Soo S. Ko

1.9k total citations
32 papers, 1.5k citations indexed

About

Soo S. Ko is a scholar working on Molecular Biology, Organic Chemistry and Infectious Diseases. According to data from OpenAlex, Soo S. Ko has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 15 papers in Organic Chemistry and 7 papers in Infectious Diseases. Recurrent topics in Soo S. Ko's work include Chemical Synthesis and Analysis (7 papers), HIV/AIDS drug development and treatment (7 papers) and HIV Research and Treatment (5 papers). Soo S. Ko is often cited by papers focused on Chemical Synthesis and Analysis (7 papers), HIV/AIDS drug development and treatment (7 papers) and HIV Research and Treatment (5 papers). Soo S. Ko collaborates with scholars based in United States, Germany and Sweden. Soo S. Ko's co-authors include N. MINAMI, Yoshito Kishi, Robert K. Boeckman, Ronald M. Klabe, Susan Erickson‐Viitanen, George L. Trainor, John Ding‐E Young, Z A Cohn, Beverly C. Cordova and Lee T. Bacheler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Soo S. Ko

32 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Soo S. Ko United States	20	841	561	169	132	131	32	1.5k
Keith Biggadike United Kingdom	19	605 0.7×	621 1.1×	305 1.8×	114 0.9×	45 0.3×	45	1.4k
Christiane Yoakim Canada	28	1.1k 1.3×	624 1.1×	306 1.8×	46 0.3×	111 0.8×	51	1.8k
Yvan Guindon Canada	28	1.3k 1.6×	744 1.3×	107 0.6×	122 0.9×	139 1.1×	88	2.0k
Yves Ducharme Canada	18	541 0.6×	362 0.6×	107 0.6×	68 0.5×	85 0.6×	33	1.2k
Francis X. Wilson United Kingdom	26	1.4k 1.7×	1.2k 2.1×	118 0.7×	128 1.0×	55 0.4×	65	2.1k
Jay Wrobel United States	33	1.5k 1.8×	876 1.6×	150 0.9×	89 0.7×	127 1.0×	76	2.8k
Wallace T. Ashton United States	22	588 0.7×	767 1.4×	226 1.3×	49 0.4×	66 0.5×	59	1.8k
Nicola Mongelli Italy	26	822 1.0×	1.2k 2.2×	126 0.7×	64 0.5×	47 0.4×	81	2.1k
Yuichi Yoshimura Japan	24	1.1k 1.4×	937 1.7×	424 2.5×	112 0.8×	47 0.4×	127	1.8k
Elizabeth A. Lunney United States	25	583 0.7×	1.0k 1.9×	119 0.7×	33 0.3×	40 0.3×	59	1.8k

Countries citing papers authored by Soo S. Ko

Since Specialization

Citations

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

Fields of papers citing papers by Soo S. Ko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Soo S. Ko. 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 Soo S. Ko. The network helps show where Soo S. Ko may publish in the future.

Co-authorship network of co-authors of Soo S. Ko

This figure shows the co-authorship network connecting the top 25 collaborators of Soo S. Ko. A scholar is included among the top collaborators of Soo S. Ko 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 Soo S. Ko. Soo S. Ko 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

Campbell, Carlton L., et al.. (2009). Enantioselective Synthesis of Benzyl (1S,2R,4R)-4-(tert-Butoxycarbonylamino)-2-(hydroxymethyl)cyclohexylcarbamate Using an Iodolactamization As the Key Step. The Journal of Organic Chemistry. 74(16). 6368–6370. 26 indexed citations

Gardner, Daniel S., Joseph B. Santella, Andrew J. Tebben, et al.. (2007). From rigid cyclic templates to conformationally stabilized acyclic scaffolds. Part II: Acyclic replacements for the (3S)-3-benzylpiperidine in a series of potent CCR3 antagonists. Bioorganic & Medicinal Chemistry Letters. 18(2). 586–595. 9 indexed citations

Watson, Paul S., Bin Jiang, Maryanne Covington, et al.. (2006). 2,4-Disubstituted piperidines as selective CC chemokine receptor 3 (CCR3) antagonists: Synthesis and selectivity. Bioorganic & Medicinal Chemistry Letters. 16(21). 5695–5699. 13 indexed citations

Das, Anuk, Krishna Vaddi, Kimberly A. Solomon, et al.. (2006). Selective Inhibition of Eosinophil Influx into the Lung by Small Molecule CC Chemokine Receptor 3 Antagonists in Mouse Models of Allergic Inflammation. Journal of Pharmacology and Experimental Therapeutics. 318(1). 411–417. 30 indexed citations

Varnes, Jeffrey, Daniel S. Gardner, Joseph B. Santella, et al.. (2004). Discovery of N-propylurea 3-benzylpiperidines as selective CC chemokine receptor-3 (CCR3) antagonists. Bioorganic & Medicinal Chemistry Letters. 14(7). 1645–1649. 21 indexed citations

Suh, Jeong, et al.. (2003). Triacylglycerol, 1-Palmitoyl-2-Linoleoyl-3-Acetyl-<i>rac </i> -Glycerol Isolated from Bovine Udder and its Synthetic Enantiomer can Potentiate the Mitogenic Activity for Mouse Peritoneal Macrophages. Cellular Physiology and Biochemistry. 13(6). 415–422. 9 indexed citations

Wacker, Dean A., Joseph B. Santella, Daniel S. Gardner, et al.. (2002). CCR3 antagonists: a potential new therapy for the treatment of asthma. Discovery and structure–activity relationships. Bioorganic & Medicinal Chemistry Letters. 12(13). 1785–1789. 35 indexed citations

Cocuzza, Anthony J., Dennis R. Chidester, Beverly C. Cordova, et al.. (2001). 4,1-Benzoxazepinone analogues of efavirenz (Sustiva™) as HIV-1 reverse transcriptase inhibitors. Bioorganic & Medicinal Chemistry Letters. 11(11). 1389–1392. 18 indexed citations

Corbett, Jeffrey W., Soo S. Ko, James D. Rodgers, et al.. (2000). Novel 2,2-dioxide-4,4-disubstituted-1,3-H-2,1,3-benzothiadiazines as non-nucleoside reverse transcriptase inhibitors. Bioorganic & Medicinal Chemistry Letters. 10(2). 193–195. 13 indexed citations

10.

Patel, Mona, James D. Rodgers, Robert J. McHugh, et al.. (1999). Unsymmetrical cyclic ureas as HIV-1 protease inhibitors: Novel biaryl indazoles as P2/P2′ substituents. Bioorganic & Medicinal Chemistry Letters. 9(22). 3217–3220. 53 indexed citations

11.

Patel, Mona, Robert J. McHugh, Beverly C. Cordova, et al.. (1999). Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVATM). Bioorganic & Medicinal Chemistry Letters. 9(22). 3221–3224. 60 indexed citations

12.

Rodgers, James D., Patrick Y. S. Lam, Barry L. Johnson, et al.. (1998). Design and selection of DMP 850 and DMP 851: the next generation of cyclic urea HIV protease inhibitors. Chemistry & Biology. 5(11). R312–R312. 1 indexed citations

13.

Ness, Gene C., Dayami Lopez, Christopher M. Chambers, et al.. (1998). Effects of 15-Oxa-32-vinyl-lanost-8-ene-3β,32 diol on the Expression of 3-Hydroxy-3-methylglutaryl Coenzyme A Reductase and Low Density Lipoprotein Receptor in Rat Liver. Archives of Biochemistry and Biophysics. 357(2). 259–264. 10 indexed citations

14.

Lucca, George V. De, Jing Liang, Beverly C. Cordova, et al.. (1998). Nonsymmetric P2/P2‘ Cyclic Urea HIV Protease Inhibitors. Structure−Activity Relationship, Bioavailability, and Resistance Profile of Monoindazole-Substituted P2 Analogues. Journal of Medicinal Chemistry. 41(13). 2411–2423. 43 indexed citations

15.

Wilde, Richard G., Jeffrey T. Billheimer, Elizabeth A. Hausner, et al.. (1996). ACAT inhibitors derived from hetero-Diels-Alder cycloadducts of thioaldehydes. Bioorganic & Medicinal Chemistry. 4(9). 1493–1513. 19 indexed citations

16.

Trzăskos, James M., Soo S. Ko, Ronald L. Magolda, et al.. (1995). Substrate-based inhibitors of lanosterol 14.alpha.-methyl demethylase: I. Assessment of inhibitor structure-activity relationship and cholesterol biosynthesis inhibition properties. Biochemistry. 34(30). 9670–9676. 29 indexed citations

17.

Baldwin, Jack E., Andrew K. Forrest, Soo S. Ko, & L Sheppard. (1987). Preparation of 2-exomethylene penam and penicillin-2-carboxylate systems. Journal of the Chemical Society Chemical Communications. 81–81. 7 indexed citations

18.

Ko, Soo S. & Pat N. Confalone. (1985). Model studies for the total synthesis of the maytansinoids based on the intramolecular nitrile oxide-olefin [3+2] cycloaddition reaction. Tetrahedron. 41(17). 3511–3518. 24 indexed citations

19.

MINAMI, N., Soo S. Ko, & Yoshito Kishi. (1982). Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonide. Journal of the American Chemical Society. 104(4). 1109–1111. 177 indexed citations

20.

Boeckman, Robert K. & Soo S. Ko. (1980). Stereocontrol in the intramolecular Diels-Alder reaction. 1. An application to the total synthesis of (.+-.) marasmic acid. Journal of the American Chemical Society. 102(23). 7146–7149. 23 indexed citations

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