Linda Roback

2.0k total citations
18 papers, 1.1k citations indexed

About

Linda Roback is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Linda Roback has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Immunology and 8 papers in Epidemiology. Recurrent topics in Linda Roback's work include Cytomegalovirus and herpesvirus research (8 papers), interferon and immune responses (5 papers) and Immune Response and Inflammation (4 papers). Linda Roback is often cited by papers focused on Cytomegalovirus and herpesvirus research (8 papers), interferon and immune responses (5 papers) and Immune Response and Inflammation (4 papers). Linda Roback collaborates with scholars based in United States and Italy. Linda Roback's co-authors include Edward S. Mocarski, William J. Kaiser, Lisa P. Daley‐Bauer, A. Louise McCormick, Hongyan Guo, Bruce H. Wainer, Grace M. Wynn, Shinya Omoto, Ganesh R. Talekar and Aarthi Sundararajan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Linda Roback

18 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Linda Roback United States 13 736 503 287 112 92 18 1.1k
Nathalie Bédard Canada 25 799 1.1× 382 0.8× 446 1.6× 155 1.4× 101 1.1× 44 1.6k
Magali Chemali Canada 8 447 0.6× 251 0.5× 528 1.8× 98 0.9× 81 0.9× 9 1.0k
Jelena Korać-Prlić Croatia 11 678 0.9× 231 0.5× 887 3.1× 319 2.8× 67 0.7× 15 1.5k
Meng Lin China 20 596 0.8× 407 0.8× 131 0.5× 48 0.4× 70 0.8× 33 1.1k
Yuexi Gu United States 13 649 0.9× 308 0.6× 805 2.8× 331 3.0× 29 0.3× 16 1.4k
Jingyue Jia United States 17 734 1.0× 301 0.6× 859 3.0× 387 3.5× 34 0.4× 27 1.5k
Hannah M. Jahn Germany 8 818 1.1× 713 1.4× 112 0.4× 49 0.4× 202 2.2× 8 1.3k
Daniel L. Tuttle United States 13 799 1.1× 278 0.6× 395 1.4× 222 2.0× 298 3.2× 14 1.5k
Paul W. Howard United States 17 495 0.7× 107 0.2× 223 0.8× 76 0.7× 54 0.6× 23 944
Aurore Claude‐Taupin France 13 465 0.6× 210 0.4× 533 1.9× 248 2.2× 21 0.2× 21 968

Countries citing papers authored by Linda Roback

Since Specialization
Citations

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

Fields of papers citing papers by Linda Roback

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linda Roback

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

All Works

18 of 18 papers shown
1.
Relation, Theresa, Joseph Stanek, Adam J. Guess, et al.. (2021). Splenic macrophage phagocytosis of intravenously infused mesenchymal stromal cells attenuates tumor localization. Cytotherapy. 23(5). 411–422. 5 indexed citations
2.
Mandal, Pratyusha, Liliana Hernández, A. Louise McCormick, et al.. (2021). Multiple Autonomous Cell Death Suppression Strategies Ensure Cytomegalovirus Fitness. Viruses. 13(9). 1707–1707. 9 indexed citations
3.
Feng, Yanjun, Lisa P. Daley‐Bauer, Linda Roback, et al.. (2019). Caspase-8 restricts natural killer cell accumulation during MCMV Infection. Medical Microbiology and Immunology. 208(3-4). 543–554. 7 indexed citations
4.
Feng, Yanjun, Lisa P. Daley‐Bauer, Linda Roback, et al.. (2019). Caspase-8 restricts antiviral CD8 T cell hyperaccumulation. Proceedings of the National Academy of Sciences. 116(30). 15170–15177. 21 indexed citations
5.
Ali, Mohammad, Linda Roback, & Edward S. Mocarski. (2018). Herpes simplex virus 1 ICP6 impedes TNF receptor 1–induced necrosome assembly during compartmentalization to detergent-resistant membrane vesicles. Journal of Biological Chemistry. 294(3). 991–1004. 14 indexed citations
6.
Feng, Yanjun, Devon Livingston‐Rosanoff, Linda Roback, et al.. (2018). Remarkably Robust Antiviral Immune Response despite Combined Deficiency in Caspase-8 and RIPK3. The Journal of Immunology. 201(8). 2244–2255. 9 indexed citations
7.
Daley‐Bauer, Lisa P., Linda Roback, A. Louise McCormick, et al.. (2017). Mouse cytomegalovirus M36 and M45 death suppressors cooperate to prevent inflammation resulting from antiviral programmed cell death pathways. Proceedings of the National Academy of Sciences. 114(13). E2786–E2795. 48 indexed citations
8.
Omoto, Shinya, Hongyan Guo, Ganesh R. Talekar, et al.. (2015). Suppression of RIP3-dependent Necroptosis by Human Cytomegalovirus. Journal of Biological Chemistry. 290(18). 11635–11648. 117 indexed citations
9.
Kang, Seokwon, Teresa Fernandes‐Alnemri, Corey Rogers, et al.. (2015). Caspase-8 scaffolding function and MLKL regulate NLRP3 inflammasome activation downstream of TLR3. Nature Communications. 6(1). 7515–7515. 214 indexed citations
10.
Kaiser, William J., Lisa P. Daley‐Bauer, Roshan J. Thapa, et al.. (2014). RIP1 suppresses innate immune necrotic as well as apoptotic cell death during mammalian parturition. Proceedings of the National Academy of Sciences. 111(21). 7753–7758. 233 indexed citations
11.
Daley‐Bauer, Lisa P., Linda Roback, Grace M. Wynn, & Edward S. Mocarski. (2014). Cytomegalovirus Hijacks CX3CR1hi Patrolling Monocytes as Immune-Privileged Vehicles for Dissemination in Mice. Cell Host & Microbe. 15(3). 351–362. 80 indexed citations
12.
McCormick, A. Louise, Linda Roback, Grace M. Wynn, & Edward S. Mocarski. (2012). Multiplicity-dependent activation of a serine protease-dependent cytomegalovirus-associated programmed cell death pathway. Virology. 435(2). 250–257. 14 indexed citations
14.
McCormick, A. Louise, Linda Roback, & Edward S. Mocarski. (2008). HtrA2/Omi Terminates Cytomegalovirus Infection and Is Controlled by the Viral Mitochondrial Inhibitor of Apoptosis (vMIA). PLoS Pathogens. 4(5). e1000063–e1000063. 45 indexed citations
15.
Weisenhorn, Daniela M. Vogt, Linda Roback, John H. Kwon, & Bruce H. Wainer. (2001). Coupling of cAMP/PKA and MAPK Signaling in Neuronal Cells Is Dependent on Developmental Stage. Experimental Neurology. 169(1). 44–55. 28 indexed citations
16.
Boss, Valerie, John D. Roback, Andrew N. Young, et al.. (2001). Nerve Growth Factor, But Not Epidermal Growth Factor, Increases Fra-2 Expression and Alters Fra-2/JunD Binding to AP-1 and CREB Binding Elements in Pheochromocytoma (PC12) Cells. Journal of Neuroscience. 21(1). 18–26. 38 indexed citations
17.
Kwon, John H., Daniela M. Vogt Weisenhorn, Martha Downen, et al.. (1998). β‐adrenergic and fibroblast growth factor receptors induce neuronal process outgrowth through different mechanisms. European Journal of Neuroscience. 10(9). 2776–2789. 11 indexed citations
18.
Edelmann, Winfried, Mark Zervas, Patrick Costello, et al.. (1996). Neuronal abnormalities in microtubule-associated protein 1B mutant mice.. Proceedings of the National Academy of Sciences. 93(3). 1270–1275. 134 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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