P. Natarajan
Genetics · Nature · 2015–2022
A researcher in the Science corpus: 14 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 214 citations into it
Whom P. Natarajan trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- Frank Dudbridge (in Genetics)
Papers from P. Natarajan's perspective
Ordered by how strongly the researchers P. Natarajan trusts endorse each paper. Same corpus, a different order for every researcher.
- ClinVar: public archive of relationships among sequence variation and human phenotype
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- Sequence variations in PCSK9, low LDL, and protection against coronary heart disease.
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Genetic variants associated with Lp(a) lipoprotein level and coronary disease. (New England Journal of Medicine)
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Fast and accurate long-range phasing in a UK Biobank cohort
- Clinical use of current polygenic risk scores may exacerbate health disparities
- Beyond GWASs: illuminating the dark road from association to function. (American Journal of Human Genetics)
Their papers
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease (2017) — 34 citations
- Lipoprotein(a) in atherosclerotic cardiovascular disease and aortic stenosis: a European Atherosclerosis Society consensus statement (2022) — 1,097 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- A statistical framework for cross-tissue transcriptome-wide association analysis (2018) — 367 citations
- Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations (2018) — 2,683 citations
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) — 80 citations
- Clonal hematopoiesis and risk for atherosclerotic cardiovascular disease (2017) — 2,178 citations
- Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity (2017) — 301 citations
- Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting (2017) — 491 citations
- Ultra-rare disruptive and damaging mutations influence educational attainment in the general population (2016) — 97 citations
- Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease (2016) — 1,197 citations
- Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia (2016) — 842 citations
- Human knockouts in a cohort with a high rate of consanguinity (2015) — 12 citations