Ana Westenberger

Ratzeburger Allee 160
Luebeck, SH 23538, Germany

Last Updated: 09/26/2026

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Found 105 publications

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Journal: medRxiv : the preprint server for health sciences
Published: July 03, 2026

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Repeat expansions in Parkinson's disease and parkinsonism across ancestries: insights from a global genetic cohort.

Journal: medRxiv : the preprint server for health sciences
Published: July 03, 2026

X-linked dystonia parkinsonism as a cause of isolated lingual dystonia (ILD).

X-linked dystonia parkinsonism as a cause of isolated lingual dystonia (ILD).

Journal: Journal of neural transmission (Vienna, Austria : 1996)
Published: June 13, 2026

Genetic Testing by Age at Onset in Parkinson Disease.

Genetic Testing by Age at Onset in Parkinson Disease.

Journal: JAMA neurology
Published: May 11, 2026

Reply to: "Unravelling the Complexity of VPS16 Splicing: Clinical Implications and Unresolved Questions".

Reply to: "Unravelling the Complexity of VPS16 Splicing: Clinical Implications and Unresolved Questions".

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 13, 2026

How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's disease.

How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's disease.

Journal: medRxiv : the preprint server for health sciences
Published: January 02, 2026

Striatal hyperechogenicity as an ultrasound imaging marker for prodromal X-linked dystonia-parkinsonism.

Striatal hyperechogenicity as an ultrasound imaging marker for prodromal X-linked dystonia-parkinsonism.

Journal: NPJ Parkinson's disease
Published: October 13, 2025

Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and Management.

Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and Management.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 01, 2025

Pathogenic or Likely Pathogenic GRN Variants Are Found in 0.1% of Parkinson's Disease Patients.

Pathogenic or Likely Pathogenic GRN Variants Are Found in 0.1% of Parkinson's Disease Patients.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: September 12, 2025

Expanding the Genetic and Phenotypic Spectrum of DYT-VPS16: The Importance of Splice-Site Variants.

Expanding the Genetic and Phenotypic Spectrum of DYT-VPS16: The Importance of Splice-Site Variants.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 30, 2025

Reply to: "Two Families with ANO10-Related Spinocerebellar Ataxia with Novel Exon Deletions: A First Report from India".

Reply to: "Two Families with ANO10-Related Spinocerebellar Ataxia with Novel Exon Deletions: A First Report from India".

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 19, 2024

FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?

FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B?

Journal: Brain : a journal of neurology
Published: November 13, 2024
Showing 1-12 of 105

Last Updated: 09/26/2026