(Q37531274)

20 August 2017

Association of the MAPT locus with Parkinson's disease (English)

1 reference

20 August 2017

1 reference

12

1 reference

20 August 2017

11

Z K Wszolek

1 reference

20 August 2017

Carles Vilariño-Güell

2

object named as

C Vilariño-Güell

1 reference

20 August 2017

8

J M Gibson

1 reference

Alexandra I Soto-Ortolaza

20 August 2017

5

object named as

A I Soto-Ortolaza

1 reference

20 August 2017

Barbara Jasinska-Myga

3

object named as

B Jasinska-Myga

1 reference

20 August 2017

9

T Lynch

1 reference

20 August 2017

C Wider

1

1 reference

20 August 2017

M G Heckman

4

1 reference

20 August 2017

S A Cobb

6

1 reference

20 August 2017

J O Aasly

7

1 reference

20 August 2017

R J Uitti

10

1 reference

20 August 2017

O A Ross

13

1 reference

20 August 2017

12 November 2009

1 reference

European Journal of Neurology

20 August 2017

1 reference

20 August 2017

17

1 reference

20 August 2017

3

1 reference

20 August 2017

483-486

1 reference

Evolutionary toggling of the MAPT 17q21.31 inversion region

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

GSK3B polymorphisms alter transcription and splicing in Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

A common inversion under selection in Europeans

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Concurrence of alpha-synuclein and tau brain pathology in the Contursi kindred

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Score tests for association between traits and haplotypes when linkage phase is ambiguous

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Tau and synuclein and their role in neuropathology

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Diagnostic criteria for Parkinson disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Tau and alpha-synuclein in susceptibility to, and dementia in, Parkinson's disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

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

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

Initiation and Synergistic Fibrillization of Tau and Alpha-Synuclein

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

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

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906622

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

2 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2009.02847.X

Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2009.02847.X

The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2009.02847.X

The tau H2 haplotype is almost exclusively Caucasian in origin

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19912324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19912324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19912324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1468-1331.2009.02847.X

1 reference

20 August 2017

1 reference

20 August 2017

1 reference