David P. Clark

6.8k total citations
110 papers, 4.8k citations indexed

About

David P. Clark is a scholar working on Molecular Biology, Genetics and Biochemistry. According to data from OpenAlex, David P. Clark has authored 110 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 32 papers in Genetics and 18 papers in Biochemistry. Recurrent topics in David P. Clark's work include Microbial Metabolic Engineering and Bioproduction (35 papers), Bacterial Genetics and Biotechnology (32 papers) and Amino Acid Enzymes and Metabolism (15 papers). David P. Clark is often cited by papers focused on Microbial Metabolic Engineering and Bioproduction (35 papers), Bacterial Genetics and Biotechnology (32 papers) and Amino Acid Enzymes and Metabolism (15 papers). David P. Clark collaborates with scholars based in United States, United Kingdom and Italy. David P. Clark's co-authors include John E. Cronan, Fairoz Mat-Jan, Philip R. Cunningham, Mário Roberto Leonardo, L. O. Ingram, Tyrrell Conway, Gavin W. Sewell, James F. Preston, Cynthia Sanville Millard and Mark I. Donnelly and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Applied and Environmental Microbiology.

In The Last Decade

David P. Clark

107 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David P. Clark United States	39	3.1k	1.0k	957	504	454	110	4.8k
Sang Jun Lee South Korea	42	3.8k 1.2×	1.1k 1.1×	734 0.8×	210 0.4×	122 0.3×	220	6.3k
Yang Ding China	35	3.4k 1.1×	956 0.9×	555 0.6×	355 0.7×	134 0.3×	108	6.9k
Sun Chang Kim South Korea	54	6.4k 2.1×	890 0.9×	943 1.0×	294 0.6×	111 0.2×	167	9.4k
M. Joost Teixeira de Mattos Netherlands	35	3.0k 1.0×	733 0.7×	619 0.6×	243 0.5×	271 0.6×	83	4.5k
Matthew Wook Chang Singapore	42	3.4k 1.1×	1.8k 1.8×	562 0.6×	635 1.3×	65 0.1×	115	6.0k
Yuichi Koga Japan	31	2.3k 0.7×	233 0.2×	439 0.5×	561 1.1×	49 0.1×	134	4.0k
Pengcheng Li China	55	2.3k 0.7×	865 0.8×	615 0.6×	624 1.2×	45 0.1×	261	9.3k
Byung‐Kwan Cho South Korea	49	5.1k 1.6×	1.0k 1.0×	1.4k 1.4×	536 1.1×	222 0.5×	222	7.1k
Sittiruk Roytrakul Thailand	40	3.4k 1.1×	405 0.4×	359 0.4×	301 0.6×	45 0.1×	557	7.6k
Yuanda Song China	37	2.8k 0.9×	1.1k 1.0×	161 0.2×	211 0.4×	316 0.7×	211	5.1k

Countries citing papers authored by David P. Clark

Since Specialization

Citations

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

Fields of papers citing papers by David P. Clark

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David P. Clark. 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 David P. Clark. The network helps show where David P. Clark may publish in the future.

Co-authorship network of co-authors of David P. Clark

This figure shows the co-authorship network connecting the top 25 collaborators of David P. Clark. A scholar is included among the top collaborators of David P. Clark 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 David P. Clark. David P. Clark 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

Clark, David P.. (2010). Molecular biology : academic cell update. Elsevier eBooks. 6 indexed citations

Espinosa, Avelina, Yan Le, Zhi Zhang, et al.. (2001). The Bifunctional Entamoeba histolytica Alcohol Dehydrogenase 2 (EhADH2) Protein Is Necessary for Amebic Growth and Survival and Requires an Intact C-terminal Domain for Both Alcohol Dehydrogenase and Acetaldehyde Dehydrogenase Activity. Journal of Biological Chemistry. 276(23). 20136–20143. 51 indexed citations

Gupta, Shashi, et al.. (2000). Acetaldehyde dehydrogenase activity of the AdhE protein ofEscherichia coliis inhibited by intermediates in ubiquinone synthesis. FEMS Microbiology Letters. 182(1). 51–55. 13 indexed citations

Clark, David P., et al.. (1997). Cutaneous Micrographic Surgery for Atypical Fibroxanthoma. Dermatologic Surgery. 23(7). 553–557. 21 indexed citations

Mat-Jan, Fairoz, et al.. (1997). Effect of chelating agents and respiratory inhibitors on regulation of the cadA gene in Escherichia coli. Archives of Microbiology. 167(4). 209–216. 9 indexed citations

Hamaker, Bruce R., et al.. (1992). AMINO-ACID AND FATTY-ACID PROFILES OF THE INCA PEANUT (PLUKENETIA-VOLUBILIS). 69(4). 461–463. 82 indexed citations

Mat-Jan, Fairoz, et al.. (1991). Mutations permitting the anaerobic growth ofEscherichia colion trehalose. FEMS Microbiology Letters. 78(2-3). 149–152. 6 indexed citations

Clark, David P.. (1990). Molybdenum cofactor negative mutants of Escherichia coli use citrate anaerobically. FEMS Microbiology Letters. 67(3). 245–249. 5 indexed citations

Clark, David P.. (1989). The fermentation pathways of Escherichia coli. FEMS Microbiology Letters. 63(3). 223–234. 97 indexed citations

10.

Cunningham, Philip R., et al.. (1989). Cloning and sequence analysis of the fermentative alcohol-dehydrogenase-encoding gene of Escherichia coli. Gene. 85(1). 209–214. 106 indexed citations

11.

Mat-Jan, Fairoz, et al.. (1989). Anaerobic growth defects resulting from gene fusions affecting succinyl-CoA synthetase in Escherichia coli K12. Molecular and General Genetics MGG. 215(2). 276–280. 14 indexed citations

12.

Clark, David P., et al.. (1988). Glucose repression of anaerobic genes ofEscherichia coliis independent of cyclic AMP. FEMS Microbiology Letters. 56(2). 231–235. 5 indexed citations

13.

Clark, David P. & C. William Hanke. (1988). Neoplasms of the Conchal Bowl: Treatment with Mohs Micrographic Surgery. The Journal of Dermatologic Surgery and Oncology. 14(11). 1223–1228. 15 indexed citations

14.

Clark, David P., et al.. (1988). Successive mutation ofE. coli for improved thiophene degradation. Applied Biochemistry and Biotechnology. 18(1). 393–401. 3 indexed citations

15.

Bracero, Luis A., et al.. (1988). Sonographic Findings in a Case of Cloverleaf Skull Deformity and Prune Belly. American Journal of Perinatology. 5(3). 239–241. 5 indexed citations

16.

Clark, David P., et al.. (1988). Mutants ofEscherichia coli defective in acid fermentation. Applied Biochemistry and Biotechnology. 17(1-3). 163–173. 11 indexed citations

17.

Clark, David P.. (1984). The number of anaerobically regulated genes in Escherichia coli. FEMS Microbiology Letters. 24(2-3). 251–254.

18.

Clark, David P.. (1984). The number of anaerobically regulated genes inEscherichia coli. FEMS Microbiology Letters. 24(2-3). 251–254. 21 indexed citations

19.

Clark, David P.. (1984). Proteins induced by high osmotic pressure in Escherichia coli. FEMS Microbiology Letters. 25(1). 81–83. 1 indexed citations

20.

Mitscher, Lester A., et al.. (1978). Antimicrobial agents from higher plants. An investigation of Hunnemannia fumariaefolia pseudoalcoholates of sanguinarine and chelerythrine.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 41(2). 145–50. 53 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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