C. Emdin
Genetics · 2015–2018
A researcher in the Science corpus: 9 papers; trusts 1 researcher and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 50 citations into it; #4,369 of 6,854 by trust here, #2,063 by citations
Whom C. Emdin trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts C. Emdin overall
Papers from C. Emdin's perspective
Ordered by how strongly the researchers C. Emdin trusts endorse each paper. Same corpus, a different order for every researcher.
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- Sequence variations in PCSK9, low LDL, and protection against coronary heart disease.
- Genetic variants associated with Lp(a) lipoprotein level and coronary disease. (New England Journal of Medicine)
- ggplot2: Elegant Graphics for Data Analysis
- 'Mendelian randomization': can genetic epidemiology contribute to understanding environmental determinants of disease? (International Journal of Epidemiology)
- ClinVar: public archive of relationships among sequence variation and human phenotype
- Chronic kidney disease: global dimension and perspectives (The Lancet)
- Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia (Journal of the American College of Cardiology)
- Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. (Journal of Clinical Lipidology)
Their papers
- Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease (2017) — 34 citations
- Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease (2018) — 80 citations
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) — 114 citations
- Mendelian Randomization. (2017) — 2,655 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
- Atrial fibrillation and risks of cardiovascular disease, renal disease, and death: systematic review and meta-analysis (2016) — 800 citations
- Blood pressure lowering for prevention of cardiovascular disease and death: a systematic review and meta-analysis. (2016) — 2,993 citations
- Blood pressure lowering in type 2 diabetes: a systematic review and meta-analysis. (2015) — 784 citations