Michael Oldridge

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

Exclusive paternal origin of new mutations in Apert syndrome

Dominique M. Moloney, Sarah R Slaney, Michael Oldridge et al. · Nature Genetics · 1996 · 316 citations

Mendelian Disorder, Genetic Disorder, Genetics +4

Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2

Ali R. Afzal, Anna Rajab, Christiane Fenske et al. · Nature Genetics · 2000 · 303 citations

Allelic Variant, Mendelian Disorder, Genetic Disorder +9

De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome

Michael Oldridge, Elaine H. Zackai, Donna M. McDonald‐McGinn et al. · The American Journal of Human Genetics · 1999 · 248 citations · Full text

Developmental Biology, Translational Biology, Bone Morphogenic Protein +11