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Showing results 1 to 6 of 6

	Title	Author(s)	Issue Date
	COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE Study): prospective cohort study and systematic review Journal:Ultrasound in Obstetrics and Gynecology	Mone, F Eberhardt, RY Morris, RK Hurles, ME McMullan, DJ Maher, ER Lord, J Chitty, LS Giordano, JL Wapner, RJ Kilby, MD The CODE Study Collaborators Chung, BHY	2021
	A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 Journal:Nature Genetics	Tomlinson, IPM Webb, E CarvajalCarmona, L Broderick, P Howarth, K Pittman, AM Spain, S Lubbe, S Walther, A Sullivan, K Jaeger, E Fielding, S Rowan, A Vijayakrishnan, J Domingo, E Chandler, I Kemp, Z Qureshi, M Farrington, SM Tenesa, A Prendergast, JGD Barnetson, RA Penegar, S Barclay, E Wood, W Martin, L Gorman, M Thomas, H Peto, J Bishop, DT Gray, R Maher, ER Lucassen, A Kerr, D Evans, DGR Schafmayer, C Buch, S Völzke, H Hampe, J Schreiber, S John, U Koessler, T Pharoah, P Van Wezel, T Morreau, H Wijnen, JT Hopper, JL Southey, MC Giles, GG Severi, G CastellvíBel, S RuizPonte, C Carracedo, A Castells, A Försti, A Hemminki, K Vodicka, P Naccarati, A Lipton, L Ho, JWC Cheng, KK Sham, PC Luk, J Agúndez, JAG Ladero, JM De La Hoya, M Caldés, T Niittymäki, I Tuupanen, S Karhu, A Aaltonen, L Cazier, JB Campbell, H Dunlop, MG Houlston, RS	2008
	Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial Journal:Lancet	Burn, J Gerdes, AM Macrae, F Mecklin, JP Moeslein, G Olschwang, S Eccles, D Evans, DG Maher, ER Bertario, L Bisgaard, ML Duniop, MG Ho, JWC Hodgson, SV Lindblom, A Lubinski, J Morrison, PJ CAPP2 Investigators, -	2011
	Obesity, aspirin, and risk of colorectal cancer in carriers of hereditary colorectal cancer: a prospective investigation in the CAPP2 study Journal:Journal of Clinical Oncology	Movahedi, M Bishop, DT Macrae, F Mecklin, JP Moeslein, G Olschwang, S Eccles, D Evans, DG Maher, ER Bertario, L Bisgaard, ML Dunlop, MG Ho, JWC Hodgson, SV Lindblom, A Lubinski, J Morrison, PJ Murday, V Ramesar, RS Side, L Scott, RJ Thomas, HJ Vasen, HF Burn, J Mathers, JC	2015
	Recurrent germline mutation in MSH2 arises frequently de novo	Desai, DC Lockman, JC Chadwick, RB Gao, X Percesepe, A Evans, DGR Miyaki, M Yuen, ST Radice, P Maher, ER Wright, FA De la chapelle, A	2000
	Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer Journal:Human Molecular Genetics	Pittman, AM Webb, E CarvajalCarmona, L Howarth, K Di Bernardo, MC Broderick, P Spain, S Walther, A Price, A Sullivan, K Twiss, P Fielding, S Rowan, A Jaeger, E Vijayakrishnan, J Chandler, I Penegar, S Qureshi, M Lubbe, S Domingo, E Kemp, Z Barclay, E Wood, W Martin, L Gorman, M Thomas, H Peto, J Bishop, T Gray, R Maher, ER Lucassen, A Kerr, D Evans, GR van Wezel, T Morreau, H Wijnen, JT Hopper, JL Southey, MC Giles, GG Severi, G CastellvíBel, S RuizPonte, C Carracedo, A Castells, A Försti, A Hemminki, K Vodicka, P Naccarati, A Lipton, L Ho, JWC Cheng, KK Sham, PC Luk, J Agúndez, JAG Ladero, JM de la Hoya, M Caldés, T Niittymäki, I Tuupanen, S Karhu, A Aaltonen, LA Cazier, JB Tomlinson, IPM Houlston, RS	2008

Showing results 1 to 6 of 6