Bernd Boidol

575 total citations
8 papers, 318 citations indexed

About

Bernd Boidol is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Bernd Boidol has authored 8 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Oncology and 1 paper in Genetics. Recurrent topics in Bernd Boidol's work include RNA modifications and cancer (2 papers), DNA Repair Mechanisms (2 papers) and Genomics and Chromatin Dynamics (2 papers). Bernd Boidol is often cited by papers focused on RNA modifications and cancer (2 papers), DNA Repair Mechanisms (2 papers) and Genomics and Chromatin Dynamics (2 papers). Bernd Boidol collaborates with scholars based in Austria, United States and Germany. Bernd Boidol's co-authors include Stefan Kubicek, Christoph Bock, Thomas Penz, Björn Nilsson, Scott A. Armstrong, David M. Weinstock, Benjamin L. Ebert, Marie McConkey, Steven R. Ellis and Magnus Jöud and has published in prestigious journals such as Nature Genetics, Oncogene and Oncotarget.

In The Last Decade

Bernd Boidol

8 papers receiving 314 citations

Peers

Bernd Boidol

MB

ONCOL

CR

PFM

IMMUN

Eric Kusnadi Australia

Julie Cahu France

Emil Aagaard Thomsen Denmark

Binny Bhandary United States

Irina Kholodnyuk Sweden

Paul van den Berk Netherlands

Benjamin T. Brett United States

Christophe Alberti France

Claudia A. Mimoso United States

Landon Wark Canada

Eric Kusnadi Australia

Bernd Boidol

284 ×1.0

MB

77 ×1.4

ONCOL

51 ×1.0

CR

20 ×0.5

PFM

21 ×0.7

IMMUN

Citations per year, relative to Bernd Boidol Bernd Boidol (= 1×) peers Eric Kusnadi

Countries citing papers authored by Bernd Boidol

Since Specialization

Citations

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

Fields of papers citing papers by Bernd Boidol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Boidol

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

All Works

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8 of 8 papers shown

1.

Schick, Sandra, André F. Rendeiro, Anna Ringler, et al.. (2019). Systematic characterization of BAF mutations provides insights into intracomplex synthetic lethalities in human cancers. Nature Genetics. 51(9). 1399–1410. 91 indexed citations

2.

Kornauth, Christoph, Charles Herbaux, Bernd Boidol, et al.. (2019). THE COMBINATION OF VENETOCLAX AND IBRUTINIB IS EFFECTIVE IN RELAPSED/REFRACTORY T‐PROLYMPHOCYTIC LEUKEMIA AND INFLUENCES BCL‐2‐FAMILY MEMBER DEPENDENCIES. Hematological Oncology. 37(S2). 482–484. 6 indexed citations

3.

Ajore, Ram, David M. Raiser, Marie McConkey, et al.. (2017). Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP 53 mutations. EMBO Molecular Medicine. 9(4). 498–507. 75 indexed citations

4.

Valent, Peter, Susanne Herndlhofer, Mathias Schneeweiss‐Gleixner, et al.. (2017). TKI rotation-induced persistent deep molecular response in multi-resistant blast crisis of Ph+ CML. Oncotarget. 8(14). 23061–23072. 9 indexed citations

5.

Ajore, Ram, David M. Raiser, Marie McConkey, et al.. (2017). Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with. DSpace@MIT (Massachusetts Institute of Technology). 1 indexed citations

6.

Englinger, Bernhard, Daniela Lötsch, Christine Pirker, et al.. (2016). Acquired nintedanib resistance in FGFR1-driven small cell lung cancer: role of endothelin-A receptor-activated ABCB1 expression. Oncotarget. 7(31). 50161–50179. 18 indexed citations

7.

Herzog, Veronika A., Adelheid Lempradl, Bernd Boidol, et al.. (2014). A strand-specific switch in noncoding transcription switches the function of a Polycomb/Trithorax response element. Nature Genetics. 46(9). 973–981. 81 indexed citations

8.

Dürnberger, Gerhard, Claudia Kerzendorfer, Bernd Boidol, et al.. (2014). NOTCH1 activation in breast cancer confers sensitivity to inhibition of SUMOylation. Oncogene. 34(29). 3780–3790. 37 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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