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Benchmarking Association Analyses of Continuous Exposures with RNA-seq in Observational Studies
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2021 |
10.1101/2021.02.12.430989 |
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Pangenomics enables genotyping of known structural variants in 5202 diverse genomes
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2021 |
10.1101/2020.12.04.412486 |
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Nakao, Tetsushi |
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
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2021 |
medRxiv |
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Sofer, Tamar |
BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion
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2021 |
10.1101/2021.01.08.21249450 |
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Wessel, Jennifer |
Whole Genome Sequence Association Analysis of Fasting Glucose and Fasting Insulin Levels in Diverse Cohorts from the NHLBI TOPMed Program
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2021 |
medrxiv |
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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics
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2021 |
10.1101/2021.03.08.434451 |
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Franceschini, Nora |
Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium
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2021 |
10.1016/j.ebiom.2020.103157 |
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Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium
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2021 |
10.1016/j.ebiom.2020.103157 |
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Li, Yun |
eSCAN: Scan Regulatory Regions for Aggregate Association Testing using Whole Genome Sequencing Data
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2020 |
10.1101/2020.11.30.405266 |
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Peloso, Gina |
Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes
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2020 |
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