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UnknownA System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program.
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S-EPMC8485147 | biostudies-literature
UnknownRare coding variants in RCN3 are associated with blood pressure.
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S-EPMC8858539 | biostudies-literature
UnknownDynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
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S-EPMC7483769 | biostudies-literature
UnknownA statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies.
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S-EPMC11981678 | biostudies-literature
UnknownSequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
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S-EPMC7875770 | biostudies-literature
UnknownPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies.
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S-EPMC10084891 | biostudies-literature
UnknownA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
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S-EPMC10008172 | biostudies-literature
UnknownMultiorgan MRI findings after hospitalisation with COVID-19 in the UK (C-MORE): a prospective, multicentre, observational cohort study.
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S-EPMC7615263 | biostudies-literature
UnknownLong term health outcomes in people with diabetes 12 months after hospitalisation with COVID-19 in the UK: a prospective cohort study.
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S-EPMC11743801 | biostudies-literature
UnknownEffect of Convalescent Plasma on Organ Support-Free Days in Critically Ill Patients With COVID-19: A Randomized Clinical Trial.
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S-EPMC8491132 | biostudies-literature
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