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Disambiguation of "Propping, Peter"

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Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

, , , , , , , , , , , , , , , , , , , , , and . BMC gastroenterology, (2010)

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Peter Propping

Ernst Propping

Dirk Propping

Stefan Propping

Walter Propping

 

Other publications of authors with the same name

Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer, , , , , , , , , and 9 other author(s). Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 8 (2): 174–182 (2010)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)Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer, , , , , , , , , and 10 other author(s). International journal of cancer. Journal international du cancer, 116 (5): 692–702 (2005)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)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)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)Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium, , , , , , , , , and 10 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 24 (26): 4285–4292 (2006)Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3, , , , , , , , , and 16 other author(s). Carcinogenesis, 35 (2): 315–323 (2014)Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome, , , , , and . Deutsches Ärzteblatt international, 110 (3): 32–38 (2013)