Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: PEX2[original query] |
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A deleterious mutation in the PEX2 gene causes Zellweger syndrome in individuals of Ashkenazi Jewish descent. Clinical genetics 2014 Apr 85 (4): 343-6. Fedick A, Jalas C, Treff N |
Associations between menarche-related genetic variants and pubertal growth in male and female adolescents. The Journal of adolescent health : official publication of the Society for Adolescent Medicine 2015 Jan 56 (1): 66-72. Tu Wanzhu, Wagner Erin K, Eckert George J, Yu Zhangsheng, Hannon Tamara, Pratt J Howard, He Chuny |
Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity. Human molecular genetics 2015 Sep . Hägg Sara, Ganna Andrea, van der Laan Sander W, Esko Tonu, Pers Tune H, Locke Adam E, Berndt Sonja I, Justice Anne E, Kahali Bratati, Siemelink Marten A, Pasterkamp Gerard, , Strachan David P, Speliotes Elizabeth K, North Kari E, Loos Ruth J F, Hirschhorn Joel N, Pawitan Yudi, Ingelsson Er |
Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Apr . Yin Xianyong, Bizon Chris, Tilson Jeffrey, Lin Yuan, Gizer Ian R, Ehlers Cindy L, Wilhelmsen Kirk |
Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study.
Arthritis & rheumatology (Hoboken, N.J.) 2021 Nov . Wang Yong-Fei, Wei Wei, Tangtanatakul Pattarin, Zheng Lichuan, Lei Yao, Lin Zhiming, Qian Chengmin, Qin Xiao, Hou Fei, Zhang Xinyu, Shao Li, Satproedprai Nusara, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Song Qin, Lau Yu Lung, Zhang Yan, Hirankarn Nattiya, Yang Wanli |
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- Page last updated:Mar 25, 2024
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