Esther M Verheyen

20PUBLICATIONS
19CO-AUTHORS
Developmental genetics (incl. sex determination)Molecular targetsEpigenetics (incl. genome methylation and epigenomics)Cancer geneticsDisease surveillance
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Publications (20)

|Jul 09, 2026
The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

|Jun 16, 2026
A Drosophila tumor model identifies a conserved Upd-JAK/STAT-Akh signaling axis associated with metabolic changes in cancer cachexia.

|Nov 18, 2025
Uncovering functional insights into human pathogenic variants in CDK19 using Drosophila models.

Karampal S Grewal, Christopher Tam, Jenny Z Liao

|Jul 02, 2025
Robinow syndrome DVL1 variants disrupt morphogenesis and appendage formation in a Drosophila disease model.

Gamze Akarsu, Katja R MacCharles, Kenneth Kin Lam Wong

|Jul 05, 2024
Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndrome.

Shruti S Tophkhane, Katherine Fu, Esther M Verheyen

|Apr 18, 2024
Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila.

Jenny Zhe Liao, Hyung-Lok Chung, Claire Shih

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Frequent Collaborators

4 joint publications

Joy M Richman

1 joint publications

David J Vocadlo

1 joint publications

Kenneth Kin Lam Wong

1 joint publications

Payel Ganguly