Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.

doi:10.1002/mds.27385

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.

Movement disorders : official journal of the Movement Disorder Society - 1 Jul 2018

Li Jiao, Ruskey Jennifer A, Arnulf Isabelle, Dauvilliers Yves, Hu Michele T M, Högl Birgit, Leblond Claire S, Zhou Sirui, Ambalavanan Amirthagowri, Ross Jay P, Bourassa Cynthia V, Spiegelman Dan, Laurent Sandra B, Stefani Ambra, Charley Monaca Christelle, Cochen De Cock Valérie, Boivin Michel, Ferini-Strambi Luigi, Plazzi Giuseppe, Antelmi Elena, Young Peter, Heidbreder Anna, Labbe Catherine, Ferman Tanis J, Dion Patrick A, Fan Dongsheng, Desautels Alex, Gagnon Jean-François, Dupré Nicolas, Fon Edward A, Montplaisir Jacques Y, Boeve Bradley F, Postuma Ronald B, Rouleau Guy A, Ross Owen A, Gan-Or Ziv

Abstract excerpt

BACKGROUND: MAPT haplotypes are associated with PD, but their association with rapid eye movement sleep behavior disorder is unclear. OBJECTIVE: To study the role of MAPT variants in rapid eye movement sleep behavior disorder. METHODS: Two cohorts were included: (A) PD (n = 600), rapid eye movement sleep behavior disorder (n = 613) patients, and controls (n = 981); (B) dementia with Lewy bodies patients with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Aged

Share to Cohort Studies

Share to Gene Frequency

Share to Lewy Body Disease

Share to Parkinson Disease

Share to Polymorphism, Single Nucleotide

Share to Principal Component Analysis

Share to tau Proteins

Source

Open in PubMed

Identifiers

PMID: 29756641
DOI: 10.1002/mds.27385

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder.PMID 29756641Read ↗

Genome-wide association study stratified byMAPThaplotypes identifies potential novel loci in Parkinson’s diseaseSemantic proximity Read ↗

Family-based association analysis of the MAPT gene in Parkinson disease.Semantic proximity Read ↗

Shared Genetic Architecture Between Parkinson’s Disease and Sleep-Related Traits Implicates theMAPTLocus on Chromosome 17Semantic proximity Read ↗

MAPTallele and haplotype frequencies in Nigerian Africans: population distribution and association with Parkinson’s disease risk and age at onsetSemantic proximity Read ↗

MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis.Semantic proximity Read ↗

Dementia risk in Parkinson disease: disentangling the role of MAPT haplotypes.Semantic proximity Read ↗

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.Semantic proximity Read ↗

Genetic Architecture of MAPT Gene Region in Parkinson Disease SubtypesSemantic proximity Read ↗

MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset.Semantic proximity Read ↗

MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies.Semantic proximity Read ↗

The Role of MAPT Haplotype H2 and Isoform 1N/4R in Parkinsonism of Older Adults.Semantic proximity Read ↗

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.