D. Terlouw

Prevalence of mismatch repair deficiency and Lynch syndrome in a cohort of unselected small bowel adenocarcinomas

H. Morreau, T. van Wezel, M. Nielsen, 2020, Journal of Clinical Pathology.

Recurrent APC splice variant c.835-8A>G in patients with unexplained colorectal polyposis fulfilling the colibactin mutational signature.

Arnoud Boot, H. Morreau, T. van Wezel, 2020, Gastroenterology.

The diverse molecular profiles of lynch syndrome-associated colorectal cancers are (highly) dependent on underlying germline mismatch repair mutations.

H. Morreau, T. van Wezel, M. Nielsen, 2021, Critical reviews in oncology/hematology.

Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy

H. Morreau, T. van Wezel, H. Vasen, 2019, European Journal of Human Genetics.

Mismatch Repair Deficiency and MUTYH Variants in Small Intestine-Neuroendocrine Tumors.

H. Morreau, T. van Wezel, M. Nielsen, 2022, Human pathology.

Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients

Arnoud Boot, H. Morreau, T. van Wezel, 2023, medRxiv.

Molecular functions of MCM8 and MCM9 and their associated pathologies

H. Morreau, T. van Wezel, Y. Goldberg, 2023, iScience.

Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers.

N. de Wind, A. Wagner, H. Morreau, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Performance of a RAD51-based functional HRD test on paraffin-embedded breast cancer tissue

N. T. Ter Haar, Lise M van Wijk, M. Vreeswijk, 2023, Breast Cancer Research and Treatment.

MLH1 Promotor Hypermethylation in Colorectal and Endometrial Carcinomas from Patients with Lynch Syndrome.

H. Morreau, T. van Wezel, T. Bosse, 2023, The Journal of molecular diagnostics : JMD.