James R. Staley
Genetics · 2016–2019
A researcher in the Science corpus: 6 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 120 citations into it
Whom James R. Staley trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts James R. Staley overall
Papers from James R. Staley's perspective
Ordered by how strongly the researchers James R. Staley trusts endorse each paper. Same corpus, a different order for every researcher.
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Genomic atlas of the human plasma proteome (Nature)
- The druggable genome and support for target identification and validation in drug development (Science Translational Medicine)
- Validating therapeutic targets through human genetics
- Connecting genetic risk to disease end points through the human blood plasma proteome (Nature Communications)
- Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study (The Lancet)
- The NCBI dbGaP database of genotypes and phenotypes (Nature Genetics)
- Clinical development success rates for investigational drugs (Nature Biotechnology)
- The role of regulatory variation in complex traits and disease (Nature reviews genetics)
- Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
Their papers
- PhenoScanner: a database of human genotype–phenotype associations (2016) — 1,277 citations
- PhenoScanner V2: an expanded tool for searching human genotype–phenotype associations (2019) — 1,762 citations
- Phenome-wide Mendelian randomization mapping the influence of the plasma proteome on complex diseases (2019) — 633 citations
- A fast and efficient colocalization algorithm for identifying shared genetic risk factors across multiple traits (2019) — 481 citations
- Genomic atlas of the human plasma proteome (2018) — 1,884 citations
- Allelic Landscape of Human Blood Cell Trait Variation and Links (2016)