Author

Senne Meynants

KU LeuvenORCID 0009-0006-7055-3737Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Ann SwilleniD· 2 shared Erika L. SoucheiD· 2 shared Jeroen BreckpotiD· 2 shared Nicolas DierckxsensiD· 2 shared Adam FrankishiD· 1 shared Alawi A.A. Alsheikh-AliiD· 1 shared Andrea GuarracinoiD· 1 shared Andrew P. BlairiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Ann SwillenORCID

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2 papers

Recent·Most cited

GenomicsNature CommunicationsPeer-reviewedApr 18, 2026

Population differences of chromosome 22q11.2 duplication structure predispose differentially to microdeletion and inversion.

David Porubskỳ, DongAhn Yoo, Nidhi Koundinya…·Todd L. Hillaker

The paper analyzes chromosome 22q11.2 haplotypes to show how structural variations in specific regions correlate with microdeletion and inversion risks across populations.

3 citationstop 1%

humanwhole-genome sequencing

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GeneticsbioRxivPreprintMar 14, 2024

Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos…·Joris Robert Vermeesch

The paper investigates the mechanisms behind the high incidence of 22q11.2 deletion syndrome by analyzing recombination events and paralogous structures in LCR22 regions.

DOI 10.1101/2024.03.14.585046

humanwhole-genome sequencing

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