Halit Ongen
Molecular Biology · 2011–2017
A researcher in the Science corpus: 8 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 124 citations into it
- Genetics — 110 citations into it
Whom Halit Ongen trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Halit Ongen's perspective
Ordered by how strongly the researchers Halit Ongen trusts endorse each paper. Same corpus, a different order for every researcher.
- An expanded view of complex traits: from polygenic to omnigenic (Cell)
- An integrated map of genetic variation from 1,092 human genomes
- A global reference for human genetic variation
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- Next-generation genotype imputation service and methods (Nature Genetics)
- Polygenic Modeling with Bayesian Sparse Linear Mixed Models (PLoS Genetics)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
- Variable Selection
- Reference-based phasing using the Haplotype Reference Consortium panel
- ClinVar: public archive of interpretations of clinically relevant variants
Their papers
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- Genetic effects on gene expression across human tissues (2017) — 3,717 citations
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015) — 4,590 citations
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2016) — 1,036 citations
- A complete tool set for molecular QTL discovery and analysis (2016) — 326 citations
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015)
- Fast and efficient QTL mapper for thousands of molecular phenotypes (2015) — 536 citations
- A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease (2011) — 669 citations