Meret Wegler

3PUBLICATIONS
84CO-AUTHORS
Developmental genetics (incl. sex determination)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (3)

|Mar 13, 2026
Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome.

Aya Abu-El-Haija, Allan Bayat, Hanifenur Mancılar

|Jan 31, 2024
Unveiling the crucial neuronal role of the proteasomal ATPase subunit gene PSMC5 in neurodevelopmental proteasomopathies.

Sébastien Küry, Janelle E Stanton, Geeske van Woerden

|Jan 07, 2021
Congenital cervical spine malformation due to bi-allelic RIPPLY2 variants in spondylocostal dysostosis type 6.

Meret Wegler, Christian Roth, Eckehard Schumann

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Frequent Collaborators

1 joint publications

Sébastien Küry

1 joint publications

Janelle E Stanton

1 joint publications

Geeske van Woerden

1 joint publications

Tzung-Chien Hsieh