FACULTAD DE CIENCIAS
Facultad
Charité
Berlín, AlemaniaPublicaciones en colaboración con investigadores/as de Charité (23)
2024
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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Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet’s Disease
Arthritis and Rheumatology, Vol. 73, Núm. 7, pp. 1244-1252
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Integrative Analysis Reveals a Molecular Stratification of Systemic Autoimmune Diseases
Arthritis and Rheumatology, Vol. 73, Núm. 6, pp. 1073-1085
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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
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Mapping the human genetic architecture of COVID-19
Nature, Vol. 600, Núm. 7889, pp. 472-477
2020
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The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
Science, Vol. 370, Núm. 6513, pp. 208-214
2019
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Large expert-curated database for benchmarking document similarity detection in biomedical literature search
Database, Vol. 2019, pp. 1-67
2018
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Inhalation of peptide-loaded nanoparticles improves heart failure
Science Translational Medicine, Vol. 10, Núm. 424
2017
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Structural basis of the oncogenic interaction of phosphatase PRL-1 with the magnesium transporter CNNM2
Journal of Biological Chemistry, Vol. 292, Núm. 3, pp. 786-801
2016
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Influence of TYK2 in systemic sclerosis susceptibility: A new locus in the IL-12 pathway
Annals of the Rheumatic Diseases, Vol. 75, Núm. 8, pp. 1521-1526
2014
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A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility
Arthritis Research and Therapy, Vol. 16, Núm. 1
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Identification of IL12RB1 as a Novel Systemic Sclerosis Susceptibility Locus
Arthritis and Rheumatology
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Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis
American Journal of Human Genetics, Vol. 94, Núm. 1, pp. 47-61
2013
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The Systemic Lupus Erythematosus IRF5 Risk Haplotype Is Associated with Systemic Sclerosis
PLoS ONE, Vol. 8, Núm. 1
2012
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A GWAS follow-up study reveals the association of the IL12RB2 gene with systemic sclerosis in Caucasian populations
Human Molecular Genetics, Vol. 21, Núm. 4, pp. 926-933
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A rare polymorphism in the gene for Toll-like receptor 2 is associated with systemic sclerosis phenotype and increases the production of inflammatory mediators
Arthritis and Rheumatism, Vol. 64, Núm. 1, pp. 264-271
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Polymorphisms in the interleukin 4, interleukin 13, and corresponding receptor genes are not associated with systemic sclerosis and do not influence gene expression
Journal of Rheumatology, Vol. 39, Núm. 1, pp. 112-118
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The autoimmune disease-associated IL2RA locus is involved in the clinical manifestations of systemic sclerosis
Genes and Immunity, Vol. 13, Núm. 2, pp. 191-196