Siân E. Piret

1.2k citations

28 papers · 593 · h-index 14

Impact in

Nephrology top 2%
- Parathyroid Disorders and Treatments
- Renal Diseases and Glomerulopathies
- Chronic Kidney Disease and Diabetes
Molecular Biology
- Renal and related cancers
- Ion Transport and Channel Regulation

Papers in

Molecular Biology 18
- Kruppel-like factors research 5
- Congenital heart defects research 3
- Renal and related cancers 3
Nephrology 9
- Parathyroid Disorders and Treatments 5
- Gout, Hyperuricemia, Uric Acid 2

Co-authors: Rajesh V. Thakker (19 shared papers)Sandeep K. Mallipattu (8 shared papers)Caroline M. Gorvin (7 shared papers)M. Andrew Nesbit (9 shared papers)Mónica P. Revelo (5 shared papers)Roger Cox (7 shared papers)Yiqing Guo (3 shared papers)John Cijiang He (3 shared papers)
Journals: PLoS ONE (3 papers)JCI Insight (2 papers)Proceedings of the National Academy of Sciences (2 papers)Endocrine Connections (2 papers)The Nephron journals/Nephron journals (2 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

Siân E. Piret

27 papers receiving 588 citations

Peers

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-authors

The 25 scholars most cited alongside Siân E. Piret, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Siân E. Piret Line = papers co-authored together Siân E. Piret links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Receptor-mediated endocytosis and endosomal acidification is impaired in proximal tubule epithelial cells of Dent disease patients Proceedings of the National Academy of Sciences ·Caroline M. Gorvin, Martijn J. Wilmer, Siân E. Piret, Brian Harding, Lambertus P. van den Heuvel, Oliver Wrong, Parmjit Jat, Jonathan D. Lippiat, Elena Levtchenko, Rajesh V. Thakker	2013	67
2	Loss of proximal tubular transcription factor Krüppel-like factor 15 exacerbates kidney injury through loss of fatty acid oxidation Kidney International ·Siân E. Piret, Ahmed A. Attallah, Xiangchen Gu, Yiqing Guo, Nehaben A. Gujarati, Justina Henein, Amy Zollman, Takashi Hato, Avi Ma’ayan, Mónica P. Revelo, Kathleen G. Dickman, Chung‐Hsin Chen, Chia‐Tung Shun, Thomas A. Rosenquist, John Cijiang He, Sandeep K. Mallipattu	2021	65
3	Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy JCI Insight ·Caroline M. Gorvin, Fadil Hannan, Sarah Howles, Valerie Babinsky, Siân E. Piret, Angela Rogers, Andrew Freidin, Michelle Stewart, Anju Paudyal, Tertius Hough, M. Andrew Nesbit, Sara Wells, Tonia L. Vincent, S.D.M. Brown, Roger Cox, Rajesh V. Thakker	2017	56
4	Krüppel-like factor 6–mediated loss of BCAA catabolism contributes to kidney injury in mice and humans Proceedings of the National Academy of Sciences ·Siân E. Piret, Yiqing Guo, Ahmed A. Attallah, Sylvia J. Horne, Amy Zollman, Daniel Owusu, Justina Henein, Viktoriya S. Sidorenko, Mónica P. Revelo, Takashi Hato, Avi Ma’ayan, John Cijiang He, Sandeep K. Mallipattu	2021	52
5	Association between Genotype and Phenotype in Uromodulin-Associated Kidney Disease Clinical Journal of the American Society of Nephrology ·Jonathan L. Moskowitz, Siân E. Piret, Karl Lhotta, Thomas M. Kitzler, Adam P. Tashman, Erin Velez, Rajesh V. Thakker, Peter Kotanko	2013	42
6	Podocyte-Specific Loss of Krüppel-Like Factor 6 Increases Mitochondrial Injury in Diabetic Kidney Disease Diabetes ·Sylvia J. Horne, Jessica M. Vasquez, Yiqing Guo, Victoria Ly, Siân E. Piret, (unknown), Jason Ling, Mónica P. Revelo, Daniel Bogenhagen, Vincent W. Yang, John Cijiang He, Sandeep K. Mallipattu	2018	33
7	Mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress Disease Models & Mechanisms ·Siân E. Piret, Eric Olinger, Adam J. Reed, M. Andrew Nesbit, Tertius Hough, Liz Bentley, Olivier Devuyst, Roger Cox, Rajesh V. Thakker	2017	32
8	Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5 PLoS ONE ·Nellie Y. Loh, Liz Bentley, Henrik Dimke, Sjoerd Verkaart, Paolo Tammaro, Caroline M. Gorvin, Michael Stechman, Bushra Ahmad, Fadil Hannan, Siân E. Piret, Holly Evans, Ilaria Bellantuono, Tertius Hough, William D. Fraser, Joost G.J. Hoenderop, Frances M. Ashcroft, Steve D. M. Brown, René J.M. Bindels, Roger Cox, Rajesh V. Thakker	2013	27
9	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 ·Michael R. Bowl, Samantha Mirczuk, I. V. Grigorieva, Siân E. Piret, Treena Cranston, Lorraine Southam, Jeremy Allgrove, S. Bahl, Caroline Brain, John Loughlin, Zulf Mughal, F Ryan, N. Shaw, Y Thakker, Dov Tiosano, M. Andrew Nesbit, Rajesh V. Thakker	2010	26
10	Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2) Journal of Bone and Mineral Research ·Siân E. Piret, Caroline M. Gorvin, Alistair T. Pagnamenta, Sarah Howles, Treena Cranston, Nigel Rust, M. Andrew Nesbit, Ben Glaser, Jenny C. Taylor, Andreas Buchs, Fadil Hannan, Rajesh V. Thakker	2016	25
11	Mouse models for inherited endocrine and metabolic disorders Journal of Endocrinology ·Siân E. Piret, Rajesh V. Thakker	2011	23
12	MEN1 Gene Replacement Therapy Reduces Proliferation Rates in a Mouse Model of Pituitary Adenomas Cancer Research ·Gerard Walls, Manuel C. Lemos, Mahsa Javid, Miriam Bazán‐Peregrino, Jeshmi Jeyabalan, Adam J. Reed, Brian Harding, Damian J. Tyler, Daniel J. Stuckey, Siân E. Piret, Paul T. Christie, Olaf Ansorge, Kieran Clarke, (unknown), Rajesh V. Thakker	2012	23
13	Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21 Human Genetics ·Siân E. Piret, Patrick Danoy, Karin Dahan, Adam J. Reed, Karena Pryce, William Wong, Rosa J. Torres, Juan Puig, Thomas Müller, Peter Kotanko, Karl Lhotta, Olivier Devuyst, Matthew A. Brown, Rajesh V. Thakker	2010	21
14	Epidemiology of Uromodulin-Associated Kidney Disease – Results from a Nation-Wide Survey PubMed ·Karl Lhotta, Siân E. Piret, Reinhard Kramar, Rajesh V. Thakker, Gere Sunder–Plassmann, Peter Kotanko	2012	20
15	Transcriptional regulation of proximal tubular metabolism in acute kidney injury Pediatric Nephrology ·Siân E. Piret, Sandeep K. Mallipattu	2022	13
16	Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation JCI Insight ·Sarah Howles, Fadil Hannan, Caroline M. Gorvin, Siân E. Piret, Anju Paudyal, Michelle Stewart, Tertius Hough, M. Andrew Nesbit, Sara Wells, S.D.M. Brown, Roger Cox, Rajesh V. Thakker	2017	12
17	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 ·Christopher T. Esapa, Siân E. Piret, M. Andrew Nesbit, Nellie Y. Loh, Gethin Thomas, Peter I. Croucher, Matthew A. Brown, Steve D. M. Brown, Roger Cox, Rajesh V. Thakker	2016	12
18	Autosomal dominant osteopetrosis associated with renal tubular acidosis is due to a CLCN7 mutation American Journal of Medical Genetics Part A ·Siân E. Piret, Caroline M. Gorvin, Anne Trinh, John Taylor, Stefano Lise, Jenny C. Taylor, Peter R. Ebeling, Rajesh V. Thakker	2016	11
19	A Mouse Model of Early-Onset Renal Failure Due to a Xanthine Dehydrogenase Nonsense Mutation PLoS ONE ·Siân E. Piret, Christopher T. Esapa, Caroline M. Gorvin, Rosie Head, Nellie Y. Loh, Olivier Devuyst, Gethin Thomas, Steve D. M. Brown, Matthew A. Brown, Peter I. Croucher, Roger Cox, Rajesh V. Thakker	2012	9
20	Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism Endocrine Connections ·Katherine U. Gaynor, I. V. Grigorieva, Samantha Mirczuk, Siân E. Piret, Kreepa Kooblall, Mark Stevenson, Karine Rizzoti, Michael R. Bowl, M. Andrew Nesbit, Paul T. Christie, William D. Fraser, Tertius Hough, Michael P. Whyte, Robin Lovell‐Badge, Rajesh V. Thakker	2020	6

About Siân E. Piret

Siân E. Piret is a scholar working on Molecular Biology, Nephrology, Genetics, Physiology and Surgery, having authored 28 papers that have together received 593 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (6 papers), Kruppel-like factors research (5 papers), Erythrocyte Function and Pathophysiology (5 papers), Parathyroid Disorders and Treatments (5 papers), Congenital heart defects research (3 papers), Renal and related cancers (3 papers), Metabolism and Genetic Disorders (2 papers) and Gout, Hyperuricemia, Uric Acid (2 papers). The work is most often cited by research in Nephrology (214 citations), Molecular Biology (253 citations), Pathology and Forensic Medicine (58 citations), Clinical Biochemistry (22 citations) and Genetics (92 citations). Siân E. Piret has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Rajesh V. Thakker, Sandeep K. Mallipattu, Caroline M. Gorvin, M. Andrew Nesbit, Mónica P. Revelo, Roger Cox, Yiqing Guo, John Cijiang He, Peter Kotanko and Tertius Hough. Their work appears in journals such as PLoS ONE, JCI Insight, Proceedings of the National Academy of Sciences, Endocrine Connections and The Nephron journals/Nephron journals.

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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Siân E. Piret

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