Nicolas Dierckxsens

6PUBLICATIONS
35CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Biological oceanographyHaematological tumoursSequence analysis
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Publications (6)

|Apr 18, 2026
Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversion.

|Nov 13, 2024
Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome.

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos

|Aug 20, 2024
Tracing Homopolymers in Oikopleura dioica's Mitogenome.

Nicolas Dierckxsens, Kosei Watanabe, Yongkai Tan

|Apr 02, 2024
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome.

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos

|May 25, 2022
Primary mediastinal large B-cell lymphoma is characterized by large-scale copy-neutral loss of heterozygosity.

Stefania Tuveri, Koen Debackere, Lukas Marcelis

|Dec 16, 2021
A benchmark of structural variation detection by long reads through a realistic simulated model.

Nicolas Dierckxsens, Tong Li, Joris R Vermeesch

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Frequent Collaborators

4 joint publications

Joris Robert Vermeesch

3 joint publications

Ann Swillen

3 joint publications

Erika Souche

2 joint publications

Hilde Van Esch