Samia B. Sassi

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 32 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

Parkinson's through a cultural lens: Diversity in disease expression and care.

Parkinson's through a cultural lens: Diversity in disease expression and care.

Journal: Journal of Parkinson's disease

Published: May 12, 2026

Primary headache disorders susceptibility is associated with fasting-related headache: evidence from a multinational study across 14 countries.

Primary headache disorders susceptibility is associated with fasting-related headache: evidence from a multinational study across 14 countries.

Journal: Frontiers in neurology

Published: April 19, 2026

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

Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural Variants.

Complementarity of Long-Reads and Optical Mapping in Parkinson's Disease for Structural Variants.

Journal: Annals of clinical and translational neurology

Published: August 26, 2025

Diffuse leptomeningeal enhancement with optic nerve involvement in a patient with intracranial hypertension as the inaugural symptom of neurosarcoidosis.

Diffuse leptomeningeal enhancement with optic nerve involvement in a patient with intracranial hypertension as the inaugural symptom of neurosarcoidosis.

Journal: Oxford medical case reports

Published: July 29, 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

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

The Genetic Architecture of Parkinson's Disease in the AfrAbia Population: Current State and Future Perspectives.

The Genetic Architecture of Parkinson's Disease in the AfrAbia Population: Current State and Future Perspectives.

Journal: Journal of integrative neuroscience

Published: February 02, 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

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

Showing 1-12 of 32

Last Updated: 09/26/2026