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- Aggf1 Specifies Hemangioblasts at the Top of Regulatory Hierarchy via Npas4l and mTOR-S6K-Emp2-ERK Signaling..Arterioscler Thromb Vasc Biol.,2023,(12):2348-2368
- Mog1 deficiency promotes cardiac contractile dysfunction and isoproterenol-induced arrhythmias associated with cardiac fibrosis and Cx43 remodeling..Biochim Biophys Acta Mol Basis Dis.,2022,(9):166429
- Mechanistic insights into the interaction of cardiac sodium channel Nav1.5 with MOG1 and a new molecular mechanism for Brugada syndrome..Heart Rhythm.,2022,(3):478-489
- Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang-Wang syndrome..Acta Physiol.,2022,(1):e13800
- KCNMA1 promotes obesity-related hypertension: Integrated analysis based on genome-wide association studies..Genes Dis.,2022,(1):58-61
- Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation..Hum Mutat.,2019,(3):310-325
- Identification of a molecular signaling gene-gene regulatory network between GWAS susceptibility genes ADTRP and MIA3/TANGO1 for coronary artery disease..Biochim Biophys Acta Mol Basis Dis.,2017,(6):1640-1653
- Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm..BMC Med Genet.,2016,(1):45
- Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family..J Hum Genet.,2009,(11):660-4
- Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.Cell.,2008,(6):1017-27
