Publications en collaboration avec des chercheurs de Instituto de Parasitología y Biomedicina López Neyra (21)

2016

  1. Analysis of plasminogen genetic variants in multiple sclerosis patients

    G3: Genes, Genomes, Genetics, Vol. 6, Núm. 7, pp. 2073-2079

2015

  1. A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosis

    Human Molecular Genetics, Vol. 24, Núm. 19, pp. 5619-5627

  2. A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bands

    Multiple Sclerosis, Vol. 21, Núm. 9, pp. 1104-1111

  3. Genome-wide significant association with seven novel multiple sclerosis risk loci

    Journal of Medical Genetics, Vol. 52, Núm. 12, pp. 848-855

  4. Influence of the LILRA3 deletion on multiple sclerosis risk: Original data and meta-analysis

    PLoS ONE, Vol. 10, Núm. 8

2014

  1. HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV

    Retrovirology, Vol. 11, Núm. 1

  2. Human endogenous retrovirus HERV-Fc1 association with multiple sclerosis susceptibility: A meta-analysis

    PLoS ONE, Vol. 9, Núm. 3

2013

  1. Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6

    PLoS ONE, Vol. 8, Núm. 4

  2. Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis

    Journal of Medical Genetics, Vol. 50, Núm. 1, pp. 25-33

  3. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

    Brain, Vol. 136, Núm. 6, pp. 1778-1782

2012

  1. A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

    Genes and Immunity, Vol. 13, Núm. 1, pp. 21-28

  2. ANKRD55 and DHCR7 are novel multiple sclerosis risk loci

    Genes and Immunity, Vol. 13, Núm. 3, pp. 253-257

  3. Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis

    Multiple Sclerosis Journal, Vol. 18, Núm. 7, pp. 983-990

  4. Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1

    PLoS ONE, Vol. 7, Núm. 5

  5. Replication study of 10 genes showing evidence for association with multiple sclerosis: Validation of TMEM39A, IL12B and CLBL genes

    Multiple Sclerosis Journal, Vol. 18, Núm. 7, pp. 959-965

2011

  1. Members 6B and 14 of the TNF receptor superfamily in multiple sclerosis predisposition

    Genes and Immunity, Vol. 12, Núm. 2, pp. 145-148

  2. Replication of top markers of a genome-wide association study in multiple sclerosis in Spain

    Genes and Immunity, Vol. 12, Núm. 2, pp. 110-115

2010

  1. Polymorphisms in the IL2, IL2RA and IL2RB genes in multiple sclerosis risk

    European Journal of Human Genetics, Vol. 18, Núm. 7, pp. 794-799

  2. STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility

    Genes and Immunity, Vol. 11, Núm. 3, pp. 264-268

  3. The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis

    Genes and Immunity, Vol. 11, Núm. 5, pp. 439-445