Susanne Bens

4.0k total citations
60 papers, 871 citations indexed

About

Susanne Bens is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Susanne Bens has authored 60 papers receiving a total of 871 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 24 papers in Pathology and Forensic Medicine and 19 papers in Genetics. Recurrent topics in Susanne Bens's work include Epigenetics and DNA Methylation (16 papers), Lymphoma Diagnosis and Treatment (13 papers) and Genetic Syndromes and Imprinting (11 papers). Susanne Bens is often cited by papers focused on Epigenetics and DNA Methylation (16 papers), Lymphoma Diagnosis and Treatment (13 papers) and Genetic Syndromes and Imprinting (11 papers). Susanne Bens collaborates with scholars based in Germany, Spain and United States. Susanne Bens's co-authors include Reiner Siebert, L. Dibbelt, Sebastian Rudolf, Ulrich Schweiger, Andreas Kordon, Reiner Siebert, Almuth Caliebe, Ole Ammerpohl, Kai G. Kahl and Kai G. Kahl and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Susanne Bens

54 papers receiving 844 citations

Peers

Countries citing papers authored by Susanne Bens

Since Specialization

Citations

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

Fields of papers citing papers by Susanne Bens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susanne Bens

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Common origin and somatic mutation patterns of composite lymphomas and leukemias 2025 ·Leukemia ·(unknown), Anna Lollies, M. Schneider, Patricia Johansson, Marc A. Weniger, (unknown), Fabio Facchetti, Stefano Ascani, (unknown), Susanne Bens, (unknown), Reiner Siebert, Wolfram Klapper, Luisa Lorenzi, Enrico Tiacci, Sylvia Hartmann, Bettina Budeus, Martin‐Leo Hansmann, Ralf Küppers	0
2	“In situ” MYC rearrangement and amplification as a secondary change in a case of High-grade B cell lymphoma with 11q aberration 2025 ·Annals of Hematology ·(unknown), Susanne Bens, (unknown), (unknown), Luca Nassi, Reiner Siebert, Raffaella Santi	0
3	The chromosomal translocation t (1;6)(p35.3;p25.2), recurrent in chronic lymphocytic leukaemia, leads to RCC1 :: IRF4 fusion 2024 ·British Journal of Haematology ·Sandrine Jayne, Cristina López, (unknown), Inga Nagel, Els Lierman, Eva Maria Murga Penas, Lucienne Michaux, Matthew J. Ahearne, Harriet S. Walter, Susanne Bens, (unknown), Monika Szczepanowski, Matthias Schlesner, Philip Rosenstiel, Iwona Włodarska, Reiner Siebert, Martin J.S. Dyer	0
4	Constitutional mosaicism of pathogenic variants in SMARCB1 in a subset of patients with sporadic rhabdoid tumors 2024 ·Neuro-Oncology ·(unknown), Karolina Nemes, (unknown), (unknown), (unknown), Susanne Bens, (unknown), Helene Kretzmer, Florian Oyen, Joachim Gerß, Martin Hasselblatt, Michael C. Frühwald, Reiner Siebert	1
5	PI3K/AKT inhibitor BEZ-235 targets CCND2 and induces G1 arrest in breast implant-associated anaplastic large cell lymphoma 2023 ·Leukemia Research ·Stefan Nagel, (unknown), Susanne Bens, (unknown), Claudia Pommerenke, Cord C. Uphoff, Margarete Zaborski, Reiner Siebert, Hilmar Quentmeier	4
6	Development of super-specific epigenome editing by targeted allele-specific DNA methylation 2023 ·Epigenetics & Chromatin ·(unknown), (unknown), Susanne Bens, Pavel Bashtrykov, Albert Jeltsch	10
7	CDKN2A-Mutated Pancreatic Ductal Organoids from Induced Pluripotent Stem Cells to Model a Cancer Predisposition Syndrome 2021 ·Cancers ·Jessica Merkle, Markus Breunig, (unknown), (unknown), Jana Krüger, (unknown), Susanne Bens, Reiner Siebert, Lukas Perkhofer, Ninel Azoitei, Thomas Seufferlein, Sandra Heller, Matthias Meier, Martin C. Müller, Alexander Kleger, Meike Hohwieler	15
8	Double-hit lymphoma of the male breast: a case report 2020 ·Journal of Medical Case Reports ·(unknown), Inga Nagel, Cristina López, Susanne Bens, Monika Szczepanowski, Rabea Wagener, Wolfram Klapper, Reiner Siebert	5
9	Epigenetic Repression of Androgen Receptor Transcription in Mutation-Negative Androgen Insensitivity Syndrome (AIS Type II) 2018 ·The Journal of Clinical Endocrinology & Metabolism ·Nadine Hornig, (unknown), Helmuth G. Dörr, Nina C. Hubner, Alexandra Kulle, (unknown), (unknown), Susanne Bens, Olaf Hiort, Ralf Werner, (unknown), (unknown), Martine Cools, (unknown), Hendrik G. Stunnenberg, Reiner Siebert, Ole Ammerpohl, Paul-Martin Holterhus	22
10	Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis 2018 ·European Journal of Human Genetics ·Till Holsten, Susanne Bens, Florian Oyen, Karolina Nemes, Martin Hasselblatt, Uwe Kordes, Reiner Siebert, Michael C. Frühwald, Reinhard Schneppenheim, Ulrich Schüller	26
11	In vivo Investigations of the Effect of Short- and Long-Term Recombinant Growth Hormone Treatment on DNA-Methylation in Humans 2015 ·PLoS ONE ·Julia Kolarova, Ole Ammerpohl, Jana Gutwein, (unknown), (unknown), Felix G. Riepe, Thomas Eggermann, Almuth Caliebe, Paul‐Martin Holterhus, Reiner Siebert, Susanne Bens	7
12	A novel large deletion of the ICR1 region including H19 and putative enhancer elements 2015 ·BMC Medical Genetics ·Helen Fryssira, (unknown), Deniz Kanber, Christalena Sofocleous, (unknown), Christina Kanaka‐Gantenbein, Flavia Cerrato, Hermann‐Josef Lüdecke, Susanne Bens, Andrea Riccio, Karin Buiting	6
13	SPAG7 is a candidate gene for the periodic fever, aphthous stomatitis, pharyngitis and adenopathy (PFAPA) syndrome 2014 ·Genes and Immunity ·Susanne Bens, Thomas Zichner, Adrian M. Stütz, Amke Caliebe, Rabea Wagener, Kirstin Hoff, Jan O. Korbel, Philipp von Bismarck, Reiner Siebert	17
14	Clinical utility gene card for: Transient Neonatal Diabetes Mellitus, 6q24-related 2014 ·European Journal of Human Genetics ·Deborah Mackay, Susanne Bens, Guiomar Pérez de Nanclares, Reiner Siebert, I. Karen Temple	19
15	Array-based DNA methylation profiling in male infertility reveals allele-specific DNA methylation in PIWIL1 and PIWIL2 2014 ·Fertility and Sterility ·(unknown), Ole Ammerpohl, Jana Gutwein, Andreas Schmutzler, Almuth Caliebe, (unknown), Sören von Otte, Reiner Siebert, Susanne Bens	32
16	Androgen Receptor Function Links Human Sexual Dimorphism to DNA Methylation 2013 ·PLoS ONE ·Ole Ammerpohl, Susanne Bens, Mahesh Appari, Ralf Werner, Bernhard Korn, Stenvert L. S. Drop, Frans W. Verheijen, (unknown), Trevor Bunch, Ieuan A. Hughes, Martine Cools, Felix G. Riepe, Olaf Hiort, Reiner Siebert, Paul‐Martin Holterhus	25
17	Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas 2013 ·Haematologica ·Idoia Martín‐Guerrero, Itziar Salaverría, Birgit Burkhardt, Monika Szczepanowski, Michael Baudis, Susanne Bens, Laurence de Leval, África García‐Orad, Heike Horn, Jasmin Lisfeld, (unknown), Wolfram Klapper, (unknown), Reiner Siebert	49
18	Mechanisms of Intracerebral Lymphoma Growth Delineated in a Syngeneic Mouse Model of Central Nervous System Lymphoma 2013 ·Journal of Neuropathology & Experimental Neurology ·Manuel Montesinos‐Rongen, (unknown), Anna Brunn, (unknown), Susanne Bens, Sandra Rodríguez, Juan C. Cigudosa, Reiner Siebert, Martina Deckert	9
19	DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples 2012 ·PLoS ONE ·Christel Eckmann-Scholz, Susanne Bens, Julia Kolarova, (unknown), Almuth Caliebe, Simone Heidemann, Constantin von Kaisenberg, (unknown), W. Jonat, Reiner Siebert, Ole Ammerpohl	24
20	Androgen Receptor Mutations Are Associated with Altered Epigenomic Programming as Evidenced by <i>HOXA5</i> Methylation 2011 ·Sexual Development ·Susanne Bens, Ole Ammerpohl, José I. Martı́n-Subero, Mahesh Appari, Julia Richter, Olaf Hiort, Ralf Werner, Felix G. Riepe, Reiner Siebert, Paul‐Martin Holterhus	9

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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