Emma von Scheibler

8PUBLICATIONS
26CO-AUTHORS
Social epidemiologyEpigenetics (incl. genome methylation and epigenomics)Child and adolescent developmentGene expression (incl. microarray and other genome-wide approaches)Neurogenetics
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Publications (8)

|Feb 07, 2025
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter Study.

Emma N M M von Scheibler, Ann Swillen, Gabriela M Repetto

|Nov 30, 2024
Obesity and metabolic syndrome in adults with a 22q11.2 microdeletion.

Hester Jaspers Faijer-Westerink, Emma N M M von Scheibler, Elisabeth F C van Rossum

|Nov 11, 2024
Cognitive, adaptive and daily life functioning in adults with 22q11.2 deletion syndrome.

Claudia Vingerhoets, Julia Ruiz-Fernandez, Emma von Scheibler

|Mar 17, 2024
Copy number variant risk loci for schizophrenia converge on the BDNF pathway.

Friederike Ehrhart, Ana Silva, Therese van Amelsvoort

|Nov 02, 2023
Hearing loss and history of otolaryngological conditions in adults with microdeletion 22q11.2.

Emma N M M von Scheibler, Josine C C Widdershoven, Denise C P B M van Barneveld

|Jan 26, 2023
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.

Emma N M M von Scheibler, Agnies M van Eeghen, Tom J de Koning

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Frequent Collaborators

6 joint publications

Erik Boot

5 joint publications

Therese van Amelsvoort

4 joint publications

Agnies M van Eeghen

2 joint publications

Claudia Vingerhoets