Priscilla K. Cooper

6.3k total citations · 2 hit papers
49 papers, 4.1k citations indexed

About

Priscilla K. Cooper is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Priscilla K. Cooper has authored 49 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 16 papers in Cancer Research and 15 papers in Genetics. Recurrent topics in Priscilla K. Cooper's work include DNA Repair Mechanisms (39 papers), Carcinogens and Genotoxicity Assessment (16 papers) and DNA and Nucleic Acid Chemistry (15 papers). Priscilla K. Cooper is often cited by papers focused on DNA Repair Mechanisms (39 papers), Carcinogens and Genotoxicity Assessment (16 papers) and DNA and Nucleic Acid Chemistry (15 papers). Priscilla K. Cooper collaborates with scholars based in United States, Netherlands and United Kingdom. Priscilla K. Cooper's co-authors include Philip C. Hanawalt, Charles A. Smith, Ann K. Ganesan, Björn Rydberg, Markus Löbrich, John A. Tainer, Jill O. Fuss, Steven A. Leadon, Eric Campeau and A.S. Arvai and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Priscilla K. Cooper

48 papers receiving 3.9k citations

Hit Papers

DNA Repair in Bacteria and Mammalian Cells 1979 2026 1994 2010 1979 2009 200 400 600

Peers

Priscilla K. Cooper
Harry Vrieling Netherlands
Randy J. Legerski United States
Veronica M. Maher United States
Thomas D. Stamato United States
Binghui Shen United States
Priscilla K. Cooper
Citations per year, relative to Priscilla K. Cooper Priscilla K. Cooper (= 1×) peers Malcolm C. Paterson

Countries citing papers authored by Priscilla K. Cooper

Since Specialization
Citations

This map shows the geographic impact of Priscilla K. Cooper'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 Priscilla K. Cooper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Priscilla K. Cooper more than expected).

Fields of papers citing papers by Priscilla K. Cooper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Priscilla K. Cooper. 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 Priscilla K. Cooper. The network helps show where Priscilla K. Cooper may publish in the future.

Co-authorship network of co-authors of Priscilla K. Cooper

This figure shows the co-authorship network connecting the top 25 collaborators of Priscilla K. Cooper. A scholar is included among the top collaborators of Priscilla K. Cooper 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 Priscilla K. Cooper. Priscilla K. Cooper is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sarker, Altaf H., Priscilla K. Cooper, & Tapas K. Hazra. (2021). DNA glycosylase NEIL2 functions in multiple cellular processes. Progress in Biophysics and Molecular Biology. 164. 72–80. 10 indexed citations
2.
Trego, Kelly S., Albert R. Davalos, Ann Christin Parplys, et al.. (2016). Non-catalytic Roles for XPG with BRCA1 and BRCA2 in Homologous Recombination and Genome Stability. Molecular Cell. 61(4). 535–546. 45 indexed citations
3.
Barnhoorn, Sander, Dick Jaarsma, Wilbert P. Vermeij, et al.. (2014). Cell-Autonomous Progeroid Changes in Conditional Mouse Models for Repair Endonuclease XPG Deficiency. PLoS Genetics. 10(10). e1004686–e1004686. 49 indexed citations
4.
Tsutakawa, Susan E., Scott Classen, B.R. Chapados, et al.. (2011). Human Flap Endonuclease Structures, DNA Double-Base Flipping, and a Unified Understanding of the FEN1 Superfamily. Cell. 145(2). 198–211. 239 indexed citations
5.
Campeau, Eric, Françis Rodier, Corey L. Smith, et al.. (2009). A Versatile Viral System for Expression and Depletion of Proteins in Mammalian Cells. PLoS ONE. 4(8). e6529–e6529. 697 indexed citations breakdown →
6.
Pluth, Janice M., et al.. (2007). DNA double-strand break and chromosomal rejoining defects with misrejoining in Nijmegen breakage syndrome cells. DNA repair. 7(1). 108–118. 17 indexed citations
7.
Tsutakawa, Susan E., et al.. (2006). Structural analysis of flexible proteins in solution by Small Angle X-ray Scattering combined with crystallography. University of North Texas Digital Library (University of North Texas). 2 indexed citations
8.
Fan, Li, A.S. Arvai, Priscilla K. Cooper, et al.. (2006). Conserved XPB Core Structure and Motifs for DNA Unwinding: Implications for Pathway Selection of Transcription or Excision Repair. Molecular Cell. 22(1). 27–37. 124 indexed citations
9.
Tsutakawa, Susan E., et al.. (2006). Structural analysis of flexible proteins in solution by small angle X-ray scattering combined with crystallography. Journal of Structural Biology. 158(2). 214–223. 57 indexed citations
10.
Wang, Junhua, Janice M. Pluth, Priscilla K. Cooper, et al.. (2005). Artemis deficiency confers a DNA double-strand break repair defect and Artemis phosphorylation status is altered by DNA damage and cell cycle progression. DNA repair. 4(5). 556–570. 81 indexed citations
11.
Sarker, Altaf H., Susan E. Tsutakawa, David Shin, et al.. (2005). Recognition of RNA Polymerase II and Transcription Bubbles by XPG, CSB, and TFIIH: Insights for Transcription-Coupled Repair and Cockayne Syndrome. Molecular Cell. 20(2). 187–198. 180 indexed citations
12.
Rydberg, Björn, Brian A. Cooper, Priscilla K. Cooper, W.R. Holley, & A. Chatterjee. (2004). Dose-dependent misrejoining of radiation-induced DNA double-strand breaks in human \nfibroblasts: Experimental and theoretical study for high and low LET radiation. eScholarship (California Digital Library). 46 indexed citations
13.
Wang, Jen‐Yeu, Altaf H. Sarker, Priscilla K. Cooper, & Michael R. Volkert. (2004). The single-strand DNA binding activity of human PC4 prevents mutagenesis and killing by \noxidative DNA damage. eScholarship (California Digital Library). 72 indexed citations
14.
Trame, Christine B., Alastair A. MacDowell, Richard Celestre, et al.. (2003). SIBYLS - A SAXS and protein crystallography beamline at the ALS. eScholarship (California Digital Library). 2 indexed citations
15.
Rydberg, Björn, L. Heilbronn, W.R. Holley, et al.. (2002). Spatial Distribution and Yield of DNA Double-Strand Breaks Induced by 3–7 MeV Helium Ions in Human Fibroblasts. Radiation Research. 158(1). 32–42. 40 indexed citations
16.
Page, Florence Le, Januário B. Cabral‐Neto, Priscilla K. Cooper, & Alain Sarasin. (2002). Transcription-Coupled Repair of 8-Oxoguanine in Human Cells. Methods in enzymology on CD-ROM/Methods in enzymology. 353. 536–547. 3 indexed citations
17.
Tsutakawa, Susan E. & Priscilla K. Cooper. (2001). Transcription-coupled repair of oxidative DNA damage in human cells: \nMechanisms and consequences. eScholarship (California Digital Library). 26 indexed citations
18.
Weinfeld, Michael, James Z. Xing, Jane Lee, et al.. (2001). Factors influencing the removal of thymine glycol from DNA in γ-irradiated human cells. Progress in nucleic acid research and molecular biology. 68. 139–149. 11 indexed citations
19.
Fouladi, Bijan, Charles A. Waldren, Björn Rydberg, & Priscilla K. Cooper. (2000). Comparison of Repair of DNA Double-Strand Breaks in Identical Sequences in Primary Human Fibroblast and Immortal Hamster–Human Hybrid Cells Harboring a Single Copy of Human Chromosome 11. Radiation Research. 153(6). 795–804. 27 indexed citations
20.
Cooper, Priscilla K. & Steven A. Leadon. (1994). Defective Repair of Ionizing Radiation Damage in Cockayne's Syndrome and Xeroderma Pigmentosum Group Ga. Annals of the New York Academy of Sciences. 726(1). 330–332. 8 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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