Guillaume Cogan

Paris, 75013, France

Last Updated: 09/26/2026

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Found 22 publications

No role of intronic expansions in HSF1 for essential tremor in Europe.

No role of intronic expansions in HSF1 for essential tremor in Europe.

Journal: Brain : a journal of neurology

Published: December 24, 2025

Author Correction: Classification of GBA1 variants and their impact on Parkinson's disease: an in silico score analysis.

Author Correction: Classification of GBA1 variants and their impact on Parkinson's disease: an in silico score analysis.

Journal: NPJ Parkinson's disease

Published: November 21, 2025

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Toward the clinical application of long-read sequencing in repeat-expansion disorders.

Journal: Nature genetics

Published: September 03, 2025

The genetic landscape of frontotemporal lobar degeneration: investigation of a diagnostic cohort of 2747 probands.

The genetic landscape of frontotemporal lobar degeneration: investigation of a diagnostic cohort of 2747 probands.

Journal: Brain : a journal of neurology

Published: July 02, 2025

The genetics of autosomal recessive early-onset Parkinson's disease.

The genetics of autosomal recessive early-onset Parkinson's disease.

Journal: Current opinion in neurobiology

Published: June 04, 2025

Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel families.

Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel families.

Journal: NPJ Parkinson's disease

Published: March 11, 2025

Screening of Hidden Pathogenic Structural Variants in PRKN.

Screening of Hidden Pathogenic Structural Variants in PRKN.

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

Published: February 28, 2025

Utility of tissue-based assays to elucidate an autoantibody-negative paraneoplastic syndrome: Lessons from a case report.

Utility of tissue-based assays to elucidate an autoantibody-negative paraneoplastic syndrome: Lessons from a case report.

Journal: Revue neurologique

Published: February 13, 2025

Classification of GBA1 variants and their impact on Parkinson's disease: an in silico score analysis.

Classification of GBA1 variants and their impact on Parkinson's disease: an in silico score analysis.

Journal: NPJ Parkinson's disease

Published: January 27, 2025

Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping Technologies.

Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping Technologies.

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

Published: November 18, 2024

Parkinson's disease: from genetics to targeted therapies

Parkinson's disease: from genetics to targeted therapies

Journal: Comptes rendus biologies

Published: November 02, 2024

Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.

Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.

Journal: medRxiv : the preprint server for health sciences

Published: August 16, 2024

Showing 1-12 of 22

Last Updated: 09/26/2026