Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy (Q29417020)

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

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scholarly article

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Europe PubMed Central

16 April 2017

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

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Europe PubMed Central

16 April 2017

genome-wide association study

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Jane Worthington

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Anna-Maria Hoffmann-Vold

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Anna-Maria Hoffmann-Vold

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Europe PubMed Central

16 April 2017

object named as

Annika Nordin

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object named as

Pravitt Gourh

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Jose-Ezequiel Martin

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Jose-Ezequiel Martin

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Laura K. Hummers

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Laura K Hummers

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Behrooz Z. Alizadeh

object named as

Behrooz Z Alizadeh

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Patricia E Carreira

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Patricia Carreira

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object named as

Paul G Shiels

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Norberto Ortego-Centeno

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Norberto Ortego-Centeno

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Ariane I. Herrick

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Ariane Herrick

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Leonid Padyukov

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Leonid Padyukov

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object named as

Javier Martin

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Elfride De Baere

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Elfride de Baere

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Peter K. Gregersen

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Peter K Gregersen

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Christopher Amos

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Christopher I Amos

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Nicolas Hunzelmann

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Nicolas Hunzelmann

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Benedicte A Lie

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Benedicte A Lie

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Francisco J. García-Hernandez

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Francisco J García-Hernández

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Paloma García de la Peña Lefebvre

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Paloma García de la Peña

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Shervin Assassi

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Shervin Assassi

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Maureen D Mayes

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Maureen D Mayes

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66

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Filemon K Tan

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Spanish Scleroderma Group

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Spanish Scleroderma Group

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Timothy R D J Radstake

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Timothy R D J Radstake

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Blanca Rueda

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Marieke J H Coenen

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Madelon C Vonk

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Annet Italiaander

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Annet Italiaander

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Roel A Ophoff

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Carmen Pilar Simeón

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Carmen P Simeon

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Miguel Angel Gonzalez-Gay

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Miguel A González-Gay

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María F González-Escribano

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María F González-Escribano

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Paolo Airo

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Roger Hesselstrand

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Roger Hesselstrand

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Filip De Keyser

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Filip de Keyser

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Fredric Houssiau

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Fredric Houssiau

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Meng May Chee

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Rajan Madhok

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Rene Westhovens

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Rene Westhovens

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Alexander Kreuter

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Alexander Kreuter

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Torsten Witte

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Lorenzo Beretta

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Lorenzo Beretta

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Monique Hinchcliff

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Bobby P C Koeleman

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Maria E Serrano-Teruel

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Maria Teruel

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Lina Marcela Diaz-Gallo

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Lina-Marcela Diaz-Gallo

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Marie Vanthuyne

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Marie Vanthuyne

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Vicente Fonollosa

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Vicente Fonollosa

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Rafaella Scorza

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Raffaella Scorza

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Claudio Lunardi

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Claudio Lunardi

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Oyvind Palm

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Gabriela Riemekasten

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M.Carmen Fonseca-Mora

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Carmen Fonseca

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Annemie J Schuerwegh

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Frank C Arnett

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Olga Y. Gorlova

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Jun Ying

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Jacob van Laar

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Vanessa Smith

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John Varga

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Annette T Lee

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Frederick M Wigley

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J Lee Nelson

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Christopher P Denton

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Sandeep Agarwal

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16 April 2017

language of work or name

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publication date

14 July 2011

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Europe PubMed Central

16 April 2017

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Europe PubMed Central

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7

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16 April 2017

e1002178

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7

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16 April 2017

copyright license

Creative Commons Attribution 2.5 Generic

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on focus list of Wikimedia project

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Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci

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

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

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

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Interaction of the Grb10 adapter protein with the Raf1 and MEK1 kinases

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

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Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

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Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

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The ERK5 and ERK1/2 signaling pathways play opposing regulatory roles during chondrogenesis of adult human bone marrow-derived multipotent progenitor cells.

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HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans

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

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Association of the C8orf13-BLK region with systemic sclerosis in North-American and European populations

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

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

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

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21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002178

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Association of HLA class II genes with systemic sclerosis in Spanish patients.

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21 January 2018

Preliminary criteria for the classification of systemic sclerosis (scleroderma)

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21 January 2018

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

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002178

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002178

21 January 2018

BANK1is a genetic risk factor for diffuse cutaneous systemic sclerosis and has additive effects withIRF5andSTAT4

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1002178

21 January 2018

Clinical, immunologic, and genetic features of familial systemic sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

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The many faces of scleroderma

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of STAT4 polymorphism with systemic sclerosis in a Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the FAM167A-BLK region with systemic sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Notch4, a non-HLA gene in the MHC is strongly associated with the most severe form of alopecia areata

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Scleroderma (systemic sclerosis): classification, subsets and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation and management of scleroderma lung disease using bronchoalveolar lavage

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary pulmonary hypertension

1 reference

https://pubmed.ncbi.nlm.nih.gov/21779181

12 December 2020

based on heuristic

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Identifiers

10.1371/JOURNAL.PGEN.1002178

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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