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Hugh Christian Watkins

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Hugh Christian Watkins
FRS FRCP FMedSci
Watkins in 2017
Born (1959-06-07) 7 June 1959 (age 65)
EducationGresham's School
Alma materSt Bartholomew's Hospital Medical College
University of London
Scientific career
InstitutionsUniversity of Oxford
Harvard Medical School
ThesisDemonstration that cardiac troponin T mutations cause hypertrophic cardiomyopathy (1996)
Notable studentsBongani Mayosi
Websitewww.rdm.ox.ac.uk/principal-investigators/researcher/hugh-watkins

Hugh Christian Watkins (born 7 June 1959) is a British cardiologist. He is a Fellow of Merton College, Oxford, an associate editor of Circulation Research, and was Field Marshal Alexander Professor of Cardiovascular Medicine in the University of Oxford between 1996 and 2013.

Early life and education

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The son of Dr David Watkins, a Norfolk physician, and his wife Gillian Mary, Watkins was educated at Gresham's School, Holt, Norfolk and the St Bartholomew's Hospital Medical College, graduating in 1983 with both Bachelor of Science and Bachelor of Medicine, Bachelor of Surgery degrees. In 1984 he gained the Brackenbury & Bourne Prize in General Medicine.[1] He was awarded a PhD from the University of London in 1995.[1]

Career and Research

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Watkins was a house physician in the Professorial Medical Unit at St Bartholomew's Hospital in 1984–1985, then a senior house officer in Medicine at the John Radcliffe Hospital, Oxford, from 1985 to 1987. He was then briefly a senior house officer in Neurology at St Bartholomew's, before two years as a Registrar in Medicine and Cardiology at St Thomas's Hospital, London, from 1987 to 1989. His next posts were as a lecturer in Cardiological Sciences at St George's Hospital, London, and as Resident Fellow in Medicine at the Harvard Medical School and Brigham and Women's Hospital, Boston. In 1995 he was appointed an assistant professor of medicine at the Harvard Medical School and as associate physician at the Brigham & Women's Hospital, and in 1996 as Field Marshal Alexander Professor of Cardiovascular Medicine in the University of Oxford.[1][2]

Watkins was elected to Membership of the Royal College of Physicians (MRCP) in 1987, graduated MD and PhD from the University of London in 1995, and was appointed a Fellow of the Royal College of Physicians (FRCP) in 1997.[1]

At Oxford, Watkins is the Director of the British Heart Foundation's Molecular Cardiology Laboratory in the Wellcome Trust Centre for Human Genetics and of its Centre of Research Excellence, one of six similar programmes in the United Kingdom. He is also an associate editor of the academic journal Circulation Research.[3]

Watkins's main specialism is in molecular genetic analysis of cardiovascular disease, and his most notable work is on the inheritance of heart disease, especially on hypertrophic cardiomyopathy and the genetic causes of "sudden cardiac death". He is chairman of an international group which investigates genetic susceptibility to coronary artery disease, which has funding from the European Commission.[3]

Honours and awards

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Publications

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Personal life

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In 1987, Watkins married Elizabeth Bridget Hewett, and they have one son and one daughter. In Who's Who his recreations are stated as "photography and Oriental porcelain".[1]

References

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  1. ^ a b c d e f g h i j k Anon (2017). "Watkins, Prof. Hugh Christian". Who's Who (online Oxford University Press ed.). Oxford: A & C Black. doi:10.1093/ww/9780199540884.013.39014. (Subscription or UK public library membership required.)
  2. ^ Commonwealth Universities Yearbook, vol. 2 (2006), p. 2006
  3. ^ a b c d "Hugh WatkinsMD, PhD, FRCP, FMedSci". cardiov.ox.ac.uk. Archived from the original on 28 April 2012., accessed 28 April 2012
  4. ^ Anon (2017). "Hugh Watkins FRS". royalsociety.org. Royal Society. Archived from the original on 5 May 2017. Retrieved 5 May 2017.
  5. ^ Clarke, Robert; Peden, John F.; Hopewell, Jemma C.; Kyriakou, Theodosios; Goel, Anuj; Heath, Simon C.; Parish, Sarah; Barlera, Simona; Franzosi, Maria Grazia; Rust, Stephan; Bennett, Derrick (2009-12-24). "Genetic variants associated with Lp(a) lipoprotein level and coronary disease" (PDF). The New England Journal of Medicine. 361 (26): 2518–2528. doi:10.1056/NEJMoa0902604. ISSN 1533-4406. PMID 20032323.
  6. ^ Thierfelder, L.; Watkins, H.; MacRae, C.; Lamas, R.; McKenna, W.; Vosberg, H. P.; Seidman, J. G.; Seidman, C. E. (1994-06-03). "Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere". Cell. 77 (5): 701–712. doi:10.1016/0092-8674(94)90054-x. ISSN 0092-8674. PMID 8205619. S2CID 205021038.
  7. ^ Nelson, Christopher P.; Goel, Anuj; Butterworth, Adam S.; Kanoni, Stavroula; Webb, Tom R.; Marouli, Eirini; Zeng, Lingyao; Ntalla, Ioanna; Lai, Florence Y.; Hopewell, Jemma C.; Giannakopoulou, Olga (September 2017). "Association analyses based on false discovery rate implicate new loci for coronary artery disease". Nature Genetics. 49 (9): 1385–1391. doi:10.1038/ng.3913. hdl:2381/40475. ISSN 1546-1718. PMID 28714975. S2CID 5009349.
  8. ^ Nikpay, Majid; Goel, Anuj; Won, Hong-Hee; Hall, Leanne M.; Willenborg, Christina; Kanoni, Stavroula; Saleheen, Danish; Kyriakou, Theodosios; Nelson, Christopher P.; Hopewell, Jemma C.; Webb, Thomas R. (October 2015). "A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease". Nature Genetics. 47 (10): 1121–1130. doi:10.1038/ng.3396. ISSN 1546-1718. PMC 4589895. PMID 26343387.
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