Job E. López

2.0k total citations
70 papers, 1.4k citations indexed

About

Job E. López is a scholar working on Parasitology, Infectious Diseases and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Job E. López has authored 70 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Parasitology, 58 papers in Infectious Diseases and 33 papers in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Job E. López's work include Vector-borne infectious diseases (62 papers), Viral Infections and Vectors (57 papers) and Vector-Borne Animal Diseases (32 papers). Job E. López is often cited by papers focused on Vector-borne infectious diseases (62 papers), Viral Infections and Vectors (57 papers) and Vector-Borne Animal Diseases (32 papers). Job E. López collaborates with scholars based in United States, Panama and Mexico. Job E. López's co-authors include Tom G. Schwan, Sandra J. Raffel, Hannah K. Wilder, Wendy C. Brown, Guy H. Palmer, Kelly A. Brayton, Sergio E. Bermúdez, Pete D. Teel, Junzo Norimine and Adalberto Á. Pérez de León and has published in prestigious journals such as PLoS ONE, Applied and Environmental Microbiology and Scientific Reports.

In The Last Decade

Job E. López

66 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Job E. López United States 22 1.0k 949 471 333 189 70 1.4k
Masako Andoh Japan 17 944 0.9× 627 0.7× 289 0.6× 331 1.0× 142 0.8× 38 1.1k
Ai Takano Japan 24 1.3k 1.3× 1.2k 1.3× 611 1.3× 369 1.1× 281 1.5× 89 1.6k
V. Roux France 15 1.2k 1.2× 1.0k 1.1× 421 0.9× 367 1.1× 190 1.0× 18 1.5k
Mohammad Yazid Abdad Australia 13 1.4k 1.3× 1.2k 1.2× 485 1.0× 438 1.3× 213 1.1× 31 1.6k
Andy Alhassan Japan 22 835 0.8× 494 0.5× 445 0.9× 208 0.6× 217 1.1× 36 1.3k
Hubert Bassène France 20 860 0.8× 766 0.8× 249 0.5× 457 1.4× 210 1.1× 67 1.4k
Luís Marcelo Aranha Camargo Brazil 20 1.3k 1.2× 862 0.9× 433 0.9× 509 1.5× 267 1.4× 41 1.5k
H.I.J. Roest Netherlands 17 887 0.9× 665 0.7× 515 1.1× 279 0.8× 67 0.4× 45 1.3k
Lorraine Michelet France 17 755 0.7× 794 0.8× 317 0.7× 162 0.5× 210 1.1× 40 1.2k
Roger W. Stich United States 27 1.5k 1.5× 844 0.9× 494 1.0× 246 0.7× 302 1.6× 74 2.0k

Countries citing papers authored by Job E. López

Since Specialization
Citations

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

Fields of papers citing papers by Job E. López

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Job E. López. 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 Job E. López. The network helps show where Job E. López may publish in the future.

Co-authorship network of co-authors of Job E. López

This figure shows the co-authorship network connecting the top 25 collaborators of Job E. López. A scholar is included among the top collaborators of Job E. López 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 Job E. López. Job E. López 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.
Kneubehl, Alexander R., et al.. (2025). Use of a mouse model for the isolation of Borrelia puertoricensis from soft ticks. PLoS ONE. 20(2). e0318652–e0318652.
2.
3.
Kneubehl, Alexander R., et al.. (2024). Borrelia turicatae from Ticks in Peridomestic Setting, Camayeca, Mexico. Emerging infectious diseases. 30(2). 380–383. 2 indexed citations
4.
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Bai, Ying, Sarah E. Maes, Adam J. Replogle, et al.. (2023). A serological assay to detect and differentiate rodent exposure to soft tick and hard tick relapsing fever infections in the United States. Ticks and Tick-borne Diseases. 14(4). 102167–102167.
6.
Blevins, Jon S., et al.. (2022). Characterization of the arthropod associated lipoprotein (Alp) in the tick-mammalian transmission cycle of Borrelia turicatae. Ticks and Tick-borne Diseases. 13(6). 102052–102052. 1 indexed citations
7.
Kneubehl, Alexander R., et al.. (2020). Differential Expression of Putative Ornithodoros turicata Defensins Mediated by Tick Feeding. Frontiers in Cellular and Infection Microbiology. 10. 152–152. 4 indexed citations
8.
Embers, Monica E., Bapi Pahar, Hannah K. Wilder, et al.. (2019). Immunological Responses to the Relapsing Fever Spirochete Borrelia turicatae in Infected Rhesus Macaques: Implications for Pathogenesis and Diagnosis. Infection and Immunity. 87(4). 3 indexed citations
9.
Hernández, García, et al.. (2019). Case report: A retrospective serological analysis indicating human exposure to tick-borne relapsing fever spirochetes in Sonora, Mexico. PLoS neglected tropical diseases. 13(4). e0007215–e0007215. 9 indexed citations
10.
Williamson, Brandi N., Robert J. Fischer, Job E. López, Hideki Ebihara, & Tom G. Schwan. (2019). Prevalence and Strains of Colorado Tick Fever Virus in Rocky Mountain Wood Ticks in the Bitterroot Valley, Montana. Vector-Borne and Zoonotic Diseases. 19(9). 694–702. 17 indexed citations
11.
Mans, Ben J., Jonathan Featherston, Marija Kvas, et al.. (2018). Argasid and ixodid systematics: Implications for soft tick evolution and systematics, with a new argasid species list. Ticks and Tick-borne Diseases. 10(1). 219–240. 118 indexed citations
12.
Bourret, Travis J., et al.. (2018). The relapsing fever spirochete Borrelia turicatae persists in the highly oxidative environment of its soft‐bodied tick vector. Cellular Microbiology. 21(2). e12987–e12987. 15 indexed citations
13.
León, Adalberto Á. Pérez de, Andrew Li, Iván Castro-Arellano, et al.. (2016). Assessment of the Geographic Distribution of Ornithodoros turicata (Argasidae): Climate Variation and Host Diversity. PLoS neglected tropical diseases. 10(2). e0004383–e0004383. 63 indexed citations
14.
Schwan, Tom G., Job E. López, David Safronetz, et al.. (2016). Fleas and trypanosomes of peridomestic small mammals in sub-Saharan Mali. Parasites & Vectors. 9(1). 541–541. 21 indexed citations
15.
Wilder, Hannah K., et al.. (2015). Case Report: A Retrospective Serological Analysis Indicating Human Exposure to Tick-Borne Relapsing Fever Spirochetes in Texas. PLoS neglected tropical diseases. 9(4). e0003617–e0003617. 24 indexed citations
16.
Wilder, Hannah K., et al.. (2014). Transmission Dynamics of Borrelia turicatae from the Arthropod Vector. PLoS neglected tropical diseases. 8(4). e2767–e2767. 51 indexed citations
17.
López, Job E., et al.. (2013). Sequence Analysis and Serological Responses against Borrelia turicatae BipA, a Putative Species-Specific Antigen. PLoS neglected tropical diseases. 7(9). e2454–e2454. 32 indexed citations
18.
López, Job E., et al.. (2011). Acquisition and Subsequent Transmission of Borrelia hermsii by the Soft Tick Ornithodoros hermsi. Journal of Medical Entomology. 48(4). 891–895. 19 indexed citations
19.
López, Job E., Merry E. Schrumpf, Sandra J. Raffel, et al.. (2008). Relapsing Fever Spirochetes Retain Infectivity After Prolonged in vitro Cultivation. Vector-Borne and Zoonotic Diseases. 8(6). 813–820. 25 indexed citations
20.
Toietta, Gabriele, William M. McCormack, Ian Del Conde, et al.. (2006). Modulation of TNFα, a determinant of acute toxicity associated with systemic delivery of first-generation and helper-dependent adenoviral vectors. Gene Therapy. 13(17). 1272–1280. 21 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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