Use of next-generation DNA sequencing to analyze genetic variants in rheumatic disease (Q38383803)

2 September 2017

5 references

17 June 2019

30 June 2019

14 September 2019

19 September 2019

1 May 2021

Use of next-generation DNA sequencing to analyze genetic variants in rheumatic disease (English)

1 reference

biomedical investigative technique

2 September 2017

1 reference

14 September 2019

1 reference

19 September 2019

1 reference

1 May 2021

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Patrick M Gaffney

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

author name string

Graham B Wiley

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

publication date

1 January 2014

1 reference

Arthritis Research and Therapy

2 September 2017

6 references

17 June 2019

30 June 2019

14 September 2019

19 September 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

1 May 2021

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

page(s)

490

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Creative Commons Attribution

6 June 2020

copyright license

5 references

17 June 2019

30 June 2019

14 September 2019

19 September 2019

1 May 2021

0 references

https://scigraph.springernature.com/pub.10.1186/s13075-014-0490-4

0 references

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome

6 September 2017

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Targeted resequencing of candidate genes reveals novel variants associated with severe Behçet's uveitis

6 September 2017

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6 September 2017

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Coverage bias and sensitivity of variant calling for four whole-genome sequencing technologies

6 September 2017

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Discovery of potential new gene variants and inflammatory cytokine associations with fibromyalgia syndrome by whole exome sequencing

6 September 2017

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Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferation

6 September 2017

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Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

6 September 2017

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6 September 2017

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RNA-Seq for enrichment and analysis of IRF5 transcript expression in SLE.

6 September 2017

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Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis

6 September 2017

1 reference

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RNA-seq analysis of synovial fibroblasts brings new insights into rheumatoid arthritis

6 September 2017

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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

6 September 2017

1 reference

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A rare variant in the osteoarthritis-associated locus GDF5 is functional and reveals a site that can be manipulated to modulate GDF5 expression.

6 September 2017

1 reference

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Association of two independent functional risk haplotypes in TNIP1 with systemic lupus erythematosus

6 September 2017

1 reference

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A functional haplotype of UBE2L3 confers risk for systemic lupus erythematosus

6 September 2017

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Cold urticaria, immunodeficiency, and autoimmunity related to PLCG2 deletions

6 September 2017

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6 September 2017

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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

6 September 2017

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Accurate and comprehensive sequencing of personal genomes

6 September 2017

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Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus

6 September 2017

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6 September 2017

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6 September 2017

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Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus

6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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14 September 2017

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23 June 2018

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31 August 2018

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Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family

31 August 2018

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31 August 2018

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31 August 2018

1 reference

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31 August 2018

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Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.

31 August 2018

1 reference

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Technology: The $1,000 genome

31 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FS13075-014-0490-4

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/25789374

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Deep sequencing of GDF5 reveals the absence of rare variants at this important osteoarthritis susceptibility locus

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25789374

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Resequencing of the human major histocompatibility complex in patients with rheumatoid arthritis and healthy controls in Alaska Natives of Southeast Alaska

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25789374

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S13075-014-0490-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

6 June 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25789374%20AND%20SRC:MED&resulttype=core&format=json