HuGE Literature Finder
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| Genetic analysis of patients with primary congenital glaucoma. International ophthalmology 2021 Mar . Ava Sedat, Demirtas Atilim Armagan, Karahan Mine, Erdem Seyfettin, Oral Diclehan, Keklikçi Ug |
| Analysis of variants in Chinese individuals with primary open-angle glaucoma using molecular inversion probe (MIP)-based panel sequencing. Molecular vision 2020 26 378-391. Liu Ting, Tang Chao, Shi Xiaolo |
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Nature genetics 2016 Feb 48 (2): 189-94. Bailey Jessica N Cooke, Loomis Stephanie J, Kang Jae H, Allingham R Rand, Gharahkhani Puya, Khor Chiea Chuen, Burdon Kathryn P, Aschard Hugues, Chasman Daniel I, Igo Robert P, Hysi Pirro G, Glastonbury Craig A, Ashley-Koch Allison, Brilliant Murray, Brown Andrew A, Budenz Donald L, Buil Alfonso, Cheng Ching-Yu, Choi Hyon, Christen William G, Curhan Gary, De Vivo Immaculata, Fingert John H, Foster Paul J, Fuchs Charles, Gaasterland Douglas, Gaasterland Terry, Hewitt Alex W, Hu Frank, Hunter David J, Khawaja Anthony P, Lee Richard K, Li Zheng, Lichter Paul R, Mackey David A, McGuffin Peter, Mitchell Paul, Moroi Sayoko E, Perera Shamira A, Pepper Keating W, Qi Qibin, Realini Tony, Richards Julia E, Ridker Paul M, Rimm Eric, Ritch Robert, Ritchie Marylyn, Schuman Joel S, Scott William K, Singh Kuldev, Sit Arthur J, Song Yeunjoo E, Tamimi Rulla M, Topouzis Fotis, Viswanathan Ananth C, Verma Shefali Setia, Vollrath Douglas, Wang Jie Jin, Weisschuh Nicole, Wissinger Bernd, Wollstein Gadi, Wong Tien Y, Yaspan Brian L, Zack Donald J, Zhang Kang, Study Epic-Norfolk Eye, , Weinreb Robert N, Pericak-Vance Margaret A, Small Kerrin, Hammond Christopher J, Aung Tin, Liu Yutao, Vithana Eranga N, MacGregor Stuart, Craig Jamie E, Kraft Peter, Howell Gareth, Hauser Michael A, Pasquale Louis R, Haines Jonathan L, Wiggs Janey |
| Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma. International journal of molecular medicine 2015 Oct 36 (4): 1111-7. Huang Xiaobo, Xiao Xueshan, Jia Xiaoyun, Li Shiqiang, Li Miaoling, Guo Xiangming, Liu Xing, Zhang Qingjio |
| Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences. European journal of human genetics : EJHG 2015 Jul . Medina-Trillo Cristina, Aroca-Aguilar José-Daniel, Méndez-Hernández Carmen-Dora, Morales Laura, García-Antón Maite, García-Feijoo Julián, Escribano Jul |
| Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma. Molecular vision 2013 19 . Mohanty K, Tanwar M, Dada R, Dada T |
| Common TGFß2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma. Molecular vision 2012 18 1526-39. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Fraser Scott, Sowden Jane |
| MYOC and FOXC1 gene analysis in primary congenital glaucoma. Molecular vision 2010 16 1996-2006. Tanwar Mukesh, Kumar Manoj, Dada Tanuj, Sihota Ramanjit, Dada Ri |
| The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma. Investigative ophthalmology & visual science 2009 Jan 50 (1): 75-83. Chakrabarti Subhabrata, Kaur Kiranpreet, Rao Kollu Nageswara, Mandal Anil K, Kaur Inderjeet, Parikh Rajul S, Thomas Ra |
| Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies. Molecular vision 2009 15 1366-73. Kaur Kulvinder, Ragge Nicola K, Ragoussis Jiann |
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- Page last updated:Jun 28, 2022
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