Search Results - "Chantereault C"

Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.

Authors: Senkevich K Parlar SC Chantereault C et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2026 Jun 10. Date of Electronic Publication: 2026 Jun 10.

Publication Type: Journal Article

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

Rare-variant burden across lysosomal genes implicates sialylation and ganglioside metabolism in Parkinson's disease.

Authors: Senkevich K Parlar SC Chantereault C et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2026 Feb 18. Date of Electronic Publication: 2026 Feb 18.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?

Authors: Senkevich K Parlar SC Chantereault C et al.

Source: NPJ Parkinson's disease [NPJ Parkinsons Dis] 2024 Oct 25; Vol. 10 (1), pp. 201. Date of Electronic Publication: 2024 Oct 25.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 101675390 Publication Model: Electronic Cited Medium: Print ISSN: 2373-8057 (Print) Linking ISSN: 23738057 NLM ISO Abbreviation: NPJ Parkinsons Dis Subsets: PubMed not MEDLINE