Allyson C. Potter

2.5k total citations · 1 hit paper
16 papers, 2.0k citations indexed

About

Allyson C. Potter is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Allyson C. Potter has authored 16 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Allyson C. Potter's work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Nerve injury and regeneration (4 papers). Allyson C. Potter is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (4 papers) and Nerve injury and regeneration (4 papers). Allyson C. Potter collaborates with scholars based in United Kingdom, Australia and United States. Allyson C. Potter's co-authors include Kay E. Davies, Jonathon M. Tinsley, Anne E. Deconinck, Jill A. Rafael, Laurent Metzinger, Rosie Fisher, S. Brown, J.G. Dickson, Diana J. Watt and Judith A. Skinner and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Allyson C. Potter

16 papers receiving 2.0k citations

Hit Papers

Utrophin-Dystrophin-Deficient Mice as a Model for Duchenn... 1997 2026 2006 2016 1997 200 400 600

Peers

Allyson C. Potter
L. V. B. Nicholson United Kingdom
Jill A. Rafael United States
Jane C. Lee United States
Iain W. McKinnell United Kingdom
K. Bushby United Kingdom
Glen B. Banks United States
Joseph X. DiMario United States
David A. Hutcheson United States
L. V. B. Nicholson United Kingdom
Allyson C. Potter
Citations per year, relative to Allyson C. Potter Allyson C. Potter (= 1×) peers L. V. B. Nicholson

Countries citing papers authored by Allyson C. Potter

Since Specialization
Citations

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

Fields of papers citing papers by Allyson C. Potter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allyson C. Potter. 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 Allyson C. Potter. The network helps show where Allyson C. Potter may publish in the future.

Co-authorship network of co-authors of Allyson C. Potter

This figure shows the co-authorship network connecting the top 25 collaborators of Allyson C. Potter. A scholar is included among the top collaborators of Allyson C. Potter 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 Allyson C. Potter. Allyson C. Potter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Ravenscroft, Gianina, Connie Jackaman, Caroline A. Sewry, et al.. (2011). Actin Nemaline Myopathy Mouse Reproduces Disease, Suggests Other Actin Disease Phenotypes and Provides Cautionary Note on Muscle Transgene Expression. PLoS ONE. 6(12). e28699–e28699. 28 indexed citations
2.
Tinsley, Jonathon M., Rebecca J. Fairclough, Richard Storer, et al.. (2011). Daily Treatment with SMTC1100, a Novel Small Molecule Utrophin Upregulator, Dramatically Reduces the Dystrophic Symptoms in the mdx Mouse. PLoS ONE. 6(5). e19189–e19189. 140 indexed citations
3.
Nowak, Kristen L., Connie Jackaman, Esther Lim, et al.. (2007). T.O.3 Transgenic expression of cardiac actin rescues skeletal actin-null mice. Neuromuscular Disorders. 17(9-10). 899–899. 6 indexed citations
4.
Anderson, Kirstie N., et al.. (2004). Isolation and culture of motor neurons from the newborn mouse spinal cord. Brain Research Protocols. 12(3). 132–136. 29 indexed citations
5.
Anderson, Kirstie N., Dilair Baban, Peter L. Oliver, Allyson C. Potter, & Kay E. Davies. (2004). Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit. Neuromuscular Disorders. 14(11). 711–722. 20 indexed citations
6.
Isaacs, Adrian M., Peter L. Oliver, Emma Jones, et al.. (2003). A Mutation inAf4Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse. Journal of Neuroscience. 23(5). 1631–1637. 57 indexed citations
7.
Isaacs, Adrian M., Peter L. Oliver, Emma Jones, et al.. (2003). A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.. PubMed. 23(5). 1631–7. 57 indexed citations
8.
Potter, Allyson C., Lucie Vizor, Phillip Oliver, et al.. (2000). Evaluation of neurological mouse mutants caused by ENU mutagenesis. European Journal of Neuroscience. 12. 171–171. 9 indexed citations
9.
Perkins, Kelly J., Edward A. Burton, Allyson C. Potter, & K E Davies. (2000). Analysis of the transcriptional control of utrophin promoters as a therapeutic strategy for Duchenne muscular dystrophy (DMD).. The American Journal of Human Genetics. 67. 192–192. 1 indexed citations
10.
Potter, Allyson C., et al.. (1999). Route of transfer for small, lipid insoluble molecules from blood into cerebrospinal fluid in the developing brain. eCite Digital Repository (University of Tasmania). 1 indexed citations
11.
Rafael, Jill A., et al.. (1999). Dystrophin and utrophin do not play crucial roles in nonmuscle tissues in mice. Muscle & Nerve. 22(4). 517–519. 14 indexed citations
12.
Rafael, Jill A., Jonathon M. Tinsley, Allyson C. Potter, Anne E. Deconinck, & Kay E. Davies. (1998). Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice. Nature Genetics. 19(1). 79–82. 181 indexed citations
13.
Campbell, Louise J., Allyson C. Potter, Jaakko Ignatius, Victor Dubowitz, & Kay E. Davies. (1997). Genomic Variation and Gene Conversion in Spinal Muscular Atrophy: Implications for Disease Process and Clinical Phenotype. The American Journal of Human Genetics. 61(1). 40–50. 261 indexed citations
14.
Deconinck, Anne E., Jill A. Rafael, Judith A. Skinner, et al.. (1997). Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy. Cell. 90(4). 717–727. 603 indexed citations breakdown →
15.
Deconinck, Anne E., Allyson C. Potter, Jonathon M. Tinsley, et al.. (1997). Postsynaptic Abnormalities at the Neuromuscular Junctions of Utrophin-deficient Mice. The Journal of Cell Biology. 136(4). 883–894. 192 indexed citations
16.
Tinsley, Jonathon M., et al.. (1996). Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene. Nature. 384(6607). 349–353. 402 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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