Audrey L Griffith

716 total citations · 1 hit paper
5 papers, 358 citations indexed

About

Audrey L Griffith is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Audrey L Griffith has authored 5 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Hematology. Recurrent topics in Audrey L Griffith's work include RNA and protein synthesis mechanisms (4 papers), CRISPR and Genetic Engineering (4 papers) and Evolution and Genetic Dynamics (3 papers). Audrey L Griffith is often cited by papers focused on RNA and protein synthesis mechanisms (4 papers), CRISPR and Genetic Engineering (4 papers) and Evolution and Genetic Dynamics (3 papers). Audrey L Griffith collaborates with scholars based in United States. Audrey L Griffith's co-authors include Annabel K. Sangree, Peter C. DeWeirdt, John G. Doench, Ruth E. Hanna, Mudra Hegde, Marissa N. Feeley, Kendall R Sanson, Luke W. Koblan, James T. Neal and Christian Fagre and has published in prestigious journals such as Cell, Nature Communications and Nature Genetics.

In The Last Decade

Audrey L Griffith

4 papers receiving 357 citations

Hit Papers

Massively parallel assessment of human variants with base... 2021 2026 2022 2024 2021 50 100 150 200

Peers

Audrey L Griffith
Marissa N. Feeley United States
Annabel K. Sangree United States
Christian Fagre United States
Paul C. Kirchgatterer United States
Sneha Suresh United States
Gillian C.A. Taylor United Kingdom
Marissa N. Feeley United States
Audrey L Griffith
Citations per year, relative to Audrey L Griffith Audrey L Griffith (= 1×) peers Marissa N. Feeley

Countries citing papers authored by Audrey L Griffith

Since Specialization
Citations

This map shows the geographic impact of Audrey L Griffith's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Audrey L Griffith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Audrey L Griffith more than expected).

Fields of papers citing papers by Audrey L Griffith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Audrey L Griffith. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Audrey L Griffith. The network helps show where Audrey L Griffith may publish in the future.

Co-authorship network of co-authors of Audrey L Griffith

This figure shows the co-authorship network connecting the top 25 collaborators of Audrey L Griffith. A scholar is included among the top collaborators of Audrey L Griffith based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Audrey L Griffith. Audrey L Griffith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

5 of 5 papers shown
1.
Kaplan, E L, et al.. (2025). Activity-based selection for enhanced base editor mutational scanning. Nature Genetics. 57(11). 2920–2929.
2.
Sangree, Annabel K., Audrey L Griffith, Peter C. DeWeirdt, et al.. (2022). Benchmarking of SpCas9 variants enables deeper base editor screens of BRCA1 and BCL2. Nature Communications. 13(1). 1318–1318. 30 indexed citations
3.
Hanna, Ruth E., Mudra Hegde, Christian Fagre, et al.. (2021). Massively parallel assessment of human variants with base editor screens. Cell. 184(4). 1064–1080.e20. 202 indexed citations breakdown →
4.
Lenoir, Walter F., Peter C. DeWeirdt, Megan McLaughlin, et al.. (2021). Discovery of putative tumor suppressors from CRISPR screens reveals rewired lipid metabolism in acute myeloid leukemia cells. Nature Communications. 12(1). 6506–6506. 16 indexed citations
5.
DeWeirdt, Peter C., Kendall R Sanson, Annabel K. Sangree, et al.. (2020). Optimization of AsCas12a for combinatorial genetic screens in human cells. Nature Biotechnology. 39(1). 94–104. 110 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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