Andreas Boland

1.6k total citations
23 papers, 1.0k citations indexed

About

Andreas Boland is a scholar working on Molecular Biology, Cell Biology and Structural Biology. According to data from OpenAlex, Andreas Boland has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 10 papers in Cell Biology and 2 papers in Structural Biology. Recurrent topics in Andreas Boland's work include Microtubule and mitosis dynamics (8 papers), RNA and protein synthesis mechanisms (7 papers) and RNA Research and Splicing (7 papers). Andreas Boland is often cited by papers focused on Microtubule and mitosis dynamics (8 papers), RNA and protein synthesis mechanisms (7 papers) and RNA Research and Splicing (7 papers). Andreas Boland collaborates with scholars based in Switzerland, Germany and United Kingdom. Andreas Boland's co-authors include Elisa Izaurralde, Oliver Weichenrieder, Eric Huntzinger, Chung-Te Chang, Ying Chen, Duygu Kuzuoğlu‐Öztürk, Praveen Bawankar, Belinda Loh, David Barford and Steffen Schmidt and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Andreas Boland

22 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andreas Boland Switzerland 13 889 212 126 78 72 23 1.0k
Paolo Swuec Italy 15 759 0.9× 101 0.5× 56 0.4× 48 0.6× 28 0.4× 24 857
Vesna Rapić-Otrin United States 14 1.3k 1.4× 220 1.0× 80 0.6× 77 1.0× 52 0.7× 15 1.4k
Justin L. Sparks United States 11 927 1.0× 70 0.3× 119 0.9× 71 0.9× 80 1.1× 12 1.0k
Go Watanabe United States 15 965 1.1× 109 0.5× 63 0.5× 73 0.9× 71 1.0× 23 1.1k
Else-Britt Lundström Sweden 6 1.3k 1.4× 238 1.1× 77 0.6× 90 1.2× 52 0.7× 8 1.4k
Sylvain Egloff France 19 1.6k 1.8× 135 0.6× 52 0.4× 94 1.2× 120 1.7× 25 1.8k
Vlada Philimonenko Czechia 16 972 1.1× 32 0.2× 350 2.8× 34 0.4× 74 1.0× 24 1.2k
Martin Heidemann Germany 18 2.0k 2.2× 174 0.8× 59 0.5× 117 1.5× 122 1.7× 20 2.2k
Veronika Altmannová Czechia 15 1.0k 1.1× 138 0.7× 107 0.8× 99 1.3× 35 0.5× 23 1.1k

Countries citing papers authored by Andreas Boland

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Boland

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andreas Boland. 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 Andreas Boland. The network helps show where Andreas Boland may publish in the future.

Co-authorship network of co-authors of Andreas Boland

This figure shows the co-authorship network connecting the top 25 collaborators of Andreas Boland. A scholar is included among the top collaborators of Andreas Boland 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 Andreas Boland. Andreas Boland 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.
Ghent, Chloe M., et al.. (2025). Substrate recognition by human separase. Science Advances. 11(46). eady9807–eady9807.
2.
Stengel, Florian, et al.. (2025). Positively charged specificity site in cyclin B1 is essential for mitotic fidelity. Nature Communications. 16(1). 853–853. 2 indexed citations
3.
Schäfer, Michael, et al.. (2025). A phosphate-binding pocket in cyclin B3 is essential for XErp1/Emi2 degradation in meiosis I. EMBO Reports. 26(3). 768–790. 1 indexed citations
4.
Yang, Jing, Ziguo Zhang, Leifu Chang, et al.. (2024). Cryo-EM structures of apo-APC/C and APC/CCDH1:EMI1 complexes provide insights into APC/C regulation. Nature Communications. 15(1). 10074–10074. 2 indexed citations
5.
Yu, Jun, Charlotte Martin, Antoine Koehl, et al.. (2024). Structural basis of μ-opioid receptor targeting by a nanobody antagonist. Nature Communications. 15(1). 8687–8687. 12 indexed citations
6.
Teixeira, Pryscila D. S., Christelle Veyrat‐Durebex, Emmanuel Somm, et al.. (2024). S100A9 exerts insulin-independent antidiabetic and anti-inflammatory effects. Science Advances. 10(1). eadj4686–eadj4686. 7 indexed citations
7.
Morgan, David O., et al.. (2023). The molecular mechanisms of human separase regulation. Biochemical Society Transactions. 51(3). 1225–1233. 11 indexed citations
8.
Cavalli, Andrea, Jacopo Sgrignani, Jonathan P. Sleeman, et al.. (2022). CEMIP (HYBID, KIAA1199): structure, function and expression in health and disease. FEBS Journal. 290(16). 3946–3962. 20 indexed citations
9.
Boland, Andreas, Jean‐François Côté, & David Barford. (2022). Structural biology of DOCK‐family guanine nucleotide exchange factors. FEBS Letters. 597(6). 794–810. 12 indexed citations
10.
Ghent, Chloe M., Tobias Raisch, Yashar Sadian, et al.. (2021). Structural basis of human separase regulation by securin and CDK1–cyclin B1. Nature. 596(7870). 138–142. 59 indexed citations
11.
Berndt, Alex, Jane L. Wagstaff, Madhanagopal Anandapadamanaban, et al.. (2021). Bipartite binding and partial inhibition links DEPTOR and mTOR in a mutually antagonistic embrace. eLife. 10. 9 indexed citations
12.
Chang, Leifu, Jing Yang, Andreas Boland, et al.. (2020). Structure of the DOCK2−ELMO1 complex provides insights into regulation of the auto-inhibited state. Nature Communications. 11(1). 3464–3464. 42 indexed citations
13.
Kiss, L., Jingwei Zeng, Claire F. Dickson, et al.. (2019). A tri-ionic anchor mechanism drives Ube2N-specific recruitment and K63-chain ubiquitination in TRIM ligases. Nature Communications. 10(1). 4502–4502. 35 indexed citations
14.
Boland, Andreas, Thomas G. Martin, Ziguo Zhang, et al.. (2017). Cryo-EM structure of a metazoan separase–securin complex at near-atomic resolution. Nature Structural & Molecular Biology. 24(4). 414–418. 59 indexed citations
15.
Chen, Ying, Andreas Boland, Duygu Kuzuoğlu‐Öztürk, et al.. (2014). A DDX6-CNOT1 Complex and W-Binding Pockets in CNOT9 Reveal Direct Links between miRNA Target Recognition and Silencing. Molecular Cell. 54(5). 737–750. 221 indexed citations
16.
Christie, Mary, Andreas Boland, Eric Huntzinger, Oliver Weichenrieder, & Elisa Izaurralde. (2013). Structure of the PAN3 Pseudokinase Reveals the Basis for Interactions with the PAN2 Deadenylase and the GW182 Proteins. Molecular Cell. 51(3). 360–373. 83 indexed citations
17.
Boland, Andreas, Ying Chen, Tobias Raisch, et al.. (2013). Structure and assembly of the NOT module of the human CCR4–NOT complex. Nature Structural & Molecular Biology. 20(11). 1289–1297. 96 indexed citations
18.
Braun, Joerg E., Vincent Truffault, Andreas Boland, et al.. (2012). A direct interaction between DCP1 and XRN1 couples mRNA decapping to 5′ exonucleolytic degradation. Nature Structural & Molecular Biology. 19(12). 1324–1331. 137 indexed citations
19.
Boland, Andreas, Eric Huntzinger, Steffen Schmidt, Elisa Izaurralde, & Oliver Weichenrieder. (2011). Crystal structure of the MID-PIWI lobe of a eukaryotic Argonaute protein. Proceedings of the National Academy of Sciences. 108(26). 10466–10471. 96 indexed citations
20.
Boland, Andreas, et al.. (2010). Crystal structure and ligand binding of the MID domain of a eukaryotic Argonaute protein. EMBO Reports. 11(7). 522–527. 81 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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