Jeffrey Allen Towbin - Genetic Mutations

Author Information

Jeffrey Allen Towbin is a renowned researcher affiliated with Le Bonheur Children's Hospital, St. Jude Children's Research Hospital, and the University of Tennessee Health Science Center in Memphis, Tennessee. His work spans several decades with significant contributions to the field of cardiomyopathy, particularly focusing on its genetic basis and management.

Research Contributions

Jeffrey Allen Towbin has made substantial contributions to the understanding and management of cardiomyopathies. His recent work includes state-of-the-art reviews on hypertrophic cardiomyopathy, exploring its management and diagnosis, and investigating the genetic architecture of pediatric cardiomyopathy. His research also delves into restrictive cardiomyopathy, its genetic underpinnings, and animal modeling. Towbin's studies extend to examining the impact of aging on cardiac function and the role of genetic factors in myocarditis and exercise-induced cardiac stress.

Aliases

Jeffrey Allen Towbin is known by various aliases, including Jeff Towbin, Jeffrey A. Towbin, J. Towbin, J A. Towbin, and Jeffreya Towbin. These variations are commonly found in academic and professional publications.

Publication and Citation Metrics

Metric	Value
Total Citation Count	138,573
H-index	150
Total Papers Published	878

Publications:

Management of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review.

DOI: 10.1016/j.jacc.2021.11.021

Year: 2022

The genetic architecture of pediatric cardiomyopathy

DOI: 10.1016/j.ajhg.2021.12.006

Year: 2022

Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling.

DOI: 10.31083/j.rcm2303108

Year: 2022

Progressive Reduction in Right Ventricular Contractile Function Due to Altered Actin Expression in an Aging Mouse Model of Arrhythmogenic Cardiomyopathy.

DOI: 10.1161/CIRCULATIONAHA.120.049261

Year: 2022

Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review.

DOI: 10.1016/j.jacc.2021.12.002

Year: 2022

Abstract P414: Systems Genetics Analysis Reveals Significant Eqtls Associated With Echocardiography Parameters In Genetic Reference Population Of Bxd Strains.

DOI: 10.1161/res.129.suppl_1.p414

Year: 2021

Myopathic Cardiac Genotypes Increase Risk for Myocarditis

DOI: 10.2139/SSRN.3831727

Year: 2021

Pediatric and adult dilated cardiomyopathy are distinguished by distinct biomarker profiles

DOI: 10.1038/s41390-021-01698-x

Year: 2021

Young athletes: Preventing sudden death by adopting a modern screening approach? A critical review and the opening of a debate

DOI: 10.1016/j.ijcha.2021.100790

Year: 2021

Deficiency in Nebulin Repeats of Sarcomeric Nebulette is Detrimental for Cardiomyocyte Tolerance to Exercise and Biomechanical Stress.

DOI: 10.1152/ajpheart.00732.2020

Year: 2021

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