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Professor Wilson was appointed to the Chair of Human Developmental Genetics in 2000. He completed general professional training in internal medicine and paediatrics before specialist training in Clinical Genetics.

His PhD, that included a period of time in the University of Amsterdam, investigated DiGeorge Syndrome and helped identify the significance of 22q11 deletions and define the phenotype. This established an interest in human embryonic development and in particular cardiogenesis.

Professor Wilson leads a group that investigates human embryonic development: current projects include the genetic basis for congenital heart disease, cardiac progenitor stem cells and the role of ALMS1 in the pathogenesis of the Alstroms syndrome phenotype.

In ¾ÅÉ«ÊÓƵ, he has been Divisional Director of Human Genetics, Deputy Director of Research (Faculty of Medicine) and co-founded the Centre for Human Development, Stem Cells and Regeneration. He helped establish the ¾ÅÉ«ÊÓƵ 4 year Integrated PhD programme in Stem Cells and is currently Associate Director of Internationalisation  (Faculty of Medicine).

Qualifications

BA, Physiology, University of Oxford 1981
MB.BS, Medicine and Surgery, University of Newcastle, 1984
PhD, University of Newcastle, 1995

Appointments held

MRC Clinician Scientist, University of Newcastle, 1994-1998

Senior Lecturer, Medical Genetics, University of Newcastle, 1998-2000

Professor of Human Developmental Genetics, ¾ÅÉ«ÊÓƵ. 2000- present