Carlos Alberto
Flores Infante
External Researcher
Karolinska Institute
Estocolmo, Suecia
2026
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Defective RNA Polymerase III sensing of mitochondrial DNA in pulmonary epithelial cells impairs type I IFN immunity to SARS-CoV-2
Proceedings of the National Academy of Sciences of the United States of America, Vol. 123, Núm. 12
2025
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A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity
Journal of Experimental Medicine, Vol. 222, Núm. 2
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Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2
Nature Communications , Vol. 16, Núm. 1
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The seven enigmas of SARS-CoV-2: From the past to the future
Journal of Human Immunity, Vol. 1, Núm. 4
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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SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency
Journal of Experimental Medicine, Vol. 221, Núm. 9
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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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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A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection
Nature Immunology, Vol. 23, Núm. 2, pp. 159-164
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Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis
Journal of Clinical Immunology
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
2021
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From Your Nose to Your Toes: A Review of Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic‒Associated Pernio
Journal of Investigative Dermatology, Vol. 141, Núm. 12, pp. 2791-2796
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Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use
European Respiratory Journal, Vol. 57, Núm. 5
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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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Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Science, Vol. 370, Núm. 6515
2018
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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