Hyun Min Kang
Genetics · 2008–2022
A researcher in the Science corpus: 21 papers; trusts 2 researchers and is trusted by 10 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 344 citations into it; #1,576 of 6,854 by trust here, #137 by citations
Whom Hyun Min Kang trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Jinliang Wang
- Andrey A. Shabalin
- Olivier J. Hardy
- Nick Patterson
- John A. Nelder
- Ciprian M. Crainiceanu
- J. K. Pritchard
- S. Picelli
- Heng Li
- Alkes L Price
Who trusts Hyun Min Kang overall
- Xiaoping Zhou
- Barbara Rakitsch
- Johann A. Gagnon-Bartsch
- G. Covarrubias-Pazaran
- Jeffrey B. Endelman
- Matthew Stephens
- Yang Xu
- Jiabo Wang
- Xiaolei Liu
- J. Rutkoski
Papers from Hyun Min Kang's perspective
Ordered by how strongly the researchers Hyun Min Kang trusts endorse each paper. Same corpus, a different order for every researcher.
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
- spagedi: a versatile computer program to analyse spatial genetic structure at the individual or population levels
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Supporting Online Material Materials and Methods Figs. S1 to S3 Tables S1 to S5 References Worldwide Human Relationships Inferred from Genome-wide Patterns of Variation
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
- Next-generation genotype imputation service and methods (Nature 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)
- The Human Gene Mutation Database: 2008 update
- Systematic Localization of Common Disease-Associated Variation in Regulatory DNA (Science)
- Mapping copy number variation by population scale genome sequencing (Nature)
Their papers
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes (2012) — 1,698 citations
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Analysis of 6,515 exomes reveals a recent origin of most human protein-coding variants (2012) — 970 citations
- Multiplexed droplet single-cell RNA-sequencing using natural genetic variation (2017) — 978 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 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
- Unified representation of genetic variants (2015) — 411 citations
- Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies (2017) — 1,245 citations
- Comparative Analysis of Proteome and Transcriptome Variation in Mouse (2011) — 637 citations
- Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
- Exome sequencing and analysis of 454,787 UK Biobank participants (2021) — 786 citations
- Biobank-driven genomic discovery yields new insight into atrial fibrillation biology (2018) — 749 citations
- Loss-of-Function Mutations in APOC 3 , Triglycerides , and Coronary Disease (2014) — 861 citations
- Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
- Identification of fifteen new psoriasis susceptibility loci highlights the role of innate immunity (2012) — 721 citations
- Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways (2012) — 841 citations
- Variance component model to account for sample structure in genome-wide association studies (2010) — 2,667 citations