Richard Hayward

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

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

Paul Rutland, Louise J. Pulleyn, William Reardon et al. · Nature Genetics · 1995 · 456 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Management of childhood craniopharyngioma: can the morbidity of radical surgery be predicted?

C J de Vile, David Grant, B. E. Kendall et al. · Journal of neurosurgery · 1996 · 330 citations

Pediatric Brain Tumors, Pediatric Hydrocephalus, Radical Surgery +18

Intracranial Pressure in Single-Suture Craniosynostosis

Dominic Thompson, George P. Malcolm, Barry M. Jones et al. · Pediatric Neurosurgery · 1995 · 229 citations

Intracranial Hypertension, Single Cranial Suture, Intracranial Pressure +7

The Effectiveness of Papilledema as an Indicator of Raised Intracranial Pressure in Children with Craniosynostosis

Gerald F. Tuite, W.K. Chong, Jane Evanson et al. · Neurosurgery · 1996 · 228 citations

Pediatric Hydrocephalus, Ophthalmology, Median Icp +12