Simone Zittel-Dirks

20PUBLICATIONS

141CO-AUTHORS

Gene mappingAnthropological geneticsNeurology and neuromuscular diseasesPyrometallurgyGene expression (incl. microarray and other genome-wide approaches)

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Publications (20)

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|Jul 03, 2026

Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variants.

|Jun 29, 2026

Phenotype and Genetics of Spinocerebellar Ataxia Type 27B: Novel Movement-disorder Features, Cognitive Impairment, and Repeat Expansion Findings.

|May 16, 2026

Inhibitory Circuits of the Sensorimotor Network are Not Modulated By Cerebellar Transcranial Direct Current Stimulation in Isolated Cervical Dystonia.

|Feb 14, 2026

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Oct 17, 2025

RAB32-Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe Criteria.

Teresa Kleinz, Francesco Cavallieri, Max Borsche

|Jun 03, 2025

Structure-function association of the cerebellar motor network is altered in isolated cervical dystonia.

Kai Grimm, Hanna Braaß, Fatemeh Sadeghi

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Frequent Collaborators

Kai Grimm

Alexander Münchau

Katja Lohmann

Fatemeh Sadeghihassanabadi

Anne Weissbach

Christoph Kamm

Alberto J Espay

Norbert Brüggemann

Alexander Y Pantelyat

2 joint publications

Friederike Borngräber

Frequent Collaborators

Kai Grimm

Alexander Münchau

Katja Lohmann

Fatemeh Sadeghihassanabadi