| Year |
Citation |
Score |
| 2020 |
Cahill ME, Loeb M, Dewan AT, Montgomery RR. In-Depth Analysis of Genetic Variation Associated with Severe West Nile Viral Disease. Vaccines. 8. PMID 33302579 DOI: 10.3390/vaccines8040744 |
0.314 |
|
| 2020 |
Rogne T, Damås JK, Solligård E, DeWan AT. Genome-Wide Linkage Analysis of the Risk of Contracting a Bloodstream Infection in 47 Pedigrees Followed for 23 Years Assembled From a Population-Based Cohort (the HUNT Study). Critical Care Medicine. PMID 32885941 DOI: 10.1097/Ccm.0000000000004520 |
0.329 |
|
| 2020 |
Salinas YD, Wang Z, DeWan AT. Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2. American Journal of Epidemiology. PMID 32700739 DOI: 10.1093/Aje/Kwaa144 |
0.366 |
|
| 2020 |
Rogne T, Damås JK, Flatby HM, Åsvold BO, DeWan AT, Solligård E. The Role of FER rs4957796 in the Risk of Developing and Dying from a Bloodstream Infection: A 23-Year Follow-up of the Population-based Nord-Trøndelag Health Study. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. PMID 32699877 DOI: 10.1093/Cid/Ciaa786 |
0.341 |
|
| 2020 |
Streicher SA, Klein AP, Olson SH, Kurtz RC, Amundadottir LT, DeWan AT, Zhao H, Risch HA. A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population. Human Genetics. PMID 32671597 DOI: 10.1007/S00439-020-02205-8 |
0.431 |
|
| 2019 |
Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, ... ... DeWan AT, et al. Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. Blood. PMID 31350265 DOI: 10.1182/Blood.2018890764 |
0.421 |
|
| 2019 |
de Smith AJ, Walsh KM, Morimoto LM, Francis SS, Hansen HM, Jeon S, Gonseth S, Chen M, Sun H, Luna-Fineman S, Antillón F, Girón V, Kang AY, Smirnov I, Shao X, ... ... DeWan AT, et al. Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. Leukemia. PMID 31296947 DOI: 10.1038/S41375-019-0514-9 |
0.32 |
|
| 2019 |
Spector LG, DeWan AT, Pankratz ND, Turcotte LM, Yang JJ, Scheurer ME. Race/ethnicity, socioeconomic position, and childhood acute lymphoblastic leukemia. American Journal of Epidemiology. PMID 30924856 DOI: 10.1093/Aje/Kwz075 |
0.31 |
|
| 2019 |
Monin JK, Goktas SO, Kershaw T, DeWan A. Associations between spouses' oxytocin receptor gene polymorphism, attachment security, and marital satisfaction. Plos One. 14: e0213083. PMID 30818381 DOI: 10.1371/Journal.Pone.0213083 |
0.351 |
|
| 2018 |
He Z, DeWan AT, Leal SM. MendelProb: Probability and sample size calculations for Mendelian studies of exome and whole genome sequence data. Bioinformatics (Oxford, England). PMID 30032240 DOI: 10.1093/Bioinformatics/Bty542 |
0.359 |
|
| 2018 |
Gray KJ, Kovacheva VP, Mirzakhani H, Bjonnes AC, Almoguera B, DeWan AT, Triche EW, Saftlas AF, Hoh J, Bodian DL, Klein E, Huddleston KC, Ingles SA, Lockwood CJ, Hakonarson H, et al. Gene-Centric Analysis of Preeclampsia Identifies Maternal Association at . Hypertension (Dallas, Tex. : 1979). PMID 29967039 DOI: 10.1161/Hypertensionaha.117.10688 |
0.418 |
|
| 2018 |
Cahill ME, Conley S, DeWan AT, Montgomery RR. Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis. Bmc Infectious Diseases. 18: 282. PMID 29929468 DOI: 10.1186/S12879-018-3186-6 |
0.304 |
|
| 2018 |
de Smith AJ, Walsh KM, Francis SS, Zhang C, Hansen HM, Smirnov I, Morimoto L, Whitehead TP, Kang A, Shao X, Barcellos LF, McKean-Cowdin R, Zhang L, Fu C, Wang R, ... ... Dewan AT, et al. BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia. International Journal of Cancer. PMID 29923177 DOI: 10.1002/Ijc.31622 |
0.431 |
|
| 2018 |
DeWan AT. Gene-Gene and Gene-Environment Interactions. Methods in Molecular Biology (Clifton, N.J.). 1793: 89-110. PMID 29876893 DOI: 10.1007/978-1-4939-7868-7_7 |
0.322 |
|
| 2018 |
Khalid M, Driessen TM, Lee JS, Tejwani L, Rasool A, Saqlain M, Shiaq PA, Hanif M, Nawaz A, DeWan AT, Raja GK, Lim J. Association of CACNA1C with bipolar disorder among the Pakistani population. Gene. PMID 29684488 DOI: 10.1016/J.Gene.2018.04.061 |
0.389 |
|
| 2018 |
Wiemels JL, Walsh KM, de Smith AJ, Metayer C, Gonseth S, Hansen HM, Francis SS, Ojha J, Smirnov I, Barcellos L, Xiao X, Morimoto L, McKean-Cowdin R, Wang R, Yu H, ... ... DeWan AT, et al. GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Nature Communications. 9: 286. PMID 29348612 DOI: 10.1038/S41467-017-02596-9 |
0.391 |
|
| 2018 |
Brown AL, Smith AJd, Scheurer ME, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Zwick ME, Winick N, Maloney K, Angiolillo AL, Schore R, Burke MM, Salzer WL, Heerema NA, ... ... DeWan AT, et al. Abstract 222: Genome-wide association study of acute lymphoblastic leukemia in children with Down syndrome Cancer Research. 78: 222-222. DOI: 10.1158/1538-7445.Am2018-222 |
0.384 |
|
| 2017 |
Salinas YD, Wang Z, DeWan AT. Statistical Analysis of Multiple Phenotypes in Genetic Epidemiological Studies:From Cross-Phenotype Associations to Pleiotropy. American Journal of Epidemiology. PMID 29020254 DOI: 10.1093/Aje/Kwx296 |
0.373 |
|
| 2017 |
Wang R, Metayer C, Morimoto L, Wiemels JL, DeWan AT, Kang A, Ma X. Parental age and risk of pediatric cancer in the offspring: a population-based record-linkage study in California. American Journal of Epidemiology. PMID 28535175 DOI: 10.1093/Aje/Kwx160 |
0.302 |
|
| 2017 |
Streicher SA, Klein AP, Olson SH, Kurtz RC, DeWan AT, Zhao H, Risch HA. Abstract 1326: A pooled genome-wide association study of pancreatic cancer susceptibility loci in American Jews Cancer Research. 77: 1326-1326. DOI: 10.1158/1538-7445.Am2017-1326 |
0.368 |
|
| 2016 |
Wang R, Wiemels JL, Metayer C, Morimoto L, Francis SS, Kadan-Lottick N, DeWan AT, Zhang Y, Ma X. Cesarean Section and Risk of Childhood Acute Lymphoblastic Leukemia in a Population-Based, Record-Linkage Study in California. American Journal of Epidemiology. PMID 27986703 DOI: 10.1093/Aje/Kww153 |
0.323 |
|
| 2016 |
Spracklen CN, Smith CJ, Saftlas AF, Triche EW, Bjonnes A, Keating BJ, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic predisposition to elevated levels of C-reactive protein is associated with a decreased risk for preeclampsia. Hypertension in Pregnancy. 1-10. PMID 27657194 DOI: 10.1080/10641955.2016.1223303 |
0.326 |
|
| 2016 |
Murk W, DeWan AT. Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma. Bmc Genetics. 17: 102. PMID 27387956 DOI: 10.1186/S12863-016-0376-3 |
0.36 |
|
| 2016 |
Salinas YD, Wang L, DeWan AT. Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans. Bmc Genetics. 17: 78. PMID 27296613 DOI: 10.1186/S12863-016-0387-0 |
0.376 |
|
| 2016 |
Wang L, Salinas YD, DeWan AT. Gene-based analysis identified the gene ZNF248 is associated with late-onset asthma in African Americans. Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology. PMID 27238579 DOI: 10.1016/J.Anai.2016.05.005 |
0.316 |
|
| 2016 |
Murk W, DeWan AT. Exhaustive Genome-Wide Search for SNP-SNP Interactions Across Ten Human Diseases. G3 (Bethesda, Md.). PMID 27185397 DOI: 10.1534/G3.116.028563 |
0.396 |
|
| 2016 |
Uzun A, Schuster J, McGonnigal B, Schorl C, Dewan A, Padbury J. Targeted Sequencing and Meta-Analysis of Preterm Birth. Plos One. 11: e0155021. PMID 27163930 DOI: 10.1371/Journal.Pone.0155021 |
0.375 |
|
| 2016 |
Uzun A, Triche EW, Schuster J, Dewan AT, Padbury JF. dbPEC: a comprehensive literature-based database for preeclampsia related genes and phenotypes. Database : the Journal of Biological Databases and Curation. 2016. PMID 26946289 DOI: 10.1093/Database/Baw006 |
0.354 |
|
| 2015 |
Wang L, Murk W, DeWan AT. Genome-Wide Gene by Environment Interaction Analysis Identifies Common SNPs at 17q21.2 that Are Associated with Increased Body Mass Index Only among Asthmatics. Plos One. 10: e0144114. PMID 26672748 DOI: 10.1371/Journal.Pone.0144114 |
0.428 |
|
| 2015 |
Smith CJ, Saftlas AF, Spracklen CN, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. American Journal of Hypertension. PMID 26002928 DOI: 10.1093/Ajh/Hpv069 |
0.314 |
|
| 2015 |
Murk W, Bracken MB, DeWan AT. Confronting the missing epistasis problem: on the reproducibility of gene-gene interactions. Human Genetics. 134: 837-49. PMID 25998948 DOI: 10.1007/S00439-015-1564-3 |
0.323 |
|
| 2015 |
Spracklen CN, Saftlas AF, Triche EW, Bjonnes A, Keating B, Saxena R, Breheny PJ, Dewan AT, Robinson JG, Hoh J, Ryckman KK. Genetic Predisposition to Dyslipidemia and Risk of Preeclampsia. American Journal of Hypertension. 28: 915-23. PMID 25523295 DOI: 10.1093/Ajh/Hpu242 |
0.359 |
|
| 2015 |
Jacobs DI, Lerro MC, Fu A, Qin Q, DeWan AT, Dubrow R, Claus EB, Zhu Y. Abstract 4623: piRNA and glioma risk: Evidence from a post-GWAS analysis of the GliomaScan Cohort Cancer Research. 75: 4623-4623. DOI: 10.1158/1538-7445.Am2015-4623 |
0.436 |
|
| 2014 |
Cartmel B, Dewan A, Ferrucci LM, Gelernter J, Stapleton J, Leffell DJ, Mayne ST, Bale AE. Novel gene identified in an exome-wide association study of tanning dependence. Experimental Dermatology. 23: 757-9. PMID 25041255 DOI: 10.1111/Exd.12503 |
0.403 |
|
| 2014 |
Triche EW, Uzun A, DeWan AT, Kurihara I, Liu J, Occhiogrosso R, Shen B, Parker J, Padbury JF. Bioinformatic approach to the genetics of preeclampsia. Obstetrics and Gynecology. 123: 1155-61. PMID 24807322 DOI: 10.1097/Aog.0000000000000293 |
0.354 |
|
| 2014 |
Hoang D, Broer N, Roman SA, Yao X, Abitbol N, Li F, Sosa JA, Sue GR, DeWan AT, Wong ML, Licinio J, Simpson C, Li AY, Pizzoferrato N, Narayan D. Leptin signaling and hyperparathyroidism: clinical and genetic associations. Journal of the American College of Surgeons. 218: 1239-1250.e4. PMID 24468228 DOI: 10.1016/J.Jamcollsurg.2013.11.013 |
0.359 |
|
| 2013 |
Zhao L, Bracken MB, DeWan AT. Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. Annals of Human Genetics. 77: 277-87. PMID 23551011 DOI: 10.1111/Ahg.12021 |
0.582 |
|
| 2013 |
Uzun A, Dewan AT, Istrail S, Padbury JF. Pathway-based genetic analysis of preterm birth. Genomics. 101: 163-70. PMID 23298525 DOI: 10.1016/J.Ygeno.2012.12.005 |
0.368 |
|
| 2013 |
Zhao L, Bracken MB, Dewan AT, Chen S. Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) and pre-eclampsia: a systematic review and meta-analysis. Molecular Human Reproduction. 19: 136-43. PMID 23180602 DOI: 10.1093/Molehr/Gas056 |
0.495 |
|
| 2012 |
Jacobs DI, Walsh KM, Wrensch M, Wiencke J, Jenkins R, Houlston RS, Bondy M, Simon M, Sanson M, Gousias K, Schramm J, Labussière M, Di Stefano AL, Wichmann HE, Müller-Nurasyid M, ... ... Dewan AT, et al. Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach. Frontiers in Genetics. 3: 203. PMID 23091480 DOI: 10.3389/Fgene.2012.00203 |
0.383 |
|
| 2012 |
DeWan AT, Egan KB, Hellenbrand K, Sorrentino K, Pizzoferrato N, Walsh KM, Bracken MB. Whole-exome sequencing of a pedigree segregating asthma. Bmc Medical Genetics. 13: 95. PMID 23046476 DOI: 10.1186/1471-2350-13-95 |
0.339 |
|
| 2012 |
Zhao L, Dewan AT, Bracken MB. Association of maternal AGTR1 polymorphisms and preeclampsia: a systematic review and meta-analysis. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 25: 2676-80. PMID 22758920 DOI: 10.3109/14767058.2012.708370 |
0.564 |
|
| 2012 |
Zhao L, Triche EW, Walsh KM, Bracken MB, Saftlas AF, Hoh J, Dewan AT. Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. Bmc Pregnancy and Childbirth. 12: 61. PMID 22748001 DOI: 10.1186/1471-2393-12-61 |
0.598 |
|
| 2012 |
Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, et al. Genetic signatures of exceptional longevity in humans. Plos One. 7: e29848. PMID 22279548 DOI: 10.1371/Journal.Pone.0029848 |
0.419 |
|
| 2012 |
Uzun A, Dewan A, Triche E, Kurihara S, Laliberte A, Padbury J. A novel bioinformatics approach for identifying the genetic contributions to preeclampsia Journal of Reproductive Immunology. 94: 121-122. DOI: 10.1016/J.Jri.2012.03.471 |
0.312 |
|
| 2011 |
Wu C, Walsh KM, Dewan AT, Hoh J, Wang Z. Disease risk prediction with rare and common variants. Bmc Proceedings. 5: S61. PMID 22373337 DOI: 10.1186/1753-6561-5-S9-S61 |
0.351 |
|
| 2011 |
Murk W, Walsh K, Hsu LI, Zhao L, Bracken MB, Dewan AT. Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthma. Human Heredity. 71: 97-105. PMID 21734400 DOI: 10.1159/000319536 |
0.585 |
|
| 2011 |
Wu C, DeWan A, Hoh J, Wang Z. A comparison of association methods correcting for population stratification in case-control studies. Annals of Human Genetics. 75: 418-27. PMID 21281271 DOI: 10.1111/J.1469-1809.2010.00639.X |
0.315 |
|
| 2011 |
Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, ... Dewan AT, et al. A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocrine-Related Cancer. 18: 171-80. PMID 21139019 DOI: 10.1677/Erc-10-0248 |
0.408 |
|
| 2010 |
Thorleifsson G, Walters GB, Hewitt AW, Masson G, Helgason A, DeWan A, Sigurdsson A, Jonasdottir A, Gudjonsson SA, Magnusson KP, Stefansson H, Lam DS, Tam PO, Gudmundsdottir GJ, Southgate L, et al. Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics. 42: 906-9. PMID 20835238 DOI: 10.1038/Ng.661 |
0.396 |
|
| 2010 |
Walsh KM, Bracken MB, Murk WK, Hoh J, Dewan AT. Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism. Mutation Research. 690: 89-94. PMID 20553737 DOI: 10.1016/J.Mrfmmm.2010.05.005 |
0.359 |
|
| 2009 |
Wu C, Zhang H, Liu X, Dewan A, Dubrow R, Ying Z, Yang Y, Hoh J. Detecting essential and removable interactions in genome-wide association studies. Statistics and Its Interface. 2: 161-170. PMID 21165165 DOI: 10.4310/Sii.2009.V2.N2.A6 |
0.371 |
|
| 2009 |
Jiao X, Yang Z, Yang X, Chen Y, Tong Z, Zhao C, Zeng J, Chen H, Gibbs D, Sun X, Li B, Wakins WS, Meyer C, Wang X, Kasuga D, ... ... DeWan A, et al. Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados. Proceedings of the National Academy of Sciences of the United States of America. 106: 17105-10. PMID 19805132 DOI: 10.1073/Pnas.0907564106 |
0.446 |
|
| 2009 |
SanGiovanni JP, Arking DE, Iyengar SK, Elashoff M, Clemons TE, Reed GF, Henning AK, Sivakumaran TA, Xu X, DeWan A, Agrón E, Rochtchina E, Sue CM, Wang JJ, Mitchell P, et al. Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration. Plos One. 4: e5508. PMID 19434233 DOI: 10.1371/Journal.Pone.0005508 |
0.305 |
|
| 2008 |
Zhang H, Morrison MA, Dewan A, Adams S, Andreoli M, Huynh N, Regan M, Brown A, Miller JW, Kim IK, Hoh J, Deangelis MM. The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. Bmc Medical Genetics. 9: 51. PMID 18541031 DOI: 10.1186/1471-2350-9-51 |
0.412 |
|
| 2008 |
Tam PO, Ng TK, Liu DT, Chan WM, Chiang SW, Chen LJ, DeWan A, Hoh J, Lam DS, Pang CP. HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH. Investigative Ophthalmology & Visual Science. 49: 2357-65. PMID 18316707 DOI: 10.1167/Iovs.07-1520 |
0.393 |
|
| 2008 |
Gibbs D, Yang Z, Constantine R, Ma X, Camp NJ, Yang X, Chen H, Jorgenson A, Hau V, Dewan A, Zeng J, Harmon J, Buehler J, Brand JM, Hoh J, et al. Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration. Vision Research. 48: 685-9. PMID 18207215 DOI: 10.1016/J.Visres.2007.10.022 |
0.443 |
|
| 2007 |
DeWan A, Klein RJ, Hoh J. Linkage disequilibrium mapping for complex disease genes. Methods in Molecular Biology (Clifton, N.J.). 376: 85-107. PMID 17984540 DOI: 10.1007/978-1-59745-389-9_7 |
0.332 |
|
| 2007 |
DeWan A, Bracken MB, Hoh J. Two genetic pathways for age-related macular degeneration. Current Opinion in Genetics & Development. 17: 228-33. PMID 17467263 DOI: 10.1016/J.Gde.2007.04.004 |
0.349 |
|
| 2006 |
Yang Z, Camp NJ, Sun H, Tong Z, Gibbs D, Cameron DJ, Chen H, Zhao Y, Pearson E, Li X, Chien J, Dewan A, Harmon J, Bernstein PS, Shridhar V, et al. A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration. Science (New York, N.Y.). 314: 992-3. PMID 17053109 DOI: 10.1126/Science.1133811 |
0.421 |
|
| 2006 |
Dewan A, Liu M, Hartman S, Zhang SS, Liu DT, Zhao C, Tam PO, Chan WM, Lam DS, Snyder M, Barnstable C, Pang CP, Hoh J. HTRA1 promoter polymorphism in wet age-related macular degeneration. Science (New York, N.Y.). 314: 989-92. PMID 17053108 DOI: 10.1126/Science.1133807 |
0.422 |
|
| 2004 |
Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, et al. X-linked high myopia associated with cone dysfunction. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 897-908. PMID 15197065 DOI: 10.1001/Archopht.122.6.897 |
0.335 |
|
| 2003 |
DeWan AT, Parrado AR, Leal SM. A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval Clinical Genetics. 63: 39-45. PMID 12519370 DOI: 10.1034/J.1399-0004.2003.630106.X |
0.328 |
|
| 2002 |
DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study. American Journal of Human Genetics. 71: 204-5. PMID 12068377 DOI: 10.1086/340730 |
0.344 |
|
| 2002 |
DeWan AT, Parrado AR, Matise TC, Leal SM. The map problem: a comparison of genetic and sequence-based physical maps. American Journal of Human Genetics. 70: 101-7. PMID 11706388 DOI: 10.1086/324774 |
0.304 |
|
| 2001 |
Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Human Molecular Genetics. 10: 2501-8. PMID 11709537 DOI: 10.1093/Hmg/10.22.2501 |
0.31 |
|
| 2001 |
Arnett DK, Devereux RB, Kitzman D, Oberman A, Hopkins P, Atwood L, Dewan A, Rao DC. Linkage of left ventricular contractility to chromosome 11 in humans: The HyperGEN Study. Hypertension (Dallas, Tex. : 1979). 38: 767-72. PMID 11641284 DOI: 10.1161/Hy1001.092650 |
0.322 |
|
| 2001 |
DeWan AT, Arnett DK, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt J. A genome scan for renal function among hypertensives: The HyperGEN study American Journal of Human Genetics. 68: 136-144. PMID 11115379 DOI: 10.1086/316927 |
0.32 |
|
| 2000 |
Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN). Ophthalmic Genetics. 21: 227-33. PMID 11135493 DOI: 10.1076/1381-6810(200012)21:4;1-H;Ft227 |
0.316 |
|
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