(Q35447435)

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

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Europe PubMed Central

PubMed publication ID

8 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

progressive supranuclear palsy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

Dennis W. Dickson

13

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

object named as

D Leung

8

0 references

Andrew John Lees

16

object named as

A J Lees

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

John Anthony Hardy

15

object named as

J Hardy

1 reference

Europe PubMed Central

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8 August 2017

Christopher Morris

12

object named as

C M Morris

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

author name string

A M Pittman

1

1 reference

Europe PubMed Central

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8 August 2017

A J Myers

2

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

P Abou-Sleiman

3

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

H C Fung

4

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

M Kaleem

5

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

L Marlowe

6

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

J Duckworth

7

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

D Williams

9

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

L Kilford

10

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

N Thomas

11

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

N W Wood

14

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Europe PubMed Central

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8 August 2017

R de Silva

17

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8 August 2017

language of work or name

0 references

publication date

25 March 2005

1 reference

Europe PubMed Central

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8 August 2017

Journal of Medical Genetics

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Europe PubMed Central

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8 August 2017

42

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Europe PubMed Central

PubMed publication ID

8 August 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

837-846

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

A common inversion under selection in Europeans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Tau gene and Parkinson's disease: a case-control study and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Tau haplotypes regulate transcription and are associated with Parkinson's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

A polymorphic gene nested within an intron of the tau gene: implications for Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Identification of a novel family of presenilin homologues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Clinical genetics of familial progressive supranuclear palsy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

The clinical and pathological spectrum of Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy): a reappraisal

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

Familial progressive supranuclear palsy. Description of a pedigree and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

The clinical features and natural history of the Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

27 July 2018

The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

The structure of the tau haplotype in controls and in progressive supranuclear palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

Genetic evidence for the involvement of tau in progressive supranuclear palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735957

26 September 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tau A0 allele in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tau H2 haplotype is almost exclusively Caucasian in origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/15792962

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2005.031377

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 August 2017

ResearchGate publication ID

0 references

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