Douglas Higgs

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Douglas Higgs
Born13 January 1951 Edit this on Wikidata
Alma mater
OccupationPhysician Edit this on Wikidata
Employer
Awards

Douglas Roland Higgs FRS (born 13 January 1951)[1] is a Professor of Molecular Haematology at the Weatherall Institute of Molecular Medicine, at the University of Oxford.[2] He is known for his work on the regulation of alpha-globin and the genetics of alpha-thalassemia.[3] He is currently working in understanding the mechanisms by which any mammalian gene is switched on and off during differentiation and development.

Education[edit]

He was educated at Alleyn's School and qualified in medicine at King's College Hospital Medical School in 1974, and trained as a haematologist.[1] He became a registrar in Haematology at Kings College Hospital in 1976.

Research and career[edit]

He joined the Molecular Haematology Unit of the Medical Research Council at Oxford in 1977. In 1996 he was appointed Ad Hominem Professor of Molecular Haematology. In 2001, he became a director of the MRC Molecular Haematology Unit (MHU).[1][4] In 2012, Higgs was appointed director of the Weatherall Institute of Molecular Medicine (WIMM).[4][5] In 2020, Higgs was succeeded as director of the MRC MHU and WIMM by Ketan J. Patel.[6] Higgs is a Senior Kurti Fellow at Brasenose College, Oxford.[7]

Honours and awards[edit]

Works[edit]

Gibbons, Richard J; Picketts, David J; Villard, Laurent; Higgs, Douglas R (1995). "Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome)". Cell. 80 (6): 837–845. doi:10.1016/0092-8674(95)90287-2. PMID 7697714. S2CID 16411046.

Tufarelli, Cristina; Stanley, Jackie A Sloane; Garrick, David; Sharpe, Jackie A; Ayyub, Helena; Wood, William G; Higgs, Douglas R (2003). "Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease". Nature Genetics. 34 (2): 157–165. doi:10.1038/ng1157. ISSN 1546-1718. PMID 12730694. S2CID 7226446.

Higgs, D. R.; Goodbourn, S. E. Y.; Lamb, J.; Clegg, J. B.; Weatherall, D. J.; Proudfoot, N. J. (1983). "α-Thalassaemia caused by a polyadenylation signal mutation". Nature. 306 (5941): 398–400. Bibcode:1983Natur.306..398H. doi:10.1038/306398a0. ISSN 1476-4687. PMID 6646217. S2CID 4332750.

Wilkie, Andrew O. M.; Lamb, Janette; Harris, Peter C.; Finney, Roger D.; Higgs, Douglas R. (1990). "A truncated human chromosome 16 associated with α thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)n". Nature. 346 (6287): 868–871. Bibcode:1990Natur.346..868W. doi:10.1038/346868a0. ISSN 1476-4687. PMID 1975428. S2CID 4239520.

Nicholls, R.D.; Fischel-Ghodsian, N.; Higgs, D.R. (1987). "Recombination at the human α-globin gene cluster: Sequence features and topological constraints". Cell. 49 (3): 369–378. doi:10.1016/0092-8674(87)90289-3. PMID 3032452. S2CID 54349888.

De Gobbi, Marco; Viprakasit, Vip; Hughes, Jim R.; Fisher, Chris; Buckle, Veronica J.; Ayyub, Helena; Gibbons, Richard J.; Vernimmen, Douglas; Yoshinaga, Yuko (26 May 2006). "A Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter". Science. 312 (5777): 1215–1217. Bibcode:2006Sci...312.1215D. doi:10.1126/science.1126431. ISSN 0036-8075. PMID 16728641. S2CID 16044469.

Law, Martin J.; Lower, Karen M.; Voon, Hsiao P.J.; Hughes, Jim R.; Garrick, David; Viprakasit, Vip; Mitson, Matthew; De Gobbi, Marco; Marra, Marco (2010). "ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner". Cell. 143 (3): 367–378. doi:10.1016/j.cell.2010.09.023. PMID 21029860.

Hughes, Jim R; Roberts, Nigel; McGowan, Simon; Hay, Deborah; Giannoulatou, Eleni; Lynch, Magnus; De Gobbi, Marco; Taylor, Stephen; Gibbons, Richard (2014). "Analysis of hundreds of cis-regulatory landscapes at high resolution in a single, high-throughput experiment". Nature Genetics. 46 (2): 205–212. doi:10.1038/ng.2871. hdl:2318/144575. ISSN 1546-1718. PMID 24413732. S2CID 205348099.

Higgs, Douglas R.; Gibbons, Richard J.; McDowell, Tarra L.; Raman, Sundhya; O'Rourke, Delia M.; Garrick, David; Ayyub, Helena (2000). "Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation". Nature Genetics. 24 (4): 368–371. doi:10.1038/74191. ISSN 1546-1718. PMID 10742099. S2CID 8847855.

Hay, Deborah; Hughes, Jim R; Babbs, Christian; Davies, James O J; Graham, Bryony J; Hanssen, Lars L P; Kassouf, Mira T; Oudelaar, A Marieke; Sharpe, Jacqueline A (2016). "Genetic dissection of the α-globin super-enhancer in vivo". Nature Genetics. 48 (8): 895–903. doi:10.1038/ng.3605. ISSN 1546-1718. PMC 5058437. PMID 27376235.

References[edit]

  1. ^ a b c d e "Higgs, Prof. Douglas Roland, (born 13 Jan. 1951), Professor of Haematology, since 1996, director, MRC Molecular Haematology Unit, since 2001, and director, Weatherall Institute of Molecular Medicine, since 2012, University of Oxford". Higgs, Prof. Douglas Roland. UK WHOS WHO. 2007. doi:10.1093/ww/9780199540884.013.244900.
  2. ^ "Doug Higgs — WIMM". Archived from the original on 27 September 2011. Retrieved 25 March 2011.
  3. ^ a b "Douglas Higgs". royalsociety.org. Retrieved 16 March 2018.
  4. ^ a b MRC, Medical Research Council (18 May 2017). "Top haematologist announced as new Director of MRC Weatherall Institute of Molecular Medicine". mrc.ac.uk. Retrieved 16 March 2018.
  5. ^ "New Weatherall Institute of Molecular Medicine director announced – Weatherall Institute of Molecular Medicine". University of Oxford. Retrieved 16 March 2018.
  6. ^ "MRC WIMM appoints new Director". www.imm.ox.ac.uk. Retrieved 1 December 2023.
  7. ^ "The Brazen Nose" (PDF). 2009–2010.
  8. ^ "Professor Douglas Higgs | The Academy of Medical Sciences". acmedsci.ac.uk. Archived from the original on 17 March 2018. Retrieved 16 March 2018.
  9. ^ "Buchanan Medal Awarded – Weatherall Institute of Molecular Medicine". University of Oxford. Archived from the original on 17 March 2018. Retrieved 16 March 2018.
  10. ^ "The Buchanan Medal (1897)". The Royal Society. Retrieved 12 September 2013.
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