Evangelos Evangelou
Genetics · 2007–2020
A researcher in the Science corpus: 12 papers; trusts 19 researchers and is trusted by 7 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 158 citations into it
- Molecular Biology — 100 citations into it
- Statistics and Probability — 38 citations into it; #6,298 of 12,932 by trust here, #2,261 by citations
- Surgery — 11 citations into it; #400 of 1,106 by trust here, #441 by citations
- Experimental and Cognitive Psychology — 9 citations into it
Whom Evangelos Evangelou trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- John D. Storey
- Eleftheria Zeggini
- Julian P. T. Higgins
- Cristen J. Willer
- H. Cooper
- John P. A. Ioannidis
- Itsik Pe'er
- Seunggeun Lee
- Hyun Min Kang
- Shaun Purcell
Who trusts Evangelos Evangelou overall
- David Gomez-Cabrero
- John P. A. Ioannidis
- Long Zhai
- Nicole Letourneau
- Paul T. von Hippel
- David Daniel Ebert
Papers from Evangelos Evangelou's perspective
Ordered by how strongly the researchers Evangelos Evangelou trusts endorse each paper. Same corpus, a different order for every researcher.
- Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data. (American Journal of Human Genetics)
- Quantifying heterogeneity in a meta‐analysis (Statistics in Medicine)
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (Proceedings of the National Academy of Sciences of the United States of America)
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect against Type 1 Diabetes (Science)
- Genomewide Association Analysis of Coronary Artery Disease (New England Journal of Medicine)
- Finding the missing heritability of complex diseases (Nature)
- A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. (American Journal of Human Genetics)
- The NCBI dbGaP database of genotypes and phenotypes (Nature Genetics)
- PLINK: a tool set for whole-genome association and population-based linkage analyses.
Their papers
- Uncertainty in heterogeneity estimates in meta-analyses (2007) — 1,194 citations
- Sensitivity of between-study heterogeneity in meta-analysis: proposed metrics and empirical evaluation. (2008) — 1,035 citations
- Seven New Loci Associated with Age-Related Macular Degeneration (2013) — 796 citations
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- An atlas of genetic influences on osteoporosis in humans and mice (2018) — 681 citations
- Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function (2018) — 630 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Environmental risk factors and multiple sclerosis: an umbrella review of systematic reviews and meta-analyses. (2015) — 598 citations
- Meta-analysis methods for genome-wide association studies and beyond (2013) — 584 citations
- Variable dialect switching among African American children: Inferences about working memory (2010)