Robert Kleta

13.6k total citations · 1 hit paper
147 papers, 5.7k citations indexed

About

Robert Kleta is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Nephrology. According to data from OpenAlex, Robert Kleta has authored 147 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 37 papers in Pathology and Forensic Medicine and 29 papers in Nephrology. Recurrent topics in Robert Kleta's work include Ion Transport and Channel Regulation (34 papers), Biomedical Research and Pathophysiology (27 papers) and Neonatal Health and Biochemistry (18 papers). Robert Kleta is often cited by papers focused on Ion Transport and Channel Regulation (34 papers), Biomedical Research and Pathophysiology (27 papers) and Neonatal Health and Biochemistry (18 papers). Robert Kleta collaborates with scholars based in United Kingdom, United States and Germany. Robert Kleta's co-authors include Detlef Böckenhauer, William A. Gahl, Horia Stanescu, Patricia A. Gonzales, Dmitry Tchapyjnikov, Trairak Pisitkun, Nam Sun Wang, Jason D. Hoffert, Mark A. Knepper and Robert A. Star and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Genetics.

In The Last Decade

Robert Kleta

145 papers receiving 5.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Large-Scale Proteomics and Phosphoproteomics of Urinary Exosomes

2008 592 citations Robert Kleta et al. Journal of the American Society of Nephrology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert Kleta United Kingdom	42	2.8k	1.2k	1.1k	863	851	147	5.7k
Francesco Emma Italy	41	2.4k 0.8×	1.5k 1.3×	2.7k 2.4×	812 0.9×	945 1.1×	184	6.3k
Detlef Böckenhauer United Kingdom	40	3.2k 1.1×	768 0.6×	1.6k 1.4×	1.2k 1.4×	572 0.7×	175	5.5k
Brigitte Kaissling Switzerland	58	5.5k 1.9×	665 0.6×	3.1k 2.7×	2.0k 2.4×	664 0.8×	133	9.0k
Brian Harding United Kingdom	46	2.8k 1.0×	300 0.3×	597 0.5×	503 0.6×	1.1k 1.3×	162	6.9k
Ralph Witzgall Germany	35	3.4k 1.2×	811 0.7×	857 0.8×	367 0.4×	373 0.4×	95	5.2k
Vincent H. Gattone United States	46	3.6k 1.3×	1.1k 0.9×	1.4k 1.3×	676 0.8×	819 1.0×	139	6.7k
Fiona E. Karet United Kingdom	36	4.7k 1.7×	318 0.3×	1.3k 1.2×	1.4k 1.6×	412 0.5×	100	6.1k
Carol Nelson‐Williams United States	33	6.8k 2.4×	451 0.4×	1.0k 0.9×	1.7k 2.0×	314 0.4×	56	10.4k
Masafumi Matsuo Japan	46	5.2k 1.8×	272 0.2×	505 0.4×	827 1.0×	1.1k 1.3×	395	8.3k
Luca Rampoldi Italy	32	1.5k 0.5×	446 0.4×	1.1k 1.0×	861 1.0×	628 0.7×	63	4.0k

Countries citing papers authored by Robert Kleta

Since Specialization

Citations

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

Fields of papers citing papers by Robert Kleta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Kleta

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Kleta. A scholar is included among the top collaborators of Robert Kleta 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 Robert Kleta. Robert Kleta 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

Voinescu, C, Monika Mozere, Giulio Genovese, et al.. (2024). A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy. Kidney International. 105(4). 791–798. 2 indexed citations

Wagner, Carsten A., Robert J. Unwin, Sergio Camilo Lopez-Garcia, et al.. (2023). The pathophysiology of distal renal tubular acidosis. Nature Reviews Nephrology. 19(6). 384–400. 34 indexed citations

Böckenhauer, Detlef & Robert Kleta. (2021). Tubulopathy meets Sherlock Holmes: biochemical fingerprinting of disorders of altered kidney tubular salt handling. Pediatric Nephrology. 36(8). 2553–2561. 11 indexed citations

Tekman, Mehmet, Sarah E. Flanagan, Lisa M. Guay‐Woodford, et al.. (2021). Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD). Molecular Genetics & Genomic Medicine. 9(12). e1674–e1674. 2 indexed citations

Downie, Mallory L., Sergio Camilo Lopez-Garcia, Robert Kleta, & Detlef Böckenhauer. (2020). Inherited Tubulopathies of the Kidney. Clinical Journal of the American Society of Nephrology. 16(4). 620–630. 38 indexed citations

McCafferty, Kieran, Ben Caplin, Paul Hockings, et al.. (2020). HEROIC: a 5-year observational cohort study aimed at identifying novel factors that drive diabetic kidney disease: rationale and study protocol. BMJ Open. 10(9). e033923–e033923. 1 indexed citations

Standing, Ariane, Ying Hong, Coro Paisán‐Ruiz, et al.. (2019). TRAP1 chaperone protein mutations and autoinflammation. Life Science Alliance. 3(2). e201900376–e201900376. 12 indexed citations

Ashton, Emma, Anne Debost‐Legrand, Valérie Benoît, et al.. (2018). Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. Kidney International. 93(4). 961–967. 67 indexed citations

Sharma, Sonia, Emma Ashton, Daniela Iancu, et al.. (2018). Long-term outcome in inherited nephrogenic diabetes insipidus. Clinical Kidney Journal. 12(2). 180–187. 16 indexed citations

10.

Walsh, Patrick R., Yincent Tse, Emma Ashton, et al.. (2017). Clinical and diagnostic features of Bartter and Gitelman syndromes. Clinical Kidney Journal. 11(3). 302–309. 42 indexed citations

11.

Enerbäck, Sven, Daniel Nilsson, Noel Edwards, et al.. (2017). Acidosis and Deafness in Patients with Recessive Mutations in FOXI1. Journal of the American Society of Nephrology. 29(3). 1041–1048. 72 indexed citations

12.

Kleta, Robert & Detlef Böckenhauer. (2017). Salt-Losing Tubulopathies in Children: What’s New, What’s Controversial?. Journal of the American Society of Nephrology. 29(3). 727–739. 50 indexed citations

13.

Standing, Ariane, Dessislava Malinova, Ying Hong, et al.. (2016). Autoinflammatory periodic fever, immunodeficiency, and thrombocytopenia (PFIT) caused by mutation in actin-regulatory gene WDR1 . The Journal of Experimental Medicine. 214(1). 59–71. 105 indexed citations

14.

Iancu, Daniela, et al.. (2016). EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10. PubMed. 4(1). e1195043–e1195043. 32 indexed citations

15.

Kari, Jameela A., et al.. (2014). The Case | Renal tubular acidosis and eye findings. Kidney International. 86(1). 217–218. 14 indexed citations

16.

Klootwijk, Enriko, Markus Reichold, Robert J. Unwin, et al.. (2014). Renal Fanconi syndrome: taking a proximal look at the nephron. Nephrology Dialysis Transplantation. 30(9). 1456–1460. 71 indexed citations

17.

Hussain, Sofia, Naomi Issler, Nicholas Lench, et al.. (2013). KCNJ10 Mutations Display Differential Sensitivity to Heteromerisation with KCNJ16. Nephron Physiology. 123(3-4). 7–14. 31 indexed citations

18.

Kleta, Robert, Enriko Klootwijk, Horia Stanescu, & Detlef Böckenhauer. (2011). Filtering the genes and sorting the glomerular filter: a new piece in the puzzle?. Nephrology Dialysis Transplantation. 26(9). 2743–2745. 1 indexed citations

19.

Kleta, Robert, et al.. (2009). EAST SYNDROME (EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS AND TUBULOPATHY) IS CAUSED BY MUTATIONS IN KCNJ10. Pediatric Nephrology. 1 indexed citations

20.

Kleta, Robert, Mauricio Arcos‐Burgos, Amanda Helip‐Wooley, et al.. (2005). Molecular basis of the Hartnup disorder. UCL Discovery (University College London). 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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