Melissa L Will

Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations.

Michael J Ackerman, Massimo Baldi, Iacopo Olivotto, 2010, Journal of the American College of Cardiology.

Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy.

Michael J Ackerman, Jeanne L Theis, B. Gersh, 2006, Biochemical and biophysical research communications.

Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.

Michael J Ackerman, D. Tester, M. Ackerman, 2005, Heart rhythm.

Long QT syndrome-associated mutations in intrauterine fetal death.

Michael J Ackerman, Brian Brost, Alice Ghidoni, 2013, JAMA.

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.

Michael J Ackerman, D. Tester, M. Ackerman, 2003, Mayo Clinic proceedings.