a model for the implementation of genetic information into clinical oncology practice. Cancer. PMID 26480326 DOI: 10.1002/Cncr.29758  0.317
2015 Amendola LM, Lautenbach D, Scollon S, Bernhardt B, Biswas S, East K, Everett J, Gilmore MJ, Himes P, Raymond VM, Wynn J, Hart R, Jarvik GP. Illustrative case studies in the return of exome and genome sequencing results. Personalized Medicine. 12: 283-295. PMID 26478737 DOI: 10.2217/Pme.14.89  0.348
2015 Namjou B, Marsolo K, Lingren T, Ritchie MD, Verma SS, Cobb BL, Perry C, Kitchner TE, Brilliant MH, Peissig PL, Borthwick KM, Williams MS, Grafton J, Jarvik GP, Holm IA, et al. A GWAS Study on Liver Function Test Using eMERGE Network Participants. Plos One. 10: e0138677. PMID 26413716 DOI: 10.1371/Journal.Pone.0138677  0.38
2015 Gallego CJ, Burt A, Sundaresan AS, Ye Z, Shaw C, Crosslin DR, Crane PK, Fullerton SM, Hansen K, Carrell D, Kuivaniemi H, Derr K, de Andrade M, McCarty CA, Kitchner TE, ... ... Jarvik GP, et al. Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network. American Journal of Human Genetics. PMID 26365338 DOI: 10.1016/J.Ajhg.2015.08.008  0.33
2015 Crosslin DR, Robertson PD, Carrell DS, Gordon AS, Hanna DS, Burt A, Fullerton SM, Scrol A, Ralston J, Leppig K, Hartzler A, Baldwin E, Andrade Md, Kullo IJ, Tromp G, ... ... Jarvik GP, et al. Prospective participant selection and ranking to maximize actionable pharmacogenetic variants and discovery in the eMERGE Network. Genome Medicine. 7: 67. PMID 26221186 DOI: 10.1186/S13073-015-0181-Z  0.34
2015 Bielinski SJ, Pathak J, Carrell DS, Takahashi PY, Olson JE, Larson NB, Liu H, Sohn S, Wells QS, Denny JC, Rasmussen-Torvik LJ, Pacheco JA, Jackson KL, Lesnick TG, Gullerud RE, ... ... Jarvik GP, et al. A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network. Journal of Cardiovascular Translational Research. PMID 26195183 DOI: 10.1007/S12265-015-9644-2  0.307
2015 Mosley JD, Shaffer CM, Van Driest SL, Weeke PE, Wells QS, Karnes JH, Velez Edwards DR, Wei WQ, Teixeira PL, Bastarache L, Crawford DC, Li R, Manolio TA, Bottinger EP, McCarty CA, ... ... Jarvik GP, et al. A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. The Pharmacogenomics Journal. PMID 26169577 DOI: 10.1038/Tpj.2015.51  0.375
2015 Shirts BH, Salama JS, Aronson SJ, Chung WK, Gray SW, Hindorff LA, Jarvik GP, Plon SE, Stoffel EM, Tarczy-Hornoch PZ, Van Allen EM, Weck KE, Chute CG, Freimuth RR, Grundmeier RW, et al. CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record. Journal of the American Medical Informatics Association : Jamia. PMID 26142422 DOI: 10.1093/Jamia/Ocv065  0.301
2015 Kim DS, Burt AA, Ranchalis JE, Vuletic S, Vaisar T, Li WF, Rosenthal EA, Dong W, Eintracht JF, Motulsky AG, Brunzell JD, Albers JJ, Furlong CE, Jarvik GP. PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity. Journal of Lipid Research. 56: 1351-62. PMID 26009633 DOI: 10.1194/Jlr.P058032  0.369
2015 Hall MA, Verma SS, Wallace J, Lucas A, Berg RL, Connolly J, Crawford DC, Crosslin DR, de Andrade M, Doheny KF, Haines JL, Harley JB, Jarvik GP, Kitchner T, Kuivaniemi H, et al. Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network. Genetic Epidemiology. 39: 376-84. PMID 25982363 DOI: 10.1002/Gepi.21902  0.362
2015 Auer PL, Nalls M, Meschia JF, Worrall BB, Longstreth WT, Seshadri S, Kooperberg C, Burger KM, Carlson CS, Carty CL, Chen WM, Cupples LA, DeStefano AL, Fornage M, Hardy J, ... ... Jarvik GP, et al. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project. Jama Neurology. 72: 781-8. PMID 25961151 DOI: 10.1001/Jamaneurol.2015.0582  0.313
2015 Regier DA, Peacock SJ, Pataky R, van der Hoek K, Jarvik GP, Hoch J, Veenstra D. Societal preferences for the return of incidental findings from clinical genomic sequencing: a discrete-choice experiment. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 187: E190-7. PMID 25754703 DOI: 10.1503/Cmaj.140697  0.331
2015 Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, ... ... Jarvik GP, et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15. PMID 25637381 DOI: 10.1101/Gr.183483.114  0.395
2015 Rosenthal E, Blue E, Jarvik GP. Next-generation gene discovery for variants of large impact on lipid traits. Current Opinion in Lipidology. 26: 114-9. PMID 25636063 DOI: 10.1097/Mol.0000000000000156  0.403
2015 Bennette CS, Gallego CJ, Burke W, Jarvik GP, Veenstra DL. The cost-effectiveness of returning incidental findings from next-generation genomic sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 587-95. PMID 25394171 DOI: 10.1038/Gim.2014.156  0.359
2015 Crosslin DR, Carrell DS, Burt A, Kim DS, Underwood JG, Hanna DS, Comstock BA, Baldwin E, de Andrade M, Kullo IJ, Tromp G, Kuivaniemi H, Borthwick KM, McCarty CA, Peissig PL, ... ... Jarvik GP, et al. Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Genes and Immunity. 16: 1-7. PMID 25297839 DOI: 10.1038/Gene.2014.51  0.398
2014 Verma SS, de Andrade M, Tromp G, Kuivaniemi H, Pugh E, Namjou-Khales B, Mukherjee S, Jarvik GP, Kottyan LC, Burt A, Bradford Y, Armstrong GD, Derr K, Crawford DC, Haines JL, et al. Imputation and quality control steps for combining multiple genome-wide datasets. Frontiers in Genetics. 5: 370. PMID 25566314 DOI: 10.3389/Fgene.2014.00370  0.373
2014 Malinowski JR, Denny JC, Bielinski SJ, Basford MA, Bradford Y, Peissig PL, Carrell D, Crosslin DR, Pathak J, Rasmussen L, Pacheco J, Kho A, Newton KM, Li R, Kullo IJ, ... ... Jarvik GP, et al. Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. Plos One. 9: e111301. PMID 25436638 DOI: 10.1371/Journal.Pone.0111301  0.371
2014 Crosslin DR, Tromp G, Burt A, Kim DS, Verma SS, Lucas AM, Bradford Y, Crawford DC, Armasu SM, Heit JA, Hayes MG, Kuivaniemi H, Ritchie MD, Jarvik GP, de Andrade M, et al. Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records. Frontiers in Genetics. 5: 352. PMID 25414722 DOI: 10.3389/Fgene.2014.00352  0.354
2014 Gaynor JW, Kim DS, Arrington CB, Atz AM, Bellinger DC, Burt AA, Ghanayem NS, Jacobs JP, Lee TM, Lewis AB, Mahle WT, Marino BS, Miller SG, Newburger JW, Pizarro C, ... ... Jarvik GP, et al. Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants. The Journal of Thoracic and Cardiovascular Surgery. 148: 2560-6. PMID 25282659 DOI: 10.1016/J.Jtcvs.2014.07.052  0.325
2014 Evans BJ, Dorschner MO, Burke W, Jarvik GP. Regulatory changes raise troubling questions for genomic testing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 799-803. PMID 25255365 DOI: 10.1038/Gim.2014.127  0.335
2014 Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, ... ... Jarvik GP, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491  0.356
2014 Cronin RM, Field JR, Bradford Y, Shaffer CM, Carroll RJ, Mosley JD, Bastarache L, Edwards TL, Hebbring SJ, Lin S, Hindorff LA, Crane PK, Pendergrass SA, Ritchie MD, Crawford DC, ... ... Jarvik GP, et al. Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index. Frontiers in Genetics. 5: 250. PMID 25177340 DOI: 10.3389/Fgene.2014.00250  0.37
2014 Simpson CL, Goldenberg AJ, Culverhouse R, Daley D, Igo RP, Jarvik GP, Mandal DM, Mascalzoni D, Montgomery CG, Pierce B, Plaetke R, Shete S, Goddard KA, Stein CM. Practical barriers and ethical challenges in genetic data sharing. International Journal of Environmental Research and Public Health. 11: 8383-98. PMID 25153467 DOI: 10.3390/Ijerph110808383  0.327
2014 Gallego CJ, Bennette CS, Heagerty P, Comstock B, Horike-Pyne M, Hisama F, Amendola LM, Bennett RL, Dorschner MO, Tarczy-Hornoch P, Grady WM, Fullerton SM, Trinidad SB, Regier DA, Nickerson DA, ... ... Jarvik GP, et al. Comparative effectiveness of next generation genomic sequencing for disease diagnosis: design of a randomized controlled trial in patients with colorectal cancer/polyposis syndromes. Contemporary Clinical Trials. 39: 1-8. PMID 24997220 DOI: 10.1016/J.Cct.2014.06.016  0.359
2014 Crawford DC, Crosslin DR, Tromp G, Kullo IJ, Kuivaniemi H, Hayes MG, Denny JC, Bush WS, Haines JL, Roden DM, McCarty CA, Jarvik GP, Ritchie MD. eMERGEing progress in genomics-the first seven years. Frontiers in Genetics. 5: 184. PMID 24987407 DOI: 10.3389/Fgene.2014.00184  0.366
2014 Kim DS, Burt AA, Rosenthal EA, Ranchalis JE, Eintracht JF, Hatsukami TS, Furlong CE, Marcovina S, Albers JJ, Jarvik GP. HDL-3 is a superior predictor of carotid artery disease in a case-control cohort of 1725 participants. Journal of the American Heart Association. 3: e000902. PMID 24965026 DOI: 10.1161/Jaha.114.000902  0.305
2014 Rasmussen-Torvik LJ, Stallings SC, Gordon AS, Almoguera B, Basford MA, Bielinski SJ, Brautbar A, Brilliant MH, Carrell DS, Connolly JJ, Crosslin DR, Doheny KF, Gallego CJ, Gottesman O, Kim DS, ... ... Jarvik GP, et al. Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems. Clinical Pharmacology and Therapeutics. 96: 482-9. PMID 24960519 DOI: 10.1038/Clpt.2014.137  0.344
2014 Crosby J, Peloso GM, Auer PL, Crosslin DR, Stitziel NO, Lange LA, Lu Y, Tang ZZ, Zhang H, Hindy G, Masca N, Stirrups K, Kanoni S, Do R, ... ... Jarvik GP, et al. Loss-of-function mutations in APOC3, triglycerides, and coronary disease. The New England Journal of Medicine. 371: 22-31. PMID 24941081 DOI: 10.1056/Nejmoa1307095  0.307
2014 Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, Evans BJ, Evans JP, Fullerton SM, Gallego CJ, Garrison NA, Gray SW, Holm IA, Kullo IJ, Lehmann LS, et al. Return of genomic results to research participants: the floor, the ceiling, and the choices in between. American Journal of Human Genetics. 94: 818-26. PMID 24814192 DOI: 10.1016/J.Ajhg.2014.04.009  0.352
2014 Makaryan V, Rosenthal EA, Bolyard AA, Kelley ML, Below JE, Bamshad MJ, Bofferding KM, Smith JD, Buckingham K, Boxer LA, Skokowa J, Welte K, Nickerson DA, Jarvik GP, Dale DC, et al. TCIRG1-associated congenital neutropenia. Human Mutation. 35: 824-7. PMID 24753205 DOI: 10.1002/Humu.22563  0.364
2014 Kullo IJ, Haddad R, Prows CA, Holm I, Sanderson SC, Garrison NA, Sharp RR, Smith ME, Kuivaniemi H, Bottinger EP, Connolly JJ, Keating BJ, McCarty CA, Williams MS, Jarvik GP. Return of results in the genomic medicine projects of the eMERGE network. Frontiers in Genetics. 5: 50. PMID 24723935 DOI: 10.3389/Fgene.2014.00050  0.373
2014 Kim DS, Crosslin DR, Auer PL, Suzuki SM, Marsillach J, Burt AA, Gordon AS, Meschia JF, Nalls MA, Worrall BB, Longstreth WT, Gottesman RF, Furlong CE, Peters U, Rich SS, ... ... Jarvik GP, et al. Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project. Journal of Lipid Research. 55: 1173-1178. PMID 24711634 DOI: 10.1194/Jlr.P049247  0.319
2014 Connolly JJ, Glessner JT, Almoguera B, Crosslin DR, Jarvik GP, Sleiman PM, Hakonarson H. Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts. Frontiers in Genetics. 5: 51. PMID 24672537 DOI: 10.3389/Fgene.2014.00051  0.33
2014 Ramos EM, Din-Lovinescu C, Berg JS, Brooks LD, Duncanson A, Dunn M, Good P, Hubbard TJ, Jarvik GP, O'Donnell C, Sherry ST, Aronson N, Biesecker LG, Blumberg B, Calonge N, et al. Characterizing genetic variants for clinical action. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 166: 93-104. PMID 24634402 DOI: 10.1002/Ajmg.C.31386  0.398
2014 Dorschner MO, Amendola LM, Shirts BH, Kiedrowski L, Salama J, Gordon AS, Fullerton SM, Tarczy-Hornoch P, Byers PH, Jarvik GP. Refining the structure and content of clinical genomic reports. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 166: 85-92. PMID 24616401 DOI: 10.1002/Ajmg.C.31395  0.347
2014 Lange LA, Hu Y, Zhang H, Xue C, Schmidt EM, Tang ZZ, Bizon C, Lange EM, Smith JD, Turner EH, Jun G, Kang HM, Peloso G, Auer P, Li KP, ... ... Jarvik GP, et al. Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol. American Journal of Human Genetics. 94: 233-45. PMID 24507775 DOI: 10.1016/J.Ajhg.2014.01.010  0.382
2014 Shirts BH, Jacobson A, Jarvik GP, Browning BL. Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 529-34. PMID 24357849 DOI: 10.1038/Gim.2013.187  0.386
2014 Shameer K, Denny JC, Ding K, Jouni H, Crosslin DR, de Andrade M, Chute CG, Peissig P, Pacheco JA, Li R, Bastarache L, Kho AN, Ritchie MD, Masys DR, Chisholm RL, ... ... Jarvik GP, et al. A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. Human Genetics. 133: 95-109. PMID 24026423 DOI: 10.1007/S00439-013-1355-7  0.408
2014 Berg JS, Amendola LM, Eng C, Allen EV, Gray SW, Wagle N, Rehm HL, DeChene ET, Dulik MC, Hisama FM, Burke W, Spinner NB, Garraway L, Green RC, Plon S, ... ... Jarvik GP, et al. Erratum: Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the clinical sequencing exploratory research consortium (Genetics in Medicine (2013) 15 (860-867) DOI:10.1038/gim.2013.133) Genetics in Medicine. 16. DOI: 10.1038/Gim.2013.191  0.359
2013 Mosley JD, Van Driest SL, Larkin EK, Weeke PE, Witte JS, Wells QS, Karnes JH, Guo Y, Bastarache L, Olson LM, McCarty CA, Pacheco JA, Jarvik GP, Carrell DS, Larson EB, et al. Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. Plos One. 8: e81503. PMID 24349080 DOI: 10.1371/Journal.Pone.0081503  0.385
2013 Denny JC, Bastarache L, Ritchie MD, Carroll RJ, Zink R, Mosley JD, Field JR, Pulley JM, Ramirez AH, Bowton E, Basford MA, Carrell DS, Peissig PL, Kho AN, Pacheco JA, ... ... Jarvik GP, et al. Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nature Biotechnology. 31: 1102-10. PMID 24270849 DOI: 10.1038/Nbt.2749  0.424
2013 Rosenthal EA, Ranchalis J, Crosslin DR, Burt A, Brunzell JD, Motulsky AG, Nickerson DA, Wijsman EM, Jarvik GP. Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. American Journal of Human Genetics. 93: 1035-45. PMID 24268658 DOI: 10.1016/J.Ajhg.2013.10.019  0.411
2013 Berg JS, Amendola LM, Eng C, Van Allen E, Gray SW, Wagle N, Rehm HL, DeChene ET, Dulik MC, Hisama FM, Burke W, Spinner NB, Garraway L, Green RC, Plon S, ... ... Jarvik GP, et al. Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 860-7. PMID 24195999 DOI: 10.1038/Gim.2013.133  0.386
2013 Tarczy-Hornoch P, Amendola L, Aronson SJ, Garraway L, Gray S, Grundmeier RW, Hindorff LA, Jarvik G, Karavite D, Lebo M, Plon SE, Van Allen E, Weck KE, White PS, Yang Y. A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 824-32. PMID 24071794 DOI: 10.1038/Gim.2013.120  0.309
2013 Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT, Kim JH, Rosenthal EA, Kim DS, Tabor HK, ... ... Jarvik GP, et al. Actionable, pathogenic incidental findings in 1,000 participants' exomes. American Journal of Human Genetics. 93: 631-40. PMID 24055113 DOI: 10.1016/J.Ajhg.2013.08.006  0.402
2013 Burke W, Antommaria AH, Bennett R, Botkin J, Clayton EW, Henderson GE, Holm IA, Jarvik GP, Khoury MJ, Knoppers BM, Press NA, Ross LF, Rothstein MA, Saal H, Uhlmann WR, et al. Recommendations for returning genomic incidental findings? We need to talk! Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 854-9. PMID 23907645 DOI: 10.1038/Gim.2013.113  0.401
2013 McDavid A, Crane PK, Newton KM, Crosslin DR, McCormick W, Weston N, Ehrlich K, Hart E, Harrison R, Kukull WA, Rottscheit C, Peissig P, Stefanski E, McCarty CA, Zuvich RL, ... ... Jarvik GP, et al. Enhancing the power of genetic association studies through the use of silver standard cases derived from electronic medical records. Plos One. 8: e63481. PMID 23762230 DOI: 10.1371/Journal.Pone.0063481  0.314
2013 Gottesman O, Kuivaniemi H, Tromp G, Faucett WA, Li R, Manolio TA, Sanderson SC, Kannry J, Zinberg R, Basford MA, Brilliant M, Carey DJ, Chisholm RL, Chute CG, Connolly JJ, ... ... Jarvik GP, et al. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 761-71. PMID 23743551 DOI: 10.1038/Gim.2013.72  0.359
2013 Bennette CS, Trinidad SB, Fullerton SM, Patrick D, Amendola L, Burke W, Hisama FM, Jarvik GP, Regier DA, Veenstra DL. Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT). Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 873-81. PMID 23722871 DOI: 10.1038/Gim.2013.63  0.308
2013 Schick UM, McDavid A, Crane PK, Weston N, Ehrlich K, Newton KM, Wallace R, Bookman E, Harrison T, Aragaki A, Crosslin DR, Wang SS, Reiner AP, Jackson RD, Peters U, ... ... Jarvik GP, et al. Confirmation of the reported association of clonal chromosomal mosaicism with an increased risk of incident hematologic cancer. Plos One. 8: e59823. PMID 23533652 DOI: 10.1371/Journal.Pone.0059823  0.356
2013 Kim DS, Burt AA, Ranchalis JE, Jarvik ER, Rosenthal EA, Hatsukami TS, Furlong CE, Jarvik GP. Novel gene-by-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol. Journal of Lipid Research. 54: 1512-20. PMID 23482652 DOI: 10.1194/Jlr.P035238  0.348
2013 Crosslin DR, McDavid A, Weston N, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Ritchie MD, Saip A, Crawford DC, ... ... Jarvik GP, et al. Genetic variation associated with circulating monocyte count in the eMERGE Network. Human Molecular Genetics. 22: 2119-27. PMID 23314186 DOI: 10.1093/Hmg/Ddt010  0.381
2013 Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, ... ... Jarvik GP, et al. Loci influencing blood pressure identified using a cardiovascular gene-centric array. Human Molecular Genetics. 22: 1663-78. PMID 23303523 DOI: 10.1093/Hmg/Dds555  0.366
2013 Kim DS, Burt AA, Crosslin DR, Robertson PD, Ranchalis JE, Boyko EJ, Nickerson DA, Furlong CE, Jarvik GP. Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL. Journal of Lipid Research. 54: 552-60. PMID 23160181 DOI: 10.1194/Jlr.P033266  0.39
2013 Kullo IJ, Jarvik GP, Manolio TA, Williams MS, Roden DM. Leveraging the electronic health record to implement genomic medicine. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 270-1. PMID 23018749 DOI: 10.1038/Gim.2012.131  0.356
2013 Rosenthal E, Bolyard AA, Kelley ML, Below J, Bamshad M, Bofferding KM, Smith JD, Buckingham K, Boxer LA, Skokowa J, Welte K, Nickerson DA, Jarvik GP, Dale DC. TCIRG1 Associated Congenital Neutropenia Blood. 122: 440-440. DOI: 10.1182/Blood.V122.21.440.440  0.333
2012 Trinidad SB, Fullerton SM, Bares JM, Jarvik GP, Larson EB, Burke W. Informed Consent in Genome-Scale Research: What Do Prospective Participants Think? Ajob Primary Research. 3: 3-11. PMID 23493836 DOI: 10.1080/21507716.2012.662575  0.338
2012 Rasmussen-Torvik LJ, Pacheco JA, Wilke RA, Thompson WK, Ritchie MD, Kho AN, Muthalagu A, Hayes MG, Armstrong LL, Scheftner DA, Wilkins JT, Zuvich RL, Crosslin D, Roden DM, Denny JC, ... Jarvik GP, et al. High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. Clinical and Translational Science. 5: 394-9. PMID 23067351 DOI: 10.1111/J.1752-8062.2012.00446.X  0.35
2012 Asselbergs FW, Guo Y, van Iperen EP, Sivapalaratnam S, Tragante V, Lanktree MB, Lange LA, Almoguera B, Appelman YE, Barnard J, Baumert J, Beitelshees AL, Bhangale TR, Chen YD, Gaunt TR, ... ... Jarvik GP, et al. Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. American Journal of Human Genetics. 91: 823-38. PMID 23063622 DOI: 10.1016/J.Ajhg.2012.08.032  0.353
2012 Kim DS, Stanaway IB, Rajagopalan R, Bernbaum JC, Solot CB, Burnham N, Zackai EH, Clancy RR, Nicolson SC, Gerdes M, Nickerson DA, Hakonarson H, Gaynor JW, Jarvik GP. Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy. Plos One. 7: e45936. PMID 23049896 DOI: 10.1371/Journal.Pone.0045936  0.324
2012 Fullerton SM, Trinidad SB, Jarvik GP, Burke W. Beneficence, clinical urgency, and the return of individual research results to relatives. The American Journal of Bioethics : Ajob. 12: 9-10. PMID 22974018 DOI: 10.1080/15265161.2012.699153  0.359
2012 Hotaling JM, Waggott DR, Goldberg J, Jarvik G, Paterson AD, Cleary PA, Lachin J, Sarma A, Wessells H. Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort. The Journal of Urology. 188: 514-20. PMID 22704111 DOI: 10.1016/J.Juro.2012.04.001  0.356
2012 Kim DS, Burt AA, Ranchalis JE, Richter RJ, Marshall JK, Eintracht JF, Rosenthal EA, Furlong CE, Jarvik GP. Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease. Journal of Lipids. 2012: 476316. PMID 22685667 DOI: 10.1155/2012/476316  0.325
2012 Pritchard CC, Smith C, Salipante SJ, Lee MK, Thornton AM, Nord AS, Gulden C, Kupfer SS, Swisher EM, Bennett RL, Novetsky AP, Jarvik GP, Olopade OI, Goodfellow PJ, King MC, et al. ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing. The Journal of Molecular Diagnostics : Jmd. 14: 357-66. PMID 22658618 DOI: 10.1016/J.Jmoldx.2012.03.002  0.329
2012 Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang LE, Lee JE, Barnes KC, Hansel NN, ... ... Jarvik GP, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics. 44: 642-50. PMID 22561516 DOI: 10.1038/Ng.2271  0.312
2012 Fullerton SM, Wolf WA, Brothers KB, Clayton EW, Crawford DC, Denny JC, Greenland P, Koenig BA, Leppig KA, Lindor NM, McCarty CA, McGuire AL, McPeek Hinz ER, Mirel DB, Ramos EM, ... ... Jarvik GP, et al. Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 424-31. PMID 22361898 DOI: 10.1038/Gim.2012.15  0.368
2012 Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, ... ... Jarvik GP, et al. Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American Journal of Human Genetics. 90: 410-25. PMID 22325160 DOI: 10.1016/J.Ajhg.2011.12.022  0.386
2012 Kho AN, Hayes MG, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei WQ, Bielinski SJ, Chute CG, Leibson CL, Jarvik GP, Crosslin DR, et al. Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. Journal of the American Medical Informatics Association : Jamia. 19: 212-8. PMID 22101970 DOI: 10.1136/Amiajnl-2011-000439  0.365
2012 Crosslin DR, McDavid A, Weston N, Nelson SC, Zheng X, Hart E, de Andrade M, Kullo IJ, McCarty CA, Doheny KF, Pugh E, Kho A, Hayes MG, Pretel S, Saip A, ... ... Jarvik GP, et al. Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Human Genetics. 131: 639-52. PMID 22037903 DOI: 10.1007/S00439-011-1103-9  0.398
2012 Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, Klopp N, Baumert J, Padmanabhan S, ... ... Jarvik G, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017  0.329
2011 Zuvich RL, Armstrong LL, Bielinski SJ, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes MG, Jarvik GP, Jiang L, Kullo IJ, Li R, et al. Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. Genetic Epidemiology. 35: 887-98. PMID 22125226 DOI: 10.1002/Gepi.20639  0.379
2011 Denny JC, Crawford DC, Ritchie MD, Bielinski SJ, Basford MA, Bradford Y, Chai HS, Bastarache L, Zuvich R, Peissig P, Carrell D, Ramirez AH, Pathak J, Wilke RA, Rasmussen L, ... ... Jarvik GP, et al. Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. American Journal of Human Genetics. 89: 529-42. PMID 21981779 DOI: 10.1016/J.Ajhg.2011.09.008  0.384
2011 Murray ML, Cerrato F, Bennett RL, Jarvik GP. Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 998-1005. PMID 21811163 DOI: 10.1097/Gim.0B013E318226Fc15  0.305
2011 Rosenthal EA, Ronald J, Rothstein J, Rajagopalan R, Ranchalis J, Wolfbauer G, Albers JJ, Brunzell JD, Motulsky AG, Rieder MJ, Nickerson DA, Wijsman EM, Jarvik GP. Linkage and association of phospholipid transfer protein activity to LASS4. Journal of Lipid Research. 52: 1837-46. PMID 21757428 DOI: 10.1194/Jlr.P016576  0.346
2011 Kullo IJ, Ding K, Shameer K, McCarty CA, Jarvik GP, Denny JC, Ritchie MD, Ye Z, Crosslin DR, Chisholm RL, Manolio TA, Chute CG. Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. American Journal of Human Genetics. 89: 131-8. PMID 21700265 DOI: 10.1016/J.Ajhg.2011.05.019  0.377
2011 Bookman EB, Langehorne AA, Eckfeldt JH, Glass KC, Jarvik GP, Klag M, Koski G, Motulsky A, Wilfond B, Manolio TA, Fabsitz RR, Luepker RV. Comment on "Multidimensional results reporting to participants in genomic studies: getting it right". Science Translational Medicine. 3: 70le1. PMID 21325615 DOI: 10.1126/Scitranslmed.3001516  0.309
2011 McCarty CA, Chisholm RL, Chute CG, Kullo IJ, Jarvik GP, Larson EB, Li R, Masys DR, Ritchie MD, Roden DM, Struewing JP, Wolf WA. The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies. Bmc Medical Genomics. 4: 13. PMID 21269473 DOI: 10.1186/1755-8794-4-13  0.301
2011 Turner S, Armstrong LL, Bradford Y, Carlson CS, Crawford DC, Crenshaw AT, de Andrade M, Doheny KF, Haines JL, Hayes G, Jarvik G, Jiang L, Kullo IJ, Li R, Ling H, et al. Quality control procedures for genome-wide association studies. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit1.19. PMID 21234875 DOI: 10.1002/0471142905.Hg0119S68  0.344
2011 Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Jarvik GP, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007  0.399
2011 Ronald J, Rajagopalan R, Cerrato F, Nord AS, Hatsukami T, Kohler T, Marcovina S, Heagerty P, Jarvik GP. Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk. Stroke; a Journal of Cerebral Circulation. 42: 2-9. PMID 21127300 DOI: 10.1161/Strokeaha.110.591230  0.307
2010 Fabsitz RR, McGuire A, Sharp RR, Puggal M, Beskow LM, Biesecker LG, Bookman E, Burke W, Burchard EG, Church G, Clayton EW, Eckfeldt JH, Fernandez CV, Fisher R, ... ... Jarvik GP, et al. Ethical and practical guidelines for reporting genetic research results to study participants: updated guidelines from a National Heart, Lung, and Blood Institute working group. Circulation. Cardiovascular Genetics. 3: 574-80. PMID 21156933 DOI: 10.1161/Circgenetics.110.958827  0.335
2010 Johnson AD, Bhimavarapu A, Benjamin EJ, Fox C, Levy D, Jarvik GP, O'Donnell CJ. CLIA-tested genetic variants on commercial SNP arrays: Potential for incidental findings in genome-wide association studies Genetics in Medicine. 12: 355-363. PMID 20556870 DOI: 10.1097/Gim.0B013E3181E1E2A9  0.4
2010 Trinidad SB, Fullerton SM, Bares JM, Jarvik GP, Larson EB, Burke W. Genomic research and wide data sharing: views of prospective participants. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 12: 486-95. PMID 20535021 DOI: 10.1097/Gim.0B013E3181E38F9E  0.314
2010 Wijsman EM, Rothstein JH, Igo RP, Brunzell JD, Motulsky AG, Jarvik GP. Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families. Human Genetics. 127: 705-19. PMID 20383777 DOI: 10.1007/S00439-010-0819-2  0.399
2010 Eagle KA, Ginsburg GS, Musunuru K, Aird WC, Balaban RS, Bennett SK, Blumenthal RS, Coughlin SR, Davidson KW, Frohlich ED, Greenland P, Jarvik GP, Libby P, Pepine CJ, Ruskin JN, et al. Identifying patients at high risk of a cardiovascular event in the near future: current status and future directions: report of a national heart, lung, and blood institute working group. Circulation. 121: 1447-54. PMID 20351302 DOI: 10.1161/Circulationaha.109.904029  0.306
2010 Carty CL, Heagerty P, Heckbert SR, Jarvik GP, Lange LA, Cushman M, Tracy RP, Reiner AP. Interaction between fibrinogen and IL-6 genetic variants and associations with cardiovascular disease risk in the Cardiovascular Health Study. Annals of Human Genetics. 74: 1-10. PMID 20059469 DOI: 10.1111/J.1469-1809.2009.00551.X  0.308
2010 Jarvik GP, Rajagopalan R, Rosenthal EA, Wolfbauer G, McKinstry L, Vaze A, Brunzell J, Motulsky AG, Nickerson DA, Heagerty PJ, Wijsman EM, Albers JJ. Genetic and nongenetic sources of variation in phospholipid transfer protein activity. Journal of Lipid Research. 51: 983-90. PMID 19965587 DOI: 10.1194/Jlr.M000125  0.341
2009 Ronald J, Rajagopalan R, Ranchalis JE, Marshall JK, Hatsukami TS, Heagerty PJ, Jarvik GP. Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease. Lipids in Health and Disease. 8: 52. PMID 19951432 DOI: 10.1186/1476-511X-8-52  0.39
2009 Carty CL, Heagerty P, Heckbert SR, Enquobahrie DA, Jarvik GP, Davis S, Tracy RP, Reiner AP. Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with IL6, IL1RN, IL1beta and TNF genes in the Cardiovascular Health Study. Journal of Atherosclerosis and Thrombosis. 16: 419-30. PMID 19729864 DOI: 10.5551/Jat.No968  0.313
2009 Ober C, Nord AS, Thompson EE, Pan L, Tan Z, Cusanovich D, Sun Y, Nicolae R, Edelstein C, Schneider DH, Billstrand C, Pfaffinger D, Phillips N, Anderson RL, Philips B, ... ... Jarvik GP, et al. Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. Journal of Lipid Research. 50: 798-806. PMID 19124843 DOI: 10.1194/Jlr.M800515-Jlr200  0.368
2008 Richter RJ, Jarvik GP, Furlong CE. Determination of paraoxonase 1 status without the use of toxic organophosphate substrates. Circulation. Cardiovascular Genetics. 1: 147-52. PMID 20031556 DOI: 10.1161/Circgenetics.108.811638  0.319
2008 Wurfel MM, Gordon AC, Holden TD, Radella F, Strout J, Kajikawa O, Ruzinski JT, Rona G, Black RA, Stratton S, Jarvik GP, Hajjar AM, Nickerson DA, Rieder M, Sevransky J, et al. Toll-like receptor 1 polymorphisms affect innate immune responses and outcomes in sepsis. American Journal of Respiratory and Critical Care Medicine. 178: 710-20. PMID 18635889 DOI: 10.1164/Rccm.200803-462Oc  0.31
2008 Zeltser I, Jarvik GP, Bernbaum J, Wernovsky G, Nord AS, Gerdes M, Zackai E, Clancy R, Nicolson SC, Spray TL, Gaynor JW. Genetic factors are important determinants of neurodevelopmental outcome after repair of tetralogy of Fallot. The Journal of Thoracic and Cardiovascular Surgery. 135: 91-7. PMID 18179924 DOI: 10.1016/J.Jtcvs.2007.04.074  0.306
2008 Crawford DC, Nord AS, Badzioch MD, Ranchalis J, McKinstry LA, Ahearn M, Bertucci C, Shephard C, Wong M, Rieder MJ, Schellenberg GD, Nickerson DA, Heagerty PJ, Wijsman EM, Jarvik GP. A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk. Journal of Lipid Research. 49: 588-96. PMID 18056683 DOI: 10.1194/Jlr.M700409-Jlr200  0.374
2007 Goode EL, Fridley BL, Sun Z, Atkinson EJ, Nord AS, McDonnell SK, Jarvik GP, de Andrade M, Slager SL. Comparison of tagging single-nucleotide polymorphism methods in association analyses. Bmc Proceedings. 1: S6. PMID 18466560 DOI: 10.1186/1753-6561-1-S1-S6  0.34
2007 Goode EL, Cherny SS, Christian JC, Jarvik GP, de Andrade M. Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 10: 703-11. PMID 17903110 DOI: 10.1375/Twin.10.5.703  0.318
2007 Carlson CS, Heagerty PJ, Nord AS, Pritchard DK, Ranchalis J, Boguch JM, Duan H, Hatsukami TS, Schwartz SM, Rieder MJ, Nickerson DA, Jarvik GP. TagSNP evaluation for the association of 42 inflammation loci and vascular disease: evidence of IL6, FGB, ALOX5, NFKBIA, and IL4R loci effects. Human Genetics. 121: 65-75. PMID 17115186 DOI: 10.1007/S00439-006-0289-8  0.355
2006 Bookman EB, Langehorne AA, Eckfeldt JH, Glass KC, Jarvik GP, Klag M, Koski G, Motulsky A, Wilfond B, Manolio TA, Fabsitz RR, Luepker RV. Reporting genetic results in research studies: summary and recommendations of an NHLBI working group. American Journal of Medical Genetics. Part A. 140: 1033-40. PMID 16575896 DOI: 10.1002/Ajmg.A.31195  0.382
2006 Carlson CS, Heagerty PJ, Hatsukami TS, Richter RJ, Ranchalis J, Lewis J, Bacus TJ, McKinstry LA, Schellenberg GD, Rieder M, Nickerson D, Furlong CE, Chait A, Jarvik GP. TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease. Journal of Lipid Research. 47: 1014-24. PMID 16474172 DOI: 10.1194/Jlr.M500517-Jlr200  0.348
2005 Goode EL, Badzioch MD, Jarvik GP. Bias of allele-sharing linkage statistics in the presence of intermarker linkage disequilibrium Bmc Genetics. 6: 1-7. PMID 16451697 DOI: 10.1186/1471-2156-6-S1-S82  0.378
2005 Badzioch MD, Goode EL, Jarvik GP. The role of parametric linkage methods in complex trait analyses using microsatellites Bmc Genetics. 6: 1-5. PMID 16451659 DOI: 10.1186/1471-2156-6-S1-S48  0.337
2005 Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, et al. Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. Bmc Genetics. 6: S1. PMID 16451554 DOI: 10.1186/1471-2156-6-S1-S1  0.373
2005 Goode EL, Jarvik GP. Assessment and implications of linkage disequilibrium in genome-wide single-nucleotide polymorphism and microsatellite panels. Genetic Epidemiology. 29. PMID 16342185 DOI: 10.1002/Gepi.20112  0.386
2005 Rozek LS, Hatsukami TS, Richter RJ, Ranchalis J, Nakayama K, McKinstry LA, Gortner DA, Boyko E, Schellenberg GD, Furlong CE, Jarvik GP. The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status. Journal of Lipid Research. 46: 1888-95. PMID 15995178 DOI: 10.1194/Jlr.M400489-Jlr200  0.305
2005 Xu J, Dimitrov L, Chang BL, Adams TS, Turner AR, Meyers DA, Eeles RA, Easton DF, Foulkes WD, Simard J, Giles GG, Hopper JL, Mahle L, Moller P, Bishop T, ... ... Jarvik GP, et al. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics. American Journal of Human Genetics. 77: 219-29. PMID 15988677 DOI: 10.1086/432377  0.318
2005 Gagnon F, Jarvik GP, Badzioch MD, Motulsky AG, Brunzell JD, Wijsman EM. Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia. Human Genetics. 117: 494-505. PMID 15959807 DOI: 10.1007/S00439-005-1338-4  0.344
2004 Richter RJ, Jampsa RL, Jarvik GP, Costa LG, Furlong CE. Determination of paraoxonase 1 status and genotypes at specific polymorphic sites. Current Protocols in Toxicology / Editorial Board, Mahin D. Maines (Editor-in-Chief) ... [Et Al.]. Unit4.12. PMID 20945303 DOI: 10.1002/0471140856.Tx0412S19  0.321
2004 Badzioch MD, Igo RP, Gagnon F, Brunzell JD, Krauss RM, Motulsky AG, Wijsman EM, Jarvik GP. Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan. Arteriosclerosis, Thrombosis, and Vascular Biology. 24: 1942-50. PMID 15331429 DOI: 10.1161/01.Atv.0000143499.09575.93  0.319
2004 Friedrichsen DM, Stanford JL, Isaacs SD, Janer M, Chang BL, Deutsch K, Gillanders E, Kolb S, Wiley KE, Badzioch MD, Zheng SL, Walsh PC, Jarvik GP, Hood L, Trent JM, et al. Identification of a prostate cancer susceptibility locus on chromosome 7q11-21 in Jewish families. Proceedings of the National Academy of Sciences of the United States of America. 101: 1939-44. PMID 14769943 DOI: 10.1073/Pnas.0308336100  0.313
2004 Badzioch MD, Thomas DC, Jarvik GP. Summary report: Missing data and pedigree and genotyping errors. Genetic Epidemiology. S36-42. PMID 14635167 DOI: 10.1002/Gepi.10282  0.35
2003 Janer M, Friedrichsen DM, Stanford JL, Badzioch MD, Kolb S, Deutsch K, Peters MA, Goode EL, Welti R, DeFrance HB, Iwasaki L, Li S, Hood L, Ostrander EA, Jarvik GP. Genomic scan of 254 hereditary prostate cancer families. The Prostate. 57: 309-19. PMID 14601027 DOI: 10.1002/Pros.10305  0.332
2003 Gagnon F, Jarvik GP, Motulsky AG, Deeb SS, Brunzell JD, Wijsman EM. Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment. Human Genetics. 113: 522-33. PMID 14569462 DOI: 10.1007/S00439-003-1006-5  0.334
2003 Conlon EM, Goode EL, Gibbs M, Stanford JL, Badzioch M, Janer M, Kolb S, Hood L, Ostrander EA, Jarvik GP, Wijsman EM. Oligogenic segregation analysis of hereditary prostate cancer pedigrees: Evidence for multiple loci affecting age at onset International Journal of Cancer. 105: 630-635. PMID 12740911 DOI: 10.1002/Ijc.11128  0.302
2003 Jarvik GP, Jampsa R, Richter RJ, Carlson CS, Rieder MJ, Nickerson DA, Furlong CE. Novel paraoxonase (PON1) nonsense and missense mutations predicted by functional genomic assay of PON1 status Pharmacogenetics. 13: 291-295. PMID 12724622 DOI: 10.1097/00008571-200305000-00009  0.342
2003 Kelada SN, Costa-Mallen P, Checkoway H, Viernes HA, Farin FM, Smith-Weller T, Franklin GM, Costa LG, Longstreth WT, Furlong CE, Jarvik GP, Swanson PD. Paraoxonase 1 promoter and coding region polymorphisms in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 546-7. PMID 12640090 DOI: 10.1136/Jnnp.74.4.546  0.318
2003 Costa LG, Cole TB, Jarvik GP, Furlong CE. Functional genomic of the paraoxonase (PON1) polymorphisms: effects on pesticide sensitivity, cardiovascular disease, and drug metabolism. Annual Review of Medicine. 54: 371-92. PMID 12525679 DOI: 10.1146/Annurev.Med.54.101601.152421  0.348
2002 Furlong CE, Cole TB, Jarvik GP, Costa LG. Pharmacogenomic considerations of the paraoxonase polymorphisms. Pharmacogenomics. 3: 341-8. PMID 12052142 DOI: 10.1517/14622416.3.3.341  0.325
2001 Bird TD, Jarvik GP, Wood NW. Genetic association studies: genes in search of diseases. Neurology. 57: 1153-4. PMID 11591829 DOI: 10.1212/Wnl.57.7.1153  0.401
2001 Peters MA, Janer M, Kolb S, Jarvik GP, Ostrander EA, Stanford JL. Germline mutations in the p73 gene do not predispose to familial prostate-brain cancer. The Prostate. 48: 292-6. PMID 11536309 DOI: 10.1002/Pros.1109  0.309
2001 Brophy VH, Jampsa RL, Clendenning JB, McKinstry LA, Jarvik GP, Furlong CE. Effects of 5' regulatory-region polymorphisms on paraoxonase-gene (PON1) expression. American Journal of Human Genetics. 68: 1428-1436. PMID 11335891 DOI: 10.1086/320600  0.322
2001 Brophy VH, Hastings MD, Clendenning JB, Richter RJ, Jarvik GP, Furlong CE. Polymorphisms in the human paraoxonase (PON1) promoter. Pharmacogenetics. 11: 77-84. PMID 11207034 DOI: 10.1097/00008571-200102000-00009  0.314
2000 Jarvik GP, Rozek LS, Brophy VH, Hatsukami TS, Richter RJ, Schellenberg GD, Furlong CE. Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype. Arteriosclerosis, Thrombosis, and Vascular Biology. 20: 2441-7. PMID 11073850 DOI: 10.1161/01.Atv.20.11.2441  0.344
2000 Brophy VH, Jarvik GP, Richter RJ, Rozek LS, Schellenberg GD, Furlong CE. Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype. Pharmacogenetics. 10: 453-60. PMID 10898114 DOI: 10.1097/00008571-200007000-00008  0.346
2000 Gibbs M, Stanford JL, Jarvik GP, Janer M, Badzioch M, Peters MA, Goode EL, Kolb S, Chakrabarti L, Shook M, Basom R, Ostrander EA, Hood L. A genomic scan of families with prostate cancer identifies multiple regions of interest. American Journal of Human Genetics. 67: 100-9. PMID 10820127 DOI: 10.1086/302969  0.323
2000 Drachman JG, Jarvik GP, Mehaffey MG. Autosomal dominant thrombocytopenia: incomplete megakaryocyte differentiation and linkage to human chromosome 10 Blood. 96: 118-125. DOI: 10.1182/Blood.V96.1.118.013K37_118_125  0.334
1999 Gibbs M, Stanford JL, McIndoe RA, Jarvik GP, Kolb S, Goode EL, Chakrabarti L, Schuster EF, Buckley VA, Miller EL, Brandzel S, Li S, Hood L, Ostrander EA. Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. American Journal of Human Genetics. 64: 776-87. PMID 10053012 DOI: 10.1086/302287  0.312
1999 Hokanson JE, Brunzell JD, Jarvik GP, Wijsman EM, Austin MA. Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency. American Journal of Human Genetics. 64: 608-618. PMID 9973300 DOI: 10.1086/302234  0.324
1998 Jarvik GP. Complex Segregation Analyses: Uses and Limitations American Journal of Human Genetics. 63: 942-946. PMID 9758633 DOI: 10.1086/302075  0.314
1998 Wijsman EM, Brunzell JD, Jarvik GP, Austin MA, Motulsky AG, Deeb SS. Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex. Arteriosclerosis, Thrombosis, and Vascular Biology. 18: 215-26. PMID 9484986 DOI: 10.1161/01.Atv.18.2.215  0.353
1997 Graham J, Chapman NH, Goddard KAB, Goode EL, Wijsman EM, Jarvik GP. Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees Genetic Epidemiology. 14: 999-1004. PMID 9433614 DOI: 10.1002/(Sici)1098-2272(1997)14:6<999::Aid-Gepi73>3.0.Co;2-F  0.317
1997 McIndoe RA, Stanford JL, Gibbs M, Jarvik GP, Brandzel S, Neal CL, Li S, Gammack JT, Gay AA, Goode EL, Hood L, Ostrander EA. Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25. American Journal of Human Genetics. 61: 347-53. PMID 9311739 DOI: 10.1016/S0022-5347(01)63104-5  0.312
1997 Jarvik GP. Genetic Predictors Of Common Disease : Apolipoprotein E Genotype As A Paradigm Annals of Epidemiology. 7: 357-362. PMID 9250631 DOI: 10.1016/S1047-2797(97)00028-8  0.371
1997 Jarvik GP, Goode EL, Austin MA, Auwerx J, Deeb S, Schellenberg GD, Reed T. Evidence that the apolipoprotein E-genotype effects on lipid levels can change with age in males: a longitudinal analysis. American Journal of Human Genetics. 61: 171-81. PMID 9245998 DOI: 10.1086/513902  0.304
1994 Jarvik GP, Brunzell JD, Austin MA, Krauss RM, Motulsky AG, Wijsman E. Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype. Arteriosclerosis and Thrombosis : a Journal of Vascular Biology / American Heart Association. 14: 1687-94. PMID 7947591 DOI: 10.1161/01.Atv.14.11.1687  0.377
1993 Jarvik GP, Beaty TH, Gallagher PR, Coates PM, Cortner JA. Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia Genetic Epidemiology. 10: 257-270. PMID 8224806 DOI: 10.1002/Gepi.1370100406  0.334
Low-probability matches (unlikely to be authored by this person)
2013 Kim DS, Marsillach J, Furlong CE, Jarvik GP. Pharmacogenetics of paraoxonase activity: elucidating the role of high-density lipoprotein in disease. Pharmacogenomics. 14: 1495-515. PMID 24024900 DOI: 10.2217/Pgs.13.147  0.3
2019 Pal T, Agnese D, Daly M, La Spada A, Litton J, Wick M, Klugman S, Esplin ED, Jarvik GP. Points to consider: is there evidence to support BRCA1/2 and other inherited breast cancer genetic testing for all breast cancer patients? A statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31831881 DOI: 10.1038/S41436-019-0712-X  0.3
1995 Jarvik GP, Wijsman EM, Kukull WA, Schellenberg GD, Yu C, Larson EB. Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control study. Neurology. 45: 1092-6. PMID 7783869 DOI: 10.1212/Wnl.45.6.1092  0.3
2017 Kim DS, Burt AA, Ranchalis JE, Wilmot B, Smith JD, Patterson KE, Coe BP, Li YK, Bamshad MJ, Nikolas M, Eichler EE, Swanson JM, Nigg JT, Nickerson DA, Jarvik GP, et al. Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28332277 DOI: 10.1002/Ajmg.B.32527  0.3
2003 Jarvik GP, Hatsukami TS, Carlson C, Richter RJ, Jampsa R, Brophy VH, Margolin S, Rieder M, Nickerson D, Schellenberg GD, Heagerty PJ, Furlong CE. Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 23: 1465-71. PMID 12805074 DOI: 10.1161/01.Atv.0000081635.96290.D3  0.3
2021 Glazer AM, Davogustto GE, Shaffer CM, Vanoye CG, Desai RR, Farber-Eger E, Dikilitas O, Shang N, Pacheco JA, Yang T, Muhammad A, Mosley JD, Van Driest SL, Wells QS, Shaffer LL, ... ... Jarvik GP, et al. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. Circulation. PMID 34930020 DOI: 10.1161/CIRCULATIONAHA.121.055562  0.299
2013 Hatsukami TS, Jarvik GP, Hippe DS, Ranchalis JE, Clowes AW. Potential Association of a Single Nucleotide Polymorphism in the CDNK1B Gene and Carotid Plaque Fibrous Cap Status by MRI Journal of Vascular Surgery. 58: 561. DOI: 10.1016/J.Jvs.2013.05.070  0.299
2017 Dumitrescu L, Ritchie MD, Denny JC, El Rouby NM, McDonough CW, Bradford Y, Ramirez AH, Bielinski SJ, Basford MA, Chai HS, Peissig P, Carrell D, Pathak J, Rasmussen LV, Wang X, ... ... Jarvik GP, et al. Genome-wide study of resistant hypertension identified from electronic health records. Plos One. 12: e0171745. PMID 28222112 DOI: 10.1371/Journal.Pone.0171745  0.299
2018 Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, ... ... Jarvik GP, et al. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30287922 DOI: 10.1038/S41436-018-0308-X  0.299
1999 Goddard KAB, Goode EL, Rozek LS, Jarvik GP. Impact of family structure on the power of linkage tests using sib-pair methods Genetic Epidemiology. 17. PMID 10597495 DOI: 10.1002/Gepi.1370170793  0.299
1999 Gibbs M, Chakrabarti L, Stanford JL, Goode EL, Kolb S, Schuster EF, Buckley VA, Shook M, Hood L, Jarvik GP, Ostrander EA. Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer. American Journal of Human Genetics. 64: 1087-95. PMID 10090894 DOI: 10.1086/302342  0.299
2000 Jarvik GP, Stanford JL, Goode EL, McIndoe R, Kolb S, Gibbs M, Hood L, Ostrander EA. Confirmation of prostate cancer susceptibility genes using high-risk families. Journal of the National Cancer Institute. Monographs. 81-7. PMID 10854490 DOI: 10.1093/Oxfordjournals.Jncimonographs.A024230  0.298
2000 Goode EL, Stanford JL, Chakrabarti L, Gibbs M, Kolb S, McIndoe RA, Buckley VA, Schuster EF, Neal CL, Miller EL, Brandzel S, Hood L, Ostrander EA, Jarvik GP. Linkage analysis of 150 high-risk prostate cancer families at 1q24-25. Genetic Epidemiology. 18: 251-75. PMID 10723109 DOI: 10.1002/(Sici)1098-2272(200003)18:3<251::Aid-Gepi5>3.0.Co;2-X  0.298
2013 Kim JH, Jarvik GP, Browning BL, Rajagopalan R, Gordon AS, Rieder MJ, Robertson PD, Nickerson DA, Fisher NA, Hopkins PM. Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families. Anesthesiology. 119: 1054-65. PMID 24013571 DOI: 10.1097/Aln.0B013E3182A8A998  0.298
2015 Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Jarvik GP, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157  0.296
2013 Bennette C, Trinidad S, Fullerton S, Patrick D, Amendola L, Burke W, Hisama F, Jarvik G, Regier D, Veensta D. Return Of Incidental Findings In Genomic Medicine: Measuring What Patients Value Value in Health. 16: A146. DOI: 10.1016/J.Jval.2013.03.716  0.296
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  0.295
2008 Jarvik GP, Brunzell JD, Motulsky AG. Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia. Journal of the American College of Cardiology. 52: 1554-6. PMID 19007591 DOI: 10.1016/J.Jacc.2008.08.012  0.295
1994 Jarvik GP, Austin MA, Fabsitz RR, Auwerx J, Reed T, Christian JC, Deeb S. Genetic influences on age-related change in total cholesterol, low density lipoprotein-cholesterol, and triglyceride levels: longitudinal apolipoprotein E genotype effects. Genetic Epidemiology. 11: 375-384. PMID 7813899 DOI: 10.1002/Gepi.1370110407  0.295
2011 Richards J, Sandler P, Jarvik G, Larson E. C-A3-03: Building a Biorepository: Lessons Learned from the Northwest Institute of Genetic Medicine Clinical Medicine & Research. 9: 177-177. DOI: 10.3121/Cmr.2011.1020.C-A3-03  0.295
2017 Mavroudis CD, Seung Kim D, Burnham N, Morss AH, Kim JH, Burt AA, Crosslin DR, McDonald-McGinn DM, Zackai EH, Cohen MS, Nicolson SC, Spray TL, Stanaway IB, Nickerson DA, Russell MW, ... ... Jarvik GP, et al. A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD. Cardiology in the Young. 1-7. PMID 28927471 DOI: 10.1017/S1047951117001391  0.294
2019 Ruiz A, Eastman B, Halasz L, Jarvik G, Brown L, Graber J. RARE-48. GROWING KNOWLEDGE AND EMERGING QUESTIONS RELATED TO POT-1 GERMLINE MUTATIONS AND ASSOCIATED MALIGNANCIES: A CASE REPORT Neuro-Oncology. 21: vi232-vi232. DOI: 10.1093/Neuonc/Noz175.969  0.294
2010 Richter RJ, Jarvik GP, Furlong CE. Paraoxonase 1 status as a risk factor for disease or exposure. Advances in Experimental Medicine and Biology. 660: 29-35. PMID 20221868 DOI: 10.1007/978-1-60761-350-3_4  0.294
2015 Evans BJ, Burke W, Jarvik GP. The FDA and genomic tests--getting regulation right. The New England Journal of Medicine. 372: 2258-64. PMID 26014592 DOI: 10.1056/Nejmsr1501194  0.294
2015 Kim DS, Kim JH, Burt AA, Crosslin DR, Burnham N, Kim CE, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL, Stanaway IB, Nickerson DA, Heagerty PJ, Hakonarson H, Gaynor JW, ... Jarvik GP, et al. Burden of potentially pathologic copy number variants is higher in children with isolated congenital heart disease and significantly impairs covariate-adjusted transplant-free survival. The Journal of Thoracic and Cardiovascular Surgery. PMID 26704054 DOI: 10.1016/J.Jtcvs.2015.09.136  0.293
1993 Austin MA, Jarvik GP, Hokanson JE, Edwards K. Complex segregation analysis of LDL peak particle diameter Genetic Epidemiology. 10: 599-604. PMID 8314067 DOI: 10.1002/Gepi.1370100645  0.293
2019 Cohen SA, Pritchard CC, Jarvik GP. Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology. Annual Review of Genomics and Human Genetics. PMID 30848956 DOI: 10.1146/Annurev-Genom-083118-015406  0.293
1993 Cortner JA, Coates PM, Liacouras CA, Jarvik GP. Familial combined hyperlipidemia in children: Clinical expression, metabolic defects, and management* The Journal of Pediatrics. 123: 177-184. PMID 8345411 DOI: 10.1016/S0022-3476(05)81686-5  0.292
1998 Breitner JC, Jarvik GP, Plassman BL, Saunders AM, Welsh KA. Risk of Alzheimer disease with the epsilon4 allele for apolipoprotein E in a population-based study of men aged 62-73 years. Alzheimer Disease and Associated Disorders. 12: 40-4. PMID 9539409 DOI: 10.1097/00002093-199803000-00006  0.292
2013 Ritchie MD, Denny JC, Zuvich RL, Crawford DC, Schildcrout JS, Bastarache L, Ramirez AH, Mosley JD, Pulley JM, Basford MA, Bradford Y, Rasmussen LV, Pathak J, Chute CG, Kullo IJ, ... ... Jarvik GP, et al. Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Circulation. 127: 1377-85. PMID 23463857 DOI: 10.1161/Circulationaha.112.000604  0.292
2012 Kim DS, Burt AA, Ranchalis JE, Richter RJ, Marshall JK, Nakayama KS, Jarvik ER, Eintracht JF, Rosenthal EA, Furlong CE, Jarvik GP. Dietary cholesterol increases paraoxonase 1 enzyme activity. Journal of Lipid Research. 53: 2450-8. PMID 22896672 DOI: 10.1194/Jlr.P030601  0.292
2021 Mehrotra R, Stanaway IB, Jarvik GP, Lambie M, Morelle J, Perl J, Himmelfarb J, Heimburger O, Johnson DW, Imam TH, Robinson B, Stenvinkel P, Devuyst O, Davies SJ. A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Kidney International. PMID 34197840 DOI: 10.1016/j.kint.2021.05.037  0.291
2010 Furlong CE, Suzuki SM, Stevens RC, Marsillach J, Richter RJ, Jarvik GP, Checkoway H, Samii A, Costa LG, Griffith A, Roberts JW, Yearout D, Zabetian CP. Human PON1, a biomarker of risk of disease and exposure. Chemico-Biological Interactions. 187: 355-61. PMID 20338154 DOI: 10.1016/J.Cbi.2010.03.033  0.291
2018 Williams JL, Chung WK, Fedotov A, Kiryluk K, Weng C, Connolly JJ, Harr M, Hakonarson H, Leppig KA, Larson EB, Jarvik GP, Veenstra DL, Hoell C, Smith ME, Holm IA, et al. Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs. Healthcare (Basel, Switzerland). 6. PMID 30011878 DOI: 10.3390/Healthcare6030083  0.29
1994 Cortner JA, Coates PM, Liacouras CA, Jarvik GP. Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and management. Current Problems in Pediatrics. 24: 295-305. PMID 7859485 DOI: 10.1016/0045-9380(94)90010-8  0.29
2019 Manolio TA, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Jarvik GP, McLeod HL, Mensah GA, Relling MV, Roden DM, Rowley R, Tamburro C, Williams MS, Green ED. Genomic Medicine Year in Review: 2019. American Journal of Human Genetics. 105: 1072-1075. PMID 32027834 DOI: 10.1016/J.Ajhg.2019.11.006  0.289
2018 Mosley JD, Benson MD, Smith JG, Melander O, Ngo D, Shaffer CM, Ferguson JF, Herzig MS, McCarty CA, Chute CG, Jarvik GP, Gordon AS, Palmer MR, Crosslin DR, Larson EB, et al. Probing the Virtual Proteome to Identify Novel Disease Biomarkers. Circulation. 138: 2469-2481. PMID 30571344 DOI: 10.1161/Circulationaha.118.036063  0.289
2014 Kim DS, Burt AA, Ranchalis JE, Jarvik LE, Eintracht JF, Furlong CE, Jarvik GP. Effects of dietary components on high-density lipoprotein measures in a cohort of 1,566 participants. Nutrition & Metabolism. 11: 44. PMID 25264450 DOI: 10.1186/1743-7075-11-44  0.287
2000 Cynthia WKO, Beresford SAA, Alderman B, Jarvik GP, Schulte SJ, Calhoun B, Tsuchida AM, Koepsell TD, Lee SP. Apolipoprotein E genotype and the risk of gallbladder disease in pregnancy Hepatology. 31: 18-23. PMID 10613722 DOI: 10.1002/Hep.510310105  0.287
2007 Saam T, Yuan C, Chu B, Takaya N, Underhill H, Cai J, Tran N, Polissar NL, Neradilek B, Jarvik GP, Isaac C, Garden GA, Maravilla KR, Hashimoto B, Hatsukami TS. Predictors of carotid atherosclerotic plaque progression as measured by noninvasive magnetic resonance imaging. Atherosclerosis. 194: e34-42. PMID 16978632 DOI: 10.1016/J.Atherosclerosis.2006.08.016  0.286
2016 Kim DS, Li YK, Bell GA, Burt AA, Vaisar T, Hutchins PM, Furlong CE, Otvos JD, Polak JF, Arnan MK, Kaufman JD, McClelland RL, Longstreth WT, Jarvik GP. Concentration of Smaller High-Density Lipoprotein Particle (HDL-P) Is Inversely Correlated With Carotid Intima Media Thickening After Confounder Adjustment: The Multi Ethnic Study of Atherosclerosis (MESA). Journal of the American Heart Association. 5. PMID 27207961 DOI: 10.1161/Jaha.115.002977  0.286
2023 Rajabli F, Benchek P, Tosto G, Kushch N, Sha J, Bazemore K, Zhu C, Lee WP, Haut J, Hamilton-Nelson KL, Wheeler NR, Zhao Y, Farrell JJ, Grunin MA, Leung YY, ... ... Jarvik GP, et al. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences. PMID 37461624 DOI: 10.1101/2023.07.06.23292311  0.285
2001 Peters MA, Jarvik GP, Janer M, Chakrabarti L, Kolb S, Goode EL, Gibbs M, DuBois CC, Schuster EF, Hood L, Ostrander EA, Stanford JL. Genetic linkage analysis of prostate cancer families to Xq27-28. Human Heredity. 51: 107-13. PMID 11096277 DOI: 10.1159/000022965  0.283
2020 Hu Y, Graff M, Haessler J, Buyske S, Bien SA, Tao R, Highland HM, Nishimura KK, Zubair N, Lu Y, Verbanck M, Hilliard AT, Klarin D, Damrauer SM, Ho YL, ... ... Jarvik GP, et al. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 16: e1008684. PMID 32226016 DOI: 10.1371/journal.pgen.1008684  0.283
2020 Palmer MR, Kim DS, Crosslin DR, Stanaway IB, Rosenthal EA, Carrell DS, Cronkite DJ, Gordon A, Du X, Li YK, Williams MS, Weng C, Feng Q, Li R, Pendergrass SA, ... ... Jarvik GP, et al. Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network. Genetic Epidemiology. PMID 32964493 DOI: 10.1002/gepi.22360  0.282
2022 Tcheandjieu C, Zhu X, Hilliard AT, Clarke SL, Napolioni V, Ma S, Lee KM, Fang H, Chen F, Lu Y, Tsao NL, Raghavan S, Koyama S, Gorman BR, Vujkovic M, ... ... Jarvik GP, et al. Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Nature Medicine. PMID 35915156 DOI: 10.1038/s41591-022-01891-3  0.282
2020 Amendola LM, Muenzen K, Biesecker LG, Bowling KM, Cooper GM, Dorschner MO, Driscoll C, Foreman AKM, Golden-Grant K, Greally JM, Hindorff L, Kanavy D, Jobanputra V, Johnston JJ, Kenny EE, ... ... Jarvik GP, et al. Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies. American Journal of Human Genetics. PMID 33108757 DOI: 10.1016/j.ajhg.2020.09.011  0.281
2018 Kim DS, Li YK, Kim JH, Bergquist CS, Gerdes M, Bernbaum JC, Burnham N, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL, Nickerson DA, Hakonarson H, Jarvik GP, Gaynor JW. Autosomal dominant mannose-binding lectin deficiency is associated with worse neurodevelopmental outcomes after cardiac surgery in infants. The Journal of Thoracic and Cardiovascular Surgery. 155: 1139-1147.e2. PMID 29452463 DOI: 10.1016/J.Jtcvs.2017.08.035  0.281
2012 Masys DR, Jarvik GP, Abernethy NF, Anderson NR, Papanicolaou GJ, Paltoo DN, Hoffman MA, Kohane IS, Levy HP. Technical desiderata for the integration of genomic data into Electronic Health Records. Journal of Biomedical Informatics. 45: 419-22. PMID 22223081 DOI: 10.1016/J.Jbi.2011.12.005  0.28
1998 Carmelli D, Swan GE, Reed T, Miller B, Wolf PA, Jarvik GP, Schellenberg GD. Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins. Neurology. 50: 1580-5. PMID 9633697 DOI: 10.1212/Wnl.50.6.1580  0.279
2008 Tabbutt S, Nord AS, Jarvik GP, Bernbaum J, Wernovsky G, Gerdes M, Zackai E, Clancy RR, Nicolson SC, Spray TL, Gaynor JW. Neurodevelopmental Outcomes After Staged Palliation for Hypoplastic Left Heart Syndrome Obstetrical & Gynecological Survey. 63: 419-421. DOI: 10.1097/01.Ogx.0000318137.90589.D0  0.279
1995 Goddard KAB, Jarvik GP, Graham J, McNeney B, Hsu L, Siegmund K, Grosser S, Olson J, Wijsman EM. Analysis of quantitative risk factors for a common oligogenic disease. Genetic Epidemiology. 12: 759-764. PMID 8788005 DOI: 10.1002/Gepi.1370120638  0.278
2020 Joo YY, Actkins K, Pacheco JA, Basile AO, Carroll R, Crosslin DR, Day F, Denny JC, Velez Edwards DR, Hakonarson H, Harley JB, Hebbring SJ, Ho K, Jarvik GP, Jones M, et al. A polygenic and phenotypic risk prediction for Polycystic Ovary Syndrome evaluated by Phenome-wide association studies. The Journal of Clinical Endocrinology and Metabolism. PMID 31917831 DOI: 10.1210/Clinem/Dgz326  0.278
2015 Nishimura AA, Shirts BH, Dorschner MO, Amendola LM, Smith JW, Jarvik GP, Tarczy-Hornoch P. Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25741865 DOI: 10.1038/Gim.2015.5  0.278
2011 Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, et al. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nature Genetics. 43: 436-41. PMID 21460841 DOI: 10.1038/Ng.801  0.276
2019 Zhang X, Veturi Y, Verma S, Bone W, Verma A, Lucas A, Hebbring S, Denny JC, Stanaway IB, Jarvik GP, Crosslin D, Larson EB, Rasmussen-Torvik L, Pendergrass SA, Smoller JW, et al. Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 24: 272-283. PMID 30864329  0.275
2015 Trinidad SB, Coffin TB, Fullerton SM, Ralston J, Jarvik GP, Larson EB. "Getting off the Bus Closer to Your Destination": Patients' Views about Pharmacogenetic Testing. The Permanente Journal. 19: 21-7. PMID 26057686 DOI: 10.7812/Tpp/15-046  0.275
2009 Samanta B, Bird GL, Kuijpers M, Zimmerman RA, Jarvik GP, Wernovsky G, Clancy RR, Licht DJ, Gaynor JW, Nataraj C. Prediction of periventricular leukomalacia. Part I: Selection of hemodynamic features using logistic regression and decision tree algorithms. Artificial Intelligence in Medicine. 46: 201-15. PMID 19162455 DOI: 10.1016/J.Artmed.2008.12.005  0.275
2015 Gallego CJ, Shirts BH, Bennette CS, Guzauskas G, Amendola LM, Horike-Pyne M, Hisama FM, Pritchard CC, Grady WM, Burke W, Jarvik GP, Veenstra DL. Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 33: 2084-91. PMID 25940718 DOI: 10.1200/Jco.2014.59.3665  0.275
1996 Clement SJ, Leppig KA, Jarvik GP, Kapur RP, Norwood TH. Trisomy 10p: report of an unusual mechanism of formation and critical evaluation of the clinical phenotype. American Journal of Medical Genetics. 65: 197-204. PMID 9240743 DOI: 10.1002/(Sici)1096-8628(19961028)65:3<197::Aid-Ajmg5>3.0.Co;2-N  0.275
2010 Fuller S, Rajagopalan R, Jarvik GP, Gerdes M, Bernbaum J, Wernovsky G, Clancy RR, Solot C, Nicolson SC, Spray TL, Gaynor JW. J. Maxwell Chamberlain Memorial Paper for congenital heart surgery. Deep hypothermic circulatory arrest does not impair neurodevelopmental outcome in school-age children after infant cardiac surgery. The Annals of Thoracic Surgery. 90: 1985-94; discussion . PMID 21095350 DOI: 10.1016/J.Athoracsur.2010.08.005  0.275
2016 Richards JE, Bane E, Fullerton SM, Ludman EJ, Jarvik G. Allocation of Resources to Communication of Research Result Summaries: Biobank Participant Perspectives. Journal of Empirical Research On Human Research Ethics : Jerhre. PMID 27613778 DOI: 10.1177/1556264616667126  0.274
2021 Suri P, Stanaway IB, Zhang Y, Freidin MB, Tsepilov YA, Carrell DS, Williams FMK, Aulchenko YS, Hakonarson H, Namjou B, Crosslin DR, Jarvik GP, Lee MT. Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Pain. PMID 33729212 DOI: 10.1097/j.pain.0000000000002221  0.274
2018 Wilfond BS, Kauffman TL, Jarvik GP, Reiss JA, Richards CS, McMullen C, Gilmore M, Himes P, Kraft SA, Porter KM, Schneider JL, Punj S, Leo MC, Dickerson JF, Lynch FL, et al. Lessons Learned From A Study Of Genomics-Based Carrier Screening For Reproductive Decision Making. Health Affairs (Project Hope). 37: 809-816. PMID 29733724 DOI: 10.1377/Hlthaff.2017.1578  0.274
2019 Robinson JR, Carroll RJ, Bastarache L, Chen Q, Mou Z, Wei WQ, Connolly JJ, Mentch F, Sleiman P, Crane PK, Hebbring SJ, Stanaway IB, Crosslin DR, Gordon AS, Rosenthal EA, ... ... Jarvik GP, et al. Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization. World Journal of Surgery. PMID 31605180 DOI: 10.1007/S00268-019-05202-9  0.273
2010 Ludman EJ, Fullerton SM, Spangler L, Trinidad SB, Fujii MM, Jarvik GP, Larson EB, Burke W. Glad you asked: participants' opinions of re-consent for dbGap data submission. Journal of Empirical Research On Human Research Ethics : Jerhre. 5: 9-16. PMID 20831417 DOI: 10.1525/Jer.2010.5.3.9  0.273
2018 Jarvik GP, King M. Arno G. Motulsky (1923–2018): A Founder of Medical Genetics, Creator of Pharmacogenetics, and Former ASHG President The American Journal of Human Genetics. 102: 335-339. DOI: 10.1016/J.Ajhg.2018.02.005  0.271
2003 Goode EL, Badzioch MD, Kim H, Gagnon F, Rozek LS, Edwards KL, Jarvik GP. Multiple genome-wide analyses of smoking behavior in the Framingham Heart Study. Bmc Genetics. 4: S102. PMID 14975170 DOI: 10.1186/1471-2156-4-S1-S102  0.271
2014 Kim DS, Kim JH, Burt AA, Crosslin DR, Burnham N, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL, Stanaway IB, Nickerson DA, Russell MW, Hakonarson H, Gaynor JW, Jarvik GP. Patient genotypes impact survival after surgery for isolated congenital heart disease. The Annals of Thoracic Surgery. 98: 104-10; discussion 1. PMID 24811984 DOI: 10.1016/J.Athoracsur.2014.03.017  0.269
2019 Bowen DJ, Hyams T, Laurino M, Woolley T, Cohen S, Leppig KA, Jarvik G. Development of FamilyTalk: an Intervention to Support Communication and Educate Families About Colorectal Cancer Risk. Journal of Cancer Education : the Official Journal of the American Association For Cancer Education. PMID 30737640 DOI: 10.1007/S13187-019-1484-3  0.269
1995 Edwards KL, Austin MA, Jarvik GP. Evidence for genetic influences on smoking in adult women twins Clinical Genetics. 47: 236-244. PMID 7554348 DOI: 10.1111/J.1399-0004.1995.Tb04303.X  0.269
2014 Hutchins PM, Ronsein GE, Monette JS, Pamir N, Wimberger J, He Y, Anantharamaiah GM, Kim DS, Ranchalis JE, Jarvik GP, Vaisar T, Heinecke JW. Quantification of HDL particle concentration by calibrated ion mobility analysis. Clinical Chemistry. 60: 1393-401. PMID 25225166 DOI: 10.1373/Clinchem.2014.228114  0.269
2009 Gaynor JW, Nord AS, Wernovsky G, Bernbaum J, Solot CB, Burnham N, Zackai E, Heagerty PJ, Clancy RR, Nicolson SC, Jarvik GP, Gerdes M. Apolipoprotein E genotype modifies the risk of behavior problems after infant cardiac surgery. Pediatrics. 124: 241-50. PMID 19564306 DOI: 10.1542/Peds.2008-2281  0.268
2014 Burke W, Evans BJ, Jarvik GP. Return of results: ethical and legal distinctions between research and clinical care. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 166: 105-11. PMID 24616381 DOI: 10.1002/Ajmg.C.31393  0.268
2003 Gaynor JW, Gerdes M, Zackai EH, Bernbaum J, Wernovsky G, Clancy RR, Newman MF, Saunders AM, Heagerty PJ, D'Agostino JA, McDonald-McGinn D, Nicolson SC, Spray TL, Jarvik GP. Apolipoprotein E genotype and neurodevelopmental sequelae of infant cardiac surgery. The Journal of Thoracic and Cardiovascular Surgery. 126: 1736-45. PMID 14688681 DOI: 10.1016/S0022-5223(03)01188-7  0.267
2011 Hotaling J, Wessells H, Burt A, Crosslin D, Jarvik G, Weston N, Ehrlich K, Larson E, Walsh T. 920 NOVEL SINGLE NUCLEOTIDE POLYMORPHISMS MAY PREDICT ED: DATA FROM THE GROUP HEALTH ADULT CHANGES IN THOUGHT STUDY Journal of Urology. 185. DOI: 10.1016/J.Juro.2011.02.811  0.267
2019 Salem JE, Shoemaker MB, Bastarache L, Shaffer CM, Glazer AM, Kroncke B, Wells QS, Shi M, Straub P, Jarvik GP, Larson EB, Velez Edwards DR, Edwards TL, Davis LK, Hakonarson H, et al. Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysis. Jama Cardiology. PMID 30673079 DOI: 10.1001/Jamacardio.2018.4615  0.266
2016 Furlong CE, Marsillach J, Jarvik GP, Costa LG. Paraoxonases-1, -2 and -3: What are their functions? Chemico-Biological Interactions. PMID 27238723 DOI: 10.1016/J.Cbi.2016.05.036  0.266
2017 Jarvik GP. 2016 Victor A. McKusick Leadership Award Introduction: Stanley Gartler. American Journal of Human Genetics. 100: 401-402. PMID 28257688 DOI: 10.1016/J.Ajhg.2017.01.012  0.265
2016 Suri P, Boyko EJ, Smith NL, Jarvik JG, Williams FM, Jarvik GP, Goldberg J. Modifiable Risk Factors for Chronic Back Pain: Insights Using the Co-Twin Control Design. The Spine Journal : Official Journal of the North American Spine Society. PMID 27794503 DOI: 10.1016/J.Spinee.2016.07.533  0.264
2005 Schultz AH, Jarvik GP, Wernovsky G, Bernbaum J, Clancy RR, D'Agostino JA, Gerdes M, McDonald-McGinn D, Nicolson SC, Spray TL, Zackai E, Gaynor JW. Effect of congenital heart disease on neurodevelopmental outcomes within multiple-gestation births. The Journal of Thoracic and Cardiovascular Surgery. 130: 1511-1516. PMID 16307991 DOI: 10.1016/J.Jtcvs.2005.07.040  0.264
2020 Morales A, Kinnamon DD, Jordan E, Platt J, Vatta M, Dorschner MO, Starkey C, Mead J, Ai T, Burke W, Gastier-Foster J, Jarvik GP, Rehm HL, Nickerson DA, Hershberger RE. Variant Interpretation for Dilated Cardiomyopathy (DCM): Refinement of the ACMG/ClinGen Guidelines for the DCM Precision Medicine Study. Circulation. Genomic and Precision Medicine. PMID 32160020 DOI: 10.1161/CIRCGEN.119.002480  0.263
2015 De R, Verma SS, Drenos F, Holzinger ER, Holmes MV, Hall MA, Crosslin DR, Carrell DS, Hakonarson H, Jarvik G, Larson E, Pacheco JA, Rasmussen-Torvik LJ, Moore CB, Asselbergs FW, et al. Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR). Biodata Mining. 8: 41. PMID 26674805 DOI: 10.1186/S13040-015-0074-0  0.263
2013 Pyott SM, Tran TT, Leistritz DF, Pepin MG, Mendelsohn NJ, Temme RT, Fernandez BA, Elsayed SM, Elsobky E, Verma I, Nair S, Turner EH, Smith JD, Jarvik GP, Byers PH. WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta. American Journal of Human Genetics. 92: 590-7. PMID 23499310 DOI: 10.1016/J.Ajhg.2013.02.009  0.262
2011 White KL, Rider DN, Kalli KR, Knutson KL, Jarvik GP, Goode EL. Genomics of the NF-κB signaling pathway: hypothesized role in ovarian cancer. Cancer Causes & Control : Ccc. 22: 785-801. PMID 21359843 DOI: 10.1007/S10552-011-9745-4  0.262
2016 Almoguera B, Vazquez L, Mentch F, Connolly J, Pacheco JA, Sundaresan AS, Peissig PL, Linneman JG, McCarty CA, Crosslin D, Carrell DS, Lingren T, Namjou-Khales B, Harley JB, Larson E, ... Jarvik GP, et al. Identification of Four Novel Loci in Asthma in European and African American Populations. American Journal of Respiratory and Critical Care Medicine. PMID 27611488 DOI: 10.1164/Rccm.201604-0861Oc  0.262
2018 Jarvik GP. Arno G. Motulsky, MD (1923-2018): Holocaust survivor who cofounded the field of medical genetics. Genetics in Medicine. 20: 477-479. PMID 29688222 DOI: 10.1038/Gim.2018.55  0.261
2005 Hendrickson A, McKinstry LA, Lewis JK, Lum J, Louie A, Schellenberg GD, Hatsukami TS, Chait A, Jarvik GP. Ex vivo measures of LDL oxidative susceptibility predict carotid artery disease. Atherosclerosis. 179: 147-53. PMID 15721021 DOI: 10.1016/J.Atherosclerosis.2004.09.015  0.261
2024 Lennon NJ, Kottyan LC, Kachulis C, Abul-Husn NS, Arias J, Belbin G, Below JE, Berndt SI, Chung WK, Cimino JJ, Clayton EW, Connolly JJ, Crosslin DR, Dikilitas O, Velez Edwards DR, ... ... Jarvik GP, et al. Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations. Nature Medicine. PMID 38374346 DOI: 10.1038/s41591-024-02796-z  0.261
2017 Nikroo N, Safarova, Austin EE, Andrade MDE, Li R, Robertson PD, Carrell DS, Bielinski SJ, Stallings SC, Larson EB, Linneman JG, Jarvik GP, Crosslin DR, Schaid DJ, Kullo IJ. P4472Targeted sequencing of 80 pharmacogenes reveals evidence for pleiotropic effects on serum LDL cholesterol levels European Heart Journal. 38. DOI: 10.1093/Eurheartj/Ehx504.P4472  0.261
2008 Tabbutt S, Nord AS, Jarvik GP, Bernbaum J, Wernovsky G, Gerdes M, Zackai E, Clancy RR, Nicolson SC, Spray TL, Gaynor JW. Neurodevelopmental outcomes after staged palliation for hypoplastic left heart syndrome. Pediatrics. 121: 476-83. PMID 18310195 DOI: 10.1542/Peds.2007-1282  0.26
2008 Reiner AP, Wurfel MM, Lange LA, Carlson CS, Nord AS, Carty CL, Rieder MJ, Desmarais C, Jenny NS, Iribarren C, Walston JD, Williams OD, Nickerson DA, Jarvik GP. Polymorphisms of the IL1-receptor antagonist gene (IL1RN) are associated with multiple markers of systemic inflammation. Arteriosclerosis, Thrombosis, and Vascular Biology. 28: 1407-12. PMID 18451331 DOI: 10.1161/Atvbaha.108.167437  0.26
2015 Mo H, Thompson WK, Rasmussen LV, Pacheco JA, Jiang G, Kiefer R, Zhu Q, Xu J, Montague E, Carrell DS, Lingren T, Mentch FD, Ni Y, Wehbe FH, Peissig PL, ... ... Jarvik GP, et al. Desiderata for computable representations of electronic health records-driven phenotype algorithms. Journal of the American Medical Informatics Association : Jamia. PMID 26342218 DOI: 10.1093/Jamia/Ocv112  0.259
2002 Jarvik GP, Tsai NT, McKinstry LA, Wani R, Brophy VH, Richter RJ, Schellenberg GD, Heagerty PJ, Hatsukami TS, Furlong CE. Vitamin C and E intake is associated with increased paraoxonase activity. Arteriosclerosis, Thrombosis, and Vascular Biology. 22: 1329-33. PMID 12171796 DOI: 10.1161/01.Atv.0000027101.40323.3A  0.258
2013 Mukherjee S, Walter S, Yang H, Jarvik G, Crosslin D, Lee S, Fardo D, Green R, Sherva R, Walker R, Larson E, Schellenberg G, Glymour M, Crane P. Vascular disease, vascular risk factors and risk of late-onset Alzheimer's disease: Mendelian randomization analyses in the combined ADGC dataset Alzheimers & Dementia. 9: 694. DOI: 10.1016/J.Jalz.2013.04.370  0.257
2013 Kim DS, Maden SK, Burt AA, Ranchalis JE, Furlong CE, Jarvik GP. Dietary fatty acid intake is associated with paraoxonase 1 activity in a cohort-based analysis of 1,548 subjects. Lipids in Health and Disease. 12: 183. PMID 24330840 DOI: 10.1186/1476-511X-12-183  0.257
2012 Saxena R, Elbers C, Guo Y, Peter I, Gaunt T, Mega J, Lanktree M, Tare A, Castillo B, Li Y, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight B, ... ... Jarvik G, et al. Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci The American Journal of Human Genetics. 90: 753. DOI: 10.1016/J.Ajhg.2012.03.001  0.256
2020 He Y, Ronsein GE, Tang C, Jarvik GP, Davidson WS, Kothari V, Song HD, Segrest J, Bornfeldt KE, Heinecke JW. Diabetes Impairs Cellular Cholesterol Efflux from ABCA1 to Small HDL Particles. Circulation Research. PMID 32819213 DOI: 10.1161/Circresaha.120.317178  0.254
2005 Furlong CE, Cole TB, Jarvik GP, Pettan-Brewer C, Geiss GK, Richter RJ, Shih DM, Tward AD, Lusis AJ, Costa LG. Role of paraoxonase (PON1) status in pesticide sensitivity: genetic and temporal determinants. Neurotoxicology. 26: 651-9. PMID 16112327 DOI: 10.1016/J.Neuro.2004.08.002  0.254
2001 Peters MA, Stanford JL, Badzioch MD, Kolb S, Janer M, Goode EL, Gibbs M, Hood L, Ostrander EA, Jarvik GP. Genome-wide scan for high-risk prostate cancer families with breast cancer reveals new loci for prostate cancer and breast cancer Nature Genetics. 27: 79-79. DOI: 10.1038/87246  0.254
2014 Jeff JM, Brown-Gentry K, Goodloe R, Ritchie MD, Denny JC, Kho AN, Armstrong LL, McClellan B, Mayo P, Allen M, Jin H, Gillani NB, Schnetz-Boutaud N, Dilks HH, Basford MA, ... ... Jarvik GP, et al. Replication of SCN5A Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies. Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics. Evobio (Conference), Author. 2014: 939-951. PMID 25590050 DOI: 10.1007/978-3-662-45523-4_76  0.253
2003 Badzioch MD, DeFrance HB, Jarvik GP. An examination of the genotyping error detection function of SIMWALK2 Bmc Genetics. 4: 1-6. PMID 14975108 DOI: 10.1186/1471-2156-4-S1-S40  0.252
2016 Bowdin S, Gilbert A, Bedoukian E, Carew C, Adam MP, Belmont J, Bernhardt B, Biesecker L, Bjornsson HT, Blitzer M, D'Alessandro LC, Deardorff MA, Demmer L, Elliott A, Feldman GL, ... ... Jarvik G, et al. Recommendations for the integration of genomics into clinical practice. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27171546 DOI: 10.1038/Gim.2016.17  0.251
2014 Ritchie MD, Verma SS, Hall MA, Goodloe RJ, Berg RL, Carrell DS, Carlson CS, Chen L, Crosslin DR, Denny JC, Jarvik G, Li R, Linneman JG, Pathak J, Peissig P, et al. Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci. Molecular Vision. 20: 1281-95. PMID 25352737  0.251
2024 Venner E, Patterson K, Kalra D, Wheeler MM, Chen YJ, Kalla SE, Yuan B, Karnes JH, Walker K, Smith JD, McGee S, Radhakrishnan A, Haddad A, Empey PE, Wang Q, ... ... Jarvik G, et al. The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities. Communications Biology. 7: 174. PMID 38374434 DOI: 10.1038/s42003-023-05708-y  0.251
2008 Kerwin WS, Oikawa M, Yuan C, Jarvik GP, Hatsukami TS. MR imaging of adventitial vasa vasorum in carotid atherosclerosis Magnetic Resonance in Medicine. 59: 507-514. PMID 18306402 DOI: 10.1002/Mrm.21532  0.25
2019 Hart MR, Garrison LP, Doyle DL, Jarvik GP, Watkins J, Devine B. Projected Cost-Effectiveness for 2 Gene-Drug Pairs Using a Multigene Panel for Patients Undergoing Percutaneous Coronary Intervention. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 22: 1231-1239. PMID 31708059 DOI: 10.1016/J.Jval.2019.05.015  0.249
2005 Takaya N, Yuan C, Chu B, Saam T, Polissar NL, Jarvik GP, Isaac C, McDonough J, Natiello C, Small R, Ferguson MS, Hatsukami TS. Presence of Intraplaque Hemorrhage Stimulates Progression of Carotid Atherosclerotic Plaques A High-Resolution Magnetic Resonance Imaging Study Circulation. 111: 2768-2775. PMID 15911695 DOI: 10.1161/Circulationaha.104.504167  0.248
2017 Schultz AH, Ittenbach RF, Gerdes M, Jarvik GP, Wernovsky G, Bernbaum J, Solot C, Clancy RR, Nicolson SC, Spray TL, McDonald-McGinn D, Zackai E, Gaynor JW. Effect of congenital heart disease on 4-year neurodevelopment within multiple-gestation births. The Journal of Thoracic and Cardiovascular Surgery. PMID 28320512 DOI: 10.1016/J.Jtcvs.2017.02.022  0.247
2019 Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Jarvik GP, et al. Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430. PMID 30820047 DOI: 10.1038/s41588-019-0358-2  0.247
2006 Kaltman JR, Jarvik GP, Bernbaum J, Wernovsky G, Gerdes M, Zackai E, Clancy RR, Nicolson SC, Spray TL, Gaynor JW. Neurodevelopmental outcome after early repair of a ventricular septal defect with or without aortic arch obstruction The Journal of Thoracic and Cardiovascular Surgery. 131: 792-798. PMID 16580436 DOI: 10.1016/J.Jtcvs.2005.12.023  0.247
2021 Harrison SM, Austin-Tse CA, Kim S, Lebo M, Leon A, Murdock D, Radhakrishnan A, Shirts BH, Steeves M, Venner E, Gibbs RA, Jarvik GP, Rehm HL. Harmonizing variant classification for return of results in the All of Us Research Program. Human Mutation. PMID 34923710 DOI: 10.1002/humu.24317  0.245
2009 Berg AO, Baird MA, Botkin JR, Driscoll DA, Fishman PA, Guarino PD, Hiatt RA, Jarvik GP, Millon-Underwood S, Morgan TM, Mulvihill JJ, Pollin TI, Schimmel SR, Stefanek ME, Vollmer WM, et al. National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health. Annals of Internal Medicine. 151: 872-877. DOI: 10.1059/0003-4819-151-12-200912150-00165  0.245
1999 Stanford JL, Gibbs M, McIndoe RA, Jarvik GP, Chakrabarti L, Goode EL, Kolb S, Hood L, Ostrander EA. A RARE PROSTATE CANCER SUSCEPTIBILITY LOCUS MAPPED TO THE SHORT ARM OF CHROMOSOME 1 (1p36) The Journal of Urology. 71. DOI: 10.1097/00005392-199904010-00285  0.243
2011 Trinidad SB, Fullerton SM, Ludman EJ, Jarvik GP, Larson EB, Burke W. Response--The Risks and Benefits of Re-Consent Science. 332: 306-306. DOI: 10.1126/Science.332.6027.306-B  0.242
2022 Zhang X, Lucas AM, Veturi Y, Drivas TG, Bone WP, Verma A, Chung WK, Crosslin D, Denny JC, Hebbring S, Jarvik GP, Kullo I, Larson EB, Rasmussen-Torvik LJ, Schaid DJ, et al. Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature Communications. 13: 3428. PMID 35701404 DOI: 10.1038/s41467-022-30678-w  0.242
2021 Bagheri M, Wang C, Shi M, Manouchehri A, Murray KT, Murphy MB, Shaffer CM, Singh K, Davis LK, Jarvik GP, Stanaway IB, Hebbring S, Reilly MP, Gerszten RE, Wang TJ, et al. The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene. Scientific Reports. 11: 15652. PMID 34341450 DOI: 10.1038/s41598-021-95154-9  0.242
2006 Carty CL, Heagerty P, Nakayama K, McClung EC, Lewis J, Lum D, Boespflug E, McCloud-Gehring C, Soleimani BR, Ranchalis J, Bacus TJ, Furlong CE, Jarvik GP. Inflammatory response after influenza vaccination in men with and without carotid artery disease. Arteriosclerosis, Thrombosis, and Vascular Biology. 26: 2738-44. PMID 17023683 DOI: 10.1161/01.Atv.0000248534.30057.B5  0.241
2007 Gaynor JW, Wernovsky G, Jarvik GP, Bernbaum J, Gerdes M, Zackai E, Nord AS, Clancy RR, Nicolson SC, Spray TL. Patient characteristics are important determinants of neurodevelopmental outcome at one year of age after neonatal and infant cardiac surgery. The Journal of Thoracic and Cardiovascular Surgery. 133: 1344-53, 1353.e1-3. PMID 17467455 DOI: 10.1016/J.Jtcvs.2006.10.087  0.241
1994 Jarvik GP, Wijsman EM. Alzheimer's disease and the family effect. Nature Genetics. 8: 115-115. PMID 7842007 DOI: 10.1038/Ng1094-115A  0.239
2022 Ramdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL, Chesi A, Wells A, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, ... ... Jarvik GP, et al. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American Journal of Human Genetics. 109: 1366-1387. PMID 35931049 DOI: 10.1016/j.ajhg.2022.06.012  0.239
2009 Fuller S, Nord AS, Gerdes M, Wernovsky G, Jarvik GP, Bernbaum J, Zackai E, Gaynor JW. Predictors of impaired neurodevelopmental outcomes at one year of age after infant cardiac surgery. European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association For Cardio-Thoracic Surgery. 36: 40-7. PMID 19394849 DOI: 10.1016/J.Ejcts.2009.02.047  0.238
2015 Ronsein GE, Pamir N, von Haller PD, Kim DS, Oda MN, Jarvik GP, Vaisar T, Heinecke JW. Parallel reaction monitoring (PRM) and selected reaction monitoring (SRM) exhibit comparable linearity, dynamic range and precision for targeted quantitative HDL proteomics. Journal of Proteomics. 113: 388-99. PMID 25449833 DOI: 10.1016/J.Jprot.2014.10.017  0.237
2004 Galli KK, Zimmerman RA, Jarvik GP, Wernovsky G, Kuypers MK, Clancy RR, Montenegro LM, Mahle WT, Newman MF, Saunders AM, Nicolson SC, Spray TL, Gaynor JW, Galli KK. Periventricular leukomalacia is common after neonatal cardiac surgery. The Journal of Thoracic and Cardiovascular Surgery. 127: 692-704. PMID 15001897 DOI: 10.1016/J.Jtcvs.2003.09.053  0.237
2023 Ferar K, Hall TO, Crawford DC, Rowley R, Satterfield BA, Li R, Gragert L, Karlson EW, de Andrade M, Kullo IJ, McCarty CA, Kho A, Hayes MG, Ritchie MD, Crane PK, ... ... Jarvik GP, et al. Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. Scientific Reports. 13: 18532. PMID 37898691 DOI: 10.1038/s41598-023-45649-4  0.237
2009 Richter RJ, Jarvik GP, Furlong CE. Paraoxonase 1 (PON1) status and substrate hydrolysis. Toxicology and Applied Pharmacology. 235: 1-9. PMID 19071155 DOI: 10.1016/J.Taap.2008.11.001  0.236
2022 Piekos JA, Hellwege JN, Zhang Y, Torstenson ES, Jarvik GP, Dikilitas O, Kullo IJ, Schaid DJ, Crosslin DR, Pendergrass SA, Lee MTM, Roden D, Denny JC, Edwards TL, Velez Edwards DR. Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid. Human Genetics. PMID 35226188 DOI: 10.1007/s00439-022-02442-z  0.236
2006 Gaynor JW, Jarvik GP, Bernbaum J, Gerdes M, Wernovsky G, Burnham NB, D’Agostino JA, Zackai E, McDonald-McGinn DM, Nicolson SC, Spray TL, Clancy RR. The relationship of postoperative electrographic seizures to neurodevelopmental outcome at 1 year of age after neonatal and infant cardiac surgery The Journal of Thoracic and Cardiovascular Surgery. 131: 181-189. PMID 16399310 DOI: 10.1016/J.Jtcvs.2005.08.062  0.236
2023 Vollger MR, Korlach J, Eldred KC, Swanson E, Underwood JG, Cheng YH, Ranchalis J, Mao Y, Blue EE, Schwarze U, Munson KM, Saunders CT, Wenger AM, Allworth A, Chanprasert S, ... ... Jarvik GP, et al. Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition. Biorxiv : the Preprint Server For Biology. PMID 37808736 DOI: 10.1101/2023.09.26.559521  0.235
2001 Rasgon N, Jarvik GP, Jarvik L. Affective Disorders and Alzheimer Disease: A Missing-Link Hypothesis American Journal of Geriatric Psychiatry. 9: 444-445. DOI: 10.1097/00019442-200111000-00015  0.235
2005 Gaynor JW, Nicolson SC, Jarvik GP, Wernovsky G, Montenegro LM, Burnham NB, Hartman DM, Louie A, Spray TL, Clancy RR. Increasing duration of deep hypothermic circulatory arrest is associated with an increased incidence of postoperative electroencephalographic seizures The Journal of Thoracic and Cardiovascular Surgery. 130: 1278-1286. PMID 16256779 DOI: 10.1016/J.Jtcvs.2005.02.065  0.235
2014 Gallego C, Shirts B, Garrison L, Jarvik G, Veenstra D. Can Next Generation Sequencing Save Lives and Provide a Good Economic Value in Colon Cancer Prevention? Value in Health. 17: A86-A87. DOI: 10.1016/J.Jval.2014.03.504  0.234
2009 Underhill HR, Yuan C, Yarnykh VL, Chu B, Oikawa M, Polissar NL, Schwartz SM, Jarvik GP, Hatsukami TS. Arterial remodeling in [corrected] subclinical carotid artery disease. Jacc. Cardiovascular Imaging. 2: 1381-9. PMID 20083072 DOI: 10.1016/J.Jcmg.2009.08.007  0.234
2018 Antommaria AHM, Brothers KB, Myers JA, Feygin YB, Aufox SA, Brilliant MH, Conway P, Fullerton SM, Garrison NA, Horowitz CR, Jarvik GP, Li R, Ludman EJ, McCarty CA, McCormick JB, et al. Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey. Ajob Empirical Bioethics. 1-15. PMID 30240342 DOI: 10.1080/23294515.2018.1505783  0.233
2009 Chen J, Zimmerman RA, Jarvik GP, Nord AS, Clancy RR, Wernovsky G, Montenegro LM, Hartman DM, Nicolson SC, Spray TL, Gaynor JW, Ichord R. Perioperative stroke in infants undergoing open heart operations for congenital heart disease. The Annals of Thoracic Surgery. 88: 823-9. PMID 19699905 DOI: 10.1016/J.Athoracsur.2009.03.030  0.233
2013 Gaynor JW, Jarvik GP, Gerdes M, Kim DS, Rajagopalan R, Bernbaum J, Wernovsky G, Nicolson SC, Spray TL, Clancy RR. Postoperative electroencephalographic seizures are associated with deficits in executive function and social behaviors at 4 years of age following cardiac surgery in infancy. The Journal of Thoracic and Cardiovascular Surgery. 146: 132-7. PMID 23768805 DOI: 10.1016/J.Jtcvs.2013.04.002  0.232
2018 Mercaldo ND, Brothers KB, Carrell DS, Clayton EW, Connolly JJ, Holm IA, Horowitz CR, Jarvik GP, Kitchner TE, Li R, McCarty CA, McCormick JB, McManus VD, Myers MF, Pankratz JJ, et al. Enrichment sampling for a multi-site patient survey using electronic health records and census data. Journal of the American Medical Informatics Association : Jamia. PMID 30590688 DOI: 10.1093/Jamia/Ocy164  0.232
1993 Jarvik GP, Wijsman E, Little RE, Albers JJ, Motulsky AG, Brunzell JD. Host and environmental effects on plasma apolipoprotein B. International Journal of Clinical & Laboratory Research. 23: 215-20. PMID 8123878 DOI: 10.1007/Bf02592312  0.231
2019 Kim DS, Newburger JW, Bellinger DC, Russell MW, Goldberg CS, Jarvik GP, Gaynor JW. Failure to validate association of mannose-binding lectin deficiency with adverse neurodevelopmental outcomes after cardiac surgery in infants. The Journal of Thoracic and Cardiovascular Surgery. 157: e397-e398. PMID 31307150 DOI: 10.1016/J.Jtcvs.2018.10.099  0.23
2020 Finn KS, Lynch J, Aufox S, Bland S, Chung W, Halverson C, Hebbring S, Hoell C, Holm I, Jarvik G, Kullo I, Leppig K, Myers M, Prows C, Rasouly HM, et al. Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network. American Journal of Medical Genetics. Part A. 185: 508-516. PMID 36046768 DOI: 10.1002/ajmg.a.62002  0.23
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Jarvik GP, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 29549329 DOI: 10.1038/S41588-018-0050-Y  0.229
2018 Watase H, Gao P, Sui B, Shen M, Balu N, Zhao X, Li R, Sun J, Hippe DS, Jarvik GP, Yuan C, Hatsukami TS. Abstract WP135: Location and Composition of Extracranial Carotid and Intracranial Atheroma in Symptomatic U.S. and Chinese Patients Detected by Vessel Wall Magnetic Resonance Imaging Stroke. 49. DOI: 10.1161/Str.49.Suppl_1.Wp135  0.229
2023 Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Jarvik GP, et al. Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 37237109 DOI: 10.1038/s41586-023-06194-2  0.228
2023 Xiao B, Velez Edwards DR, Lucas A, Drivas T, Gray K, Keating B, Weng C, Jarvik GP, Hakonarson H, Kottyan L, Elhadad N, Wei WQ, Luo Y, Kim D, Ritchie M, et al. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association. e026561. PMID 36846987 DOI: 10.1161/JAHA.121.026561  0.226
2021 Makhnoon S, Bowen DJ, Shirts BH, Fullerton SM, Larson EB, Ralston JD, Leppig KA, Crosslin DR, Veenstra D, Jarvik GP. The FamilyTalk randomized controlled trial: patient-reported outcomes in clinical genetic sequencing for colorectal cancer. Cancer Causes & Control : Ccc. PMID 33591484 DOI: 10.1007/s10552-021-01398-1  0.226
2019 Suri P, Boyko EJ, Smith NL, Jarvik JG, Jarvik GP, Williams FMK, Williams R, Haselkorn J, Goldberg J. Post-Traumatic Stress Disorder Symptoms are Associated with Incident Chronic Back Pain: A Longitudinal Twin Study of Older Male Veterans. Spine. PMID 30985567 DOI: 10.1097/Brs.0000000000003053  0.226
2011 Trinidad SB, Fullerton SM, Ludman EJ, Jarvik GP, Larson EB, Burke W. Research ethics. Research practice and participant preferences: the growing gulf. Science (New York, N.Y.). 331: 287-8. PMID 21252333 DOI: 10.1126/Science.1199000  0.225
2009 Samanta B, Bird GL, Kuijpers M, Zimmerman RA, Jarvik GP, Wernovsky G, Clancy RR, Licht DJ, Gaynor JW, Nataraj C. Prediction of periventricular leukomalacia. Part II: Selection of hemodynamic features using computational intelligence. Artificial Intelligence in Medicine. 46: 217-31. PMID 19162456 DOI: 10.1016/J.Artmed.2008.12.004  0.224
2000 Li W, Brophy V, Costa L, Richter R, Hagen T, Shih D, Lusis A, Jarvik G, Furlong C. Mutations in Human PON1: Role in Organophosphorus Sensitivity and Vascular Disease Biochemical Society Transactions. 28: A436-A436. DOI: 10.1042/Bst028A436A  0.224
2021 Hindy G, Dornbos P, Chaffin MD, Liu DJ, Wang M, Selvaraj MS, Zhang D, Park J, Aguilar-Salinas CA, Antonacci-Fulton L, Ardissino D, Arnett DK, Aslibekyan S, Atzmon G, Ballantyne CM, ... ... Jarvik GP, et al. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. American Journal of Human Genetics. PMID 34932938 DOI: 10.1016/j.ajhg.2021.11.021  0.224
2021 Rosenthal EA, Crosslin DR, Gordon AS, Carrell DS, Stanaway IB, Larson EB, Grafton J, Wei WQ, Denny JC, Feng QP, Shah AS, Sturm AC, Ritchie MD, Pacheco JA, Hakonarson H, ... ... Jarvik GP, et al. Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort. Bmc Medical Genomics. 14: 11. PMID 33407432 DOI: 10.1186/s12920-020-00854-2  0.223
2022 Leppig KA, Kulchak Rahm A, Appelbaum P, Aufox S, Bland ST, Buchanan A, Christensen KD, Chung WK, Clayton EW, Crosslin D, Denny J, DeVange S, Gordon A, Green RC, Hakonarson H, ... ... Jarvik GP, et al. The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35216901 DOI: 10.1016/j.gim.2022.01.015  0.222
2021 Zouk H, Yu W, Oza A, Hawley M, Vijay Kumar PK, Koch C, Mahanta LM, Harley JB, Jarvik GP, Karlson EW, Leppig KA, Myers MF, Prows CA, Williams MS, Weiss ST, et al. Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34906510 DOI: 10.1016/j.gim.2021.10.010  0.222
2022 Wiley K, Findley L, Goldrich M, Rakhra-Burris TK, Stevens A, Williams P, Bult CJ, Chisholm R, Deverka P, Ginsburg GS, Green ED, Jarvik G, Mensah GA, Ramos E, Relling MV, et al. A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources. Journal of the American Medical Informatics Association : Jamia. PMID 35485600 DOI: 10.1093/jamia/ocac057  0.222
2022 Hui D, Xiao B, Dikilitas O, Freimuth RR, Irvin MR, Jarvik GP, Kottyan L, Kullo I, Limdi NA, Liu C, Luo Y, Namjou B, Puckelwartz MJ, Schaid D, Tiwari H, et al. Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 28: 437-448. PMID 36540998  0.221
2014 Tragante V, Barnes MR, Ganesh SK, Lanktree MB, Guo W, Franceschini N, Smith EN, Johnson T, Holmes MV, Padmanabhan S, Karczewski KJ, Almoguera B, Barnard J, Baumert J, Chang YP, ... ... Jarvik GP, et al. Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American Journal of Human Genetics. 94: 349-60. PMID 24560520 DOI: 10.1016/J.Ajhg.2013.12.016  0.221
2023 Dikilitas O, Sherafati A, Saadatagah S, Satterfield BA, Kochan DC, Anderson KC, Chung WK, Hebbring SJ, Salvati ZM, Sharp RR, Sturm AC, Gibbs RA, Rowley R, Venner E, Linder JE, ... ... Jarvik GP, et al. Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results. Circulation. Genomic and Precision Medicine. 16: e003816. PMID 37071725 DOI: 10.1161/CIRCGEN.122.003816  0.22
2021 Murugan M, Babb LJ, Overby Taylor C, Rasmussen LV, Freimuth RR, Venner E, Yan F, Yi V, Granite SJ, Zouk H, Aronson SJ, Power K, Fedotov A, Crosslin DR, Fasel D, ... Jarvik GP, et al. Genomic Considerations for FHIR®; eMERGE Implementation Lessons. Journal of Biomedical Informatics. 103795. PMID 33930535 DOI: 10.1016/j.jbi.2021.103795  0.218
2021 Mittendorf KF, Kauffman TL, Amendola LM, Anderson KP, Biesecker BB, Dorschner MO, Duenas DM, Eubanks DJ, Feigelson HS, Gilmore MJ, Hunter JE, Joseph G, Kraft SA, Lee SSJ, Leo MC, ... ... Jarvik GP, et al. Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations. Contemporary Clinical Trials. 106432. PMID 33984519 DOI: 10.1016/j.cct.2021.106432  0.217
2014 Overby CL, Rasmussen LV, Hartzler A, Connolly JJ, Peterson JF, Hedberg RE, Freimuth RR, Shirts BH, Denny JC, Larson EB, Chute CG, Jarvik GP, Ralston JD, Shuldiner AR, Starren J, et al. A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 2014: 944-53. PMID 25954402  0.216
2010 Gaynor JW, Gerdes M, Nord AS, Bernbaum J, Zackai E, Wernovsky G, Clancy RR, Heagerty PJ, Solot CB, McDonald-McGinn D, Jarvik GP. Is cardiac diagnosis a predictor of neurodevelopmental outcome after cardiac surgery in infancy? The Journal of Thoracic and Cardiovascular Surgery. 140: 1230-7. PMID 20951391 DOI: 10.1016/J.Jtcvs.2010.07.069  0.215
2021 Natarajan P, Pampana A, Graham SE, Ruotsalainen SE, Perry JA, de Vries PS, Broome JG, Pirruccello JP, Honigberg MC, Aragam K, Wolford B, Brody JA, Antonacci-Fulton L, Arden M, Aslibekyan S, ... ... Jarvik GP, et al. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nature Communications. 12: 2182. PMID 33846329 DOI: 10.1038/s41467-021-22339-1  0.212
2021 Satterfield BA, Dikilitas O, Safarova MS, Clarke SL, Tcheandjieu C, Zhu X, Bastarache L, Larson EB, Justice AE, Shang N, Rosenthal EA, Shah A, Namjou-Khales B, Urbina EM, Wei WQ, ... ... Jarvik GP, et al. Associations of Genetically Predicted Lipoprotein (a) Levels with Cardiovascular Traits in Individuals of European and African Ancestry. Circulation. Genomic and Precision Medicine. PMID 34282949 DOI: 10.1161/CIRCGEN.120.003354  0.211
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, 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  0.21
2021 Eric V, Yi V, Murdock D, Kalla SE, Wu TJ, Sabo A, Li S, Meng Q, Tian X, Murugan M, Cohen M, Kovar C, Wei WQ, Chung WK, Weng C, ... ... Jarvik GP, et al. Neptune: an environment for the delivery of genomic medicine. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34257418 DOI: 10.1038/s41436-021-01230-w  0.206
2012 Allen M, Zou F, Chai HS, Younkin CS, Crook J, Pankratz VS, Carrasquillo MM, Rowley CN, Nair AA, Middha S, Maharjan S, Nguyen T, Ma L, Malphrus KG, Palusak R, ... ... Jarvik GP, et al. Novel late-onset Alzheimer disease loci variants associate with brain gene expression. Neurology. 79: 221-8. PMID 22722634 DOI: 10.1212/Wnl.0B013E3182605801  0.203
2023 Lennon NJ, Kottyan LC, Kachulis C, Abul-Husn N, Arias J, Belbin G, Below JE, Berndt S, Chung W, Cimino JJ, Clayton EW, Connolly JJ, Crosslin D, Dikilitas O, Velez Edwards DR, ... ... Jarvik GP, et al. Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations. Medrxiv : the Preprint Server For Health Sciences. PMID 37333246 DOI: 10.1101/2023.05.25.23290535  0.2
2022 Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, Zajac GJM, Wu KH, Ntalla I, ... ... Jarvik GP, et al. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology. 23: 268. PMID 36575460 DOI: 10.1186/s13059-022-02837-1  0.197
2022 Amendola LM, Shuster E, Leo MC, Dorschner MO, Rolf BA, Shirts BH, Gilmore MJ, Okuyama S, Zepp JM, Kauffman TL, Mittendorf KF, Bellcross C, Jenkins CL, Joseph G, Riddle L, ... ... Jarvik GP, et al. Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35305866 DOI: 10.1016/j.gim.2022.02.006  0.196
2021 Khan SS, Hoell C, Castillo LM, Connolly JJ, Crosslin DR, Chung WK, Gordon AS, Harr M, Jarvik GP, Kullo I, Larson EB, Leppig KA, Manolio T, Pacheco JA, Ralston JD, et al. Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network. Circulation. Heart Failure. CIRCHEARTFAILURE1200. PMID 33951936 DOI: 10.1161/CIRCHEARTFAILURE.120.008155  0.194
2024 Hu J, Korchina V, Zouk H, Harden MV, Murdock D, Macbeth A, Harrison SM, Lennon N, Kovar C, Balasubramanian A, Zhang L, Chandanavelli G, Pasham D, Rowley R, Wiley K, ... ... Jarvik GP, et al. Genetic sex validation for sample tracking in next-generation sequencing clinical testing. Bmc Research Notes. 17: 62. PMID 38433186 DOI: 10.1186/s13104-024-06723-w  0.194
2021 Shang N, Khan A, Polubriaginof F, Zanoni F, Mehl K, Fasel D, Drawz PE, Carrol RJ, Denny JC, Hathcock MA, Arruda-Olson AM, Peissig PL, Dart RA, Brilliant MH, Larson EB, ... ... Jarvik GP, et al. Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. Npj Digital Medicine. 4: 70. PMID 33850243 DOI: 10.1038/s41746-021-00428-1  0.193
2022 Khan A, Turchin MC, Patki A, Srinivasasainagendra V, Shang N, Nadukuru R, Jones AC, Malolepsza E, Dikilitas O, Kullo IJ, Schaid DJ, Karlson E, Ge T, Meigs JB, Smoller JW, ... ... Jarvik GP, et al. Genome-wide polygenic score to predict chronic kidney disease across ancestries. Nature Medicine. PMID 35710995 DOI: 10.1038/s41591-022-01869-1  0.193
2022 Zeng C, Bastarache LA, Tao R, Venner E, Hebbring S, Andujar JD, Bland ST, Crosslin DR, Pratap S, Cooley A, Pacheco JA, Christensen KD, Perez E, Zawatsky CLB, Witkowski L, ... ... Jarvik GP, et al. Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases. Jama Oncology. PMID 35446370 DOI: 10.1001/jamaoncol.2022.0373  0.192
2021 Liu G, Shi M, Mosley JD, Weng C, Zhang Y, Lee MTM, Jarvik GP, Hakonarson H, Namjou-Khales B, Sleiman P, Luo Y, Mentch F, Denny JC, Linton MF, Wei WQ, et al. A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes. Jama Network Open. 4: e2112820. PMID 34097045 DOI: 10.1001/jamanetworkopen.2021.12820  0.19
2023 Hu J, Korchina V, Zouk H, Harden MV, Murdock D, Macbeth A, Harrison SM, Lennon N, Kovar C, Balasubramanian A, Zhang L, Chandanavelli G, Pasham D, Rowley R, Wiley K, ... ... Jarvik GP, et al. Genetic Sex Validation for Sample Tracking in Clinical Testing. Research Square. PMID 37790445 DOI: 10.21203/rs.3.rs-3304685/v1  0.187
2022 Liles EG, Leo MC, Freed AS, Porter KM, Zepp JM, Kauffman TL, Keast E, McMullen CK, Gruß I, Biesecker BB, Muessig KR, Eubanks DJ, Amendola LM, Dorschner MO, Rolf BA, ... Jarvik GP, et al. ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35522237 DOI: 10.1016/j.gim.2022.04.008  0.185
2022 Namjou B, Lape M, Malolepsza E, DeVore SB, Weirauch MT, Dikilitas O, Jarvik GP, Kiryluk K, Kullo IJ, Liu C, Luo Y, Satterfield BA, Smoller JW, Walunas TL, Connolly J, et al. Multiancestral polygenic risk score for pediatric asthma. The Journal of Allergy and Clinical Immunology. PMID 35595084 DOI: 10.1016/j.jaci.2022.03.035  0.185
2022 Ge T, Irvin MR, Patki A, Srinivasasainagendra V, Lin YF, Tiwari HK, Armstrong ND, Benoit B, Chen CY, Choi KW, Cimino JJ, Davis BH, Dikilitas O, Etheridge B, Feng YA, ... ... Jarvik GP, et al. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. Genome Medicine. 14: 70. PMID 35765100 DOI: 10.1186/s13073-022-01074-2  0.184
2023 Jordan E, Kinnamon DD, Haas GJ, Hofmeyer M, Kransdorf E, Ewald GA, Morris AA, Owens A, Lowes B, Stoller D, Tang WHW, Garg S, Trachtenberg BH, Shah P, Pamboukian SV, ... ... Jarvik GP, et al. Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry. Jama. 330: 432-441. PMID 37526719 DOI: 10.1001/jama.2023.11970  0.181
2022 Patel HV, Henrikson NB, Ralston JD, Leppig K, Scrol A, Jarvik GP, DeVange S, Larson EB, Hartzler AL. Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance. Amia ... Annual Symposium Proceedings. Amia Symposium. 2021: 950-958. PMID 35309003  0.181
2021 Jujjavarapu C, Anandasakaran J, Amendola LM, Haas C, Zampino E, Henrikson NB, Jarvik GP, Mooney SD. ShareDNA: a smartphone app to facilitate family communication of genetic results. Bmc Medical Genomics. 14: 10. PMID 33407467 DOI: 10.1186/s12920-020-00864-0  0.18
2023 Linder JE, Allworth A, Bland ST, Caraballo PJ, Chisholm RL, Clayton EW, Crosslin DR, Dikilitas O, DiVietro A, Esplin ED, Forman S, Freimuth RR, Gordon AS, Green R, Harden MV, ... ... Jarvik GP, et al. Returning integrated genomic risk and clinical recommendations: the eMERGE study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100006. PMID 36621880 DOI: 10.1016/j.gim.2023.100006  0.178
2022 Robinson JR, Carroll RJ, Bastarache L, Chen Q, Pirruccello J, Mou Z, Wei WQ, Connolly J, Mentch F, Crane PK, Hebbring SJ, Crosslin DR, Gordon AS, Rosenthal EA, Stanaway IB, ... ... Jarvik GP, et al. Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics. Obesity (Silver Spring, Md.). PMID 36372681 DOI: 10.1002/oby.23561  0.177
2021 Henrikson NB, Scrol A, Leppig KA, Ralston JD, Larson EB, Jarvik GP. Preferences of biobank participants for receiving actionable genomic test results: results of a recontacting study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 33603197 DOI: 10.1038/s41436-021-01111-2  0.174
2012 Ding K, Shameer K, Jouni H, Masys DR, Jarvik GP, Kho AN, Ritchie MD, McCarty CA, Chute CG, Manolio TA, Kullo IJ. Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. Mayo Clinic Proceedings. 87: 461-74. PMID 22560525 DOI: 10.1016/j.mayocp.2012.01.016  0.174
2020 Jarvik GP, Wang X, Fontanillas P, Kim E, Chanprasert S, Gordon AS, Bastarache L, Kowdley KV, Harrison T, Rosenthal EA, Stanaway IB, Bézieau S, Weinstein SJ, Newcomb PA, Casey G, et al. Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis. Hgg Advances. 1: 100010. PMID 35047832 DOI: 10.1016/j.xhgg.2020.100010  0.173
2015 Bennette CS, Burke W, Jarvik GP, Veenstra DL. Response to Phillips et al. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 315. PMID 25835196 DOI: 10.1038/Gim.2015.11  0.172
2021 De T, Zhang H, Alarcon C, Lec B, Avitia J, Smithberger E, Chen C, Horvath M, Kwan S, Young M, Adhikari S, Kwon J, Pacheco J, Jarvik G, Wei WQ, et al. Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease. Pharmacogenetics and Genomics. PMID 34380996 DOI: 10.1097/FPC.0000000000000445  0.172
2023 Linder JE, Tao R, Chung WK, Kiryluk K, Liu C, Weng C, Connolly JJ, Hakonarson H, Harr M, Leppig KA, Jarvik GP, Veenstra DL, Aufox S, Chisholm RL, Gordon AS, et al. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing. American Journal of Human Genetics. PMID 37883979 DOI: 10.1016/j.ajhg.2023.10.006  0.171
2022 Shadrina AS, Elgaeva EE, Stanaway IB, Jarvik GP, Namjou B, Wei WQ, Glessner J, Hakonarson H, Suri P, Tsepilov YA. Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities. Plos One. 17: e0268725. PMID 35594287 DOI: 10.1371/journal.pone.0268725  0.171
2022 Joseph G, Leo MC, Riddle L, Guerra C, Amendola LM, Gilmore MJ, Rolf BA, Dorschner MO, Zepp J, Biesecker BB, Caruncho M, Hunter JE, Keast E, Lewis HS, Duenas D, ... ... Jarvik GP, et al. An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 36053287 DOI: 10.1016/j.gim.2022.07.025  0.166
2019 Kunkle BW, Grenier-Boley B, Sims R, Bis JC, Damotte V, Naj AC, Boland A, Vronskaya M, van der Lee SJ, Amlie-Wolf A, Bellenguez C, Frizatti A, Chouraki V, Martin ER, Sleegers K, ... ... Jarvik GP, et al. Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. PMID 31417202 DOI: 10.1038/s41588-019-0495-7  0.164
2023 Bhatraju PK, Stanaway IB, Palmer MR, Menon R, Schaub JA, Menez S, Srivastava A, Wilson FP, Kiryluk K, Palevsky PM, Naik AS, Sakr SS, Jarvik GP, Parikh CR, Ware LB, et al. Genome-wide Association Study for Acute Kidney Injury. Kidney360. PMID 37273234 DOI: 10.34067/KID.0000000000000175  0.164
2015 Amendola LM, Horike-Pyne M, Trinidad SB, Fullerton SM, Evans BJ, Burke W, Jarvik GP. Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death. The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics. 43: 476-85. PMID 26479557 DOI: 10.1111/jlme.12290  0.163
2018 Rosenthal EA, Shirts BH, Amendola LM, Horike-Pyne M, Robertson PD, Hisama FM, Bennett RL, Dorschner MO, Nickerson DA, Stanaway IB, Nassir R, Vickers KT, Li C, Grady WM, Peters U, ... Jarvik GP, et al. Rare loss of function variants in candidate genes and risk of colorectal cancer. Human Genetics. PMID 30267214 DOI: 10.1007/s00439-018-1938-4  0.162
2023 Thomas M, Su YR, Rosenthal EA, Sakoda LC, Schmit SL, Timofeeva MN, Chen Z, Fernandez-Rozadilla C, Law PJ, Murphy N, Carreras-Torres R, Diez-Obrero V, van Duijnhoven FJ, Jiang S, Shin A, ... ... Jarvik GP, et al. Combining Asian-European Genome-Wide Association Studies of Colorectal Cancer Improves Risk Prediction Across Race and Ethnicity. Medrxiv : the Preprint Server For Health Sciences. PMID 36789420 DOI: 10.1101/2023.01.19.23284737  0.161
2023 Rosenthal EA, Hsu L, Thomas M, Peters U, Kachulis C, Patterson K, Jarvik GP. Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score. Medrxiv : the Preprint Server For Health Sciences. PMID 37961088 DOI: 10.1101/2023.10.23.23296753  0.16
2023 Thomas M, Su YR, Rosenthal EA, Sakoda LC, Schmit SL, Timofeeva MN, Chen Z, Fernandez-Rozadilla C, Law PJ, Murphy N, Carreras-Torres R, Diez-Obrero V, van Duijnhoven FJB, Jiang S, Shin A, ... ... Jarvik GP, et al. Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. Nature Communications. 14: 6147. PMID 37783704 DOI: 10.1038/s41467-023-41819-0  0.157
2022 Knerr S, Guo B, Mittendorf KF, Feigelson HS, Gilmore MJ, Jarvik GP, Kauffman TL, Keast E, Lynch FL, Muessig KR, Okuyama S, Veenstra DL, Zepp JM, Goddard KAB, Devine B. Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system. Cancer. PMID 35679147 DOI: 10.1002/cncr.34349  0.156
2019 Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, ... ... Jarvik GP, et al. Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30670880 DOI: 10.1038/s41436-019-0440-2  0.155
2022 Sherafati A, Elsekaily O, Saadatagah S, Kochan DC, Lee C, Wiesner GL, Liu C, Dellefave-Castillo L, Namjou B, Perez EF, Salvati ZM, Connolly JJ, Hakonarson H, Williams MS, Jarvik GP, et al. Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 35943490 DOI: 10.1016/j.gim.2022.07.007  0.155
2023 Manolio TA, Narula J, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Green ED, Hooker G, Jarvik GP, Mensah GA, Ramos EM, Roden DM, Rowley R, Williams MS. Genomic medicine year in review: 2023. American Journal of Human Genetics. 110: 1992-1995. PMID 38065071 DOI: 10.1016/j.ajhg.2023.11.001  0.151
2022 Manolio TA, Narula J, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Goldrich M, Green ED, Jarvik GP, Mensah GA, Ramos EM, Relling MV, Roden DM, Rowley R, Williams MS. Genomic Medicine Year in Review: 2022. American Journal of Human Genetics. 109: 2101-2104. PMID 36459977 DOI: 10.1016/j.ajhg.2022.11.003  0.15
2021 Manolio TA, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Goldrich M, Jarvik GP, Mensah GA, Ramos EM, Relling MV, Roden DM, Rowley R, Williams MS, Green ED. Genomic medicine year in review: 2021. American Journal of Human Genetics. 108: 2210-2214. PMID 34861172 DOI: 10.1016/j.ajhg.2021.11.006  0.15
2020 Manolio TA, Bult CJ, Chisholm RL, Deverka PA, Ginsburg GS, Goldrich M, Jarvik GP, Mensah GA, Relling MV, Roden DM, Rowley R, Tamburro C, Williams MS, Green ED. Genomic Medicine Year in Review: 2020. American Journal of Human Genetics. 107: 1007-1010. PMID 33275910 DOI: 10.1016/j.ajhg.2020.11.005  0.15
2021 Haas CB, Scrol A, Jujjavarapu C, Jarvik GP, Henrikson NB. Usefulness of mobile apps for communication of genetic test results to at-risk family members in a U.S. integrated health system: a qualitative approach from user-testing. Health Policy and Technology. 10. PMID 34040952 DOI: 10.1016/j.hlpt.2021.100511  0.15
2023 Jasper EA, Hellwege JN, Breeyear JH, Xiao B, Jarvik GP, Stanaway IB, Leppig KA, Chittoor G, Hayes MG, Dikilitas O, Kullo IJ, Holm IA, Verma SS, Edwards TL, Velez Edwards DR. Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia. Medrxiv : the Preprint Server For Health Sciences. PMID 36824881 DOI: 10.1101/2023.02.09.23285734  0.148
2023 Knerr S, Guo B, Wernli KJ, Mittendorf KF, Feigelson HS, Gilmore MJ, Jarvik GP, Kauffman TL, Keast E, Liles EG, Lynch FL, Muessig KR, Okuyama S, Veenstra DL, Zepp JM, et al. Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system. Breast Cancer Research and Treatment. PMID 37470892 DOI: 10.1007/s10549-023-07007-w  0.147
2021 Bowen DJ, Makhnoon S, Shirts BH, Fullerton SM, Larson E, Ralston JD, Leppig K, Crosslin DR, Veenstra D, Jarvik GP. What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk? Patient Education and Counseling. PMID 33455827 DOI: 10.1016/j.pec.2021.01.001  0.145
2021 Rolf BA, Schneider JL, Amendola LM, Davis JV, Mittendorf KF, Schmidt MA, Jarvik GP, Wilfond BS, Goddard KAB, Ezzell Hunter J. Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment. Journal of Genetic Counseling. PMID 34302314 DOI: 10.1002/jgc4.1476  0.143
2022 Muenzen KD, Amendola LM, Kauffman TL, Mittendorf KF, Bensen JT, Chen F, Green R, Powell BC, Kvale M, Angelo F, Farnan L, Fullerton SM, Robinson JO, Li T, Murali P, ... ... Jarvik GP, et al. Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience. Hgg Advances. 3: 100120. PMID 35707062 DOI: 10.1016/j.xhgg.2022.100120  0.138
2020 Riddle L, Amendola LM, Gilmore MJ, Guerra C, Biesecker B, Kauffman TL, Anderson K, Rope AF, Leo MC, Caruncho M, Jarvik GP, Wilfond B, Goddard KAB, Joseph G. Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model. Patient Education and Counseling. PMID 33549385 DOI: 10.1016/j.pec.2020.12.017  0.136
2015 Borthwick KM, Smelser DT, Bock JA, Elmore JR, Ryer EJ, Ye Z, Pacheco JA, Carrell DS, Michalkiewicz M, Thompson WK, Pathak J, Bielinski SJ, Denny JC, Linneman JG, Peissig PL, ... ... Jarvik GP, et al. ePhenotyping for Abdominal Aortic Aneurysm in the Electronic Medical Records and Genomics (eMERGE) Network: Algorithm Development and Konstanz Information Miner Workflow. International Journal of Biomedical Data Mining. 4. PMID 27054044  0.13
2022 Jarvik GP. 2021 ASHG presidential address-Imagination and daring: Past, present, and future. American Journal of Human Genetics. 109: 381-383. PMID 35245471 DOI: 10.1016/j.ajhg.2021.11.023  0.126
2023 Ferar K, Hall TO, Crawford DC, Rowley R, Satterfield BA, Li R, Gragert L, Karlson EW, de Andrade M, Kullo IJ, McCarty CA, Kho A, Hayes MG, Ritchie MD, Crane PK, ... ... Jarvik GP, et al. Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. Scientific Reports. 13: 19972. PMID 37968452 DOI: 10.1038/s41598-023-47359-3  0.126
2022 Mittendorf KF, Kauffman TL, Amendola LM, Anderson KP, Biesecker BB, Dorschner MO, Duenas DM, Eubanks DJ, Feigelson HS, Gilmore MJ, Hunter JE, Joseph G, Kraft SA, Lee SSJ, Leo MC, ... ... Jarvik GP, et al. Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432]. Contemporary Clinical Trials. 106682. PMID 35123916 DOI: 10.1016/j.cct.2022.106682  0.12
2022 Leppig KA, Plon SE, Milewicz DM, Levy-Lahad E, Jarvik GP. The annual ASHG dinner. American Journal of Human Genetics. 109: 377-378. PMID 35245469 DOI: 10.1016/j.ajhg.2021.11.024  0.118
2021 Liu C, Zeinomar N, Chung WK, Kiryluk K, Gharavi AG, Hripcsak G, Crew KD, Shang N, Khan A, Fasel D, Manolio TA, Jarvik GP, Rowley R, Justice AE, Rahm AK, et al. Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. Jama Network Open. 4: e2119084. PMID 34347061 DOI: 10.1001/jamanetworkopen.2021.19084  0.109
2023 Pujol-Giménez J, Mirzaa G, Blue EE, Albano G, Miller DE, Allworth A, Bennett JT, Byers PH, Chanprasert S, Chen J, Doherty D, Folta AB, Gillentine MA, Glass I, Hing A, ... ... Jarvik GP, et al. Dominant-negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome. Annals of Clinical and Translational Neurology. PMID 37194416 DOI: 10.1002/acn3.51786  0.108
2021 Fan X, Wynn J, Shang N, Liu C, Fedotov A, Hallquist MLG, Buchanan AH, Williams MS, Smith ME, Hoell C, Rasmussen-Torvik LJ, Peterson JF, Wiesner GL, Murad AM, Jarvik GP, et al. Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network. Jnci Cancer Spectrum. 5: pkab044. PMID 34377931 DOI: 10.1093/jncics/pkab044  0.107
2009 Berg AO, Baird MA, Botkin JR, Driscoll DA, Fishman PA, Guarino PD, Hiatt RA, Jarvik GP, Millon-Underwood S, Morgan TM, Mulvihill JJ, Pollin TI, Schimmel SR, Stefanek ME, Vollmer WM, et al. National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health. Annals of Internal Medicine. 151: 872-7. PMID 19884615 DOI: 10.7326/0003-4819-151-12-200912150-00165  0.107
2023 Stergachis AB, Blue EE, Gillentine MA, Wang LK, Schwarze U, Cortés AS, Ranchalis J, Allworth A, Bland AE, Chanprasert S, Chen J, Doherty D, Folta AB, Glass I, Horike-Pyne M, ... ... Jarvik GP, et al. Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A. Biorxiv : the Preprint Server For Biology. PMID 36798371 DOI: 10.1101/2023.02.07.526487  0.097
2023 Stergachis AB, Blue EE, Gillentine MA, Wang LK, Schwarze U, Cortés AS, Ranchalis J, Allworth A, Bland AE, Chanprasert S, Chen J, Doherty D, Folta AB, Glass I, Horike-Pyne M, ... ... Jarvik GP, et al. Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A. Neurology. Genetics. 9: e200090. PMID 37560121 DOI: 10.1212/NXG.0000000000200090  0.096
2023 Sathe NA, Xian S, Mabrey FL, Crosslin DR, Mooney SD, Morrell ED, Lybarger K, Yetisgen M, Jarvik GP, Bhatraju PK, Wurfel MM. Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach. Bmc Pulmonary Medicine. 23: 292. PMID 37559024 DOI: 10.1186/s12890-023-02560-y  0.091
2022 Gaynor JW, Burnham NB, Ittenbach RF, Gerdes M, Bernbaum JC, Zackai E, Licht DJ, Russell WW, Zullo EE, Miller T, Hakonarson H, Clarke KA, Jarvik GP, Calafat AM, Bradman A, et al. Childhood exposures to environmental chemicals and neurodevelopmental outcomes in congenital heart disease. Plos One. 17: e0277611. PMID 36395323 DOI: 10.1371/journal.pone.0277611  0.09
2020 Klarin D, Verma SS, Judy R, Dikilitas O, Wolford BN, Paranjpe I, Levin MG, Pan C, Tcheandjieu C, Spin JM, Lynch J, Assimes TL, Nyrønning LÅ, Mattsson E, Edwards TL, ... ... Jarvik GP, et al. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Circulation. PMID 32981348 DOI: 10.1161/CIRCULATIONAHA.120.047544  0.089
2019 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Jarvik GP, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 31160809 DOI: 10.1038/s41588-019-0447-2  0.085
2022 Bhatraju PK, Morrell ED, Stanaway IB, Sathe NA, Srivastava A, Postelnicu R, Green R, Andrews A, Gonzalez M, Kratochvil CJ, Kumar VK, Hsiang TY, Gale M, Anesi GL, Wyles D, ... ... Jarvik GP, et al. Angiopoietin-Like4 Is a Novel Marker of COVID-19 Severity. Critical Care Explorations. 5: e0827. PMID 36600780 DOI: 10.1097/CCE.0000000000000827  0.08
2009 Berg AO, Baird MA, Botkin JR, Driscoll DA, Fishman PA, Guarino PD, Hiatt RA, Jarvik GP, Millon-Underwood S, Morgan TM, Mulvihill JJ, Pollin TI, Schimmel SR, Stefanek ME, Vollmer WM, et al. National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009. Nih Consensus and State-of-the-Science Statements. 26: 1-19. PMID 19721470  0.075
2018 Turcot V, Lu Y, Highland HM, Schurmann C, Justice AE, Fine RS, Bradfield JP, Esko T, Giri A, Graff M, Guo X, Hendricks AE, Karaderi T, Lempradl A, Locke AE, ... ... Jarvik GP, et al. Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Nature Genetics. PMID 29549330 DOI: 10.1038/s41588-018-0082-3  0.073
2020 Watase H, Shen M, Sui B, Gao P, Zhang D, Sun J, Balu N, Hippe DS, Jarvik GP, Zhao X, Li R, Chen S, Yuan C, Hatsukami TS. Differences in atheroma between Caucasian and Asian subjects with anterior stroke: A vessel wall MRI study. Stroke and Vascular Neurology. PMID 32792458 DOI: 10.1136/svn-2020-000370  0.065
2023 Plon S, Jarvik G. Ten Years of Incidental, Secondary, and Actionable Findings. The New England Journal of Medicine. 389: 1813-1814. PMID 37937782 DOI: 10.1056/NEJMe2310263  0.051
2021 Thomas M, Sakoda LC, Hoffmeister M, Rosenthal EA, Lee JK, van Duijnhoven FJB, Platz EA, Wu AH, Dampier CH, de la Chapelle A, Wolk A, Joshi AD, Burnett-Hartman A, Gsur A, Lindblom A, ... ... Jarvik GP, et al. Response to Li and Hopper. American Journal of Human Genetics. 108: 527-529. PMID 33667396 DOI: 10.1016/j.ajhg.2021.02.003  0.011
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