World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
98
Citations
127560
World Ranking
787
National Ranking
394

Medicine

D-Index
98
Citations
127547
World Ranking
8712
National Ranking
4493

Overview

Yun Li is affiliated with the University of North Carolina at Chapel Hill in the United States. Their research primarily spans the fields of Biochemistry, Genetics, and Molecular Biology, as well as Medicine. Within these broad disciplines, their work focuses intensively on Molecular Biology, Genetics, Cancer Research, Epidemiology, and Pulmonary and Respiratory Medicine.

The research topics covered by Yun Li include Genetic Associations and Epidemiology, Epigenetics and DNA Methylation, Single-cell and Spatial Transcriptomics, Genomics and Chromatin Dynamics, Genetic Mapping and Diversity in Plants and Animals, Genomics and Rare Diseases, and Gene Expression and Cancer Classification.

The scientist has contributed extensively to multiple publication venues. Notable among these are UNC Libraries, bioRxiv (Cold Spring Harbor Laboratory), The American Journal of Human Genetics, Nature Communications, and Briefings in Bioinformatics.

Yun Li has coauthored publications frequently with several researchers, including Laura M. Raffield, Quan Sun, Jia Wen, Ming Hu, and Charles Kooperberg.

Some of Yun Li's recent research papers include:

  • The Polygenic and Monogenic Basis of Blood Traits and Diseases, 2020, Cell
  • Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations, 2020, Cell
  • Common genetic variation influencing human white matter microstructure, 2021, Science
  • Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases, 2020, Molecular Cell
  • Heart-brain connections: Phenotypic and genetic insights from magnetic resonance images, 2023, Science

Best Publications

  • A global reference for human genetic variation.

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

  • A second generation human haplotype map of over 3.1 million SNPs

    Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds

  • METAL: fast and efficient meta-analysis of genomewide association scans.

    Cristen J. Willer;Yun Li;Gonçalo R. Abecasis

  • A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

    Laura J. Scott;Karen L. Mohlke;Lori L. Bonnycastle;Cristen J. Willer

  • Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski

  • Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

    Michael C. Wu;Seunggeun Lee;Tianxi Cai;Yun Li

  • New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

    Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena

  • Genome-wide detection and characterization of positive selection in human populations

    Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller

  • Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

    E Zeggini;L J Scott;R Saxena;B F Voight

  • MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

    Yun Li;Cristen J. Willer;Jun Ding;Paul A Scheet

  • An epigenetic biomarker of aging for lifespan and healthspan

    Morgan E. Levine;Ake T. Lu;Austin Quach;Brian H. Chen

  • Newly identified loci that influence lipid concentrations and risk of coronary artery disease

    Cristen J. Willer;Serena Sanna;Anne U. Jackson;Angelo Scuteri

  • A genome-wide association search for type 2 diabetes genes in African Americans.

    N D Palmer;C W McDonough;P J Hicks;B H Roh

  • Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways

    Rajan P. Nair;Kristina Callis Duffin;Cynthia Helms;Jun Ding

  • Common variants at 30 loci contribute to polygenic dyslipidemia.

    Sekar Kathiresan;Sekar Kathiresan;Sekar Kathiresan;Cristen J. Willer;Gina M. Peloso;Serkalem Demissie

  • DNA methylation GrimAge strongly predicts lifespan and healthspan.

    Ake T. Lu;Austin Quach;James G. Wilson;Alex P. Reiner

  • Genotype imputation.

    Unknown

  • 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 Compendium of Chromatin Contact Maps Reveals Spatially Active Regions in the Human Genome

    Anthony D. Schmitt;Ming Hu;Inkyung Jung;Zheng Xu

  • An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

    Matthew R. Nelson;Daniel Wegmann;Margaret G. Ehm;Darren Kessner

Frequent Co-Authors

Alexander P. Reiner
Alexander P. Reiner University of Washington
Hakon Hakonarson
Hakon Hakonarson Children's Hospital of Philadelphia
Eric Boerwinkle
Eric Boerwinkle The University of Texas Health Science Center at Houston
Leslie A. Lange
Leslie A. Lange University of Colorado Anschutz Medical Campus
Bruce M. Psaty
Bruce M. Psaty University of Washington
Gonçalo R. Abecasis
Gonçalo R. Abecasis University of Michigan–Ann Arbor
Brendan J. Keating
Brendan J. Keating University of Pennsylvania
Myriam Fornage
Myriam Fornage The University of Texas Health Science Center at Houston
Jerome I. Rotter
Jerome I. Rotter UCLA Medical Center
James G. Wilson
James G. Wilson University of Mississippi Medical Center

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