Ben E. Black

11.0k total citations · 2 hit papers
100 papers, 8.3k citations indexed

About

Ben E. Black is a scholar working on Molecular Biology, Plant Science and Cell Biology. According to data from OpenAlex, Ben E. Black has authored 100 papers receiving a total of 8.3k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Molecular Biology, 56 papers in Plant Science and 27 papers in Cell Biology. Recurrent topics in Ben E. Black's work include Chromosomal and Genetic Variations (56 papers), Genomics and Chromatin Dynamics (51 papers) and Microtubule and mitosis dynamics (26 papers). Ben E. Black is often cited by papers focused on Chromosomal and Genetic Variations (56 papers), Genomics and Chromatin Dynamics (51 papers) and Microtubule and mitosis dynamics (26 papers). Ben E. Black collaborates with scholars based in United States, France and Canada. Ben E. Black's co-authors include Don W. Cleveland, Daniel R. Foltz, Lars E.T. Jansen, Bryce M. Paschal, Emily Bassett, Aaron O. Bailey, Nikolina Sekulić, John R. Yates, Tanya Panchenko and James M. Holaska and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Ben E. Black

97 papers receiving 8.2k citations

Hit Papers

The human CENP-A centromeric nucleosome-associated complex 2006 2026 2012 2019 2006 2009 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ben E. Black United States 52 7.0k 3.8k 2.3k 1.0k 929 100 8.3k
Tarun M. Kapoor United States 59 9.0k 1.3× 1.3k 0.3× 7.8k 3.4× 625 0.6× 1.2k 1.3× 136 12.1k
Anna Shevchenko Germany 45 8.3k 1.2× 934 0.2× 2.7k 1.2× 775 0.8× 1.1k 1.2× 63 10.0k
Klaus Scheffzek Germany 43 5.2k 0.7× 582 0.2× 1.5k 0.6× 528 0.5× 991 1.1× 78 7.1k
Brian Schaffhausen United States 43 5.3k 0.8× 871 0.2× 1.0k 0.4× 1.5k 1.5× 3.1k 3.4× 107 7.9k
Ronald Berezney United States 49 6.9k 1.0× 662 0.2× 980 0.4× 996 1.0× 590 0.6× 120 8.0k
Stéfan Dimitrov France 47 6.2k 0.9× 1.0k 0.3× 703 0.3× 727 0.7× 566 0.6× 139 7.0k
Stephen P. Bell United States 56 14.3k 2.0× 1.4k 0.4× 2.2k 0.9× 2.8k 2.8× 1.4k 1.5× 110 16.0k
Michiel Vermeulen Netherlands 53 10.5k 1.5× 583 0.2× 916 0.4× 1.3k 1.3× 1.1k 1.2× 182 12.2k
Daniel E. Gottschling United States 48 11.1k 1.6× 1.9k 0.5× 719 0.3× 943 0.9× 375 0.4× 74 12.6k
Hongtao Yu United States 74 14.6k 2.1× 2.1k 0.5× 7.5k 3.3× 1.0k 1.0× 2.4k 2.6× 172 17.0k

Countries citing papers authored by Ben E. Black

Since Specialization
Citations

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

Fields of papers citing papers by Ben E. Black

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ben E. Black. 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 Ben E. Black. The network helps show where Ben E. Black may publish in the future.

Co-authorship network of co-authors of Ben E. Black

This figure shows the co-authorship network connecting the top 25 collaborators of Ben E. Black. A scholar is included among the top collaborators of Ben E. Black 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 Ben E. Black. Ben E. Black 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.
Billur, Ramya, et al.. (2025). A PARP2 active site helix melts to permit DNA damage-induced enzymatic activation. Molecular Cell. 85(5). 865–876.e4. 3 indexed citations
2.
Chang, Yi‐Wei, et al.. (2025). Centromeric chromatin clearings demarcate the site of kinetochore formation. Cell. 188(5). 1280–1296.e19. 5 indexed citations
3.
Dawicki-McKenna, Jennine M., et al.. (2025). Satellite DNA shapes dictate pericentromere packaging in female meiosis. Nature. 638(8051). 814–822. 8 indexed citations
4.
Manske, Gabriel, Rajesh Ranjan, Lindsay Moritz, et al.. (2025). Maternal CENP-C restores centromere symmetry in mammalian zygotes to ensure proper chromosome segregation. Developmental Cell. 61(1). 146–163.e10. 1 indexed citations
5.
Gibson, Daniel G., et al.. (2025). Rapid assembly of functional modules for generating human artificial chromosome constructs compatible with epigenetic centromere seeding. Chromosome Research. 33(1). 29–29. 1 indexed citations
6.
Creekmore, Benjamin C., et al.. (2024). Ultrastructure of human brain tissue vitrified from autopsy revealed by cryo-ET with cryo-plasma FIB milling. Nature Communications. 15(1). 2660–2660. 12 indexed citations
7.
Velagapudi, Uday Kiran, et al.. (2024). Novel modifications of PARP inhibitor veliparib increase PARP1 binding to DNA breaks. Biochemical Journal. 481(6). 437–460. 3 indexed citations
8.
Gambogi, Craig W., Jennine M. Dawicki-McKenna, Mikhail Liskovykh, et al.. (2023). Centromere innovations within a mouse species. Science Advances. 9(46). eadi5764–eadi5764. 3 indexed citations
9.
Dawicki-McKenna, Jennine M., et al.. (2023). The structural basis of the multi-step allosteric activation of Aurora B kinase. eLife. 12. 6 indexed citations
10.
Iwata‐Otsubo, Aiko, et al.. (2022). Epigenetic, genetic and maternal effects enable stable centromere inheritance. Nature Cell Biology. 24(5). 748–756. 13 indexed citations
11.
Langelier, Marie-France, Ramya Billur, Aleksandr Sverzhinsky, Ben E. Black, & John M. Pascal. (2021). HPF1 dynamically controls the PARP1/2 balance between initiating and elongating ADP-ribose modifications. Nature Communications. 12(1). 6675–6675. 54 indexed citations
12.
Allu, Praveen Kumar, Glennis A. Logsdon, Jennine M. Dawicki-McKenna, et al.. (2021). Gene replacement strategies validate the use of functional tags on centromeric chromatin and invalidate an essential role for CENP-AK124ub. Cell Reports. 37(5). 109924–109924. 3 indexed citations
13.
Zandarashvili, Levani, Marie-France Langelier, Uday Kiran Velagapudi, et al.. (2020). Structural basis for allosteric PARP-1 retention on DNA breaks. Science. 368(6486). 233 indexed citations
14.
Karch, Kelly R., Mariel Coradin, Levani Zandarashvili, et al.. (2018). Hydrogen-Deuterium Exchange Coupled to Top- and Middle-Down Mass Spectrometry Reveals Histone Tail Dynamics before and after Nucleosome Assembly. Structure. 26(12). 1651–1663.e3. 34 indexed citations
15.
Sekulić, Nikolina & Ben E. Black. (2016). Preparation of Recombinant Centromeric Nucleosomes and Formation of Complexes with Nonhistone Centromere Proteins. Methods in enzymology on CD-ROM/Methods in enzymology. 573. 67–96. 9 indexed citations
16.
Bailey, Aaron O., Tanya Panchenko, Jeffrey Shabanowitz, et al.. (2015). Identification of the Post-translational Modifications Present in Centromeric Chromatin. Molecular & Cellular Proteomics. 15(3). 918–931. 42 indexed citations
17.
Keramisanou, Dimitra, et al.. (2014). CENP-A Arrays Are More Condensed than Canonical Arrays at Low Ionic Strength. Biophysical Journal. 106(4). 875–882. 13 indexed citations
18.
Panchenko, Tanya, Troy C. Sorensen, Christopher L. Woodcock, et al.. (2011). Replacement of histone H3 with CENP-A directs global nucleosome array condensation and loosening of nucleosome superhelical termini. Proceedings of the National Academy of Sciences. 108(40). 16588–16593. 83 indexed citations
19.
Kuich, P. Henning J. L., et al.. (2011). HJURP is a CENP-A chromatin assembly factor sufficient to form a functional de novo kinetochore. The Journal of Cell Biology. 194(2). 229–243. 258 indexed citations
20.
Foltz, Daniel R., Lars E.T. Jansen, Ben E. Black, et al.. (2006). The human CENP-A centromeric nucleosome-associated complex. Nature Cell Biology. 8(5). 458–469. 566 indexed citations breakdown →

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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