Valeriia Haberland
Genetics · 2018–2020
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 86 citations into it
Whom Valeriia Haberland trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Valeriia Haberland's perspective
Ordered by how strongly the researchers Valeriia Haberland trusts endorse each paper. Same corpus, a different order for every researcher.
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Efficient Design for Mendelian Randomization Studies: Subsample and 2-Sample Instrumental Variable Estimators (American Journal of Epidemiology)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression (International Journal of Epidemiology)
- Genome-wide genetic data on ~500,000 UK Biobank participants (bioRxiv)
- Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator (Genetic Epidemiology)
- Triangulation in aetiological epidemiology (International Journal of Epidemiology)
Their papers
- The MRC IEU OpenGWAS data infrastructure (2020) — 798 citations
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) — 633 citations
- The MR-Base platform supports systematic causal inference across the human phenome (2018) — 6,483 citations