Petr Vyleťal

1.4k total citations
10 papers, 312 citations indexed

About

Petr Vyleťal is a scholar working on Molecular Biology, Nephrology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Petr Vyleťal has authored 10 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Nephrology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Petr Vyleťal's work include Ion Transport and Channel Regulation (7 papers), Kidney Stones and Urolithiasis Treatments (4 papers) and Pediatric Urology and Nephrology Studies (3 papers). Petr Vyleťal is often cited by papers focused on Ion Transport and Channel Regulation (7 papers), Kidney Stones and Urolithiasis Treatments (4 papers) and Pediatric Urology and Nephrology Studies (3 papers). Petr Vyleťal collaborates with scholars based in Czechia, United States and United Kingdom. Petr Vyleťal's co-authors include Stanislav Kmoch, Anthony J. Bleyer, Helena Hůlková, Blanka Stibůrková, Kateřina Hodaňová, M. Elleder, Jacek Majewski, Gopalakrishnan Venkat‐Raman, Jakub Sikora and J Živný and has published in prestigious journals such as Kidney International, Clinica Chimica Acta and European Journal of Human Genetics.

In The Last Decade

Petr Vyleťal

10 papers receiving 306 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Petr Vyleťal Czechia 9 184 152 94 64 40 10 312
Martina Živná Czechia 9 127 0.7× 101 0.7× 49 0.5× 30 0.5× 46 1.1× 16 216
Kimberley Veraar Netherlands 7 87 0.5× 126 0.8× 25 0.3× 54 0.8× 110 2.8× 9 395
Weizhen Tan United States 8 274 1.5× 190 1.3× 120 1.3× 78 1.2× 72 1.8× 12 418
Alexandru R. Constantinescu United States 7 74 0.4× 87 0.6× 42 0.4× 13 0.2× 49 1.2× 21 255
T Matsuo Japan 11 205 1.1× 101 0.7× 87 0.9× 26 0.4× 28 0.7× 22 353
Shinya Ishiko Japan 11 89 0.5× 195 1.3× 44 0.5× 16 0.3× 85 2.1× 31 343
Silvia B. Campos-Bilderback United States 9 156 0.8× 91 0.6× 24 0.3× 20 0.3× 10 0.3× 12 286
C. Cazeneuve France 10 59 0.3× 242 1.6× 156 1.7× 57 0.9× 16 0.4× 16 498
Manga Motrapu Germany 8 107 0.6× 92 0.6× 44 0.5× 14 0.2× 32 0.8× 12 259
María Helena Vaisbich Brazil 9 89 0.5× 107 0.7× 39 0.4× 69 1.1× 22 0.6× 34 282

Countries citing papers authored by Petr Vyleťal

Since Specialization
Citations

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

Fields of papers citing papers by Petr Vyleťal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petr Vyleťal

This figure shows the co-authorship network connecting the top 25 collaborators of Petr Vyleťal. A scholar is included among the top collaborators of Petr Vyleťal 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 Petr Vyleťal. Petr Vyleťal 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.
Jorge, Sofía, Kendrah Kidd, Petr Vyleťal, et al.. (2023). Bi-allelic REN Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD. Kidney International Reports. 8(5). 1112–1116. 1 indexed citations
2.
Živná, Martina, Pratiti Bhadra, Veronika Barešová, et al.. (2022). Phenylbutyrate rescues the transport defect of the Sec61α mutations V67G and T185A for renin. Life Science Alliance. 5(4). e202101150–e202101150. 10 indexed citations
3.
Jedličková, Ivana, Maxime Cadieux‐Dion, Anna Přistoupilová, et al.. (2020). Autosomal-dominant adult neuronal ceroid lipofuscinosis caused by duplication in DNAJC5 initially missed by Sanger and whole-exome sequencing. European Journal of Human Genetics. 28(6). 783–789. 11 indexed citations
4.
5.
Vyleťal, Petr, Anthony J. Bleyer, & Stanislav Kmoch. (2010). Uromodulin Biology and Pathophysiology – An Update. Kidney & Blood Pressure Research. 33(6). 456–475. 67 indexed citations
6.
Bleyer, Anthony J., Martina Živná, Helena Hůlková, et al.. (2010). Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone. Clinical Nephrology. 74(12). 411–422. 30 indexed citations
7.
Vyleťal, Petr, Helena Hůlková, Martina Živná, et al.. (2008). Abnormal expression and processing of uromodulin in Fabry disease reflects tubular cell storage alteration and is reversible by enzyme replacement therapy. Journal of Inherited Metabolic Disease. 31(4). 508–517. 24 indexed citations
8.
Vyleťal, Petr, Marie Hubálek Kalbáčová, Kateřina Hodaňová, et al.. (2006). Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome. Kidney International. 70(6). 1155–1169. 89 indexed citations
9.
Hodaňová, Kateřina, Jacek Majewski, Petr Vyleťal, et al.. (2005). Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41. Kidney International. 68(4). 1472–1482. 26 indexed citations
10.
Stibůrková, Blanka, Jacek Majewski, Kateřina Hodaňová, et al.. (2003). Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes. European Journal of Human Genetics. 11(2). 145–154. 19 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

Breakdown of academic impact, for papers by Martina Živná Breakdown of academic impact, for papers by Kimberley Veraar Breakdown of academic impact, for papers by Weizhen Tan Breakdown of academic impact, for papers by Alexandru R. Constantinescu Breakdown of academic impact, for papers by T Matsuo Breakdown of academic impact, for papers by Shinya Ishiko Breakdown of academic impact, for papers by Silvia B. Campos-Bilderback Breakdown of academic impact, for papers by C. Cazeneuve Breakdown of academic impact, for papers by Manga Motrapu Breakdown of academic impact, for papers by María Helena Vaisbich
Rankless by CCL
2026