Jiangchuan Ye

发表

Prolyl hydroxylase domain protein 2 regulates the intracellular cyclic AMP level in cardiomyocytes through its interaction with phosphodiesterase 4D.

Yi Liu, Dandan Liang, Z. Huo, 2012, Biochemical and biophysical research communications.

Tom70 serves as a molecular switch to determine pathological cardiac hypertrophy

Luying Peng, Jian Huang, Yi-Han Chen, 2014, Cell Research.

Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy

P. Ellinor, M. Kost-Alimova, K. Margulies, 2022, Nature.

Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation

K. Lunetta, A. Hofman, A. Uitterlinden, 2014, Circulation.

Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

Robert W. Mills, Manolis Kellis, P. Ellinor, 2016, eLife.

Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy

Robert W. Mills, P. Ellinor, S. Lubitz, 2017, Circulation. Cardiovascular genetics.

Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential

Robert W. Mills, K. Lunetta, L. Mirny, 2017, Circulation. Cardiovascular genetics.

A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a.

P. Ellinor, S. Lubitz, N. Tucker, 2016, American journal of human genetics.

Dynamin-2 mediates heart failure by modulating Ca2+ -dependent cardiomyocyte apoptosis.

Yunfu Sun, Luying Peng, Li Li, 2013, International journal of cardiology.

SNX13 reduction mediates heart failure through degradative sorting of apoptosis repressor with caspase recruitment domain

Luying Peng, Yingyu Cui, Yi-Han Chen, 2014, Nature Communications.

Physical activity and mental health in children and youth during COVID-19: a systematic review and meta-analysis

X. Tong, Xiao Zhou, J. J. Yu, 2023, Child and Adolescent Psychiatry and Mental Health.

Aberrant dynamin 2-dependent Na+/H+ exchanger-1 trafficking contributes to cardiomyocyte apoptosis

Xia Li, Luying Peng, Jing Wang, 2013, Journal of cellular and molecular medicine.

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Robert W. Mills, A J Agopian, Jonathan H. Chung, 2017, Circulation. Cardiovascular genetics.

Loss of the Atrial Fibrillation-Related Gene, Zfhx3, Results in Atrial Dilation and Arrhythmias

Robert W. Mills, P. Ellinor, D. Milan, 2023, Circulation research.

Gain-of-function mutations in GATA6 lead to atrial fibrillation.

E. Benjamin, P. Ellinor, D. Milan, 2017, Heart rhythm.

Author ’ s Accepted Manuscript Gain of function mutations in GATA 6 lead to atrial fibrillation

E. Benjamin, P. Ellinor, D. Milan, 2016 .

Prolyl hydroxylase domain protein 2 regulates the intracellular cyclic AMP level in cardiomyocytes through its interaction with phosphodiesterase 4D.

Yi Liu, Dandan Liang, Z. Huo, 2012, Biochemical and biophysical research communications.

Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation

D. Chasman, V. Gudnason, P. Ellinor, 2014, Circulation.