Irish-British physician and scientist (born 1958)
Sir Stephen Patrick O'Rahilly FRS FRCP FRCPI FRCPath FMedSci FRSB MRIA (born 1 April 1958) is an Irish-British physician and scientist known for his research into the molecular pathogenesis of human obesity , insulin resistance and related metabolic and endocrine disorders.[ 2] [ 3] [ 4] [ 5] [ 6] [ 7] [ 8] [ 9] [ 10]
^ a b c "O'RAHILLY, Prof. Stephen" . Who's Who . Vol. 2015 (online Oxford University Press ed.). A & C Black. (Subscription or UK public library membership required.)
^ Neill, U. S. (2013). "A conversation with Stephen O'Rahilly" . Journal of Clinical Investigation . 123 (6): 2335–2336. doi :10.1172/JCI70726 . PMC 3668822 . PMID 23722908 .
^ Weston, K. (2011). "Translating metabolic biochemistry into the clinic: An interview with Steve O'Rahilly" . Disease Models & Mechanisms . 4 (2): 141–144. doi :10.1242/dmm.007641 . PMC 3046085 . PMID 21357759 .
^ Gerken, T.; Girard, C. A.; Tung, Y. -C. L.; Webby, C. J.; Saudek, V.; Hewitson, K. S.; Yeo, G. S. H.; McDonough, M. A.; Cunliffe, S.; McNeill, L. A.; Galvanovskis, J.; Rorsman, P. ; Robins, P.; Prieur, X.; Coll, A. P.; Ma, M.; Jovanovic, Z.; Farooqi, I. S. ; Sedgwick, B.; Barroso, I.; Lindahl, T. ; Ponting, C. P. ; Ashcroft, F. M. ; O'Rahilly, S. ; Schofield, C. J. (2007). "The Obesity-Associated FTO Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase" . Science . 318 (5855): 1469–1472. Bibcode :2007Sci...318.1469G . doi :10.1126/science.1151710 . PMC 2668859 . PMID 17991826 .
^ Stephen O'Rahilly's publications indexed by the Scopus bibliographic database. (subscription required)
^ Oʼrahilly, Stephen; Montague, C. T.; Farooqi, I. S. ; Whitehead, J. P.; Soos, M. A.; Rau, H.; Wareham, N. J.; Sewter, C. P.; Digby, J. E.; Mohammed, S. N.; Hurst, J. A.; Cheetham, C. H.; Earley, A. R.; Barnett, A. H.; Prins, J. B. (1997). "Congenital leptin deficiency is associated with severe early-onset obesity in humans" . Nature . 387 (6636): 903–8. Bibcode :1997Natur.387..903M . doi :10.1038/43185 . PMID 9202122 . S2CID 205032762 .
^ Seminara, S. B.; Messager, S.; Chatzidaki, E. E.; Thresher, R. R.; Acierno, J. S.; Shagoury, J. K.; Bo-Abbas, Y.; Kuohung, W.; Schwinof, K. M.; Hendrick, A. G.; Zahn, D.; Dixon, J.; Kaiser, U. B.; Slaugenhaupt, S. A.; Gusella, J. F.; O'Rahilly, S.; Carlton, M. B. L.; Crowley, W. F.; Aparicio, S. A. J. R.; Colledge, W. H. (2003). "TheGPR54Gene as a Regulator of Puberty" . New England Journal of Medicine . 349 (17): 1614–27. doi :10.1056/NEJMoa035322 . PMID 14573733 .
^ Farooqi, I. S ; Jebb, S. A.; Langmack, G.; Lawrence, E.; Cheetham, C. H.; Prentice, A. M.; Hughes, I. A.; McCamish, M. A.; O'Rahilly, S. (1999). "Effects of Recombinant Leptin Therapy in a Child with Congenital Leptin Deficiency" . New England Journal of Medicine . 341 (12): 879–84. doi :10.1056/NEJM199909163411204 . PMID 10486419 .
^ Payne, F.; Lim, K.; Girousse, A.; Brown, R. J.; Kory, N.; Robbins, A.; Xue, Y.; Sleigh, A.; Cochran, E.; Adams, C.; Dev Borman, A.; Russel-Jones, D.; Gorden, P.; Semple, R. K.; Saudek, V.; O'Rahilly, S.; Walther, T. C.; Barroso, I.; Savage, D. B. (2014). "Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease" . Proceedings of the National Academy of Sciences . 111 (24): 8901–8906. Bibcode :2014PNAS..111.8901P . doi :10.1073/pnas.1408523111 . PMC 4066527 . PMID 24889630 .
^ "Professor Steve O'Rahilly, Head of Department and Professor of Clinical Biochemistry and Medicine" . University of Cambridge. Archived from the original on 13 April 2014.