Lisa Ehlers

12PUBLICATIONS
121CO-AUTHORS
AutoimmunityGene expression (incl. microarray and other genome-wide approaches)Haematological tumoursDevelopmental genetics (incl. sex determination)Infant and child health
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Publications (12)

|Aug 04, 2026
Adenosine deaminase type 2 deficiency: From rare to common.

|Jun 18, 2026
ADA2 genotype and enzyme activity may predict vasculitic or hematologic DADA2 phenotype.

|Mar 23, 2026
ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

Lisa Ehlers, Marjon Wouters, Bethany Pillay

|Aug 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Marjon Wouters, Lisa Ehlers, Wout Van Eynde

|Mar 13, 2025
TGFβ links EBV to multisystem inflammatory syndrome in children.

Carl Christoph Goetzke, Mona Massoud, Stefan Frischbutter

|Dec 23, 2024
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Marjon Wouters, Lisa Ehlers, Wout Van Eynde

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Frequent Collaborators

5 joint publications

Isabelle Meyts

3 joint publications

Marjon Wouters

3 joint publications

Christian Dejaco

3 joint publications

Giorgia Bucciol