Sekar Kathiresan
Genetics · 2007–2021
A researcher in the Science corpus: 54 papers; trusts 5 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 667 citations into it; #2,591 of 6,854 by trust here, #58 by citations
- Surgery — 186 citations into it; #389 of 1,106 by trust here, #78 by citations
- Cancer Research — 104 citations into it
- Economics and Econometrics — 19 citations into it
Whom Sekar Kathiresan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Sekar Kathiresan overall
Papers from Sekar Kathiresan's perspective
Ordered by how strongly the researchers Sekar Kathiresan trusts endorse each paper. Same corpus, a different order for every researcher.
- Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology (Statistics in Medicine)
- Newly identified loci that influence lipid concentrations and risk of coronary artery disease (Nature Genetics)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (Nature Genetics)
- SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap (Bioinform.)
- Sex Hormone–Binding Globulin and Risk of Type 2 Diabetes in Women and Men (New England Journal of Medicine)
- Principal components analysis corrects for stratification in genome-wide association studies
- Next-generation genotype imputation service and methods (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9 (Nature Genetics)
Their papers
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus (2010) — 1,164 citations
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Testing for an Unusual Distribution of Rare Variants (2011) — 617 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels (2007) — 2,928 citations
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease (2017) — 34 citations
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores (2015) — 1,263 citations
- Searching for missing heritability: Designing rare variant association studies (2014) — 633 citations
- In vivo CRISPR base editing of PCSK9 durably lowers cholesterol in primates (2021) — 676 citations
- The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2012) — 551 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) — 1,140 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies (2011) — 531 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Polygenic prediction of weight and obesity trajectories from birth to adulthood (2019) — 657 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations