2026 Kelly A. Frazer: Genetics Researcher – H-Index, Publications & Awards

Discipline name	D-Index	World Ranking	Current World Ranking	National Ranking	Current National Ranking	Publications	Citations
Genetics	78	1659	1577	762	718	238	45757

Overview

Kelly A. Frazer is affiliated with the University of California, San Diego in the United States. Their research encompasses various aspects of biochemistry, genetics, and molecular biology, with significant contributions to medicine as well. The scientist has published extensively across key subfields including molecular biology, genetics, immunology, surgery, and oncology.

Their work covers a broad spectrum of topics, with a particular focus on genetic associations and epidemiology, single-cell and spatial transcriptomics, pluripotent stem cells research, pancreatic function and diabetes, CRISPR and genetic engineering, RNA research and splicing, and genomics and chromatin dynamics.

Kelly A. Frazer has published papers in prominent venues, frequently contributing to bioRxiv (Cold Spring Harbor Laboratory), Nature Communications, Cell Genomics, Zenodo (CERN European Organization for Nuclear Research), and Nature. Notable recent publications include:

"Systematic analysis of binding of transcription factors to noncoding variants" (2021, Nature)
"Interleukin-6 Signaling Effects on Ischemic Stroke and Other Cardiovascular Outcomes" (2020, Circulation Genomic and Precision Medicine)
"Enhancer release and retargeting activates disease-susceptibility genes" (2021, Nature)
"Cellular deconvolution of GTEx tissues powers discovery of disease and cell-type associated regulatory variants" (2020, Nature Communications)
"Properties of structural variants and short tandem repeats associated with gene expression and complex traits" (2020, Nature Communications)

Their research collaborations feature frequent coauthors such as Matteo D'Antonio, Agnieszka D'Antonio-Chronowska, Hiroko Matsui, Timothy D. Arthur, and Jennifer Nguyen. These collaborations reflect a diverse and interdisciplinary approach to biomedical research.

Best Publications

A haplotype map of the human genome

John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol

5528
Citations
A second generation human haplotype map of over 3.1 million SNPs

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

5383
Citations
VISTA: computational tools for comparative genomics

Kelly A. Frazer;Lior Pachter;Alexander Poliakov;Edward M. Rubin

2540
Citations
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

2437
Citations
Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21

Nila Patil;Anthony J. Berno;David A. Hinds;Wade A. Barrett

1531
Citations
Whole-Genome Patterns of Common DNA Variation in Three Human Populations

David A. Hinds;David A. Hinds;Laura L. Stuve;Laura L. Stuve;Geoffrey B. Nilsen;Geoffrey B. Nilsen;Eran Halperin;Eran Halperin

1457
Citations
PipMaker—A Web Server for Aligning Two Genomic DNA Sequences

Scott Schwartz;Zheng Zhang;Kelly A. Frazer;Arian Smit

1423
Citations
Human genetic variation and its contribution to complex traits.

Kelly A. Frazer;Sarah S. Murray;Nicholas J. Schork;Eric J. Topol

1351
Citations
VISTA : visualizing global DNA sequence alignments of arbitrary length.

Chris Mayor;Michael Brudno;Jody R. Schwartz;Alexander Poliakov

1252
Citations
PI3Kγ is a molecular switch that controls immune suppression

Megan M. Kaneda;Karen S. Messer;Natacha Ralainirina;Hongying Li

1040
Citations
Identification of a Coordinate Regulator of Interleukins 4, 13, and 5 by Cross-Species Sequence Comparisons

Gabriela G. Loots;Gabriela G. Loots;Richard M. Locksley;Catherine M. Blankespoor;Zhi-En Wang

1019
Citations
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana.

Richard M. Clark;Gabriele Schweikert;Christopher Toomajian;Stephan Ossowski

870
Citations
Common vs. rare allele hypotheses for complex diseases.

Nicholas J Schork;Sarah S Murray;Kelly A Frazer;Eric J Topol

855
Citations
Evaluation of next generation sequencing platforms for population targeted sequencing studies

Olivier Harismendy;Pauline C Ng;Robert L Strausberg;Xiaoyun Wang

766
Citations
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response

Olivier Harismendy;Dimple Notani;Xiaoyuan Song;Nazli G. Rahim

739
Citations
Genomewide SNP variation reveals relationships among landraces and modern varieties of rice

Kenneth L. McNally;Kevin L. Childs;Regina Bohnert;Rebecca M. Davidson

723
Citations
Microdroplet-based PCR enrichment for large-scale targeted sequencing

Ryan Tewhey;Ryan Tewhey;Jason B Warner;Masakazu Nakano;Masakazu Nakano;Brian Libby

640
Citations
Implementing genomic medicine in the clinic: the future is here

Teri A. Manolio;Rex L Chisholm;Brad Ozenberger;Dan M. Roden

605
Citations
High-Resolution Whole-Genome Association Study of Parkinson Disease

Demetrius M. Maraganore;Mariza de Andrade;Timothy G. Lesnick;Kari J. Strain

600
Citations
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

Kelly A. Frazer;Eleazar Eskin;Hyun Min Kang;Molly A. Bogue

550
Citations

Frequent Co-Authors

Erin N. Smith University of California, San Diego

David R. Cox University of Oxford

Eric J. Topol Scripps Research Institute

Oliver Stegle German Cancer Research Center

Frank B. Furnari University of California, San Diego

David A. Hinds 23andMe (United States)

Vineet Bafna University of California, San Diego

Marc Jan Bonder University of Groningen

Paul S. Mischel Stanford University

Marco A. Marra University of British Columbia

External Links

Wikipedia of Kelly A. Frazer Personal website of Kelly A. Frazer

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