Andrew O.M. Wilkie
John Radcliffe Hospital(GB)University of Oxford(GB)MRC Weatherall Institute of Molecular Medicine(GB)MRC Human Immunology Unit(GB)Oxford BioMedica (United Kingdom)(GB)Oxford University Hospitals NHS Trust(GB)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Cleft Lip and Palate Research, Genomic variations and chromosomal abnormalities, Connective tissue disorders research, Genomics and Rare Diseases
Most-Cited Works
- → Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications(2014)1,174 cited
- → Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome(1995)929 cited
- → The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data(2013)837 cited
- → Craniosynostosis: genes and mechanisms(1997)526 cited
- → The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation(1995)508 cited
- → Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies(2005)475 cited