Benedict C. S. Cross

1.5k total citations · 1 hit paper
18 papers, 1.0k citations indexed

About

Benedict C. S. Cross is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Benedict C. S. Cross has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Cell Biology and 2 papers in Genetics. Recurrent topics in Benedict C. S. Cross's work include Endoplasmic Reticulum Stress and Disease (8 papers), RNA regulation and disease (4 papers) and CRISPR and Genetic Engineering (4 papers). Benedict C. S. Cross is often cited by papers focused on Endoplasmic Reticulum Stress and Disease (8 papers), RNA regulation and disease (4 papers) and CRISPR and Genetic Engineering (4 papers). Benedict C. S. Cross collaborates with scholars based in United Kingdom, United States and Netherlands. Benedict C. S. Cross's co-authors include Stephen High, David Ron, Heather P. Harding, Ian R. Baxendale, Peter J. Bond, Babal K. Jha, Thomas A. Neubert, Jonathan M. Goodman, Robert H. Silverman and Paweł Sadowski and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Reviews Molecular Cell Biology and The Journal of Cell Biology.

In The Last Decade

Benedict C. S. Cross

18 papers receiving 1.0k citations

Hit Papers

The molecular basis for s... 2012 2026 2016 2021 2012 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Benedict C. S. Cross United Kingdom 13 636 591 272 143 121 18 1.0k
Robert Gauss Germany 12 790 1.2× 667 1.1× 292 1.1× 63 0.4× 144 1.2× 13 1.1k
Steffen Preißler United Kingdom 18 1.1k 1.8× 648 1.1× 251 0.9× 188 1.3× 179 1.5× 22 1.5k
Claude Nuoffer United States 15 1.4k 2.2× 1.4k 2.5× 190 0.7× 125 0.9× 98 0.8× 19 2.1k
Anton Schmitz Germany 18 697 1.1× 387 0.7× 86 0.3× 61 0.4× 127 1.0× 26 1.1k
Kevin E. Knockenhauer United States 14 998 1.6× 222 0.4× 135 0.5× 94 0.7× 93 0.8× 21 1.3k
Michele Santoro Italy 13 801 1.3× 671 1.1× 123 0.5× 89 0.6× 98 0.8× 18 1.2k
Van Dat Nguyen Finland 7 525 0.8× 394 0.7× 78 0.3× 83 0.6× 106 0.9× 13 829
Stefan Schorr Germany 12 705 1.1× 514 0.9× 90 0.3× 134 0.9× 106 0.9× 16 945
Laurel Mydock‐McGrane United States 14 815 1.3× 147 0.2× 234 0.9× 124 0.9× 98 0.8× 16 1.3k
Geoffrey T. Smith United States 14 860 1.4× 306 0.5× 230 0.8× 76 0.5× 49 0.4× 20 1.2k

Countries citing papers authored by Benedict C. S. Cross

Since Specialization
Citations

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

Fields of papers citing papers by Benedict C. S. Cross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Benedict C. S. Cross. 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 Benedict C. S. Cross. The network helps show where Benedict C. S. Cross may publish in the future.

Co-authorship network of co-authors of Benedict C. S. Cross

This figure shows the co-authorship network connecting the top 25 collaborators of Benedict C. S. Cross. A scholar is included among the top collaborators of Benedict C. S. Cross 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 Benedict C. S. Cross. Benedict C. S. Cross is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Bellail, Anita C., Dae-Ho Kim, Carlos le Sage, et al.. (2021). Ubiquitination and degradation of SUMO1 by small-molecule degraders extends survival of mice with patient-derived tumors. Science Translational Medicine. 13(615). eabh1486–eabh1486. 18 indexed citations
2.
Martin, Glynn, Carlos le Sage, Steffen Lawo, et al.. (2020). A Flexible, Pooled CRISPR Library for Drug Development Screens. The CRISPR Journal. 3(3). 211–222. 6 indexed citations
3.
Sage, Carlos le, Steffen Lawo, & Benedict C. S. Cross. (2019). CRISPR: A Screener’s Guide. SLAS DISCOVERY. 25(3). 233–240. 13 indexed citations
4.
Sage, Carlos le, Steffen Lawo, Syed Asad Rahman, et al.. (2017). Dual direction CRISPR transcriptional regulation screening uncovers gene networks driving drug resistance. Scientific Reports. 7(1). 17693–17693. 34 indexed citations
5.
Cross, Benedict C. S., Steffen Lawo, C Archer, et al.. (2016). Increasing the performance of pooled CRISPR–Cas9 drop-out screening. Scientific Reports. 6(1). 31782–31782. 24 indexed citations
6.
Harding, Heather P., et al.. (2013). Selective inhibition of the unfolded protein response: targeting catalytic sites for Schiff base modification. Molecular BioSystems. 9(10). 2408–2416. 24 indexed citations
7.
Avezov, Edward, Benedict C. S. Cross, Gabriele S. Kaminski Schierle, et al.. (2013). Lifetime imaging of a fluorescent protein sensor reveals surprising stability of ER thiol redox. The Journal of Cell Biology. 201(2). 337–349. 86 indexed citations
8.
Cross, Benedict C. S., Peter J. Bond, Paweł Sadowski, et al.. (2012). The molecular basis for selective inhibition of unconventional mRNA splicing by an IRE1-binding small molecule. 9 indexed citations
9.
Ron, David, et al.. (2012). Establishing a Flow Process to Coumarin‐8‐Carbaldehydes as Important Synthetic Scaffolds. Chemistry - A European Journal. 18(32). 9901–9910. 39 indexed citations
10.
Cross, Benedict C. S. & David Ron. (2012). New twists in the unfolded protein response. eLife. 1. e00243–e00243. 3 indexed citations
11.
Öjemalm, Karin, Helen Watson, Peristera Roboti, et al.. (2012). Positional editing of transmembrane domains during ion channel assembly. Journal of Cell Science. 126(2). 464–472. 9 indexed citations
12.
Cross, Benedict C. S., Peter J. Bond, Paweł Sadowski, et al.. (2012). The molecular basis for selective inhibition of unconventional mRNA splicing by an IRE1-binding small molecule. Proceedings of the National Academy of Sciences. 109(15). E869–78. 452 indexed citations breakdown →
13.
Cross, Benedict C. S., Craig McKibbin, Anna C. Callan, et al.. (2009). Eeyarestatin I inhibits Sec61-mediated protein translocation at the endoplasmic reticulum. Journal of Cell Science. 122(23). 4393–4400. 87 indexed citations
14.
Cross, Benedict C. S., et al.. (2009). Endoplasmic reticulum-associated degradation of a degron-containing polytopic membrane protein. Molecular Membrane Biology. 26(8). 448–464. 11 indexed citations
15.
Cross, Benedict C. S., Irmgard Sinning, Joen Luirink, & Stephen High. (2009). Delivering proteins for export from the cytosol. Nature Reviews Molecular Cell Biology. 10(4). 255–264. 159 indexed citations
16.
Cross, Benedict C. S. & Stephen High. (2009). Dissecting the physiological role of selective transmembrane-segment retention at the ER translocon. Journal of Cell Science. 122(11). 1768–1777. 25 indexed citations
17.
Ismail, Nurzian, Samuel G. Crawshaw, Benedict C. S. Cross, Anna C. Haagsma, & Stephen High. (2008). Specific transmembrane segments are selectively delayed at the ER translocon during opsin biogenesis. Biochemical Journal. 411(3). 495–506. 34 indexed citations
18.
Crawshaw, Samuel G., Benedict C. S. Cross, Cornelia M. Wilson, & Stephen High. (2007). The oligomeric state of Derlin-1 is modulated by endoplasmic reticulum stress. Molecular Membrane Biology. 24(2). 113–120. 12 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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