(Q34299422)

1 August 2017

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

1 reference

genome-wide association study

1 August 2017

main subject

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author

Dennis W. Dickson

30

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Margaret A. Pericak-Vance

1 August 2017

24

Margaret A Pericak-Vance

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Nilüfer Ertekin-Taner

32

Nilüfer Ertekin-Taner

1 reference

1 August 2017

Christopher N Rowley

8

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Sumit Middha

Sumit Middha

10

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Lindsay A. Farrer

Lindsay A Farrer

25

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Richard Mayeux

23

Richard Mayeux

1 reference

1 August 2017

28

Ronald C Petersen

1 reference

1 August 2017

22

Jonathan L Haines

1 reference

1 August 2017

0 references

5

Julia Crook

1 reference

1 August 2017

Minerva M Carrasquillo

7

Minerva M Carrasquillo

1 reference

1 August 2017

Gerard D Schellenberg

26

Gerard D Schellenberg

1 reference

1 August 2017

Neill R Graff-Radford

29

Neill R Graff-Radford

1 reference

Alzheimer's Disease Genetics Consortium

1 August 2017

27

Alzheimer's Disease Genetics Consortium

1 reference

1 August 2017

4

Mariet Allen

1 reference

1 August 2017

1

Fanggeng Zou

1 reference

1 August 2017

3

Curtis S Younkin

1 reference

1 August 2017

6

V Shane Pankratz

1 reference

1 August 2017

14

Kimberly G Malphrus

1 reference

1 August 2017

17

Gina Bisceglio

1 reference

1 August 2017

Christopher P Kolbert

20

Christopher P Kolbert

1 reference

1 August 2017

21

Jin Jen

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1 August 2017

11

Sooraj Maharjan

1 reference

1 August 2017

15

Ryan Palusak

1 reference

1 August 2017

18

Constantin Georgescu

1 reference

1 August 2017

19

Naomi Kouri

1 reference

1 August 2017

31

Steven G Younkin

1 reference

1 August 2017

16

Sarah Lincoln

1 reference

1 August 2017

High Seng Chai

2

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1 August 2017

Asha A Nair

9

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1 August 2017

Thuy Nguyen

12

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1 August 2017

Li Ma

13

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1 August 2017

publication date

7 June 2012

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1 August 2017

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1 August 2017

volume

8

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1 August 2017

issue

6

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1 August 2017

page(s)

e1002707

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Creative Commons Attribution 4.0 International

1 August 2017

copyright license

start time

7 June 2012

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

based on heuristic

inferred from title

cites work

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

1 reference

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Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans

6 July 2018

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

6 July 2018

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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

6 July 2018

1 reference

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

6 July 2018

1 reference

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Gene expression endophenotypes: a novel approach for gene discovery in Alzheimer's disease

6 July 2018

1 reference

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

6 July 2018

1 reference

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Global analysis of the impact of environmental perturbation on cis-regulation of gene expression

6 July 2018

1 reference

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Gene expression in skin and lymphoblastoid cells: Refined statistical method reveals extensive overlap in cis-eQTL signals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

6 July 2018

1 reference

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METAL: fast and efficient meta-analysis of genomewide association scans

6 July 2018

1 reference

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Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genome-wide analysis of genetic loci associated with Alzheimer disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Intratumor heterogeneity and precision of microarray-based predictors of breast cancer biology and clinical outcome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Common regulatory variation impacts gene expression in a cell type-dependent manner

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetic control of human brain transcript expression in Alzheimer disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Mapping the genetic architecture of gene expression in human liver

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetics of gene expression and its effect on disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Model-based variance-stabilizing transformation for Illumina microarray data.

6 July 2018

1 reference

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A genome-wide association study of global gene expression

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Population genomics of human gene expression

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Haplotype-specific expression of the N-terminal exons 2 and 3 at the human MAPT locus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Methodological considerations for gene expression profiling of human brain.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Relative impact of nucleotide and copy number variation on gene expression phenotypes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genome-wide associations of gene expression variation in humans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

A haplotype map of the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Mapping determinants of human gene expression by regional and genome-wide association

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Polymorphisms in human organic anion-transporting polypeptide 1A2 (OATP1A2): implications for altered drug disposition and central nervous system drug entry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetic inheritance of gene expression in human cell lines

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetic analysis of genome-wide variation in human gene expression

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Statistical significance for genomewide studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Genetics of gene expression surveyed in maize, mouse and man

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Multiple tests for genetic effects in association studies.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

Neuropathological stageing of Alzheimer-related changes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3369937

A survey of genetic human cortical gene expression

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002707

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002707

Natural variation in human gene expression assessed in lymphoblastoid cells

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22685416

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22685416

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1002707

1 reference

1 August 2017

1 reference

1 August 2017

1 reference