Martin D. Tobin

Nature · 2005–2018

A researcher in the Science corpus: 11 papers; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Whom Martin D. Tobin trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Donald B. Rubin

Papers from Martin D. Tobin's perspective

Ordered by how strongly the researchers Martin D. Tobin trusts endorse each paper. Same corpus, a different order for every researcher.

1. INFERENCE AND MISSING DATA
2. Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
3. Analysis of Incomplete Multivariate Data (Technometrics)
4. Standardisation of spirometry (European Respiratory Journal)
5. Meta-analyses of genome-wide association studies identify multiple novel loci associated with pulmonary function (Nature Genetics)
6. Integrated detection and population-genetic analysis of SNPs and copy number variation (Nature Genetics)
7. Copy Number Variation in Human Health, Disease, and Evolution (Annual review of genomics and human genetics (Print))
8. Hypertension prevalence and blood pressure levels in 6 European countries, Canada, and the United States. (Journal of the American Medical Association (JAMA))
9. Value of low dose combination treatment with blood pressure lowering drugs: analysis of 354 randomised trials (British medical journal)
10. Bankruptcy Prediction With Industry Effects

Their papers

• Genomewide Association Analysis of Coronary Artery Disease (2007) — 2,121 citations
• The UK10K project identifies rare variants in health and disease (2015) — 1,063 citations
• Haplotype estimation for biobank scale datasets (2016) — 226 citations
• Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
• Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel (2015) — 384 citations
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank (2015) — 386 citations
• Identification of seven loci affecting mean telomere length and their association with disease (2013) — 909 citations
• Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls (2010) — 710 citations
• Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure. (2009) — 1,206 citations
• Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (2007) — 9,550 citations
• Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure (2005) — 699 citations