Adam S. Butterworth
Genetics · 2010–2023
A researcher in the Science corpus: 25 papers; trusts 13 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 345 citations into it; #462 of 6,854 by trust here, #663 by citations
- Statistics and Probability — 39 citations into it
- Rheumatology — 25 citations into it
- Economics and Econometrics — 16 citations into it
- Pediatrics, Perinatology and Child Health — 14 citations into it
- Sociology and Political Science — 6 citations into it
Whom Adam S. Butterworth trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Vanessa Didelez
- George Davey Smith
- R. D. Blander
- Brandon L. Pierce
- Stephen Burgess
- Joshua D. Angrist
- Christopher F. Baum
- Nuala Sheehan
- Shah Ebrahim
- M. Bolland
Who trusts Adam S. Butterworth overall
- Stephen Burgess
- J. Bowden
- George Davey Smith
- E. Sanderson
- S. Thompson
- F. Hartwig
- F. Del Greco M
- O. Yavors’ka
- Cosetta Minelli
- N. Davies
Papers from Adam S. Butterworth's perspective
Ordered by how strongly the researchers Adam S. Butterworth trusts endorse each paper. Same corpus, a different order for every researcher.
- Power and instrument strength requirements for Mendelian randomization studies using multiple genetic variants. (International Journal of Epidemiology)
- Instrumental Variables and GMM: Estimation and Testing
- 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)
- Instrumental Variables Regression with Weak Instruments
- Mendelian randomization: prospects, potentials, and limitations. (International Journal of Epidemiology)
- An integrated map of genetic variation from 1,092 human genomes
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- Using multiple genetic variants as instrumental variables for modifiable risk factors (Statistical Methods in Medical Research)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
Their papers
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- PhenoScanner: a database of human genotype–phenotype associations (2016) — 1,277 citations
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 citations
- Association of Cardiometabolic Multimorbidity With Mortality. (2015) — 954 citations
- Mendelian randomization for cardiovascular diseases: principles and applications (2023) — 637 citations
- Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets (2023) — 622 citations
- SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe. (2021) — 1,383 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations (2019) — 1,762 citations
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) — 633 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Genomic atlas of the human plasma proteome (2018) — 1,884 citations
- Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (2018) — 1,405 citations
- Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies (2018) — 1,035 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Polygenic risk score identifies subgroup with higher burden of atherosclerosis and greater relative benefit from statin therapy in the primary prevention setting (2017) — 491 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
- Allelic Landscape of Human Blood Cell Trait Variation and Links (2016)