(Q36012302)

11 August 2017

Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up (English)

1 reference

genome-wide association study

11 August 2017

0 references

0 references

31

1 reference

11 August 2017

Jose-Ezequiel Martin

1

0 references

Luis Rodriguez-Rodriguez

Luis Rodriguez-Rodriguez

8

0 references

Patricia E Carreira

Patricia Carreira

15

0 references

Norberto Ortego-Centeno

Norberto Ortego-Centeno

11

0 references

Ariane I. Herrick

Ariane Herrick

32

0 references

Javier Martin

Javier Martin

41

0 references

Nicolas Hunzelmann

26

Nicolas Hunzelmann

1 reference

Francisco J. García-Hernandez

11 August 2017

13

Francisco J García-Hernández

1 reference

Paloma García de la Peña Lefebvre

11 August 2017

14

Paloma García de la Peña

1 reference

11 August 2017

36

Shervin Assassi

1 reference

11 August 2017

38

Maureen D Mayes

1 reference

11 August 2017

34

Filemon K Tan

1 reference

Spanish Scleroderma Group

11 August 2017

16

Spanish Scleroderma Group

1 reference

11 August 2017

Timothy R D J Radstake

39

Timothy R D J Radstake

1 reference

11 August 2017

6

Madelon C Vonk

1 reference

11 August 2017

17

Alexandre E Voskuyl

1 reference

11 August 2017

2

Jasper C Broen

1 reference

11 August 2017

19

Piet L C M van Riel

1 reference

11 August 2017

7

Ruben van 't Slot

1 reference

11 August 2017

5

Carmen P Simeon

1 reference

Miguel Angel Gonzalez-Gay

11 August 2017

12

Miguel A González-Gay

1 reference

11 August 2017

23

Paolo Airo

1 reference

11 August 2017

30

Meng May Chee

1 reference

11 August 2017

20

Alexander Kreuter

1 reference

11 August 2017

21

Torsten Witte

1 reference

11 August 2017

28

Lorenzo Beretta

1 reference

11 August 2017

40

Bobby P C Koeleman

1 reference

11 August 2017

Maria E Serrano-Teruel

4

Maria Teruel

1 reference

11 August 2017

10

Vicente Fonollosa

1 reference

11 August 2017

24

Raffaella Scorza

1 reference

11 August 2017

25

Claudio Lunardi

1 reference

11 August 2017

22

Gabriella Riemekasten

1 reference

11 August 2017

M.Carmen Fonseca-Mora

37

Carmen Fonseca

1 reference

11 August 2017

27

Jörg H W Distler

1 reference

11 August 2017

18

Annemie J Schuerwegh

1 reference

11 August 2017

35

Frank C Arnett

1 reference

11 August 2017

F David Carmona

3

1 reference

11 August 2017

Esther Vicente

9

1 reference

11 August 2017

Jacob van Laar

29

1 reference

11 August 2017

Christopher Denton

33

1 reference

11 August 2017

9 March 2012

1 reference

11 August 2017

Human Molecular Genetics

1 reference

11 August 2017

21

1 reference

11 August 2017

12

1 reference

11 August 2017

2825-2835

1 reference

describes a project that uses

11 August 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

1 reference

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Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy

2 October 2017

1 reference

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Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis

2 October 2017

1 reference

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Genetics and pathogenesis of inflammatory bowel disease

2 October 2017

1 reference

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The genetics of systemic sclerosis: an update.

2 October 2017

1 reference

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The genetics of systemic lupus erythematosus and implications for targeted therapy

2 October 2017

1 reference

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The genetics of scleroderma

2 October 2017

1 reference

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Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus

2 October 2017

1 reference

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Association of TNFSF4 (OX40L) polymorphisms with susceptibility to systemic sclerosis

2 October 2017

1 reference

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European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups

2 October 2017

1 reference

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Major histocompatibility complex (MHC) class II alleles, haplotypes and epitopes which confer susceptibility or protection in systemic sclerosis: analyses in 1300 Caucasian, African-American and Hispanic cases and 1000 controls

2 October 2017

1 reference

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Genetics and genomic studies in scleroderma (systemic sclerosis).

2 October 2017

1 reference

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

2 October 2017

1 reference

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A new multipoint method for genome-wide association studies by imputation of genotypes

2 October 2017

1 reference

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Src protein tyrosine kinase family and acute inflammatory responses.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Racial variation in clinical and immunological manifestations of systemic sclerosis.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Modulation of prosurvival signaling in fibroblasts by a protein kinase inhibitor protects against fibrotic tissue injury.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Haploview: analysis and visualization of LD and haplotype maps

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Src-family kinases: rheostats of immune cell signaling

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Following the molecular pathways toward an understanding of the pathogenesis of systemic sclerosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Criteria for the classification of early systemic sclerosis.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

NF-kappaB: a key role in inflammatory diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Nuclear factor-kappaB: a pivotal transcription factor in chronic inflammatory diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Preliminary criteria for the classification of systemic sclerosis (scleroderma). Subcommittee for scleroderma criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee

2 October 2017

1 reference

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BANK1 functional variants are associated with susceptibility to diffuse systemic sclerosis in Caucasians

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

NFKB1 -94 insertion/deletion ATTG polymorphism contributes to risk of systemic lupus erythematosus.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Association of a functional polymorphism in the IRF5 region with systemic sclerosis in a Japanese population.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Src kinases in systemic sclerosis: central roles in fibroblast activation and in skin fibrosis

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Analysis of the functional NFKB1 promoter polymorphism in rheumatoid arthritis and systemic lupus erythematosus.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

Myofibroblast differentiation by transforming growth factor-beta1 is dependent on cell adhesion and integrin signaling via focal adhesion kinase.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3368627

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort

23 September 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS099

Preliminary criteria for the classification of systemic sclerosis (scleroderma)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS099

STAT4is a genetic risk factor for systemic sclerosis having additive effects withIRF5on disease susceptibility and related pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS099

Association of the TNFAIP3 rs5029939 variant with systemic sclerosis in the European Caucasian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS099

Association between theIRF5rs2004640 functional polymorphism and systemic sclerosis: A new perspective for pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS099

Clinical, immunologic, and genetic features of familial systemic sclerosis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22407130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The many faces of scleroderma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22407130

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDS099

1 reference

11 August 2017

1 reference

11 August 2017

1 reference