Erika Souche

4PUBLICATIONS
30CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Molecular targets
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Publications (4)

|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

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

Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos

|Nov 12, 2017
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.

Maria A Rujano, Magda Cannata Serio, Ganna Panasyuk

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Frequent Collaborators

3 joint publications

Ann Swillen

3 joint publications

Joris R Vermeesch

3 joint publications

Nicolas Dierckxsens

2 joint publications

Anne S Bassett