|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
|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
|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
|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
|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
|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
|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
|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
|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
|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
|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), 2009
|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
|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
|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
|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
|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
|p53 responsive elements in human retrotransposons|
CR Harris, A Dewan, A Zupnick, R Normart, A Gabriel, C Prives, ...
Oncogene 28 (44), 3857-3865, 2009
|The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration|
H Zhang, MA Morrison, A DeWan, S Adams, M Andreoli, N Huynh, ...
BMC medical genetics 9 (1), 51, 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), 61, 2012
|Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of Barbados|
X Jiao, Z Yang, X Yang, Y Chen, Z Tong, C Zhao, J Zeng, H Chen, ...
Proceedings of the National Academy of Sciences 106 (40), 17105-17110, 2009