Siân E. Piret

1.2k total citations
28 papers, 570 citations indexed

About

Siân E. Piret is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Siân E. Piret has authored 28 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Nephrology and 8 papers in Genetics. Recurrent topics in Siân E. Piret's work include Genetic Syndromes and Imprinting (6 papers), Parathyroid Disorders and Treatments (6 papers) and Erythrocyte Function and Pathophysiology (5 papers). Siân E. Piret is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Parathyroid Disorders and Treatments (6 papers) and Erythrocyte Function and Pathophysiology (5 papers). Siân E. Piret collaborates with scholars based in United Kingdom, United States and Australia. Siân E. Piret's co-authors include Rajesh V. Thakker, Sandeep K. Mallipattu, Caroline M. Gorvin, M. Andrew Nesbit, Roger Cox, Yiqing Guo, John Cijiang He, Mónica P. Revelo, Peter Kotanko and Karl Lhotta and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Siân E. Piret

24 papers receiving 565 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Siân E. Piret United Kingdom 14 277 234 103 89 64 28 570
Beata S. Lipska‐Ziętkiewicz Poland 13 254 0.9× 205 0.9× 138 1.3× 76 0.9× 73 1.1× 41 538
M. Mengel Germany 11 336 1.2× 328 1.4× 64 0.6× 104 1.2× 47 0.7× 20 810
Éva Dizin Switzerland 15 446 1.6× 150 0.6× 115 1.1× 88 1.0× 70 1.1× 19 768
Silvia Berra Italy 10 178 0.6× 229 1.0× 52 0.5× 56 0.6× 39 0.6× 21 529
Ziyuan Ma United States 13 501 1.8× 285 1.2× 91 0.9× 129 1.4× 23 0.4× 24 873
China Nagano Japan 15 361 1.3× 161 0.7× 154 1.5× 87 1.0× 63 1.0× 79 630
Nicola Wanner Germany 16 515 1.9× 495 2.1× 163 1.6× 112 1.3× 89 1.4× 25 1.0k
Ling Hou China 14 344 1.2× 89 0.4× 100 1.0× 83 0.9× 43 0.7× 69 736
Yoichiro Ikeda Japan 11 266 1.0× 145 0.6× 81 0.8× 38 0.4× 39 0.6× 22 599
Mato Nagel Germany 13 278 1.0× 230 1.0× 121 1.2× 62 0.7× 38 0.6× 41 707

Countries citing papers authored by Siân E. Piret

Since Specialization
Citations

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

Fields of papers citing papers by Siân E. Piret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Siân E. Piret. 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 Siân E. Piret. The network helps show where Siân E. Piret may publish in the future.

Co-authorship network of co-authors of Siân E. Piret

This figure shows the co-authorship network connecting the top 25 collaborators of Siân E. Piret. A scholar is included among the top collaborators of Siân E. Piret 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 Siân E. Piret. Siân E. Piret 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
1.
Piret, Siân E., et al.. (2025). Krüppel-Like Factor 6 Induces RNA Polymerase II Subunit RPB1 to Promote Kidney Injury. Journal of the American Society of Nephrology. 36(10). 1914–1927.
2.
DiMartino, Stephen J., Mónica P. Revelo, Sandeep K. Mallipattu, & Siân E. Piret. (2024). Activation of branched chain amino acid catabolism protects against nephrotoxic acute kidney injury. American Journal of Physiology-Renal Physiology. 328(1). F152–F163.
3.
Piret, Siân E.. (2023). Roles of Krüppel-Like Transcription Factors KLF6 and KLF15 in Proximal Tubular Metabolism. ˜The œNephron journals/Nephron journals. 147(12). 766–768. 1 indexed citations
4.
Piret, Siân E., Sobia Khan, Chang Kyung Kim, et al.. (2023). Endotoxemia Correlates with Kidney Function and Length of Stay in Critically Ill Patients. Blood Purification. 53(1). 30–39.
5.
Piret, Siân E. & Sandeep K. Mallipattu. (2022). Transcriptional regulation of proximal tubular metabolism in acute kidney injury. Pediatric Nephrology. 38(4). 975–986. 10 indexed citations
6.
Piret, Siân E., Yiqing Guo, Ahmed A. Attallah, et al.. (2021). Krüppel-like factor 6–mediated loss of BCAA catabolism contributes to kidney injury in mice and humans. Proceedings of the National Academy of Sciences. 118(23). 48 indexed citations
7.
Piret, Siân E., Ahmed A. Attallah, Xiangchen Gu, et al.. (2021). Loss of proximal tubular transcription factor Krüppel-like factor 15 exacerbates kidney injury through loss of fatty acid oxidation. Kidney International. 100(6). 1250–1267. 58 indexed citations
8.
Piret, Siân E. & Sandeep K. Mallipattu. (2020). Proximal Tubular Transcription Factors in Acute Kidney Injury: Recent Advances. ˜The œNephron journals/Nephron journals. 144(12). 613–615. 4 indexed citations
9.
Howles, Sarah, Fadil Hannan, Caroline M. Gorvin, et al.. (2017). Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation. JCI Insight. 2(20). 12 indexed citations
10.
Gorvin, Caroline M., Fadil Hannan, Sarah Howles, et al.. (2017). Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy. JCI Insight. 2(3). e91103–e91103. 55 indexed citations
11.
Piret, Siân E., Caroline M. Gorvin, Anne Trinh, et al.. (2016). Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation. American Journal of Medical Genetics Part A. 170(11). 2988–2992. 10 indexed citations
12.
Esapa, Christopher T., Siân E. Piret, M. Andrew Nesbit, et al.. (2016). Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway. PLoS ONE. 11(12). e0167916–e0167916. 12 indexed citations
13.
Gorvin, Caroline M., Martijn J. Wilmer, Siân E. Piret, et al.. (2013). Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients. Proceedings of the National Academy of Sciences. 110(17). 7014–7019. 67 indexed citations
14.
Loh, Nellie Y., Liz Bentley, Henrik Dimke, et al.. (2013). Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5. PLoS ONE. 8(1). e55412–e55412. 27 indexed citations
15.
Piret, Siân E., et al.. (2013). Association between Genotype and Phenotype in Uromodulin-Associated Kidney Disease. Clinical Journal of the American Society of Nephrology. 8(8). 1349–1357. 42 indexed citations
16.
Piret, Siân E., Christopher T. Esapa, Caroline M. Gorvin, et al.. (2012). A Mouse Model of Early-Onset Renal Failure Due to a Xanthine Dehydrogenase Nonsense Mutation. PLoS ONE. 7(9). e45217–e45217. 8 indexed citations
17.
Lhotta, Karl, Siân E. Piret, Reinhard Kramar, et al.. (2012). Epidemiology of Uromodulin-Associated Kidney Disease – Results from a Nation-Wide Survey. SHILAP Revista de lepidopterología. 2(1). 147–158. 20 indexed citations
18.
Piret, Siân E. & Rajesh V. Thakker. (2011). Mouse models for inherited endocrine and metabolic disorders. Journal of Endocrinology. 211(3). 211–230. 23 indexed citations
19.
Piret, Siân E., Patrick Danoy, Karin Dahan, et al.. (2010). Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21. Human Genetics. 129(1). 51–58. 21 indexed citations
20.
Bowl, Michael R., Samantha Mirczuk, I. V. Grigorieva, et al.. (2010). Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism. Human Molecular Genetics. 19(10). 2028–2038. 26 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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