Robert J. Roberts

Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy

Hideshi Niimura, Linda L. Bachinski, Somkiat Sangwatanaroj et al. · New England Journal of Medicine · 1998 · 759 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Identification of a Gene Responsible for Familial Wolff–Parkinson–White Syndrome

Michael H. Gollob, Anthony Tang, Tanya N. Gollob et al. · New England Journal of Medicine · 2001 · 674 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

Majid Nikpay, Anuj Goel, Hong‐Hee Won et al. · EUR Research Repository (Erasmus University Rotterdam) · 2015 · 588 citations

Life Sciences, Bioinformatics, Genetics +16

American College of Endocrinology Position Statement on Inpatient Diabetes and Metabolic Control

Alan J. Garber, Etie S. Moghissi, Edwin D. Bransome et al. · Endocrine Practice · 2004 · 410 citations

Medicine, Endocrinology, Internal Medicine +16

Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy

Michael H. Gollob, John J. Seger, Tanya N. Gollob et al. · Circulation · 2001 · 280 citations

Life Sciences, Genetics, Molecular Genetics +17