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UnknownAn explainable model of host genetic interactions linked to COVID-19 severity.
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S-EPMC9606365 | biostudies-literature
UnknownCommon, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity.
Not available
S-EPMC8661833 | biostudies-literature
UnknownRare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients.
Not available
S-EPMC8703210 | biostudies-literature
UnknownUltra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder.
Not available
S-EPMC10276396 | biostudies-literature
UnknownGain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes.
Not available
S-EPMC9776607 | biostudies-literature
UnknownA first update on mapping the human genetic architecture of COVID-19.
Not available
S-EPMC9352569 | biostudies-literature
UnknownWhole-genome sequencing reveals host factors underlying critical COVID-19.
Not available
S-EPMC9259496 | biostudies-literature
UnknownMapping the human genetic architecture of COVID-19.
Not available
S-EPMC8674144 | biostudies-literature
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