John W. Chase

3.8k total citations · 1 hit paper
71 papers, 3.3k citations indexed

About

John W. Chase is a scholar working on Molecular Biology, Genetics and Ecology. According to data from OpenAlex, John W. Chase has authored 71 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 20 papers in Genetics and 13 papers in Ecology. Recurrent topics in John W. Chase's work include DNA Repair Mechanisms (26 papers), DNA and Nucleic Acid Chemistry (26 papers) and Bacterial Genetics and Biotechnology (19 papers). John W. Chase is often cited by papers focused on DNA Repair Mechanisms (26 papers), DNA and Nucleic Acid Chemistry (26 papers) and Bacterial Genetics and Biotechnology (19 papers). John W. Chase collaborates with scholars based in United States, Australia and Russia. John W. Chase's co-authors include Kenneth R. Williams, Charles C. Richardson, J B Murphy, Igor B. Dawid, John W. Winchester, Robert F. Whittier, Charles D. Coryell, Aziz Sancar, W. Dean Rupp and Eleanor K. Spicer 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

John W. Chase

69 papers receiving 3.1k citations

Hit Papers

SINGLE-STRANDED DNA BINDING PROTEINS REQUIRED FOR DNA REP... 1986 2026 1999 2012 1986 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
John W. Chase United States 31 2.7k 1.3k 615 190 158 71 3.3k
L. Elizabeth Bertani Sweden 20 1.0k 0.4× 458 0.4× 732 1.2× 96 0.5× 58 0.4× 34 1.6k
Rick Russell United States 35 3.5k 1.3× 240 0.2× 440 0.7× 229 1.2× 152 1.0× 157 4.9k
L. Waters United States 17 1.8k 0.7× 772 0.6× 454 0.7× 211 1.1× 198 1.3× 51 3.1k
Hyman Hartman United States 30 1.6k 0.6× 335 0.3× 455 0.7× 233 1.2× 217 1.4× 67 2.9k
Éric Larquet France 26 1.2k 0.4× 638 0.5× 225 0.4× 450 2.4× 159 1.0× 63 3.0k
Antonio Lazcano Mexico 38 2.8k 1.0× 469 0.4× 504 0.8× 503 2.6× 386 2.4× 124 4.8k
Alain Bernadac France 30 1.9k 0.7× 961 0.7× 694 1.1× 158 0.8× 273 1.7× 70 3.1k
John Abelson United States 73 15.3k 5.6× 2.0k 1.6× 1.5k 2.4× 417 2.2× 824 5.2× 212 16.3k
Jane K. Setlow United States 31 2.6k 1.0× 628 0.5× 548 0.9× 105 0.6× 472 3.0× 115 3.9k
Arash Komeili United States 33 3.1k 1.1× 269 0.2× 233 0.4× 554 2.9× 167 1.1× 52 4.1k

Countries citing papers authored by John W. Chase

Since Specialization
Citations

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

Fields of papers citing papers by John W. Chase

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John W. Chase. 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 John W. Chase. The network helps show where John W. Chase may publish in the future.

Co-authorship network of co-authors of John W. Chase

This figure shows the co-authorship network connecting the top 25 collaborators of John W. Chase. A scholar is included among the top collaborators of John W. Chase 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 John W. Chase. John W. Chase 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.
Dayan, N., et al.. (2010). Skin moisturization by hydrogenated polyisobutene—Quantitative and visual evaluation. International Journal of Cosmetic Science. 32(1). 81–82. 3 indexed citations
2.
Davis, Maria C., Kristine M. Hujer, Jacques Ravel, et al.. (1996). A Survey of the Genome of the Hyperthermophilic Archaeon, Pyrococcus furiosus. 1(2). 37–46. 18 indexed citations
4.
Thorn, Jennifer M., Paul D. Carr, John W. Chase, Nicholas E. Dixon, & David L. Ollis. (1994). Crystallization and Low Temperature Diffraction Studies of the DNA Binding Domain of the Single-stranded DNA Binding Protein from Escherichia coli. Journal of Molecular Biology. 240(4). 396–399. 7 indexed citations
5.
Shuai, Ke, et al.. (1992). Purification and characterization of an endo-exonuclease from adult flies ofDrosophila melanogaster. Nucleic Acids Research. 20(6). 1379–1385. 13 indexed citations
6.
Ruvolo, Peter P., Kathleen M. Keating, Kenneth R. Williams, & John W. Chase. (1991). Single‐stranded DNA binding proteins (SSBs) from prokaryotic transmissible plasmids. Proteins Structure Function and Bioinformatics. 9(2). 120–134. 19 indexed citations
7.
Tsao, Désirée H.H., August H. Maki, & John W. Chase. (1990). Energy transfer in complexes of E. coli single‐stranded DNA‐binding protein with single‐stranded poly‐(2‐thiouridylic acid). FEBS Letters. 261(2). 389–391.
8.
Muniyappa, K., et al.. (1990). Active nucleoprotein filaments of single-stranded binding protein and recA protein on single-stranded DNA have a regular repeating structure. Nucleic Acids Research. 18(13). 3967–3973. 27 indexed citations
9.
Tsao, Désirée H.H., José R. Casas‐Finet, August H. Maki, & John W. Chase. (1989). Triplet state properties of tryptophan residues in complexes of mutated Escherichia coli single-stranded DNA binding proteins with single-stranded polynucleotides. Biophysical Journal. 55(5). 927–936. 24 indexed citations
13.
Khamis, Mustafa, José R. Casas‐Finet, August H. Maki, Peter P. Ruvolo, & John W. Chase. (1987). Optically detected magnetic resonance of tryptophan residues in complexes formed between a bacterial single-stranded DNA binding protein and heavy atom-modified poly(uridylic acid). Biochemistry. 26(12). 3347–3354. 12 indexed citations
14.
Casas‐Finet, José R., Mustafa Khamis, August H. Maki, Peter P. Ruvolo, & John W. Chase. (1987). Optically detected magnetic resonance of tryptophan residues in Escherichia coli ssb gene product and E. coli plasmid-encoded single-stranded DNA-binding proteins and their complexes with poly(deoxythymidylic) acid.. Journal of Biological Chemistry. 262(18). 8574–8583. 20 indexed citations
15.
Egner, Carol, et al.. (1987). Effects of various single-stranded-DNA-binding proteins on reactions promoted by RecA protein. Journal of Bacteriology. 169(8). 3422–3428. 22 indexed citations
16.
Prigodich, Richard V., Yousif Shamoo, Kenneth R. Williams, et al.. (1986). Proton NMR (500 MHz) identification of aromatic residues of gene 32 protein involved in DNA binding by use of protein containing perdeuterated aromatic residues and by site-directed mutagenesis. Biochemistry. 25(12). 3666–3672. 49 indexed citations
17.
Williams, Kenneth R., Eleanor K. Spicer, M B LoPresti, R A Guggenheimer, & John W. Chase. (1983). Limited proteolysis studies on the Escherichia coli single-stranded DNA binding protein. Evidence for a functionally homologous domain in both the Escherichia coli and T4 DNA binding proteins.. Journal of Biological Chemistry. 258(5). 3346–3355. 182 indexed citations
18.
Chase, John W., et al.. (1980). Synthesis of recA protein and induction of bacteriophage lambda in single-strand deoxyribonucleic acid-binding protein mutants of Escherichia coli. Journal of Bacteriology. 144(2). 489–498. 58 indexed citations
19.
Chase, John W., Warren E. Masker, & J B Murphy. (1979). Pyrimidine dimer excision in Escherichia coli strains deficient in exonucleases V and VII and in the 5' leads to 3' exonuclease of DNA polymerase I. Journal of Bacteriology. 137(1). 234–242. 15 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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