Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: TRIOBP[original query] |
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Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations. Clinical genetics 2015 Jun 87 (6): 588-93. Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li |
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.
Genetic epidemiology 2015 Mar 39 (3): 207-16. Springelkamp Henriët, Mishra Aniket, Hysi Pirro G, Gharahkhani Puya, Höhn René, Khor Chiea-Chuen, Cooke Bailey Jessica N, Luo Xiaoyan, Ramdas Wishal D, Vithana Eranga, Koh Victor, Yazar Seyhan, Xu Liang, Forward Hannah, Kearns Lisa S, Amin Najaf, Iglesias Adriana I, Sim Kar-Seng, van Leeuwen Elisabeth M, Demirkan Ayse, van der Lee Sven, Loon Seng-Chee, Rivadeneira Fernando, Nag Abhishek, Sanfilippo Paul G, Schillert Arne, de Jong Paulus T V M, Oostra Ben A, Uitterlinden André G, Hofman Albert, , Zhou Tiger, Burdon Kathryn P, Spector Timothy D, Lackner Karl J, Saw Seang-Mei, Vingerling Johannes R, Teo Yik-Ying, Pasquale Louis R, Wolfs Roger C W, Lemij Hans G, Tai E-Shyong, Jonas Jost B, Cheng Ching-Yu, Aung Tin, Jansonius Nomdo M, Klaver Caroline C W, Craig Jamie E, Young Terri L, Haines Jonathan L, MacGregor Stuart, Mackey David A, Pfeiffer Norbert, Wong Tien-Yin, Wiggs Janey L, Hewitt Alex W, van Duijn Cornelia M, Hammond Christopher |
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.
PLoS genetics 2016 Oct 12 (10): e1006371. Hoffmann Thomas J, Keats Bronya J, Yoshikawa Noriko, Schaefer Catherine, Risch Neil, Lustig Lawrence |
Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment. Hearing research 2017 1 347 56-62. Wesdorp Mieke, van de Kamp Jiddeke M, Hensen Erik F, Schraders Margit, Oostrik Jaap, Yntema Helger G, Feenstra Ilse, Admiraal Ronald J C, Kunst Henricus P M, Tekin Mustafa, Kanaan Moien, Kremer Hannie, Pennings Ronald J |
Novel Variants Identified in Multiple Sclerosis Patients From Southern China. Frontiers in neurology 2018 8 9 582. Wang Hongxuan, Pardeshi Lakhansing Arun, Rong Xiaoming, Li Enqin, Wong Koon Ho, Peng Ying, Xu Ren- |
Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis. BioMed research international 2018 3 2018 3103986. Shang Haiqiong, Yan Denise, Tayebi Naeimeh, Saeidi Kolsoum, Sahebalzamani Afsaneh, Feng Yong, Blanton Susan, Liu Xuezho |
Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients. Clinical genetics 2019 9 97 (2): 352-356. Zou Songfeng, Mei Xueshuang, Yang Weiqiang, Zhu Rvfei, Yang Tao, Hu Hong |
Panel-Based Nuclear and Mitochondrial Next-Generation Sequencing Outcomes of an Ethnically Diverse Pediatric Patient Cohort with Mitochondrial Disease. The Journal of molecular diagnostics : JMD 2019 3 21 (3): 503-513. Schoonen Maryke, Smuts Izelle, Louw Roan, Elson Joanna L, van Dyk Etresia, Jonck Lindi-Maryn, Rodenburg Richard J T, van der Westhuizen Francois |
Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family. Frontiers in genetics 2021 12 12 766973. Zhou Cong, Xiao Yuanyuan, Xie Hanbing, Wang Jing, Liu Shanli |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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