Jessica D. Kushner

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

P. Rahko, R. Hershberger, P. Jakobs, 2008, American heart journal.

Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

R. Hershberger, P. Jakobs, D. Nauman, 2008, Clinical and translational science.

Return of Genetic Results in the Familial Dilated Cardiomyopathy Research Project

N. Norton, Duanxiang Li, A. Morales, 2013, Journal of Genetic Counseling.

Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy.

Michael Jerosch-Herold, Rami Alharethi, David C. Sheridan, 2008, American journal of physiology. Heart and circulatory physiology.

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

Marni J. Falk, E. Zackai, C. Cytrynbaum, 2021, American journal of medical genetics. Part A.

Clinical characteristics of 304 kindreds evaluated for familial dilated cardiomyopathy.

R. Hershberger, G. Pantely, D. Nauman, 2006, Journal of cardiac failure.

Clinical Investigations Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy

R. Hershberger, G. Pantely, D. Nauman, 2006 .

Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

J. Potter, R. Hershberger, Duanxiang Li, 2009, Circulation. Cardiovascular genetics.

Tay-Sachs disease carrier screening: a 21-year experience.

G. D’Souza, J. Kushner, J. Hedrick, 2000, Genetic testing.

At the Heart of the Pregnancy: What Prenatal and Cardiovascular Genetic Counselors Need to Know about Maternal Heart Disease

S. Fitzgerald-Butt, H. Tandri, A. Morales, 2017, Journal of Genetic Counseling.

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

Michael Litt, R. Hershberger, C. Allen, 2006, American journal of human genetics.