Michael H. Muders

4.1k total citations
79 papers, 2.7k citations indexed

About

Michael H. Muders is a scholar working on Molecular Biology, Oncology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Michael H. Muders has authored 79 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 35 papers in Oncology and 24 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Michael H. Muders's work include Angiogenesis and VEGF in Cancer (14 papers), Prostate Cancer Treatment and Research (14 papers) and Lymphatic System and Diseases (13 papers). Michael H. Muders is often cited by papers focused on Angiogenesis and VEGF in Cancer (14 papers), Prostate Cancer Treatment and Research (14 papers) and Lymphatic System and Diseases (13 papers). Michael H. Muders collaborates with scholars based in Germany, United States and Slovakia. Michael H. Muders's co-authors include Kaustubh Datta, Anna Dubrovska, Monica Cojoc, Katrin Mäbert, Heyu Zhang, Donald J. Tindall, Pia Hönscheid, Udo Loehrs, Konstantin Nikolaou and Maximilian F. Reiser and has published in prestigious journals such as Journal of Clinical Investigation, Blood and Gastroenterology.

In The Last Decade

Michael H. Muders

77 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael H. Muders Germany	30	1.3k	904	554	502	401	79	2.7k
Qichun Wei China	30	1.2k 0.9×	903 1.0×	620 1.1×	487 1.0×	423 1.1×	138	3.2k
Rainer Kehlbach Germany	25	1.1k 0.9×	815 0.9×	507 0.9×	367 0.7×	410 1.0×	57	2.4k
Frits Thorsen Norway	36	1.6k 1.3×	955 1.1×	648 1.2×	972 1.9×	320 0.8×	84	4.0k
Debabrata Saha United States	29	1.1k 0.9×	676 0.7×	576 1.0×	471 0.9×	275 0.7×	111	2.4k
Deliang Fu China	28	994 0.8×	1.3k 1.5×	342 0.6×	621 1.2×	160 0.4×	99	2.7k
Hao Xiong United States	29	2.0k 1.6×	1.6k 1.8×	412 0.7×	377 0.8×	210 0.5×	132	4.4k
Jonathan B. Fitzgerald United States	22	1.0k 0.8×	643 0.7×	243 0.4×	205 0.4×	357 0.9×	50	2.4k
Yuri Sheinin United States	29	1.2k 0.9×	1.1k 1.2×	867 1.6×	453 0.9×	150 0.4×	60	2.9k
Gilbert Spizzo Austria	29	2.1k 1.6×	1.7k 1.9×	488 0.9×	723 1.4×	351 0.9×	70	3.8k
Ling Geng United States	28	1.9k 1.5×	981 1.1×	539 1.0×	866 1.7×	339 0.8×	50	3.1k

Countries citing papers authored by Michael H. Muders

Since Specialization

Citations

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

Fields of papers citing papers by Michael H. Muders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael H. Muders. 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 Michael H. Muders. The network helps show where Michael H. Muders may publish in the future.

Co-authorship network of co-authors of Michael H. Muders

This figure shows the co-authorship network connecting the top 25 collaborators of Michael H. Muders. A scholar is included among the top collaborators of Michael H. Muders 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 Michael H. Muders. Michael H. Muders 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

Mayr, Thomas, Saskia von Stillfried, Sarah Förster, et al.. (2025). Differential expression of viral entry protein neuropilin 1 (NRP1) and neuropilin 2 (NRP2) in fatal COVID-19. Journal of Virology. 99(11). e0138425–e0138425.

Boecker, Werner, Katharina Tiemann, Joerg Boecker, et al.. (2020). Cellular organization and histogenesis of adenosquamous carcinoma of the pancreas: evidence supporting the squamous metaplasia concept. Histochemistry and Cell Biology. 154(1). 97–105. 9 indexed citations

Schulz, Alexander, et al.. (2019). Silencing of Neuropilins and GIPC1 in pancreatic ductal adenocarcinoma exerts multiple cellular and molecular antitumor effects. Scientific Reports. 9(1). 15471–15471. 9 indexed citations

Roy, Sohini, Arup K. Bag, Samikshan Dutta, et al.. (2018). Macrophage-Derived Neuropilin-2 Exhibits Novel Tumor-Promoting Functions. Cancer Research. 78(19). 5600–5617. 58 indexed citations

Zhao, Chenming, Yuri Tolkach, Doris Schmidt, et al.. (2018). Mitochondrial PIWI-interacting RNAs are novel biomarkers for clear cell renal cell carcinoma. World Journal of Urology. 37(8). 1639–1647. 27 indexed citations

Galli, Roberta, et al.. (2017). Sex-specific differences in age-dependent progression of aortic dysfunction and related cardiac remodeling in spontaneously hypertensive rats. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 312(5). R835–R849. 21 indexed citations

Schulz, Alexander, et al.. (2017). Role of neuropilin-2 in the immune system. Molecular Immunology. 90. 239–244. 47 indexed citations

Peitzsch, Claudia, Monica Cojoc, Ina Kurth, et al.. (2016). An Epigenetic Reprogramming Strategy to Resensitize Radioresistant Prostate Cancer Cells. Cancer Research. 76(9). 2637–2651. 57 indexed citations

Möller, Frank, Sebastian T. Soukup, Oliver Zierau, et al.. (2016). Soy isoflavone exposure through all life stages accelerates 17β-estradiol-induced mammary tumor onset and growth, yet reduces tumor burden, in ACI rats. Archives of Toxicology. 90(8). 1907–1916. 11 indexed citations

10.

Dutta, Samikshan, Sohini Roy, Gustavo Baretton, et al.. (2016). NRP2 transcriptionally regulates its downstream effector WDFY1. Scientific Reports. 6(1). 23588–23588. 19 indexed citations

11.

Kunz‐Schughart, Leoni A., Anna Dubrovska, Claudia Peitzsch, et al.. (2016). Nanoparticles for radiooncology: Mission, vision, challenges. Biomaterials. 120. 155–184. 94 indexed citations

12.

Zierau, Oliver, Dana Macejová, Michael H. Muders, et al.. (2016). The phytoestrogenic Cyclopia extract, SM6Met, increases median tumor free survival and reduces tumor mass and volume in chemically induced rat mammary gland carcinogenesis. The Journal of Steroid Biochemistry and Molecular Biology. 163. 129–135. 5 indexed citations

13.

Dutta, Samikshan, Sohini Roy, Heyu Zhang, et al.. (2015). Neuropilin-2 Regulates Endosome Maturation and EGFR Trafficking to Support Cancer Cell Pathobiology. Cancer Research. 76(2). 418–428. 47 indexed citations

14.

Dutta, Samikshan, Heyu Zhang, Alexey A. Leontovich, et al.. (2012). Autophagy Control by the VEGF-C/NRP-2 Axis in Cancer and Its Implication for Treatment Resistance. Cancer Research. 73(1). 160–171. 73 indexed citations

15.

Singer, Adam D., Yvonne Deuse, U. Koch, et al.. (2012). Impact of the adaptor protein GIPC1/Synectin on radioresistance and survival after irradiation of prostate cancer. Strahlentherapie und Onkologie. 188(12). 1125–1132. 1 indexed citations

16.

Rowley, Matthew, Akihiro Ohashi, Gourish Mondal, et al.. (2011). Inactivation of Brca2 Promotes Trp53-Associated but Inhibits KrasG12D-Dependent Pancreatic Cancer Development in Mice. Gastroenterology. 140(4). 1303–1313.e3. 59 indexed citations

17.

Muders, Michael H., Heyu Zhang, Enfeng Wang, Donald J. Tindall, & Kaustubh Datta. (2009). Vascular Endothelial Growth Factor-C Protects Prostate Cancer Cells from Oxidative Stress by the Activation of Mammalian Target of Rapamycin Complex-2 and AKT-1. Cancer Research. 69(15). 6042–6048. 54 indexed citations

18.

Patra, Chitta Ranjan, Resham Bhattacharya, Enfeng Wang, et al.. (2008). Targeted Delivery of Gemcitabine to Pancreatic Adenocarcinoma Using Cetuximab as a Targeting Agent. Cancer Research. 68(6). 1970–1978. 296 indexed citations

19.

Muders, Michael H., Shamit K. Dutta, Ling Wang, et al.. (2006). Expression and Regulatory Role of GAIP-Interacting Protein GIPC in Pancreatic Adenocarcinoma. Cancer Research. 66(21). 10264–10268. 37 indexed citations

20.

Kopp, Reinhard, Maximilian I. Ruge, H Arnholdt, et al.. (2003). Clinical Implications of the EGF Receptor/Ligand System for Tumor Progression and Survival in Gastrointestinal Carcinomas: Evidence for New Therapeutic Options. Recent results in cancer research. 162. 115–132. 55 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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