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Jennifer A. Doudna

Jennifer A. Doudna

· Howard Hughes Medical Institute Investigator, Li Ka Shing Chancellor's Chair in Biomedical and Health Sciences, Professor of Molecular Therapeutics

University of California, Berkeley · Department of Chemical and Biomolecular Engineering

Active 1987–2026

h-index230
Citations288.7k
Papers1.5k547 last 5y
Funding

Academic metrics are sourced from OpenAlex and public funding records; values may differ from Google Scholar.

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About

Jennifer A. Doudna is a Professor of Chemistry at the University of California, Berkeley, holding the Li Ka Shing Chancellor’s Chair in Biomedical and Health Sciences. She is a Nobel Laureate in Chemistry, recognized for her pioneering work in the discovery of CRISPR, a revolutionary gene-editing technology. Her research focuses on advancing society through education and research in the fields of chemical biology, molecular and cell biology, and biomedical sciences. Doudna's academic career includes post-doctoral work at the University of Colorado, followed by positions at Yale University, where she served as an assistant, associate, and full professor before joining UC Berkeley in 2002. She has been a Howard Hughes Medical Investigator since 1997 and has received numerous awards, including the NSF Alan T. Waterman Award in 2000, and membership in prestigious organizations such as the National Academy of Sciences, the American Academy of Arts and Sciences, and the Institute of Medicine of the National Academies. Her groundbreaking research has significantly contributed to the development and understanding of CRISPR technology, impacting the fields of genetics, molecular biology, and biomedical sciences.

Research topics

  • Biology
  • Computational biology
  • Genetics
  • Cell biology
  • Chemistry

Selected publications

  • CRISPR technology: A decade of genome editing is only the beginning

    Science · 2023-01-19 · 1006 citations

    reviewSenior authorCorresponding

    The advent of clustered regularly interspaced short palindromic repeat (CRISPR) genome editing, coupled with advances in computing and imaging capabilities, has initiated a new era in which genetic diseases and individual disease susceptibilities are both predictable and actionable. Likewise, genes responsible for plant traits can be identified and altered quickly, transforming the pace of agricultural research and plant breeding. In this Review, we discuss the current state of CRISPR-mediated g…

  • Viral delivery of an RNA-guided genome editor for transgene-free germline editing in Arabidopsis

    Nature Plants · 2025-04-22 · 70 citations

    articleOpen access

    Abstract Genome editing is transforming plant biology by enabling precise DNA modifications. However, delivery of editing systems into plants remains challenging, often requiring slow, genotype-specific methods such as tissue culture or transformation 1 . Plant viruses, which naturally infect and spread to most tissues, present a promising delivery system for editing reagents. However, many viruses have limited cargo capacities, restricting their ability to carry large CRISPR-Cas systems. Here w…

  • An updated evolutionary classification of CRISPR–Cas systems including rare variants

    Nature Microbiology · 2025-11-06 · 44 citations

    reviewOpen access

    The known diversity of CRISPR-Cas systems continues to expand. To encompass new discoveries, here we present an updated evolutionary classification of CRISPR-Cas systems. The updated CRISPR-Cas classification includes 2 classes, 7 types and 46 subtypes, compared with the 6 types and 33 subtypes in our previous survey 5 years ago. In addition, a classification of the cyclic oligoadenylate-dependent signalling pathway in type III systems is presented. We also discuss recently characterized alterna…

  • CRISPRi-ART enables functional genomics of diverse bacteriophages using RNA-binding dCas13d

    Nature Microbiology · 2025-02-26 · 22 citations

    articleOpen accessCorresponding

    Bacteriophages constitute one of the largest reservoirs of genes of unknown function in the biosphere. Even in well-characterized phages, the functions of most genes remain unknown. Experimental approaches to study phage gene fitness and function at genome scale are lacking, partly because phages subvert many modern functional genomics tools. Here we leverage RNA-targeting dCas13d to selectively interfere with protein translation and to measure phage gene fitness at a transcriptome-wide scale. W…

  • Phage-based delivery of CRISPR-associated transposases for targeted bacterial editing

    Proceedings of the National Academy of Sciences · 2025-07-25 · 19 citations

    articleOpen access

    Phage λ, a well-characterized temperate phage, has been recently leveraged for bacterial genome editing by selectively delivering base editors into targeted bacterial species. We extend this concept by engineering phage λ to deliver CRISPR-guided transposases, accomplishing large insertions and targeted gene disruptions. To achieve this, we engineered phage λ using homologous recombination paired with Cas13a-based counterselection for precise phage modifications. Initially, we established the ut…

Frequent coauthors

  • Jillian F. Banfield

    University of California, Berkeley

    331 shared
  • Abdullah M. Syed

    Gladstone Institutes

    311 shared
  • Alison Ciling

    University of California, Berkeley

    294 shared
  • Eva Nogales

    Howard Hughes Medical Institute

    294 shared
  • Mélanie Ott

    Gladstone Institutes

    284 shared
  • Benjamin A. Adler

    Innovative Genomics Institute

    277 shared
  • Gavin J. Knott

    Monash University

    260 shared
  • Marena Trinidad

    Howard Hughes Medical Institute

    254 shared

Awards & honors

  • Howard Hughes Medical Investigator (1997 to present)
  • Packard Foundation Fellow Award (1996)
  • NSF Alan T. Waterman Award (2000)
  • Member, National Academy of Sciences (2002)
  • Member, American Academy of Arts and Sciences (2003)

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