Wouter N. Leonhard
Impact in
- Genetics top 1%
- Genetic and Kidney Cyst Diseases
- Genetic Syndromes and Imprinting
- Nephrology top 2%
- Renal Diseases and Glomerulopathies
Papers in
- Genetics 30
- Genetic and Kidney Cyst Diseases 30
- Genetic Syndromes and Imprinting 10
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- Renal and related cancers 20
- Hedgehog Signaling Pathway Studies 7
- Advanced biosensing and bioanalysis techniques 2
- CRISPR and Genetic Engineering 2
- Co-authors
- Dorien J.M. Peters (33 shared papers)Emile de Heer (12 shared papers)Martijn H. Breuning (11 shared papers)Irma S Lantinga‐van Leeuwen (7 shared papers)Annemieke van der Wal (4 shared papers)H. Kevin Happe (4 shared papers)M.H. Breuning (2 shared papers)Steven J. Kunnen (6 shared papers)
- Journals
- Journal of the American Society of Nephrology (5 papers)Human Molecular Genetics (3 papers)American Journal of Physiology-Renal Physiology (3 papers)The Journal of Pathology (2 papers)Kidney International (2 papers)
- Partner nations
- NetherlandsUnited StatesCanada
In The Last Decade
Wouter N. Leonhard
34 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 81
- Genetics 1.3k
- Nephrology 220
- Pathology and Forensic Medicine 376
- Molecular Biology 1.2k
- Cell Biology 122
Countries citing papers authored by Wouter N. Leonhard
This map shows the geographic impact of Wouter N. Leonhard'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 Wouter N. Leonhard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wouter N. Leonhard more than expected).
Fields of papers citing papers by Wouter N. Leonhard
This network shows the impact of papers produced by Wouter N. Leonhard. 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 Wouter N. Leonhard. The network helps show where Wouter N. Leonhard may publish in the future.
Co-authors
The 25 scholars most cited alongside Wouter N. Leonhard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 263 | |
| 2 | 2007 | 164 | |
| 3 | 2009 | 117 | |
| 4 | 2011 | 102 | |
| 5 | 2011 | 100 | |
| 6 | 2010 | 84 | |
| 7 | 2012 | 83 | |
| 8 | 2014 | 62 | |
| 9 | 2019 | 61 | |
| 10 | 2011 | 60 | |
| 11 | 2006 | 57 | |
| 12 | 2016 | 55 | |
| 13 | 2016 | 45 | |
| 14 | 2017 | 40 | |
| 15 | 2016 | 37 | |
| 16 | 2017 | 35 | |
| 17 | 2005 | 32 | |
| 18 | 2017 | 29 | |
| 19 | 2017 | 29 | |
| 20 | 2013 | 27 |
About Wouter N. Leonhard
Wouter N. Leonhard is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Nephrology and Urology, having authored 34 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (30 papers), Renal and related cancers (20 papers), Genetic Syndromes and Imprinting (10 papers), Hedgehog Signaling Pathway Studies (7 papers), Biomedical Research and Pathophysiology (6 papers), Renal Diseases and Glomerulopathies (4 papers), Advanced biosensing and bioanalysis techniques (2 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Genetics (1.3k citations), Nephrology (220 citations), Pathology and Forensic Medicine (376 citations), Molecular Biology (1.2k citations) and Cell Biology (122 citations). Wouter N. Leonhard has collaborated with scholars based in Netherlands, United States and Canada. Frequent co-authors include Dorien J.M. Peters, Emile de Heer, Martijn H. Breuning, Irma S Lantinga‐van Leeuwen, Annemieke van der Wal, H. Kevin Happe, M.H. Breuning, Steven J. Kunnen, Sjef Verbeek and Hans J. Baelde. Their work appears in journals such as Journal of the American Society of Nephrology, Human Molecular Genetics, American Journal of Physiology-Renal Physiology, The Journal of Pathology and Kidney International.
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.