Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: PACS1[original query] |
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Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Nature genetics 2013 May 45 (5): 513-7. Wheeler Eleanor, Huang Ni, Bochukova Elena G, Keogh Julia M, Lindsay Sarah, Garg Sumedha, Henning Elana, Blackburn Hannah, Loos Ruth J F, Wareham Nick J, O'Rahilly Stephen, Hurles Matthew E, Barroso Inês, Farooqi I Sad |
Association Study of Three Gene Polymorphisms Recently Identified by a Genome-Wide Association Study with Obesity-Related Phenotypes in Chinese Children. Obesity facts 2017 Jun 10 (3): 179-190. Song Qi-Ying, Song Jie-Yun, Wang Yang, Wang Shuo, Yang Yi-De, Meng Xiang-Rui, Ma Jun, Wang Hai-Jun, Wang Y |
A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study. Journal of personalized medicine 2020 12 10 (4): . Hong Syuan-Yu, Yang Jiann-Jou, Li Shuan-Yow, Lee Inn-C |
Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants. Genome medicine 2022 5 14 (1): 53. Chen Rui, Yang Zhihui, Liu Jiewei, Cai Xin, Huo Yongxia, Zhang Zhijun, Li Ming, Chang Hong, Luo Xiong-Ji |
[Prenatal diagnosis of a case with Schuurs-Hoeijmakers syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2023 10 40 (11): 1373-1376. Lisha Su, Xiaofan Zhu, Qinghua Wu, Xiangdong Ko |
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