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Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
Cancer Research|November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndromeD J Marsh, S Roth, K L Lunetta, et al.
British Journal of Cancer|July 17, 2003
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndromeW Lim, N Hearle, B Shah, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|September 19, 2022
Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genesC Loveday, A Garrett, P Law, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
British Journal of Cancer|March 24, 2011
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2A Osorio, R L Milne, R Alonso, et al.
BJU International|September 16, 2010
Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT studyAnita V Mitra, Elizabeth K Bancroft, Yolanda Barbachano, et al.
British Journal of Cancer|June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter studyA Jakubowska, D Rozkrut, A Antoniou, et al.
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