HuGE Literature Finder
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| A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India. European journal of ophthalmology 2022 3 32 (3): 1361-1369. Chakravarty Mrigyanka, Ponnam Surya Prakash Goud, Bardoloi Narayan, Kumar Subhash, Saikia Prasan |
| Absence of significant genetic alterations in the VSX1, SOD1, TIMP3, and LOX genes in Brazilian patients with Keratoconus. Ophthalmic genetics 2021 11 43 (1): 73-79. Lopes Alessandro Garcia, de Almeida Gildásio Castello, Miola Marcos Paulo, Teixeira Ronan Marques, Pires Francielly Camilla Bazilio Laurindo, Miani Rodolfo Andrade, de Mattos Luiz Carlos, Brandão Cinara Cássia, Castiglioni Lili |
| [A novel VSX1 gene mutation identified in a sporadic keratoconus patient from China]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2018 3 54 (3): 212-217. Guan T, Wu H J, Zhang L J, Xu D J, Zheng L B, Yao Y |
| Analysis of VSX1 Variations in Brazilian Subjects with Keratoconus. Journal of ophthalmic & vision research 2018 8 13 (3): 266-273. da Silva Dulceria Costa, Gadelha Bianca Nery Benevides, Feitosa Alex Felipe Barbosa, da Silva Rafaela Gomes, Albuquerque Tarsila Livia Paz E, Santos Débora Christina Pereira Fernandes, Gadelha Diego Nery Benevides, Fonseca Schamber-Reis Bruno Lu |
| Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. PloS one 2018 13 (6): e0199178. Lucas Sionne E M, Zhou Tiger, Blackburn Nicholas B, Mills Richard A, Ellis Jonathan, Leo Paul, Souzeau Emmanuelle, Ridge Bronwyn, Charlesworth Jac C, Lindsay Richard, Craig Jamie E, Burdon Kathryn |
| Analysis of the VSX1 gene in sporadic keratoconus patients from China. BMC ophthalmology 2017 Sep 17 (1): 173. Guan Tao, Wang Xue, Zheng Li-Bin, Wu Hai-Jian, Yao Yu-Fe |
| Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus. Ophthalmic genetics 2015 Sep 36 (3): 213-7. Moschos Marilita M, Kokolakis Nikolaos, Gazouli Maria, Chatziralli Irini P, Droutsas Dimitrios, Anagnou Nicholas P, Ladas Ioannis |
| Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification. Ophthalmic genetics 2015 Aug 1-7. Karolak Justyna A, Polakowski Piotr, Szaflik Jerzy, Szaflik Jacek P, Gajecka Marze |
| 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 |
| Common single nucleotide polymorphisms and keratoconus in the Han Chinese population. Ophthalmic genetics 2013 Jan . Wang Y, Jin T, Zhang X, Wei W, Cui Y, Geng T, Liu Q, Gao J, Liu M, Chen C, Zhang C, Zhu X |
| Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus. BMC research notes 2013 6 103. Verma Anshuman, Das Manoranjan, Srinivasan Muthiah, Prajna Namperumalsamy V, Sundaresan Periasa |
| Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant. Molecular vision 2013 19 852-60. Vincent Andrea L, Jordan Charlotte, Sheck Leo, Niederer Rachel, Patel Dipika V, McGhee Charles N |
| Study of VSX1 mutations in patients with keratoconus in southwest Iran using PCR-single-strand conformation polymorphism/heteroduplex analysis and sequencing method. Acta cytologica 2013 57 (6): 646-51. Dehkordi Fatemeh Azadegan, Rashki Ahmad, Bagheri Nader, Chaleshtori Minoo Hashemzadeh, Memarzadeh Ezzatollah, Salehi Ali, Ghatreh Homan, Zandi Farid, Yazdanpanahi Nasrin, Tabatabaiefar Mohammad Amin, Chaleshtori Morteza Hashemzad |
| VSX1 gene and keratoconus: genetic analysis in Korean patients. Cornea 2012 Jul 31 (7): 746-50. Jeoung Jin Wook, Kim Mee Kum, Park Sung Sup, Kim Sung Yeun, Ko Hyun Soo, Wee Won Ryang, Lee Jin H |
| Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus. Cornea 2010 Feb 29 (2): 172-6. Stabuc-Silih Mirna, Strazisar Mojca, Hawlina Marko, Glavac Damj |
| Genetics and clinical characteristics of keratoconus. Acta dermatovenerologica Alpina, Pannonica, et Adriatica 2010 19 (2): 3-10. Stabuc-Silih Mirna, Strazisar Mojca, Ravnik-Glavac Metka, Hawlina Marko, Glavac Damj |
| VSX1 gene analysis in keratoconus. Molecular vision 2010 16 2395-401. Tanwar Mukesh, Kumar Manoj, Nayak Bhagabat, Pathak Dhananjay, Sharma Namrata, Titiyal Jeewan S, Dada Ri |
| A novel VSX1 mutation identified in an individual with keratoconus in India. Molecular vision 2009 15 2475-9. Paliwal Preeti, Singh Anuradha, Tandon Radhika, Titiyal Jeevan S, Sharma Arundha |
| Three VSX1 gene mutations, L159M, R166W, and H244R, are not associated with keratoconus. Cornea 2008 Feb 27 (2): 189-92. Tang Yongming G, Picornell Yoana, Su Xiaowen, Li Xiaohui, Yang Huiying, Rabinowitz Yaron |
| VSX1 gene variants are associated with keratoconus in unrelated Korean patients. Journal of human genetics 2008 53 (9): 842-9. Mok Jee-Won, Baek Sun-Jin, Joo Choun- |
| VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Investigative ophthalmology & visual science 2005 Jan 46 (1): 39-45. Bisceglia Luigi, Ciaschetti Marilena, De Bonis Patrizia, Campo Pablo Alberto Perafan, Pizzicoli Costantina, Scala Costanza, Grifa Michele, Ciavarella Pio, Delle Noci Nicola, Vaira Filippo, Macaluso Claudio, Zelante Leopol |
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- Page last updated:Mar 28, 2023
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