Martin Farrall
Genetics · 2005–2018
A researcher in the Science corpus: 29 papers; trusts 8 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 336 citations into it
- Rheumatology — 14 citations into it
Whom Martin Farrall trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Martin Farrall's perspective
Ordered by how strongly the researchers Martin Farrall trusts endorse each paper. Same corpus, a different order for every researcher.
- Searching for genetic determinants in the new millennium (Nature)
- THE CONTROL OF THE FALSE DISCOVERY RATE IN MULTIPLE TESTING UNDER DEPENDENCY
- Estimation of Significance Thresholds for Genomewide Association Scans (Genetic Epidemiology)
- Genome-wide association studies for common diseases and complex traits (Nature reviews genetics)
- Association study designs for complex diseases (Nature reviews genetics)
- Association mapping in structured populations. (American Journal of Human Genetics)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Identification of ten loci associated with height highlights new biological pathways in human growth (Nature Genetics)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
Their papers
- A genome-wide association study of global gene expression (2007) — 1,046 citations
- Genome-wide association analysis identifies 20 loci that influence adult height (2008) — 819 citations
- Genetic Loci Influencing C-reactive Protein Levels and Risk of Coronary Heart Disease (2009) — 643 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
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease (2017) — 244 citations
- Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia (2016) — 842 citations
- Reassessment Of Mendelian Gene Pathogenicity Using 7,855 Cardiomyopathy Cases And 60,706 Reference Samples (2016) — 703 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
- Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data (2014) — 637 citations
- Mendelian randomization of blood lipids for coronary heart disease (2014) — 726 citations
- Supplementary Material 7 (2014)
- Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) — 652 citations
- Bayesian refinement of association signals for 14 loci in 3 common diseases (2012) — 508 citations
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) — 841 citations