Ann Swillen

23PUBLICATIONS
110CO-AUTHORS
Infant and child healthSocial program evaluationEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Data mining and knowledge discovery
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Publications (23)

|Oct 09, 2026
'A Constant Battle for Services': Parents' Experiences on Healthcare Services for Children With 22q11 Deletion Syndrome.

|Aug 07, 2026
Multicenter retrospective study on perceived effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndrome.

|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

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Frequent Collaborators

9 joint publications

Donna M McDonald-McGinn

8 joint publications

Anne S Bassett

8 joint publications

Jeroen Breckpot

6 joint publications

Joris Robert Vermeesch