(Q35750009)

10 August 2017

title

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

1 reference

genome-wide association study

10 August 2017

main subject

0 references

progressive supranuclear palsy

1 reference

54

1 reference

10 August 2017

Nilüfer Ertekin-Taner

50

Nilüfer Ertekin-Taner

1 reference

10 August 2017

Evan T Geller

21

0 references

Jungsu Kim

Jungsu Kim

10

0 references

Irene Litvan

Irene Litvan

47

0 references

Gregor Wenning

Gregor K Wenning

34

0 references

Charles L White

Charles L White

35

0 references

John Q. Trojanowski

32

John Q Trojanowski

1 reference

10 August 2017

31

Steven E Arnold

1 reference

10 August 2017

45

Ryan J Uitti

1 reference

10 August 2017

44

Zbigniew K Wszolek

1 reference

10 August 2017

28

Murray Grossman

1 reference

10 August 2017

17

Jordan Grafman

1 reference

10 August 2017

51

Rosa Rademakers

1 reference

10 August 2017

2

Owen A Ross

1 reference

10 August 2017

12

Catriona A McLean

1 reference

10 August 2017

42

Bradley F Boeve

1 reference

10 August 2017

13

Bernardino Ghetti

1 reference

10 August 2017

18

Edward D Huey

1 reference

10 August 2017

Neill R Graff-Radford

46

Neill R Graff-Radford

1 reference

10 August 2017

Gerard D Schellenberg

53

Gerard D Schellenberg

1 reference

Alexandra I Soto-Ortolaza

10 August 2017

6

Alexandra Soto-Ortolaza

1 reference

10 August 2017

43

Keith A Josephs

1 reference

10 August 2017

40

Julia Crook

1 reference

10 August 2017

3

Beth Dombroski

1 reference

10 August 2017

Jean Paul G Vonsattel

26

Jean Paul G Vonsattel

1 reference

10 August 2017

39

Lawrence I Golbe

1 reference

10 August 2017

36

Günter U Höglinger

1 reference

10 August 2017

29

Howard I Hurtig

1 reference

10 August 2017

30

Rachel G Gross

1 reference

10 August 2017

15

Laura B Cantwell

1 reference

10 August 2017

38

Bernie Devlin

1 reference

10 August 2017

5

Daniel J Serie

1 reference

10 August 2017

11

Shinsuke Fujioka

1 reference

10 August 2017

Vivianna M Van Deerlin

27

Vivianna M Van Deerlin

1 reference

10 August 2017

41

Joseph E Parisi

1 reference

10 August 2017

1

Naomi Kouri

1 reference

10 August 2017

23

Sigrun Roeber

1 reference

10 August 2017

25

Jorge L Juncos

1 reference

10 August 2017

22

Hans A Kretzschmar

1 reference

10 August 2017

16

Martin R Farlow

1 reference

10 August 2017

24

Marla Gearing

1 reference

10 August 2017

Curtis S Younkin

4

1 reference

10 August 2017

Matthew Baker

7

1 reference

10 August 2017

Ni Cole A Finch

8

1 reference

10 August 2017

Hyejin Yoon

9

1 reference

10 August 2017

Salvatore Spina

14

1 reference

10 August 2017

Mi Ryung Han

19

1 reference

10 August 2017

Sherry Beecher

20

1 reference

10 August 2017

Virginia M Lee

33

1 reference

10 August 2017

Ulrich Müller

37

1 reference

10 August 2017

Steven G Younkin

48

1 reference

10 August 2017

Li-San Wang

49

1 reference

10 August 2017

Hakon Hakonarsen

52

1 reference

10 August 2017

language of work or name

English

0 references

publication date

16 June 2015

1 reference

10 August 2017

published in

Nature Communications

1 reference

10 August 2017

volume

6

1 reference

10 August 2017

issue

1

0 references

page(s)

7247

1 reference

Creative Commons Attribution 4.0 International

10 August 2017

copyright license

start time

16 June 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

genome-wide association study

1 reference

Three sib-pairs of autopsy-confirmed progressive supranuclear palsy

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Haplotype estimation using sequencing reads

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Criteria for the diagnosis of corticobasal degeneration

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

An integrated map of genetic variation from 1,092 human genomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Genotype imputation with thousands of genomes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Corticobasal degeneration: a pathologically distinct 4R tauopathy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

LocusZoom: regional visualization of genome-wide association scan results

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Does corticobasal degeneration exist? A clinicopathological re-evaluation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

PLINK: a tool set for whole-genome association and population-based linkage analyses

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Signature tau neuropathology in gray and white matter of corticobasal degeneration

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Phosphoprotein phosphatase activities in Alzheimer disease brain

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Cloning and expression of myelin-associated oligodendrocytic basic protein. A novel basic protein constituting the central nervous system myelin

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

A novel mitogen-activated protein kinase phosphatase. Structure, expression, and regulation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Corticodentatonigral Degeneration With Neuronal Achromasia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

KIF13B enhances the endocytosis of LRP1 by recruiting LRP1 to caveolae.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Mapping and analysis of chromatin state dynamics in nine human cell types

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Transport of PIP3 by GAKIN, a kinesin-3 family protein, regulates neuronal cell polarity

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Structural evidence for feedback activation by Ras.GTP of the Ras-specific nucleotide exchange factor SOS

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

The tau gene A0 allele and progressive supranuclear palsy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4469997

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

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNCOMMS8247

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%2FNCOMMS8247

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NCOMMS8247

1 reference

10 August 2017

0 references

1 reference

10 August 2017

1 reference