Robert J. Barbuch

2.9k total citations
63 papers, 2.3k citations indexed

About

Robert J. Barbuch is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Robert J. Barbuch has authored 63 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 16 papers in Organic Chemistry and 13 papers in Pharmacology. Recurrent topics in Robert J. Barbuch's work include Fungal and yeast genetics research (14 papers), Pharmacogenetics and Drug Metabolism (11 papers) and Plant biochemistry and biosynthesis (10 papers). Robert J. Barbuch is often cited by papers focused on Fungal and yeast genetics research (14 papers), Pharmacogenetics and Drug Metabolism (11 papers) and Plant biochemistry and biosynthesis (10 papers). Robert J. Barbuch collaborates with scholars based in United States, Italy and Singapore. Robert J. Barbuch's co-authors include Martin Bard, N. Douglas Lees, James A. Eckstein, C. A. Pierson, Daniel Gachotte, Palaniappan Kulanthaivel, Norton P. Peet, Jennifer B. Dennison, Stephen D. Hall and William J. Ehlhardt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cell Metabolism and Genetics.

In The Last Decade

Robert J. Barbuch

60 papers receiving 2.2k citations

Peers

Robert J. Barbuch
G. Willemsens Belgium
Yi Ding China
Yuzo Yoshida Japan
Rolf D. Walter Germany
W Cools Belgium
Masayoshi Arai Japan
Xiao Ding China
Kunio Ando Japan
Pei‐Wen Hsiao Taiwan
Yoshinori Kitagawa Japan
G. Willemsens Belgium
Robert J. Barbuch
Citations per year, relative to Robert J. Barbuch Robert J. Barbuch (= 1×) peers G. Willemsens

Countries citing papers authored by Robert J. Barbuch

Since Specialization
Citations

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

Fields of papers citing papers by Robert J. Barbuch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert J. Barbuch. 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 Robert J. Barbuch. The network helps show where Robert J. Barbuch may publish in the future.

Co-authorship network of co-authors of Robert J. Barbuch

This figure shows the co-authorship network connecting the top 25 collaborators of Robert J. Barbuch. A scholar is included among the top collaborators of Robert J. Barbuch 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 Robert J. Barbuch. Robert J. Barbuch 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.
Zamek‐Gliszczynski, Maciej J., Trent L. Abraham, Palaniappan Kulanthaivel, et al.. (2013). Pharmacokinetics, Metabolism, and Excretion of the Glycogen Synthase Kinase-3 Inhibitor LY2090314 in Rats, Dogs, and Humans: A Case Study in Rapid Clearance by Extensive Metabolism with Low Circulating Metabolite Exposure. Drug Metabolism and Disposition. 41(4). 714–726. 36 indexed citations
2.
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Bhuiyan, M. Shah Alam, Stephen K. Randall, Robert J. Barbuch, et al.. (2008). Genetic analyses involving interactions between the ergosterol biosynthetic enzymes, lanosterol synthase (Erg7p) and 3-ketoreductase (Erg27p), in the yeast Saccharomyces cerevisiae. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1781(8). 359–366. 10 indexed citations
4.
Willger, Sven D., Srisombat Puttikamonkul, Kwang‐Hyung Kim, et al.. (2008). A Sterol-Regulatory Element Binding Protein Is Required for Cell Polarity, Hypoxia Adaptation, Azole Drug Resistance, and Virulence in Aspergillus fumigatus. PLoS Pathogens. 4(11). e1000200–e1000200. 275 indexed citations
5.
Dennison, Jennifer B., Michael A. Mohutsky, Robert J. Barbuch, Steven Wrighton, & Stephen D. Hall. (2008). Apparent High CYP3A5 Expression Is Required for Significant Metabolism of Vincristine by Human Cryopreserved Hepatocytes. Journal of Pharmacology and Experimental Therapeutics. 327(1). 248–257. 28 indexed citations
6.
Hughes, Adam L., David W. Powell, Martin Bard, et al.. (2007). Dap1/PGRMC1 Binds and Regulates Cytochrome P450 Enzymes. Cell Metabolism. 5(2). 143–149. 189 indexed citations
7.
Dennison, Jennifer B., Palaniappan Kulanthaivel, Robert J. Barbuch, et al.. (2006). SELECTIVE METABOLISM OF VINCRISTINE IN VITRO BY CYP3A5. Drug Metabolism and Disposition. 34(8). 1317–1327. 143 indexed citations
8.
Burkey, Jennifer, et al.. (2006). Disposition of [14C]Ruboxistaurin in Humans. Drug Metabolism and Disposition. 34(11). 1909–1917. 9 indexed citations
9.
Bard, Martin, C. A. Pierson, Sarah C. Nabinger, et al.. (2005). Sterol uptake in Candida glabrata: Rescue of sterol auxotrophic strains. Diagnostic Microbiology and Infectious Disease. 52(4). 285–293. 44 indexed citations
10.
Barbuch, Robert J., Kristina Campanale, Chad E. Hadden, et al.. (2005). IN VIVO METABOLISM OF [14C]RUBOXISTAURIN IN DOGS, MICE, AND RATS FOLLOWING ORAL ADMINISTRATION AND THE STRUCTURE DETERMINATION OF ITS METABOLITES BY LIQUID CHROMATOGRAPHY/MASS SPECTROMETRY AND NMR SPECTROSCOPY. Drug Metabolism and Disposition. 34(2). 213–224. 11 indexed citations
11.
Pierson, C. A., Nan Jia, Caiqing Mo, et al.. (2004). Isolation, characterization, and regulation of theCandidaalbicansERG27gene encoding the sterol 3-keto reductase. Medical Mycology. 42(5). 461–473. 14 indexed citations
12.
Pierson, C. A., et al.. (2004). Ergosterol gene expression in wild-type and ergosterol-deficient mutants ofCandidaalbicans. Medical Mycology. 42(4). 385–389. 16 indexed citations
13.
Kennedy, Matthew A., Robert J. Barbuch, & Martin Bard. (1999). Transcriptional regulation of the squalene synthase gene (ERG9) in the yeast Saccharomyces cerevisiae. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1445(1). 110–122. 72 indexed citations
14.
Dage, Jeffrey L., Bradley L. Ackermann, Robert J. Barbuch, et al.. (1997). Evidence for a Novel Pentyl Radical Adduct of the Cyclic Nitrone Spin Trap MDL 101,002. Free Radical Biology and Medicine. 22(5). 807–812. 6 indexed citations
15.
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Barbuch, Robert J., et al.. (1995). Spectral analysis and structural identification of a major deflazacort metabolite in man. Xenobiotica. 25(2). 175–183. 3 indexed citations
17.
Ackermann, Bradley L., Robert J. Barbuch, John E. Coutant, John L. Krstenansky, & Thomas J. Owen. (1992). Evidence for a lysine‐specific fragmentation in fast‐atom bombardment mass spectra of peptides. Rapid Communications in Mass Spectrometry. 6(4). 257–264. 4 indexed citations
18.
Skatrud, Paul L., et al.. (1991). Cloning, disruption and sequence of the gene encoding yeast C-5 sterol desaturase. Gene. 102(1). 39–44. 127 indexed citations
19.
20.
Coutant, John E., et al.. (1987). Identification in man of urinary metabolites of a new bronchodilator, MDL 257, using triple stage quadrupole mass spectrometry-mass spectrometry. Journal of Mass Spectrometry. 14(7). 325–330. 9 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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