John Rogers

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

Correlated gene expression supports synchronous activity in brain networks

Jonas Richiardi, André Altmann, Anna-Clare Milazzo et al. · Science · 2015 · 675 citations · Full text

Brain Organization, Social Sciences, Neurology +16

Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda

Ági K. Gedeon, Alison Colley, Robyn V. Jamieson et al. · Nature Genetics · 1999 · 187 citations

Somatic Variant, Genetic Disorder, Genetics +7

Vascular burden and Alzheimer disease pathologic progression

Raymond Y. Lo, William J. Jagust, Michael W. Weiner et al. · Neurology · 2012 · 153 citations · Full text

Fibrodysplasia ossificans progressiva. A survey of forty-two cases.

John Rogers, W. Blair Geho · Journal of Bone and Joint Surgery · 1979 · 137 citations

Bone Disease, Thumb Hypoplasia, Great Toe +13