Publications by authors named "Jezabel Varade"

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Central Role of Semaphorin 3B in a Serum-Induced Arthritis Model and Reduced Levels in Patients With Rheumatoid Arthritis.
Ana Igea, Tiago Carvalheiro, Beatriz Malvar-Fernández, Sara Martinez-Ramos, Carlos Rafael-Vidal

Arthritis Rheumatol· June 2022

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and Genes are Associated With Selective IgA Deficiency.
Che Kang Lim, Paola G Bronson, Jezabel Varade, Timothy W Behrens, Lennart Hammarström

Front Genet· December 2021

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Human immunology and immunotherapy: main achievements and challenges.
Jezabel Varadé, Susana Magadán, África González-Fernández

Cell Mol Immunol· April 2021

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Fucosyltransferase Gene Polymorphisms and Lewisb-Negative Status Are Frequent in Swedish Newborns, With Implications for Infectious Disease Susceptibility and Personalized Medicine.
Jovanka R King, Jezabel Varadé, Lennart Hammarström

J Pediatric Infect Dis Soc· December 2019

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Functional implications of single nucleotide polymorphisms rs662 and rs854860 on the antioxidative activity of paraoxonase1 (PON1) in patients with rheumatoid arthritis.
Arkaitz Mucientes, Benjamín Fernández-Gutiérrez, Eva Herranz, Luis Rodriguez-Rodriguez, Jezabel Varadé

Clin Rheumatol· May 2019

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Novel genetic loci associated HLA-B*08:01 positive myasthenia gravis.
Jezabel Varade, Ning Wang, Che Kang Lim, Tao Zhang, Yuanwei Zhang

J Autoimmun· March 2018

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A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis.
Fuencisla Matesanz, Victor Potenciano, Maria Fedetz, Priscila Ramos-Mozo, María del Mar Abad-Grau

Hum Mol Genet· October 2015

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A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands.
Mercedes Delgado-García, Fuencisla Matesanz, Antonio Alcina, María Fedetz, María Isabel García-Sánchez

Mult Scler· August 2015

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Multiple sclerosis retrovirus-like envelope gene: Role of the chromosome 20 insertion.
Jezabel Varadé, Marta García-Montojo, Belén de la Hera, Iris Camacho, M Ángel García-Martínez

BBA Clin· June 2015

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Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: a meta-analysis.
Belén de la Hera, Jezabel Varadé, Marta García-Montojo, Antonio Alcina, María Fedetz

PLoS One· January 2015

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HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV.
Marta García-Montojo, Belén de la Hera, Jezabel Varadé, Ana de la Encarnación, Iris Camacho

Retrovirology· January 2014

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Candidate gene study of TRAIL and TRAIL receptors: association with response to interferon beta therapy in multiple sclerosis patients.
Carlos López-Gómez, Almudena Pino-Ángeles, Teresa Órpez-Zafra, María Jesús Pinto-Medel, Begoña Oliver-Martos

PLoS One· December 2013

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Role of the human endogenous retrovirus HERV-K18 in autoimmune disease susceptibility: study in the Spanish population and meta-analysis.
Belén de la Hera, Jezabel Varadé, Marta García-Montojo, José Ramón Lamas, Ana de la Encarnación

PLoS One· November 2013

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Alternative splicing and proteolytic rupture contribute to the generation of soluble IL-6 receptors (sIL-6R) in rheumatoid arthritis.
José Ramón Lamas, Luis Rodríguez-Rodríguez, Pilar Tornero-Esteban, Esther Villafuertes, José Hoyas

Cytokine· March 2013

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Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis.
Antonio Alcina, Maria Fedetz, Oscar Fernández, Albert Saiz, Guillermo Izquierdo

J Med Genet· January 2013

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Combined influence of genetic and environmental factors in age of rheumatoid arthritis onset.
Luis Rodríguez-Rodríguez, José Ramón Lamas, Jezabel Varadé, Pilar Tornero-Esteban, Lydia Abasolo

Rheumatol Int· October 2012

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Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes.
Jezabel Varadé, Manuel Comabella, Miguel A Ortiz, Rafael Arroyo, Oscar Fernández

Mult Scler· July 2012

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TRAIL/TRAIL receptor system and susceptibility to multiple sclerosis.
Carlos López-Gómez, Oscar Fernández, Juan Antonio García-León, María Jesús Pinto-Medel, Begoña Oliver-Martos

PLoS One· December 2011

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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
Gosia Trynka, Karen A Hunt, Nicholas A Bockett, Jihane Romanos, Vanisha Mistry

Nat Genet· November 2011

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Analysis of the REL polymorphism rs13031237 in autoimmune diseases.
Jezabel Varadé, Rogelio Palomino-Morales, Norberto Ortego-Centeno, Manuel Díaz-Rubio, Benjamín Fernández-Gutiérrez

Ann Rheum Dis· April 2011

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Plasma soluble IL-6 receptor concentration in rheumatoid arthritis: associations with the rs8192284 IL6R polymorphism and with disease activity.
Luis Rodríguez-Rodríguez, José Ramón Lamas, Jezabel Varadé, Pedro López-Romero, Pilar Tornero-Esteban

Rheumatol Int· March 2011

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Influence of IL6R rs8192284 polymorphism status in disease activity in rheumatoid arthritis.
José Ramón Lamas, Luis Rodríguez-Rodríguez, Jezabel Varadé, Pedro López-Romero, Pilar Tornero-Esteban

J Rheumatol· August 2010

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NO role of NOS2A susceptibility polymorphisms in rheumatoid arthritis.
Jezabel Varadé, José Ramón Lamas, Miguel Fernández-Arquero, Juan Angel Jover, Emilio G de la Concha

Nitric Oxide· January 2010

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Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients.
Ana Márquez, Jezabel Varadé, Gema Robledo, Alfonso Martínez, Juan Luis Mendoza

Eur J Hum Genet· October 2009

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Shared epitope and anti-cyclic citrullinated peptide antibodies: relationship with age at onset and duration of disease in rheumatoid arthritis.
Jezabel Varadé, Estíbaliz Loza-Santamaría, Miguel Fernández-Arquero, Jose Ramón Lamas, Maria de Los Angeles Figueredo

J Rheumatol· May 2009

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