Author of the publication

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study

, , , , , , , , , , , , , and . The Lancet. Oncology, 6 (8): 566–572 (2005)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed. You can also use the button next to the name to display some publications already assigned to the person.

 

Other publications of authors with the same name

N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC), , , , , , , , , and 3 other author(s). Cancer letters, 241 (1): 150–157 (2006)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)Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study, , , , , , , , , and 4 other author(s). The Lancet. Oncology, 6 (8): 566–572 (2005)'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate., , , , , , , , , and . Bioinform., 28 (23): 3027-3033 (2012)Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium, , , , , , , , , and 3 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 22 (22): 4486–4494 (2004)HNPCC-associated small bowel cancer: clinical and molecular characteristics, , , , , , , , , and 8 other author(s). Gastroenterology, 128 (3): 590–599 (2005)Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue, , , , , , , , , and 4 other author(s). Human mutation, 23 (3): 285 (2004)Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer, , , , , , , , , and 10 other author(s). International journal of cancer. Journal international du cancer, 118 (1): 115–122 (2006)Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives., , , , , , , , , and . Bioinform., 30 (15): 2189-2196 (2014)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)