Suzanne M. Deschênes

1.6k total citations
12 papers, 1.2k citations indexed

About

Suzanne M. Deschênes is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pathology and Forensic Medicine. According to data from OpenAlex, Suzanne M. Deschênes has authored 12 papers receiving a total of 1.2k 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 3 papers in Pathology and Forensic Medicine. Recurrent topics in Suzanne M. Deschênes's work include Hereditary Neurological Disorders (5 papers), DNA Repair Mechanisms (3 papers) and Genetic factors in colorectal cancer (3 papers). Suzanne M. Deschênes is often cited by papers focused on Hereditary Neurological Disorders (5 papers), DNA Repair Mechanisms (3 papers) and Genetic factors in colorectal cancer (3 papers). Suzanne M. Deschênes collaborates with scholars based in United States and France. Suzanne M. Deschênes's co-authors include R. Michael Liskay, Sean M. Baker, Andrew B. Buermeyer, Kenneth H. Fischbeck, Steven S. Scherer, Linda S. Musil, Judy K. VanSlyke, Jennifer M. Puck, Paula S. Henthorn and T Wexler and has published in prestigious journals such as Journal of Neuroscience, Human Molecular Genetics and Annual Review of Genetics.

In The Last Decade

Suzanne M. Deschênes

12 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suzanne M. Deschênes United States 11 772 323 233 224 190 12 1.2k
Christy J. Fryer United States 13 1.4k 1.8× 127 0.4× 80 0.3× 323 1.4× 222 1.2× 15 1.7k
Catherine L. Keck United States 12 821 1.1× 75 0.2× 299 1.3× 262 1.2× 60 0.3× 20 1.3k
Stephanie Lerach United States 9 901 1.2× 348 1.1× 35 0.2× 131 0.6× 172 0.9× 13 1.5k
Ivana L. de la Serna United States 18 1.6k 2.1× 287 0.9× 44 0.2× 164 0.7× 146 0.8× 29 1.7k
Reinhard Grausenburger Austria 14 702 0.9× 60 0.2× 106 0.5× 92 0.4× 126 0.7× 25 1.1k
J. Inazawa Japan 17 892 1.2× 81 0.3× 58 0.2× 168 0.8× 128 0.7× 25 1.2k
Adrienne Brown United States 14 478 0.6× 49 0.2× 228 1.0× 66 0.3× 350 1.8× 26 977
M D Erisman United States 10 435 0.6× 226 0.7× 115 0.5× 61 0.3× 54 0.3× 14 836
Cole Ferguson United States 17 616 0.8× 59 0.2× 143 0.6× 365 1.6× 136 0.7× 28 1.3k
Sabine Endele Germany 14 701 0.9× 88 0.3× 74 0.3× 309 1.4× 74 0.4× 22 908

Countries citing papers authored by Suzanne M. Deschênes

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne M. Deschênes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suzanne M. Deschênes. 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 Suzanne M. Deschênes. The network helps show where Suzanne M. Deschênes may publish in the future.

Co-authorship network of co-authors of Suzanne M. Deschênes

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

All Works

12 of 12 papers shown
1.
Deschênes, Suzanne M., et al.. (2015). Which Came First, the Mutation or the Antibiotic?: Understanding Antibiotic Resistance Through Fluctuation Analysis. 1 indexed citations
2.
Erdeniz, Naz, et al.. (2007). Mutations affecting a putative MutLα endonuclease motif impact multiple mismatch repair functions. DNA repair. 6(10). 1463–1470. 41 indexed citations
3.
Scherer, Steven S., Linda Jo Bone, Suzanne M. Deschênes, et al.. (2007). The Role of the Gap Junction Protein Connexin32 in the Pathogenesis of X‐Linked Charcot‐Marie‐Tooth Disease. Novartis Foundation symposium. 219. 175–187. 10 indexed citations
4.
Deschênes, Suzanne M., et al.. (2006). The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair. Cancer Letters. 249(2). 148–156. 28 indexed citations
5.
VanSlyke, Judy K., Suzanne M. Deschênes, & Linda S. Musil. (2000). Intracellular Transport, Assembly, and Degradation of Wild-Type and Disease-linked Mutant Gap Junction Proteins. Molecular Biology of the Cell. 11(6). 1933–1946. 181 indexed citations
6.
Buermeyer, Andrew B., Suzanne M. Deschênes, Sean M. Baker, & R. Michael Liskay. (1999). Mammalian DNA Mismatch Repair. Annual Review of Genetics. 33(1). 533–564. 360 indexed citations
7.
Bone, Linda Jo, Suzanne M. Deschênes, Rita J. Balice‐Gordon, Kenneth H. Fischbeck, & Steven S. Scherer. (1997). Connexin32 and X-linked Charcot–Marie–Tooth Disease. Neurobiology of Disease. 4(3-4). 221–230. 110 indexed citations
8.
Deschênes, Suzanne M., et al.. (1997). Altered Trafficking of Mutant Connexin32. Journal of Neuroscience. 17(23). 9077–9084. 182 indexed citations
9.
Hoffmann, George, et al.. (1996). Mutagenicity of acridines in a reversion assay based on tetracycline resistance in plasmid pBR322 in Escherichia coli. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 351(1). 33–43. 22 indexed citations
10.
Fischbeck, Kenneth H., Suzanne M. Deschênes, Linda Jo Bone, & Steven S. Scherer. (1996). Connexin32 and X-linked Charcot-Marie-Tooth disease.. PubMed. 61. 673–7. 14 indexed citations
11.
Deschênes, Suzanne M., et al.. (1994). Comparative Mapping of Canine and Human Proximal Xq and Genetic Analysis of Canine X-Linked Severe Combined Immunodeficiency. Genomics. 23(1). 62–68. 34 indexed citations
12.
Puck, Jennifer M., Suzanne M. Deschênes, Joanne C. Porter, et al.. (1993). The interleukin-2 receptor γ chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1. Human Molecular Genetics. 2(8). 1099–1104. 213 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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