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Ann Swillen

21PUBLICATIONS

90CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Data mining and knowledge discoveryEarly English languagesSocial epidemiology

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Publications (21)

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|Apr 18, 2026

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

|Mar 27, 2026

Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome.

Jhih-Rong Lin, Daniella Miller, Dana Luong

|Dec 08, 2025

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22-23 Deletions.

Tanner J Nelson, Daniel E McGinn, T Blaine Crowley

|Aug 20, 2025

MINDDS-connect: a federated data platform integrating biobanks for meta cohort building and analysis.

Benjamin Huremagic, Nishkala Sattanathan, Mathilde Geysens

|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

|Oct 17, 2024

Language Profiles of School-Age Children With 16p11.2 Copy Number Variants in a Clinically Ascertained Cohort.

Jente Verbesselt, Jeroen Breckpot, Inge Zink

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Frequent Collaborators

9 joint publications

Donna M McDonald-McGinn

8 joint publications

Jeroen Breckpot

8 joint publications

Anne S Bassett

6 joint publications

Joris Robert Vermeesch

5 joint publications

Jente Verbesselt

5 joint publications

T Blaine Crowley

4 joint publications

Inge Zink

4 joint publications

Beverly S Emanuel

4 joint publications

Carrie E Bearden

4 joint publications

Michael J Owen

Frequent Collaborators

9 joint publications

Donna M McDonald-McGinn

8 joint publications

Jeroen Breckpot

8 joint publications

Anne S Bassett

6 joint publications

Joris Robert Vermeesch

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