Rolf H. Sijmons

Groningen, GR, Netherlands

Last Updated: 09/26/2026

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Found 91 publications

Metastatic mismatch repair deficient oesophageal squamous cell carcinoma leading to diagnosis of Lynch syndrome with a complete response to nivolumab treatment.

Metastatic mismatch repair deficient oesophageal squamous cell carcinoma leading to diagnosis of Lynch syndrome with a complete response to nivolumab treatment.

Journal: Virchows Archiv : an international journal of pathology

Published: August 04, 2025

Systemic barriers and opportunities for equity in early implementation of genetic testing and counseling for cardiomyopathies in Tanzania.

Systemic barriers and opportunities for equity in early implementation of genetic testing and counseling for cardiomyopathies in Tanzania.

Journal: Communications medicine

Published: December 23, 2024

Men with metastatic prostate cancer carrying a pathogenic germline variant in breast cancer genes: disclosure of genetic test results to relatives.

Men with metastatic prostate cancer carrying a pathogenic germline variant in breast cancer genes: disclosure of genetic test results to relatives.

Journal: Familial cancer

Published: December 15, 2023

Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.

Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.

Journal: Hereditary cancer in clinical practice

Published: August 13, 2023

PMS2-associated Lynch syndrome: Past, present and future.

PMS2-associated Lynch syndrome: Past, present and future.

Journal: Frontiers in oncology

Published: December 19, 2022

Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.

Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.

Journal: Annals of surgical oncology

Published: November 16, 2022

Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.

Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.

Journal: Cells

Published: November 02, 2022

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.

Journal: EClinicalMedicine

Published: October 12, 2022

AXIN2-related oligodontia-colorectal cancer syndrome with cleft palate as a possible new feature.

AXIN2-related oligodontia-colorectal cancer syndrome with cleft palate as a possible new feature.

Journal: Molecular genetics & genomic medicine

Published: August 02, 2022

Is HLA type a possible cancer risk modifier in Lynch syndrome?

Is HLA type a possible cancer risk modifier in Lynch syndrome?

Journal: International journal of cancer

Published: July 15, 2022

SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnostics.

SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnostics.

Journal: Gene

Published: February 20, 2022

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.

Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.

Journal: Hereditary cancer in clinical practice

Published: December 03, 2021

Showing 1-12 of 91

Last Updated: 09/26/2026