Greg P. Boivin

1.5k total citations
23 papers, 1.2k citations indexed

About

Greg P. Boivin is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Biomedical Engineering. According to data from OpenAlex, Greg P. Boivin has authored 23 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Cardiology and Cardiovascular Medicine and 2 papers in Biomedical Engineering. Recurrent topics in Greg P. Boivin's work include Cardiomyopathy and Myosin Studies (16 papers), Muscle Physiology and Disorders (12 papers) and Cardiovascular Effects of Exercise (8 papers). Greg P. Boivin is often cited by papers focused on Cardiomyopathy and Myosin Studies (16 papers), Muscle Physiology and Disorders (12 papers) and Cardiovascular Effects of Exercise (8 papers). Greg P. Boivin collaborates with scholars based in United States, Belgium and Poland. Greg P. Boivin's co-authors include David F. Wieczorek, R. John Solaro, Ingrid L. Grupp, Rethinasamy Prabhakar, Grace M. Arteaga, Beata M. Wolska, Natalia Petrashevskaya, Timothy E. Hewett, Brian D. Hoit and Ganapathy Jagatheesan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

Greg P. Boivin

23 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
Greg P. Boivin United States 16 864 739 87 80 74 23 1.2k
Jasmine Healy Canada 17 709 0.8× 301 0.4× 86 1.0× 131 1.6× 38 0.5× 31 1.0k
Seda Eminaga United States 11 592 0.7× 396 0.5× 142 1.6× 86 1.1× 47 0.6× 18 909
Tie Ke China 16 704 0.8× 258 0.3× 89 1.0× 40 0.5× 62 0.8× 35 913
Kenneth W. Hewett United States 18 710 0.8× 768 1.0× 46 0.5× 60 0.8× 37 0.5× 40 1.1k
Patrick G. Burgon Canada 20 748 0.9× 418 0.6× 60 0.7× 36 0.5× 114 1.5× 36 1.2k
Po‐Hsien Chu Taiwan 11 763 0.9× 730 1.0× 26 0.3× 32 0.4× 107 1.4× 22 1.1k
Tyler L. Taigen United States 13 908 1.1× 819 1.1× 39 0.4× 110 1.4× 73 1.0× 38 1.4k
A. Subramaniam United States 6 853 1.0× 552 0.7× 40 0.5× 42 0.5× 64 0.9× 11 1.0k
Mitsuo Iwatate Japan 13 575 0.7× 600 0.8× 24 0.3× 98 1.2× 64 0.9× 18 959
Priyatansh Gurha United States 23 1.1k 1.3× 572 0.8× 353 4.1× 70 0.9× 109 1.5× 44 1.7k

Countries citing papers authored by Greg P. Boivin

Since Specialization
Citations

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

Fields of papers citing papers by Greg P. Boivin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Greg P. Boivin

This figure shows the co-authorship network connecting the top 25 collaborators of Greg P. Boivin. A scholar is included among the top collaborators of Greg P. Boivin 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 Greg P. Boivin. Greg P. Boivin 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.
Jagatheesan, Ganapathy, Sudarsan Rajan, Rafeeq Ahmed, et al.. (2010). Striated muscle tropomyosin isoforms differentially regulate cardiac performance and myofilament calcium sensitivity. Journal of Muscle Research and Cell Motility. 31(3). 227–239. 17 indexed citations
2.
Rajan, Sudarsan, Ganapathy Jagatheesan, Marco Stephan Lofrano‐Alves, et al.. (2010). Molecular and Functional Characterization of a Novel Cardiac-Specific Human Tropomyosin Isoform. Circulation. 121(3). 410–418. 73 indexed citations
3.
Bossuyt, Wouter, Avedis Kazanjian, Natalie De Geest, et al.. (2009). Atonal homolog 1 Is a Tumor Suppressor Gene. PLoS Biology. 7(2). e1000039–e1000039. 89 indexed citations
4.
Rajan, Sudarsan, Karen M. D’Souza, Shahab A. Akhter, et al.. (2009). Molecular and Functional Characterization of a Novel Cardiac Specific Human Tropomyosin Isoform. Biophysical Journal. 96(3). 224a–224a. 4 indexed citations
5.
Jagatheesan, Ganapathy, Sudarsan Rajan, Emily Schulz, et al.. (2009). An internal domain of β-tropomyosin increases myofilament Ca2+sensitivity. American Journal of Physiology-Heart and Circulatory Physiology. 297(1). H181–H190. 10 indexed citations
6.
Rajan, Sudarsan, Rafeeq Ahmed, Ganapathy Jagatheesan, et al.. (2007). Dilated Cardiomyopathy Mutant Tropomyosin Mice Develop Cardiac Dysfunction With Significantly Decreased Fractional Shortening and Myofilament Calcium Sensitivity. Circulation Research. 101(2). 205–214. 83 indexed citations
7.
Jagatheesan, Ganapathy, Sudarsan Rajan, Natalia Petrashevskaya, et al.. (2007). Rescue of tropomyosin-induced familial hypertrophic cardiomyopathy mice by transgenesis. American Journal of Physiology-Heart and Circulatory Physiology. 293(2). H949–H958. 40 indexed citations
8.
Leonis, Mike A., Arlene E. Dent, Meredith A. Olson, et al.. (2006). Short-form Ron receptor is required for normal IFN-γ production in concanavalin A-induced acute liver injury. American Journal of Physiology-Gastrointestinal and Liver Physiology. 292(1). G253–G261. 12 indexed citations
9.
Butler, David L., Natalia Juncosa‐Melvin, Greg P. Boivin, et al.. (2006). Functional Tissue Engineering to Repair Tendon & Other Musculoskeletal Tissues. Molecular & cellular biomechanics. 3(4). 127–130. 2 indexed citations
10.
Jagatheesan, Ganapathy, Sudarsan Rajan, Natalia Petrashevskaya, et al.. (2004). Physiological significance of troponin T binding domains in striated muscle tropomyosin. American Journal of Physiology-Heart and Circulatory Physiology. 287(4). H1484–H1494. 17 indexed citations
11.
Jagatheesan, Ganapathy, Sudarsan Rajan, Natalia Petrashevskaya, et al.. (2003). Functional Importance of the Carboxyl-terminal Region of Striated Muscle Tropomyosin. Journal of Biological Chemistry. 278(25). 23204–23211. 31 indexed citations
12.
Prabhakar, Rethinasamy, Natalia Petrashevskaya, Arnold Schwartz, et al.. (2003). A mouse model of familial hypertrophic cardiomyopathy caused by a α-tropomyosin mutation. Molecular and Cellular Biochemistry. 251(1-2). 33–42. 35 indexed citations
13.
Arteaga, Grace M., R. John Solaro, Ingrid L. Grupp, et al.. (2002). Tropomyosin 3 expression leads to hypercontractility and attenuates myofilament length-dependent Ca2+activation. American Journal of Physiology-Heart and Circulatory Physiology. 283(4). H1344–H1353. 49 indexed citations
14.
Prabhakar, Rethinasamy, Greg P. Boivin, Ingrid L. Grupp, et al.. (2001). A Familial Hypertrophic Cardiomyopathy α -Tropomyosin Mutation Causes Severe Cardiac Hypertrophy and Death in Mice. Journal of Molecular and Cellular Cardiology. 33(10). 1815–1828. 108 indexed citations
15.
Prabhakar, Rethinasamy, Greg P. Boivin, Brian D. Hoit, & David F. Wieczorek. (1999). Rescue of High Expression β-Tropomyosin Transgenic Mice by 5-Propyl-2-thiouracil. Journal of Biological Chemistry. 274(41). 29558–29563. 5 indexed citations
16.
Muthuchamy, Mariappan, Rethinasamy Prabhakar, Brian D. Hoit, et al.. (1999). Mouse Model of a Familial Hypertrophic Cardiomyopathy Mutation in α-Tropomyosin Manifests Cardiac Dysfunction. Circulation Research. 85(1). 47–56. 122 indexed citations
17.
Prabhakar, Rethinasamy, Mariappan Muthuchamy, Timothy E. Hewett, et al.. (1998). Molecular and Physiological Effects of α-Tropomyosin Ablation in the Mouse. Circulation Research. 82(1). 116–123. 90 indexed citations
18.
Stambrook, Peter J., Changshun Shao, Michael Stockelman, et al.. (1996). Other transgenic mutation assays:APRT: A versatile in vivo resident reporter of local mutation and loss of heterozygosity. Environmental and Molecular Mutagenesis. 28(4). 471–482. 56 indexed citations
19.
Boivin, Greg P., et al.. (1996). Eradication of Aspiculuris tetraptera, using fenbendazole-medicated food.. PubMed. 35(2). 69–70. 9 indexed citations
20.
Jones, W. Keith, Ingrid L. Grupp, Thomas Doetschman, et al.. (1996). Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart.. Journal of Clinical Investigation. 98(8). 1906–1917. 175 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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