P. van der Harst
Genetics · 2012–2021
A researcher in the Science corpus: 15 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 273 citations into it
- Surgery — 40 citations into it
- Cardiology and Cardiovascular Medicine — 35 citations into it
Whom P. van der Harst trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from P. van der Harst's perspective
Ordered by how strongly the researchers P. van der Harst trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (Nature)
- 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
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Clinical use of current polygenic risk scores may exacerbate health disparities
- Second-generation PLINK: rising to the challenge of larger and richer datasets (GigaScience)
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- Fast and accurate long-range phasing in a UK Biobank cohort
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
Their papers
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (2016) — 815 citations
- Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease (2017) — 946 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- EU-Wide Cross-Sectional Observational Study of Lipid-Modifying Therapy Use in Secondary and Primary Care: the DA VINCI study. (2020) — 692 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation (2018) — 699 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (2014) — 637 citations
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) — 652 citations
- The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis (2012) — 1,018 citations