(Q43339552)

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

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scholarly article

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19 November 2017

MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium (English)

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19 November 2017

Alzheimer's disease

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19 November 2017

Alfredo Ramirez

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19 November 2017

Miguel Ángel Fernández-Blázquez

object named as

Miguel Ángel Fernández-Blázquez

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Eva Carro

10

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Marian M. de Pancorbo

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Marian M de Pancorbo

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Pau Pastor

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María A Pastor

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María A Pastor

31

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Jaime Kulisevsky

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Jaime Kulisevsky

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12

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Eliecer Coto

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author name string

Fermín Moreno

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Jordi Clarimón

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Agustín Ruiz

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Onofre Combarros

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Adolfo López de Munain

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Maria J Bullido

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Anna Antonell

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Sara Ortega-Cubero

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Isabel Hernandez

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Lluís Tárraga

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Mercè Boada

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Alberto Lleó

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Oriol Dols-Icardo

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José Luis Vázquez-Higuera

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Jon Infante

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Alberto Rábano

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Meritxell Valentí

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Begoña Indakoetxea

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Myriam Barandiarán

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Ana Gorostidi

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Ana Frank-García

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Isabel Sastre

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Elena Lorenzo

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Xabier Elcoroaristizabal

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Martina Lennarz

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Wolfang Maier

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Manuel Serrano-Ríos

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Suzee E Lee

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Pascual Sánchez-Juan

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19 November 2017

Dementia Genetic Spanish Consortium (DEGESCO)

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19 November 2017

publication date

29 September 2015

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19 November 2017

Journal of Alzheimer's Disease

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19 November 2017

49

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2

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343-352

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19 November 2017

Tau protein and neurodegeneration

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Interface between tauopathies and synucleinopathies: A tale of two proteins

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Colocalization of Tau and Alpha-Synuclein Epitopes in Lewy Bodies

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Genetic evidence for the involvement of tau in progressive supranuclear palsy

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Association between the extended tau haplotype and frontotemporal dementia.

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Genome-wide association study reveals genetic risk underlying Parkinson's disease

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

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https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Neurodegenerative disease phenotypes in carriers of MAPT p.A152T, a risk factor for frontotemporal dementia spectrum disorders and Alzheimer disease

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

"Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation.

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Overcoming the winner's curse: estimating penetrance parameters from case-control data

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Deciphering the mechanism underlying late-onset Alzheimer disease

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

The Effect of MAPT H1 and APOE ε4 on Transition from Mild Cognitive Impairment to Dementia

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Comment: Double mutants of frontotemporal dementia genes--Simple co-occurrence?

1 reference

https://api.crossref.org/works/10.3233%2FJAD-150555

21 January 2018

Identifiers

10.3233/JAD-150555

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Europe PubMed Central

PubMed publication ID

19 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

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19 November 2017

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