(Q33832877)

29 July 2017

title

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

1 reference

Margaret A. Pericak-Vance

29 July 2017

0 references

12

Margaret A Pericak-Vance

0 references

John D. Rioux

John D Rioux

7

0 references

Alastair Compston

9

Alastair Compston

1 reference

29 July 2017

10

David A Hafler

1 reference

29 July 2017

11

Stephen J Sawcer

1 reference

29 July 2017

13

Jonathan L Haines

1 reference

29 July 2017

6

Philip L De Jager

1 reference

29 July 2017

2

Stacy Caillier

1 reference

29 July 2017

17

Lisa F Barcellos

1 reference

29 July 2017

16

Jorge R Oksenberg

1 reference

29 July 2017

15

Stephen L Hauser

1 reference

29 July 2017

4

Jacob L McCauley

1 reference

International Multiple Sclerosis Genetics Consortium

29 July 2017

14

International Multiple Sclerosis Genetics Consortium

1 reference

29 July 2017

8

Adrian J Ivinson

1 reference

29 July 2017

5

Rebecca L Zuvich

1 reference

29 July 2017

Paola G Bronson

1

1 reference

29 July 2017

Patricia P Ramsay

3

1 reference

29 July 2017

publication date

8 March 2010

1 reference

29 July 2017

number of pages

10

1 reference

inferred from page(s)

published in

Human Molecular Genetics

1 reference

29 July 2017

volume

19

1 reference

29 July 2017

issue

11

1 reference

29 July 2017

page(s)

2331-2340

1 reference

A comparison of case-only designs for detecting gene x gene interaction in rheumatoid arthritis using genome-wide case-control data in Genetic Analysis Workshop 16

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Genetic mapping in human disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

PGA: power calculator for case-control genetic association analyses.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Conditional genotype analysis: detecting secondary disease loci in linkage disequilibrium with a primary disease locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Discerning the ancestry of European Americans in genetic association studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for association

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Risk alleles for multiple sclerosis identified by a genomewide study

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Role of the MHC2TA gene in autoimmune diseases.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Evolutionary relationships of vertebrate NACHT domain-containing proteins

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A haplotype map of the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Familial risk of multiple sclerosis: a nationwide cohort study

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A high-density screen for linkage in multiple sclerosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A note on exact tests of Hardy-Weinberg equilibrium

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Parental phenotypes in family-based association analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Mini-review: Specificity and expression of CIITA, the master regulator of MHC class II genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Statistical aspects of the analysis of data from retrospective studies of disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

The structure of haplotype blocks in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Score tests for association between traits and haplotypes when linkage phase is ambiguous

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Predicting deleterious amino acid substitutions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Human autoimmunity genes in mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

General score tests for associations of genetic markers with disease using cases and their parents.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Class II transactivator regulates the expression of multiple genes involved in antigen presentation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Mapping disease genes: family-based association studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

The two novel MHC class II transactivators RFX5 and CIITA both control expression of HLA-DM genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Meta-analysis in clinical trials

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Twin concordance and sibling recurrence rates in multiple sclerosis.

28 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Refining genetic associations in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

The role of the CD58 locus in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Expression of MHC class II molecules in different cellular and functional compartments is controlled by differential usage of multiple promoters of the transactivator CIITA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Single nucleotide polymorphisms in MHC2TA, the gene encoding the MHC class II transactivator (CIITA).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Some Methods for Strengthening the Common χ 2 Tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Inference of population structure using multilocus genotype data: linked loci and correlated allele frequencies

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

Case-only design to measure gene-gene interaction.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2865376

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

29 October 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

HLA-DQB1*0602 Determines Disease Susceptibility in a New "Humanized" Multiple Sclerosis Model in HLA-DR15 (DRB1*1501;DQB1*0602) Transgenic Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

A full genome search in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

Case-Only Design to Measure Gene-Gene Interaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ101

MHC2TA rs4774C and HHV-6A active replication in multiple sclerosis patients

21 January 2018

1 reference

12 December 2020

Environment-gene interaction in multiple sclerosis: human herpesvirus 6 and MHC2TA

1 reference

12 December 2020

Genetic susceptibility to multiple sclerosis: detection of polymorphic nucleotides and an intron in the 3' untranslated region of the major histocompatibility complex class II transactivator gene

1 reference

12 December 2020

Vra4 congenic rats with allelic differences in the class II transactivator gene display altered susceptibility to experimental autoimmune encephalomyelitis

1 reference

12 December 2020

On estimating HLA/disease association with application to a study of aplastic anemia

1 reference

12 December 2020

The MHC2TA-168A/G and +1614G/C polymorphisms and risk for multiple sclerosis or chronic inflammatory arthropathies

1 reference

12 December 2020

Promoter polymorphism rs3087456 in the MHC class II transactivator gene is not associated with susceptibility for selected autoimmune diseases in German patient groups

1 reference

12 December 2020

Re: "Familial risk of multiple sclerosis: a nationwide cohort study"

1 reference

12 December 2020

Mice lacking the MHC class II transactivator (CIITA) show tissue-specific impairment of MHC class II expression

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDQ101

1 reference

29 July 2017

1 reference

29 July 2017

1 reference