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Disambiguation of "Holinski-Feder, Elke"

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Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

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Elke Holinski-Feder

Detlef Holinski

Rüdiger Holinski

Sebastian Holinski

Rajae Elkehal

 

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)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)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)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)Risks of less common cancers in proven mutation carriers with lynch syndrome, , , , , , , , , and 14 other author(s). Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 30 (35): 4409–4415 (2012)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)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)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)Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer, , , , , , , , , and 4 other author(s). Cancer letters, 236 (2): 191–197 (2006)