Human Genome Epidemiology Literature Finder
|
Records 1 - 14 (of 14 Records) |
| Query Trace: Deafness and WFS1[original query] |
|---|
| Testing of diabetes-associated WFS1 polymorphisms in the Diabetes Prevention Program. Diabetologia 2008 Mar 51 (3): 451-7. Florez J C, Jablonski K A, McAteer J, Sandhu M S, Wareham N J, Barroso I, Franks P W, Altshuler D, Knowler W C, |
| A WFS1 haplotype consisting of the minor alleles of rs752854, rs10010131, and rs734312 shows a protective role against type 2 diabetes in Russian patients. The review of diabetic studies : RDS 2011 6 7 (4): 285-92. Chistiakov Dimitry A, Khodyrev Dmitry S, Smetanina Svetlana A, Bel'chikova Larisa N, Suplotova Lyudmila A, Nosikov Valery |
| Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of translational medicine 2014 12 (1): 311. Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi |
Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
Clinical cancer research : an official journal of the American Association for Cancer Research 2016 Dec . Wheeler Heather E, Gamazon Eric R, Frisina Robert D, Perez-Cervantes Carlos, El Charif Omar, Mapes Brandon, Fossa Sophie D, Feldman Darren R, Hamilton Robert J, Vaughn David J, Beard Clair J, Fung Chunkit, Kollmannsberger Christian, Kim Jeri, Mushiroda Taisei, Kubo Michiaki, Ardeshir-Rouhani-Fard Shirin, Einhorn Lawrence H, Cox Nancy J, Dolan M Eileen, Travis Lois |
| Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan. PloS one 2019 1 14 (1): e0211261. Liu Wei-Hsiu, Chang Pi-Yueh, Chang Shih-Cheng, Lu Jang-Jih, Wu Che-Mi |
| Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss. Molecular genetics & genomic medicine 2020 6 8 (8): e1367. Guan Jing, Wang Hongyang, Lan Lan, Wu Yusen, Chen Guohui, Zhao Cui, Wang Dayong, Wang Qiu |
| A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations. Human genetics 2020 5 139 (10): 1315-1323. Walls W Daniel, Moteki Hideaki, Thomas Taylor R, Nishio Shin-Ya, Yoshimura Hidekane, Iwasa Yoichiro, Frees Kathy L, Nishimura Carla J, Azaiez Hela, Booth Kevin T, Marini Robert J, Kolbe Diana L, Weaver A Monique, Schaefer Amanda M, Wang Kai, Braun Terry A, Usami Shin-Ichi, Barr-Gillespie Peter G, Richardson Guy P, Smith Richard J, Casavant Thomas |
| Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome. BMC endocrine disorders 2021 8 21 (1): 166. Ren Ziyu, Yi Jixiu, Zhong Min, Wang Yunting, Liu Qicong, Wang Xuan, Liu Dongfang, Ren W |
| Single gene variants causing deafness in Asian Indians. Journal of genetics 2021 7 100 . Panigrahi Inusha, Kumari Divya, Anil Kumar B |
| Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China. Frontiers in genetics 2021 12 637096. Cai Luhang, Liu Ya, Xu Yaping, Yang Hang, Lv Lihui, Li Yang, Chen Qiongqiong, Lin Xiaojiang, Yang Yihui, Hu Guangwei, Zheng Guofeng, Zhou Jing, Qian Qiyong, Xu Mei-Ai, Fang Jin, Ding Jianjun, Chen Wei, Gao Jio |
| Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype. BioMed research international 2021 7 2021 6624744. Li Jinying, Xu Hongen, Sun Jianfeng, Tian Yongan, Liu Danhua, Qin Yaping, Liu Huanfei, Li Ruijun, Neng Lingling, Deng Xiaohua, Xue Binbin, Yu Changyun, Tang Wenx |
| Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG 2021 Nov . Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel |
| The miR-668 binding site variant rs1046322 on WFS1 is associated with obesity in Southeast Asians. Frontiers in endocrinology 2023 10 14 1185956. Maha M Hammad, Mohamed Abu-Farha, Prashantha Hebbar, Emil Anoop, Betty Chandy, Motasem Melhem, Arshad Channanath, Fahd Al-Mulla, Thangavel Alphonse Thanaraj, Jehad Abubak |
| Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel. Human genomics 2023 1 17 (1): 1. Ma Jing, Ma Xiuli, Lin Ken, Huang Rui, Bi Xianyun, Ming Cheng, Li Li, Li Xia, Li Guo, Zhao Liping, Yang Tao, Gao Yingqin, Zhang Tieso |
- Page last reviewed:Feb 1, 2024
- Content source: