Gregory J. LaRosa

7.3k total citations · 2 hit papers
38 papers, 6.2k citations indexed

About

Gregory J. LaRosa is a scholar working on Immunology, Molecular Biology and Oncology. According to data from OpenAlex, Gregory J. LaRosa has authored 38 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Immunology, 14 papers in Molecular Biology and 10 papers in Oncology. Recurrent topics in Gregory J. LaRosa's work include Chemokine receptors and signaling (8 papers), HIV Research and Treatment (7 papers) and Vagus Nerve Stimulation Research (7 papers). Gregory J. LaRosa is often cited by papers focused on Chemokine receptors and signaling (8 papers), HIV Research and Treatment (7 papers) and Vagus Nerve Stimulation Research (7 papers). Gregory J. LaRosa collaborates with scholars based in United States, Netherlands and United Kingdom. Gregory J. LaRosa's co-authors include Paul Ponath, Charles R. Mackay, Hyeryun Choe, Michael Farzan, Barrett J. Rollins, Nancy Sullivan, Ying Sun, Lijun Wu, Joseph Sodroski and Craig Gérard and has published in prestigious journals such as Science, Cell and Journal of Biological Chemistry.

In The Last Decade

Gregory J. LaRosa

38 papers receiving 6.0k citations

Hit Papers

The β-Chemokine Receptors CCR3 and CCR5 Facilitate Infect... 1990 2026 2002 2014 1996 1990 500 1000 1.5k

Peers

Gregory J. LaRosa
Comparison fields: 5 of 118
  • Immunology 2.8k
  • Virology 2.3k
  • Molecular Biology 1.9k
  • Oncology 1.1k
  • Infectious Diseases 978
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Citations per field, relative to Gregory J. LaRosa
Gregory J. LaRosa · 1×
Citations per year, relative to Gregory J. LaRosa
Gregory J. LaRosa · 1×

Countries citing papers authored by Gregory J. LaRosa

Since Specialization
Citations

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

Fields of papers citing papers by Gregory J. LaRosa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory J. LaRosa. 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 Gregory J. LaRosa. The network helps show where Gregory J. LaRosa may publish in the future.

Co-authorship network of co-authors of Gregory J. LaRosa

This figure shows the co-authorship network connecting the top 25 collaborators of Gregory J. LaRosa. A scholar is included among the top collaborators of Gregory J. LaRosa 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 Gregory J. LaRosa. Gregory J. LaRosa 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
# Work Indexed citations
1 24
2 38
3 221
4 187
5 293
6 185
7 22
8 17
9 307
10 154
11 50
12 59
13 34
14 47
15 198
16 157
17
The β-Chemokine Receptors CCR3 and CCR5 Facilitate Infection by Primary HIV-1 Isolates breakdown →
1957
18 19
19 24
20 13

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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