DeeAnn M. Reeder

11.5k total citations · 2 hit papers
63 papers, 7.4k citations indexed

About

DeeAnn M. Reeder is a scholar working on Ecology, Evolution, Behavior and Systematics, Infectious Diseases and Ecology. According to data from OpenAlex, DeeAnn M. Reeder has authored 63 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Ecology, Evolution, Behavior and Systematics, 27 papers in Infectious Diseases and 12 papers in Ecology. Recurrent topics in DeeAnn M. Reeder's work include Bat Biology and Ecology Studies (43 papers), Viral Infections and Vectors (26 papers) and Yersinia bacterium, plague, ectoparasites research (11 papers). DeeAnn M. Reeder is often cited by papers focused on Bat Biology and Ecology Studies (43 papers), Viral Infections and Vectors (26 papers) and Yersinia bacterium, plague, ectoparasites research (11 papers). DeeAnn M. Reeder collaborates with scholars based in United States, Finland and Belgium. DeeAnn M. Reeder's co-authors include Don E. Wilson, Rudolf Schmid, Kristin M. Kramer, Gregory G. Turner, Jeremy T. H. Coleman, Carol U. Meteyer, David S. Blehert, Melissa Behr, Kenneth A. Field and Alan C. Hicks and has published in prestigious journals such as Nature, The Journal of Immunology and PLoS ONE.

In The Last Decade

DeeAnn M. Reeder

61 papers receiving 7.0k citations

Hit Papers

Mammal Species of the World: A Taxonomic and Geographic R... 1993 2026 2004 2015 1993 2011 1000 2.0k 3.0k 4.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
DeeAnn M. Reeder United States 29 3.9k 3.4k 1.9k 1.7k 1.4k 63 7.4k
Emma C. Teeling Ireland 40 3.5k 0.9× 2.0k 0.6× 1.8k 0.9× 1.7k 1.0× 1.2k 0.9× 111 7.4k
Robert S. Sikes United States 19 3.1k 0.8× 5.5k 1.6× 1.5k 0.8× 782 0.5× 582 0.4× 34 7.7k
Steven M. Goodman United States 45 4.3k 1.1× 3.4k 1.0× 2.0k 1.0× 1.7k 1.0× 1.1k 0.8× 385 9.7k
Don E. Wilson United States 38 5.7k 1.5× 6.4k 1.9× 2.2k 1.1× 3.3k 2.0× 638 0.5× 173 11.3k
Robert C. Fleischer United States 58 3.9k 1.0× 5.7k 1.7× 4.9k 2.5× 832 0.5× 1.1k 0.8× 304 12.4k
Nancy B. Simmons United States 36 3.7k 1.0× 2.1k 0.6× 645 0.3× 2.1k 1.3× 567 0.4× 167 5.2k
Bruce D. Patterson United States 47 4.1k 1.1× 5.3k 1.6× 1.5k 0.8× 2.5k 1.5× 487 0.4× 186 9.7k
Paul A. Racey United Kingdom 55 7.2k 1.9× 6.1k 1.8× 1.2k 0.6× 659 0.4× 775 0.6× 235 9.9k
Elisabeth K. V. Kalko Germany 63 8.8k 2.3× 6.3k 1.9× 756 0.4× 924 0.5× 783 0.6× 183 11.5k
Thomas B. Smith United States 69 5.5k 1.4× 6.9k 2.0× 4.6k 2.4× 854 0.5× 791 0.6× 237 14.8k

Countries citing papers authored by DeeAnn M. Reeder

Since Specialization
Citations

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

Fields of papers citing papers by DeeAnn M. Reeder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by DeeAnn M. Reeder. 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 DeeAnn M. Reeder. The network helps show where DeeAnn M. Reeder may publish in the future.

Co-authorship network of co-authors of DeeAnn M. Reeder

This figure shows the co-authorship network connecting the top 25 collaborators of DeeAnn M. Reeder. A scholar is included among the top collaborators of DeeAnn M. Reeder 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 DeeAnn M. Reeder. DeeAnn M. Reeder 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.
Pannkuk, Evan L., Marianne Moore, Shivani Bansal, et al.. (2024). White adipose tissue remodeling in Little Brown Myotis (Myotis lucifugus) with white-nose syndrome. Metabolomics. 20(5). 100–100. 1 indexed citations
2.
Sánchez, Cecilia A., Kendra L. Phelps, Hannah K. Frank, et al.. (2024). Advances in understanding bat infection dynamics across biological scales. Proceedings of the Royal Society B Biological Sciences. 291(2018). 20232823–20232823. 4 indexed citations
3.
Twort, Victoria, Veronika N. Laine, Kenneth A. Field, et al.. (2024). Signals of positive selection in genomes of palearctic Myotis-bats coexisting with a fungal pathogen. BMC Genomics. 25(1). 828–828.
4.
Reeder, DeeAnn M., et al.. (2023). Interdisciplinary Insights from the Plague of Cyprian.
5.
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
6.
Geiselman, Cullen, Jorrit H. Poelen, Nancy B. Simmons, et al.. (2023). A Standardized Review of Bat Names Across Multiple Taxonomic Authorities. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
7.
Groom, Quentin, et al.. (2021). Using iNaturalist to monitor adherence to best practices in bat handling. ZooKeys. 9. e68052–e68052. 7 indexed citations
8.
Reeder, DeeAnn M., et al.. (2020). Hepatocystis. Trends in Parasitology. 37(5). 456–457. 4 indexed citations
9.
Kurta, Allen, et al.. (2020). Exceptional Longevity in Little Brown Bats Still Occurs, despite Presence of White-Nose Syndrome. Journal of Fish and Wildlife Management. 11(2). 583–587. 4 indexed citations
10.
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
11.
Vallo, Peter, DeeAnn M. Reeder, Megan E. Vodzak, & Petr Benda. (2019). Resurrection of an East African house bat species Scotophilus altilis Allen, 1914 (Chiroptera: Vespertilionidae). Zootaxa. 4577(1). zootaxa.4577.1.9–zootaxa.4577.1.9. 1 indexed citations
12.
Lilley, Thomas M., Riley F. Bernard, Emma V. Willcox, et al.. (2017). Molecular Detection of Candidatus Bartonella mayotimonensis in North American Bats. Vector-Borne and Zoonotic Diseases. 17(4). 243–246. 34 indexed citations
13.
Lilley, Thomas M., Joseph S. Johnson, Lasse Ruokolainen, et al.. (2016). White-nose syndrome survivors do not exhibit frequent arousals associated with Pseudogymnoascus destructans infection. Frontiers in Zoology. 13(1). 12–12. 52 indexed citations
14.
Court, Michael H., et al.. (2016). Pharmacokinetics of terbinafine in little brown myotis (Myotis lucifugus) infected with Pseudogymnoascus destructans. American Journal of Veterinary Research. 78(1). 90–99. 16 indexed citations
15.
Pearson, Brandon L., DeeAnn M. Reeder, & Peter G. Judge. (2015). Crowding increases salivary cortisol but not self‐directed behavior in captive baboons. American Journal of Primatology. 77(4). 462–467. 26 indexed citations
16.
Johnson, Joseph S., DeeAnn M. Reeder, Melissa B. Meierhofer, et al.. (2014). Host, Pathogen, and Environmental Characteristics Predict White-Nose Syndrome Mortality in Captive Little Brown Myotis (Myotis lucifugus). PLoS ONE. 9(11). e112502–e112502. 58 indexed citations
17.
Reeder, DeeAnn M., et al.. (2013). A new genus for a rare African vespertilionid bat: insights from South Sudan. ZooKeys. 285. 89–115. 9 indexed citations
18.
Reeder, DeeAnn M., Craig L. Frank, Gregory G. Turner, et al.. (2012). Frequent Arousal from Hibernation Linked to Severity of Infection and Mortality in Bats with White-Nose Syndrome. PLoS ONE. 7(6). e38920–e38920. 244 indexed citations
19.
Wilson, Don E. & DeeAnn M. Reeder. (2011). Class Mammalia Linnaeus, 1758. Zootaxa. 56. 8 indexed citations
20.
Reeder, DeeAnn M.. (2001). The biology of parenting in the monogamous titi monkey (Callicebus moloch). Bell & Howell Information and Learning eBooks. 5 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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