S. Stringer
Genetics · 2018–2019
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 103 citations into it
Whom S. Stringer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from S. Stringer's perspective
Ordered by how strongly the researchers S. Stringer trusts endorse each paper. Same corpus, a different order for every researcher.
- Pitfalls of predicting complex traits from SNPs
- Estimation of Significance Thresholds for Genomewide Association Scans (Genetic Epidemiology)
- Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
- Rare and Common Variants: Twenty arguments (Nature reviews genetics)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- FTO Obesity Variant Circuitry and Adipocyte Browning in Humans (New England Journal of Medicine)
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Their papers
- A global overview of pleiotropy and genetic architecture in complex traits (2019) — 1,107 citations
- Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk (2019) — 2,006 citations
- Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways (2019) — 705 citations
- A tutorial on conducting genome‐wide association studies: Quality control and statistical analysis (2018) — 684 citations
- Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways (2018) — 685 citations