R. Scott
Genetics · Nature Genetics · 2012–2019
A researcher in the Science corpus: 13 papers; trusts 2 researchers and is trusted by 4 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 231 citations into it; #2,792 of 6,854 by trust here, #620 by citations
Whom R. Scott trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts R. Scott overall
Papers from R. Scott's perspective
Ordered by how strongly the researchers R. Scott trusts endorse each paper. Same corpus, a different order for every researcher.
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
- Large-scale association analyses identifies 13 new susceptibility loci for coronary artery disease (Nature Genetics)
- Mendelian randomization as an instrumental variable approach to causal inference (Statistical Methods in Medical Research)
- Avoiding bias from weak instruments in Mendelian randomization studies. (International Journal of Epidemiology)
- Mendelian randomization: prospects, potentials, and limitations. (International Journal of Epidemiology)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Instruments for Causal Inference: An Epidemiologist's Dream?
- Instrumental Variables and GMM: Estimation and Testing
- Genomic atlas of the human plasma proteome (Nature)
- The druggable genome and support for target identification and validation in drug development (Science Translational Medicine)
Their papers
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) — 633 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes (2017) — 401 citations
- Using published data in Mendelian randomization: a blueprint for efficient identification of causal risk factors (2015) — 1,618 citations
- Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) — 841 citations