Dilys D. Weijers

Utrecht, UT, Netherlands

Last Updated: 09/26/2026

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Found 9 publications

Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Paris, France, November 16th 2022.

Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C4CMMRD), Paris, France, November 16th 2022.

Journal: Familial cancer
Published: May 16, 2024

T-cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD): Exploring treatment opportunities.

T-cell lymphoblastic lymphoma in constitutional mismatch repair deficiency (CMMRD): Exploring treatment opportunities.

Journal: HemaSphere
Published: February 26, 2024

Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency.

Unraveling mutagenic processes influencing the tumor mutational patterns of individuals with constitutional mismatch repair deficiency.

Journal: Nature communications
Published: November 22, 2023

Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations.

Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations.

Journal: International journal of cancer
Published: June 30, 2023

Clinical and laboratory diversity of diffuse large B-cell lymphomas in children with Nijmegen breakage syndrome.

Clinical and laboratory diversity of diffuse large B-cell lymphomas in children with Nijmegen breakage syndrome.

Journal: Haematologica
Published: November 20, 2022

High Prevalence of Constitutional Mismatch Repair Deficiency in a Pediatric T-cell Lymphoblastic Lymphoma Cohort.

High Prevalence of Constitutional Mismatch Repair Deficiency in a Pediatric T-cell Lymphoblastic Lymphoma Cohort.

Journal: HemaSphere
Published: September 08, 2021

Challenges of Neoantigen Targeting in Lynch Syndrome and Constitutional Mismatch Repair Deficiency Syndrome.

Challenges of Neoantigen Targeting in Lynch Syndrome and Constitutional Mismatch Repair Deficiency Syndrome.

Journal: Cancers
Published: April 07, 2021

De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.

De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.

Journal: American journal of human genetics
Published: April 09, 2020

Maternal inflammation has a profound effect on cortical interneuron development in a stage and subtype-specific manner.

Maternal inflammation has a profound effect on cortical interneuron development in a stage and subtype-specific manner.

Journal: Molecular psychiatry
Published: August 15, 2018
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Last Updated: 09/26/2026