Maria Gomes‐Solecki

1.8k total citations
49 papers, 1.1k citations indexed

About

Maria Gomes‐Solecki is a scholar working on Parasitology, Infectious Diseases and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Maria Gomes‐Solecki has authored 49 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Parasitology, 26 papers in Infectious Diseases and 9 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Maria Gomes‐Solecki's work include Vector-borne infectious diseases (27 papers), Viral Infections and Vectors (23 papers) and Leptospirosis research and findings (17 papers). Maria Gomes‐Solecki is often cited by papers focused on Vector-borne infectious diseases (27 papers), Viral Infections and Vectors (23 papers) and Leptospirosis research and findings (17 papers). Maria Gomes‐Solecki collaborates with scholars based in United States, France and Portugal. Maria Gomes‐Solecki's co-authors include Raymond J. Dattwyler, Catherine Werts, Dustin Brisson, Luciana Richer, Ignacio Santecchia, Rita Melo, Miguel Aroso, Richard S. Ostfeld, Beatriz del Río and Jos F. M. L. Seegers and has published in prestigious journals such as PLoS ONE, Scientific Reports and The FASEB Journal.

In The Last Decade

Maria Gomes‐Solecki

48 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
Maria Gomes‐Solecki United States 21 804 590 186 135 111 49 1.1k
Pedro Fernández‐Soto Spain 23 775 1.0× 417 0.7× 275 1.5× 127 0.9× 80 0.7× 66 1.2k
Hiromi Ikadai Japan 21 905 1.1× 400 0.7× 259 1.4× 328 2.4× 206 1.9× 77 1.3k
Isabelle Vallée France 22 602 0.7× 660 1.1× 96 0.5× 46 0.3× 92 0.8× 80 1.4k
Jason Mott United States 19 668 0.8× 553 0.9× 195 1.0× 156 1.2× 105 0.9× 20 1.2k
Manish Kumar India 14 562 0.7× 394 0.7× 103 0.6× 132 1.0× 219 2.0× 55 770
Aya Matsuu Japan 22 523 0.7× 573 1.0× 211 1.1× 249 1.8× 101 0.9× 70 1.2k
Reginaldo G. Bastos United States 19 586 0.7× 428 0.7× 104 0.6× 327 2.4× 141 1.3× 63 996
Sunlian Feng United States 18 1.2k 1.5× 981 1.7× 196 1.1× 312 2.3× 245 2.2× 32 1.3k
Hege Brun‐Hansen Norway 11 319 0.4× 346 0.6× 89 0.5× 168 1.2× 60 0.5× 20 633
R van Vugt United States 7 770 1.0× 534 0.9× 71 0.4× 253 1.9× 339 3.1× 8 999

Countries citing papers authored by Maria Gomes‐Solecki

Since Specialization
Citations

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

Fields of papers citing papers by Maria Gomes‐Solecki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Gomes‐Solecki. 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 Maria Gomes‐Solecki. The network helps show where Maria Gomes‐Solecki may publish in the future.

Co-authorship network of co-authors of Maria Gomes‐Solecki

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Gomes‐Solecki. A scholar is included among the top collaborators of Maria Gomes‐Solecki 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 Maria Gomes‐Solecki. Maria Gomes‐Solecki 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.
Nair, Nisha, et al.. (2024). Intranasal vaccine for Lyme disease provides protection against tick transmitted Borrelia burgdorferi beyond one year. npj Vaccines. 9(1). 33–33. 7 indexed citations
3.
Kim, Sangsik, et al.. (2023). A portable immunosensor provides sensitive and rapid detection of Borrelia burgdorferi antigen in spiked blood. Scientific Reports. 13(1). 7546–7546. 3 indexed citations
5.
Dattwyler, Raymond J. & Maria Gomes‐Solecki. (2022). The year that shaped the outcome of the OspA vaccine for human Lyme disease. npj Vaccines. 7(1). 10–10. 28 indexed citations
6.
Gomes, Charles, et al.. (2022). Enzyme immunoassays (EIA) for serodiagnosis of human leptospirosis: specific IgG3/IgG1 isotyping may further inform diagnosis of acute disease. PLoS neglected tropical diseases. 16(2). e0010241–e0010241. 5 indexed citations
7.
Ivanova, Larisa, et al.. (2021). Maximum antigen diversification in a lyme bacterial population and evolutionary strategies to overcome pathogen diversity. The ISME Journal. 16(2). 447–464. 8 indexed citations
8.
Nair, Nisha, et al.. (2021). Borrelia burgdorferi (Spirochaetales: Spirochaetaceae) Infection Prevalence and Host Associations of Ticks Found on Peromyscus spp. in Maryland. Journal of Medical Entomology. 59(2). 752–757. 7 indexed citations
9.
Nair, Nisha, et al.. (2021). Maternal transfer of neutralizing antibodies to B. burgdorferi OspA after oral vaccination of the rodent reservoir. Vaccine. 39(31). 4320–4327. 2 indexed citations
10.
Nair, Nisha, et al.. (2021). Role of TLR4 in Persistent Leptospira interrogans Infection: A Comparative In Vivo Study in Mice. Frontiers in Immunology. 11. 572999–572999. 6 indexed citations
11.
Kundu, Suman, et al.. (2021). Inflammatory Signatures of Pathogenic and Non-Pathogenic Leptospira Infection in Susceptible C3H-HeJ Mice. Frontiers in Cellular and Infection Microbiology. 11. 677999–677999. 17 indexed citations
12.
Santecchia, Ignacio, Frédérique Vernel-Pauillac, Orhan Raşid, et al.. (2019). Innate immune memory through TLR2 and NOD2 contributes to the control of Leptospira interrogans infection. PLoS Pathogens. 15(5). e1007811–e1007811. 61 indexed citations
13.
14.
Gomes‐Solecki, Maria. (2014). Blocking pathogen transmission at the source: reservoir targeted OspA-based vaccines against Borrelia burgdorferi. Frontiers in Cellular and Infection Microbiology. 4. 136–136. 24 indexed citations
15.
Río, Beatriz del, Jos F. M. L. Seegers, & Maria Gomes‐Solecki. (2010). Immune Response to Lactobacillus plantarum Expressing Borrelia burgdorferi OspA Is Modulated by the Lipid Modification of the Antigen. PLoS ONE. 5(6). e11199–e11199. 23 indexed citations
16.
Schwanz, Lisa E., Dustin Brisson, Maria Gomes‐Solecki, & Richard S. Ostfeld. (2010). Linking disease and community ecology through behavioural indicators: immunochallenge of white-footed mice and its ecological impacts. Journal of Animal Ecology. 80(1). 204–214. 15 indexed citations
17.
Río, Beatriz del, et al.. (2010). Platform technology to deliver prophylactic molecules orally: An example using the Class A select agent Yersinia pestis. Vaccine. 28(41). 6714–6722. 13 indexed citations
18.
Ivanova, Larisa, Iva Christova, Vera Neves, et al.. (2009). Comprehensive seroprofiling of sixteen B. burgdorferi OspC: Implications for Lyme disease diagnostics design. Clinical Immunology. 132(3). 393–400. 29 indexed citations
19.
Gomes‐Solecki, Maria, Dustin Brisson, & Raymond J. Dattwyler. (2005). Oral vaccine that breaks the transmission cycle of the Lyme disease spirochete can be delivered via bait. Vaccine. 24(20). 4440–4449. 63 indexed citations
20.
Gomes‐Solecki, Maria, Gary P. Wormser, & Raymond J. Dattwyler. (2002). IFNγ production in peripheral blood of early Lyme disease patients to hLFAαL (aa326-345). BMC Musculoskeletal Disorders. 3(1). 25–25. 3 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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