Pathway and network-based analysis of genome-wide association studies in multiple sclerosis (Q37183962)

18 August 2017

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis (English)

1 reference

genome-wide association study

18 August 2017

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Rachel A Gibson

14

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Michael R. Barnes

object named as

Michael R Barnes

16

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Paul M. Matthews

object named as

Paul M Matthews

12

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Pouya Khankhanian

4

object named as

Pouya Khankhanian

1 reference

18 August 2017

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Ludwig Kappos

1 reference

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Jorge R Oksenberg

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18 August 2017

13

Stephen L Hauser

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1

Sergio E Baranzini

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5

Raija Lindberg

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18 August 2017

8

Bernard M J Uitdehaag

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11

Chris H Polman

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18 August 2017

Nicholas W Galwey

2

1 reference

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Joanne Wang

3

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18 August 2017

Daniel Pelletier

6

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Wen Wu

7

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GeneMSA Consortium

10

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13 March 2009

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18 August 2017

Human Molecular Genetics

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18

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2078-2090

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11

1 reference

describes a project that uses

18 August 2017

Cytoscape

1 reference

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

1 reference

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

6 September 2017

1 reference

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Genetic mapping in human disease

6 September 2017

1 reference

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Pathway analysis of seven common diseases assessed by genome-wide association

6 September 2017

1 reference

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

6 September 2017

1 reference

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Segregation of axial motor and sensory pathways via heterotypic trans-axonal signaling

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission

6 September 2017

1 reference

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eQED: an efficient method for interpreting eQTL associations using protein networks

6 September 2017

1 reference

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Pathway-based approaches for analysis of genomewide association studies

6 September 2017

1 reference

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Integration of biological networks and gene expression data using Cytoscape

6 September 2017

1 reference

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Novel methods for detecting epistasis in pharmacogenomics studies

6 September 2017

1 reference

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TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study

6 September 2017

1 reference

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Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Risk alleles for multiple sclerosis identified by a genomewide study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Detecting association using epistatic information

6 September 2017

1 reference

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A genomic pathway approach to a complex disease: axon guidance and Parkinson disease

6 September 2017

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

6 September 2017

1 reference

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The human disease network

6 September 2017

1 reference

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A human phenome-interactome network of protein complexes implicated in genetic disorders

6 September 2017

1 reference

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The neurobiology of multiple sclerosis: genes, inflammation, and neurodegeneration

6 September 2017

1 reference

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Functional epistasis on a common MHC haplotype associated with multiple sclerosis

6 September 2017

1 reference

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Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes

6 September 2017

1 reference

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Towards a proteome-scale map of the human protein–protein interaction network

6 September 2017

1 reference

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BiNGO: a Cytoscape plugin to assess overrepresentation of gene ontology categories in biological networks

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Genome-wide association studies: theoretical and practical concerns

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

A functional and structural basis for TCR cross-reactivity in multiple sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Discovering regulatory and signalling circuits in molecular interaction networks

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Multiple sclerosis: genomic rewards

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

6 September 2017

1 reference

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Gene ontology: tool for the unification of biology

6 September 2017

1 reference

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Glutamate as a neurotransmitter in the brain: review of physiology and pathology

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.

6 September 2017

1 reference

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An integrative approach for causal gene identification and gene regulatory pathway inference

3 September 2018

1 reference

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Genome-wide strategies for detecting multiple loci that influence complex diseases.

3 September 2018

1 reference

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Ephrin A receptors and ligands in lesions and normal-appearing white matter in multiple sclerosis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Inferring pathways from gene lists using a literature-derived network of biological relationships.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Multiple sclerosis: altered glutamate homeostasis in lesions correlates with oligodendrocyte and axonal damage

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2678928

A full genome search in multiple sclerosis

20 October 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDP120

A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDP120

Glutamate excitotoxicity in a model of multiple sclerosis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19286671

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19286671

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDP120

1 reference

18 August 2017

1 reference

18 August 2017

1 reference