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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ... Nature genetics 48 (2), 134-143, 2016 | 1407 | 2016 |
Seven new loci associated with age-related macular degeneration Nature genetics 45 (4), 433-439, 2013 | 857 | 2013 |
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration W Chen, D Stambolian, AO Edwards, KE Branham, M Othman, ... Proceedings of the National Academy of Sciences 107 (16), 7401-7406, 2010 | 605 | 2010 |
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration A Kanda, W Chen, M Othman, KEH Branham, M Brooks, R Khanna, S He, ... Proceedings of the National Academy of Sciences 104 (41), 16227-16232, 2007 | 516 | 2007 |
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration S Zareparsi, KEH Branham, M Li, S Shah, RJ Klein, J Ott, J Hoh, ... The American Journal of Human Genetics 77 (1), 149-153, 2005 | 491 | 2005 |
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration M Li, P Atmaca-Sonmez, M Othman, KEH Branham, R Khanna, MS Wade, ... Nature genetics 38 (9), 1049-1054, 2006 | 413 | 2006 |
Next‐generation genetic testing for retinitis pigmentosa K Neveling, RWJ Collin, C Gilissen, RAC Van Huet, L Visser, MP Kwint, ... Human mutation 33 (6), 963-972, 2012 | 330 | 2012 |
E2-2 protein and Fuchs's corneal dystrophy KH Baratz, N Tosakulwong, E Ryu, WL Brown, K Branham, W Chen, ... New England Journal of Medicine 363 (11), 1016-1024, 2010 | 305 | 2010 |
High-resolution imaging with adaptive optics in patients with inherited retinal degeneration JL Duncan, Y Zhang, J Gandhi, C Nakanishi, M Othman, KEH Branham, ... Investigative ophthalmology & visual science 48 (7), 3283-3291, 2007 | 285 | 2007 |
Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements F Wang, H Wang, HF Tuan, DH Nguyen, V Sun, V Keser, SJ Bowne, ... Human genetics 133, 331-345, 2014 | 242 | 2014 |
Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease GR Abecasis, BM Yashar, Y Zhao, NM Ghiasvand, S Zareparsi, ... The American Journal of Human Genetics 74 (3), 482-494, 2004 | 235 | 2004 |
Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits A Swaroop, KEH Branham, W Chen, G Abecasis Human Molecular Genetics 16 (R2), R174-R182, 2007 | 230 | 2007 |
Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration S Zareparsi, M Buraczynska, KEH Branham, S Shah, D Eng, M Li, ... Human molecular genetics 14 (11), 1449-1455, 2005 | 225 | 2005 |
Biomarkers of cardiovascular disease as risk factors for age-related macular degeneration AK Vine, J Stader, K Branham, DC Musch, A Swaroop Ophthalmology 112 (12), 2076-2080, 2005 | 202 | 2005 |
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration X Zhan, DE Larson, C Wang, DC Koboldt, YV Sergeev, RS Fulton, ... Nature genetics 45 (11), 1375-1379, 2013 | 190 | 2013 |
Association of apolipoprotein E alleles with susceptibility to age-related macular degeneration in a large cohort from a single center S Zareparsi, AC Reddick, KEH Branham, KB Moore, L Jessup, S Thoms, ... Investigative ophthalmology & visual science 45 (5), 1306-1310, 2004 | 172 | 2004 |
Ancestry estimation and control of population stratification for sequence-based association studies C Wang, X Zhan, J Bragg-Gresham, HM Kang, D Stambolian, EY Chew, ... Nature genetics 46 (4), 409-415, 2014 | 155 | 2014 |
Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa JD Churchill, SJ Bowne, LS Sullivan, RA Lewis, DK Wheaton, DG Birch, ... Investigative ophthalmology & visual science 54 (2), 1411-1416, 2013 | 151 | 2013 |
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration JS Friedman, B Chang, C Kannabiran, C Chakarova, HP Singh, S Jalali, ... The American Journal of Human Genetics 79 (6), 1059-1070, 2006 | 149 | 2006 |