Shantie Jagmohan–Changur

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

Apc1638N: A mouse model for familial adenomatous polyposis–associated desmoid tumors and cutaneous cysts

Ron Smits, Willemien van der Houven van Oordt, Arne Luz et al. · Gastroenterology · 1998 · 134 citations

Tumor Biology, Tumoral Pathology, Cutaneous Cysts +9

Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor)

Raymond Poon, Ron Smits, Catherine Li et al. · Oncogene · 2001 · 106 citations · Full text

Tumor Biology, Desmoid Tumor, Fibrosis +4

SomaticApc mutations are selected upon their capacity to inactivate the ?-catenin downregulating activity

Ron Smits, Nandy Hofland, Winfried Edelmann et al. · Genes Chromosomes and Cancer · 2000 · 91 citations

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.

Shantie Jagmohan–Changur, Taija Poikonen, Susa Vilkki et al. · PubMed · 2003 · 68 citations

Genome Instability, European Crc Patients, Cancer Risk +14