个人简介
Chris Talbot was born in Hong Kong, but went to school in High Wycombe, Buckinghamshire. After a BSc at Imperial College in London, he worked first at St. Mary’s Hospital in Paddington with John Hardy on the genetics of Alzheimer’s disease. He then carried out a PhD as an external student of London University, working at Washington University in St. Louis. The project, supervised by Alison Goate, continued the work on Alzheimer’s disease. Subsequently he returned to the UK to carry out a three year postdoc with Jonathan Flint at the Wellcome Trust Centre for Human Genetics at Oxford University. This work in psychiatric genetics aimed to find quantitative trait loci for anxiety in mice. He obtained a lectureship in the Department of Genetics in the University of Leicester in 2001.
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Hainsworth AH, Allsopp RC, Jim A, Potter JF, Lowe J, Talbot CJ, Prettyman RJ. Death-associated protein kinase (DAPK1) in cerebral cortex of late-onset Alzheimer's disease patients and aged controls. Neuropathol Appl Neurobiol. 2010 Feb;36(1):17-24.
Tanteles GA, Whitworth J, Mills J, Peat I, Osman A, McCann GP, Chan S, Barwell JG, Talbot CJ, Symonds RP. Can cutaneous telangiectasiae as late normal-tissue injury predict cardiovascular disease in women receiving radiotherapy for breast cancer? Br J Cancer. 2009 Aug 4;101(3):403-9.
Sandhu J, Kaur B, Armstrong C, Talbot CJ, Steward WP, Farmer PB, Singh R. Determination of 5-methyl-2'-deoxycytidine in genomic DNA using high performance liquid chromatography-ultraviolet detection. J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Jul 1;877(20-21):1957-61.
Giotopoulos G, Armstrong C, Osman A, Peat I, Symonds RP, Talbot CJ. Refining the evidence for GSTA1 and eNOS genetic effects on risk of radiotherapy-induced telangiectasia. Int J Cancer. 2008 Dec 15;123(12):2973-4.
Jawad M, Cole C, Zanker A, Giotopoulos G, Fitch S, Talbot CJ, Plumb M. QTL analyses of lineage-negative mouse bone marrow cells labeled with Sca-1 and c-Kit. Mamm Genome. 2008 Mar;19(3):190-8.
Jawad M, Giotopoulos G, Fitch S, Cole C, Plumb M, Talbot CJ. Mouse bone marrow and peripheral blood erythroid cell counts are regulated by different autosomal genetic loci. Blood Cells Mol Dis. 2007 Mar-Apr;38(2):69-77.
Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, HunterDG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus. Nat Genet. 2006 Nov;38(11):1242-4