Constanze Pagenstecher

High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas et al. · Human Mutation · 2005 · 285 citations

Life Sciences, Genetics, Molecular Genetics +17

Lower Incidence of Colorectal Cancer and Later Age of Disease Onset in 27 Families With Pathogenic <i>MSH6</i> Germline Mutations Compared With Families With <i>MLH1</i> or <i>MSH2</i> Mutations: The German Hereditary Nonpolyposis Colorectal Cancer Consortium

Jens Plaschke, Christoph Engel, Stefan Krüger et al. · Journal of Clinical Oncology · 2004 · 245 citations · Full text

Life Sciences, Genetics, Oncology +17

HNPCC-associated small bowel cancer: Clinical and molecular characteristics

Karsten Schulmann, Frank Brasch, Erdmute Kunstmann et al. · Gastroenterology · 2005 · 199 citations · Full text

Medicine, Molecular Biology, Oncology +14

<i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

Stefan Aretz, Siegfried Uhlhaas, Heike Goergens et al. · International Journal of Cancer · 2006 · 195 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genotype-Phenotype Comparison of German <i>MLH1</i> and <i>MSH2</i> Mutation Carriers Clinically Affected With Lynch Syndrome: A Report by the German HNPCC Consortium

Timm O. Goecke, Karsten Schulmann, Christoph Engel et al. · Journal of Clinical Oncology · 2006 · 151 citations · Full text

Life Sciences, Genetics, Oncology +12