Wouter N. Leonhard

2.2k total citations
34 papers, 1.7k citations indexed

About

Wouter N. Leonhard is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Wouter N. Leonhard has authored 34 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 27 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Wouter N. Leonhard's work include Genetic and Kidney Cyst Diseases (30 papers), Renal and related cancers (20 papers) and Genetic Syndromes and Imprinting (10 papers). Wouter N. Leonhard is often cited by papers focused on Genetic and Kidney Cyst Diseases (30 papers), Renal and related cancers (20 papers) and Genetic Syndromes and Imprinting (10 papers). Wouter N. Leonhard collaborates with scholars based in Netherlands, United States and Canada. Wouter N. Leonhard's 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 and has published in prestigious journals such as Scientific Reports, Journal of Controlled Release and Kidney International.

In The Last Decade

Wouter N. Leonhard

34 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Wouter N. Leonhard Netherlands	21	1.3k	1.2k	376	220	160	34	1.7k
Anna‐Rachel Gallagher United States	19	1.2k 0.9×	1.1k 0.9×	330 0.9×	69 0.3×	113 0.7×	29	1.5k
Katharina Hopp United States	24	1.6k 1.2×	1.4k 1.1×	505 1.3×	271 1.2×	350 2.2×	40	2.2k
Daniela A. Braun Germany	16	522 0.4×	711 0.6×	129 0.3×	287 1.3×	298 1.9×	25	1.2k
Shengqiang Yu China	16	501 0.4×	474 0.4×	218 0.6×	178 0.8×	87 0.5×	28	908
Serge Garbay France	14	353 0.3×	787 0.6×	103 0.3×	118 0.5×	132 0.8×	19	1.1k
Tomoko Horinouchi Japan	15	207 0.2×	472 0.4×	71 0.2×	217 1.0×	99 0.6×	83	804
Giacomo Quilici Italy	12	410 0.3×	448 0.4×	162 0.4×	81 0.4×	50 0.3×	24	758
Zubaida Saifudeen United States	23	210 0.2×	882 0.7×	34 0.1×	72 0.3×	219 1.4×	49	1.2k
N Livni Israel	16	213 0.2×	242 0.2×	160 0.4×	300 1.4×	53 0.3×	42	1.0k
Andrew R. Baker United States	6	453 0.3×	347 0.3×	622 1.7×	23 0.1×	40 0.3×	7	1.0k

Countries citing papers authored by Wouter N. Leonhard

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Wouter N. Leonhard

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

All Works

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20 of 20 papers shown

Song, Xuewen, et al.. (2023). Preclinical evaluation of tolvaptan and salsalate combination therapy in a Pkd1-mouse model. Frontiers in Molecular Biosciences. 10. 1058825–1058825. 5 indexed citations

Gastel, Maatje D.A. van, Harry van Goor, Kenneth R. Hallows, et al.. (2022). Effects of Hydrochlorothiazide and Metformin on Aquaresis and Nephroprotection by a Vasopressin V2 Receptor Antagonist in ADPKD. Clinical Journal of the American Society of Nephrology. 17(4). 507–517. 25 indexed citations

Malas, Tareq B., Wouter N. Leonhard, Zoraide Granchi, et al.. (2019). Prioritization of novel ADPKD drug candidates from disease-stage specific gene expression profiles. EBioMedicine. 51. 102585–102585. 20 indexed citations

Leonhard, Wouter N., Xuewen Song, Ioan-Andrei Iliuta, et al.. (2019). Salsalate, but not metformin or canagliflozin, slows kidney cyst growth in an adult-onset mouse model of polycystic kidney disease. EBioMedicine. 47. 436–445. 61 indexed citations

Shi, Haili, Wouter N. Leonhard, Mies J. van Steenbergen, et al.. (2018). Folate-dactolisib conjugates for targeting tubular cells in polycystic kidneys. Journal of Controlled Release. 293. 113–125. 20 indexed citations

Leonhard, Wouter N., Caro Bos, Joost G.J. Hoenderop, et al.. (2018). Polycystin-1 dysfunction impairs electrolyte and water handling in a renal precystic mouse model for ADPKD. American Journal of Physiology-Renal Physiology. 315(3). F537–F546. 17 indexed citations

Fragiadaki, Maria, Madeleine Themanns, Barbara Maurer, et al.. (2017). STAT5 drives abnormal proliferation in autosomal dominant polycystic kidney disease. Kidney International. 91(3). 575–586. 40 indexed citations

Booij, Tijmen H., Wouter N. Leonhard, Kuan Yan, et al.. (2017). High-Throughput Phenotypic Screening of Kinase Inhibitors to Identify Drug Targets for Polycystic Kidney Disease. SLAS DISCOVERY. 22(8). 974–984. 35 indexed citations

Leonhard, Wouter N., H. Kevin Happe, & Dorien J.M. Peters. (2016). Variable Cyst Development in Autosomal Dominant Polycystic Kidney Disease: The Biologic Context. Journal of the American Society of Nephrology. 27(12). 3530–3538. 37 indexed citations

10.

Leonhard, Wouter N., Dmitri Firsov, Hassib Chehade, et al.. (2015). Urine Fetuin-A is a biomarker of autosomal dominant polycystic kidney disease progression. Journal of Translational Medicine. 13(1). 103–103. 17 indexed citations

11.

Leonhard, Wouter N., Malu Zandbergen, Kimberley Veraar, et al.. (2014). Scattered Deletion of PKD1 in Kidneys Causes a Cystic Snowball Effect and Recapitulates Polycystic Kidney Disease. Journal of the American Society of Nephrology. 26(6). 1322–1333. 62 indexed citations

12.

Happe, H. Kevin, Daniela Salvatori, Wouter N. Leonhard, et al.. (2013). Cyst expansion and regression in a mouse model of polycystic kidney disease. Kidney International. 83(6). 1099–1108. 27 indexed citations

13.

Novalić, Zlata, Wouter N. Leonhard, Gudrun E. Koehl, et al.. (2012). Dose-Dependent Effects of Sirolimus on mTOR Signaling and Polycystic Kidney Disease. Journal of the American Society of Nephrology. 23(5). 842–853. 83 indexed citations

14.

Happe, H. Kevin, Wouter N. Leonhard, Steven J. Kunnen, et al.. (2011). Altered Hippo signalling in polycystic kidney disease. The Journal of Pathology. 224(1). 133–142. 102 indexed citations

15.

Meijer, Esther, R. T. Gansevoort, Paul E. de Jong, et al.. (2011). Therapeutic potential of vasopressin V2 receptor antagonist in a mouse model for autosomal dominant polycystic kidney disease: optimal timing and dosing of the drug. Nephrology Dialysis Transplantation. 26(8). 2445–2453. 60 indexed citations

16.

Leonhard, Wouter N., Annemieke van der Wal, Lukas J.A.C. Hawinkels, et al.. (2010). Elevated TGFβ–Smad signalling in experimental Pkd1 models and human patients with polycystic kidney disease. The Journal of Pathology. 222(1). 21–31. 84 indexed citations

17.

Ohnesorg, Thomas, Stefanie Eggers, Wouter N. Leonhard, Andrew Sinclair, & Stefan J. White. (2009). Rapid high-throughput analysis of DNaseI hypersensitive sites using a modified Multiplex Ligation-dependent Probe Amplification approach. BMC Genomics. 10(1). 412–412. 6 indexed citations

18.

Happe, H. Kevin, Wouter N. Leonhard, Annemieke van der Wal, et al.. (2009). Toxic tubular injury in kidneys from Pkd1-deletion mice accelerates cystogenesis accompanied by dysregulated planar cell polarity and canonical Wnt signaling pathways. Human Molecular Genetics. 18(14). 2532–2542. 117 indexed citations

19.

Leonhard, Wouter N., Jeroen Roelfsema, Irma S Lantinga‐van Leeuwen, Martijn H. Breuning, & Dorien J.M. Peters. (2008). Quantification of Cre-mediated recombination by a novel strategy reveals a stable extra-chromosomal deletion-circle in mice. BMC Biotechnology. 8(1). 18–18. 10 indexed citations

20.

Leeuwen, Irma S Lantinga‐van, Wouter N. Leonhard, Annemieke van der Wal, et al.. (2007). Kidney-specific inactivation of the Pkd1 gene induces rapid cyst formation in developing kidneys and a slow onset of disease in adult mice. Human Molecular Genetics. 16(24). 3188–3196. 164 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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