Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Sclerosis and CNTN4[original query] |
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Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
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 |
| GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans. BMC genomics 2016 Apr 17 276. Chittoor Geetha, Kent Jack W, Almeida Marcio, Puppala Sobha, Farook Vidya S, Cole Shelley A, Haack Karin, Göring Harald H H, MacCluer Jean W, Curran Joanne E, Carless Melanie A, Johnson Matthew P, Moses Eric K, Almasy Laura, Mahaney Michael C, Lehman Donna M, Duggirala Ravindranath, Comuzzie Anthony G, Blangero John, Voruganti Venkata Saro |
| 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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