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Online Research @ Cardiff

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Number of items: 15.

West, Hannah, Coffey, Michelle, Wagner, Michael J., McLeod, Howard L., Colley, James P., Adams, Richard A., Fleck, Oliver, Maughan, Timothy S., Fisher, David, Kaplan, Richard S., Harris, Rebecca and Cheadle, Jeremy P. 2018. Role for nucleotide-excision repair gene variants in oxaliplatin-induced peripheral neuropathy. JCO Precision Oncology 2 , pp. 1-18. 10.1200/PO.18.00090

Madi, Ayman, Fisher, David, Maughan, Timothy S., Colley, James P., Meade, Angela M., Maynard, Julie, Humphreys, Vikki, Wasan, Harpreet, Adams, Richard A., Idziaszczyk, Shelley, Harris, Rebecca, Kaplan, Richard S. and Cheadle, Jeremy P. 2018. Pharmacogenetic analyses of 2,183 patients with advanced colorectal cancer; Potential role for common dihydropyrimidine dehydrogenase variants in toxicity to chemotherapy. European Journal of Cancer 102 , pp. 31-39. 10.1016/j.ejca.2018.07.009

Smith, Chris, Naven, Marc, Harris, Rebecca, Colley, James, West, Hannah, Li, Ning, Liu, Yuan, Adams, Richard Alexander, Maughan, Timothy S., Nichols, Laura, Kaplan, Richard, Wagner, Michael J., McLeod, Howard L. and Cheadle, Jeremy Peter 2013. Exome resequencing identifies potential tumor-suppressor genes that predispose to colorectal cancer. Human Mutation 34 (7) , pp. 1026-1034. 10.1002/humu.22333

Bell, W., Colley, James, Evans, W.D., Darlington, S.E. and Cooper, S.-M. 2012. ACTN3 genotypes of Rugby Union players: distribution, power output and body composition. Annals of Human Biology 39 (1) , pp. 19-27. 10.3109/03014460.2011.632648

Colley, James P. M. 2012. The development and application of SNP discovery technologies from 2005 to 2012. PhD Thesis, Cardiff University.
Item availability restricted.

Houlston, Richard S, Cheadle, Jeremy Peter, Dobbins, Sara E., Tenesa, Albert, Jones, Angela M., Howarth, Kimberley, Spain, Sarah L., Broderick, Peter, Domingo, Enric, Farrington, Susan, Prendergast, James G. D., Pittman, Alan M., Theodoratou, Evi, Smith, Chris, Olver, Bianca, Walther, Axel, Barnetson, Rebecca A., Churchman, Michael, Jaeger, Emma E. M., Penegar, Steven, Barclay, Ella, Martin, Lynn, Gorman, Maggie, Mager, Rachel, Johnstone, Elaine, Midgley, Rachel, Niittymäki, Iina, Tuupanen, Sari, Colley, James, Idziaszczyk, Shelley Alexis, Thomas, Huw J. W., Lucassen, Anneke M., Evans, D. Gareth R., Maher, Eamonn R., Maughan, Timothy Stanley, Dimas, Antigone, Dermitzakis, Emmanouil, Cazier, Jean-Baptiste, Aaltonen, Lauri A., Pharoah, Paul, Kerr, David J., Carvajal-Carmona, Luis G., Campbell, Harry, Dunlop, Malcolm G. and Tomlinson, Ian P. M. 2010. Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 [Letter]. Nature Genetics 42 (11) , pp. 973-977. 10.1038/ng.670

Bell, W., Colley, James, Gwynne, J. R., Glazier, P., Evans, William D. and Darlington, Sarah E. 2010. ACE ID genotype and leg power in Rugby Union players. Journal of Sports Medicine and Physical Fitness 50 (3) , pp. 350-355.

Azzopardi, Duncan Lee, Dallosso, Anthony Richard, Eliason, Kristilyn, Hendrickson, Brant C., Jones, Natalie, Rawstorne, Edward Charles, Colley, James, Escott-Price, Valentina, Frye, Cynthia, Sampson, Julian Roy, Wenstrup, Richard, Scholl, Thomas and Cheadle, Jeremy Peter 2008. Multiple rare nonsynonymous variants in the 'adenomatous polyposis coli' gene predispose to colorectal adenomas. Cancer Research 68 (2) , pp. 358-363. 10.1158/0008-5472.CAN-07-5733

Dallosso, Anthony Richard, Dolwani, Sunil, Jones, N., Jones, Sian, Colley, James, Maynard, Julie Helen, Idziaszczyk, Shelley Alexis, Humphreys, Vikki, Arnold, J., Donaldson, A., Eccles, D., Ellis, A., Evans, D. G., Frayling, Ian, Hes, F. J., Houlston, R S, Maher, E R, Nielsen, M, Parry, S, Tyler, E, Escott-Price, Valentina, Cheadle, Jeremy Peter and Sampson, Julian Roy 2008. Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3. Gut 57 (9) , pp. 1252-1255. 10.1136/gut.2007.145748

Wilson, Catherine Helen, Bonnet, Cleo, Guy, Carol, Idziaszczyk, Shelley Alexis, Colley, James, Humphreys, Vikki, Maynard, Julie Helen, Sampson, Julian Roy and Cheadle, Jeremy Peter 2006. Tsc1 Haploinsufficiency without Mammalian Target of Rapamycin Activation Is Sufficient for Renal Cyst Formation in Tsc1+/- Mice. Cancer Research 66 (16) , pp. 7934-8. 10.1158/0008-5472.CAN-06-1740

Wilson, Catherine Helen, Idziaszczyk, Shelley Alexis, Colley, James, Humphreys, Vikki, Guy, Carol, Maynard, Julie Helen, Sampson, Julian Roy and Cheadle, Jeremy Peter 2005. Induction of renal tumorigenesis with elevated levels of somatic loss of heterozygosity in Tsc1+/- mice on a Blm-deficient background. Cancer Research 65 (22) , pp. 10179-10182. 10.1158/0008-5472.CAN-05-2688

Colley, James, Jones, Sian, Dallosso, Anthony R., Maynard, Julie Helen, Humphreys, Vikki, Dolwani, Sunil, Sampson, Julian Roy and Cheadle, Jeremy Peter 2005. Rapid recognition of aberrant dHPLC elution profiles using the Transgenomic NavigatorTM software. Human Mutation 26 (2) , p. 165. 10.1002/humu.9354

Evans, Julie C., Archer, Hayley Louise, Colley, James, Ravn, Kirstine, Nielsen, Jytte Bieber, Kerr, Alison, Williams, Elizabeth, Christodoulou, John, Gécz, Jozef, Jardine, Philip E., Wright, Michael J., Pilz, Daniela, Lazarou, Lazarus, Cooper, David Neil, Sampson, Julian Roy, Butler, Rachel, Whatley, Sharon D. and Clarke, Angus John 2005. Early onset seizures and Rett-like features associated with mutations in CDKL5. European Journal of Human Genetics 13 (10) , pp. 1113-1120. 10.1038/sj.ejhg.5201451

Ridley, Andrew J., Colley, James, Wynford-Thomas, David and Jones, Christopher J. 2005. Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects. Journal of Human Genetics 50 (3) , pp. 151-154. 10.1007/s10038-004-0228-2

Low, Jin Hong, Williams, Fiona A., Yang, Xuesong, Cullen, Sue, Colley, James, Ling, Khoon Lin, Armuzzi, Alessandro, Ahmad, Tariq, Neville, Matt J., Dechairo, Bryan M., Walton, Robert, Lench, Nick J. and Jewell, Derek P. 2004. Inflammatory bowel disease is linked to 19p13 and associated with ICAM-1. Inflammatory Bowel Diseases 10 (3) , pp. 173-181. 10.1097/00054725-200405000-00001

This list was generated on Mon Jul 6 06:29:37 2020 BST.

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