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Andrew O.M. Wilkie | Researchclopedia

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Andrew O.M. Wilkie

John Radcliffe Hospital ORCID

465

Works

29,205

Citations

89

h-index

252

i10-index

Research Topics

Craniofacial Disorders and Treatments Cleft Lip and Palate Research Genomic variations and chromosomal abnormalities

Affiliations

Tulane University2000–2000

Tokyo Medical and Dental University2005–2005

National Health Service2007–2017

Hôpital Necker-Enfants Malades1993–1993

Boston Children's Hospital2013–2013

Top Works

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

Andy Rimmer,Hang Phan,et al.

20141,174 citations

Connective tissue disorders research

Genomics and Rare Diseases

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Andrew O.M. Wilkie,Sarah F. Slaney,et al.

1995929 citations

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

Sebastian Köhler,Sandra C. Doelken,et al.

2013837 citations

Craniosynostosis: genes and mechanisms

Andrew O.M. Wilkie

1997526 citations

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

Jonathan Flint,Andrew O.M. Wilkie,et al.

1995508 citations

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

Gillian Morriss‐Kay,Andrew O.M. Wilkie

2005475 citations

Craniosynostosis

David Johnson,Andrew O.M. Wilkie

2011458 citations

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

Paul Rutland,Louise J. Pulleyn,et al.

1995456 citations

A review of the molecular genetics of the human alpha-globin gene cluster

DR Higgs,Mark A. Vickers,et al.

1989447 citations