Publications by authors named "Antonio Catala-Rabasa"

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A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria.
Fuencisla Matesanz, María Fedetz, Cristina Barrionuevo, Mohamad Karaky, Antonio Catalá-Rabasa

Eur J Hum Genet· November 2016

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High ACSL5 transcript levels associate with systemic lupus erythematosus and apoptosis in Jurkat T lymphocytes and peripheral blood cells.
Antonio Catalá-Rabasa, Dorothy Ndagire, Jose Mario Sabio, Maria Fedetz, Fuencisla Matesanz

PLoS One· July 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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Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.
Antonio Alcina, María Del Mar Abad-Grau, María Fedetz, Guillermo Izquierdo, Miguel Lucas

PLoS One· May 2012

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Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.
Antonio Alcina, Oscar Fernández, Juan Ramón Gonzalez, Antonio Catalá-Rabasa, María Fedetz

Eur J Hum Genet· July 2010

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Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis.
Antonio Alcina, Sreeram V Ramagopalan, Oscar Fernández, Antonio Catalá-Rabasa, María Fedetz

Eur J Hum Genet· May 2010

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