Rainer Spang

13.4k total citations · 2 hit papers
148 papers, 7.3k citations indexed

About

Rainer Spang is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Rainer Spang has authored 148 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 32 papers in Pathology and Forensic Medicine and 28 papers in Oncology. Recurrent topics in Rainer Spang's work include Gene expression and cancer classification (40 papers), Lymphoma Diagnosis and Treatment (29 papers) and Bioinformatics and Genomic Networks (26 papers). Rainer Spang is often cited by papers focused on Gene expression and cancer classification (40 papers), Lymphoma Diagnosis and Treatment (29 papers) and Bioinformatics and Genomic Networks (26 papers). Rainer Spang collaborates with scholars based in Germany, United States and Switzerland. Rainer Spang's co-authors include Florian Markowetz, Harry Zuzan, Joseph R. Nevins, Erich Huang, Mike West, Seiichi Ishida, Peter J. Oefner, Carrie Blanchette, Jeffrey R. Marks and John A. Olson and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Rainer Spang

140 papers receiving 7.1k citations

Hit Papers

Predicting the clinical status of human breast cancer by ... 2001 2026 2009 2017 2001 2014 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rainer Spang Germany 40 4.6k 1.6k 913 906 702 148 7.3k
Michael Reich United States 22 6.5k 1.4× 1.2k 0.8× 1.3k 1.4× 852 0.9× 1.0k 1.5× 42 9.6k
Tero Aittokallio Finland 54 6.3k 1.4× 1.4k 0.9× 1.1k 1.2× 351 0.4× 1.1k 1.6× 244 10.2k
Sampsa Hautaniemi Finland 49 4.9k 1.1× 1.5k 1.0× 1.6k 1.7× 534 0.6× 529 0.8× 186 7.6k
John E. Tomaszewski United States 51 2.0k 0.4× 1.5k 1.0× 1.3k 1.5× 685 0.8× 804 1.1× 203 9.4k
Kevin R. Coombes United States 53 6.8k 1.5× 1.7k 1.1× 2.1k 2.3× 625 0.7× 873 1.2× 241 10.2k
David A. Fishman United States 53 6.3k 1.4× 2.2k 1.4× 2.0k 2.2× 557 0.6× 817 1.2× 157 11.4k
Kenneth N. Ross United States 33 7.2k 1.6× 1.3k 0.8× 1.7k 1.9× 301 0.3× 617 0.9× 60 10.7k
David E. Misek United States 53 7.1k 1.6× 2.0k 1.3× 2.0k 2.2× 527 0.6× 1.6k 2.2× 95 11.1k
Julio Sáez-Rodríguez Germany 58 8.9k 2.0× 1.1k 0.7× 1.2k 1.3× 287 0.3× 1.2k 1.7× 249 12.4k
Balasubramanian Narasimhan United States 30 2.4k 0.5× 687 0.4× 733 0.8× 402 0.4× 434 0.6× 67 5.5k

Countries citing papers authored by Rainer Spang

Since Specialization
Citations

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

Fields of papers citing papers by Rainer Spang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rainer Spang

This figure shows the co-authorship network connecting the top 25 collaborators of Rainer Spang. A scholar is included among the top collaborators of Rainer Spang 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 Rainer Spang. Rainer Spang 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.
Simeth, Jakob, Roman Mayr, Florian Weber, et al.. (2025). Lipid metabolism of clear cell renal cell carcinoma predicts survival and affects intratumoral CD8 T cells. Translational Oncology. 61. 102513–102513.
2.
Simeth, Jakob, et al.. (2024). Virtual tissue expression analysis. Bioinformatics. 40(12).
4.
Grasedyck, Lars, et al.. (2024). Taming numerical imprecision by adapting the KL divergence to negative probabilities. Statistics and Computing. 34(5). 1 indexed citations
5.
Richter, Julia, Katharina John, Annette M. Staiger, et al.. (2021). Epstein–Barr virus status of sporadic Burkitt lymphoma is associated with patient age and mutational features. British Journal of Haematology. 196(3). 681–689. 16 indexed citations
6.
Meyer, Katharina, Julia C. Engelmann, Rainer Spang, et al.. (2021). Learning from Embryogenesis—A Comparative Expression Analysis in Melanoblast Differentiation and Tumorigenesis Reveals miRNAs Driving Melanoma Development. Journal of Clinical Medicine. 10(11). 2259–2259. 5 indexed citations
7.
Simeth, Jakob, Paul V. Heinrich, Tilo Wettig, et al.. (2020). DTD: An R Package for Digital Tissue Deconvolution. Journal of Computational Biology. 27(3). 386–389. 3 indexed citations
8.
Wettig, Tilo, et al.. (2019). Modelling cancer progression using Mutual Hazard Networks. Bioinformatics. 36(1). 241–249. 22 indexed citations
9.
Heinrich, Paul V., Christian Köhler, Lisa Ellmann, et al.. (2018). Correcting for natural isotope abundance and tracer impurity in MS-, MS/MS- and high-resolution-multiple-tracer-data from stable isotope labeling experiments with IsoCorrectoR. Scientific Reports. 8(1). 17910–17910. 97 indexed citations
10.
Riquelme, Paloma, Jan Haarer, Lisa Walter, et al.. (2018). TIGIT+ iTregs elicited by human regulatory macrophages control T cell immunity. Nature Communications. 9(1). 2858–2858. 99 indexed citations
11.
Szczepanowski, Monika, J. Lange, Christian Köhler, et al.. (2017). Cell‐of‐origin classification by gene expression and MYC‐rearrangements in diffuse large B‐cell lymphoma of children and adolescents. British Journal of Haematology. 179(1). 116–119. 12 indexed citations
12.
Holler, Ernst, Karin Schmid‐Zalaudek, Christian Hundsrucker, et al.. (2014). Metagenomic analysis of the stool microbiome in patients receiving allogeneic SCT: Loss of diversity is associated with use of systemic antibiotics and more pronounced in gastrointestinal GvHD. University of Regensburg Publication Server (University of Regensburg). 4 indexed citations
13.
Yang, Moon Hee, Gaëlle Laurent, Alexandra S. Bause, et al.. (2013). HDAC6 and SIRT2 Regulate the Acetylation State and Oncogenic Activity of Mutant K-RAS. Molecular Cancer Research. 11(9). 1072–1077. 110 indexed citations
14.
Vockerodt, Martina, Frederike von Bonin, Wolfram Klapper, et al.. (2013). Aberrant Lymphocyte Enhancer–Binding Factor 1 Expression Is Characteristic for Sporadic Burkitt’s Lymphoma. American Journal Of Pathology. 182(4). 1092–1098. 29 indexed citations
15.
Hertwig, Falk, Katharina Meyer, Sebastian Braun, et al.. (2012). Definition of Genetic Events Directing the Development of Distinct Types of Brain Tumors from Postnatal Neural Stem/Progenitor Cells. Cancer Research. 72(13). 3381–3392. 12 indexed citations
16.
Engelmann, Julia C. & Rainer Spang. (2012). A Least Angle Regression Model for the Prediction of Canonical and Non-Canonical miRNA-mRNA Interactions. PLoS ONE. 7(7). e40634–e40634. 19 indexed citations
17.
Lottaz, Claudio, Dagmar Beier, Katharina Meyer, et al.. (2010). Transcriptional Profiles of CD133+ and CD133− Glioblastoma-Derived Cancer Stem Cell Lines Suggest Different Cells of Origin. Cancer Research. 70(5). 2030–2040. 207 indexed citations
18.
Bentink, Stefan, Swen Weßendorf, Carsten Schwäenen, et al.. (2008). Conserved oncogenic module activation patterns (COMAPS) identify biologically homogeneous groups of diffuse large B-cell lymphomas and clearly define Burkitt lymphoma. Annals of Oncology. 19. 83–83. 2 indexed citations
19.
Koczan, Dirk, Hans‐Juergen Thiesen, Saleh Ibrahim, et al.. (2007). Gene Expression Signatures for Tumor Progression, Tumor Subtype, and Tumor Thickness in Laser-Microdissected Melanoma Tissues. Clinical Cancer Research. 13(3). 806–815. 175 indexed citations
20.
Kirschner‐Schwabe, Renate, Claudio Lottaz, Peter Rhein, et al.. (2006). Expression of Late Cell Cycle Genes and an Increased Proliferative Capacity Characterize Very Early Relapse of Childhood Acute Lymphoblastic Leukemia. Clinical Cancer Research. 12(15). 4553–4561. 32 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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