ENRIQUE GERMÁN
RAYA ÁLVAREZ
PROFESOR TITULAR DE UNIVERSIDAD
Instituto de Parasitología y Biomedicina López Neyra
Armilla, EspañaPublicacións en colaboración con investigadores/as de Instituto de Parasitología y Biomedicina López Neyra (24)
2024
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Molecular subtypes explain lupus epigenomic heterogeneity unveiling new regulatory genetic risk variants
npj Genomic Medicine, Vol. 9, Núm. 1
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Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study
The Lancet Rheumatology, Vol. 6, Núm. 6, pp. e374-e383
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Single-cell transcriptomic profiling reveals a pathogenic role of cytotoxic CD4+ T cells in giant cell arteritis
Journal of Autoimmunity, Vol. 142
2022
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Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
npj Genomic Medicine, Vol. 7, Núm. 1
2021
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A new molecular classification to drive precision treatment strategies in primary Sjögren’s syndrome
Nature Communications, Vol. 12, Núm. 1
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Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature
Scientific Reports, Vol. 11, Núm. 1
2014
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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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Lack of validation of genetic variants associated with anti-tumor necrosis factor therapy response in rheumatoid arthritis: A genome-wide association study replication and meta-analysis
Arthritis Research and Therapy, Vol. 16, Núm. 2
2013
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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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Influence of the STAT3 genetic variants in the susceptibility to psoriatic arthritis and Behcet's disease
Human Immunology, Vol. 74, Núm. 2, pp. 230-233
2012
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NPSR1 gene is associated with reduced risk of rheumatoid arthritis
Journal of Rheumatology, Vol. 39, Núm. 6, pp. 1166-1170
2011
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Evidence for PTPN22 R620W polymorphism as the sole common risk variant for rheumatoid arthritis in the 1p13.2 region
Journal of Rheumatology, Vol. 38, Núm. 11, pp. 2290-2296
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No evidence of association of the KLF12 gene with rheumatoid arthritis in Spanish and Dutch cohorts and a meta-analysis of published data
Human Immunology, Vol. 72, Núm. 9, pp. 779-782
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The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples
Arthritis and Rheumatism, Vol. 63, Núm. 2, pp. 365-372
2010
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Association study of ghrelin receptor gene polymorphisms in rheumatoid arthritis
Clinical and Experimental Rheumatology, Vol. 28, Núm. 1, pp. 25-29
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Deletion of the late cornified envelope genes, LCE3C and LCE3B, is associated with rheumatoid arthritis
Arthritis and Rheumatism, Vol. 62, Núm. 5, pp. 1246-1251
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Identification of HAVCR1 gene haplotypes associated with mRNA expression levels and susceptibility to autoimmune diseases
Human Genetics, Vol. 128, Núm. 2, pp. 221-229
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Identification of the oxidative stress-related gene MSRA as a rheumatoid arthritis susceptibility locus by genome-wide pathway analysis
Arthritis and Rheumatism, Vol. 62, Núm. 11, pp. 3183-3190
2008
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Investigation of CD69 as a new candidate gene for rheumatoid arthritis
Tissue Antigens, Vol. 72, Núm. 3, pp. 206-210
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The IL23R Arg381Gln non-synonymous polymorphism confers susceptibility to ankylosing spondylitis
Annals of the Rheumatic Diseases, Vol. 67, Núm. 10, pp. 1451-1454