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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 5, 2023. (Total: 223688Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Vision and VEGFA[original query]
Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss.
Journal of medical genetics 2009 May 46 (5): 300-7.
Francis P J, Hamon S C, Ott J, Weleber R G, Klein M
Vascular endothelial growth factor gene polymorphisms as prognostic markers for ocular manifestations in pseudoxanthoma elasticum.
Human molecular genetics 2009 Sep 18 (17): 3344-51.
Zarbock Ralf, Hendig Doris, Szliska Christiane, Kleesiek Knut, Götting Christi
Genetic association with response to intravitreal ranibizumab in patients with neovascular AMD.
Investigative ophthalmology & visual science 2011 Jun 52 (7): 4694-702.
Kloeckener-Gruissem Barbara, Barthelmes Daniel, Labs Stephan, Schindler Christian, Kurz-Levin Malaika, Michels Stephan, Fleischhauer Johannes, Berger Wolfgang, Sutter Florian, Menghini More
Common variant in VEGFA and response to anti-VEGF therapy for neovascular age-related macular degeneration.
Current molecular medicine 2013 Jul 13 (6): 6.
Zhao L, Grob S, Avery R, Kimura A, Pieramici D, Lee J, Rabena M, Ortiz S, Quach J, Cao G, Luo H, Zhang M, Pei M, Song Y, Tornambe P, Goldbaum M, Ferreyra H, Kozak I, Zhang K
TCF7L2 variation and proliferative diabetic retinopathy.
Diabetes 2013 Jul 62 (7): 2613-7.
Luo Jing, Zhao Ling, Chen Aaron Yun, Zhang Xiaohui, Zhu Jin, Zhao Jiagang, Ouyang Hong, Luo Hongrong, Song Yaojun, Lee Janet, Patel Sherrina H, Shaw Peter X, Sadda Srinivas, Zhuo Yehong, Rosenfeld Michael G, Zhang Ka
Set-based joint test of interaction between SNPs in the VEGF pathway and exogenous estrogen finds association with age-related macular degeneration.
Investigative ophthalmology & visual science 2014 Jul .
Courtenay Monique D, Cade William, Schwartz Stephen G, Kovach Jaclyn L, Agarwal Anita, Wang Gaofeng, Haines Jonathan L, Pericak-Vance Margaret A, Scott Wiliam
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.
Investigative ophthalmology & visual science 2014 Jun 55 (6): 3543-54.
Owen Leah A, Morrison Margaux A, Ahn Jeeyun, Woo Se Joon, Sato Hajime, Robinson Rosann, Morgan Denise J, Zacharaki Fani, Simeonova Marina, Uehara Hironori, Chakravarthy Usha, Hogg Ruth E, Ambati Balamurali K, Kotoula Maria, Baehr Wolfgang, Haider Neena B, Silvestri Giuliana, Miller Joan W, Tsironi Evangelia E, Farrer Lindsay A, Kim Ivana K, Park Kyu Hyung, DeAngelis Margaret
VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticum.
Clinical genetics 2020 4 98 (1): 74-79.
De Vilder Eva Y G, Hosen Mohammad J, Martin Ludovic, De Zaeytijd Julie, Leroy Bart P, Ebran Jean-Marc, Coucke Paul J, De Paepe Anne, Vanakker Olivier
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