Bernhard Zabel

929 total citations
10 papers, 654 citations indexed

About

Bernhard Zabel is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Urology. According to data from OpenAlex, Bernhard Zabel has authored 10 papers receiving a total of 654 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 2 papers in Urology. Recurrent topics in Bernhard Zabel's work include Renal and related cancers (4 papers), Renal cell carcinoma treatment (2 papers) and Urological Disorders and Treatments (2 papers). Bernhard Zabel is often cited by papers focused on Renal and related cancers (4 papers), Renal cell carcinoma treatment (2 papers) and Urological Disorders and Treatments (2 papers). Bernhard Zabel collaborates with scholars based in Germany, United States and Canada. Bernhard Zabel's co-authors include Jerry Pelletier, Nabeel Bardeesy, Maria Cássia Ferreira de Aguiar, Mohammed Adam, Paul E. Grundy, Norma J. Nowak, Stéfan Wirth, H Trübel, Patrick Gerner and Ekkehart Lausch and has published in prestigious journals such as Nature Genetics, Hepatology and Biochemical and Biophysical Research Communications.

In The Last Decade

Bernhard Zabel

10 papers receiving 641 citations

Peers

Bernhard Zabel
M J Mayol Spain
Bernhard Zabel
Citations per year, relative to Bernhard Zabel Bernhard Zabel (= 1×) peers M J Mayol

Countries citing papers authored by Bernhard Zabel

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard Zabel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Zabel

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

All Works

10 of 10 papers shown
1.
Enklaar, Thorsten, et al.. (2000). Mapping and Structure of DMXL1, a Human Homologue of the DmX Gene from Drosophila melanogaster Coding for a WD Repeat Protein. Genomics. 64(1). 97–101. 17 indexed citations
2.
Bahn, Andrew, Dirk Prawitt, Glen Reid, et al.. (2000). Genomic Structure and in Vivo Expression of the Human Organic Anion Transporter 1 (hOAT1) Gene. Biochemical and Biophysical Research Communications. 275(2). 623–630. 35 indexed citations
3.
Friedt, Michael, Patrick Gerner, Ekkehart Lausch, et al.. (1999). Mutations in the Basic Core Promotor and the Precore Region of Hepatitis B Virus and Their Selection in Children With Fulminant and Chronic Hepatitis B. Hepatology. 29(4). 1252–1258. 101 indexed citations
4.
Dreyer, Sandra D., Mark V. Clough, Wafaa Eyaid, et al.. (1998). Mutation Analysis of LMX1B Gene in Nail-Patella Syndrome Patients. The American Journal of Human Genetics. 63(6). 1651–1658. 117 indexed citations
5.
Dreyer, Sandra D., Mirta A. Machado, William A. Horton, et al.. (1998). Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndrome. Mammalian Genome. 9(6). 458–462. 19 indexed citations
6.
Bardeesy, Nabeel, Norma J. Nowak, Bernhard Zabel, et al.. (1994). Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations. Nature Genetics. 7(1). 91–97. 234 indexed citations
7.
Winterpacht, Andreas, et al.. (1994). Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasia. Human Molecular Genetics. 3(10). 1891–1893. 24 indexed citations
8.
Bardeesy, Nabeel, Bernhard Zabel, Klaus Schmitt, & Jerry Pelletier. (1994). WT1 Mutations Associated with Incomplete Denys-Drash Syndrome Define a Domain Predicted to Behave in a Dominant-Negative Fashion. Genomics. 21(3). 663–665. 52 indexed citations
9.
Davis, Lisa M., Bernhard Zabel, Gabriele Senger, et al.. (1991). A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus. Genomics. 10(3). 588–592. 17 indexed citations
10.
Royer‐Pokora, Brigitte, Susanne Ragg, Katherine M. Call, et al.. (1991). Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare. Genes Chromosomes and Cancer. 3(2). 89–100. 38 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026