Cargando…
Novel Common Variants Associated with Obesity and Type 2 Diabetes Detected Using a cFDR Method
Genome-wide association studies (GWASs) have been performed extensively in diverse populations to identify single nucleotide polymorphisms (SNPs) associated with complex diseases or traits. However, to date, the SNPs identified fail to explain a large proportion of the variance of the traits/disease...
Autores principales: | Zhang, Qiang, Wu, Ke-Hao, He, Jing-Yang, Zeng, Yong, Greenbaum, Jonathan, Xia, Xin, Liu, Hui-Min, Lv, Wan-Qiang, Lin, Xu, Zhang, Wei-Dong, Xi, Yuan-Lin, Shi, Xue-Zhong, Sun, Chang-Qing, Deng, Hong-Wen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703959/ https://www.ncbi.nlm.nih.gov/pubmed/29180724 http://dx.doi.org/10.1038/s41598-017-16722-6 |
Ejemplares similares
-
Identification of novel genetic loci for osteoporosis and/or rheumatoid arthritis using cFDR approach
por: Zhou, Rou, et al.
Publicado: (2017) -
Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method
por: Mao, Xiang-Jie, et al.
Publicado: (2019) -
CORRIGENDUM FOR “Identification of Novel Potentially Pleiotropic Variants Associated With Osteoporosis and Obesity Using the cFDR Method”
Publicado: (2018) -
Identification of novel SNPs associated with coronary artery disease and birth weight using a pleiotropic cFDR method
por: Wu, Xinrui, et al.
Publicado: (2020) -
Leveraging auxiliary data from arbitrary distributions to boost GWAS discovery with Flexible cFDR
por: Hutchinson, Anna, et al.
Publicado: (2021)