Yvonne Tiersma
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
An accurate cellular assay to determine pathogenicity of coding and noncoding variants in Lynch syndrome genes.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: January 16, 2026
High resolution clonal architecture of hypomutated Wilms tumours.
Journal: Nature communications
Published: January 08, 2025
Predictive functional assay-based classification of PMS2 variants in Lynch syndrome.
Journal: Human mutation
Published: November 09, 2021
Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer.
Journal: Genes, chromosomes & cancer
Published: March 04, 2020
Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation.
Journal: Frontiers in genetics
Published: February 20, 2020
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 10, 2019
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 27, 2018
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
Journal: Human mutation
Published: February 19, 2016
Increased numbers of CD5+ B lymphocytes with a regulatory phenotype in spondylarthritis.
Journal: Arthritis and rheumatism
Published: January 11, 2012
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Last Updated: 09/26/2026