Human Genome Epidemiology Literature Finder
|
Records 1 - 17 (of 17 Records) |
| Query Trace: Glaucoma and FOXC1[original query] |
|---|
| Molecular basis of Peters anomaly in Saudi Arabia. Ophthalmic genetics 2004 12 25 (4): 257-70. Edward Deepak, Al Rajhi Ali, Lewis Richard Alan, Curry Stacey, Wang Zongren, Bejjani Bass |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
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 Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome. Current eye research 2018 6 43 (11): 1334-1341. Wang Xun, Liu Xing, Huang Liqin, Fang Shaohua, Jia Xiaoyun, Xiao Xueshan, Li Shiqiang, Guo Xiangmi |
| Molecular analysis of Cypriot families with aniridia reveals a novel PAX6 mutation. Molecular medicine reports 2018 6 18 (2): 1623-1627. Syrimis Andreas, Nicolaou Nayia, Alexandrou Angelos, Papaevripidou Ioannis, Nicolaou Michael, Loukianou Eleni, Sismani Carolina, Malas Stavros, Christophidou-Anastasiadou Violetta, Tanteles George |
| 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 |
| Genetic analysis of patients with primary congenital glaucoma. International ophthalmology 2021 Mar . Ava Sedat, Demirta? At?l?m Arma?an, Karahan Mine, Erdem Seyfettin, Oral Diclehan, Keklikçi U? |
| TXNRD2 (rs35934224) CT genotype and primary open-angle glaucoma: correspondenceReply to "TXNRD2 (rs35934224) CT genotype and primary open-angle glaucoma: correspondence"Primary open-angle glaucomaGenome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucomaGenome-wide association study of primary open-angle glaucoma in continental and admixed African populations. Arquivos brasileiros de oftalmologia 2022 4 85 (2): 214-215. Sookaromdee Pathum, Wiwanitkit Vir |
| Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome. Experimental eye research 2022 11 226 109307. Zhou Lin, Wang Xiaoli, An Jingqi, Zhang Yao, He Mengxia, Tang |
| First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association. Journal of clinical medicine 2022 1 11 (1): . Stingl Julia V, Diederich Stefan, Diel Heidi, Schuster Alexander K, Wagner Felix M, Chronopoulos Panagiotis, Aghayeva Fidan, Grehn Franz, Winter Jennifer, Schweiger Susann, Hoffmann Esther |
| Analysis of glaucoma genes in Finnish patients with juvenile open-angle glaucoma. Acta ophthalmologica 2023 4 . Liuska Perttu J, Tadji Abdessallam, Repo Pauliina, Hiltunen Juho, Backlund Michael, Järvinen Reetta-Stiina, Ojanen Eeva, Majander Anna, Kivelä Tero T, Harju Mika, Turunen Joni |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
- Content source: