(Q29417026)

22 June 2017

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy (English)

1 reference

progressive supranuclear palsy

22 June 2017

1 reference

1 reference

39

Hakon Hakonarson

1 reference

22 June 2017

26

Allissa Dillman

0 references

Jana Vandrovcova

15

Jana Vandrovcova

1 reference

22 June 2017

Stefano Goldwurm

19

0 references

John Van Swieten

John C van Swieten

11

0 references

Irene Litvan

Irene Litvan

9

0 references

Pau Pastor

Pau Pastor

22

0 references

Matthew J. Farrer

Matthew J Farrer

32

0 references

Dennis W. Dickson

Dennis W Dickson

3

0 references

Lambertus Klei

6

Lambertus Klei

1 reference

22 June 2017

14

Ryan J Uitti

1 reference

22 June 2017

13

Zbigniew K Wszolek

1 reference

22 June 2017

20

Eduardo Tolosa

1 reference

22 June 2017

18

Walter Maetzler

1 reference

22 June 2017

37

Andrew J Lees

1 reference

22 June 2017

12

Peter Heutink

1 reference

22 June 2017

36

John Hardy

1 reference

22 June 2017

21

Barbara Borroni

1 reference

22 June 2017

7

Rosa Rademakers

1 reference

22 June 2017

29

Mark R Cookson

1 reference

22 June 2017

31

Andrew B Singleton

1 reference

22 June 2017

30

Dena G Hernandez

1 reference

ORCID Public Data File 2021

22 June 2017

1 reference

Daniela Berg

1 reference

ORCID Public Data File 2021

Gerard D Schellenberg

41

Gerard D Schellenberg

1 reference

22 June 2017

34

Lawrence I Golbe

1 reference

22 June 2017

1

Günter U Höglinger

1 reference

22 June 2017

16

Howard I Hurtig

1 reference

22 June 2017

17

Rachel G Gross

1 reference

22 June 2017

24

Laura B Cantwell

1 reference

22 June 2017

38

Bernie Devlin

1 reference

22 June 2017

28

J Raphael Gibbs

1 reference

22 June 2017

Nadine M Melhem

2

1 reference

22 June 2017

Patrick M A Sleiman

4

1 reference

22 June 2017

Li-San Wang

5

1 reference

22 June 2017

Rohan de Silva

8

1 reference

22 June 2017

David E Riley

10

1 reference

22 June 2017

PSP Genetics Study Group

23

1 reference

22 June 2017

Mi Ryung Han

25

1 reference

22 June 2017

Marcel P van der Brug

27

1 reference

22 June 2017

Chang-En Yu

33

1 reference

22 June 2017

Tamas Revesz

35

1 reference

22 June 2017

Ulrich Müller

40

1 reference

22 June 2017

language of work or name

English

0 references

publication date

19 June 2011

1 reference

22 June 2017

1 reference

22 June 2017

43

1 reference

22 June 2017

699-705

1 reference

22 June 2017

7

1 reference

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

22 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Genome-wide association study reveals genetic risk underlying Parkinson's disease

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Evolutionary toggling of the MAPT 17q21.31 inversion region

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

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

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Principal components analysis corrects for stratification in genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

SNAREs--engines for membrane fusion

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Replicating genotype-phenotype associations

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

A common inversion under selection in Europeans

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

A systematic review of the incidence and prevalence of long-term neurological conditions in the UK

18 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Rational therapeutic approaches to progressive supranuclear palsy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Genome-wide analysis of genetic loci associated with Alzheimer disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Screen and clean: a tool for identifying interactions in genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

The unfolded protein response is activated in pretangle neurons in Alzheimer's disease hippocampus

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Endoplasmic reticulum protein quality control in neurodegenerative disease: the good, the bad and the therapy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Analysis and application of European genetic substructure using 300 K SNP information

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Progressive supranuclear palsy: pathology and genetics

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Haplotype-specific expression of exon 10 at the human MAPT locus

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Myelin-associated oligodendrocytic basic protein: a family of abundant CNS myelin proteins in search of a function

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Cellular abnormalities linked to endoplasmic reticulum dysfunction in cerebrovascular disease--therapeutic potential

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Update on progressive supranuclear palsy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Accuracy of clinical diagnosis of progressive supranuclear palsy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Syntaxin 6: the promiscuous behaviour of a SNARE protein.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Follow-up study of risk factors in progressive supranuclear palsy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

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

3 June 2018

1 reference

Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.

21 January 2018

1 reference

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

21 January 2018

1 reference

Activation of the unfolded protein response in Parkinson's disease.

21 January 2018

1 reference

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

21 January 2018

1 reference

A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies

21 January 2018

1 reference

Discovering genetic ancestry using spectral graph theory

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3125476

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21685912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Endoplasmic reticulum stress features are prominent in Alzheimer disease but not in prion diseases in vivo

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21685912

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.859

1 reference

Dimensions Publication ID

22 June 2017

1039099140

0 references

OpenCitations bibliographic resource ID

558263

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference