Nicholas J. Timpson
Genetics · 2007–2021
A researcher in the Science corpus: 30 papers; trusts 9 researchers and is trusted by 13 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 525 citations into it; #926 of 6,854 by trust here, #57 by citations
- Statistics and Probability — 53 citations into it
- Pediatrics, Perinatology and Child Health — 43 citations into it
- Rheumatology — 29 citations into it; #58 of 221 by trust here, #32 by citations
- Economics and Econometrics — 26 citations into it
Whom Nicholas J. Timpson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Nicholas J. Timpson overall
Papers from Nicholas J. Timpson's perspective
Ordered by how strongly the researchers Nicholas J. Timpson trusts endorse each paper. Same corpus, a different order for every researcher.
- A Survey of Weak Instruments and Weak Identification in Generalized Method of Moments
- LARGE SAMPLE PROPERTIES OF GENERALIZED METHOD OF
- Instruments for Causal Inference: An Epidemiologist's Dream?
- Mendelian randomization as an instrumental variable approach to causal inference (Statistical Methods in Medical Research)
- Major Lipids, Apolipoproteins, and Risk of Vascular Disease
- Mendelian randomization: prospects, potentials, and limitations. (International Journal of Epidemiology)
- Efficient Design for Mendelian Randomization Studies: Subsample and 2-Sample Instrumental Variable Estimators (American Journal of Epidemiology)
- Avoiding bias from weak instruments in Mendelian randomization studies. (International Journal of Epidemiology)
- Power and instrument strength requirements for Mendelian randomization studies using multiple genetic variants. (International Journal of Epidemiology)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
Their papers
- Using multiple genetic variants as instrumental variables for modifiable risk factors (2012) — 1,190 citations
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (2008) — 1,910 citations
- The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
- Multiple type 2 diabetes susceptibility genes following genome-wide association scan in UK samples (2007) — 2,209 citations
- HMG-coenzyme A reductase inhibition, type 2 diabetes, and bodyweight: evidence from genetic analysis and randomised trials (2015) — 671 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Strengthening the reporting of observational studies in epidemiology using mendelian randomisation (STROBE-MR): explanation and elaboration (2021) — 1,401 citations
- Strengthening the Reporting of Observational Studies in Epidemiology Using Mendelian Randomization: The STROBE-MR Statement. (2021) — 3,318 citations
- Large-scale association analyses identify host factors influencing human gut microbiome composition (2021) — 1,459 citations
- Polygenic prediction of weight and obesity trajectories from birth to adulthood (2019) — 657 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- The Avon Longitudinal Study of Parents and Children (ALSPAC): an update on the enrolled sample of index children in 2019 (2019) — 734 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- The MR-Base platform supports systematic causal inference across the human phenome (2018) — 6,483 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Genome-wide analysis identifies 12 loci influencing human reproductive behavior (2016) — 129 citations
- Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses (2016) — 986 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