Marjo van Puijenbroek

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

Yvonne Hendriks, Anja Wagner, Hans Morreau et al. · Gastroenterology · 2004 · 427 citations · Full text

Somatic Variant, Cancer Epidemiology, Cancer Risk +10

The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC

Andrea E. van der Meulen‐de Jong, Hans Morreau, Marjo van Puijenbroek et al. · Gastroenterology · 2003 · 216 citations

Gene Therapies, Genome Instability, Mendelian Disorder +8

Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

Andrea E. van der Meulen‐de Jong, Marjo van Puijenbroek, Yvonne Hendriks et al. · Clinical Cancer Research · 2004 · 212 citations · Full text

Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 Gene

Anja Wagner, Alicia Barrows, Juul Wijnen et al. · The American Journal of Human Genetics · 2003 · 207 citations · Full text

Oncology, Somatic Variant, Medicine +11

Heterozygous Mutations in PMS2 Cause Hereditary Nonpolyposis Colorectal Carcinoma (Lynch Syndrome)

Yvonne Hendriks, Shantie Jagmohan–Changur, Heleen M. van der Klift et al. · Gastroenterology · 2006 · 153 citations · Full text

Lynch Syndrome, Genetic Disorder, Genetics +6