Omri Gottesman
Endocrinology, Diabetes and Metabolism · 2013–2018
A researcher in the Science corpus: 10 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Endocrinology, Diabetes and Metabolism — 33 citations into it
Whom Omri Gottesman trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Omri Gottesman overall
Papers from Omri Gottesman's perspective
Ordered by how strongly the researchers Omri Gottesman trusts endorse each paper. Same corpus, a different order for every researcher.
- The NCBI dbGaP database of genotypes and phenotypes (Nature Genetics)
- Genome-partitioning of genetic variation for complex traits using common SNPs (Nature Genetics)
- Next-generation phenotyping of electronic health records
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
- Topology and data
- Common genetic variation and human traits. (New England Journal of Medicine)
- PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene–disease associations
- A review of approaches to identifying patient phenotype cohorts using electronic health records
- Regression Shrinkage and Selection via the Lasso
Their papers
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- Identification of type 2 diabetes subgroups through topological analysis of patient similarity (2015) — 544 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- The Electronic Medical Records and Genomics (eMERGE) Network: Past, Present and Future (2013) — 680 citations
- PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability (2016) — 347 citations
- A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease (2018) — 665 citations
- Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease (2017) — 750 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
- Defining the role of common variation in the genomic and biological architecture of adult human height (2014)