Patricia Delai

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

Life Sciences, Genetics, Molecular Genetics +11

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 · 448 citations

Medicine, Genetics, Molecular Genetics +15

The Phenotype of Fibrodysplasia Ossificans Progressiva

Frederick S. Kaplan, David L. Glaser, Eileen M. Shore et al. · Clinical Reviews in Bone and Mineral Metabolism · 2005 · 117 citations

Medicine, Pathobiology, Pathology +5

Reduction of New Heterotopic Ossification ( <scp>HO</scp> ) in the <scp>Open‐Label</scp> , Phase 3 <scp>MOVE</scp> Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva ( <scp>FOP</scp> )

Robert J. Pignolo, Edward C. Hsiao, Mona Al Mukaddam et al. · Journal of Bone and Mineral Research · 2022 · 66 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +7

Neurological symptoms in individuals with fibrodysplasia ossificans progressiva

Joseph A. Kitterman, Jonathan B. Strober, Lixin Kan et al. · Journal of Neurology · 2012 · 54 citations

Medicine, Neurology, Neuroscience +6