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Scientific Reports|February 10, 2017
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery DiseaseDan Yin, Duraid Hamied Naji, Yunlong Xia, et al.Scientific Reports|February 21, 2018
Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial FibrillationPengxia Wang, Weixi Qin, Pengyun Wang, et al.Annals of Human Genetics|March 2, 2019
Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4-subunit SCN4B with atrial fibrillationHongbo Xiong, Qin Yang, Xiaoping Zhang, et al.Human Molecular Genetics|June 2, 2019
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypesLina Liang, Xia Li, Sébastien Moutton, et al.Circulation. Cardiovascular Genetics|September 25, 2014
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery diseaseChengqi Xu, Qin Yang, Hongbo Xiong, et al.Plos Genetics|August 13, 2015
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial FibrillationYufeng Huang, Chuchu Wang, Yufeng Yao, et al.Pageof 12