Andrew DeWan
Andrew DeWan
Associate Professor of Epidemiology, Yale School of Public Health
Verified email at - Homepage
Cited by
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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
p53 responsive elements in human retrotransposons
CR Harris, A Dewan, A Zupnick, R Normart, A Gabriel, C Prives, ...
Oncogene 28 (44), 3857-3865, 2009
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
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 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
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
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
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
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
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
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
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
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
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