Libin Wang

发表

Truncations of titin causing dilated cardiomyopathy.

L. Mestroni, J. Seidman, D. Pennell, 2012, The New England journal of medicine.

Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin‐2 Mutation

J. Seidman, C. Seidman, C. Berul, 2011, Journal of cardiovascular electrophysiology.

Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.

Kristin A. Maloney, R. Virmani, A. Finn, 2021, JAMA cardiology.

Genetics of Unexplained Sudden Cardiac Death in Adult Caucasian and African American Individuals Living in the State of Maryland

R. Virmani, A. Finn, F. Kolodgie, 2019 .

Functional Characterization of a Novel Mutation in NKX2-5 Associated With Congenital Heart Disease and Adult-Onset Cardiomyopathy

Milena B. Furtado, Mauro W. Costa, N. Rosenthal, 2013, Circulation. Cardiovascular genetics.

Eya4 regulation of Na+/K+-ATPase is required for sensory system development in zebrafish

L. Zon, J. Seidman, C. Seidman, 2008, Development.

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

L. Zon, J. Seidman, A. Mungall, 2005, Nature Genetics.

Pheochromocytoma-Induced Cardiomyopathy is Modulated by the Synergistic Effects of Cell-Secreted Factors

J. Seidman, E. Edelman, A. Baker, 2009, Circulation. Heart failure.

LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

J. Seidman, W. Roberts, B. Maron, 2021, Journal of the American Heart Association.

FUNCTIONAL CHARACTERIZATION OF A NOVEL MUTATION IN NKX 2-5 ASSOCIATED WITH CONGENITAL HEART DISEASE AND ADULT-ONSET CARDIOMYOPATHY . Costa : NKX 2-5 mutation in familial DCM

Milena B. Furtado, Mauro W. Costa, J. Seidman, 2015 .

Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort

Yi-Ju Chen, J. Perry, Y. Chun, 2022, Frontiers in Genetics.

Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.

Roger R Markwald, Christine E Seidman, J. Schmitt, 2010, The Journal of clinical investigation.

Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.

Ferhaan Ahmad, J. Seidman, G. Fishman, 2008, Journal of molecular and cellular cardiology.

Narrative Review: Harnessing Molecular Genetics for the Diagnosis and Management of Hypertrophic Cardiomyopathy

J. Seidman, C. Seidman, Libin Wang, 2010, Annals of Internal Medicine.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

Deborah A Nickerson, Stephan Züchner, Eden Martin, 2011, American journal of human genetics.

Heterogeneous myocyte enhancer factor-2 (Mef2) activation in myocytes predicts focal scarring in hypertrophic cardiomyopathy

J. Seidman, E. Olson, C. Seidman, 2010, Proceedings of the National Academy of Sciences.

Truncations of titin causing dilated cardiomyopathy.

L. Mestroni, J. Seidman, D. Pennell, 2012, The New England journal of medicine.

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.

M. Rieder, D. Nickerson, S. Züchner, 2011, American journal of human genetics.

Heterogeneous myocyte enhancer factor-2 (Mef2) activation in myocytes predicts focal scarring in hypertrophic cardiomyopathy

J. Seidman, E. Olson, C. Seidman, 2010, Proceedings of the National Academy of Sciences.

Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin‐2 Mutation

J. Seidman, C. Seidman, C. Berul, 2011, Journal of cardiovascular electrophysiology.

Harnessing Molecular Genetics for the Diagnosis and Management of Hypertrophic Cardiomyopathy

J. Seidman, C. Seidman, Libin Wang, 2010 .