Sekar Kathiresan


Ontology type: schema:Person     


Person Info

NAME

Sekar

SURNAME

Kathiresan

Publications in SciGraph latest 50 shown

  • 2021-12-09 The power of genetic diversity in genome-wide association studies of lipids in NATURE
  • 2021-11-08 Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases in NATURE METABOLISM
  • 2021-11-02 Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response in NATURE GENETICS
  • 2021-10-05 A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response in NATURE GENETICS
  • 2021-05-19 In vivo CRISPR base editing of PCSK9 durably lowers cholesterol in primates in NATURE
  • 2021-05-11 Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic test in GENETICS IN MEDICINE
  • 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices in NATURE COMMUNICATIONS
  • 2021-03-11 Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes in NATURE
  • 2021-02-03 Author Correction: A structural variation reference for medical and population genetics in NATURE
  • 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease in NATURE COMMUNICATIONS
  • 2020-10-14 Inherited causes of clonal haematopoiesis in 97,691 whole genomes in NATURE
  • 2020-08-24 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale in NATURE GENETICS
  • 2020-08-20 Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions in NATURE COMMUNICATIONS
  • 2020-05-27 A structural variation reference for medical and population genetics in NATURE
  • 2020-05-07 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy in NATURE COMMUNICATIONS
  • 2020-04-01 Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2020-01-08 A brief history of human disease genetics in NATURE
  • 2019-11-26 Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores in GENOME MEDICINE
  • 2019-11-01 Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease in NATURE GENETICS
  • 2019-07-08 Genome-wide association study of peripheral artery disease in the Million Veteran Program in NATURE MEDICINE
  • 2019-06-03 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2019-02-25 Biological and clinical insights from genetics of insomnia symptoms in NATURE GENETICS
  • 2018-11-14 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-10-01 Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia in GENETICS IN MEDICINE
  • 2018-10-01 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program in NATURE GENETICS
  • 2018-09-17 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-08-23 Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2018-08-23 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals in NATURE COMMUNICATIONS
  • 2018-08-13 Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations in NATURE GENETICS
  • 2018-07-04 Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries in NATURE COMMUNICATIONS
  • 2018-06-13 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-06-11 Multi-ethnic genome-wide association study for atrial fibrillation in NATURE GENETICS
  • 2018-04-24 Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease in NATURE COMMUNICATIONS
  • 2018-04-09 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-03-16 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-03-16 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12-22 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-10-30 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-10-30 Exome chip meta-analysis identifies novel loci and East Asian–specific coding variants that contribute to lipid levels and coronary artery disease in NATURE GENETICS
  • 2017-08-23 Putative medicines that mimic mutations in NATURE
  • 2017-08-21 A human APOC3 missense variant and monoclonal antibody accelerate apoC-III clearance and lower triglyceride-rich lipoprotein levels in NATURE MEDICINE
  • 2017-07-17 Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease in NATURE GENETICS
  • 2017-07-14 Is ANGPTL3 the next PCSK9? in NATURE REVIEWS ENDOCRINOLOGY
  • 2017-05-22 Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms in NATURE GENETICS
  • 2017-04-17 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-04-13 Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity in NATURE
  • 2017-03-13 Genetics of coronary artery disease: discovery, biology and clinical translation in NATURE REVIEWS GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-11-08 Gene-gene Interaction Analyses for Atrial Fibrillation in SCIENTIFIC REPORTS
  • 2016-10-17 Prospective functional classification of all possible missense variants in PPARG in NATURE GENETICS
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