(Q34144851)

31 July 2017

A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles (English)

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systemic lupus erythematosus

31 July 2017

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J Wither

20

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Christine A Peschken

object named as

C Peschken

11

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Dafna D. Gladman

8

object named as

D Gladman

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ORCID Public Data File 2021

31 July 2017

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author name string

M L Budarf

1

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31 July 2017

P Goyette

2

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31 July 2017

G Boucher

3

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31 July 2017

J Lian

4

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31 July 2017

R R Graham

5

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31 July 2017

J O Claudio

6

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31 July 2017

T Hudson

7

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31 July 2017

A E Clarke

9

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31 July 2017

J E Pope

10

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31 July 2017

C D Smith

12

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31 July 2017

J Hanly

13

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31 July 2017

E Rich

14

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31 July 2017

G Boire

15

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31 July 2017

S G Barr

16

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31 July 2017

M Zummer

17

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31 July 2017

GenES Investigators

18

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31 July 2017

P R Fortin

19

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31 July 2017

J D Rioux

21

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31 July 2017

21 October 2010

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31 July 2017

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31 July 2017

12

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31 July 2017

1

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31 July 2017

51-58

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https://scigraph.springernature.com/pub.10.1038/gene.2010.47

31 July 2017

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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

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Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX

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Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus

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Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci

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Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus

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A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus

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

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The ubiquitin-editing enzyme A20 (TNFAIP3) is a central regulator of immunopathology

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Triad3A, an E3 ubiquitin-protein ligase regulating Toll-like receptors

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Targeting HER proteins in cancer therapy and the role of the non-target HER3.

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Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus.

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Defining the role of the MHC in autoimmunity: a review and pooled analysis

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Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

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Identification of two independent risk factors for lupus within the MHC in United Kingdom families

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

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

21 January 2018

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Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosus

21 January 2018

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Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus

21 January 2018

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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

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

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Evidence for CTLA4 as a susceptibility gene for systemic lupus erythematosus

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Evidence for unique association signals in SLE at the CD28-CTLA4-ICOS locus in a family-based study

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Association of the CT60 marker of the CTLA4 gene with systemic lupus erythematosus

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

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Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

21 January 2018

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

21 January 2018

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

21 January 2018

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A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

21 January 2018

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Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

21 January 2018

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

21 January 2018

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Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases

21 January 2018

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Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis

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Risk alleles for multiple sclerosis identified by a genomewide study

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Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

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Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

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

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

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

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inferred from DOI database lookup

7 January 2021

based on heuristic

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2010.47

21 January 2018

Identifiers

DOI

10.1038/GENE.2010.47

1 reference

Dimensions Publication ID

31 July 2017

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1 reference