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Kari Branham
Kari Branham
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Cited by
Cited by
Year
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
28532016
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
14072016
Seven new loci associated with age-related macular degeneration
Nature genetics 45 (4), 433-439, 2013
8572013
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
6052010
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
5162007
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
4912005
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
4132006
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
3302012
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
3052010
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
2852007
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
2422014
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
2352004
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
2302007
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
2252005
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
2022005
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
1902013
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
1722004
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
1552014
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
1512013
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
1492006
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