Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: GRM6[original query] |
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Genotyping microarray for CSNB-associated genes. Investigative ophthalmology & visual science 2009 Dec 50 (12): 5919-26. Zeitz Christina, Labs Stephan, Lorenz Birgit, Forster Ursula, Uksti Janne, Kroes Hester Y, De Baere Elfride, Leroy Bart P, Cremers Frans P M, Wittmer Mariana, van Genderen Maria M, Sahel José-Alain, Audo Isabelle, Poloschek Charlotte M, Mohand-Saïd Saddek, Fleischhauer Johannes C, Hüffmeier Ulrike, Moskova-Doumanova Veselina, Levin Alex V, Hamel Christian P, Leifert Dorothee, Munier Francis L, Schorderet Daniel F, Zrenner Eberhart, Friedburg Christoph, Wissinger Bernd, Kohl Susanne, Berger Wolfga |
Sequence variations of GRM6 in patients with high myopia. Molecular vision 2009 15 2094-100. Xu Xiaoyu, Li Shiqiang, Xiao Xueshan, Wang Panfeng, Guo Xiangming, Zhang Qingjio |
Response to methadone maintenance treatment is associated with the MYOCD and GRM6 genes. Molecular diagnosis & therapy 2010 Jun 14 (3): 171-8. Fonseca Francina, Gratacòs Mònica, Escaramís Geòrgia, De Cid Rafael, Martín-Santos Rocío, Fernández-Espejo Emilio, Estivill Xavier, Torrens Mar |
Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness. Ophthalmic genetics 2016 Jul 1-5. Dan Handong, Song Xiusheng, Li Jiazhang, Xing Yiqiao, Li T |
Association of ZNF644, GRM6, and CTNND2 genes with high myopia in the Han Chinese population: Jiangsu Eye Study. Eye (London, England) 2016 Apr . Wang H, Su S, Yang M, Hu N, Yao Y, Zhu R, Zhou J, Liang C, Guan |
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort. Scientific reports 2017 Mar 7 44155. Guo Hui, Peng Yu, Hu Zhengmao, Li Ying, Xun Guanglei, Ou Jianjun, Sun Liangdan, Xiong Zhimin, Liu Yanling, Wang Tianyun, Chen Jingjing, Xia Lu, Bai Ting, Shen Yidong, Tian Qi, Hu Yiqiao, Shen Lu, Zhao Rongjuan, Zhang Xuejun, Zhang Fengyu, Zhao Jingping, Zou Xiaobing, Xia K |
Impacts of GRIN3A, GRM6 and TPH2 genetic polymorphisms on quality of life in methadone maintenance therapy population. PloS one 2018 13 (7): e0201408. Wang Ruey-Yun, Chen Hsiu-Ju, Huang Chieh-Liang, Wang Jiun-Yi, Lee Tsui-Er, Lee Hsiang-Yen, Hung Chin-Chu |
Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine veterinary journal 2020 7 53 (2): 316-323. Hack Yael L, Crabtree Elizabeth E, Avila Felipe, Sutton Roger B, Grahn Robert, Oh Annie, Gilger Brian, Bellone Rebecca |
Congenital Stationary Night Blindness: Clinical and Genetic Features. International journal of molecular sciences 2022 12 23 (23): . Kim Angela H, Liu Pei-Kang, Chang Yin-Hsi, Kang Eugene Yu-Chuan, Wang Hung-Hsuan, Chen Nelson, Tseng Yun-Ju, Seo Go Hun, Lee Hane, Liu Laura, Chao An-Ning, Chen Kuan-Jen, Hwang Yih-Shiou, Wu Wei-Chi, Lai Chi-Chun, Tsang Stephen H, Hsiao Meng-Chang, Wang Nan-K |
Metabotropic glutamate receptor genetic variants and peripheral receptor expression affects trait scores of autistic probands. Scientific reports 2024 4 14 (1): 8558. Nilanjana Dutta, Mahasweta Chatterjee, Sharmistha Saha, Swagata Sinha, Kanchan Mukhopadhy |
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- Page last updated:Apr 22, 2024
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