Emily C. Glassberg
Genetics · 2018
A researcher in the Science corpus: 1 paper; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 19 citations into it
Whom Emily C. Glassberg trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Emily C. Glassberg's perspective
Ordered by how strongly the researchers Emily C. Glassberg trusts endorse each paper. Same corpus, a different order for every researcher.
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- LUMPY: a probabilistic framework for structural variant discovery (Genome Biology)
- Population genomics of human gene expression (Nature Genetics)
- Improved heritability estimation from genome-wide SNPs. (American Journal of Human Genetics)
- Analysis of protein-coding genetic variation in 60,706 humans
- Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS (PLoS Genetics)
- Colocalization of GWAS and eQTL Signals Detects Target Genes (bioRxiv)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
Their papers
- Evidence for Weak Selective Constraint on Human Gene Expression (2018) — 68 citations