Jodie P. Simard

653 total citations
8 papers, 484 citations indexed

About

Jodie P. Simard is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine. According to data from OpenAlex, Jodie P. Simard has authored 8 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Jodie P. Simard's work include Genetic Neurodegenerative Diseases (5 papers), DNA Repair Mechanisms (4 papers) and Mitochondrial Function and Pathology (4 papers). Jodie P. Simard is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), DNA Repair Mechanisms (4 papers) and Mitochondrial Function and Pathology (4 papers). Jodie P. Simard collaborates with scholars based in Canada, United Kingdom and United States. Jodie P. Simard's co-authors include Christopher E. Pearson, Meghan M. Slean, Gagan B. Panigrahi, Stéphanie Tomé, O. Gileadi, Pierre Hilven, Patrick Haentjens, Meera Swami, Anna Seriola and Peggy Shelbourne and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Cell Science.

In The Last Decade

Jodie P. Simard

8 papers receiving 481 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jodie P. Simard Canada 8 444 306 69 63 47 8 484
Stéphanie Tomé France 11 534 1.2× 416 1.4× 93 1.3× 53 0.8× 91 1.9× 17 591
Edith Lopez United States 7 579 1.3× 506 1.7× 76 1.1× 39 0.6× 147 3.1× 8 681
Sherman Ku United States 6 314 0.7× 168 0.5× 53 0.8× 13 0.2× 19 0.4× 8 337
Holly A. Hung United States 9 255 0.6× 210 0.7× 38 0.6× 12 0.2× 33 0.7× 10 447
Beatriz Llamusí Spain 15 590 1.3× 455 1.5× 18 0.3× 24 0.4× 76 1.6× 33 691
Ryan W. O’Meara Canada 10 177 0.4× 99 0.3× 53 0.8× 33 0.5× 20 0.4× 11 354
Saïd Ghandour France 9 264 0.6× 114 0.4× 34 0.5× 30 0.5× 18 0.4× 12 420
Mateusz de Mezer Poland 8 505 1.1× 304 1.0× 69 1.0× 9 0.1× 39 0.8× 20 630
Kyriaki Markoullis Cyprus 9 219 0.5× 119 0.4× 43 0.6× 62 1.0× 54 1.1× 11 375
Adrianne Kolpak United States 7 260 0.6× 124 0.4× 53 0.8× 35 0.6× 24 0.5× 7 432

Countries citing papers authored by Jodie P. Simard

Since Specialization
Citations

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

Fields of papers citing papers by Jodie P. Simard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jodie P. Simard. 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 Jodie P. Simard. The network helps show where Jodie P. Simard may publish in the future.

Co-authorship network of co-authors of Jodie P. Simard

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

All Works

8 of 8 papers shown
1.
Tomé, Stéphanie, Kevin Manley, Jodie P. Simard, et al.. (2013). MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice. PLoS Genetics. 9(2). e1003280–e1003280. 109 indexed citations
2.
Tomé, Stéphanie, Jodie P. Simard, Randell T. Libby, et al.. (2013). Expression levels of DNA replication and repair genes predict regional somatic repeat instability in the brain but are not altered by polyglutamine disease protein expression or age. Human Molecular Genetics. 23(6). 1606–1618. 41 indexed citations
3.
Hick, Aurore, Marie Wattenhofer‐Donzé, Satyan Chintawar, et al.. (2012). Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia. Disease Models & Mechanisms. 6(3). 608–21. 120 indexed citations
4.
Tomé, Stéphanie, Jodie P. Simard, Meghan M. Slean, et al.. (2012). Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues. DNA repair. 12(1). 46–52. 28 indexed citations
5.
Panigrahi, Gagan B., Meghan M. Slean, Jodie P. Simard, & Christopher E. Pearson. (2012). Human Mismatch Repair Protein hMutLα Is Required to Repair Short Slipped-DNAs of Trinucleotide Repeats. Journal of Biological Chemistry. 287(50). 41844–41850. 31 indexed citations
6.
Simard, Jodie P., et al.. (2011). Overexpression of HSP70 inhibits cofilin phosphorylation and promotes lymphocyte migration in heat-stressed cells. Journal of Cell Science. 124(14). 2367–2374. 19 indexed citations
7.
Panigrahi, Gagan B., Meghan M. Slean, Jodie P. Simard, O. Gileadi, & Christopher E. Pearson. (2010). Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSβ, but clustered slip-outs are poorly repaired. Proceedings of the National Academy of Sciences. 107(28). 12593–12598. 66 indexed citations
8.
Seriola, Anna, Claudia Spits, Jodie P. Simard, et al.. (2010). Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiation. Human Molecular Genetics. 20(1). 176–185. 70 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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