Mato Nagel

1.5k total citations
41 papers, 707 citations indexed

About

Mato Nagel is a scholar working on Molecular Biology, Nephrology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Mato Nagel has authored 41 papers receiving a total of 707 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Nephrology and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Mato Nagel's work include Renal and related cancers (9 papers), Cell Adhesion Molecules Research (7 papers) and Ion Transport and Channel Regulation (6 papers). Mato Nagel is often cited by papers focused on Renal and related cancers (9 papers), Cell Adhesion Molecules Research (7 papers) and Ion Transport and Channel Regulation (6 papers). Mato Nagel collaborates with scholars based in Germany, United States and Austria. Mato Nagel's co-authors include Marie Loh, Pengbo Liu, Adrian Mondry, Oliver Groß, Anja Büscher, Stefanie Weber, Peter F. Hoyer, Maik Gollasch, Elisabet Ars and Lev Shagam and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Kidney International.

In The Last Decade

Mato Nagel

36 papers receiving 682 citations

Peers

Mato Nagel
Tetsuo Morioka Japan
Marcel Blot-Chabaud France
Taku Miyoshi Japan
Samantha Moore United Kingdom
Clément E. Tagoe United States
Saori Miwa Japan
Mary Blonski United States
Jukka Tienari Finland
Masakuni Noda Japan
Mariko Fukui Japan
Tetsuo Morioka Japan
Mato Nagel
Citations per year, relative to Mato Nagel Mato Nagel (= 1×) peers Tetsuo Morioka

Countries citing papers authored by Mato Nagel

Since Specialization
Citations

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

Fields of papers citing papers by Mato Nagel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mato Nagel

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

All Works

20 of 20 papers shown
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Hoefele, Julia, Korbinian M. Riedhammer, Mato Nagel, et al.. (2022). Lifelong effect of therapy in young patients with the COL4A5 Alport missense variant p.(Gly624Asp): a prospective cohort study. Nephrology Dialysis Transplantation. 37(12). 2496–2504. 20 indexed citations
3.
Rothe, H., et al.. (2021). Epitheloides Angiomyolipom der Niere nach stattgehabtem malignem Melanom. Der Urologe. 61(2). 183–186. 1 indexed citations
4.
Schönauer, Ria, et al.. (2021). Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics. Frontiers in Genetics. 12. 682565–682565. 3 indexed citations
5.
Cicinelli, Maria Vittoria, Markus Ritter, Cybele Ghossein, et al.. (2021). THE SPECTRUM OF INTERNAL LIMITING MEMBRANE DISEASE IN ALPORT SYNDROME. Retina. 42(2). 274–282. 6 indexed citations
6.
Kettwig, Matthias, H. Zappel, Johannes Hofer, et al.. (2019). Kidney Injury by Variants in the COL4A5 Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental Glomerulosclerosis. International Journal of Molecular Sciences. 20(3). 519–519. 11 indexed citations
7.
Accogli, Andrea, Marcello Scala, Annalisa Calcagno, et al.. (2018). CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations. European Journal of Medical Genetics. 62(3). 198–203. 22 indexed citations
8.
Savige, Judy, Francesca Ariani, Francesca Mari, et al.. (2018). Expert consensus guidelines for the genetic diagnosis of Alport syndrome. Pediatric Nephrology. 34(7). 1175–1189. 85 indexed citations
9.
Savige, Judy, Helen Storey, Hae Il Cheong, et al.. (2016). X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations. PLoS ONE. 11(9). e0161802–e0161802. 63 indexed citations
10.
Zitt, Emanuel, et al.. (2016). Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will find. Wiener klinische Wochenschrift. 128(7-8). 291–294. 4 indexed citations
11.
Wołyniec, Wojciech, et al.. (2015). A case report of Gitelman syndrome resulting from two novel mutations in SLC12A3 gene. Nefrología. 36(3). 304–309. 5 indexed citations
12.
Mann, W. Alexander, Déborah Morris-Rosendahl, Mato Nagel, et al.. (2015). Mutation in the V2 vasopressin receptor gene, AVPR2, causes nephrogenic syndrome of inappropriate diuresis. Kidney International. 88(5). 1070–1078. 39 indexed citations
13.
Vester, Udo, Thurid Ahlenstiel, Ulrich Budde, et al.. (2013). Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS). Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 462(4). 455–464. 8 indexed citations
14.
Loomba‐Albrecht, Lindsey A., et al.. (2011). Familial hypomagnesemia with hypercalciuria and nephrocalcinosis in three siblings having the same genetic lesion but different clinical presentations. World Journal of Pediatrics. 8(2). 177–180. 14 indexed citations
15.
Loomba‐Albrecht, Lindsey A., Mato Nagel, & Andrew A. Bremer. (2010). Pseudohypoaldosteronism Type 1 due to a Novel Mutation in the Mineralocorticoid Receptor Gene. Hormone Research in Paediatrics. 73(6). 482–486. 4 indexed citations
16.
Hoefele, Julia, Bärbel Lange-Sperandio, Judith Glöckner-Pagel, et al.. (2010). Novel heterozygous COL4A3 mutation in a family with late-onset ESRD. Pediatric Nephrology. 25(8). 1539–1542. 11 indexed citations
17.
18.
Nagel, Mato, et al.. (2005). Novel COL4A5, COL4A4, and COL4A3 mutations in Alport syndrome. Human Mutation. 26(1). 60–60. 42 indexed citations
19.
Zumkeller, W, A. Jassoy, Simon Lebek, & Mato Nagel. (2001). Clinical, Endocrinological and Radiological Features in a Child with McCune-Albright Syndrome and Pituitary Adenoma. Journal of Pediatric Endocrinology and Metabolism. 14(5). 553–9. 11 indexed citations
20.
Nagel, Mato, et al.. (1967). [Action of 1-triiodothyronine on protein-bound iodine in the blood (PBI 127) of patients suffering from hyperthyroidism with diffuse thyroid hyperplasia].. PubMed. 28(2). 214–9. 1 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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