Uwe Kordes

4.1k total citations
58 papers, 1.6k citations indexed

About

Uwe Kordes is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Uwe Kordes has authored 58 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 26 papers in Genetics and 15 papers in Pathology and Forensic Medicine. Recurrent topics in Uwe Kordes's work include Chromatin Remodeling and Cancer (20 papers), Glioma Diagnosis and Treatment (18 papers) and Cancer Mechanisms and Therapy (13 papers). Uwe Kordes is often cited by papers focused on Chromatin Remodeling and Cancer (20 papers), Glioma Diagnosis and Treatment (18 papers) and Cancer Mechanisms and Therapy (13 papers). Uwe Kordes collaborates with scholars based in Germany, United States and United Kingdom. Uwe Kordes's co-authors include Claus Scheidereit, Daniel Krappmann, Martin Hasselblatt, Reinhard Schneppenheim, Michael C. Frühwald, WD Ludwig, Vigo Heissmeyer, Reiner Siebert, Florian Oyen and Bernd Dörken and has published in prestigious journals such as Journal of Clinical Oncology, Blood and Cancer.

In The Last Decade

Uwe Kordes

55 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Uwe Kordes Germany 21 1.1k 585 356 322 256 58 1.6k
Christina Halsey United Kingdom 19 599 0.6× 194 0.3× 239 0.7× 147 0.5× 176 0.7× 36 1.3k
Elvis Terci Valera Brazil 18 725 0.7× 118 0.2× 368 1.0× 186 0.6× 57 0.2× 108 1.4k
Marc Shuman United States 11 396 0.4× 317 0.5× 259 0.7× 257 0.8× 62 0.2× 20 1.1k
Carolina Vicente‐Dueñas Spain 18 728 0.7× 208 0.4× 110 0.3× 244 0.8× 147 0.6× 41 1.2k
Xiao-Yan Zhou China 23 1.0k 1.0× 297 0.5× 189 0.5× 819 2.5× 230 0.9× 44 1.9k
Debra Saxe United States 20 578 0.5× 170 0.3× 244 0.7× 106 0.3× 204 0.8× 45 1.4k
Akihide Yoshimi Japan 23 994 0.9× 103 0.2× 250 0.7× 244 0.8× 229 0.9× 64 1.6k
Sílvia Regina Caminada de Toledo Brazil 23 654 0.6× 77 0.1× 333 0.9× 287 0.9× 95 0.4× 68 1.4k
Ana Carrió Spain 22 491 0.5× 312 0.5× 398 1.1× 71 0.2× 179 0.7× 59 1.3k
Nadia Carboni Italy 23 628 0.6× 231 0.4× 171 0.5× 191 0.6× 116 0.5× 51 1.4k

Countries citing papers authored by Uwe Kordes

Since Specialization
Citations

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

Fields of papers citing papers by Uwe Kordes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Uwe Kordes

This figure shows the co-authorship network connecting the top 25 collaborators of Uwe Kordes. A scholar is included among the top collaborators of Uwe Kordes 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 Uwe Kordes. Uwe Kordes 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.
Warmuth‐Metz, Monika, Camelia‐Maria Monoranu, Torsten Pietsch, et al.. (2025). Leptomeningeal Dissemination in Choroid Plexus Tumors: Magnetic Resonance Imaging Appearance and Risk Factors. Children. 12(1). 82–82.
2.
Obrecht, Denise, Pablo Hernáiz Driever, Axel Sauerbrey, et al.. (2024). Medulloblastoma in children with Fanconi anemia: Association with FA-D1/FA-N, SHH type and poor survival independent of treatment strategies. Neuro-Oncology. 26(11). 2125–2139. 1 indexed citations
3.
4.
Bies, Juraj, Iris Lange, Arjen R. Mensenkamp, et al.. (2024). A germline PDGFRB splice site variant associated with infantile myofibromatosis and resistance to imatinib. Genetics in Medicine. 27(2). 101334–101334. 1 indexed citations
5.
Wößmann, Wilhelm, et al.. (2023). Generalized Infantile Myofibromatosis with Extensive Small Bowel Involvement in a Neonate. Zeitschrift für Geburtshilfe und Neonatologie. 227(3). 231–235. 1 indexed citations
6.
7.
Frühwald, Michael C., Karolina Nemes, Heidrun Boztug, et al.. (2021). Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group. Familial Cancer. 20(4). 305–316. 25 indexed citations
8.
Thomas, Christian, et al.. (2020). Epigenetics impacts upon prognosis and clinical management of choroidplexus tumors. Journal of Neuro-Oncology. 148(1). 39–45. 10 indexed citations
9.
Holsten, Till, Susanne Bens, Florian Oyen, et al.. (2018). Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis. European Journal of Human Genetics. 26(8). 1083–1093. 26 indexed citations
10.
Holsten, Till, Konstantinos Tsiakas, Uwe Kordes, et al.. (2017). Group 3 medulloblastoma in a patient with a GYS2 germline mutation and glycogen storage disease 0a. Child s Nervous System. 34(3). 581–584. 1 indexed citations
11.
Koehne, Till, Reinhard E. Friedrich, Uwe Kordes, et al.. (2017). Differences in maxillomandibular morphology among patients with mucopolysaccharidoses I, II, III, IV and VI: a retrospective MRI study. Clinical Oral Investigations. 22(3). 1541–1549. 6 indexed citations
12.
Kordes, Uwe, et al.. (2011). Ectopic Craniopharyngioma. Klinische Pädiatrie. 223(3). 176–177. 21 indexed citations
13.
Schneppenheim, Reinhard, Michael C. Frühwald, Stefan Gesk, et al.. (2010). Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome. The American Journal of Human Genetics. 86(2). 279–284. 222 indexed citations
14.
Kordes, Uwe, Andréa Richter, René Santer, et al.. (2010). Neonatal cholestasis and glucose‐6‐P‐dehydrogenase deficiency. Pediatric Blood & Cancer. 54(5). 758–760. 7 indexed citations
15.
Bug, Stefanie, Jan Dürig, Florian Oyen, et al.. (2009). Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A–TCRAD juxtaposition. Cancer Genetics and Cytogenetics. 192(1). 44–47. 14 indexed citations
16.
Distelmaier, Felix, Gabriele Calaminus, D. Harms, et al.. (2006). Ovarian small cell carcinoma of the hypercalcemic type in children and adolescents. Cancer. 107(9). 2298–2306. 46 indexed citations
17.
Meo, Anna, et al.. (2005). Long‐term treatment with deferiprone in a L1 veteran. European Journal Of Haematology. 74(6). 523–525. 1 indexed citations
18.
Kordes, Uwe, Yi‐Chuan Cheng, & Paul J. Scotting. (2005). Sox group E gene expression distinguishes different types and maturational stages of glial cells in developing chick and mouse. Developmental Brain Research. 157(2). 209–213. 30 indexed citations
19.
Zabelina, Tatjana, Helmut Renges, Uwe Kordes, et al.. (2002). Long-term follow-up of allogeneic stem cell transplantation in patients with severe aplastic anemia after conditioning with cyclophosphamide plus antithymocyte globulin. Annals of Hematology. 81(11). 627–631. 22 indexed citations
20.
Nielsen, Peter, et al.. (2002). SQUID-Biosuszeptometrie bei Eisenüberladungskrankheiten in der Hämatologie. Klinische Pädiatrie. 214(4). 218–222. 8 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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