Rim Amouri

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 26 publications

The Age at Onset of LRRK2 p.Gly2019Ser Parkinson's Disease Across Ancestries and Countries of Origin.

The Age at Onset of LRRK2 p.Gly2019Ser Parkinson's Disease Across Ancestries and Countries of Origin.

Journal: Annals of neurology

Published: September 04, 2025

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease.

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson's Disease.

Journal: medRxiv : the preprint server for health sciences

Published: July 17, 2025

Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease.

Rare but Relevant? Assessing Variants in Dystonia-Linked Genes in Parkinson's Disease.

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

Published: July 07, 2025

A Mild Ataxia-Dominant Phenotype of Phosphomannomutase 2-Congenital Disorder of Glycosylation in a Tunisian Family: Broadening the Geographical Scope.

A Mild Ataxia-Dominant Phenotype of Phosphomannomutase 2-Congenital Disorder of Glycosylation in a Tunisian Family: Broadening the Geographical Scope.

Journal: Journal of movement disorders

Published: April 18, 2025

Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase.

Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin Reductase.

Journal: International journal of molecular sciences

Published: March 13, 2025

The Evolution of Genetic Variability at the LRRK2 Locus.

The Evolution of Genetic Variability at the LRRK2 Locus.

Journal: Genes

Published: May 28, 2024

A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.

A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.

Journal: medRxiv : the preprint server for health sciences

Published: January 31, 2024

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.

RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.

Journal: The Lancet. Neurology

Published: January 05, 2024

Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes.

Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes.

Journal: Journal of neurogenetics

Published: December 18, 2023

Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab-Berbers.

Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab-Berbers.

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

Published: November 20, 2023

Challenges of Parkinson's disease GWASs in African people.

Challenges of Parkinson's disease GWASs in African people.

Journal: The Lancet. Neurology

Published: September 10, 2023

Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism.

Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism.

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

Published: January 18, 2023

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Last Updated: 09/26/2026