Oliver Bischof

7.0k total citations
32 papers, 2.4k citations indexed

About

Oliver Bischof is a scholar working on Molecular Biology, Physiology and Oncology. According to data from OpenAlex, Oliver Bischof has authored 32 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 11 papers in Physiology and 7 papers in Oncology. Recurrent topics in Oliver Bischof's work include Telomeres, Telomerase, and Senescence (11 papers), Advanced biosensing and bioanalysis techniques (5 papers) and Cancer-related Molecular Pathways (5 papers). Oliver Bischof is often cited by papers focused on Telomeres, Telomerase, and Senescence (11 papers), Advanced biosensing and bioanalysis techniques (5 papers) and Cancer-related Molecular Pathways (5 papers). Oliver Bischof collaborates with scholars based in France, United States and Germany. Oliver Bischof's co-authors include Anne Dejean, Judith Campisi, Utz Herbig, Moussa Benhamed, Ricardo Iván Martínez‐Zamudio, Pavan Kumar P, M. Haddad, Weidong Xu, Estela E. Medrano and Karen H. Vousden and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Oliver Bischof

30 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oliver Bischof France 20 1.9k 519 475 375 298 32 2.4k
Fernando G. Osorio Spain 26 2.1k 1.1× 329 0.6× 378 0.8× 324 0.9× 286 1.0× 32 2.8k
Jamila Laoukili Netherlands 20 1.7k 0.9× 548 1.1× 315 0.7× 256 0.7× 293 1.0× 30 2.5k
Yoko Itahana United States 24 2.0k 1.1× 896 1.7× 516 1.1× 321 0.9× 160 0.5× 40 2.6k
Pierre H. Vachon Canada 31 1.7k 0.9× 676 1.3× 318 0.7× 148 0.4× 307 1.0× 46 2.8k
Yoshikazu Johmura Japan 20 1.3k 0.7× 310 0.6× 180 0.4× 397 1.1× 236 0.8× 47 1.9k
Greg Hannon United States 14 1.9k 1.0× 1.1k 2.1× 515 1.1× 500 1.3× 239 0.8× 21 2.6k
Laura Lintault United States 7 2.3k 1.2× 877 1.7× 1.4k 2.9× 267 0.7× 347 1.2× 8 3.1k
Matthieu Lacroix France 18 1.1k 0.6× 516 1.0× 302 0.6× 142 0.4× 261 0.9× 28 2.0k
Jason Howitt Australia 23 1.7k 0.9× 201 0.4× 541 1.1× 97 0.3× 208 0.7× 34 2.2k

Countries citing papers authored by Oliver Bischof

Since Specialization
Citations

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

Fields of papers citing papers by Oliver Bischof

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oliver Bischof

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver Bischof. A scholar is included among the top collaborators of Oliver Bischof 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 Oliver Bischof. Oliver Bischof 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.
Nemazanyy, Ivan, Susanne Brodesser, Gregory J. Dore, et al.. (2024). A homoeostatic switch causing glycerol-3-phosphate and phosphoethanolamine accumulation triggers senescence by rewiring lipid metabolism. Nature Metabolism. 6(2). 323–342. 34 indexed citations
2.
Martínez‐Zamudio, Ricardo Iván, Themistoklis Vasilopoulos, Mark Simpson, et al.. (2023). Escape from oncogene-induced senescence is controlled by POU2F2 and memorized by chromatin scars. Cell Genomics. 3(4). 100293–100293. 22 indexed citations
3.
Martínez‐Zamudio, Ricardo Iván, Pierre‐François Roux, Lucas Robinson, et al.. (2020). Author Correction: AP-1 imprints a reversible transcriptional programme of senescent cells. Nature Cell Biology. 22(10). 1286–1288. 1 indexed citations
4.
Martínez‐Zamudio, Ricardo Iván, Pierre‐François Roux, Lucas Robinson, et al.. (2020). AP-1 imprints a reversible transcriptional programme of senescent cells. Nature Cell Biology. 22(7). 842–855. 123 indexed citations
5.
Müller‐Deubert, Sigrid, Melanie Krug, Jutta Meißner-Weigl, et al.. (2020). Phosphodiesterase 10A Is a Mediator of Osteogenic Differentiation and Mechanotransduction in Bone Marrow-Derived Mesenchymal Stromal Cells. Stem Cells International. 2020. 1–11. 4 indexed citations
6.
Chen, Yan, Heidi Braumüller, Ellen Brenner, et al.. (2018). Nuclear Translocation of Argonaute 2 in Cytokine-Induced Senescence. Cellular Physiology and Biochemistry. 51(3). 1103–1118. 12 indexed citations
7.
Fernández‐Rebollo, Eduardo, Birgit Mentrup, Regina Ebert, et al.. (2017). Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells. Scientific Reports. 7(1). 5132–5132. 65 indexed citations
8.
Martínez‐Zamudio, Ricardo Iván, Lucas Robinson, Pierre‐François Roux, & Oliver Bischof. (2017). SnapShot: Cellular Senescence Pathways. Cell. 170(4). 816–816.e1. 101 indexed citations
9.
Cui, Hengxiang, Michela Esposito, Elena Mylonas, et al.. (2017). Senescence is a Spi1-induced anti-proliferative mechanism in primary hematopoietic cells. Haematologica. 102(11). 1850–1860. 19 indexed citations
10.
Martínez‐Zamudio, Ricardo Iván, Lucas Robinson, Pierre‐François Roux, & Oliver Bischof. (2017). SnapShot: Cellular Senescence in Pathophysiology. Cell. 170(5). 1044–1044.e1. 15 indexed citations
11.
P, Pavan Kumar, Pascal Pineau, Agnès Marchio, et al.. (2014). Long noncoding RNA PANDA and scaffold-attachment-factor SAFA control senescence entry and exit. Nature Communications. 5(1). 5323–5323. 159 indexed citations
12.
Neyret‐Kahn, Hélène, Moussa Benhamed, Tao Ye, et al.. (2013). Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation. Genome Research. 23(10). 1563–1579. 105 indexed citations
13.
Martin, Nadine, Moussa Benhamed, Karim Nacerddine, et al.. (2011). Physical and functional interaction between PML and TBX2 in the establishment of cellular senescence. The EMBO Journal. 31(1). 95–109. 33 indexed citations
14.
Martin, Nadine, Klaus Schwamborn, Valérie Schreiber, et al.. (2009). PARP‐1 transcriptional activity is regulated by sumoylation upon heat shock. The EMBO Journal. 28(22). 3534–3548. 98 indexed citations
15.
Bischof, Oliver, Anne Dejean, & Pascal Pineau. (2009). Une re-vue de la sénescence cellulaire. médecine/sciences. 25(2). 153–160. 13 indexed citations
16.
Seeler, Jacob-S., Oliver Bischof, Karim Nacerddine, & Anne Dejean. (2007). SUMO, the Three Rs and Cancer. Current topics in microbiology and immunology. 313. 49–71. 62 indexed citations
17.
Bischof, Oliver, et al.. (2007). C-terminal modifications regulate MDM2 dissociation and nuclear export of p53. Nature Cell Biology. 9(4). 428–435. 189 indexed citations
18.
Bischof, Oliver & Anne Dejean. (2007). SUMO is Growing Senescent. Cell Cycle. 6(6). 677–681. 31 indexed citations
19.
Bischof, Oliver. (2002). Deconstructing PML-induced premature senescence. The EMBO Journal. 21(13). 3358–3369. 182 indexed citations
20.
Xu, Weidong, Limin Gong, M. Haddad, et al.. (2000). Regulation of Microphthalmia-Associated Transcription Factor MITF Protein Levels by Association with the Ubiquitin-Conjugating Enzyme hUBC9. Experimental Cell Research. 255(2). 135–143. 209 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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