Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease (Q57619872)

6

object named as

Christine Klein

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Vladimir S. Kostić

5

object named as

Vladimir Kostic

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author name string

Susan Winkler

1

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Katja Lohmann-Hedrich

3

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Peter Vieregge

European Journal of Human Genetics

4

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publication date

18 July 2007

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published in

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volume

15

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page(s)

1163-1168

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issue

11

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201901

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cites work

The genetics of Parkinson disease: Implications for neurological care

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

The Tau Gene Haplotype H1 Confers a Susceptibility to Parkinson’s Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Linkage disequilibrium and association of MAPT H1 in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

A comparison of clinical and pathological features of young- and old-onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

DYT1 mutation in primary torsion dystonia in a Serbian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Case-control study of the extended tau gene haplotype in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

7 January 2021

Association of the Tau haplotype with Parkinson's disease in the Greek population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

7 January 2021

Prevalence of parkinsonism and Parkinson's disease in Europe: the EUROPARKINSON Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

7 January 2021

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201901

7 January 2021