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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Disease and SHANK3[original query]
Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936.
Genes, brain, and behavior 2009 Mar 8 (2): 238-47.
Houlihan L M, Harris S E, Luciano M, Gow A J, Starr J M, Visscher P M, Deary I
Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.
BMC medical genetics 2009 10 61.
Qin Jian, Jia Meixiang, Wang Lifang, Lu Tianlan, Ruan Yan, Liu Jing, Guo Yanqing, Zhang Jishui, Yang Xiaoling, Yue Weihua, Zhang D
High-throughput sequencing of mGluR signaling pathway genes reveals enrichment of rare variants in autism.
PloS one 2012 7 (4): e35003.
Kelleher Raymond J, Geigenmüller Ute, Hovhannisyan Hayk, Trautman Edwin, Pinard Robert, Rathmell Barbara, Carpenter Randall, Margulies Dav
Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
PloS one 2013 8 (2): e56639.
Liu Yanyan, Du Yasong, Liu Wenwen, Yang Caohua, Liu Yan, Wang Hongyan, Gong Xiaoho
Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder.
Frontiers in genetics 2018 9 594.
Du Xiujuan, Gao Xueren, Liu Xin, Shen Lixiao, Wang Kai, Fan Yanjie, Sun Yu, Luo Xiaomei, Liu Huili, Wang Lili, Wang Yu, Gong Zhuwen, Wang Jianguo, Yu Yongguo, Li F
Association of SHANK3 Gene Polymorphism and Parkinson Disease in the North of Iran.
Basic and clinical neuroscience 2021 5 12 (1): 57-62.
Mizban Nahid, Vousooghi Nasim, Mizban Nasr
Genetic Overlap Between Attention Deficit/Hyperactivity Disorder and Autism Spectrum Disorder in SHANK2 Gene.
Frontiers in neuroscience 2021 5 15 649588.
Ma Suk-Ling, Chen Lu Hua, Lee Chi-Chiu, Lai Kelly Y C, Hung Se-Fong, Tang Chun-Pan, Ho Ting-Pong, Shea Caroline, Mo Flora, Mak Timothy S H, Sham Pak-Chung, Leung Patrick W
Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy.
Epileptic disorders : international epilepsy journal with videotape 2021 Jul .
Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji
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