Gregory G. Turner

3.1k total citations · 1 hit paper
35 papers, 2.1k citations indexed

About

Gregory G. Turner is a scholar working on Ecology, Evolution, Behavior and Systematics, Infectious Diseases and Genetics. According to data from OpenAlex, Gregory G. Turner has authored 35 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Ecology, Evolution, Behavior and Systematics, 23 papers in Infectious Diseases and 12 papers in Genetics. Recurrent topics in Gregory G. Turner's work include Bat Biology and Ecology Studies (27 papers), Viral Infections and Vectors (20 papers) and Yersinia bacterium, plague, ectoparasites research (11 papers). Gregory G. Turner is often cited by papers focused on Bat Biology and Ecology Studies (27 papers), Viral Infections and Vectors (20 papers) and Yersinia bacterium, plague, ectoparasites research (11 papers). Gregory G. Turner collaborates with scholars based in United States, Czechia and Finland. Gregory G. Turner's co-authors include Alan C. Hicks, Winifred F. Frick, Kate E. Langwig, DeeAnn M. Reeder, Thomas Kunz, D. Scott Reynolds, Jacob F. Pollock, Jeremy T. H. Coleman, David S. Blehert and Carol U. Meteyer and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Gregory G. Turner

33 papers receiving 2.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An Emerging Disease Causes Regional Population Collapse of a Common North American Bat Species

2010 698 citations Winifred F. Frick, Gregory G. Turner et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gregory G. Turner United States	19	1.6k	841	737	709	271	35	2.1k
Jeremy T. H. Coleman United States	13	1.1k 0.7×	582 0.7×	652 0.9×	484 0.7×	170 0.6×	22	1.7k
Kate E. Langwig United States	23	2.1k 1.3×	1.3k 1.5×	894 1.2×	1.1k 1.5×	314 1.2×	42	2.9k
Alan C. Hicks United States	12	2.3k 1.4×	1.1k 1.3×	987 1.3×	978 1.4×	320 1.2×	20	2.9k
Jan Zukal Czechia	20	1.2k 0.8×	477 0.6×	725 1.0×	415 0.6×	199 0.7×	86	1.7k
Joseph R. Hoyt United States	18	1.2k 0.8×	760 0.9×	455 0.6×	685 1.0×	153 0.6×	38	1.7k
Marco Tschapka Germany	28	1.7k 1.1×	578 0.7×	936 1.3×	320 0.5×	516 1.9×	125	2.7k
Thomas M. Lilley Finland	26	982 0.6×	518 0.6×	635 0.9×	358 0.5×	224 0.8×	86	1.7k
Tomáš Bartonička Czechia	22	1.1k 0.7×	530 0.6×	570 0.8×	409 0.6×	200 0.7×	92	1.4k
Elizabeth L. Buckles United States	16	928 0.6×	555 0.7×	520 0.7×	470 0.7×	111 0.4×	33	2.0k
Andrea Gargas United States	26	2.3k 1.5×	615 0.7×	575 0.8×	666 0.9×	145 0.5×	40	3.6k

Countries citing papers authored by Gregory G. Turner

Since Specialization

Citations

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

Fields of papers citing papers by Gregory G. Turner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gregory G. Turner

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

All Works

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20 of 20 papers shown

Field, Kenneth A., Tomáš Bartonička, Veronika N. Laine, et al.. (2025). Bat species tolerant and susceptible to fungal infection show transcriptomic differences in late hibernation and healing. Journal of Experimental Biology. 229(1).

Turner, Gregory G., et al.. (2024). Long-term trends in the extent of Pseudogymnoascus destructans infection in little brown myotis. Biological Conservation. 302. 110954–110954. 1 indexed citations

Turner, Gregory G., et al.. (2024). Dietary flexibility of insectivorous bats, Eptesicus fuscus and Myotis lucifugus, during Magicicada spp. Brood X emergence. Canadian Journal of Zoology. 102(11). 888–895. 1 indexed citations

Chothe, Shubhada K., Santhamani Ramasamy, Abhinay Gontu, et al.. (2023). Little Brown Bats (Myotis lucifugus) Support the Binding of SARS-CoV-2 Spike and Are Likely Susceptible to SARS-CoV-2 Infection. Viruses. 15(5). 1103–1103. 2 indexed citations

Sewall, Brent J., Gregory G. Turner, Joseph S. Johnson, et al.. (2023). Environmental control reduces white‐nose syndrome infection in hibernating bats. Animal Conservation. 26(5). 642–653. 5 indexed citations

Hartzler, Lynn K., et al.. (2023). Long‐term exposure to an invasive fungal pathogen decreases Eptesicus fuscus body mass with increasing latitude. Ecosphere. 14(2). 3 indexed citations

Brown, Justin D., et al.. (2022). Unrecognized diversity of mammalian orthoreoviruses in North American bats. Virology. 571. 1–11. 7 indexed citations

Duchamp, Joseph E., et al.. (2022). A novel SNP assay reveals increased genetic variability and abundance following translocations to a remnant Allegheny woodrat population. SHILAP Revista de lepidopterología. 22(1). 137–137. 2 indexed citations

Turner, Gregory G., et al.. (2021). Cooling of bat hibernacula to mitigate white‐nose syndrome. Conservation Biology. 36(2). e13803–e13803. 21 indexed citations

10.

Turner, Gregory G., et al.. (2021). Phylogeographic analysis of Pseudogymnoascus destructans partitivirus-pa explains the spread dynamics of white-nose syndrome in North America. PLoS Pathogens. 17(3). e1009236–e1009236. 8 indexed citations

11.

Lilley, Thomas M., Kenneth A. Field, DeeAnn M. Reeder, et al.. (2020). Genome-Wide Changes in Genetic Diversity in a Population of Myotis lucifugus Affected by White-Nose Syndrome. G3 Genes Genomes Genetics. 10(6). 2007–2020. 13 indexed citations

12.

Bernard, Riley F., Jonathan D. Reichard, Jeremy T. H. Coleman, et al.. (2020). Identifying research needs to inform white‐nose syndrome management decisions. Conservation Science and Practice. 2(8). 27 indexed citations

13.

Turner, Gregory G., et al.. (2020). Ultrasonic Acoustic Surveys of State Endangered Northern Flying Squirrels in the Pocono Mountains, Pennsylvania. Journal of Fish and Wildlife Management. 11(2). 644–653. 5 indexed citations

14.

Lilley, Thomas M., Jenni M. Prokkola, Anna S. Blomberg, et al.. (2019). Resistance is futile: RNA-sequencing reveals differing responses to bat fungal pathogen in Nearctic Myotis lucifugus and Palearctic Myotis myotis. Oecologia. 191(2). 295–309. 31 indexed citations

15.

Pikula, Jiří, Sybill K. Amelon, Hana Banďouchová, et al.. (2017). White-nose syndrome pathology grading in Nearctic and Palearctic bats. PLoS ONE. 12(8). e0180435–e0180435. 42 indexed citations

16.

Chothe, Shubhada K., Ruth H. Nissly, Justin D. Brown, et al.. (2017). Avian and human influenza virus compatible sialic acid receptors in little brown bats. Scientific Reports. 7(1). 660–660. 21 indexed citations

17.

Turner, Gregory G., et al.. (2016). Using a Novel Partitivirus in Pseudogymnoascus destructans to Understand the Epidemiology of White-Nose Syndrome. PLoS Pathogens. 12(12). e1006076–e1006076. 40 indexed citations

18.

Mascuch, Samantha J., Wilna J. Moree, Cheng‐Chih Hsu, et al.. (2015). Direct Detection of Fungal Siderophores on Bats with White-Nose Syndrome via Fluorescence Microscopy-Guided Ambient Ionization Mass Spectrometry. PLoS ONE. 10(3). e0119668–e0119668. 26 indexed citations

19.

Zukal, Jan, Hana Banďouchová, Tomáš Bartonička, et al.. (2014). White-Nose Syndrome Fungus: A Generalist Pathogen of Hibernating Bats. PLoS ONE. 9(5). e97224–e97224. 68 indexed citations

20.

Cossart, Yvonne E., Elizabeth Gillespie, Dianne Jones, et al.. (1968). Infection Risks of Haemodialysis—Some Preventive Aspects. BMJ. 3(5616). 454–460. 16 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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