Author: Pradeep Natarajan

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Preprints

Analysis of protein-coding genetic variation in 60,706 humans

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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease

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Androgen regulates SARS-CoV-2 receptor levels and is associated with severe COVID-19 symptoms in men

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A statistical framework for cross-tissue transcriptome-wide association analysis

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Human knockouts in a cohort with a high rate of consanguinity

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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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Inherited Causes of Clonal Hematopoiesis of Indeterminate Potential in TOPMed Whole Genomes

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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

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Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

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Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

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Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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Heart Rate Variability with Photoplethysmography in 8 Million Individuals: Results and Scaling Relations with Age, Gender, and Time of Day

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Genetic Association of Arterial Stiffness Index with Blood Pressure and Coronary Artery Disease

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Heterozygous ATP-binding Cassette Transporter G5 Gene Deficiency and Risk of Coronary Artery Disease

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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

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Genome-Wide Screening Reveals CSDE1 as a Novel Regulator of the LDL Receptor

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