Selina Reich

4PUBLICATIONS
12CO-AUTHORS
Neurology and neuromuscular diseasesCardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (4)

|Apr 01, 2025
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism.

Holger Hengel, Shabab B Hannan, Selina Reich

|Dec 12, 2024
Elevated cholesterol is a common phenotype for dominant and recessive ATAD3-associated disorders.

Ann-Sophie Kiesel, Lucia Laugwitz, Rebecca Buchert

|Aug 01, 2022
Repeat expansions nested within tandem CNVs: a unique structural change in GLS exemplifies the diagnostic challenges of non-coding pathogenic variation.

Sarah Fazal, Matt C Danzi, André B P van Kuilenburg

|Jun 23, 2021
Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans.

Jack J Collier, Claire Guissart, Monika Oláhová

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Frequent Collaborators

3 joint publications

Matthis Synofzik

1 joint publications

Fumi Suomi

1 joint publications

Fowzan S Alkuraya

1 joint publications

Robert W Taylor