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 · 564 citations

Medicine, Cardiology, Genetics +15

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 · 427 citations

Medicine, Cardiology, Genetics +14

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 · 417 citations

Life Sciences, Cardiology, Genetics +17

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 · 295 citations · Full text

Medicine, Cardiology, Genetics +15

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 Jones et al. · Mayo Clinic Proceedings · 2003 · 294 citations

Medicine, Cardiology, Genetics +17