Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: DFNA5[original query] |
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A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing loss. Annals of human genetics 2014 Mar 78 (2): 83-91. Nishio Ayako, Noguchi Yoshihiro, Sato Tatsuya, Naruse Taeko K, Kimura Akinori, Takagi Akira, Kitamura K |
Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study. Environmental health : a global access science source 2015 14 (1): 77. Zhang Xuhui, Liu Yi, Zhang Lei, Yang Zhangping, Yang Luoxian, Wang Xuchu, Jiang CaiXia, Wang Qiang, Xia Yuyong, Chen Yanjuan, Wu Ou, Zhu Yim |
APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease. Molecular psychiatry 2015 Dec . Vélez J I, Lopera F, Sepulveda-Falla D, Patel H R, Johar A S, Chuah A, Tobón C, Rivera D, Villegas A, Cai Y, Peng K, Arkell R, Castellanos F X, Andrews S J, Silva Lara M F, Creagh P K, Easteal S, de Leon J, Wong M L, Licinio J, Mastronardi C A, Arcos-Burgos |
Association of DFNA5, SYK, and NELL1 variants along with HPV infection in oral cancer among the prolonged tobacco-chewers. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2018 Aug 40 (8): 1010428318793023. Kundu Sharbadeb, Ramshankar Vijayalakshmi, Verma Akalesh Kumar, Thangaraj Soundara Viveka, Krishnamurthy Arvind, Kumar Rajeev, Kannan Ravi, Ghosh Sankar Kum |
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 |
Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing. Gene 2022 2 819 146258. Liu Ya, Tan Meihua, Cai Luhang, Lv Lihui, Chen Qingqing, Chen Wei, Yang Hang, Xu Yapi |
Identification of the First Single GSDME Exon 8 Structural Variants Associated with Autosomal Dominant Hearing Loss. Diagnostics (Basel, Switzerland) 2022 1 12 (1): . Mansard Luke, Vaché Christel, Bianchi Julie, Baudoin Corinne, Perthus Isabelle, Isidor Bertrand, Blanchet Catherine, Baux David, Koenig Michel, Kalatzis Vasiliki, Roux Anne-Françoi |
Tissue-specific gene expression of genome-wide significant loci associated with major depressive disorder subtypes. Progress in neuro-psychopharmacology & biological psychiatry 2024 4 133 111019. Kaai Torii, Kazutaka Ohi, Daisuke Fujikane, Kentaro Takai, Ayumi Kuramitsu, Yukimasa Muto, Shunsuke Sugiyama, Toshiki Shioi |
Replication of previous autism-GWAS hits suggests the association between NAA1, SORCS3, and GSDME and autism in the Han Chinese population. Heliyon 2024 1 10 (1): e23677. Fen Lin, Jun Li, Ziqi Wang, Tian Zhang, Tianlan Lu, Miaomiao Jiang, Kang Yang, Meixiang Jia, Dai Zhang, Lifang Wa |
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- Page last updated:May 20, 2024
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