Michael Oldridge
Oxford University Hospitals NHS Trust(GB)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Cleft Lip and Palate Research, Connective tissue disorders research, Wnt/β-catenin signaling in development and cancer, Developmental Biology and Gene Regulation
Most-Cited Works
- → Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome(1995)929 cited
- → Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes(1995)456 cited
- → Exclusive paternal origin of new mutations in Apert syndrome(1996)318 cited
- → Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2(2000)303 cited
- → De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome(1999)250 cited
- Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome.(1996)
- → Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B(2000)232 cited
- → A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1(1998)230 cited
- → Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome(2000)204 cited
- → Distinct Mutations in the Receptor Tyrosine Kinase Gene ROR2 Cause Brachydactyly Type B(2000)190 cited