ANA M.
MARQUEZ ORTIZ
Hospital Clínico San Carlos de Madrid
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Hospital Clínico San Carlos de Madrid (27)
2020
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A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease
Scientific Reports, Vol. 10, Núm. 1
2018
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Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations
Genome Medicine, Vol. 10, Núm. 1
2017
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A combined large-scale meta-Analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus
Annals of the Rheumatic Diseases, Vol. 76, Núm. 1, pp. 286-294
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New insights into the genetic component of non-infectious uveitis through an Immunochip strategy
Journal of Medical Genetics, Vol. 54, Núm. 1, pp. 38-46
2016
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LILRA3 deficiency is not involved in the giant cell arteritis and systemic sclerosis predisposition
Clinical and Experimental Rheumatology
2015
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Specific association of IL17A genetic variants with panuveitis
British Journal of Ophthalmology, Vol. 99, Núm. 4, pp. 566-570
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Study of association of CTLA4 gene variants to non-anterior uveitis
Tissue Antigens, Vol. 86, Núm. 5, pp. 373-376
2014
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A candidate gene approach identifies an IL33 genetic variant as a novel genetic risk factor for GCA
PLoS ONE, Vol. 9, Núm. 11
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Analysis of two autoimmunity genes, IRAK1 and MECP2, in giant cell arteritis
Clinical and Experimental Rheumatology, Vol. 32, Núm. SUPPL.82
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Influence of the IL17A locus in giant cell arteritis susceptibility
Annals of the Rheumatic Diseases, Vol. 73, Núm. 9, pp. 1742-1745
2013
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Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition
BMC Medical Genetics, Vol. 14, Núm. 1
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Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis
Annals of the Rheumatic Diseases, Vol. 72, Núm. 11, pp. 1882-1886
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Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis
Molecular Vision, Vol. 19, pp. 638-643
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No evidence of association between common autoimmunity STAT4 and IL23R risk polymorphisms and non-anterior uveitis
PLoS ONE, Vol. 8, Núm. 11
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Two Functional Variants of IRF5 Influence the Development of Macular Edema in Patients with Non-Anterior Uveitis
PLoS ONE, Vol. 8, Núm. 10
2010
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STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility
Genes and Immunity, Vol. 11, Núm. 3, pp. 264-268
2009
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Effect of BSN-MST1 locus on inflammatory bowel disease and multiple sclerosis susceptibility
Genes and Immunity, Vol. 10, Núm. 7, pp. 631-635
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Novel association of the interleukin 2-interleukin 21 region with inflammatory bowel disease
American Journal of Gastroenterology, Vol. 104, Núm. 8, pp. 1968-1975
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Role of ATG16L1 Thr300Ala polymorphism in inflammatory bowel disease: A study in the spanish population and a meta-analysis
Inflammatory Bowel Diseases, Vol. 15, Núm. 11, pp. 1697-1704
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Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15- Crohn's disease patients
European Journal of Human Genetics, Vol. 17, Núm. 10, pp. 1304-1308