J. Thompson
Genetics · Nature Genetics · 2002–2019
A researcher in the Science corpus: 20 papers; trusts 10 researchers and is trusted by 11 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 202 citations into it; #840 of 6,854 by trust here, #97 by citations
- Surgery — 61 citations into it
- Statistics and Probability — 30 citations into it; #12,199 of 12,932 by trust here, #7,508 by citations
- Pediatrics, Perinatology and Child Health — 15 citations into it
- Rheumatology — 14 citations into it
Whom J. Thompson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- George Davey Smith
- Stephen Burgess
- J. Bowden
- S. Thompson
- Julian P. T. Higgins
- Vanessa Didelez
- Shah Ebrahim
Who trusts J. Thompson overall
Papers from J. Thompson's perspective
Ordered by how strongly the researchers J. Thompson trusts endorse each paper. Same corpus, a different order for every researcher.
- Mendelian randomization as an instrumental variable approach to causal inference (Statistical Methods in Medical Research)
- Mendelian randomization: prospects, potentials, and limitations. (International Journal of Epidemiology)
- Power and instrument strength requirements for Mendelian randomization studies using multiple genetic variants. (International Journal of Epidemiology)
- On Instrumental Variables Estimation of Causal Odds Ratios
- Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression (International Journal of Epidemiology)
- Avoiding bias from weak instruments in Mendelian randomization studies. (International Journal of Epidemiology)
- Instrumental Variables Estimation With Some Invalid Instruments and its Application to Mendelian Randomization
- Mendelian randomization: genetic anchors for causal inference in epidemiological studies (Human Molecular Genetics)
- Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator (Genetic Epidemiology)
- Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data (Genetic Epidemiology)
Their papers
- Genomewide Association Analysis of Coronary Artery Disease (2007) — 2,121 citations
- Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption (2018) — 879 citations
- Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants (2009) — 1,094 citations
- DNA methylation and body-mass index: a genome-wide analysis. (2014) — 729 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- White Cell Telomere Length and Risk of Premature Myocardial Infarction (2003) — 616 citations
- Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies (2011) — 531 citations
- Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults Implications for Primary Prevention (2019)
- Improving the visualization, interpretation and analysis of two-sample summary data Mendelian randomization via the Radial plot and Radial regression (2018) — 561 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Assessing the suitability of summary data for two-sample Mendelian randomization analyses using MR-Egger regression: the role of the I2 statistic (2016) — 1,508 citations
- Detecting pleiotropy in Mendelian randomisation studies with summary data and a continuous outcome (2015) — 1,439 citations
- Identification of seven loci affecting mean telomere length and their association with disease (2013) — 909 citations
- Large-scale association analyses identifies 13 new susceptibility loci for coronary artery disease (2011) — 1,948 citations
- Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior (2010) — 726 citations
- Biological, Clinical, and Population Relevance of 95 Loci for Blood Lipids (2010) — 3,781 citations
- Telomere length, risk of coronary heart disease, and statin treatment in the West of Scotland Primary Prevention Study: a nested case-control study. (2007) — 686 citations
- Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations
- Telomere shortening in atherosclerosis. (2002) — 621 citations