Peutz–Jeghers syndrome: a systematic review and recommendations for management von Beggs, A D, Latchford, A R, Vasen, H F A, Moslein, G, Alonso, A, Aretz, S, Bertario, L, Blanco, I, Bülow, S, Burn, J, Capella, G, Colas, C, Friedl, W, Møller, P, Hes, F J, Järvinen, H, Mecklin, J-P, Nagengast, F M, Parc, Y, Phillips, R K S, Hyer, W, Ponz de Leon, M, Renkonen-Sinisalo, L, Sampson, J R, Stormorken, A, Tejpar, S, Thomas, H J W, Wijnen, J T, Clark, S K, Hodgson, S V

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Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations von Pollard, P.J., Brière, J.J., Alam, N.A., Barwell, J., Barclay, E., Wortham, N.C., Hunt, T., Mitchell, M., Olpin, S., Moat, S.J., Hargreaves, I.P., Heales, S.J., Chung, Y.L., Griffiths, J.R., Dalgleish, A., McGrath, J.A., Gleeson, M.J., Hodgson, S.V., Poulsom, R., Rustin, P., Tomlinson, I.P.M.

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Expression and DNA methylation of TNF, IFNG and FOXP3 in colorectal cancer and their prognostic significance von Ganapathi, S K, Beggs, A D, Hodgson, S V, Kumar, D

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Fanconi anaemia von Tischkowitz, M D, Hodgson, S V

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

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Refining the Amsterdam Criteria and Bethesda Guidelines: Testing Algorithms for the Prediction of Mismatch Repair Mutation Status in the Familial Cancer Clinic von LIPTON, L. R, JOHNSON, V, THOMAS, H. J. W, TOMLINSON, I. P. M, CUMMINGS, C, FISHER, S, RISBY, P, EFTEKHAR SADAT, A. T, CRANSTON, T, IZATT, L, SASIENI, P, HODGSON, S. V

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The risk of subsequent primary cancers after colorectal cancer in southeast England von Evans, H S, Møller, H, Robinson, D, Lewis, C M, Bell, C M J, Hodgson, S V

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Deletion and reduced expression of the fanconi anemia FANCA gene in sporadic acute myeloid leukemia von TISCHKOWITZ, M. D, MORGAN, N. V, GRIMWADE, D, EDDY, C, BALL, S, VORECHOVSKY, I, LANGABEER, S, STÖGER, R, HODGSON, S. V, MATHEW, C. G

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Incidence of multiple primary cancers in a cohort of women diagnosed with breast cancer in southeast England von EVANS, H. S, LEWIS, C. M, ROBINSON, D, BELL, C. M. J, MØLLER, H, HODGSON, S. V

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Second primary cancers after cervical intraepithelial neoplasia III and invasive cervical cancer in Southeast England von Evans, H.S, Newnham, A, Hodgson, S.V, Møller, H

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An Ancestral Ashkenazi Haplotype at the HMPS/CRAC1 Locus on 15q13–q14 Is Associated with Hereditary Mixed Polyposis Syndrome von Jaeger, E.E.M., Woodford-Richens, K.L., Lockett, M., Rowan, A.J., Sawyer, E.J., Heinimann, K., Rozen, P., Murday, V.A., Whitelaw, S.C., Ginsberg, A., Atkin, W.S., Lynch, H.T., Southey, M.C., Debinski, H., Eng, C., Bodmer, W.F., Talbot, I.C., Hodgson, S.V., Thomas, H.J.W., Tomlinson, I.P.M.

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Analysis of Chromosomal Instability in Human Colorectal Adenomas with Two Mutational Hits at APC von Sieber, O. M., Heinimann, K., Gorman, P., Lamlum, H., Crabtree, M., Simpson, C. A., Davies, D., Neale, K., Hodgson, S. V., Roylance, R. R., Phillips, R. K. S., Bodmer, W. F., Tomlinson, I. P. M.

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Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome von Lim, W, Hearle, N, Shah, B, Murday, V, Hodgson, S V, Lucassen, A, Eccles, D, Talbot, I, Neale, K, Lim, A G, O'Donohue, J, Donaldson, A, Macdonald, R C, Young, I D, Robinson, M H, Lee, P W R, Stoodley, B J, Tomlinson, I, Alderson, D, Holbrook, A G, Vyas, S, Swarbrick, E T, Lewis, A A M, Phillips, R K S, Houlston, R S

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Polyclonal Origin of Colonic Adenomas in an XO/XY Patient with FAP von Novelli, M. R., Williamson, J. A., Tomlinson, I. P. M., Elia, G., Hodgson, S. V., Talbot, I. C., Bodmer, W. F., Wright, N. A.

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Analysis of genetic and phenotypic heterogeneity in juvenile polyposis von Woodford-Richens, K, Bevan, S, Churchman, M, Dowling, B, Jones, D, Norbury, C G, Hodgson, S V, Desai, D, Neale, K, Phillips, R K S, Young, J, Leggett, B, Dunlop, M, Rozen, P, Eng, C, Markie, D, Rodriguez-Bigas, M A, Sheridan, E, Iwama, T, Eccles, D, Smith, G T, Kim, J C, Kim, K M, Sampson, J R, Evans, G, Tejpar, S, Bodmer, W F, Tomlinson, I P M, Houlston, R S

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Analysis of candidate modifier loci for the severity of colonic familial adenomatous polyposis, with evidence for the importance of the N-acetyl transferases von Crabtree, M D, Fletcher, C, Churchman, M, Hodgson, S V, Neale, K, Phillips, R K S, Tomlinson, I P M

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Germline PTEN mutations in Cowden syndrome-like families von Marsh, D J, Dahia, P L, Caron, S, Kum, J B, Frayling, I M, Tomlinson, I P, Hughes, K S, Eeles, R A, Hodgson, S V, Murday, V A, Houlston, R, Eng, C

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Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome von Hearle, N C M, Rudd, M F, Lim, W, Murday, V, Lim, A G, Phillips, R K, Lee, P W, O’Donohue, J, Morrison, P J, Norman, A, Hodgson, S V, Lucassen, A, Houlston, R S

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Explaining variation in familial adenomatous polyposis: relationship between genotype and phenotype and evidence for modifier genes von Crabtree, M D, Tomlinson, I P M, Hodgson, S V, Neale, K, Phillips, R K S, Houlston, R S

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Clinical and molecular features of the hereditary mixed polyposis syndrome von Whitelaw, SC, Murday, VA, Tomlinson, IP, Thomas, HJ, Cottrell, S, Ginsberg, A, Bukofzer, S, Hodgson, SV, Skudowitz, RB, Jass, JR, Talbot, IC, Northover, JM, Bodmer, WF, Solomon, E

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