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Genetics

D-Index
94
Citations
96544
World Ranking
914
National Ranking
455

Overview

Hyun Min Kang is affiliated with the University of Michigan-Ann Arbor in the United States. Their research spans predominantly the fields of Biochemistry, Genetics and Molecular Biology, with a significant focus also on Medicine. The scientist's work covers several subfields including Genetics, Molecular Biology, Immunology, Infectious Diseases, and Cancer Research.

The primary research topics explored by Hyun Min Kang encompass Genetic Associations and Epidemiology, Genomics and Rare Diseases, Single-cell and Spatial Transcriptomics, Cancer Genomics and Diagnostics, SARS-CoV-2 and COVID-19 Research, Genomic Variations and Chromosomal Abnormalities, as well as Bioinformatics and Genomic Networks.

Hyun Min Kang has contributed to numerous publications featured in various scientific venues. Frequent publication outlets include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • UNC Libraries
  • Nature Communications
  • Nature
  • Zenodo (CERN European Organization for Nuclear Research)

Their notable recent papers illustrate a range of collaborative projects within high-impact journals. These include:

  • Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program, 2021, Nature
  • Plasma proteomic associations with genetics and health in the UK Biobank, 2023, Nature
  • Exome sequencing and analysis of 454,787 UK Biobank participants, 2021, Nature
  • Rare coding variants in ten genes confer substantial risk for schizophrenia, 2022, Nature
  • Microscopic examination of spatial transcriptome using Seq-Scope, 2021, Cell

Hyun Min Kang has collaborated extensively with several frequent co-authors, reflecting long-term research partnerships. These co-authors include:

  • Gonçalo R. Abecasis
  • Adam E. Locke
  • Joelle Mbatchou
  • Jeffrey G. Reid
  • Charles Kooperberg

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Table S2: Trans-factors and trinucleotide repeat instability Trans-factor

    Arturo López Castel;John D Cleary;Christopher E Pearson

  • A reference panel of 64,976 haplotypes for genotype imputation

    Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau

  • Variance component model to account for sample structure in genome-wide association studies

    Hyun Min Kang;Jae Hoon Sul;Noah A. Zaitlen

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

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

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

    Andrew P Morris;Benjamin F Voight;Benjamin F Voight;Tanya M Teslovich;Teresa Ferreira

  • Efficient Control of Population Structure in Model Organism Association Mapping

    Hyun Min Kang;Noah A. Zaitlen;Claire M. Wade;Claire M. Wade;Andrew Kirby;Andrew Kirby

  • Evolution and functional impact of rare coding variation from deep sequencing of human exomes

    Jacob A. Tennessen;Abigail W. Bigham;Timothy D. O'Connor;Wenqing Fu

  • Large-scale association analysis identifies new risk loci for coronary artery disease

    Panos Deloukas;Stavroula Kanoni;Christina Willenborg;Martin Farrall

  • Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

    Wei Zhou;Jonas B. Nielsen;Lars G. Fritsche;Rounak Dey

  • Mapping copy number variation by population-scale genome sequencing

    Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan

  • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Lam C. Tsoi;Sarah L. Spain;Sarah L. Spain;Jo Knight;Eva Ellinghaus;Eva Ellinghaus

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

    Wenqing Fu;Timothy D. O’Connor;Goo Jun;Hyun Min Kang

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

    Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

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

    Daniel Taliun;Daniel N. Harris;Michael D. Kessler;Jedidiah Carlson;Jedidiah Carlson

  • The genetic architecture of type 2 diabetes

    Christian Fuchsberger;Jason Flannick;Tanya M. Teslovich;Anubha Mahajan

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

    Anubha Mahajan;Min Jin Go;Weihua Zhang;Jennifer E. Below

Frequent Co-Authors

Gonçalo R. Abecasis
Gonçalo R. Abecasis University of Michigan–Ann Arbor
Michael Boehnke
Michael Boehnke University of Michigan–Ann Arbor
David Altshuler
David Altshuler Harvard University
Tonu Esko
Tonu Esko University of Tartu
Christian Fuchsberger
Christian Fuchsberger University of Lübeck
Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Leif Groop
Leif Groop Lund University
Ruth J. F. Loos
Ruth J. F. Loos University of Copenhagen
Kristian Hveem
Kristian Hveem Norwegian University of Science and Technology

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