Marissa G. Viola

640 total citations
13 papers, 426 citations indexed

About

Marissa G. Viola is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Marissa G. Viola has authored 13 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Cell Biology. Recurrent topics in Marissa G. Viola's work include Bacterial Genetics and Biotechnology (7 papers), Cellular transport and secretion (4 papers) and Bacteriophages and microbial interactions (3 papers). Marissa G. Viola is often cited by papers focused on Bacterial Genetics and Biotechnology (7 papers), Cellular transport and secretion (4 papers) and Bacteriophages and microbial interactions (3 papers). Marissa G. Viola collaborates with scholars based in United States, France and Australia. Marissa G. Viola's co-authors include Jodi L. Camberg, Alan H. Beggs, Christopher R. Pierson, Hui Meng, Michael W. Lawlor, Pankaj B. Agrawal, Behzad Moghadaszadeh, Gianina Ravenscroft, Beril Talim and Mugdha Joshi and has published in prestigious journals such as PLoS ONE, FEBS Letters and Journal of Bacteriology.

In The Last Decade

Marissa G. Viola

12 papers receiving 419 citations

Peers

Marissa G. Viola
Akif Uzman United States
Amanda J. Wilson United Kingdom
Nagesh Pulicherla United States
Conor J Howard United States
M B LoPresti United States
Sven U. Heinrich United States
Jonathan A. Atwater United States
Akif Uzman United States
Marissa G. Viola
Citations per year, relative to Marissa G. Viola Marissa G. Viola (= 1×) peers Akif Uzman

Countries citing papers authored by Marissa G. Viola

Since Specialization
Citations

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

Fields of papers citing papers by Marissa G. Viola

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marissa G. Viola. 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 Marissa G. Viola. The network helps show where Marissa G. Viola may publish in the future.

Co-authorship network of co-authors of Marissa G. Viola

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

All Works

13 of 13 papers shown
1.
Viola, Marissa G., et al.. (2022). An enhancer sequence in the intrinsically disordered region of FtsZ promotes polymer‐guided substrate processing by ClpXP protease. Protein Science. 31(5). e4306–e4306. 4 indexed citations
2.
Eswara, Prahathees J., Robert Brzozowski, Marissa G. Viola, et al.. (2018). An essential Staphylococcus aureus cell division protein directly regulates FtsZ dynamics. eLife. 7. 45 indexed citations
3.
Viola, Marissa G., et al.. (2018). MinC N- and C-Domain Interactions Modulate FtsZ Assembly, Division Site Selection, and MinD-Dependent Oscillation in Escherichia coli. Journal of Bacteriology. 201(4). 17 indexed citations
4.
Viola, Marissa G., et al.. (2017). FtsA reshapes membrane architecture and remodels the Z‐ring in Escherichia coli. Molecular Microbiology. 107(4). 558–576. 34 indexed citations
5.
Viola, Marissa G., et al.. (2017). Proteolysis-Dependent Remodeling of the Tubulin Homolog FtsZ at the Division Septum in Escherichia coli. PLoS ONE. 12(1). e0170505–e0170505. 16 indexed citations
6.
Viola, Marissa G., et al.. (2017). The Protein Chaperone ClpX Targets Native and Non-native Aggregated Substrates for Remodeling, Disassembly, and Degradation with ClpP. Frontiers in Molecular Biosciences. 4. 26–26. 33 indexed citations
7.
Camberg, Jodi L., et al.. (2014). Location of Dual Sites in E. coli FtsZ Important for Degradation by ClpXP; One at the C-Terminus and One in the Disordered Linker. PLoS ONE. 9(4). e94964–e94964. 28 indexed citations
8.
Viola, Marissa G., et al.. (2014). The bacterial cell division regulators MinD and MinC form polymers in the presence of nucleotide. FEBS Letters. 589(2). 201–206. 21 indexed citations
9.
Agrawal, Pankaj B., Christopher R. Pierson, Mugdha Joshi, et al.. (2014). SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy. The American Journal of Human Genetics. 95(2). 218–226. 115 indexed citations
10.
Lawlor, Michael W., Marissa G. Viola, Hui Meng, et al.. (2014). Differential Muscle Hypertrophy Is Associated with Satellite Cell Numbers and Akt Pathway Activation Following Activin Type IIB Receptor Inhibition in Mtm1 p.R69C Mice. American Journal Of Pathology. 184(6). 1831–1842. 26 indexed citations
11.
Lawlor, Michael W., Dustin Armstrong, Marissa G. Viola, et al.. (2013). Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy. Human Molecular Genetics. 22(8). 1525–1538. 54 indexed citations
12.
Lawlor, Michael W., Matthew S. Alexander, Marissa G. Viola, et al.. (2012). Myotubularin-Deficient Myoblasts Display Increased Apoptosis, Delayed Proliferation, and Poor Cell Engraftment. American Journal Of Pathology. 181(3). 961–968. 33 indexed citations
13.
Agrawal, Pankaj B., Kathryn H. Schmitz, Elizabeth T. DeChene, et al.. (2012). C.O.6 Complete genetic analysis by whole exome sequencing of a cohort with centronuclear myopathy identifies titin gene mutations. Neuromuscular Disorders. 22(9-10). 840–840.

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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