(Q43537186)

24 November 2017

Genetic variants in the JAK1 gene confer higher risk of Behcet's disease with ocular involvement in Han Chinese (English)

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24 November 2017

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8

Aize Kijlstra

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24 November 2017

Shengping Hou

1

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24 November 2017

Jian Qi

2

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24 November 2017

Qi Zhang

3

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24 November 2017

Dan Liao

4

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24 November 2017

Qi Li

5

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24 November 2017

Ke Hu

6

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24 November 2017

Yan Zhou

7

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24 November 2017

Peizeng Yang

9

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24 November 2017

15 May 2013

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24 November 2017

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24 November 2017

132

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24 November 2017

9

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24 November 2017

1049-1058

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https://scigraph.springernature.com/pub.10.1007/s00439-013-1312-5

24 November 2017

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cites work

Behcet's syndrome: a family study and the elucidation of a genetic role

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

A family study of Behcet's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

JAK1 gene polymorphisms are associated with the outcomes of hepatitis B virus infection, but not with α interferon therapy response in a Han Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

HLA-B51/B5 and the risk of Behçet's disease: a systematic review and meta-analysis of case-control genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Autoimmunity vs autoinflammation in Behcet's disease: do we oversimplify a complex disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Familial aggregation of Behçet's disease in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Replication study confirms the association between UBAC2 and Behçet's disease in two independent Chinese sets of patients and controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Genetic variant on PDGFRL associated with Behçet disease in Chinese Han populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

JAK-1 rs2780895 C-related genotype and allele but not JAK-1 rs10789166, rs4916008, rs2780885, rs17127114, and rs3806277 are associated with higher susceptibility to asthma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behçet's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Epidemiology of Behçet disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Familial aggregation in Behçet's disease: high frequency in siblings and parents of pediatric probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Ocular involvement is associated with HLA-B51 in Adamantiades-Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

The 5q31 variants associated with psoriasis and Crohn's disease are distinct

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Relationships of HLA-B51 or B5 genotype with Behcet's disease clinical characteristics: systematic review and meta-analyses of observational studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Behçet's disease--a contemporary review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Pathogenic gene responsible for the predisposition of Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Genetic susceptibility to Behcet's disease: role of genes belonging to the MHC region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Defining a tissue stem cell-driven Runx1/Stat3 signalling axis in epithelial cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Dengue hemorrhagic fever is associated with polymorphisms in JAK1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

AAV2-mediated subretinal gene transfer of hIFN-α attenuates experimental autoimmune uveoretinitis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

AAV2-mediated combined subretinal delivery of IFN-α and IL-4 reduces the severity of experimental autoimmune uveoretinitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Clinical characteristics of Behçet's disease in China.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Mutational analysis of JAK1 gene in human hepatocellular carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-013-1312-5

Criteria for diagnosis of Behçet's disease. International Study Group for Behçet's Disease

21 January 2018

1 reference

12 December 2020

Evidence for linkage of the HLA-B locus in Behçet's disease, obtained using the transmission disequilibrium test

1 reference

12 December 2020

Localization of the pathogenic gene of Behçet's disease by microsatellite analysis of three different populations

1 reference

12 December 2020

SLC22A4 and RUNX1: identification of RA susceptible genes

1 reference

12 December 2020

Association analysis between the MIC-A and HLA-B alleles in Japanese patients with Behçet's disease

1 reference

12 December 2020

Behçet's disease associated with one of the HLA-B51 subantigens, HLA-B* 5101

1 reference

12 December 2020

CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population

1 reference

12 December 2020

Cytokine gene polymorphisms in Behçet's disease and their association with clinical and laboratory findings

1 reference

12 December 2020

HLA-DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation

1 reference

12 December 2020

Thalidomide neuropathy incidence and clinico-electrophysiologic findings in 42 patients

1 reference

12 December 2020

Two independent genetic factors responsible for the associations of the IBD5 locus with Crohnʼs disease in the Czech population

1 reference

12 December 2020

HLA class I and II typing of the patients with Behçet's disease in Saudi Arabia

1 reference

12 December 2020

AliBaba2: context specific identification of transcription factor binding sites.

1 reference

12 December 2020

IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population

1 reference

12 December 2020

Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: a meta-analysis

1 reference

12 December 2020

10.1007/S00439-013-1312-5

Identifiers

DOI

1 reference

Dimensions Publication ID

24 November 2017

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1 reference