David C. Bouck

2.0k total citations
21 papers, 1.2k citations indexed

About

David C. Bouck is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, David C. Bouck has authored 21 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Cell Biology and 4 papers in Plant Science. Recurrent topics in David C. Bouck's work include Microtubule and mitosis dynamics (9 papers), Genomics and Chromatin Dynamics (7 papers) and Ubiquitin and proteasome pathways (5 papers). David C. Bouck is often cited by papers focused on Microtubule and mitosis dynamics (9 papers), Genomics and Chromatin Dynamics (7 papers) and Ubiquitin and proteasome pathways (5 papers). David C. Bouck collaborates with scholars based in United States and Japan. David C. Bouck's co-authors include Kerry Bloom, Ajit P. Joglekar, Edward D. Salmon, Jeffrey N. Molk, Leocadia V. Paliulis, Julian Haase, Taosheng Chen, Eric S. Lightcap, Jonathan L. Blank and Khristofer Garcia and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

David C. Bouck

21 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David C. Bouck United States 15 1.0k 682 345 130 75 21 1.2k
Emily R. Hildebrandt United States 17 698 0.7× 329 0.5× 88 0.3× 87 0.7× 32 0.4× 31 881
Andrew Bloecher United States 13 1.1k 1.0× 415 0.6× 146 0.4× 281 2.2× 26 0.3× 17 1.2k
Craig W. Vander Kooi United States 11 969 1.0× 82 0.1× 76 0.2× 173 1.3× 11 0.1× 13 1.2k
Javier Valdez Taubas Argentina 14 769 0.8× 472 0.7× 121 0.4× 69 0.5× 3 0.0× 24 978
Jennifer Haynes United States 12 557 0.5× 139 0.2× 78 0.2× 108 0.8× 6 0.1× 24 785
Carmen De Lemos-Chiarandini United States 11 599 0.6× 575 0.8× 21 0.1× 83 0.6× 109 1.5× 12 913
David Montefusco United States 16 461 0.5× 156 0.2× 47 0.1× 28 0.2× 9 0.1× 20 602
Ben Moree United States 13 1.3k 1.3× 949 1.4× 519 1.5× 107 0.8× 8 0.1× 16 1.5k
Otto Hudecz Austria 16 943 0.9× 407 0.6× 77 0.2× 121 0.9× 2 0.0× 20 1.1k

Countries citing papers authored by David C. Bouck

Since Specialization
Citations

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

Fields of papers citing papers by David C. Bouck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David C. Bouck

This figure shows the co-authorship network connecting the top 25 collaborators of David C. Bouck. A scholar is included among the top collaborators of David C. Bouck 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 C. Bouck. David C. Bouck 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.
Bouck, David C., et al.. (2018). Engineering Novel Lab Devices Using 3D Printing and Microcontrollers. SLAS TECHNOLOGY. 23(5). 448–455. 10 indexed citations
2.
Lightcap, Eric S., et al.. (2015). Acoustic Liquid Handling for Rapid siRNA Transfection Optimization. SLAS DISCOVERY. 20(8). 957–964. 3 indexed citations
3.
Bouck, David C., Khristofer Garcia, Jonathan L. Blank, et al.. (2015). Abstract C55: Nedd8-activating enzyme inhibitor pevonedistat synergizes with cisplatin and carboplatin through interference with nucleotide excision repair and interstrand cross-link repair mechanisms in non-small cell lung cancer. Molecular Cancer Therapeutics. 14(12_Supplement_2). C55–C55. 1 indexed citations
4.
Garcia, Khristofer, Jonathan L. Blank, David C. Bouck, et al.. (2014). Nedd8-Activating Enzyme Inhibitor MLN4924 Provides Synergy with Mitomycin C through Interactions with ATR, BRCA1/BRCA2, and Chromatin Dynamics Pathways. Molecular Cancer Therapeutics. 13(6). 1625–1635. 45 indexed citations
5.
Blank, Jonathan L., Katherine Cosmopoulos, David C. Bouck, et al.. (2012). Novel DNA Damage Checkpoints Mediating Cell Death Induced by the NEDD8-Activating Enzyme Inhibitor MLN4924. Cancer Research. 73(1). 225–234. 85 indexed citations
6.
Bouck, David C., et al.. (2011). A High-Content Screen Identifies Inhibitors of Nuclear Export of Forkhead Transcription Factors. SLAS DISCOVERY. 16(4). 394–404. 12 indexed citations
7.
Sappal, Darshan S., Neil Bence, Paul Fleming, et al.. (2011). Cellular and biochemical characterization of an inhibitor of the Ubiquitin Activating Enzyme (UAE). 2. 1 indexed citations
8.
Liao, Hua, Jonathan L. Blank, David C. Bouck, et al.. (2011). Quantitative Proteomic Analysis of Cellular Protein Modulation upon Inhibition of the NEDD8-Activating Enzyme by MLN4924. Molecular & Cellular Proteomics. 10(11). M111.009183–M111.009183. 58 indexed citations
9.
Young, Brandon, Janice L. Hyatt, David C. Bouck, et al.. (2010). Structure−Activity Relationships of Substituted 1-Pyridyl-2-phenyl-1,2-ethanediones: Potent, Selective Carboxylesterase Inhibitors. Journal of Medicinal Chemistry. 53(24). 8709–8715. 21 indexed citations
10.
Joglekar, Ajit P., David C. Bouck, Xingkun Liu, et al.. (2008). Molecular architecture of the kinetochore-microtubule attachment site is conserved between point and regional centromeres. The Journal of Cell Biology. 181(4). 587–594. 129 indexed citations
11.
Yeh, Elaine, Julian Haase, Leocadia V. Paliulis, et al.. (2008). Pericentric Chromatin Is Organized into an Intramolecular Loop in Mitosis. Current Biology. 18(2). 81–90. 132 indexed citations
12.
Merker, Jason D., Margaret Dominska, Patricia W. Greenwell, et al.. (2008). The histone methylase Set2p and the histone deacetylase Rpd3p repress meiotic recombination at the HIS4 meiotic recombination hotspot in Saccharomyces cerevisiae. DNA repair. 7(8). 1298–1308. 38 indexed citations
13.
Gardner, Melissa K., David C. Bouck, Leocadia V. Paliulis, et al.. (2008). Chromosome Congression by Kinesin-5 Motor-Mediated Disassembly of Longer Kinetochore Microtubules. Cell. 135(5). 894–906. 132 indexed citations
14.
Lin, Wenwei, et al.. (2008). Cyclin-dependent Kinase 2 Negatively Regulates Human Pregnane X Receptor-mediated CYP3A4 Gene Expression in HepG2 Liver Carcinoma Cells. Journal of Biological Chemistry. 283(45). 30650–30657. 92 indexed citations
15.
Bouck, David C., Ajit P. Joglekar, & Kerry Bloom. (2008). Design Features of a Mitotic Spindle: Balancing Tension and Compression at a Single Microtubule Kinetochore Interface in Budding Yeast. Annual Review of Genetics. 42(1). 335–359. 44 indexed citations
16.
Bouck, David C. & Kerry Bloom. (2007). Pericentric Chromatin Is an Elastic Component of the Mitotic Spindle. Current Biology. 17(9). 741–748. 71 indexed citations
17.
Joglekar, Ajit P., David C. Bouck, Jeffrey N. Molk, Kerry Bloom, & Edward D. Salmon. (2006). Molecular architecture of a kinetochore–microtubule attachment site. Nature Cell Biology. 8(6). 581–585. 233 indexed citations
18.
Bouck, David C. & Kerry Bloom. (2005). The role of centromere-binding factor 3 (CBF3) in spindle stability, cytokinesis, and kinetochore attachment. Biochemistry and Cell Biology. 83(6). 696–702. 14 indexed citations
19.
Bouck, David C. & Kerry Bloom. (2005). The kinetochore protein Ndc10p is required for spindle stability and cytokinesis in yeast. Proceedings of the National Academy of Sciences. 102(15). 5408–5413. 45 indexed citations
20.
Rodrigo-Brenni, Monica C., Scott C. Thomas, David C. Bouck, & Kenneth B. Kaplan. (2004). Sgt1p and Skp1p Modulate the Assembly and Turnover of CBF3 Complexes Required for Proper Kinetochore Function. Molecular Biology of the Cell. 15(7). 3366–3378. 39 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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