Results 1 to 4 of 4
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TypeTitleAuthor(s)YearViews
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, -2011177
 
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Journal:
Nature Genetics
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.genetics.nature.com
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, RS2008404
 
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer
Journal:
Human Molecular Genetics
Publisher:
Oxford University Press. The Journal's web site is located at http://hmg.oxfordjournals.org/
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, RS2008472
 
Recurrent germline mutation in MSH2 arises frequently de novo
Publisher:
B M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/
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, A2000436
 
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