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No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients, , , , , , , , , and 3 other author(s). European journal of human genetics : EJHG, 16 (5): 587–592 (2008)Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies, , , , , , , , , and 8 other author(s). Familial cancer, 10 (2): 273–284 (2011)Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families, , , , , , , , , and 16 other author(s). Cancer letters, 271 (1): 153–157 (2008)Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study, , , , , , , , , and 12 other author(s). BMC gastroenterology, (2010)Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility, , , , , , , , , and 24 other author(s). Carcinogenesis, 31 (9): 1612–1619 (2010)Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin, , , , , , , , , and 14 other author(s). PloS one, 6 (6): e20464 (2011)Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications, , , , , , , , , and 19 other author(s). International journal of molecular epidemiology and genetics, 2 (1): 36–50 (2011)