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Article

MAPT H1 haplotype is a risk factor for essential tremor and multiple system atrophy.

Neurology - 15 Feb 2011

Vilariño-Güell C, Soto-Ortolaza A I, Rajput A, Mash D C, Papapetropoulos S, Pahwa R, Lyons K E, Uitti R J, Wszolek Z K, Dickson D W, Farrer M J, Ross O A

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 21321341
DOI: 10.1212/WNL.0b013e31820c30c1
PMCID: PMC3053340

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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

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Linkage disequilibrium and association of MAPT H1 in Parkinson disease.Semantic proximity Read ↗

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.Semantic proximity Read ↗

Navigating the ALS Genetic Labyrinth: The Role of MAPT Haplotypes.Semantic proximity Read ↗

Exploring MAPT-containing H1 and H2 haplotypes in Parkinson’s disease across diverse populationsSemantic proximity Read ↗

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.Semantic proximity Read ↗

Genome-wide association study stratified by<i>MAPT</i>haplotypes identifies potential novel loci in Parkinson’s diseaseSemantic proximity Read ↗

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