| HTRA1 promoter polymorphism in wet age-related macular degeneration A DeWan, M Liu, S Hartman, SSM Zhang, DTL Liu, C Zhao, POS Tam, ... Science 314 (5801), 989-992, 2006 | 1094 | 2006 |
| A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration Z Yang, NJ Camp, H Sun, Z Tong, D Gibbs, DJ Cameron, H Chen, Y Zhao, ... Science 314 (5801), 992-993, 2006 | 969 | 2006 |
| Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ... Nature genetics 42 (10), 906-909, 2010 | 458 | 2010 |
| Brain-derived neurotrophic factor mediates the activity-dependent regulation of inhibition in neocortical cultures LC Rutherford, A DeWan, HM Lauer, GG Turrigiano Journal of Neuroscience 17 (12), 4527-4535, 1997 | 458 | 1997 |
| Genetic signatures of exceptional longevity in humans P Sebastiani, N Solovieff, AT DeWan, KM Walsh, A Puca, SW Hartley, ... PloS one 7 (1), e29848, 2012 | 451 | 2012 |
| Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss IN Bespalova, G Van Camp, S JH Bom, DJ Brown, K Cryns, AT DeWan, ... Human molecular genetics 10 (22), 2501-2508, 2001 | 316 | 2001 |
| Mutations in the γ-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26) M Zhu, T Yang, S Wei, AT DeWan, RJ Morell, JL Elfenbein, RA Fisher, ... The American Journal of Human Genetics 73 (5), 1082-1091, 2003 | 252 | 2003 |
| Evidence for a putative bipolar disorder locus on 2p13–16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21–24, 13q32, 14q21 and 17q11–12 J Liu, SH Juo, A Dewan, A Grunn, X Tong, M Brito, N Park, JE Loth, ... Molecular psychiatry 8 (3), 333-342, 2003 | 151 | 2003 |
| Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration JP SanGiovanni, DE Arking, SK Iyengar, M Elashoff, TE Clemons, ... PLoS One 4 (5), e5508, 2009 | 118 | 2009 |
| p53 responsive elements in human retrotransposons CR Harris, A Dewan, A Zupnick, R Normart, A Gabriel, C Prives, ... Oncogene 28 (44), 3857-3865, 2009 | 116 | 2009 |
| HTRA1 promoter polymorphism predisposes Japanese to age-related macular degeneration T Yoshida, A DeWan, H Zhang, R Sakamoto, H Okamoto, M Minami, ... Molecular vision 13, 545, 2007 | 114 | 2007 |
| A comparison of association methods correcting for population stratification in case–control studies C Wu, A DeWan, J Hoh, Z Wang Annals of human genetics 75 (3), 418-427, 2011 | 109 | 2011 |
| X-linked high myopia associated with cone dysfunction TL Young, SS Deeb, SM Ronan, AT Dewan, AB Alvear, GS Scavello, ... Archives of Ophthalmology 122 (6), 897-908, 2004 | 109 | 2004 |
| HTRA1 variants in exudative age-related macular degeneration and interactions with smoking and CFH POS Tam, TK Ng, DTL Liu, WM Chan, SWY Chiang, LJ Chen, A DeWan, ... Investigative ophthalmology & visual science 49 (6), 2357-2365, 2008 | 102 | 2008 |
| Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients L Zhao, EW Triche, KM Walsh, MB Bracken, AF Saftlas, J Hoh, AT Dewan BMC pregnancy and childbirth 12, 1-10, 2012 | 95 | 2012 |
| A genome scan for renal function among hypertensives: the HyperGEN study AT DeWan, DK Arnett, LD Atwood, MA Province, CE Lewis, SC Hunt, ... The American Journal of Human Genetics 68 (1), 136-144, 2001 | 94 | 2001 |
| Further refinement of the MYP2 locus for autosomal dominant high myopia by linkage disequilibrium analysis TL Young, LD Atwood, SM Ronan, AT Dewan, AB Alvear, J Peterson, ... Ophthalmic genetics 22 (2), 69-75, 2001 | 88 | 2001 |
| Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse … L Zhao, MB Bracken, AT DeWan Annals of human genetics 77 (4), 277-287, 2013 | 87 | 2013 |
| Joint effects of polymorphisms in the HTRA1, LOC387715/ARMS2, and CFH genes on AMD in a Caucasian population PJ Francis, H Zhang, A DeWan, J Hoh, ML Klein Molecular vision 14, 1395, 2008 | 86 | 2008 |
| GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24. 21 JL Wiemels, KM Walsh, AJ de Smith, C Metayer, S Gonseth, HM Hansen, ... Nature communications 9 (1), 286, 2018 | 83 | 2018 |
