George Feldman

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

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita Quaderi, Susann Schweiger, Karin Gaudenz et al. · Nature Genetics · 1997 · 367 citations

Developmental Anomaly, Opitz G/bbb Syndrome, Developmental Biology +7

Mutations in <i>FGFR1</i> and <i>FGFR2</i> cause familial and sporadic Pfeiffer syndrome

Ute Schell, Andreas Hehr, George Feldman et al. · Human Molecular Genetics · 1995 · 232 citations

Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

Nathaniel H. Robin, George Feldman, Adam Aronson et al. · Nature Genetics · 1995 · 122 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

The Genetics of Fibrodysplasia Ossificans Progressiva

Eileen M. Shore, George Feldman, Meiqi Xu et al. · Clinical Reviews in Bone and Mineral Metabolism · 2005 · 121 citations

Fibrosis, Bone Morphogenic Protein, Genetics +4