Goo Jun
Genetics · 2012–2017
A researcher in the Science corpus: 9 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 145 citations into it
Whom Goo Jun trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Goo Jun's perspective
Ordered by how strongly the researchers Goo Jun trusts endorse each paper. Same corpus, a different order for every researcher.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Exome sequencing as a tool for Mendelian disease gene discovery
- The Human Gene Mutation Database: 2008 update
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- Diversity of Human Copy Number Variation and Multicopy Genes (Science)
- An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people (Science)
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (Nature Genetics)
- Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians (Nature Genetics)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
- An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data (2015) — 409 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations