Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex (Q35155990)

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English	Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex	scientific article

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scholarly article

1 reference

Europe PubMed Central

6 August 2017

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex (English)

1 reference

Europe PubMed Central

6 August 2017

multiple sclerosis

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Margaret A. Pericak-Vance

12

object named as

Margaret A Pericak-Vance

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object named as

William S Bush

2

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Alastair Compston

8

object named as

Alastair Compston

1 reference

Europe PubMed Central

6 August 2017

David A. Hafler

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David A Hafler

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Europe PubMed Central

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11

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Stephen J Sawcer

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Europe PubMed Central

6 August 2017

Jonathan L Haines

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object named as

Jonathan L Haines

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Europe PubMed Central

6 August 2017

Philip L. De Jager

5

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Philip L De Jager

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Europe PubMed Central

6 August 2017

Lisa F Barcellos

13

object named as

Lisa F Barcellos

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Europe PubMed Central

6 August 2017

Stephen L. Hauser

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object named as

Stephen L Hauser

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Europe PubMed Central

6 August 2017

Rebecca L Zuvich

1

object named as

Rebecca L Zuvich

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Europe PubMed Central

6 August 2017

Jacob L McCauley

3

object named as

Jacob L McCauley

1 reference

Europe PubMed Central

6 August 2017

Adrian J. Ivinson

7

object named as

Adrian J Ivinson

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Europe PubMed Central

6 August 2017

author name string

Ashley H Beecham

4

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Europe PubMed Central

6 August 2017

International Multiple Sclerosis Genetics Consortium

6

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Europe PubMed Central

6 August 2017

Douglas P Mortlock

14

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Europe PubMed Central

6 August 2017

publication date

8 June 2011

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Europe PubMed Central

6 August 2017

Human Molecular Genetics

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Europe PubMed Central

6 August 2017

20

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Europe PubMed Central

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17

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Europe PubMed Central

6 August 2017

3517-3524

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Europe PubMed Central

6 August 2017

Gene-environment interactions in human disease: nuisance or opportunity?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci

1 reference

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28 July 2018

The UCSC Genome Browser database: update 2010

1 reference

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28 July 2018

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Common vs. rare allele hypotheses for complex diseases

1 reference

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28 July 2018

Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

The expanding genetic overlap between multiple sclerosis and type I diabetes

1 reference

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28 July 2018

Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci

1 reference

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28 July 2018

CD226 Gly307Ser association with multiple autoimmune diseases

1 reference

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28 July 2018

High-resolution mapping of expression-QTLs yields insight into human gene regulation

1 reference

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28 July 2018

The complex genetics of multiple sclerosis: pitfalls and prospects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Gene polymorphisms and male infertility--a meta-analysis and literature review

1 reference

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28 July 2018

Risk alleles for multiple sclerosis identified by a genomewide study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

Genome-wide maps of chromatin state in pluripotent and lineage-committed cells

1 reference

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28 July 2018

Genome-wide association studies: theoretical and practical concerns

1 reference

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28 July 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

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28 July 2018

Locus control regions: coming of age at a decade plus

1 reference

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28 July 2018

The significance of the association between HLA and multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

28 July 2018

A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

27 September 2018

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

27 September 2018

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

27 September 2018

ENCODE whole-genome data in the UCSC Genome Browser

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

27 September 2018

Silencing of SOCS1 in macrophages suppresses tumor development by enhancing antitumor inflammation.

1 reference

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27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3153306

27 September 2018

Refining genetic associations in multiple sclerosis

1 reference

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Suppressors of cytokine signaling and immunity

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Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis

1 reference

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

1 reference

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27 September 2018

HL-A antigen frequencies in multiple sclerosis. Significant increase of HL-A3, HL-A10 and W5, and decrease of HL-A12

1 reference

https://pubmed.ncbi.nlm.nih.gov/21653641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple Sclerosis: Association with HL—A3

1 reference

https://pubmed.ncbi.nlm.nih.gov/21653641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suppressor of cytokine signaling-1 in T cells and macrophages is critical for preventing lethal inflammation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21653641

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDR250

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

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