Medicina
Facultad
Howard Hughes Medical Institute
Chevy Chase, Estados UnidosPublicaciones en colaboración con investigadores/as de Howard Hughes Medical Institute (31)
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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Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children
The Journal of experimental medicine, Vol. 221, Núm. 2
2023
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Inherited human ezrin deficiency impairs adaptive immunity
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 4, pp. 997-1009.e11
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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
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Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs
Science immunology, Vol. 8, Núm. 90, pp. eabp8966
2022
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Autoantibodies against type I IFNs in patients with critical influenza pneumonia
The Journal of experimental medicine, Vol. 219, Núm. 11
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Human genetic and immunological determinants of critical COVID-19 pneumonia
Nature, Vol. 603, Núm. 7902, pp. 587-598
2021
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Clinical and Immunological Features of Human BCL10 Deficiency
Frontiers in Immunology, Vol. 12
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Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain
Journal of Clinical Immunology, Vol. 41, Núm. 5, pp. 914-922
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SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Journal of Experimental Medicine, Vol. 218, Núm. 6
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Spread of a SARS-CoV-2 variant through Europe in the summer of 2020
Nature, Vol. 595, Núm. 7869, pp. 707-712
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Vision, challenges and opportunities for a plant cell atlas
eLife, Vol. 10
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X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19
Science immunology, Vol. 6, Núm. 62
2020
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Autoantibodies against type I IFNs in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
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Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants
American Heart Journal, Vol. 225, pp. 108-119
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Human BCL10 Deficiency due to Homozygosity for a Rare Allele
Journal of Clinical Immunology, Vol. 40, Núm. 2, pp. 388-398
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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
2019
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Mutations in foregut SOX2+ cells induce efficient proliferation via CXCR2 pathway
Protein and Cell, Vol. 10, Núm. 7, pp. 485-495
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The genomic history of the Iberian Peninsula over the past 8000 years
Science, Vol. 363, Núm. 6432, pp. 1230-1234
2017
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Molecular definitions of autophagy and related processes
EMBO Journal, Vol. 36, Núm. 13, pp. 1811-1836