Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Blindness and HLA-B[original query] |
---|
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study. Lancet (London, England) 2008 Nov 372 (9652): 1828-34. Ennis Sarah, Jomary Catherine, Mullins Robert, Cree Angela, Chen Xiaoli, Macleod Alex, Jones Stephen, Collins Andrew, Stone Edwin, Lotery Andr |
Human leukocyte antigen (HLA)-B, DRB1, and DQB1 allotypes associated with disease and protection of trachoma endemic villagers. Investigative ophthalmology & visual science 2009 Apr 50 (4): 1734-8. Abbas Muneer, Bobo Linda D, Hsieh Yu-Hsiang, Berka Noureddine, Dunston Georgia, Bonney George E, Apprey Victor, Quinn Thomas C, West Sheila |
Replication of a microsatellite genome-wide association study of Behcet's disease in a Korean population. Rheumatology (Oxford, England) 2012 Jun 51 (6): 983-6. Horie Yukihiro, Meguro Akira, Kitaichi Nobuyoshi, Lee Eun Bong, Kanda Atsuhiro, Noda Kousuke, Song Yeong Wook, Park Kyung Sook, Namba Kenichi, Ota Masao, Inoko Hidetoshi, Mizuki Nobuhisa, Ishida Susumu, Ohno Shigea |
Genetic and non-genetic factors affecting the visual outcome of ocular Behcet's disease. Human immunology 2013 Oct 74 (10): 1363-7. Kang Eun Ha, Park Jun Won, Park Chaerin, Yu Hyeong Gon, Lee Eun Bong, Park Myoung Hee, Song Yeong Wo |
Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Human genetics 2014 Oct 133 (10): 1319-30. Bailey Jessica N Cooke, Yaspan Brian L, Pasquale Louis R, Hauser Michael A, Kang Jae H, Loomis Stephanie J, Brilliant Murray, Budenz Donald L, Christen William G, Fingert John, Gaasterland Douglas, Gaasterland Terry, Kraft Peter, Lee Richard K, Lichter Paul R, Liu Yutao, McCarty Catherine A, Moroi Sayoko E, Richards Julia E, Realini Tony, Schuman Joel S, Scott William K, Singh Kuldev, Sit Arthur J, Vollrath Douglas, Wollstein Gadi, Zack Donald J, Zhang Kang, Pericak-Vance Margaret A, Allingham R Rand, Weinreb Robert N, Haines Jonathan L, Wiggs Janey |
Conjunctival scarring in trachoma is associated with the HLA-C ligand of KIR and is exacerbated by heterozygosity at KIR2DL2/KIR2DL3. PLoS neglected tropical diseases 2014 Mar 8 (3): e2744. Roberts Chrissy H, Molina Sandra, Makalo Pateh, Joof Hassan, Harding-Esch Emma M, Burr Sarah E, Mabey David C W, Bailey Robin L, Burton Matthew J, Holland Martin |
PTPN22 R620W minor allele is a genetic risk factor for giant cell arteritis. RMD open 2016 2 (1): e000246. Lester Susan, Hewitt Alex W, Ruediger Carlee D, Bradbury Linda, De Smit Elisabeth, Wiese Michael D, Black Rachel, Harrison Andrew, Jones Graeme, Littlejohn Geoffrey O, Merriman Tony R, Shenstone Bain, Smith Malcolm D, Rischmueller Maureen, Brown Matthew A, Hill Catherine |
Lack of association of C3 gene with uveitis: additional insights into the genetic profile of uveitis regarding complement pathway genes. Scientific reports 2017 Apr 7 (1): 879. Yang Ming Ming, Wang Jun, Dong Li, Kong De Ju, Teng Yan, Liu Ping, Fan Jiao Jie, Yu Xu H |
Variability at the 3' untranslated region of the HLA-G gene: a study on patients with AIDS and cytomegalovirus retinochoroiditis. Scientific reports 2020 10 10 (1): 18646. Vicente Luciana de Morais, Castelli Erick C, Veronese Rodrigues Maria de Lourdes, Deghaide Neifi Hassan Saloum, Mendes-Junior Celso Teixeira, Furtado João M, Donadi Eduardo Anton |
Human leukocyte antigen B*0702 is protective against ocular Stevens-Johnson syndrome/toxic epidermal necrolysis in the UK population. Scientific reports 2021 Feb 11 (1): 2928. Butt Gibran F, Hassan Ali, Wallace Graham R, Kinoshita Shigeru, Ahmad Sajjad, Ueta Mayumi, Rauz Saae |
Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study. Clinical and experimental immunology 2021 Jan . Elfishawi M, Mossallam G, Augusto D G, Montero-Martin G, de Bruin H, Van de Pasch L, Norman P J, Rozemuller E, Fernandez-Vina M, Abrudescu A, Hollenbach J A, Zaky K, Elfishawi |
Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma.
Nature communications 2022 11 13 (1): 7376. Gao Xiaoyi Raymond, Chiariglione Marion, Arch Alexander |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: