Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy (Q35750009)

10 August 2017

title

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy (English)

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genome-wide association study

10 August 2017

main subject

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progressive supranuclear palsy

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54

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Nilüfer Ertekin-Taner

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Nilüfer Ertekin-Taner

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Evan T Geller

21

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Jungsu Kim

Jungsu Kim

10

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Irene Litvan

Irene Litvan

47

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Gregor Wenning

Gregor K Wenning

34

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Charles L White

Charles L White

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John Q. Trojanowski

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John Q Trojanowski

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Steven E Arnold

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Ryan J Uitti

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Zbigniew K Wszolek

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Murray Grossman

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Jordan Grafman

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Rosa Rademakers

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Owen A Ross

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Catriona A McLean

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Bradley F Boeve

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Bernardino Ghetti

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Edward D Huey

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Neill R Graff-Radford

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Neill R Graff-Radford

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Gerard D Schellenberg

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Gerard D Schellenberg

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Alexandra I Soto-Ortolaza

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Alexandra Soto-Ortolaza

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Keith A Josephs

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Julia Crook

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Beth Dombroski

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Jean Paul G Vonsattel

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Jean Paul G Vonsattel

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Lawrence I Golbe

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Günter U Höglinger

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Howard I Hurtig

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Rachel G Gross

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Laura B Cantwell

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Bernie Devlin

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Daniel J Serie

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Shinsuke Fujioka

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Vivianna M Van Deerlin

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Vivianna M Van Deerlin

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Joseph E Parisi

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Naomi Kouri

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Sigrun Roeber

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Jorge L Juncos

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Hans A Kretzschmar

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Martin R Farlow

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Marla Gearing

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Curtis S Younkin

4

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Matthew Baker

7

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Ni Cole A Finch

8

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Hyejin Yoon

9

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Salvatore Spina

14

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Mi Ryung Han

19

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Sherry Beecher

20

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Virginia M Lee

33

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Ulrich Müller

37

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Steven G Younkin

48

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Li-San Wang

49

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Hakon Hakonarsen

52

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10 August 2017

language of work or name

English

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publication date

16 June 2015

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10 August 2017

published in

Nature Communications

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10 August 2017

volume

6

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10 August 2017

issue

1

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page(s)

7247

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Creative Commons Attribution 4.0 International

10 August 2017

copyright license

start time

16 June 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

genome-wide association study

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Three sib-pairs of autopsy-confirmed progressive supranuclear palsy

inferred from title

cites work

1 reference

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Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome

27 July 2018

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Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

27 July 2018

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Corticobasal degeneration: a pathologically distinct 4R tauopathy

27 July 2018

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27 July 2018

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Does corticobasal degeneration exist? A clinicopathological re-evaluation

27 July 2018

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Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank

27 July 2018

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Signature tau neuropathology in gray and white matter of corticobasal degeneration

27 July 2018

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GAKIN, a novel kinesin-like protein associates with the human homologue of the Drosophila discs large tumor suppressor in T lymphocytes

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

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25 September 2018

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

25 September 2018

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Crossref

https://api.crossref.org/works/10.1038/NCOMMS8247

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26077951

12 December 2020

inferred from PubMed ID database lookup

An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26077951

12 December 2020

inferred from PubMed ID database lookup

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26077951

12 December 2020

inferred from PubMed ID database lookup

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

1 reference

Crossref

https://api.crossref.org/works/10.1038/NCOMMS8247

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NCOMMS8247

1 reference

10 August 2017

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1 reference

10 August 2017

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