Joshua M. Akey
Molecular Biology · 2002–2017
A researcher in the Science corpus: 13 papers; trusts 4 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 159 citations into it
- Genetics — 139 citations into it; #5,568 of 6,854 by trust here, #238 by citations
- Artificial Intelligence — 11 citations into it
- Statistics and Probability — 8 citations into it
Whom Joshua M. Akey trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Joshua M. Akey overall
- J. Storz
- J. Stinchcombe
- MARK A. Beaumont
- P. Villemereuil
- Noah A. Rosenberg
- Gordon Luikart
- Oscar E. Gaggiotti
- H. Hoekstra
- David J. Balding
- Christian Schlötterer
Papers from Joshua M. Akey's perspective
Ordered by how strongly the researchers Joshua M. Akey trusts endorse each paper. Same corpus, a different order for every researcher.
- Gene Ontology: tool for the unification of biology
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms (Nature)
- High-resolution haplotype structure in the human genome (Nature Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Positive and negative selection on the human genome. (Genetics)
- Approximate Bayesian inference for latent Gaussian models by using integrated nested Laplace approximations
- Polygenic Modeling with Bayesian Sparse Linear Mixed Models (PLoS Genetics)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations (PLoS Genetics)
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus (Nature)
Their papers
- The accessible chromatin landscape of the human genome (2012) — 2,728 citations
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- An expansive human regulatory lexicon encoded in transcription factor footprints (2012) — 841 citations
- Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- Trans-acting regulatory variation in Saccharomyces cerevisiae and the role of transcription factors (2003) — 673 citations
- Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders (2012) — 1,254 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- Impacts of Neanderthal-introgressed sequences on the landscape of human gene expression (2017) — 158 citations
- Great ape genetic diversity and population history (2013) — 858 citations
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations (2012) — 2,200 citations
- From the Cover: Tracking footprints of artificial selection in the dog genome (2010) — 342 citations
- Interrogating a high-density SNP map for signatures of natural selection. (2002) — 930 citations