Molecular genetics in gastroenterology: from research success to clinical application? by Satsangi, J, Campbell, H, Dunlop, MG, Porteous, MEM

Investigation of the effects of DNA repair gene polymorphisms on the risk of colorectal cancer. by Tomlinson, I, Houlston, R, Montgomery, G, Sieber, O, Dunlop, MG

A novel test for gene-ancestry interactions in genome-wide association data by Davies, J, Cazier, J, Dunlop, MG, Houlston, R, Tomlinson, I, Holmes, C

Imputation as a method to fine map cancer susceptibility loci by Whiffin, N, Dobbins, SE, Broderick, P, Dunlop, MG, Tomlinson, I, Houlston, R

The TERT variant rs2736100 is associated with colorectal cancer risk. by Kinnersley, B, Migliorini, G, Broderick, P, Whiffin, N, Dobbins, SE, Casey, G, Hopper, J, Sieber, O, Lipton, L, Kerr, D, Dunlop, MG, Tomlinson, I, Houlston, R

The TERT variant rs2736100 is associated with colorectal cancer risk by Kinnersley, B, Migliorini, G, Broderick, P, Whiffin, N, Dobbins, SE, Casey, G, Hopper, J, Sieber, O, Lipton, L, Kerr, D, Dunlop, MG, Tomlinson, I, Houlston, R

Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer. by Chubb, D, Broderick, P, Dobbins, SE, Frampton, M, Kinnersley, B, Penegar, S, Price, A, Ma, YP, Sherborne, AL, Palles, C, Timofeeva, MN, Bishop, DT, Dunlop, MG, Tomlinson, I, Houlston, RS

TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres by Jones, A, Beggs, A, Carvajal-Carmona, L, Farrington, S, Tenesa, A, Walker, M, Howarth, K, Ballereau, S, Hodgson, S, Zauber, A, Bertagnolli, M, Midgley, R, Campbell, H, Kerr, D, Dunlop, MG, Tomlinson, I

TERC polymorphisms are associated both with susceptibility to colorectal cancer and with longer telomeres. by Jones, A, Beggs, A, Carvajal-Carmona, L, Farrington, S, Tenesa, A, Walker, M, Howarth, K, Ballereau, S, Hodgson, S, Zauber, A, Bertagnolli, M, Midgley, R, Campbell, H, Kerr, D, Dunlop, MG, Tomlinson, I

Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)... by Monahan, KJ, Bradshaw, N, Dolwani, S, Desouza, B, Dunlop, MG, East, JE, Ilyas, M, Kaur, A, Lalloo, F, Latchford, A, Rutter, MD, Tomlinson, I, Thomas, HJW, Hill, J, Hereditary CRC Guidelines Edelphi Consensus Group

Altered DNA methylation within DNMT3A, AHRR, LTA/TNF loci mediates the effect of smoking on inflammatory bowel disease by Zhang, H, Kalla, R, Chen, J, Zhao, J, Zhou, X, Adams, A, Noble, A, Ventham, NT, Wellens, J, Ho, G-T, Dunlop, MG, Nowak, JK, Ding, Y, Liu, Z, Satsangi, J, Theodoratou, E, Li, X

Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis. by Kinnersley, B, Buch, S, Castellví-Bel, S, Farrington, S, Forsti, A, Hampe, J, Hemminki, K, Hofstra, R, Northwood, E, Palles, C, Pinheiro, M, Ruiz-Ponte, C, Schafmayer, C, Teixeira, MR, Westers, H, Wezel, T, Bishop, D, Tomlinson, I, Dunlop, MG, Houlston, R

Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas by Sieber, O, Lamlum, H, Crabtree, MD, Rowan, A, Barclay, E, Lipton, L, Hodgson, S, Thomas, H, Neale, K, Phillips, R, Farrington, S, Dunlop, MG, Mueller, H, Bisgaard, M, Bulow, S, Fidalgo, P, Albuquerque, C, Scarano, M, Bodmer, W, Tomlinson, I, Heinimann, K

Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas. by Sieber, O, Lamlum, H, Crabtree, MD, Rowan, A, Barclay, E, Lipton, L, Hodgson, S, Thomas, H, Neale, K, Phillips, R, Farrington, S, Dunlop, MG, Mueller, H, Bisgaard, M, Bulow, S, Fidalgo, P, Albuquerque, C, Scarano, M, Bodmer, W, Tomlinson, I, Heinimann, K

Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer. by Whiffin, N, Dobbins, SE, Hosking, F, Palles, C, Tenesa, A, Wang, Y, Farrington, S, Jones, A, Broderick, P, Campbell, H, Newcomb, P, Casey, G, Conti, D, Schumacher, F, Gallinger, S, Lindor, N, Hopper, J, Jenkins, M, Dunlop, MG, Tomlinson, I, Houlston, R

Contribution of the NOD1/CARD4 insertion/deletion polymorphism +32656 to inflammatory bowel disease in Northern Europe by Van Limbergen, J, Russell, RK, Nimmo, ER, Törkvist, L, Lees, CW, Drummond, HE, Smith, L, Anderson, NH, Gillett, PM, McGrogan, P, Hassan, K, Weaver, LT, Bisset, WM, Mahdi, G, Arnott, ID, Sjöqvist, U, Lördal, M, Farrington, SM, Dunlop, MG, Wilson, DC, Satsangi, J

Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment. by Kirin, M, Chandra, A, Charteris, D, Hayward, C, Campbell, S, Celap, I, Bencic, G, Vatavuk, Z, Kirac, I, Richards, A, Tenesa, A, Snead, M, Fleck, B, Singh, J, Harsum, S, Maclaren, R, den Hollander, A, Dunlop, MG, Hoyng, C, Wright, A, Campbell, H, Vitart, V, Mitry, D

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk by Dunlop, MG, Dobbins, SE, Farrington, S, Jones, A, Palles, C, Whiffin, N, Tenesa, A, Spain, S, Broderick, P, Ooi, L, Domingo, E, Smillie, C, Henrion, M, Frampton, M, Martin, L, Grimes, G, Gorman, M, Semple, C, Ma, Y, Barclay, E, Prendergast, J, Cazier, J, Olver, B, Penegar, S, Lubbe, S

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. by Dunlop, MG, Dobbins, SE, Farrington, S, Jones, A, Palles, C, Whiffin, N, Tenesa, A, Spain, S, Broderick, P, Ooi, L, Domingo, E, Smillie, C, Henrion, M, Frampton, M, Martin, L, Grimes, G, Gorman, M, Semple, C, Ma, Y, Barclay, E, Prendergast, J, Cazier, J, Olver, B, Penegar, S, Lubbe, S

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome. by Marsh, D, Roth, S, Lunetta, K, Hemminki, A, Dahia, P, Sistonen, P, Zheng, Z, Caron, S, van Orsouw, N, Bodmer, W, Cottrell, SE, Dunlop, MG, Eccles, D, Hodgson, S, Järvinen, H, Kellokumpu, I, Markie, D, Neale, K, Phillips, R, Rozen, P, Syngal, S, Vijg, J, Tomlinson, I, Aaltonen, L, Eng, C