Benno Küsters

6.4k total citations
125 papers, 3.9k citations indexed

About

Benno Küsters is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Benno Küsters has authored 125 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 24 papers in Surgery and 24 papers in Genetics. Recurrent topics in Benno Küsters's work include Glioma Diagnosis and Treatment (14 papers), Cancer, Hypoxia, and Metabolism (14 papers) and Adrenal and Paraganglionic Tumors (13 papers). Benno Küsters is often cited by papers focused on Glioma Diagnosis and Treatment (14 papers), Cancer, Hypoxia, and Metabolism (14 papers) and Adrenal and Paraganglionic Tumors (13 papers). Benno Küsters collaborates with scholars based in Netherlands, United States and Germany. Benno Küsters's co-authors include Pieter Wesseling, William P. J. Leenders, Robert M.W. de Waal, Marcel M. Verbeek, Arend Heerschap, H. Bea Kuiperij, Dirk J. Ruiter, Patricia J.T.A. Groenen, Jurgen A.H.R. Claassen and Willeke A.M. Blokx and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Benno Küsters

118 papers receiving 3.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Benno Küsters 1.7k 806 755 751 543 125 3.9k
Peter Pytel 1.8k 1.0× 620 0.8× 619 0.8× 359 0.5× 308 0.6× 126 3.7k
Christian Hagel 1.1k 0.7× 1.5k 1.9× 707 0.9× 342 0.5× 482 0.9× 202 4.0k
Takanori Ohnishi 1.1k 0.7× 775 1.0× 715 0.9× 485 0.6× 325 0.6× 146 3.5k
Patrick N. Harter 1.9k 1.1× 476 0.6× 1.5k 1.9× 971 1.3× 655 1.2× 181 4.8k
Sonika Dahiya 1.6k 1.0× 846 1.0× 1.2k 1.6× 950 1.3× 701 1.3× 142 4.2k
Martin Hasselblatt 3.0k 1.8× 1.2k 1.5× 2.2k 2.9× 528 0.7× 626 1.2× 164 6.1k
Kazunari Yoshida 1.6k 1.0× 1.7k 2.1× 1.1k 1.4× 605 0.8× 577 1.1× 336 6.2k
Hideaki Yokoo 981 0.6× 578 0.7× 1000 1.3× 374 0.5× 444 0.8× 181 2.7k
Wolfgang Roggendorf 1.5k 0.9× 1.2k 1.5× 1.2k 1.6× 491 0.7× 324 0.6× 109 4.7k
Valérie Rigau 893 0.5× 531 0.7× 1.4k 1.9× 382 0.5× 654 1.2× 123 3.6k

Countries citing papers authored by Benno Küsters

Since Specialization
Citations

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

Fields of papers citing papers by Benno Küsters

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Benno Küsters

This figure shows the co-authorship network connecting the top 25 collaborators of Benno Küsters. A scholar is included among the top collaborators of Benno Küsters 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 Benno Küsters. Benno Küsters 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.
Verhoeven, Jamie I., Jürgen Seeger, J. Molenaar, et al.. (2024). Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait. Neurology. 102(5). e209164–e209164. 1 indexed citations
2.
Geenen, Bram, Benno Küsters, Jurgen A.H.R. Claassen, et al.. (2024). Deep learning‐based segmentation in MRI‐(immuno)histological examination of myelin and axonal damage in normal‐appearing white matter and white matter hyperintensities. Brain Pathology. 35(2). e13301–e13301. 2 indexed citations
3.
Gorissen, Marnix, Richard J. Rodenburg, Antonius E. van Herwaarden, et al.. (2024). Characterisation of an Adult Zebrafish Model for SDHB-Associated Phaeochromocytomas and Paragangliomas. International Journal of Molecular Sciences. 25(13). 7262–7262.
4.
Groothuis, Jan T., Corrie E. Erasmus, Michael A. Gaytant, et al.. (2024). A cross-sectional study in 18 patients with typical and mild forms of nemaline myopathy in the Netherlands. Neuromuscular Disorders. 43. 29–38. 1 indexed citations
5.
Geenen, Bram, José Gutierrez, Benno Küsters, et al.. (2023). Association between hypertension and neurovascular inflammation in both normal-appearing white matter and white matter hyperintensities. Acta Neuropathologica Communications. 11(1). 31 indexed citations
6.
Geurts, Birgit S., Laurien J. Zeverijn, Gijs F. de Wit, et al.. (2023). Efficacy and Safety of Panitumumab in Patients With RAF/RAS-Wild-Type Glioblastoma: Results From the Drug Rediscovery Protocol. The Oncologist. 29(5). 431–440. 3 indexed citations
7.
Grunsven, Adriana C. H. van Engen–van, Johan Bussink, Cathelijne Frielink, et al.. (2022). [18F]FDG Uptake and Expression of Immunohistochemical Markers Related to Glycolysis, Hypoxia, and Proliferation in Indeterminate Thyroid Nodules. Molecular Imaging and Biology. 25(3). 483–494. 7 indexed citations
8.
Erasmus, Corrie E., Maartje Pennings, Meyke Schouten, et al.. (2021). Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands. Clinical Genetics. 100(6). 692–702. 8 indexed citations
9.
Sabatella, Mariangela, Tuomo Mantere, Esmé Waanders, et al.. (2021). Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors. The Journal of Pathology. 255(2). 202–211. 28 indexed citations
11.
Lassche, Saskia, Nicol C. Voermans, Robbert van der Pijl, et al.. (2020). Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy. Neurology. 94(11). e1157–e1170. 8 indexed citations
12.
Boldt, Henning B., Jeanette Krogh Petersen, David Scheie, et al.. (2020). Brain tumour diagnostics using a DNA methylation‐based classifier as a diagnostic support tool. Neuropathology and Applied Neurobiology. 46(5). 478–492. 68 indexed citations
13.
Wortmann, Saskia B., Charlotte A. Haaxma, Peter M. van Hasselt, et al.. (2020). Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction. Clinical Genetics. 97(4). 556–566. 23 indexed citations
14.
Lassche, Saskia, Benno Küsters, Arend Heerschap, et al.. (2020). Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD. Journal of Neuromuscular Diseases. 7(4). 495–504. 25 indexed citations
15.
Lenting, Krissie, Remco C. de Boer, Elizabeth A. Tindall, et al.. (2019). Mapping actionable pathways and mutations in brain tumours using targeted RNA next generation sequencing. Acta Neuropathologica Communications. 7(1). 185–185. 6 indexed citations
16.
Udd, Bjarne, Werner Stenzel, Anders Oldfors, et al.. (2019). 1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018. Neuromuscular Disorders. 29(6). 483–485. 34 indexed citations
17.
Pedersen, Malin, Heidi V.N. Küsters‐Vandevelde, Amaya Virós, et al.. (2013). Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes. Cancer Discovery. 3(4). 458–469. 51 indexed citations
18.
Rao, Jyotsna U., Udo F. H. Engelke, Richard J. Rodenburg, et al.. (2013). Genotype-Specific Abnormalities in Mitochondrial Function Associate with Distinct Profiles of Energy Metabolism and Catecholamine Content in Pheochromocytoma and Paraganglioma. Clinical Cancer Research. 19(14). 3787–3795. 44 indexed citations
19.
Kleinnijenhuis, Michiel, et al.. (2013). Detailed laminar characteristics of the human neocortex revealed by NODDI and histology. Human Brain Mapping. 4. 3815–3815. 8 indexed citations
20.
Kleinnijenhuis, Michiel, Markus Barth, Valerio Zerbi, et al.. (2011). Layer-specific diffusion weighted imaging in human primary visual cortex in vitro.. Human Brain Mapping. 2509–2509. 1 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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