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Page 1
Colorectal cancer risk in monoallelic carriers of MYH variants.
Webb EL, Rudd MF, Houlston RS. Webb EL, et al. Among authors: rudd mf. Am J Hum Genet. 2006 Oct;79(4):768-71; author reply 771-2. doi: 10.1086/507912. Am J Hum Genet. 2006. PMID: 16960817 Free PMC article. No abstract available.
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
Hearle NC, Rudd MF, Lim W, Murday V, Lim AG, Phillips RK, Lee PW, O'donohue J, Morrison PJ, Norman A, Hodgson SV, Lucassen A, Houlston RS. Hearle NC, et al. Among authors: rudd mf. J Med Genet. 2006 Apr;43(4):e15. doi: 10.1136/jmg.2005.036830. J Med Genet. 2006. PMID: 16582077 Free PMC article.
Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
Webb EL, Rudd MF, Sellick GS, El Galta R, Bethke L, Wood W, Fletcher O, Penegar S, Withey L, Qureshi M, Johnson N, Tomlinson I, Gray R, Peto J, Houlston RS. Webb EL, et al. Among authors: rudd mf. Hum Mol Genet. 2006 Nov 1;15(21):3263-71. doi: 10.1093/hmg/ddl401. Epub 2006 Sep 25. Hum Mol Genet. 2006. PMID: 17000706
Variants in the GH-IGF axis confer susceptibility to lung cancer.
Rudd MF, Webb EL, Matakidou A, Sellick GS, Williams RD, Bridle H, Eisen T, Houlston RS; GELCAPS Consortium. Rudd MF, et al. Genome Res. 2006 Jun;16(6):693-701. doi: 10.1101/gr.5120106. Genome Res. 2006. PMID: 16741161 Free PMC article.
15 results