Roland Penzel

8.5k total citations
134 papers, 4.4k citations indexed

About

Roland Penzel is a scholar working on Oncology, Pulmonary and Respiratory Medicine and Molecular Biology. According to data from OpenAlex, Roland Penzel has authored 134 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Oncology, 49 papers in Pulmonary and Respiratory Medicine and 47 papers in Molecular Biology. Recurrent topics in Roland Penzel's work include Cancer Genomics and Diagnostics (36 papers), Lung Cancer Treatments and Mutations (29 papers) and Genetic factors in colorectal cancer (16 papers). Roland Penzel is often cited by papers focused on Cancer Genomics and Diagnostics (36 papers), Lung Cancer Treatments and Mutations (29 papers) and Genetic factors in colorectal cancer (16 papers). Roland Penzel collaborates with scholars based in Germany, United States and France. Roland Penzel's co-authors include Peter Schirmacher, Wilko Weichert, Albrecht Stenzinger, Arne Warth, Volker Endris, Sebastian Aulmann, Herwart F. Otto, Hendrik Bläker, Ralf J. Rieker and Nicole Pfarr and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Hepatology.

In The Last Decade

Roland Penzel

131 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roland Penzel Germany 40 1.8k 1.7k 1.5k 1.3k 771 134 4.4k
Darrell R. Borger United States 35 1.7k 1.0× 1.7k 1.0× 1.2k 0.8× 1.1k 0.8× 585 0.8× 86 4.1k
David S. Rickman United States 34 1.4k 0.8× 2.8k 1.7× 1.6k 1.1× 1.6k 1.2× 855 1.1× 63 5.6k
Nina N. Nupponen Finland 35 999 0.6× 2.2k 1.3× 1.4k 1.0× 1.1k 0.9× 507 0.7× 64 4.5k
Lukas C. Heukamp Germany 44 1.9k 1.1× 3.4k 2.0× 1.7k 1.1× 1.5k 1.2× 506 0.7× 175 6.1k
Núria Viñolas Spain 33 1.5k 0.9× 1.6k 1.0× 1.5k 1.0× 1.2k 0.9× 634 0.8× 123 4.3k
Enrique de Álava Spain 40 1.9k 1.0× 2.7k 1.6× 3.8k 2.6× 953 0.7× 1.0k 1.3× 186 6.9k
Volker Endris Germany 35 1.7k 1.0× 1.2k 0.7× 1.1k 0.7× 1.4k 1.0× 676 0.9× 99 3.4k
Maria Cristina Manara Italy 45 1.6k 0.9× 2.9k 1.7× 2.4k 1.6× 1.3k 1.0× 614 0.8× 117 5.5k
Birgit Geoerger France 43 2.0k 1.1× 2.6k 1.5× 1.4k 1.0× 1.1k 0.9× 700 0.9× 209 6.2k
Hans‐Ulrich Schildhaus Germany 32 1.7k 0.9× 995 0.6× 2.0k 1.4× 686 0.5× 432 0.6× 190 4.2k

Countries citing papers authored by Roland Penzel

Since Specialization
Citations

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

Fields of papers citing papers by Roland Penzel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roland Penzel

This figure shows the co-authorship network connecting the top 25 collaborators of Roland Penzel. A scholar is included among the top collaborators of Roland Penzel 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 Roland Penzel. Roland Penzel 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
2.
Buchhalter, Ivo, Eugen Rempel, Volker Endris, et al.. (2018). Size matters: Dissecting key parameters for panel‐based tumor mutational burden analysis. International Journal of Cancer. 144(4). 848–858. 117 indexed citations
4.
Christopoulos, Petros, Volker Endris, Farastuk Bozorgmehr, et al.. (2018). EML4‐ALK fusion variant V3 is a high‐risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK+ non‐small cell lung cancer. International Journal of Cancer. 142(12). 2589–2598. 79 indexed citations
5.
Leichsenring, Jonas, Anna‐Lena Volckmar, Martina Kirchner, et al.. (2017). Targeted deep sequencing of effusion cytology samples is feasible, informs spatiotemporal tumor evolution, and has clinical and diagnostic utility. Genes Chromosomes and Cancer. 57(2). 70–79. 13 indexed citations
6.
Pfarr, Nicole, Silvia Darb‐Esfahani, Jonas Leichsenring, et al.. (2017). Mutational profiles of Brenner tumors show distinctive features uncoupling urothelial carcinomas and ovarian carcinoma with transitional cell histology. Genes Chromosomes and Cancer. 56(10). 758–766. 16 indexed citations
7.
Pfarr, Nicole, Roland Penzel, Volker Endris, et al.. (2016). Targeted next‐generation sequencing enables reliable detection of HER2 (ERBB2) status in breast cancer and provides ancillary information of clinical relevance. Genes Chromosomes and Cancer. 56(4). 255–265. 16 indexed citations
8.
Kreuter, Michael, D Kirsten, Thomas Bahmer, et al.. (2015). Screening for <b><i>Helicobacter pylori</i></b> in Idiopathic Pulmonary Fibrosis Lung Biopsies. Respiration. 91(1). 3–8. 12 indexed citations
9.
Fassunke, Jana, Florian Haller, Evgeny A. Moskalev, et al.. (2015). Utility of different massive parallel sequencing platforms for mutation profiling in clinical samples and identification of pitfalls using FFPE tissue. International Journal of Molecular Medicine. 36(5). 1233–1243. 11 indexed citations
10.
Laffert, Maximilian von, Roland Penzel, Peter Schirmacher, et al.. (2014). Multicenter ALK Testing in Non–Small-Cell Lung Cancer: Results of a Round Robin Test. Journal of Thoracic Oncology. 9(10). 1464–1469. 16 indexed citations
11.
Andrulis, Mindaugas, Nicola Lehners, David Capper, et al.. (2013). Targeting the BRAF V600E Mutation in Multiple Myeloma. Cancer Discovery. 3(8). 862–869. 171 indexed citations
12.
Breinig, Marco, Philipp Mayer, Benjamin Goeppert, et al.. (2011). Heat Shock Protein 90-Sheltered Overexpression of Insulin-Like Growth Factor 1 Receptor Contributes to Malignancy of Thymic Epithelial Tumors. Clinical Cancer Research. 17(8). 2237–2249. 21 indexed citations
13.
Warth, Arne, Stephan Macher‐Goeppinger, Thomas Muley, et al.. (2011). Clonality of multifocal nonsmall cell lung cancer: implications for staging and therapy. European Respiratory Journal. 39(6). 1437–1442. 79 indexed citations
14.
Singer, Stephan, Mona Malz, Esther Herpel, et al.. (2009). Coordinated Expression of Stathmin Family Members by Far Upstream Sequence Element-Binding Protein-1 Increases Motility in Non–Small Cell Lung Cancer. Cancer Research. 69(6). 2234–2243. 83 indexed citations
15.
Macher‐Goeppinger, Stephan, Sebastian Aulmann, Katrin E. Tagscherer, et al.. (2009). Prognostic Value of Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand (TRAIL) and TRAIL Receptors in Renal Cell Cancer. Clinical Cancer Research. 15(2). 650–659. 56 indexed citations
16.
Mechtersheimer, Gunhild, Roland Penzel, Wolfgang Hofmann, & Peter Schirmacher. (2006). Primäre Sarkome und Sarkommetastasen in der Leber. Der Pathologe. 27(4). 251–262. 2 indexed citations
17.
Kayed, Hany, Jörg Kleeff, Armin Kolb, et al.. (2005). FXYD3 is overexpressed in pancreatic ductal adenocarcinoma and influences pancreatic cancer cell growth. International Journal of Cancer. 118(1). 43–54. 58 indexed citations
18.
Esposito, Iréne, Andrea S. Bauer, Jörg Kleeff, et al.. (2004). Microcystic tubulopapillary carcinoma of the pancreas: a new tumor entity?. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 444(5). 447–453. 26 indexed citations
19.
Sergi, Consolato, Roland Penzel, Johannes Uhl, et al.. (2001). Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal α-N-acetyl-neuraminidase (sialidase) gene. Human Genetics. 109(4). 421–428. 16 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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