Vincent Huin

Lille, France

Last Updated: 09/26/2026

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Found 39 publications

Large-scale functional annotation establishes a reference framework for human LRRK2 variants.

Large-scale functional annotation establishes a reference framework for human LRRK2 variants.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Expanding the Phenotype of PARK-PRKN to Spastic Paraplegia: A Report of Two Cases.

Expanding the Phenotype of PARK-PRKN to Spastic Paraplegia: A Report of Two Cases.

Journal: Movement disorders clinical practice

Published: November 25, 2025

Blood-based biomarkers of ferroptosis in Parkinson's disease.

Blood-based biomarkers of ferroptosis in Parkinson's disease.

Journal: Neurobiology of disease

Published: October 31, 2025

RPGRorf15 nanopore long-read sequencing improves retinitis pigmentosa molecular diagnosis for men and women.

RPGRorf15 nanopore long-read sequencing improves retinitis pigmentosa molecular diagnosis for men and women.

Journal: Human genetics

Published: April 23, 2025

Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series.

Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series.

Journal: Journal of neurology

Published: April 21, 2025

Conservative iron chelation for VAC14: Two-year clinical-radiological follow-up.

Conservative iron chelation for VAC14: Two-year clinical-radiological follow-up.

Journal: Journal of Parkinson's disease

Published: April 13, 2025

Two case reports of RAB39B deletion displaying highly variable parkinsonism.

Two case reports of RAB39B deletion displaying highly variable parkinsonism.

Journal: Parkinsonism & related disorders

Published: December 12, 2024

HMGA1 deficiency: a pathogenic link between tau pathology and insulin resistance.

HMGA1 deficiency: a pathogenic link between tau pathology and insulin resistance.

Journal: EBioMedicine

Published: November 08, 2024

Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report.

Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report.

Journal: BMC neurology

Published: June 06, 2024

Reply to: "Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1-Related Syndrome".

Reply to: "Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1-Related Syndrome".

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

Published: May 18, 2024

Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognition.

Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognition.

Journal: Neurobiology of disease

Published: April 22, 2024

Late-onset Kjellin syndrome: Diagnosis of SPG11 on fundus examination.

Late-onset Kjellin syndrome: Diagnosis of SPG11 on fundus examination.

Journal: European journal of ophthalmology

Published: April 13, 2024

Showing 1-12 of 39

Last Updated: 09/26/2026