List of works by Hyun Min Kang

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

scientific article published on 24 March 2017

A central role for GRB10 in regulation of islet function in man.

scientific article published on 3 April 2014

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

scientific article

A high-resolution association mapping panel for the dissection of complex traits in mice

scientific article

A reference panel of 64,976 haplotypes for genotype imputation

scientific article

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

scientific article published on 28 November 2012

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

scientific article published on 24 January 2020

Discovery of common and rare genetic risk variants for colorectal cancer

scientific article published on 03 December 2018

Erratum: Corrigendum: Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

scientific article published in Nature

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 23 January 2018

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes

scientific article

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

scientific article

Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

article

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

scientific article

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

scientific article

Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project

scientific article

Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits

scientific article

Identification of the niche and mobilization mechanism for tissue-protective multipotential bone marrow ILC progenitors

scientific article published in 2022

In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

scientific article

Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population

scientific article

Integrating comprehensive functional annotations to boost power and accuracy in gene-based association analysis

scientific article published on 15 December 2020

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

scientific article

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

scientific article

Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis

scientific article

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 19 December 2017

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

scientific article published on 6 March 2019

Single-Cell RNA Sequencing Resolves Molecular Relationships Among Individual Plant Cells

article

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

scientific article

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

scientific article

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