Bitten Schönewolf-Greulich

7PUBLICATIONS
54CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Gene and molecular therapy
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Publications (7)

|May 22, 2024
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA.

Nicole Revencu, Astrid Eijkelenboom, Claire Bracquemart

|Aug 20, 2021
Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders.

Miriam Nøstvik, Sarah M Kateta, Bitten Schönewolf-Greulich

|Jul 23, 2021
Decline in gross motor skills in adult Rett syndrome; results from a Danish longitudinal study.

Anne-Marie Bisgaard, Kingsley Wong, Anne-Katrine Højfeldt

|Jul 03, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.

Stephanie Oates, Michael Absoud, Sushma Goyal

|Jul 12, 2020
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A).

Simranpreet Kaur, Nicole J Van Bergen, Kristen J Verhey

|Nov 13, 2018
Mosaic MECP2 variants in males with classical Rett syndrome features, including stereotypical hand movements.

Bitten Schönewolf-Greulich, Anne-Marie Bisgaard, Morten Dunø

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Frequent Collaborators

3 joint publications

Zeynep Tümer

1 joint publications

Simranpreet Kaur

1 joint publications

Nicole J Van Bergen

1 joint publications

Kristen J Verhey