Name
Designations
Role
GMC number
Medicine is a science of uncertainty and an art of probability
Dr William Osler
My current role
I spend half my time doing clinical work for the NHS and half my time doing research at the University of Cambridge. I am the clinical lead for cancer genetics services. I see a mix of patients in cancer genetics clinics and general adult / paediatric genetics clinics. My clinics are at Addenbrooke's hospital and Norfolk and Norwich University hospital.
My research is focussed on hereditary breast and ovarian cancer, hereditary gastric cancer and rare cancer syndromes such as Fanconi anaemia, ataxia telangiectasia and PTEN hamartoma tumour syndrome. I have a special interest in translating the recent advances in genomic technology into clinical practice.
Previous history
Before joining CUH I was a consultant (attending staff) at the Jewish general hospital in Montreal, and I was an associate professor at McGill University, Montreal, Canada.
Prior to this, I did my medical training in the UK and my PhD at Kings College, London.
Membership and accreditations
I am a trustee of the Fanconi Hope charity and the editor of BJC Reports, a medical journal focused on new advances in cancer.
Personal interests
I enjoy teaching students, healthcare professionals and other doctors about cancer genetics.
In my spare time I enjoy playing tennis, badminton, bridge and chess.
Publications
-
Hereditary diffuse gastric cancer: updated clinical practice guidelines.
-
European experts consensus: BRCA/homologous recombination deficiency testing in first-line ovarian cancer
-
Prevalence and architecture of de novo mutations in developmental disorders
-
Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
-
Whole-genome sequencing of patients with rare diseases in a national health system