Janice D. Pata

1.2k total citations
32 papers, 825 citations indexed

About

Janice D. Pata is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Janice D. Pata has authored 32 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 12 papers in Genetics and 11 papers in Infectious Diseases. Recurrent topics in Janice D. Pata's work include DNA Repair Mechanisms (13 papers), DNA and Nucleic Acid Chemistry (8 papers) and Bacterial Genetics and Biotechnology (8 papers). Janice D. Pata is often cited by papers focused on DNA Repair Mechanisms (13 papers), DNA and Nucleic Acid Chemistry (8 papers) and Bacterial Genetics and Biotechnology (8 papers). Janice D. Pata collaborates with scholars based in United States, Canada and Italy. Janice D. Pata's co-authors include Thomas A. Steitz, Karla Kirkegaard, S.C. Schultz, Joachim Jäger, William G. Stirtan, Steven W. Goldstein, Indrajit Lahiri, Marcus Jackson, Yifeng Wu and Nebojša Janjić and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Janice D. Pata

32 papers receiving 810 citations

Peers

Janice D. Pata

GENET

PHEOH

VIROL

David Alderton United Kingdom

J. Stephen Lodmell United States

Jason E. Comer United States

Krystal A. Fontaine United States

Jason D. Graci United States

Guanghui Yi United States

Alexander F. A. Keszei Canada

Simon Daefler United States

Miguel Ángel Cuesta-Geijo Spain

Xiulian Sun China

David Alderton United Kingdom

Janice D. Pata

512 ×0.8

135 ×0.7

GENET

221 ×1.1

68 ×0.8

PHEOH

127 ×1.7

VIROL

Citations per year, relative to Janice D. Pata Janice D. Pata (= 1×) peers David Alderton

Countries citing papers authored by Janice D. Pata

Since Specialization

Citations

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

Fields of papers citing papers by Janice D. Pata

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janice D. Pata. 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 Janice D. Pata. The network helps show where Janice D. Pata may publish in the future.

Co-authorship network of co-authors of Janice D. Pata

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

All Works

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20 of 20 papers shown

Kuo, Lili, Janice D. Pata, Alan P. Dupuis, et al.. (2023). Maintenance of a host-specific minority mutation in the West Nile virus NS3. iScience. 26(8). 107468–107468. 1 indexed citations

Lasek‐Nesselquist, Erica, Zhuo Ma, J. Nicholas O’Donnell, et al.. (2022). Phenotypic and genetic changes associated with the seesaw effect in MRSA strain N315 in a bioreactor model. Journal of Global Antimicrobial Resistance. 28. 249–253. 1 indexed citations

Pata, Janice D., et al.. (2022). The Role of the Flavivirus Replicase in Viral Diversity and Adaptation. Viruses. 14(5). 1076–1076. 8 indexed citations

Dangerfield, Tyler L., et al.. (2021). Pyrophosphate release acts as a kinetic checkpoint during high-fidelity DNA replication by the Staphylococcus aureus replicative polymerase PolC. Nucleic Acids Research. 49(14). 8324–8338. 10 indexed citations

Wu, Yifeng, et al.. (2020). Heterotrimeric PCNA increases the activity and fidelity of Dbh, a Y-family translesion DNA polymerase prone to creating single-base deletion mutations. DNA repair. 96. 102967–102967. 3 indexed citations

Lasek‐Nesselquist, Erica, Zhuo Ma, Vincenzo Russo, et al.. (2019). Insights Into the Evolution of Staphylococcus aureus Daptomycin Resistance From an in vitro Bioreactor Model. Frontiers in Microbiology. 10. 345–345. 10 indexed citations

Ma, Zhuo, Erica Lasek‐Nesselquist, Janice D. Pata, et al.. (2018). Characterization of genetic changes associated with daptomycin nonsusceptibility in Staphylococcus aureus. PLoS ONE. 13(6). e0198366–e0198366. 19 indexed citations

Cheung, Jonah, et al.. (2017). Novel structural features drive DNA binding properties of Cmr, a CRP family protein in TB complex mycobacteria. Nucleic Acids Research. 46(1). 403–420. 7 indexed citations

Pata, Janice D., et al.. (2014). Cytosine Unstacking and Strand Slippage at an Insertion–Deletion Mutation Sequence in an Overhang-Containing DNA Duplex. Biochemistry. 53(23). 3807–3816. 5 indexed citations

10.

Lahiri, Indrajit, et al.. (2013). Kinetic Characterization of Exonuclease-Deficient Staphylococcus aureus PolC, a C-family Replicative DNA Polymerase. PLoS ONE. 8(5). e63489–e63489. 11 indexed citations

11.

Lahiri, Indrajit, et al.. (2013). Human polymerase kappa uses a template-slippage deletion mechanism, but can realign the slipped strands to favour base substitution mutations over deletions. Nucleic Acids Research. 41(9). 5024–5035. 20 indexed citations

12.

Jackson, Marcus, et al.. (2012). Y-Family Polymerase Conformation Is a Major Determinant of Fidelity and Translesion Specificity. Structure. 21(1). 20–31. 31 indexed citations

13.

Pata, Janice D.. (2010). Structural diversity of the Y-family DNA polymerases. Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1804(5). 1124–1135. 67 indexed citations

14.

Evans, Ronald J., D.R. Davies, James M. Bullard, et al.. (2008). Structure of PolC reveals unique DNA binding and fidelity determinants. Proceedings of the National Academy of Sciences. 105(52). 20695–20700. 74 indexed citations

15.

Pata, Janice D., et al.. (2008). Structural Insights into the Generation of Single-Base Deletions by the Y Family DNA Polymerase Dbh. Molecular Cell. 29(6). 767–779. 44 indexed citations

16.

Bai, Guangchun, Janice D. Pata, Kathleen A. McDonough, Andrey Golubov, & Eric A. Smith. (2007). Differential Gene Regulation in Yersinia pestis versus Yersinia pseudotuberculosis: Effects of Hypoxia and Potential Role of a Plasmid Regulator. Advances in experimental medicine and biology. 603. 131–144. 6 indexed citations

17.

Nag, Dilip K., et al.. (2006). Both conserved and non-conserved regions of Spo11 are essential for meiotic recombination initiation in yeast. Molecular Genetics and Genomics. 276(4). 313–321. 12 indexed citations

18.

Pata, Janice D.. (2002). Assembly, purification and crystallization of an active HIV-1 reverse transcriptase initiation complex. Nucleic Acids Research. 30(22). 4855–4863. 6 indexed citations

19.

Pata, Janice D., et al.. (2001). Crystal Structure of a DinB Lesion Bypass DNA Polymerase Catalytic Fragment Reveals a Classic Polymerase Catalytic Domain. Molecular Cell. 8(2). 427–437. 162 indexed citations

20.

Rice, Charles M., Ruedi Aebersold, David B. Teplow, et al.. (1986). Partial N-terminal amino acid sequences of three nonstructural proteins of two flaviviruses. Virology. 151(1). 1–9. 47 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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