Manfred Beier

929 total citations
36 papers, 641 citations indexed

About

Manfred Beier is a scholar working on Molecular Biology, Electrical and Electronic Engineering and Oncology. According to data from OpenAlex, Manfred Beier has authored 36 papers receiving a total of 641 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 7 papers in Electrical and Electronic Engineering and 5 papers in Oncology. Recurrent topics in Manfred Beier's work include Renal and related cancers (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). Manfred Beier is often cited by papers focused on Renal and related cancers (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). Manfred Beier collaborates with scholars based in Germany, Spain and United States. Manfred Beier's co-authors include Brigitte Royer‐Pokora, Hans‐Dieter Royer, Barbara Hildebrandt, Maike Busch, Angela Weirich, Kati Servan, Valerié Schumacher, Vicki Huff, Rita Alam and Niels Eckstein and has published in prestigious journals such as PLoS ONE, Cancer and Cancer Research.

In The Last Decade

Manfred Beier

36 papers receiving 631 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manfred Beier Germany 12 388 120 101 94 91 36 641
Süleyman Coşkun United States 10 333 0.9× 75 0.6× 70 0.7× 54 0.6× 136 1.5× 14 652
Rumi Satoh Japan 12 249 0.6× 206 1.7× 31 0.3× 26 0.3× 129 1.4× 14 1.0k
Barbara Ziegler Austria 16 541 1.4× 112 0.9× 232 2.3× 84 0.9× 89 1.0× 26 865
Geraldine Jackson United States 8 349 0.9× 205 1.7× 304 3.0× 35 0.4× 71 0.8× 10 699
Roger Cohen United States 12 218 0.6× 319 2.7× 174 1.7× 53 0.6× 53 0.6× 17 772
Michael F. Haller United States 13 216 0.6× 82 0.7× 14 0.1× 25 0.3× 64 0.7× 16 638
Xiaoli Xie China 11 215 0.6× 41 0.3× 74 0.7× 64 0.7× 17 0.2× 51 505
Cicely A. Williams United States 8 263 0.7× 46 0.4× 90 0.9× 52 0.6× 174 1.9× 9 668
Matteo Vecellio United Kingdom 17 361 0.9× 73 0.6× 44 0.4× 25 0.3× 162 1.8× 40 832
Gregory Cesarone United States 9 304 0.8× 260 2.2× 65 0.6× 142 1.5× 9 0.1× 13 653

Countries citing papers authored by Manfred Beier

Since Specialization
Citations

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

Fields of papers citing papers by Manfred Beier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manfred Beier

This figure shows the co-authorship network connecting the top 25 collaborators of Manfred Beier. A scholar is included among the top collaborators of Manfred Beier 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 Manfred Beier. Manfred Beier 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.
Royer‐Pokora, Brigitte, Wasco Wruck, James Adjaye, & Manfred Beier. (2023). Gene expression studies of WT1 mutant Wilms tumor cell lines in the frame work of published kidney development data reveals their early kidney stem cell origin. PLoS ONE. 18(1). e0270380–e0270380. 6 indexed citations
2.
Beier, Manfred, et al.. (2022). ADAM10 and ADAM17—Novel Players in Retinoblastoma Carcinogenesis. International Journal of Molecular Sciences. 23(20). 12621–12621. 3 indexed citations
3.
Busch, Maike, Eva Biewald, Nikolaos E. Bechrakis, et al.. (2022). TFF1 in Aqueous Humor—A Potential New Biomarker for Retinoblastoma. Cancers. 14(3). 677–677. 14 indexed citations
4.
Sproll, Christoph, Sarah Schumacher, Norbert R. Kübler, et al.. (2021). Genetic analysis of single disseminated tumor cells in the lymph nodes and bone marrow of patients with head and neck squamous cell carcinoma. Molecular Oncology. 16(2). 333–346. 4 indexed citations
5.
Royer‐Pokora, Brigitte, Maike Busch, Mathias Schmidt, et al.. (2020). Comprehensive Biology and Genetics Compendium of Wilms Tumor Cell Lines with Different WT1 Mutations. Cancers. 13(1). 60–60. 7 indexed citations
6.
Skowron, Margaretha A., Patrick Petzsch, Karin Hardt, et al.. (2019). Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines. Scientific Reports. 9(1). 14476–14476. 10 indexed citations
7.
Royer‐Pokora, Brigitte, Manfred Beier, Maike Busch, et al.. (2018). Chemotherapy and terminal skeletal muscle differentiation in WT1‐mutant Wilms tumors. Cancer Medicine. 7(4). 1359–1368. 10 indexed citations
8.
Busch, Maike, Manfred Beier, Harald Stephan, et al.. (2017). Reduction of the tumorigenic potential of human retinoblastoma cell lines byTFF1overexpression involves p53/caspase signaling and miR-18a regulation. International Journal of Cancer. 141(3). 549–560. 35 indexed citations
9.
Rausch, Valentin, Andreas Krieg, Jordi Camps, et al.. (2017). Array comparative genomic hybridization of 18 pancreatic ductal adenocarcinomas and their autologous metastases. BMC Research Notes. 10(1). 560–560. 7 indexed citations
10.
Beier, Manfred, Barbara Leube, Carmen de Torres, et al.. (2016). Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15. PLoS ONE. 11(5). e0155561–e0155561. 6 indexed citations
11.
Busch, Maike, Manfred Beier, Paul J. Romaniuk, et al.. (2014). Classification of a frameshift/extended and a stop mutation in WT1 as gain-of-function mutations that activate cell cycle genes and promote Wilms tumour cell proliferation. Human Molecular Genetics. 23(15). 3958–3974. 13 indexed citations
12.
Koch, Martin, Manfred Beier, Ulrich Jaehde, et al.. (2013). Overcoming chemotherapy resistance of ovarian cancer cells by liposomal cisplatin: Molecular mechanisms unveiled by gene expression profiling. Biochemical Pharmacology. 85(8). 1077–1090. 37 indexed citations
13.
14.
Royer‐Pokora, Brigitte, Maike Busch, Manfred Beier, et al.. (2010). Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm. Human Molecular Genetics. 19(9). 1651–1668. 52 indexed citations
15.
Eckstein, Niels, Kati Servan, Barbara Hildebrandt, et al.. (2009). Hyperactivation of the Insulin-like Growth Factor Receptor I Signaling Pathway Is an Essential Event for Cisplatin Resistance of Ovarian Cancer Cells. Cancer Research. 69(7). 2996–3003. 134 indexed citations
16.
Royer‐Pokora, Brigitte, Angela Weirich, Valerié Schumacher, et al.. (2008). Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin‐associated protein β1 gene CTNNB1 for patients with Wilms tumors. Cancer. 113(5). 1080–1089. 34 indexed citations
17.
Evers, Christina, Manfred Beier, Barbara Hildebrandt, et al.. (2007). Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH. Genes Chromosomes and Cancer. 46(12). 1119–1128. 36 indexed citations
18.
Trost, Detlef, et al.. (2006). Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia. Cancer Genetics and Cytogenetics. 165(1). 51–63. 18 indexed citations
19.
Royer‐Pokora, Brigitte, et al.. (2006). Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia. Cancer Genetics and Cytogenetics. 167(1). 66–69. 6 indexed citations
20.
Royer‐Pokora, Brigitte, Manfred Beier, Rita Alam, et al.. (2004). Twenty‐four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development. American Journal of Medical Genetics Part A. 127A(3). 249–257. 93 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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