HuGE Literature Finder
Records
1
-
8
| Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis. Molecular medicine reports 2021 2 23 (4): . Zhou Yijing, Guo Dongwei, Cao Qianzhong, Zhang Xinyu, Jin Guangming, Zheng Danyi |
| Genotype-Phenotype Correlation in Children: The Impact of FBN1 Variants on Pediatric Marfan Care. Genes 2020 7 11 (7): . Stark Veronika C, Hensen Flemming, Kutsche Kerstin, Kortüm Fanny, Olfe Jakob, Wiegand Peter, von Kodolitsch Yskert, Kozlik-Feldmann Rainer, Müller Götz C, Mir Thomas |
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Nature communications 2018 May 9 (1): 1864. Iglesias Adriana I, Mishra Aniket, Vitart Veronique, Bykhovskaya Yelena, Höhn René, Springelkamp Henriët, Cuellar-Partida Gabriel, Gharahkhani Puya, Bailey Jessica N Cooke, Willoughby Colin E, Li Xiaohui, Yazar Seyhan, Nag Abhishek, Khawaja Anthony P, Polašek Ozren, Siscovick David, Mitchell Paul, Tham Yih Chung, Haines Jonathan L, Kearns Lisa S, Hayward Caroline, Shi Yuan, van Leeuwen Elisabeth M, Taylor Kent D, , Bonnemaijer Pieter, Rotter Jerome I, Martin Nicholas G, Zeller Tanja, Mills Richard A, Staffieri Sandra E, Jonas Jost B, Schmidtmann Irene, Boutin Thibaud, Kang Jae H, Lucas Sionne E M, Wong Tien Yin, Beutel Manfred E, Wilson James F, , , Uitterlinden André G, Vithana Eranga N, Foster Paul J, Hysi Pirro G, Hewitt Alex W, Khor Chiea Chuen, Pasquale Louis R, Montgomery Grant W, Klaver Caroline C W, Aung Tin, Pfeiffer Norbert, Mackey David A, Hammond Christopher J, Cheng Ching-Yu, Craig Jamie E, Rabinowitz Yaron S, Wiggs Janey L, Burdon Kathryn P, van Duijn Cornelia M, MacGregor Stua |
| Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia. Investigative ophthalmology & visual science 2018 1 59 (1): 338-348. Flitcroft D Ian, Loughman James, Wildsoet Christine F, Williams Cathy, Guggenheim Jeremy A, |
| Marfan syndrome: ocular findings and novel mutations-in pursuit of genotype-phenotype associations. Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2016 Apr 51 (2): 113-8. Latasiewicz Marta, Fontecilla Christian, Millá Elena, Sánchez Auro |
| Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.
Nature communications 2016 7 11008. Fan Qiao, Verhoeven Virginie J M, Wojciechowski Robert, Barathi Veluchamy A, Hysi Pirro G, Guggenheim Jeremy A, Höhn René, Vitart Veronique, Khawaja Anthony P, Yamashiro Kenji, Hosseini S Mohsen, Lehtimäki Terho, Lu Yi, Haller Toomas, Xie Jing, Delcourt Cécile, Pirastu Mario, Wedenoja Juho, Gharahkhani Puya, Venturini Cristina, Miyake Masahiro, Hewitt Alex W, Guo Xiaobo, Mazur Johanna, Huffman Jenifer E, Williams Katie M, Polasek Ozren, Campbell Harry, Rudan Igor, Vatavuk Zoran, Wilson James F, Joshi Peter K, McMahon George, St Pourcain Beate, Evans David M, Simpson Claire L, Schwantes-An Tae-Hwi, Igo Robert P, Mirshahi Alireza, Cougnard-Gregoire Audrey, Bellenguez Céline, Blettner Maria, Raitakari Olli, Kähönen Mika, Seppala Ilkka, Zeller Tanja, Meitinger Thomas, , Ried Janina S, Gieger Christian, Portas Laura, van Leeuwen Elisabeth M, Amin Najaf, Uitterlinden André G, Rivadeneira Fernando, Hofman Albert, Vingerling Johannes R, Wang Ya Xing, Wang Xu, Tai-Hui Boh Eileen, Ikram M Kamran, Sabanayagam Charumathi, Gupta Preeti, Tan Vincent, Zhou Lei, Ho Candice E H, Lim Wan'e, Beuerman Roger W, Siantar Rosalynn, Tai E-Shyong, Vithana Eranga, Mihailov Evelin, Khor Chiea-Chuen, Hayward Caroline, Luben Robert N, Foster Paul J, Klein Barbara E K, Klein Ronald, Wong Hoi-Suen, Mitchell Paul, Metspalu Andres, Aung Tin, Young Terri L, He Mingguang, Pärssinen Olavi, van Duijn Cornelia M, Jin Wang Jie, Williams Cathy, Jonas Jost B, Teo Yik-Ying, Mackey David A, Oexle Konrad, Yoshimura Nagahisa, Paterson Andrew D, Pfeiffer Norbert, Wong Tien-Yin, Baird Paul N, Stambolian Dwight, Wilson Joan E Bailey, Cheng Ching-Yu, Hammond Christopher J, Klaver Caroline C W, Saw Seang-Mei, Rahi Jugnoo S, Korobelnik Jean-François, Kemp John P, Timpson Nicholas J, Smith George Davey, Craig Jamie E, Burdon Kathryn P, Fogarty Rhys D, Iyengar Sudha K, Chew Emily, Janmahasatian Sarayut, Martin Nicholas G, MacGregor Stuart, Xu Liang, Schache Maria, Nangia Vinay, Panda-Jonas Songhomitra, Wright Alan F, Fondran Jeremy R, Lass Jonathan H, Feng Sheng, Zhao Jing Hua, Khaw Kay-Tee, Wareham Nick J, Rantanen Taina, Kaprio Jaakko, Pang Chi Pui, Chen Li Jia, Tam Pancy O, Jhanji Vishal, Young Alvin L, Döring Angela, Raffel Leslie J, Cotch Mary-Frances, Li Xiaohui, Yip Shea Ping, Yap Maurice K H, Biino Ginevra, Vaccargiu Simona, Fossarello Maurizio, Fleck Brian, Yazar Seyhan, Tideman Jan Willem L, Tedja Milly, Deangelis Margaret M, Morrison Margaux, Farrer Lindsay, Zhou Xiangtian, Chen Wei, Mizuki Nobuhisa, Meguro Akira, Mäkelä Kari Mat |
| Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes. Investigative ophthalmology & visual science 2015 Dec 56 (13): 8365-72. Sun Wenmin, Huang Li, Xu Yan, Xiao Xueshan, Li Shiqiang, Jia Xiaoyun, Gao Bei, Wang Panfeng, Guo Xiangming, Zhang Qingjio |
| A DNA pooling-based case-control study of myopia candidate genes COL11A1, COL18A1, FBN1, and PLOD1 in a Chinese population. Molecular vision 2011 17 810-21. Yip Shea Ping, Leung Kim Hung, Fung Wai Yan, Ng Po Wah, Sham Pak Chung, Yap Maurice K |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 31, 2023
- Content source: