HuGE Literature Finder
Records
1
-
17
| Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations. Cornea 2019 5 38 (8): 1033-1039. Zhang Wenlin, Margines J Ben, Jacobs Deborah S, Rabinowitz Yaron S, Hanser Evelyn Maryam, Chauhan Tulika, Chung Doug, Bykhovskaya Yelena, Gaster Ronald N, Aldave Anthony |
| Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent. Investigative ophthalmology & visual science 2017 Dec 58 (14): 6248-6256. Lucas Sionne E M, Zhou Tiger, Blackburn Nicholas B, Mills Richard A, Ellis Jonathan, Leo Paul, Souzeau Emmanuelle, Ridge Bronwyn, Charlesworth Jac C, Brown Matthew A, Lindsay Richard, Craig Jamie E, Burdon Kathryn |
| Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort. BMC research notes 2017 Nov 10 (1): 652. Kalantan Hatem, Kondkar Altaf A, Sultan Tahira, Azad Taif A, Alsabaani Nasser A, AlQahtani Masoud Ali, Almummar Abdulrahman, Liu Yuato, Abu-Amero Khaled |
| Genetic associations for keratoconus: a systematic review and meta-analysis. Scientific reports 2017 Jul 7 (1): 4620. Rong Shi Song, Ma Sarah Tsz Ue, Yu Xin Ting, Ma Li, Chu Wai Kit, Chan Tommy Chung Yan, Wang Yu Meng, Young Alvin L, Pang Chi Pui, Jhanji Vishal, Chen Li J |
| Novel Zinc Finger Protein Gene 469 (ZNF469) Variants in Advanced Keratoconus. Current eye research 2017 Jun 1-5. Yildiz Elvin, Bardak Handan, Gunay Murat, Bardak Yavuz, Imamoglu Serhat, Ozbas Halil, Bagci Ozk |
| Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population. Molecular vision 2017 23 296-305. Yu Xiaoning, Chen Binbin, Zhang Xin, Shentu Xingch |
| Replication of SNP associations with keratoconus in a Czech cohort. PloS one 2017 12 (2): e0172365. Liskova Petra, Dudakova Lubica, Krepelova Anna, Klema Jiri, Hysi Pirro |
| Evidence against ZNF469 being causative for keratoconus in Polish patients. Acta ophthalmologica 2016 May 94 (3): 289-94. Karolak Justyna A, Gambin Tomasz, Rydzanicz Malgorzata, Szaflik Jacek P, Polakowski Piotr, Frajdenberg Agata, Mrugacz Malgorzata, Podfigurna-Musielak Monika, Stankiewicz Pawel, Gajecka Marze |
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.
Human molecular genetics 2016 11 25 (22): 5035-5045. Gao Xiaoyi, Nannini Drew R, Corrao Kristen, Torres Mina, Chen Yii-Der I, Fan Bao J, Wiggs Janey L, , Taylor Kent D, Gauderman W James, Rotter Jerome I, Varma Roh |
| Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population. Ophthalmic genetics 2015 Jun 36 (2): 132-6. Hao Xiao-Dan, Chen Peng, Chen Zhao-Li, Li Su-Xia, Wang |
| Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus. Investigative ophthalmology & visual science 2015 1 56 (1): 578-86. Davidson Alice E, Borasio Edmondo, Liskova Petra, Khan Arif O, Hassan Hala, Cheetham Michael E, Plagnol Vincent, Alkuraya Fowzan S, Tuft Stephen J, Hardcastle Alison |
| Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population. Journal of negative results in biomedicine 2015 14 10. Abu-Amero Khaled K, Helwa Inas, Al-Muammar Abdulrahman, Strickland Shelby, Hauser Michael A, Allingham R Rand, Liu Yut |
| Enrichment of pathogenic alleles in the brittle cornea gene, ZNF469, in keratoconus. Human molecular genetics 2014 Oct 23 (20): 5527-35. Lechner Judith, Porter Louise F, Rice Aine, Vitart Veronique, Armstrong David J, Schorderet Daniel F, Munier Francis L, Wright Alan F, Inglehearn Chris F, Black Graeme C, Simpson David A, Manson Forbes, Willoughby Colin |
| Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus. Investigative ophthalmology & visual science 2014 Sep 55 (9): 5629-35. Vincent Andrea L, Jordan Charlotte A, Cadzow Murray J, Merriman Tony R, McGhee Charles |
| Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population. Investigative ophthalmology & visual science 2013 Nov . Sahebjada S, Schache M, Richardson AJ, Macgregor S, Snibson GR, Daniell M, Baird PN |
| A genome-wide association study of central corneal thickness in Latinos.
Investigative ophthalmology & visual science 2013 Apr 54 (4): 2435-43. Gao Xiaoyi, Gauderman W James, Liu Yutao, Marjoram Paul, Torres Mina, Haritunians Talin, Kuo Jane Z, Chen Yii-Der I, Allingham R Rand, Hauser Michael A, Taylor Kent D, Rotter Jerome I, Varma Roh |
| New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.
Human molecular genetics 2010 Nov 19 (21): 4304-11. Vitart Veronique, Benci? Goran, Hayward Caroline, Skunca Herman Jelena, Huffman Jennifer, Campbell Susan, Bu?an Kajo, Navarro Pau, Gunjaca Grgo, Marin Josipa, Zgaga Lina, Kolci? Ivana, Polasek Ozren, Kirin Mirna, Hastie Nicholas D, Wilson James F, Rudan Igor, Campbell Harry, Vatavuk Zoran, Fleck Brian, Wright Al |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 22, 2023
- Content source: