D C LaPorte

3.8k total citations · 1 hit paper
53 papers, 3.2k citations indexed

About

D C LaPorte is a scholar working on Molecular Biology, Materials Chemistry and Genetics. According to data from OpenAlex, D C LaPorte has authored 53 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 21 papers in Materials Chemistry and 14 papers in Genetics. Recurrent topics in D C LaPorte's work include Enzyme Structure and Function (21 papers), Protein Structure and Dynamics (14 papers) and Bacterial Genetics and Biotechnology (12 papers). D C LaPorte is often cited by papers focused on Enzyme Structure and Function (21 papers), Protein Structure and Dynamics (14 papers) and Bacterial Genetics and Biotechnology (12 papers). D C LaPorte collaborates with scholars based in United States, Russia and France. D C LaPorte's co-authors include Daniel R. Storm, Daniel E. Koshland, Kenneth A. Walsh, John E. Cronan, Charles H. Keller, David J. Klumpp, William A. Toscano, C S Stueland, Peter E. Thorsness and Theodore D. Chung and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

D C LaPorte

52 papers receiving 3.0k citations

Hit Papers

Calcium-induced exposure ... 1980 2026 1995 2010 1980 100 200 300 400

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
D C LaPorte 2.5k 786 713 240 214 53 3.2k
Octavian Bârzu 2.5k 1.0× 815 1.0× 709 1.0× 251 1.0× 181 0.8× 124 3.6k
R.E. Huber 2.0k 0.8× 712 0.9× 422 0.6× 133 0.6× 240 1.1× 106 3.1k
Rosalind Kim 3.6k 1.4× 1.1k 1.4× 565 0.8× 275 1.1× 204 1.0× 87 4.4k
Robert L. Switzer 3.4k 1.4× 1.2k 1.5× 856 1.2× 250 1.0× 268 1.3× 126 4.1k
Charles Gilvarg 2.2k 0.9× 621 0.8× 521 0.7× 219 0.9× 413 1.9× 80 3.1k
Hans Jörnvall 2.9k 1.1× 397 0.5× 504 0.7× 660 2.8× 348 1.6× 97 4.6k
T. Hastings Wilson 2.3k 0.9× 585 0.7× 1.4k 1.9× 173 0.7× 809 3.8× 80 3.3k
Robert Simoni 2.5k 1.0× 408 0.5× 412 0.6× 313 1.3× 447 2.1× 209 3.4k
Gerald Böhm 1.9k 0.7× 728 0.9× 241 0.3× 207 0.9× 88 0.4× 28 2.5k
Thomas Acton 2.7k 1.1× 754 1.0× 377 0.5× 195 0.8× 114 0.5× 110 3.6k

Countries citing papers authored by D C LaPorte

Since Specialization
Citations

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

Fields of papers citing papers by D C LaPorte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D C LaPorte

This figure shows the co-authorship network connecting the top 25 collaborators of D C LaPorte. A scholar is included among the top collaborators of D C LaPorte 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 D C LaPorte. D C LaPorte 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.
Miller, Steven P., et al.. (2003). Multiple Positive and Negative Elements Involved in the Regulation of Expression of GSY1 in Saccharomyces cerevisiae. Journal of Biological Chemistry. 278(29). 26450–26457. 28 indexed citations
2.
Miller, Stephen P., et al.. (2002). Bacillus subtilis Isocitrate Dehydrogenase. Journal of Biological Chemistry. 277(9). 7567–7573. 28 indexed citations
3.
Sunnarborg, Susan W., et al.. (2001). Expression of the yeast glycogen phosphorylase gene is regulated by stress‐response elements and by the HOG MAP kinase pathway. Yeast. 18(16). 1505–1514. 35 indexed citations
4.
Singh, Satinder K., Kiyoshi Matsuno, D C LaPorte, & Leonard Banaszak. (2001). Crystal Structure of Bacillus subtilis Isocitrate Dehydrogenase at 1.55 Å. Journal of Biological Chemistry. 276(28). 26154–26163. 50 indexed citations
5.
Miller, Stephen P., et al.. (2000). Locations of the Regulatory Sites for Isocitrate Dehydrogenase Kinase/Phosphatase. Journal of Biological Chemistry. 275(2). 833–839. 20 indexed citations
7.
Miller, Stephen P., et al.. (1996). Isocitrate Dehydrogenase Kinase/Phosphatase. Journal of Biological Chemistry. 271(32). 19124–19128. 18 indexed citations
8.
Resnik, Ernesto, et al.. (1996). Integration host factor amplifies the induction of the aceBAK operon of Escherichia coli by relieving IclR repression. Journal of Bacteriology. 178(9). 2715–2717. 31 indexed citations
9.
LaPorte, D C, et al.. (1995). Response of a yeast glycogen synthase gene to stress. Molecular Microbiology. 16(6). 1197–1205. 44 indexed citations
10.
LaPorte, D C. (1993). The isocitrate dehydrogenase phosphorylation cycle: Regulation and enzymology. Journal of Cellular Biochemistry. 51(1). 14–18. 71 indexed citations
11.
Rowen, D, et al.. (1992). GLC3 and GHA1 of Saccharomyces cerevisiae Are Allelic and Encode the Glycogen Branching Enzyme. Molecular and Cellular Biology. 12(1). 22–29. 4 indexed citations
12.
Rowen, D, Martina C. Meinke, & D C LaPorte. (1992). GLC3 and GHA1 of Saccharomyces cerevisiae are allelic and encode the glycogen branching enzyme.. Molecular and Cellular Biology. 12(1). 22–29. 51 indexed citations
13.
Ikeda, Timothy P., et al.. (1992). Isocitrate dehydrogenase kinase/phosphatase: identification of mutations which selectively inhibit phosphatase activity. Journal of Bacteriology. 174(4). 1414–1416. 14 indexed citations
14.
Perentesis, John P., Lon Phan, William B. Gleason, et al.. (1992). Saccharomyces cerevisiae elongation factor 2. Genetic cloning, characterization of expression, and G-domain modeling.. Journal of Biological Chemistry. 267(2). 1190–1197. 66 indexed citations
15.
Resnik, Ernesto & D C LaPorte. (1991). Introduction of single-copy sequences into the chromosome of Escherichia coli: application to gene and operon fusions. Gene. 107(1). 19–25. 10 indexed citations
16.
LaPorte, D C, C S Stueland, & Timothy P. Ikeda. (1989). Isocitrate dehydrogenase kinase/phosphatase. Biochimie. 71(9-10). 1051–1057. 37 indexed citations
17.
Koshland, Daniel E., Kenneth A. Walsh, & D C LaPorte. (1985). Sensitivity of Metabolic Fluxes to Covalent Control. Current topics in cellular regulation. 27. 13–22. 65 indexed citations
18.
LaPorte, D C & Daniel E. Koshland. (1983). Phosphorylation of isocitrate dehydrogenase as a demonstration of enhanced sensitivity in covalent regulation. Nature. 305(5932). 286–290. 163 indexed citations
19.
LaPorte, D C, et al.. (1980). Calcium-induced exposure of a hydrophobic surface on calmodulin. Biochemistry. 19(16). 3814–3819. 445 indexed citations breakdown →
20.
LaPorte, D C, Susan Gidwitz, Michael J. Weber, & Daniel R. Storm. (1979). Relationship between changes in the calcium dependent regulatory protein and adenylate cyclase during viral transformation. Biochemical and Biophysical Research Communications. 86(4). 1169–1177. 50 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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