M. Docteur BAPTISTE COUSTET

Bibliographie

• Comparaison de l'échographique des enthèses dans la polyarthrite rhumatoïde et la spondyloarthrite

  2019

  ArticleRevue du Rhumatisme

• Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

  2017

  ArticleEuropean Respiratory Journal

• Reply to the comment of Brinster et al. “Acquired hemophilia, rheumatoid arthritis, and TNFα antagonists”

  2015

  ArticleJoint Bone Spine

• Identification of Secreted Phosphoprotein 1 Gene as a new Rheumatoid Arthritis Susceptibility Gene

  2014

  ArticleAnnals of the Rheumatic Diseases

• Independent Replication and Metaanalysis of Association Studies Establish TNFSF4 as a Susceptibility Gene Preferentially Associated with the Subset of Anticentromere-positive Patients with Systemic Sclerosis

  2012

  ArticleJournal of Rheumatology

• C8orf13-BLK Is a Genetic Risk Locus for Systemic Sclerosis and Has Additive Effects With BANK1: Results From a Large French Cohort and Meta-Analysis

  2011

  ArticleArthritis and Rheumatism

• Association Study of ITGAM, ITGAX, and CD58 Autoimmune Risk Loci in Systemic Sclerosis: Results from 2 Large European Caucasian Cohorts

  2011

  ArticleJournal of Rheumatology

Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).

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Top publications · les plus citées

• 1

  Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis

  The European respiratory journal · 2017

  📚 186 citations🎯 RCR 7.39Top 4% NIH🔓 Open Access📄 PDF gratuit ↗

  Lire l'abstract Crossref ↓

  Despite its high prevalence and mortality, little is known about the pathogenesis of rheumatoid arthritis-associated interstitial lung disease (RA-ILD). Given that familial pulmonary fibrosis (FPF) and RA-ILD frequently share the usual pattern of interstitial pneumonia and common environmental risk factors, we hypothesised that the two diseases might share additional risk factors, including FPF-linked genes. Our aim was to identify coding mutations of FPF-risk genes associated with RA-ILD.We used whole exome sequencing (WES), followed by restricted analysis of a discrete number of FPF-linked genes and performed a burden test to assess the excess number of mutations in RA-ILD patients compared to controls.Among the 101 RA-ILD patients included, 12 (11.9%) had 13 WES-identified heterozygous mutations in theTERT,RTEL1,PARNorSFTPCcoding regions.The burden test, based on 81 RA-ILD patients and 1010 controls of European ancestry, revealed an excess ofTERT,RTEL1,PARNorSFTPCmutations in RA-ILD patients (OR 3.17, 95% CI 1.53–6.12; p=9.45×10−4). Telomeres were shorter in RA-ILD patients with aTERT,RTEL1orPARNmutation than in controls (p=2.87×10−2).Our results support the contribution of FPF-linked genes to RA-ILD susceptibility.

• 2

  Positron emission tomography and computed tomography angiography for the diagnosis of giant cell arteritis: A real-life prospective study

  Medicine · 2016

  📚 102 citations🎯 RCR 5.28Top 7% NIH🔓 Open Access
• 3

  C8orf13-BLK is a genetic risk locus for systemic sclerosis and has additive effects with BANK1: results from a large french cohort and meta-analysis

  Arthritis and rheumatism · 2011

  📚 43 citations🎯 RCR 1.10🔓 Open Access📄 PDF gratuit ↗

Publications scientifiques (18) — classées par pathologie

Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).

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