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Search Results to Rasika Ann Mathias

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Mathias, Rasika

One or more keywords matched the following items that are connected to Mathias, Rasika

Item Type	Name
Academic Article	On the threshold from genome-wide association studies to whole-genome sequencing. Looking for signal in all the right places.
Academic Article	Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data.
Academic Article	High-Throughput Sequencing in Respiratory, Critical Care, and Sleep Medicine Research. An Official American Thoracic Society Workshop Report.
Academic Article	Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
Academic Article	Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.
Concept	Whole Genome Sequencing
Academic Article	Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
Academic Article	De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
Academic Article	Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
Academic Article	Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
Academic Article	Transcriptional profile of platelets and iPSC-derived megakaryocytes from whole-genome and RNA sequencing.
Academic Article	Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium.
Academic Article	Whole genome sequencing identifies novel genetic mutations in patients with eczema herpeticum.
Academic Article	Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Academic Article	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.
Academic Article	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Academic Article	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Academic Article	Genome sequencing unveils a regulatory landscape of platelet reactivity.
Academic Article	Multiethnic genome-wide and HLA association study of total serum IgE level.
Academic Article	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Academic Article	Rare coding variants in RCN3 are associated with blood pressure.
Academic Article	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.
Academic Article	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.
Academic Article	A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Academic Article	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.
Academic Article	Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.
Academic Article	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.
Academic Article	Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium.
Academic Article	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Academic Article	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.
Academic Article	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.

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Whole Genome Sequencing