Ian Smyth

7.3k total citations
80 papers, 3.1k citations indexed

About

Ian Smyth is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ian Smyth has authored 80 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Molecular Biology, 29 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ian Smyth's work include Renal and related cancers (27 papers), Hedgehog Signaling Pathway Studies (16 papers) and Birth, Development, and Health (9 papers). Ian Smyth is often cited by papers focused on Renal and related cancers (27 papers), Hedgehog Signaling Pathway Studies (16 papers) and Birth, Development, and Health (9 papers). Ian Smyth collaborates with scholars based in Australia, United States and United Kingdom. Ian Smyth's co-authors include Kieran M. Short, John F. Bertram, Carol Wicking, Brandon J. Wainwright, A. Bale, Peter Scambler, Alexander N. Combes, Tia DiTommaso, Ian J. Jackson and Fiona M. Watt and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Communications.

In The Last Decade

Ian Smyth

78 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ian Smyth Australia 32 2.1k 922 451 331 323 80 3.1k
Carol Wicking Australia 37 3.4k 1.6× 1.4k 1.6× 460 1.0× 176 0.5× 381 1.2× 78 4.1k
Gabriele Richard United States 41 3.2k 1.5× 1.6k 1.7× 1.3k 2.8× 277 0.8× 193 0.6× 90 5.2k
Gen Kondoh Japan 36 2.8k 1.3× 855 0.9× 625 1.4× 228 0.7× 563 1.7× 95 5.2k
Pleasantine Mill United Kingdom 20 2.5k 1.1× 814 0.9× 577 1.3× 105 0.3× 403 1.2× 33 3.4k
Cynthia A. Loomis United States 25 1.8k 0.8× 450 0.5× 429 1.0× 208 0.6× 218 0.7× 55 2.8k
Tom Strachan United Kingdom 36 4.2k 2.0× 1.7k 1.8× 632 1.4× 134 0.4× 185 0.6× 69 5.7k
Chia‐Yang Liu United States 49 2.3k 1.1× 773 0.8× 1.3k 2.8× 328 1.0× 427 1.3× 188 6.5k
Concepción Rodrı́guez Esteban United States 34 4.0k 1.9× 749 0.8× 361 0.8× 313 0.9× 203 0.6× 48 4.9k
Spiro Getsios United States 37 1.9k 0.9× 259 0.3× 868 1.9× 163 0.5× 389 1.2× 70 4.0k
John M. Levorse United States 29 4.2k 1.9× 1.8k 1.9× 609 1.4× 102 0.3× 481 1.5× 40 5.3k

Countries citing papers authored by Ian Smyth

Since Specialization
Citations

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

Fields of papers citing papers by Ian Smyth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ian Smyth

This figure shows the co-authorship network connecting the top 25 collaborators of Ian Smyth. A scholar is included among the top collaborators of Ian Smyth 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 Ian Smyth. Ian Smyth 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.
Hort, Yvonne, Chirag Patel, John A. Sayer, et al.. (2025). PKD1 5’UTR variants are a rare cause of disease in ADPKD and suggest a new focus for therapeutic development. European Journal of Human Genetics. 34(1). 61–69. 1 indexed citations
2.
Cottle, Denny L., Kieran M. Short, Lynelle K. Jones, et al.. (2024). Deletion of Aurora kinase A prevents the development of polycystic kidney disease in mice. Nature Communications. 15(1). 371–371. 12 indexed citations
3.
4.
Cottle, Denny L., Lynelle K. Jones, Helen Cumming, et al.. (2023). Modulating inflammation with interleukin 37 treatment ameliorates murine Autosomal Dominant Polycystic Kidney Disease. Kidney International. 105(4). 731–743. 7 indexed citations
5.
Jhala, Gaurang, Balasubramanian Krishnamurthy, Thomas C. Brodnicki, et al.. (2022). Interferons limit autoantigen-specific CD8+ T-cell expansion in the non-obese diabetic mouse. Cell Reports. 39(4). 110747–110747. 5 indexed citations
6.
Short, Kieran M. & Ian Smyth. (2020). Branching morphogenesis as a driver of renal development. The Anatomical Record. 303(10). 2578–2587. 15 indexed citations
7.
Cottle, Denny L., et al.. (2020). Topical Aminosalicylic Acid Improves Keratinocyte Differentiation in an Inducible Mouse Model of Harlequin Ichthyosis. Cell Reports Medicine. 1(8). 100129–100129. 3 indexed citations
8.
Rutledge, Elisabeth A., Riana K. Parvez, Kieran M. Short, Ian Smyth, & Andrew P. McMahon. (2019). Morphogenesis of the kidney and lung requires branch-tip directed activity of the Adamts18 metalloprotease. Developmental Biology. 454(2). 156–169. 28 indexed citations
9.
O’Brien, Lori L., Alexander N. Combes, Kieran M. Short, et al.. (2018). Wnt11 directs nephron progenitor polarity and motile behavior ultimately determining nephron endowment. eLife. 7. 45 indexed citations
10.
Lefevre, James, Kieran M. Short, Timothy O. Lamberton, et al.. (2017). Branching morphogenesis in the developing kidney is governed by rules that pattern the ureteric tree. Development. 144(23). 4377–4385. 27 indexed citations
11.
Dyson, Jennifer M., Sarah E. Conduit, Sandra J. Feeney, et al.. (2016). INPP5E regulates phosphoinositide-dependent cilia transition zone function. The Journal of Cell Biology. 216(1). 247–263. 87 indexed citations
12.
Short, Kieran M. & Ian Smyth. (2015). A morphological investigation of sexual and lateral dimorphism in the developing metanephric kidney. Scientific Reports. 5(1). 15209–15209. 4 indexed citations
13.
Liakath‐Ali, Kifayathullah, Valerie E. Vancollie, Emma Heath, et al.. (2014). Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen. Nature Communications. 5(1). 3540–3540. 44 indexed citations
14.
DiTommaso, Tia, Lynelle K. Jones, Denny L. Cottle, et al.. (2014). Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse. PLoS Genetics. 10(10). e1004705–e1004705. 20 indexed citations
15.
Short, Kieran M., Alexander N. Combes, James Lefevre, et al.. (2014). Global Quantification of Tissue Dynamics in the Developing Mouse Kidney. Developmental Cell. 29(2). 188–202. 186 indexed citations
16.
DiTommaso, Tia, Denny L. Cottle, Helen Pearson, et al.. (2014). Keratin 76 Is Required for Tight Junction Function and Maintenance of the Skin Barrier. PLoS Genetics. 10(10). e1004706–e1004706. 30 indexed citations
17.
Hokke, Stacey, James A. Armitage, Victor G. Puelles, et al.. (2013). Altered Ureteric Branching Morphogenesis and Nephron Endowment in Offspring of Diabetic and Insulin-Treated Pregnancy. PLoS ONE. 8(3). e58243–e58243. 54 indexed citations
18.
Takeda, Hikaru, Stephen Lyle, Alexander J. Lazar, et al.. (2006). Human sebaceous tumors harbor inactivating mutations in LEF1. Nature Medicine. 12(4). 395–397. 106 indexed citations
19.
Evans, Timothy, Waranya Boonchai, Susan Shanley, et al.. (2000). The spectrum ofpatched mutations in a collection of Australian basal cell carcinomas. Human Mutation. 16(1). 43–48. 20 indexed citations
20.

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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