HuGE Literature Finder
Records 1-23
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An evaluation of genetic causes and environmental risks for bilateral optic atrophy.
PloS one 2019 14 (11): e0225656. Chen Andrew T, Brady Lauren, Bulman Dennis E, Sundaram Arun N E, Rodriguez Amadeo R, Margolin Edward, Waye John S, Tarnopolsky Mark |
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Association between Mitofusin 2 Gene Polymorphisms and Late-Onset Alzheimer's Disease in the Korean Population.
Psychiatry investigation 2017 Jan 14 (1): 81-85. Kim Young Jong, Park Jin Kyung, Kang Won Sub, Kim Su Kang, Han Changsu, Na Hae Ri, Park Hae Jeong, Kim Jong Woo, Kim Young Youl, Park Moon Ho, Paik Jong-W |
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The OPA1 Gene Mutations Are Frequent in Han Chinese Patients with Suspected Optic Neuropathy.
Molecular neurobiology 2016 Feb . Zhang A-Mei, Bi Rui, Hu Qiu-Xiang, Fan Yu, Zhang Qingjiong, Yao Yong-Ga |
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Identification of copy number variation in the gene for autosomal dominant optic atrophy, OPA1, in a Chinese pedigree.
Genetics and molecular research : GMR 2015 14 (3): 10961-72. Jin X, Chen Y H, Liu Z, Deng Y, Li N N, Huang H, Qi M, Yi X, Zhu |
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Mutation screening of mitochondrial DNA as well as OPA1 and OPA3 in a Chinese cohort with suspected hereditary optic atrophy.
Investigative ophthalmology & visual science 2014 Oct 55 (10): 6987-95. Chen Jieqiong, Xu Ke, Zhang Xiaohui, Jiang Feng, Liu Lijuan, Dong Bing, Ren Yanfan, Li Ya |
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Mutation survey of the optic atrophy 1 gene in 193 Chinese families with suspected hereditary optic neuropathy.
Molecular vision 2013 19 292-302. Chen Yabin, Jia Xiaoyun, Wang Panfeng, Xiao Xueshan, Li Shiqiang, Guo Xiangming, Zhang Qingjio |
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Association of OPA1 polymorphisms with NTG and HTG: a meta-analysis.
PloS one 2012 7 (8): e42387. Guo Yatu, Chen Xia, Zhang Hongtuan, Li Ningdong, Yang Xiong, Cheng Wenbo, Zhao Kanxi |
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Genetic screening for OPA1 and OPA3 mutations in patients with suspected inherited optic neuropathies.
Ophthalmology 2011 Mar 118 (3): 558-63. Yu-Wai-Man Patrick, Shankar Suma P, Biousse Valérie, Miller Neil R, Bean Lora J H, Coffee Bradford, Hegde Madhuri, Newman Nancy |
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Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma.
Investigative ophthalmology & visual science 2010 Aug 51 (8): 4110-6. Fan Bao Jian, Liu Ke, Wang Dan Yi, Tham Clement C Y, Tam Pancy O S, Lam Dennis S C, Pang Chi P |
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OPA1 increases the risk of normal but not high tension glaucoma.
Journal of medical genetics 2010 Feb 47 (2): 120-5. Yu-Wai-Man P, Stewart J D, Hudson G, Andrews R M, Griffiths P G, Birch M K, Chinnery P |
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Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy.
Molecular vision 2010 16 2760-4. Hudson Gavin, Yu-Wai-Man Patrick, Griffiths Phillip G, Caporali Leonardo, Salomao Solange S, Berezovsky Adriana, Carelli Valerio, Zeviani Massimo, Chinnery Patrick |
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Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 Novel OPA1 mutations.
Human mutation 2009 Mar . Ferré M, Bonneau D, Milea D, Chevrollier A, Verny C, Dollfus H, Ayuso C, Defoort S, Vignal C, Zanlonghi X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P |
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Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study.
BMC medical genetics 2009 10 91. Wolf Christiane, Gramer Eugen, Müller-Myhsok Bertram, Pasutto Francesca, Reinthal Eva, Wissinger Bernd, Weisschuh Nico |
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OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.
BMC medical genetics 2009 10 (1): 70. Pierron Denis, Ferré Marc, Rocher Christophe, Chevrollier Arnaud, Murail Pascal, Thoraval Didier, Amati-Bonneau Patrizia, Reynier Pascal, Letellier Thier |
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Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
Journal of neurology 2008 Sep 255 (9): 1384-91. Virgilio Roberta, Ronchi Dario, Hadjigeorgiou Georgios M, Bordoni Andreina, Saladino Francesca, Moggio Maurizio, Adobbati Laura, Kafetsouli Demetra, Tsironi Evangelia, Previtali Stefano, Papadimitriou Alexandros, Bresolin Nereo, Comi Giacomo |
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The OPA1 gene polymorphism is associated with normal tension and high tension glaucoma.
American journal of ophthalmology 2007 Jan 143 (1): 125-130. Mabuchi F, Tang S, Kashiwagi K, Yamagata Z, Iijima H, Tsukahara S |
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No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations.
Molecular vision 2007 13 2137-41. Liu Yutao, Schmidt Silke, Qin Xuejun, Gibson Jason, Munro Drew, Wiggs Janey L, Hauser Michael A, Allingham R Ra |
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Investigation of the association between OPA1 polymorphisms and normal-tension glaucoma in Korea.
Journal of glaucoma 2004 Dec 13 (6): 492-5. Woo Se Joon, Kim Dong Myung, Kim Ji Yeon, Park Sung Sup, Ko Hyun Soo, Yoo Taiw |
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OPA1 gene mutations in Japanese patients with bilateral optic atrophy unassociated with mitochondrial DNA mutations at nt 11778, 3460, and 14484.
Japanese journal of ophthalmology 2003 47 (4): 409-11. Yamada T, Hayasaka S, Matsumoto M, Esa T, Hayasaka Y, Endo M, Nagaki Y, Fujiki K, Murakami A, Kanai A |
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The phenotype of normal tension glaucoma patients with and without OPA1 polymorphisms.
The British journal of ophthalmology 2003 Feb 87 (2): 149-52. Aung T, Okada K, Poinoosawmy D, Membrey L, Brice G, Child A H, Bhattacharya S S, Lehmann O J, Garway-Heath D F, Hitchings R |
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Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma.
Human genetics 2002 May 110 (5): 513-4. Aung Tin, Ocaka Louise, Ebenezer Neil D, Morris Alex G, Brice Glen, Child Anne H, Hitchings Roger A, Lehmann Ordan J, Bhattacharya Shomi |
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A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
Human genetics 2002 Jan 110 (1): 52-6. Aung Tin, Ocaka Louise, Ebenezer Neil D, Morris Alex G, Krawczak Michael, Thiselton Dawn L, Alexander Christiane, Votruba Marcela, Brice Glen, Child Anne H, Francis Peter J, Hitchings Roger A, Lehmann Ordan J, Bhattacharya Shomi |
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Polymorphism Analysis of GSTM1 and OPA1 Genes in Greek Patients with Primary Open-angle Glaucoma.
In vivo (Athens, Greece) 0 30 (4): 473-477. Lavaris Anastasios, Gazouli Maria, Brouzas Dimitrios, Moschos Marilita |
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- Page last updated:Mar 02, 2021
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