Jeffrey Robbins

31.0k total citations · 5 hit papers
272 papers, 24.0k citations indexed

About

Jeffrey Robbins is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Jeffrey Robbins has authored 272 papers receiving a total of 24.0k indexed citations (citations by other indexed papers that have themselves been cited), including 202 papers in Molecular Biology, 160 papers in Cardiology and Cardiovascular Medicine and 44 papers in Cell Biology. Recurrent topics in Jeffrey Robbins's work include Cardiomyopathy and Myosin Studies (123 papers), Cardiovascular Effects of Exercise (54 papers) and Muscle Physiology and Disorders (53 papers). Jeffrey Robbins is often cited by papers focused on Cardiomyopathy and Myosin Studies (123 papers), Cardiovascular Effects of Exercise (54 papers) and Muscle Physiology and Disorders (53 papers). Jeffrey Robbins collaborates with scholars based in United States, Australia and Germany. Jeffrey Robbins's co-authors include James Gulick, Jeffery D. Molkentin, Hanna Osińska, Timothy E. Hewett, Raisa Klevitsky, Eric N. Olson, Atsushi Sanbe, Katherine E. Yutzey, Xuejun Wang and James A. Richardson and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Jeffrey Robbins

272 papers receiving 23.7k citations

Hit Papers

A Calcineurin-Dependent Transcriptional Pathway for Cardi... 1998 2026 2007 2016 1998 2005 2016 2007 2012 500 1000 1.5k 2.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey Robbins United States 80 16.7k 11.0k 2.8k 2.7k 2.3k 272 24.0k
Seigo Izumo United States 82 15.6k 0.9× 10.4k 0.9× 1.8k 0.6× 2.0k 0.7× 3.0k 1.3× 161 24.1k
Richard P. Lifton United States 92 20.6k 1.2× 4.9k 0.4× 1.4k 0.5× 1.3k 0.5× 4.2k 1.8× 276 35.1k
Kenneth R. Chien United States 110 29.4k 1.8× 15.0k 1.4× 2.5k 0.9× 2.7k 1.0× 6.9k 3.0× 303 41.1k
Takeshi Nakano Japan 57 10.2k 0.6× 3.6k 0.3× 1.4k 0.5× 3.5k 1.3× 1.8k 0.8× 509 19.6k
Gary K. Owens United States 88 15.2k 0.9× 4.3k 0.4× 1.4k 0.5× 2.3k 0.8× 3.7k 1.6× 227 26.6k
Fumiaki Marumo Japan 89 13.4k 0.8× 7.3k 0.7× 3.6k 1.3× 859 0.3× 2.5k 1.1× 626 28.0k
Wolfgang Dillmann United States 71 9.9k 0.6× 5.2k 0.5× 961 0.3× 1.4k 0.5× 1.6k 0.7× 212 16.2k
Mark L. Entman United States 88 10.4k 0.6× 10.0k 0.9× 1.3k 0.5× 1.1k 0.4× 6.0k 2.6× 295 23.9k
Yoshio Yazaki Japan 93 17.8k 1.1× 10.2k 0.9× 1.8k 0.7× 2.9k 1.1× 4.5k 2.0× 442 35.5k
Masaaki Ito Japan 54 9.7k 0.6× 3.9k 0.4× 746 0.3× 3.9k 1.4× 1.4k 0.6× 365 16.5k

Countries citing papers authored by Jeffrey Robbins

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey Robbins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey Robbins. 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 Jeffrey Robbins. The network helps show where Jeffrey Robbins may publish in the future.

Co-authorship network of co-authors of Jeffrey Robbins

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey Robbins. A scholar is included among the top collaborators of Jeffrey Robbins 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 Jeffrey Robbins. Jeffrey Robbins 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.
Lowey, Susan, Peteranne B. Joel, Kathleen M. Trybus, et al.. (2018). Hypertrophic cardiomyopathy R403Q mutation in rabbit β-myosin reduces contractile function at the molecular and myofibrillar levels. Proceedings of the National Academy of Sciences. 115(44). 11238–11243. 24 indexed citations
2.
Meng, Qinghang, Md. Shenuarin Bhuiyan, J. Howard James, et al.. (2018). Myofibroblast-Specific TGFβ Receptor II Signaling in the Fibrotic Response to Cardiac Myosin Binding Protein C-Induced Cardiomyopathy. Circulation Research. 123(12). 1285–1297. 36 indexed citations
3.
4.
Bhuiyan, Md. Shenuarin, James Gulick, Hanna Osińska, Manish Gupta, & Jeffrey Robbins. (2012). Determination of the critical residues responsible for cardiac myosin binding protein C's interactions. Journal of Molecular and Cellular Cardiology. 53(6). 838–847. 42 indexed citations
5.
Mun, Ji Young, James Gulick, Jeffrey Robbins, et al.. (2011). Electron Microscopy and 3D Reconstruction of F-Actin Decorated with Cardiac Myosin-Binding Protein C (cMyBP-C). Journal of Molecular Biology. 410(2). 214–225. 61 indexed citations
6.
Nakamura, Tomoki, et al.. (2009). Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations. Proceedings of the National Academy of Sciences. 106(36). 15436–15441. 66 indexed citations
7.
Topkara, Veli K., Wei Wang, Feng Gao, et al.. (2009). Abstract 3731: Overlapping Patterns of Gene Expression in Experimental and Clinical Models of Myocardial Recovery. Circulation. 120(suppl_18). 1 indexed citations
8.
Sadayappan, Sakthivel, James Gulick, Lisa Martin, et al.. (2009). Abstract 3846: Hierarchical and Critical Functions of Ser282 Phosphorylation in Cardiac Myosin Binding Protein-C Phosphorylation and Cardiac Function. Circulation. 120(18). 2 indexed citations
9.
Heineke, Joerg, Kai C. Wollert, Hanna Osińska, et al.. (2009). Calcineurin protects the heart in a murine model of dilated cardiomyopathy. Journal of Molecular and Cellular Cardiology. 48(6). 1080–1087. 35 indexed citations
10.
Pattison, J. Scott, Atsushi Sanbe, Alina Maloyan, et al.. (2008). Cardiomyocyte Expression of a Polyglutamine Preamyloid Oligomer Causes Heart Failure. Circulation. 117(21). 2743–2751. 116 indexed citations
11.
Gálvez, Anita, Abhinav Diwan, Amy Odley, et al.. (2007). Cardiomyocyte Degeneration With Calpain Deficiency Reveals a Critical Role in Protein Homeostasis. Circulation Research. 100(7). 1071–1078. 109 indexed citations
12.
Maloyan, Alina, James Gulick, Charles Glabe, Rakez Kayed, & Jeffrey Robbins. (2007). Exercise reverses preamyloid oligomer and prolongs survival in αB-crystallin-based desmin-related cardiomyopathy. Proceedings of the National Academy of Sciences. 104(14). 5995–6000. 68 indexed citations
13.
Purcell, Nicole H., Benjamin J. Wilkins, Allen J. York, et al.. (2007). Genetic inhibition of cardiac ERK1/2 promotes stress-induced apoptosis and heart failure but has no effect on hypertrophy in vivo. Proceedings of the National Academy of Sciences. 104(35). 14074–14079. 197 indexed citations
14.
Wang, Hao, et al.. (2006). PKC-βII sensitizes cardiac myofilaments to Ca2+ by phosphorylating troponin I on threonine-144. Journal of Molecular and Cellular Cardiology. 41(5). 823–833. 79 indexed citations
15.
Levine, Wilton C., et al.. (2005). Usability factors in the organization and display of disparate information sources in the operative environment.. Europe PMC (PubMed Central). 1025–1025. 4 indexed citations
16.
Nakayama, Masaaki, Xinhua Yan, Robert L. Price, et al.. (2004). Chronic ventricular myocyte-specific overexpression of angiotensin II type 2 receptor results in intrinsic myocyte contractile dysfunction. American Journal of Physiology-Heart and Circulatory Physiology. 288(1). H317–H327. 23 indexed citations
17.
Sze, Raymond W., Bernard J. Dardzinski, Scott Dunn, et al.. (2001). Three-dimensional MR microscopy of a transgenic mouse model of dilated cardiomyopathy. Pediatric Radiology. 31(2). 55–61. 7 indexed citations
18.
Nelson, David P., D. Greg Hall, Steven M. Schwartz, et al.. (2000). Proinflammatory consequences of transgenic Fas ligand expression in the heart. Journal of Clinical Investigation. 105(9). 1199–1208. 73 indexed citations
19.
Parenteau, Chantal S., et al.. (1999). Seated Weight Distribution of Adults and Children in Normal and Non-Normal Positions. Europe PMC (PubMed Central). 43(3). 383–397. 6 indexed citations
20.
Gulick, James, et al.. (1995). Remodeling the mammalian heart using transgenesis.. PubMed. 41(6). 501–9. 19 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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