(Q37034965)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

Small ubiquitin-like modifier 4 (SUMO4) polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome in the Chinese Han population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

7

Aize Kijlstra

1 reference

17 August 2017

Shengping Hou

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Peizeng Yang

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Liping Du

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Hongyan Zhou

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Xiaomin Lin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Xiaoli Liu

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Aize Kijlstra

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

31 December 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

2597-2603

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

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

19 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association of small ubiquitin-like modifier 4 (SUMO4) variant, located in IDDM5 locus, with type 2 diabetes in the Japanese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

SUMO4 M55V variant is associated with diabetic nephropathy in type 2 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Evidence for the role of small ubiquitin-like modifier 4 as a general autoimmunity locus in the Japanese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Genetic heterogeneity in association of the SUMO4 M55V variant with susceptibility to type 1 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Haploview: analysis and visualization of LD and haplotype maps

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

A 212-kb region on chromosome 6q25 containing the TAB2 gene is associated with susceptibility to type 1 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

HLA-DPB1 glutamate 69: a genetic marker of beryllium disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Echographic features of the Vogt-Koyanagi-Harada syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association of HLA antigens with Vogt-Koyanagi-Harada syndrome in a Han Chinese population

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Vogt-Koyanagi-Harada disease in monozygotic twins

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and -DR4 in Hispanic patients living in southern California.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2613071

Association study of NFKB1 and SUMO4 polymorphisms in Chinese patients with psoriasis vulgaris

20 October 2018

1 reference

12 December 2020

Choroidal neovascularization in long-standing case of Vogt-Koyanagi-Harada disease

1 reference

12 December 2020

Profiling human leukocyte antigens in Vogt-Koyanagi-Harada syndrome

1 reference

12 December 2020

Identification of the HLA-DRB1*04, -DRB1*07, and -DRB1*09 alleles by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours

1 reference

12 December 2020

HLA class II genes in Vogt-Koyanagi-Harada disease

1 reference

12 December 2020

Simultaneous onset of Vogt-Koyanagi-Harada syndrome in monozygotic twins

1 reference

12 December 2020

Vogt-Koyanagi-Harada disease in identical twins

1 reference

12 December 2020

Vogt-Koyanagi-Harada syndrome

1 reference

12 December 2020

[The association of HLA-DR4 gene subtypes with Vogt-Koyanagi-Harada syndrome]

1 reference

12 December 2020

Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19122825%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

PubMed publication ID

19122825

1 reference