Y. Tiersma

发表

Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome

Andrea Rakushin Lee, N. de Wind, L. Rasmussen, 2020, Genetics in Medicine.

Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation

N. de Wind, A. Spurdle, S. Tavtigian, 2020, Frontiers in Genetics.

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

N. de Wind, H. Morreau, T. van Wezel, 2020, Genes, chromosomes & cancer.

Functional assay-based classification of PMS2 variants in Lynch Syndrome

N. de Wind, A. Spurdle, B. Thompson, 2021 .

β-Lactamase-producing bacteriaHow can I resist you?

A. Fleming, Y. Tiersma, 2013 .

A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

Rolf H. Sijmons, Amanda B. Spurdle, Sean V. Tavtigian, 2018, Genetics in Medicine.

Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

P. Devilee, C. Asperen, S. Verhoef, 2016, Human mutation.

Increased numbers of CD5+ B lymphocytes with a regulatory phenotype in spondylarthritis.

P. Tak, N. de Vries, M. Doorenspleet, 2012, Arthritis and rheumatism.

A functional assay–based procedure to classify mismatch repair gene variants in Lynch syndrome

L. Rasmussen, A. Spurdle, J. Osinga, 2018, Genetics in Medicine.

Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome

Andrea Rakushin Lee, N. de Wind, L. Rasmussen, 2020, Genetics in Medicine.

Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome

A. Spurdle, B. Thompson, M. Drost, 2022, Human mutation.