Fanni Gergely

5.2k total citations
48 papers, 3.8k citations indexed

About

Fanni Gergely is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Fanni Gergely has authored 48 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 35 papers in Cell Biology and 11 papers in Genetics. Recurrent topics in Fanni Gergely's work include Microtubule and mitosis dynamics (33 papers), Epigenetics and DNA Methylation (10 papers) and DNA Repair Mechanisms (8 papers). Fanni Gergely is often cited by papers focused on Microtubule and mitosis dynamics (33 papers), Epigenetics and DNA Methylation (10 papers) and DNA Repair Mechanisms (8 papers). Fanni Gergely collaborates with scholars based in United Kingdom, United States and Ireland. Fanni Gergely's co-authors include Alexis R. Barr, Jordan W. Raff, John V. Kilmartin, Viji M. Draviam, C. Geoffrey Woods, Pavithra L. Chavali, Michael J. Lee, Sew‐Yeu Peak‐Chew, Ivan H. Still and Christina Karlsson and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Fanni Gergely

48 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fanni Gergely United Kingdom 30 3.0k 2.3k 765 487 345 48 3.8k
Susana A. Godinho United Kingdom 15 2.6k 0.8× 2.3k 1.0× 589 0.8× 832 1.7× 346 1.0× 27 3.5k
Anna Philpott United Kingdom 37 3.6k 1.2× 862 0.4× 638 0.8× 864 1.8× 196 0.6× 97 4.4k
Jadranka Lončarek United States 31 2.4k 0.8× 2.4k 1.0× 677 0.9× 264 0.5× 422 1.2× 58 3.2k
Jan‐Michael Peters Austria 20 4.5k 1.5× 2.5k 1.1× 414 0.5× 628 1.3× 985 2.9× 22 5.1k
Yuki Katou Japan 42 5.7k 1.9× 1.4k 0.6× 668 0.9× 389 0.8× 1.1k 3.1× 62 6.1k
Andrew J. Holland United States 38 4.4k 1.5× 3.7k 1.6× 1.1k 1.4× 978 2.0× 950 2.8× 67 5.6k
Renata Basto France 24 2.4k 0.8× 2.5k 1.1× 713 0.9× 317 0.7× 521 1.5× 44 3.0k
Paola Vagnarelli United Kingdom 29 3.7k 1.2× 2.0k 0.9× 356 0.5× 574 1.2× 1.1k 3.3× 63 4.1k
Kei‐ichiro Ishiguro Japan 22 2.8k 0.9× 1.1k 0.5× 412 0.5× 252 0.5× 629 1.8× 62 3.2k
Anna Elisabetta Salcini Italy 28 3.8k 1.2× 1.4k 0.6× 462 0.6× 459 0.9× 109 0.3× 46 4.6k

Countries citing papers authored by Fanni Gergely

Since Specialization
Citations

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

Fields of papers citing papers by Fanni Gergely

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fanni Gergely

This figure shows the co-authorship network connecting the top 25 collaborators of Fanni Gergely. A scholar is included among the top collaborators of Fanni Gergely 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 Fanni Gergely. Fanni Gergely 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.
Holder, James, Jennifer A. Miles, Matthew Batchelor, et al.. (2024). CEP192 localises mitotic Aurora-A activity by priming its interaction with TPX2. The EMBO Journal. 43(22). 5381–5420. 5 indexed citations
2.
Gogola, Ewa, James A. West, Rachel Seear, et al.. (2023). A histone deacetylase 3 and mitochondrial complex I axis regulates toxic formaldehyde production. Science Advances. 9(20). eadg2235–eadg2235. 8 indexed citations
3.
Carden, Sarah, et al.. (2020). Accessorizing the centrosome: new insights into centriolar appendages and satellites. Current Opinion in Structural Biology. 66. 148–155. 21 indexed citations
4.
Stojic, Lovorka, Aaron T. L. Lun, Patrice Mascalchi, et al.. (2020). A high-content RNAi screen reveals multiple roles for long noncoding RNAs in cell division. Nature Communications. 11(1). 1851–1851. 46 indexed citations
5.
Quarantotti, Valentina, Jia‐Xuan Chen, Clive S. D’Santos, et al.. (2019). Centriolar satellites are acentriolar assemblies of centrosomal proteins. The EMBO Journal. 38(14). e101082–e101082. 55 indexed citations
6.
Burgess, Selena G., Sarah Sabir, Nimesh Joseph, et al.. (2018). Mitotic spindle association of TACC3 requires Aurora‐A‐dependent stabilization of a cryptic α‐helix. The EMBO Journal. 37(8). 43 indexed citations
7.
Chavali, Pavithra L., Lovorka Stojic, Luke W. Meredith, et al.. (2017). Neurodevelopmental protein Musashi-1 interacts with the Zika genome and promotes viral replication. Science. 357(6346). 83–88. 117 indexed citations
8.
Chavali, Pavithra L., G. Chandrasekaran, Alexis R. Barr, et al.. (2016). A CEP215–HSET complex links centrosomes with spindle poles and drives centrosome clustering in cancer. Nature Communications. 7(1). 11005–11005. 63 indexed citations
9.
Chandrasekaran, G., Péter Tátrai, & Fanni Gergely. (2015). Hitting the brakes: targeting microtubule motors in cancer. British Journal of Cancer. 113(5). 693–698. 69 indexed citations
10.
Lalor, Pierce, et al.. (2013). Abnormal centrosomal structure and duplication in Cep135-deficient vertebrate cells. Molecular Biology of the Cell. 24(17). 2645–2654. 23 indexed citations
11.
Richards, Frances M., Andreas Bender, Peter J. Bond, et al.. (2013). Design, Synthesis, and Biological Evaluation of an Allosteric Inhibitor of HSET that Targets Cancer Cells with Supernumerary Centrosomes. Chemistry & Biology. 20(11). 1399–1410. 92 indexed citations
12.
Jacoby, Monique, James J. Cox, Stéphanie Gayral, et al.. (2009). INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse. Nature Genetics. 41(9). 1027–1031. 277 indexed citations
13.
Gergely, Fanni, et al.. (2009). Centrosome function in cancer: guilty or innocent?. Trends in Cell Biology. 19(7). 334–346. 123 indexed citations
14.
Weyden, Louise van der, Mark J. Arends, Oliver M. Dovey, et al.. (2008). Loss of Rassf1a cooperates with ApcMin to accelerate intestinal tumourigenesis. Oncogene. 27(32). 4503–4508. 28 indexed citations
15.
Gergely, Fanni, et al.. (2004). Targeting of Inositol 1,4,5-Trisphosphate Receptors to the Endoplasmic Reticulum by Multiple Signals within Their Transmembrane Domains. Journal of Biological Chemistry. 279(22). 23797–23805. 37 indexed citations
16.
Vandenberg, Cassandra J., Fanni Gergely, Paul Pace, et al.. (2003). BRCA1-Independent Ubiquitination of FANCD2. Molecular Cell. 12(1). 247–254. 107 indexed citations
17.
Gergely, Fanni, Viji M. Draviam, & Jordan W. Raff. (2003). The ch-TOG/XMAP215 protein is essential for spindle pole organization in human somatic cells. Genes & Development. 17(3). 336–341. 229 indexed citations
18.
Gergely, Fanni. (2002). Centrosomal TACCtics. BioEssays. 24(10). 915–925. 67 indexed citations
19.
Lee, Michael J., et al.. (2001). Msps/XMAP215 interacts with the centrosomal protein D-TACC to regulate microtubule behaviour. Nature Cell Biology. 3(7). 643–649. 222 indexed citations
20.
Micklem, David, Ramanuj DasGupta, Fanni Gergely, et al.. (1997). The mago nashi gene is required for the polarisation of the oocyte and the formation of perpendicular axes in Drosophila. Current Biology. 7(7). 468–478. 174 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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