Robin M. Winter

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge et al. · Nature Genetics · 1995 · 925 citations

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +9

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

William Reardon, Robin M. Winter, Paul Rutland et al. · Nature Genetics · 1994 · 766 citations

Fibrosis, Mendelian Disorder, Human Growth +6

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

Maximilian Muenke, Ute Schell, Andreas Hehr et al. · Nature Genetics · 1994 · 622 citations

Fibrosis, Mendelian Disorder, Common Mutation +8

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

Xianhua Piao, R. Sean Hill, Adria Bodell et al. · Science · 2004 · 519 citations

Developmental Cognitive Neuroscience, Cellular Neurobiology, Social Sciences +16

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

Jonathan Flint, Andrew O.M. Wilkie, Veronica J. Buckle et al. · Nature Genetics · 1995 · 508 citations · Full text

Chromatin, Mendelian Disorder, Psychiatry +10