Melissa L. Will

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

David J. Tester, Melissa L. Will, Carla M. Haglund et al. · Heart Rhythm · 2005 · 563 citations

Channelopathies, Genetic Disorder, Genetics +7

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Sara L. Van Driest, Vlad C. Vasile, Steve R. Ommen et al. · Journal of the American College of Cardiology · 2004 · 426 citations

Cardiac Muscle, Cardiomyopathy, Heart Failure +11

Most LQT2 Mutations Reduce Kv11.1 (hERG) Current by a Class 2 (Trafficking-Deficient) Mechanism

Corey L. Anderson, Brian P. Delisle, Blake D. Anson et al. · Circulation · 2006 · 409 citations

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

Francesca Girolami, Carolyn Y. Ho, Christopher Semsarian et al. · Journal of the American College of Cardiology · 2010 · 294 citations · Full text

Cardiac Muscle, Cardiomyopathy, Genetics +7

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, David J. Tester, Gregg S. Jones et al. · Mayo Clinic Proceedings · 2003 · 292 citations

Cardiomyopathy, Genetic Testing, Cardiovascular Disease +12