Juul T. Wijnen

Leiden, ZH, Netherlands

Last Updated: 09/26/2026

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Found 66 publications

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.

A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.

Journal: Scientific reports

Published: November 10, 2020

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material.

The complexity of screening PMS2 in DNA isolated from formalin-fixed paraffin-embedded material.

Journal: European journal of human genetics : EJHG

Published: September 25, 2018

Cancer Risks for PMS2-Associated Lynch Syndrome.

Cancer Risks for PMS2-Associated Lynch Syndrome.

Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology

Published: August 31, 2018

Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue.

Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue.

Journal: The Journal of molecular diagnostics : JMD

Published: March 06, 2018

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Journal: British journal of cancer

Published: January 24, 2018

SNP association study in PMS2-associated Lynch syndrome.

SNP association study in PMS2-associated Lynch syndrome.

Journal: Familial cancer

Published: November 18, 2017

Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.

Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.

Journal: International journal of cancer

Published: November 15, 2017

Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer.

Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer.

Journal: Familial cancer

Published: November 11, 2017

RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing.

RNA analysis of cancer predisposing genes in formalin-fixed paraffin-embedded tissue determines aberrant splicing.

Journal: European journal of human genetics : EJHG

Published: August 18, 2017

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.

Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report.

Journal: Hereditary cancer in clinical practice

Published: June 08, 2017

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia.

Journal: British journal of cancer

Published: March 21, 2017

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.

Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database.

Journal: Gut

Published: February 28, 2017

Showing 1-12 of 66

Last Updated: 09/26/2026