Joanne Trinh

Ratzeburger Allee 160
Luebeck, SH 23562, Germany

Last Updated: 09/26/2026

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Found 102 publications

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

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

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

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

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

PSMF1 Variants in a German Parkinson's Disease Cohort.

PSMF1 Variants in a German Parkinson's Disease Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: May 04, 2026

Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease.

Massive-scale single-nucleus multi-omics identifies novel rare noncoding drivers of Parkinson's disease.

Journal: bioRxiv : the preprint server for biology

Published: March 23, 2026

Lifestyle interventions for Parkinson's disease - Authors' reply.

Lifestyle interventions for Parkinson's disease - Authors' reply.

Journal: The Lancet. Neurology

Published: February 12, 2026

Phenotypic spectrum of FGF14-related late-onset ataxia: predominant tremor and cognitive decline as key features of SCA27A.

Phenotypic spectrum of FGF14-related late-onset ataxia: predominant tremor and cognitive decline as key features of SCA27A.

Journal: Journal of neurology

Published: January 29, 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

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 23, 2025

Validation of a Mitochondrial Polygenic Score for Parkinson's Disease.

Validation of a Mitochondrial Polygenic Score for Parkinson's Disease.

Journal: medRxiv : the preprint server for health sciences

Published: October 01, 2025

Showing 1-12 of 102

Last Updated: 09/26/2026