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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 12, 2024. (Total: 232444Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Amyotrophic Lateral Sclerosis and CNTN4[original query]
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. GWAS Catalog
Neurobiology of aging 2014 Jul 35 (7): 1778.e9-1778.e23.
Xie Tong, Deng Libin, Mei Puming, Zhou Yiyi, Wang Bo, Zhang Jie, Lin Jiari, Wei Yi, Zhang Xiong, Xu Rens
Polymorphism of rs3737597 in DISC1 Gene on Chromosome 1q42.2 in sALS Patients: a Chinese Han Population Case-Control Study.
Molecular neurobiology 2016 Apr .
Deng Libin, Hou Liwei, Zhang Jie, Tang Xiaoli, Cheng Zhujun, Li Gang, Fang Xin, Xu Jinsong, Zhang Xiong, Xu Rens
The rs2619566, rs10260404, and rs79609816 Polymorphisms Are Associated With Sporadic Amyotrophic Lateral Sclerosis in Individuals of Han Ancestry From Mainland China.
Frontiers in genetics 2021 12 679204.
Zhang Jie, Qiu Weiwen, Hu Fan, Zhang Xiong, Deng Youqing, Nie Hongbing, Xu Rens
Effect of the Minor C Allele of CNTN4 rs2619566 on Medial Hypothalamic Connectivity in Early-Stage Patients of Chinese Han Ancestry with Sporadic Amyotrophic Lateral Sclerosis.
Neuropsychiatric disease and treatment 2022 3 18 437-448.
Wang Yao, He Yujie, Zhu Yanyan, He Ting, Xu Jie, Kuang Qinmei, Ji Yuqi, Xu Renshi, Li Fangjun, Zhou Fuqi
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