Barbara E. Stranger
Genetics · 2007–2020
A researcher in the Science corpus: 12 papers; trusts 7 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 252 citations into it
Whom Barbara E. Stranger trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- J. K. Pritchard
- David J. Balding
- Lon R. Cardon
- John Hardy
- Jonathan Marchini
- Robert M. Plenge
- David Altshuler
- J. Bell
- Peter Donnelly
- Matthew Stephens
Who trusts Barbara E. Stranger overall
- Lee H. Dicker
- Alessia David
- Oliver Stegle
- Daniel Money
- Stephen B. Montgomery
- Benjamin A. Logsdon
- Magnus Ingelman-Sundberg
- Rozami Razali
- Leopold Parts
- Kyle M. Gardner
Papers from Barbara E. Stranger's perspective
Ordered by how strongly the researchers Barbara E. Stranger trusts endorse each paper. Same corpus, a different order for every researcher.
- Linkage disequilibrium in humans: models and data. (American Journal of Human Genetics)
- 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)
- A genome-wide association study of global gene expression (Nature Genetics)
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Nature Genetics)
- High-resolution haplotype structure in the human genome (Nature Genetics)
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- Association mapping in structured populations. (American Journal of Human Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
Their papers
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- A second generation human haplotype map of over 3.1 million SNPs (2007) — 4,677 citations
- Candidate Causal Regulatory Effects by Integration of Expression QTLs with Complex Trait Genetic Associations (2010) — 461 citations
- Population genomics of human gene expression (2007) — 1,231 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- The GTEx Consortium atlas of genetic regulatory effects across human tissues (2019) — 4,770 citations
- The transcriptional landscape of age in human peripheral blood (2015) — 654 citations
- Common regulatory variation impacts gene expression in a cell type dependent manner (2009) — 829 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- The impact of sex on gene expression across human tissues (2020) — 618 citations
- Progress and Promise of Genome-Wide Association Studies for Human Complex Trait Genetics (2011) — 613 citations
- Relative impact of nucleotide and copy number variation on gene expression phenotypes (2007) — 1,794 citations