Instituto Universitario de Tecnologías Biomédicas
Instituto de investigación
Charité
Berlín, AlemaniaPublicaciones en colaboración con investigadores/as de Charité (30)
2024
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Erratum: Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19 (Genome medicine (2023) 15 1 (22))
Genome medicine
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Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1
Kidney International Reports, Vol. 9, Núm. 1, pp. 114-133
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
Nature, Vol. 623, Núm. 7988, pp. 803-813
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European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
Nature Communications, Vol. 14, Núm. 1
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Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
Journal of Experimental Medicine, Vol. 220, Núm. 5
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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
Genome Medicine, Vol. 15, Núm. 1
2022
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Effects of Chronic Kidney Disease on Nanomechanics of the Endothelial Glycocalyx Are Mediated by the Mineralocorticoid Receptor
International Journal of Molecular Sciences, Vol. 23, Núm. 18
2021
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Epigenomic and transcriptional profiling identifies impaired glyoxylate detoxification in NAFLD as a risk factor for hyperoxaluria
Cell Reports, Vol. 36, Núm. 8
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
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Light-dependent effects of prefrontal rTMS on emotional working memory
Brain Sciences, Vol. 11, Núm. 4
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
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
2018
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AmpliSeq screening of genes encoding the C-type lectin receptors and their signaling components reveals a common variant in MASP1 associated with pulmonary tuberculosis in an Indian population
Frontiers in Immunology, Vol. 9, Núm. FEB
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Erratum to: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis (Nature Genetics, (2018), 50, 8, (1072-1080), 10.1038/s41588-018-0157-1)
Nature Genetics
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Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Nature Genetics
2017
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Association between telomere length and risk of cancer and non-neoplastic diseases a mendelian randomization study
JAMA Oncology, Vol. 3, Núm. 5, pp. 636-651
2016
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A phase III, randomized, controlled trial of apremilast in patients with psoriatic arthritis: Results of the PALACE 2 trial
Journal of Rheumatology, Vol. 43, Núm. 9, pp. 1724-1734
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222