Stefan Wiemann

17.1k total citations · 1 hit paper
186 papers, 8.8k citations indexed

About

Stefan Wiemann is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Stefan Wiemann has authored 186 papers receiving a total of 8.8k indexed citations (citations by other indexed papers that have themselves been cited), including 140 papers in Molecular Biology, 28 papers in Cancer Research and 25 papers in Oncology. Recurrent topics in Stefan Wiemann's work include RNA and protein synthesis mechanisms (27 papers), RNA modifications and cancer (16 papers) and MicroRNA in disease regulation (15 papers). Stefan Wiemann is often cited by papers focused on RNA and protein synthesis mechanisms (27 papers), RNA modifications and cancer (16 papers) and MicroRNA in disease regulation (15 papers). Stefan Wiemann collaborates with scholars based in Germany, United Kingdom and United States. Stefan Wiemann's co-authors include Annemarie Poustka, Özgür Şahin, Jitao David Zhang, Rainer Pepperkok, Ulrike Korf, Jeremy C. Simpson, Aoife Ward, Nina S. Heiss, Sabine M. Klauck and Philip J. Mason and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Stefan Wiemann

185 papers receiving 8.7k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

1998 708 citations Nina S. Heiss, S. W. Knight et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefan Wiemann Germany	51	5.8k	2.1k	1.2k	810	778	186	8.8k
Paolo Fortina United States	47	4.7k 0.8×	1.9k 0.9×	1.4k 1.2×	614 0.8×	576 0.7×	208	9.2k
Ching C. Lau Hong Kong	50	4.8k 0.8×	1.8k 0.9×	2.0k 1.6×	909 1.1×	634 0.8×	155	8.4k
Sherry L. Jenkins United States	13	5.2k 0.9×	1.4k 0.7×	881 0.7×	725 0.9×	1.2k 1.6×	23	8.4k
Yunlong Liu United States	49	6.1k 1.1×	2.3k 1.1×	1.2k 1.0×	559 0.7×	829 1.1×	366	9.6k
Andrew D. Rouillard United States	12	4.9k 0.9×	1.3k 0.6×	821 0.7×	711 0.9×	1.1k 1.4×	17	8.1k
David Liu United States	38	4.4k 0.8×	1.4k 0.7×	1.5k 1.2×	720 0.9×	893 1.1×	148	8.0k
Connie R. Jiménez Netherlands	56	4.8k 0.8×	1.4k 0.7×	1.3k 1.1×	496 0.6×	655 0.8×	240	8.6k
Gregory W. Gundersen United States	10	4.7k 0.8×	1.3k 0.6×	801 0.6×	701 0.9×	1.1k 1.4×	11	7.6k
Senji Shirasawa Japan	48	5.8k 1.0×	2.0k 1.0×	2.7k 2.2×	775 1.0×	920 1.2×	191	9.3k
Marc Vooijs Netherlands	45	4.9k 0.9×	1.4k 0.7×	2.0k 1.6×	994 1.2×	633 0.8×	108	8.0k

Countries citing papers authored by Stefan Wiemann

Since Specialization

Citations

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

Fields of papers citing papers by Stefan Wiemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Wiemann

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Voutetakis, Konstantinos, Vivian Kosmidou, Kymberleigh A. Pagel, et al.. (2025). Molecular and functional profiling unravels targetable vulnerabilities in colorectal cancer. Molecular Oncology. 19(6). 1751–1774. 1 indexed citations

Borgoni, Simone, Birgitta E. Michels, Sara Burmester, et al.. (2023). Clonal heterogeneity in ER+ breast cancer reveals the proteasome and PKC as potential therapeutic targets. npj Breast Cancer. 9(1). 97–97.

Marrocco, Ilaria, Ashish Noronha, Mary Luz Uribe, et al.. (2021). Host-Dependent Phenotypic Resistance to EGFR Tyrosine Kinase Inhibitors. Cancer Research. 81(14). 3862–3875. 6 indexed citations

Haller, Florian, Fulvia Ferrazzi, Michael Michal, et al.. (2021). Lipomatous Solitary Fibrous Tumors Harbor Rare NAB2-STAT6 Fusion Variants and Show Up-Regulation of the Gene PPARG, Encoding for a Regulator of Adipocyte Differentiation. American Journal Of Pathology. 191(7). 1314–1324. 6 indexed citations

Korallı, Panagiota, Maria Goulielmaki, Stella Arelaki, et al.. (2021). Rational design of aqueous conjugated polymer nanoparticles as potential theranostic agents of breast cancer. Materials Chemistry Frontiers. 5(13). 4950–4962. 12 indexed citations

Saatci, Özge, Simone Borgoni, Özge Akbulut, et al.. (2018). Targeting PLK1 overcomes T-DM1 resistance via CDK1-dependent phosphorylation and inactivation of Bcl-2/xL in HER2-positive breast cancer. Oncogene. 37(17). 2251–2269. 66 indexed citations

Giotti, Bruno, Mark Barnett, Tim Regan, et al.. (2018). Assembly of a parts list of the human mitotic cell cycle machinery. Journal of Molecular Cell Biology. 11(8). 703–718. 55 indexed citations

Ansari, Suhail A., Umar Raza, Pelin G. Ersan, et al.. (2018). Reactivation of cAMP Pathway by PDE4D Inhibition Represents a Novel Druggable Axis for Overcoming Tamoxifen Resistance in ER-positive Breast Cancer. Clinical Cancer Research. 24(8). 1987–2001. 44 indexed citations

Quandt, Jasmin, Michael Bartoschek, Rainer Will, et al.. (2018). Long-peptide vaccination with driver gene mutations in p53 and Kras induces cancer mutation-specific effector as well as regulatory T cell responses. OncoImmunology. 7(12). e1500671–e1500671. 35 indexed citations

10.

Enuka, Yehoshua, Morris E. Feldman, Animesh Chowdhury, et al.. (2017). Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormone. Nucleic Acids Research. 45(22). 12681–12699. 18 indexed citations

11.

Bure, Irina V., Alexander Braun, Helene Geddert, et al.. (2017). The expression of hematopoietic progenitor cell antigen CD34 is regulated by DNA methylation in a site‐dependent manner in gastrointestinal stromal tumours. International Journal of Cancer. 141(11). 2296–2304. 6 indexed citations

12.

Agaimy, Abbas, Matthias Bieg, Michael Michal, et al.. (2016). Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and Myopericytomas. The American Journal of Surgical Pathology. 41(2). 195–203. 62 indexed citations

13.

Lauriola, Mattia, Yehoshua Enuka, Amit Zeisel, et al.. (2014). Diurnal suppression of EGFR signalling by glucocorticoids and implications for tumour progression and treatment. Nature Communications. 5(1). 5073–5073. 49 indexed citations

14.

Spaich, Sebastian, Rainer Will, Steffen Just, et al.. (2012). F-Box and Leucine-Rich Repeat Protein 22 Is a Cardiac-Enriched F-Box Protein That Regulates Sarcomeric Protein Turnover and Is Essential for Maintenance of Contractile Function In Vivo. Circulation Research. 111(12). 1504–1516. 47 indexed citations

15.

Löbke, Christian, Mark Laible, Markus Ruschhaupt, et al.. (2008). Contact spotting of protein microarrays coupled with spike‐in of normalizer protein permits time‐resolved analysis of ERBB receptor signaling. PROTEOMICS. 8(8). 1586–1594. 12 indexed citations

16.

Sansone, Susanna‐Assunta, Philippe Rocca‐Serra, Marco Brandizi, et al.. (2008). The First RSBI (ISA-TAB) Workshop: “Can a Simple Format Work for Complex Studies?”. OMICS A Journal of Integrative Biology. 12(2). 143–149. 58 indexed citations

17.

Schumann, Günter, Dan Rujescu, Andrea Szegedi, et al.. (2001). Alcohol dependence is associated with a NMDA-receptor 2B gene variant. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 105(7). 1 indexed citations

18.

Heiss, Nina S., S. W. Knight, Tom Vulliamy, et al.. (1998). X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nature Genetics. 19(1). 32–38. 708 indexed citations breakdown →

19.

Zimmermann, J., Hartmut Voss, Stefan Wiemann, et al.. (1993). Cycle sequencing protocol with fluorescein-12-dCTP. 4(1). 27–28. 1 indexed citations

20.

Zimmermann, J., Hartmut Voss, Stefan Wiemann, et al.. (1993). Direct sequencing of PCR products using magnetic beads and fluorescein-15-dATP. 4(1). 29–32. 3 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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