Frederick S. Kaplan

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

Eileen M. Shore, Meiqi Xu, George Feldman et al. · Nature Genetics · 2006 · 1.2K citations

Recurrent Mutation, Fibrosis, Signal Transduction +11

Bone Formation and Inflammation in Cardiac Valves

Emile R. Mohler, Francis H. Gannon, Carol Reynolds et al. · Circulation · 2001 · 1K citations

Risk Factors for Falls as a Cause of Hip Fracture in Women

Jeane Ann Grisso, Jennifer L. Kelsey, Brian L. Strom et al. · New England Journal of Medicine · 1991 · 865 citations · Full text

Conversion of vascular endothelial cells into multipotent stem-like cells

Damian Medici, Eileen M. Shore, Vitali Lounev et al. · Nature Medicine · 2010 · 657 citations

Regenerative Medicine, Angiogenesis, Medicine +6

Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

Frederick S. Kaplan, Meiqi Xu, Petra Seemann et al. · Human Mutation · 2008 · 436 citations