Verena Passerini

1.3k total citations
13 papers, 674 citations indexed

About

Verena Passerini is a scholar working on Molecular Biology, Cell Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Verena Passerini has authored 13 papers receiving a total of 674 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cell Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Verena Passerini's work include Microtubule and mitosis dynamics (5 papers), Lymphoma Diagnosis and Treatment (4 papers) and DNA Repair Mechanisms (3 papers). Verena Passerini is often cited by papers focused on Microtubule and mitosis dynamics (5 papers), Lymphoma Diagnosis and Treatment (4 papers) and DNA Repair Mechanisms (3 papers). Verena Passerini collaborates with scholars based in Germany, United Kingdom and United States. Verena Passerini's co-authors include Zuzana Štorchová, Neysan Donnelly, Milena Dürrbaum, Mirjam S. de Pagter, Wigard P. Kloosterman, Batsheva Kerem, E. Ozeri-Galai, Jason M. Sheltzer, Nicole M. Sayles and Julie H. Ko and has published in prestigious journals such as Nature Communications, The EMBO Journal and Blood.

In The Last Decade

Verena Passerini

12 papers receiving 668 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Verena Passerini Germany	8	394	273	214	159	139	13	674
Mirjam S. de Pagter Netherlands	6	331 0.8×	172 0.6×	187 0.9×	126 0.8×	153 1.1×	7	557
Ofer Shoshani United States	11	679 1.7×	230 0.8×	318 1.5×	115 0.7×	160 1.2×	16	895
Ángel Martínez‐Ramírez Spain	17	564 1.4×	90 0.3×	153 0.7×	122 0.8×	159 1.1×	26	843
Henri J. van de Vrugt Netherlands	12	819 2.1×	107 0.4×	247 1.2×	110 0.7×	197 1.4×	18	888
Brian Freie United States	15	588 1.5×	80 0.3×	155 0.7×	140 0.9×	111 0.8×	23	782
Joel E. Straughen United States	6	1.2k 3.0×	88 0.3×	322 1.5×	215 1.4×	238 1.7×	9	1.4k
Deborah M. Ketterer United States	6	294 0.7×	90 0.3×	120 0.6×	111 0.7×	242 1.7×	6	585
Namrata S. Chandhok United States	8	519 1.3×	461 1.7×	81 0.4×	173 1.1×	62 0.4×	29	718
Petra van der Lelij Austria	13	969 2.5×	97 0.4×	86 0.4×	77 0.5×	122 0.9×	13	1.1k
Sarah Sabir United Kingdom	6	354 0.9×	174 0.6×	76 0.4×	163 1.0×	61 0.4×	6	540

Countries citing papers authored by Verena Passerini

Since Specialization

Citations

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

Fields of papers citing papers by Verena Passerini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verena Passerini

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

All Works

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13 of 13 papers shown

Barbon, Silvia, Verena Passerini, Sergio Angeli, et al.. (2024). Innate immune response in COVID-19: single-cell multi-omics profile of NK lymphocytes in a clinical case series. Cell Communication and Signaling. 22(1). 496–496. 2 indexed citations

Passerini, Verena, Vindi Jurinović, Christopher R. Bolen, et al.. (2021). An EZH2 Gene Expression Signature Is Predictive of Differential Efficacy of Chemotherapy Irrespective of EZH2 Mutation Status in Patients with Follicular Lymphoma Treated within the Gallium Trial. Blood. 138(Supplement 1). 39–39. 2 indexed citations

Bararia, Deepak, Michael Heide, Verena Passerini, et al.. (2021). ARID1A Controls a Novel Transcriptional Network Regulating FAS in Follicular Lymphoma. Blood. 138(Supplement 1). 3492–3492.

Passerini, Verena, Vindi Jurinović, Axel Lechner, et al.. (2021). CHOP but Not Bendamustine Reverses EZH2 Y641 Mutation Induced MHC-I/II Loss in Human Lymphoma Models. Blood. 138(Supplement 1). 2391–2391. 4 indexed citations

Jurinović, Vindi, Verena Passerini, Mikkel Z. Oestergaard, et al.. (2019). Evaluation of the m7-FLIPI in Patients with Follicular Lymphoma Treated within the Gallium Trial: EZH2 mutation Status May be a Predictive Marker for Differential Efficacy of Chemotherapy. Blood. 134(Supplement_1). 122–122. 36 indexed citations

Keuper, Kristina, Mirjam S. de Pagter, Markus J. van Roosmalen, et al.. (2019). Micronuclei-based model system reveals functional consequences of chromothripsis in human cells. eLife. 8. 69 indexed citations

Qu, Xiaoyu, Hongli Li, Rita M. Braziel, et al.. (2018). Genomic alterations important for the prognosis in patients with follicular lymphoma treated in SWOG study S0016. Blood. 133(1). 81–93. 39 indexed citations

Passerini, Verena, Michael Boesl, Michael Heide, et al.. (2018). PARP14 Is a Novel Therapeutic Target in STAT6 mutant Follicular Lymphoma. Blood. 132(Supplement 1). 2842–2842. 1 indexed citations

Sheltzer, Jason M., Julie H. Ko, Nicole M. Sayles, et al.. (2017). Single-chromosome Gains Commonly Function as Tumor Suppressors. Cancer Cell. 31(2). 240–255. 138 indexed citations

10.

Passerini, Verena, E. Ozeri-Galai, Mirjam S. de Pagter, et al.. (2016). The presence of extra chromosomes leads to genomic instability. Nature Communications. 7(1). 10754–10754. 205 indexed citations

11.

Passerini, Verena & Zuzana Štorchová. (2016). Too much to handle — how gaining chromosomes destabilizes the genome. Cell Cycle. 15(21). 2867–2874. 7 indexed citations

12.

Dürrbaum, Milena, et al.. (2014). Unique features of the transcriptional response to model aneuploidy in human cells. BMC Genomics. 15(1). 139–139. 75 indexed citations

13.

Donnelly, Neysan, et al.. (2014). HSF 1 deficiency and impaired HSP 90‐dependent protein folding are hallmarks of aneuploid human cells. The EMBO Journal. 33(20). 2374–2387. 96 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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