Jie Zheng
Genetics · bioRxiv · 2016–2020
A researcher in the Science corpus: 5 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 150 citations into it
Whom Jie Zheng trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- George Davey Smith
- Stephen Burgess
- J. Bowden
- Gibran Hemani
- Jian Yang
- Frank Dudbridge
- Deborah Lawlor
- O. Yavors’ka
- F. Hartwig
- Peter M. Visscher
Who trusts Jie Zheng overall
Papers from Jie Zheng's perspective
Ordered by how strongly the researchers Jie Zheng 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)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Power and Predictive Accuracy of Polygenic Risk Scores (PLoS Genetics)
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
- Efficient Design for Mendelian Randomization Studies: Subsample and 2-Sample Instrumental Variable Estimators (American 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)
- Overcoming the winner's curse: estimating penetrance parameters from case-control data.
Their papers
- Recent Developments in Mendelian Randomization Studies (2017) — 945 citations
- 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
- LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis (2016) — 890 citations