Stephen A. Wood

5.4k total citations
85 papers, 3.5k citations indexed

About

Stephen A. Wood is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Stephen A. Wood has authored 85 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 24 papers in Genetics and 17 papers in Cell Biology. Recurrent topics in Stephen A. Wood's work include Ubiquitin and proteasome pathways (36 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Stephen A. Wood is often cited by papers focused on Ubiquitin and proteasome pathways (36 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Parkinson's Disease Mechanisms and Treatments (7 papers). Stephen A. Wood collaborates with scholars based in Australia, United States and Japan. Stephen A. Wood's co-authors include Lachlan A. Jolly, George D. Mellick, P. L. Kaye, Jozef Gécz, Wendy J. Brown, Masami Kanai‐Azuma, Mariyam Murtaza, Kozo Kaibuchi, Anna B. Auerbach and András Nagy and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Stephen A. Wood

85 papers receiving 3.5k citations

Peers

Stephen A. Wood
Egon Ogris Austria
Ryoji Yao Japan
C. James Hastie United Kingdom
Sheelagh Frame United Kingdom
Shaun M. Cowley United Kingdom
Juan A. Osés-Prieto United States
Hilary McLauchlan United Kingdom
Nicholas A. Morrice United Kingdom
Egon Ogris Austria
Stephen A. Wood
Citations per year, relative to Stephen A. Wood Stephen A. Wood (= 1×) peers Egon Ogris

Countries citing papers authored by Stephen A. Wood

Since Specialization
Citations

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

Fields of papers citing papers by Stephen A. Wood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen A. Wood. 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 Stephen A. Wood. The network helps show where Stephen A. Wood may publish in the future.

Co-authorship network of co-authors of Stephen A. Wood

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen A. Wood. A scholar is included among the top collaborators of Stephen A. Wood 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 Stephen A. Wood. Stephen A. Wood 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.
Pierens, Gregory K., Linlin Ma, Des R. Richardson, et al.. (2022). Meeting the Challenge 2: Identification of Potential Chemical Probes for Parkinson’s Disease from Ligusticum chuanxiong Hort Using Cytological Profiling. ACS Chemical Neuroscience. 13(17). 2565–2578. 6 indexed citations
2.
Murakami, Kiichi, Andrew Elia, Yukiko Shibahara, et al.. (2021). Therapeutic inhibition of USP9x-mediated Notch signaling in triple-negative breast cancer. Proceedings of the National Academy of Sciences. 118(38). 49 indexed citations
3.
Bentley, Steven R., Suliman Khan, Javed Fowdar, et al.. (2020). Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism. Frontiers in Neurology. 11. 331–331. 4 indexed citations
4.
Khan, Omar M., Joana Carvalho, Bradley Spencer‐Dene, et al.. (2018). The deubiquitinase USP9X regulates FBW7 stability and suppresses colorectal cancer. Journal of Clinical Investigation. 128(4). 1326–1337. 87 indexed citations
5.
Rouquié, Nelly, et al.. (2017). Grb2-Mediated Recruitment of USP9X to LAT Enhances Themis Stability following Thymic Selection. The Journal of Immunology. 199(8). 2758–2766. 9 indexed citations
6.
Uchida, Aya, Hinako M. Takase, Hitomi Suzuki, et al.. (2017). Spermatogonial deubiquitinase USP9X is essential for proper spermatogenesis in mice. Reproduction. 154(2). 135–143. 23 indexed citations
7.
Murtaza, Mariyam, Nicholas Matigian, Michael Todorovic, et al.. (2016). Rotenone Susceptibility Phenotype in Olfactory Derived Patient Cells as a Model of Idiopathic Parkinson’s Disease. PLoS ONE. 11(4). e0154544–e0154544. 23 indexed citations
8.
Murtaza, Mariyam, Lachlan A. Jolly, Jozef Gécz, & Stephen A. Wood. (2015). La FAM fatale: USP9X in development and disease. Cellular and Molecular Life Sciences. 72(11). 2075–2089. 142 indexed citations
9.
Grkovic, Tanja, Rebecca H. Pouwer, Luca Gambini, et al.. (2014). NMR Fingerprints of the Drug‐like Natural‐Product Space Identify Iotrochotazine A: A Chemical Probe to Study Parkinson’s Disease. Angewandte Chemie International Edition. 53(24). 6070–6074. 58 indexed citations
10.
Follett, Jordan, Suzanne J. Norwood, Nicholas Hamilton, et al.. (2013). The Vps35 D620N Mutation Linked to Parkinson's Disease Disrupts the Cargo Sorting Function of Retromer. Traffic. 15(2). 230–244. 176 indexed citations
11.
Stegeman, Shane, Lachlan A. Jolly, Jozef Gécz, et al.. (2013). Loss of Usp9x Disrupts Cortical Architecture, Hippocampal Development and TGFβ-Mediated Axonogenesis. PLoS ONE. 8(7). e68287–e68287. 62 indexed citations
12.
Osmond-McLeod, Megan J., Ronald I. W. Osmond, Yalchin Oytam, et al.. (2013). Surface coatings of ZnO nanoparticles mitigate differentially a host of transcriptional, protein and signalling responses in primary human olfactory cells. Particle and Fibre Toxicology. 10(1). 54–54. 30 indexed citations
13.
Jolly, Lachlan A., Verdon Taylor, & Stephen A. Wood. (2009). USP9X Enhances the Polarity and Self-Renewal of Embryonic Stem Cell-derived Neural Progenitors. Molecular Biology of the Cell. 20(7). 2015–2029. 48 indexed citations
14.
Tucker, Ben, et al.. (2007). Evolutionary and Expression Analysis of the Zebrafish Deubiquitylating Enzyme, Usp9. Zebrafish. 4(2). 95–101. 11 indexed citations
15.
Murray, Rachael Z., Lachlan A. Jolly, & Stephen A. Wood. (2004). The FAM Deubiquitylating Enzyme Localizes to Multiple Points of Protein Trafficking in Epithelia, where It Associates with E-cadherin and β-catenin. Molecular Biology of the Cell. 15(4). 1591–1599. 69 indexed citations
16.
Kanai, Yoshiakira, Masami Kanai‐Azuma, Maki Ishii, et al.. (2002). Stage- and sex-dependent expressions of Usp9x, an X-linked mouse ortholog of Drosophila Fat facets, during gonadal development and oogenesis in mice. Mechanisms of Development. 119. S91–S95. 24 indexed citations
17.
Pantaleon, Marie, Masami Kanai‐Azuma, John S. Mattick, et al.. (2001). FAM deubiquitylating enzyme is essential for preimplantation mouse embryo development. Mechanisms of Development. 109(2). 151–160. 49 indexed citations
18.
Hargrave, Murray, Asanka Karunaratne, Liza L. Cox, et al.. (2000). The HMG Box Transcription Factor Gene Sox14 Marks a Novel Subset of Ventral Interneurons and Is Regulated by Sonic Hedgehog. Developmental Biology. 219(1). 142–153. 50 indexed citations
19.
Wood, Stephen A., Wendy S. Pascoe, Kelin Ru, et al.. (1997). Cloning and expression analysis of a novel mouse gene with sequence similarity to the Drosophila fat facets gene. Mechanisms of Development. 63(1). 29–38. 74 indexed citations
20.
Sedgwick, Jonathon D., et al.. (1995). Gene knock-out technology: a methodological overview for the interested novice. Journal of Immunological Methods. 181(1). 1–15. 58 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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