William Reardon

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

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford, Andrew J. Sharp, Carl Baker et al. · New England Journal of Medicine · 2008 · 803 citations · Full text

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

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Helen G. Harley, J. David Brook, S.A. Rundle et al. · Nature · 1992 · 727 citations

Phenotypic Variation, Mendelian Disorder, Genetic Disorder +7

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