Verena Klämbt

642 total citations
9 papers, 143 citations indexed

About

Verena Klämbt is a scholar working on Nephrology, Molecular Biology and Genetics. According to data from OpenAlex, Verena Klämbt has authored 9 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Nephrology, 3 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Verena Klämbt's work include Renal Diseases and Glomerulopathies (5 papers), Renal and related cancers (3 papers) and Adenosine and Purinergic Signaling (2 papers). Verena Klämbt is often cited by papers focused on Renal Diseases and Glomerulopathies (5 papers), Renal and related cancers (3 papers) and Adenosine and Purinergic Signaling (2 papers). Verena Klämbt collaborates with scholars based in Germany, United States and Saudi Arabia. Verena Klämbt's co-authors include Jacqueline A. Valeri, Francisco M. Marty, Isadora T. Lape, Michael M. Kaminski, Leonardo V. Riella, James J. Collins, Enver Akalin, Jamil Azzi, Miguel A. Alcantar and Jan Hülsdünker and has published in prestigious journals such as The Journal of Immunology, American Journal of Physiology-Cell Physiology and Molecular Therapy.

In The Last Decade

Verena Klämbt

6 papers receiving 141 citations

Peers

Verena Klämbt

MB

IMMUN

BE

HEMAT

ID

Senthil Velan Bhoopalan United States

Lisa Baldwin Switzerland

Sydney Stein United States

Lloyd D. W. King United Kingdom

Ian Bilmon Australia

Marti Cabanes‐Creus Australia

Sabrina Bouyer France

Priyanka Kambli India

Stella Hermann Germany

Andy Roemhild Germany

Senthil Velan Bhoopalan United States

Verena Klämbt

134 ×1.7

MB

21 ×0.7

IMMUN

6 ×0.2

BE

50 ×2.2

HEMAT

16 ×0.7

ID

Citations per year, relative to Verena Klämbt Verena Klämbt (= 1×) peers Senthil Velan Bhoopalan

Countries citing papers authored by Verena Klämbt

Since Specialization

Citations

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

Fields of papers citing papers by Verena Klämbt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Verena Klämbt

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

All Works

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9 of 9 papers shown

1.

Gellermann, Jutta, Johannes Holle, Caroline Kempf, et al.. (2025). Outcomes and prognostic factors in childhood-onset steroid-resistant nephrotic syndrome: a retrospective single-center study. Pediatric Nephrology. 40(7). 2239–2252.

2.

Yılmaz, Duygu Elif, Ria Schönauer, Kai‐Uwe Eckardt, et al.. (2025). In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney disease. Molecular Therapy. 33(11). 5373–5382.

3.

Shang, Lin, et al.. (2024). Ciliopathy organoid models: a comprehensive review. American Journal of Physiology-Cell Physiology. 327(6). C1604–C1625. 2 indexed citations

4.

Klämbt, Verena, Charlotte Gimpel, Martin Bald, et al.. (2020). Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis. Pediatric Nephrology. 36(2). 463–471. 4 indexed citations

5.

Klämbt, Verena, Ronen Schneider, Florian Buerger, et al.. (2020). Generation of Monogenic Candidate Genes for Human Nephrotic Syndrome Using 3 Independent Approaches. Kidney International Reports. 6(2). 460–471. 2 indexed citations

6.

Kaminski, Michael M., Miguel A. Alcantar, Isadora T. Lape, et al.. (2020). A CRISPR-based assay for the detection of opportunistic infections post-transplantation and for the monitoring of transplant rejection. Nature Biomedical Engineering. 4(6). 601–609. 89 indexed citations

7.

Klämbt, Verena, Max Werth, Thomas M. Kitzler, et al.. (2020). Mutations in transcription factor CP2-like 1 may cause a novel syndrome with distal renal tubulopathy in humans. Nephrology Dialysis Transplantation. 36(2). 237–246.

8.

Klämbt, Verena, Marcus Panning, Maximilian Seidl, Karsten Häffner, & Martin Pöhl. (2018). Ribavirin therapy of hepatitis E infection may cause hyporegenerative anemia in pediatric renal transplant patients. Pediatric Transplantation. 22(4). e13195–e13195. 4 indexed citations

9.

Klämbt, Verena, Sebastian A. Wohlfeil, Jan Hülsdünker, et al.. (2015). A Novel Function for P2Y2 in Myeloid Recipient–Derived Cells during Graft-versus-Host Disease. The Journal of Immunology. 195(12). 5795–5804. 42 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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