Shanshan Chen

发表

Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in mice

Qiang Sun, Xingxu Huang, Zhen Liu, 2020, Cell Death & Disease.

Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease

Y. Liu, X. Tu, Qiuyun Chen, 2017, Scientific Reports.

Significant genetic association of a functional TFPI variant with circulating fibrinogen levels and coronary artery disease

Qiuyun Chen, Chengqi Xu, Q. Wang, 2017, Molecular Genetics and Genomics.

De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia

Qing Kenneth Wang, J. Pu, X. Tu, 2017, Journal of the American Heart Association.

Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population

X. Tu, Chengqi Xu, Q. Wang, 2015, PloS one.

New Insights into the Functions of MicroRNAs in Cardiac Fibrosis: From Mechanisms to Therapeutic Strategies

D. Du, Zhishui Chen, Yuanyuan Zhao, 2022, Genes.

Common variant rs 7597774 in ADD 2 is associated with dilated cardiomyopathy in Chinese Han population

X. Tu, Chengqi Xu, Yunlong Xia, 2015 .

Elevated serum chloride is an independent risk factor for coronary heart disease: A retrospective study of more than 13,000 Han Chinese.

X. Tu, Min Liu, Luosha Zhao, 2015, International journal of cardiology.

Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population

X. Tu, Qiuyun Chen, Chengqi Xu, 2016, Molecular Genetics and Genomics.

Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4‐subunit SCN4B with atrial fibrillation

Y. Liu, T. Ke, X. Tu, 2019, Annals of human genetics.

Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population

X. Tu, Chengqi Xu, Q. Wang, 2015, Journal of the American Heart Association.

Signi fi cant Association Between CAV 1 Variant rs 3807989 on 7 p 31 and Atrial Fibrillation in a Chinese Han Population

X. Tu, Chengqi Xu, Q. Wang, 2015 .

BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3

Y. Zhang, Tangchun Wu, Fan Wang, 2014, Human Genetics.

Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.

Fan Wang, X. Tu, Qiuyun Chen, 2016, Atherosclerosis.

Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke.

X. Tu, Qiuyun Chen, Chengqi Xu, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Minor Allele C of Chromosome 1p32 Single Nucleotide Polymorphism rs11206510 Confers Risk of Ischemic Stroke in the Chinese Han Population

Cong Li, Fan Wang, X. Tu, 2010, Stroke.

Candidate Pathway-Based Genome-Wide Association Studies Identify Novel Associations of Genomic Variants in the Complement System Associated With Coronary Artery Disease

Tangchun Wu, J. Chen, Y. Liu, 2014, Circulation. Cardiovascular genetics.

Efficient base editing in G/C-rich regions to model androgen insensitivity syndrome

Hanhui Ma, Qiang Sun, Xingxu Huang, 2019, Cell Research.

Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation

R. Elston, Shaoqi Rao, Chunyan Luo, 2015, PLoS genetics.

Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease.

Y. Zhang, Fan Wang, X. Tu, 2013, Atherosclerosis.

Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population

X. Tu, Qiuyun Chen, Chengqi Xu, 2015, Molecular Genetics and Genomics.