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Genetics and Functional Genomics of Spondyloarthritis

Frontiers in immunology, 2018-12, Vol.9, p.2933-2933

2018

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Dissecting the phenotypic and functional heterogeneity of mouse inflammatory osteoclasts by the expression of Cx3cr1

eLife, 2020-05, Vol.9

2020

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Prevalence of spondyloarthritis in reference to HLA-B27 in the French population: results of the GAZEL cohort

Annals of the rheumatic diseases, 2015-04, Vol.74 (4), p.689-693

2015

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Genetic Factors in Autoimmune Myasthenia Gravis

Annals of the New York Academy of Sciences, 2008-06, Vol.1132 (1), p.180-192

2008

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ERAP1 Gene Expression Is Influenced by Nonsynonymous Polymorphisms Associated With Predisposition to Spondyloarthritis

Arthritis & rheumatology (Hoboken, N.J.), 2015-06, Vol.67 (6), p.1525-1534

2015

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Monocyte transcriptomes from patients with axial spondyloarthritis reveal dysregulated monocytopoiesis and a distinct inflammatory imprint

Arthritis research & therapy, 2021-09, Vol.23 (1), p.246-246, Article 246

2021

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Use of Whole‐Blood Transcriptomic Profiling to Highlight Several Pathophysiologic Pathways Associated With Response to Rituximab in Patients With Rheumatoid Arthritis: Data From a Randomized, Controlled, Open‐Label Trial

Arthritis & rheumatology (Hoboken, N.J.), 2014-08, Vol.66 (8), p.2015-2025

2014

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CARMN‐NOTCH2 fusion transcript drives high NOTCH2 expression in glomus tumors of the upper digestive tract

Genes chromosomes & cancer, 2021-11, Vol.60 (11), p.723-732

2021

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STAT1 deficiency underlies a proinflammatory imprint of naive CD4+ T cells in spondyloarthritis

Frontiers in immunology, 2023-10, Vol.14, p.1227281-1227281

2023

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Monocyte distribution width as a biomarker of resistance to corticosteroids in patients with sepsis: the MOCORSEP observational study

Intensive care medicine, 2021-10, Vol.47 (10), p.1161-1164

2021

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What Have We Learned From Family-Based Studies About Spondyloarthritis?

Frontiers in genetics, 2021-06, Vol.12, p.671306-671306

2021

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Cynomolgus macaque IL37 polymorphism and control of SIV infection

Scientific reports, 2019-05, Vol.9 (1), p.7981-7981, Article 7981

2019

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In-Host Adaptation of Salmonella enterica Serotype Dublin during Prosthetic Hip Joint Infection

Emerging infectious diseases, 2018-12, Vol.24 (12), p.2360-2363

2018

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An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus

Nature (London), 2007-08, Vol.448 (7156), p.934-937

2007

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Brief Report: The IL23R Nonsynonymous Polymorphism rs11209026 Is Associated With Radiographic Sacroiliitis in Spondyloarthritis

Arthritis & rheumatology (Hoboken, N.J.), 2013-10, Vol.65 (10), p.2655-2660

2013

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Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations

Molecular medicine (Cambridge, Mass.), 2015-01, Vol.21 (1), p.769-781

2015

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Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Basic and clinical andrology, 2021-11, Vol.31 (1), p.1-27, Article 27

2021

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Association of the PTPN22R620W polymorphism with autoimmune myasthenia gravis

Annals of neurology, 2006-02, Vol.59 (2), p.404-407

2006

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Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France

Human mutation, 2003-12, Vol.22 (6), p.496-496

2003

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Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis

PLoS genetics, 2009-06, Vol.5 (6), p.e1000528-e1000528

2009

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Epigenetics of spondyloarthritis

Joint, bone, spine : revue du rhumatisme, 2020-12, Vol.87 (6), p.565-571

2020

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A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in mice

PloS one, 2024-09, Vol.19 (9), p.e0309974

2024

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Increased thymic development of regulatory T cells in NOD mice is functionally dissociated from type I diabetes susceptibility

European journal of immunology, 2013-05, Vol.43 (5), p.1356-1362

2013

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stringgaussnet: from differentially expressed genes to semantic and Gaussian networks generation

Bioinformatics (Oxford, England), 2015-12, Vol.31 (23), p.3865-3867

2015

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Genetics and Functional Genomics of Spondyloarthritis

Dissecting the phenotypic and functional heterogeneity of mouse inflammatory osteoclasts by the expression of Cx3cr1

Prevalence of spondyloarthritis in reference to HLA-B27 in the French population: results of the GAZEL cohort

Genetic Factors in Autoimmune Myasthenia Gravis

ERAP1 Gene Expression Is Influenced by Nonsynonymous Polymorphisms Associated With Predisposition to Spondyloarthritis

Monocyte transcriptomes from patients with axial spondyloarthritis reveal dysregulated monocytopoiesis and a distinct inflammatory imprint

Use of Whole‐Blood Transcriptomic Profiling to Highlight Several Pathophysiologic Pathways Associated With Response to Rituximab in Patients With Rheumatoid Arthritis: Data From a Randomized, Controlled, Open‐Label Trial

CARMN‐NOTCH2 fusion transcript drives high NOTCH2 expression in glomus tumors of the upper digestive tract

Specific targeting of inflammatory osteoclastogenesis by the probiotic yeast S. boulardii CNCM I-745 reduces bone loss in osteoporosis

STAT1 deficiency underlies a proinflammatory imprint of naive CD4+ T cells in spondyloarthritis

Monocyte distribution width as a biomarker of resistance to corticosteroids in patients with sepsis: the MOCORSEP observational study

What Have We Learned From Family-Based Studies About Spondyloarthritis?

Cynomolgus macaque IL37 polymorphism and control of SIV infection

In-Host Adaptation of Salmonella enterica Serotype Dublin during Prosthetic Hip Joint Infection

An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus

Brief Report: The IL23R Nonsynonymous Polymorphism rs11209026 Is Associated With Radiographic Sacroiliitis in Spondyloarthritis

Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Association of the PTPN22R620W polymorphism with autoimmune myasthenia gravis

Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France

Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis

Epigenetics of spondyloarthritis

A partial deletion within the meiosis-specific sporulation domain SPO22 of Tex11 is not associated with infertility in mice

Increased thymic development of regulatory T cells in NOD mice is functionally dissociated from type I diabetes susceptibility

stringgaussnet: from differentially expressed genes to semantic and Gaussian networks generation

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