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Environmental and physiological correlates of the severity of clinical signs of snake fungal disease in a population of pigmy rattlesnakes,Sistrurus miliarius
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Disentangling host, pathogen, and environmental determinants of a recently emerged wildlife disease: lessons from the first 15 years of amphibian chytridiomycosis research
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Changes in lifetime immunocompetence in male and female Gryllus texensis (formerly G. integer): trade-offs between immunity and reproduction
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Annual Cycle of Plasma Testosterone in Male Copperheads,Agkistrodon contortrix(Serpentes, Viperidae): Relationship to Timing of Spermatogenesis, Mating, and Agonistic Behavior
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Testing the immunocompetence handicap hypothesis: a review of the evidence
inferredcites →https://doi.org/10.1016/j.anbehav.2004.09.028openalex-snapshot
Sympatric rattlesnakes with contrasting mating systems show differences in seasonal patterns of plasma sex steroids
inferredcites →https://doi.org/10.1016/j.biocon.2010.12.001openalex-snapshot
Decline of an isolated timber rattlesnake (Crotalus horridus) population: Interactions between climate change, disease, and loss of genetic diversity
inferredcites →https://doi.org/10.1016/j.cbpa.2011.08.011openalex-snapshot
Bioenergetic components of reproductive effort in viviparous snakes: Costs of vitellogenesis exceed costs of pregnancy
inferredcites →https://doi.org/10.1016/j.funeco.2015.05.003openalex-snapshot
The natural history, ecology, and epidemiology of Ophidiomyces ophiodiicola and its potential impact on free-ranging snake populations
inferredcites →https://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot
The ecology and impact of chytridiomycosis: an emerging disease of amphibians
inferredcites →https://doi.org/10.1016/j.tree.2010.11.002openalex-snapshot
Horizon scan of global conservation issues for 2011
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A horizon scan of global conservation issues for 2014
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Seasonal steroid hormone levels and their relation to reproduction in the Western Diamond-backed Rattlesnake, Crotalus atrox (Serpentes: Viperidae)
inferredcites →https://doi.org/10.1016/j.ygcen.2007.04.007openalex-snapshot
Immune function varies with reproductive stage and context in female and male tree lizards, Urosaurus ornatus
inferredcites →https://doi.org/10.1016/j.ygcen.2010.01.026openalex-snapshot
The relationship between plasma steroid hormone concentrations and the reproductive cycle in the Northern Pacific rattlesnake, Crotalus oreganus
inferredcites →https://doi.org/10.1016/j.ygcen.2011.09.015openalex-snapshot
Innate immune performance and steroid hormone profiles of pregnant versus nonpregnant cottonmouth snakes (Agkistrodon piscivorus)
inferredcites →https://doi.org/10.1016/j.yhbeh.2009.09.019openalex-snapshot
Food supplementation and testosterone interact to influence reproductive behavior and immune function in Sceloporus graciosus
inferredcites →https://doi.org/10.1038/nature10947openalex-snapshot
Emerging fungal threats to animal, plant and ecosystem health
inferredcites →https://doi.org/10.1046/j.1365-2435.2000.00387.xopenalex-snapshot
The metabolic cost of reproduction in an oviparous lizard
inferredcites →https://doi.org/10.1086/284547openalex-snapshot
Acquisition and Allocation of Resources: Their Influence on Variation in Life History Tactics
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Trade‐Offs between the Reproductive and Immune Systems: Facultative Responses to Resources or Obligate Responses to Reproduction?
inferredcites →https://doi.org/10.1086/683058openalex-snapshot
Male Snakes Allocate Time and Energy according to Individual Energetic Status: Body Condition, Steroid Hormones, and Reproductive Behavior in Timber Rattlesnakes,Crotalus horridus
inferredcites →https://doi.org/10.1098/rspb.2000.1289openalex-snapshot
Testosterone, ticks and travels: a test of the immunocompetence-handicap hypothesis in free-ranging male sand lizards
inferredcites →https://doi.org/10.1098/rspb.2002.2265openalex-snapshot
Variation in immune defence as a question of evolutionary ecology
inferredcites →https://doi.org/10.1098/rstb.2007.2142openalex-snapshot
Seasonal changes in vertebrate immune activity: mediation by physiological trade-offs
inferredcites →https://doi.org/10.1098/rstb.2015.0457openalex-snapshot
Snake fungal disease: an emerging threat to wild snakes
inferredcites →https://doi.org/10.1111/j.0269-8463.2004.00916.xopenalex-snapshot
Seasonal variation in the contribution of different behavioural mechanisms to lizard thermoregulation
inferredcites →https://doi.org/10.1111/j.0908-8857.2005.03342.xopenalex-snapshot
Brood size and immunity costs in zebra finches Taeniopygia guttata
inferredcites →https://doi.org/10.1111/j.1365-2435.2007.01311.xopenalex-snapshot
Immune activity suppresses reproduction in food‐limited female tree lizards Urosaurus ornatus
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01756.xopenalex-snapshot
Experimental evidence for physiological costs underlying the trade‐off between reproduction and survival
inferredcites →https://doi.org/10.1111/j.1461-0248.2005.00879.xopenalex-snapshot
Seasonality and the dynamics of infectious diseases
inferredcites →https://doi.org/10.1111/j.1469-7998.2006.00220.xopenalex-snapshot
Large‐scale seasonal variation in the prevalence and severity of chytridiomycosis
inferredcites →https://doi.org/10.1111/j.1523-1739.2005.00255.xopenalex-snapshot
The Novel and Endemic Pathogen Hypotheses: Competing Explanations for the Origin of Emerging Infectious Diseases of Wildlife
inferredcites →https://doi.org/10.1111/j.1523-1739.2010.01638.xopenalex-snapshot
Investigating and Managing the Rapid Emergence of White‐Nose Syndrome, a Novel, Fatal, Infectious Disease of Hibernating Bats
inferredcites →https://doi.org/10.1111/j.1751-0813.2004.tb11137.xopenalex-snapshot
Effect of season and temperature on mortality in amphibians due to chytridiomycosis
inferredcites →https://doi.org/10.1126/science.1114347openalex-snapshot
Export-Mediated Assembly of Mycobacterial Glycoproteins Parallels Eukaryotic Pathways
inferredcites →https://doi.org/10.1126/science.1163874openalex-snapshot
Bat White-Nose Syndrome: An Emerging Fungal Pathogen?
inferredcites →https://doi.org/10.1126/science.184.4140.1001openalex-snapshot
Behavioral Thermoregulation in Lizards: Importance of Associated Costs
inferredcites →https://doi.org/10.1128/jcm.01465-13openalex-snapshot
Molecular Characterization of Reptile Pathogens Currently Known as Members of the Chrysosporium Anamorph of Nannizziopsis vriesii Complex and Relationship with Some Human-Associated Isolates
inferredcites →https://doi.org/10.1128/mbio.01534-15openalex-snapshot
Experimental Infection of Snakes with Ophidiomyces ophiodiicola Causes Pathological Changes That Typify Snake Fungal Disease
inferredcites →https://doi.org/10.1139/cjz-78-2-254openalex-snapshot
The winter immunoenhancement hypothesis: associations among immunity, density, and survival in prairie vole (Microtus ochrogaster) populations
inferredcites →https://doi.org/10.1139/z99-203openalex-snapshot
The winter immunoenhancement hypothesis: associations among immunity, density, and survival in prairie vole (Microtus ochrogaster) populations
inferredcites →https://doi.org/10.1186/1742-9994-8-8openalex-snapshot
Mitigating amphibian disease: strategies to maintain wild populations and control chytridiomycosis
inferredcites →https://doi.org/10.1371/journal.pone.0038920openalex-snapshot
Frequent Arousal from Hibernation Linked to Severity of Infection and Mortality in Bats with White-Nose Syndrome
inferredcites →https://doi.org/10.1371/journal.pone.0071737openalex-snapshot
Temperature Alters Host Genotype-Specific Susceptibility to Chytrid Infection
inferredcites →https://doi.org/10.1371/journal.ppat.1002808openalex-snapshot
Fungi and the Rise of Mammals
inferredcites →https://doi.org/10.1371/journal.ppat.1004367openalex-snapshot
Chrysosporium-Related Fungi and Reptiles: A Fatal Attraction
inferredcites →https://doi.org/10.15368/theses.2009.66openalex-snapshot
The Relationship Between Plasma Steroid Hormone Concentrations and the Reproductive Cycle of the Northern Pacific Rattlesnake, Crotalus oreganus
inferredcites →https://doi.org/10.1655/herpmonographs-d-11-00003.1openalex-snapshot
Growth Patterns of Dusky Pygmy Rattlesnakes (Sistrurus miliarius barbouri) from Central Florida
inferredcites →https://doi.org/10.1890/080187openalex-snapshot
Could localized warm areas inside cold caves reduce mortality of hibernating bats affected by white‐nose syndrome?
inferredcites →https://doi.org/10.2307/1446855openalex-snapshot
Seasonal Abundance and Activity of a Rattlesnake (Sistrurus miliarius barbouri) in Central Florida
inferredcites →https://doi.org/10.2307/1565081openalex-snapshot
Reproduction in the Rattlesnake, Sistrurus miliarius barbouri, in Central Florida
inferredcites →https://doi.org/10.2307/3761981openalex-snapshot
Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians
inferredcites →https://doi.org/10.3201/eid1712.110240openalex-snapshot
Chrysosporiumsp. Infection in Eastern Massasauga Rattlesnakes
inferredcites →https://doi.org/10.3201/eid2106.150123openalex-snapshot
Invasion Dynamics of White-Nose Syndrome Fungus, Midwestern United States, 2012–2014
inferredcites →https://doi.org/10.7589/0090-3558-39.2.329openalex-snapshot
AN OUTBREAK OF FUNGAL DERMATITIS AND STOMATITIS IN A FREE-RANGING POPULATION OF PIGMY RATTLESNAKES (SISTRURUS MILIARIUS BARBOURI) IN FLORIDA
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1093/jmammal/gyae064zenodo-depositor-declared
Summer cave use by tricolored bats declined in response to white-nose syndrome despite persistence in winter hibernacula in the southeastern United States
inferred← citeshttps://doi.org/10.1002/eap.2251openalex-snapshot
Effects of snake fungal disease on short‐term survival, behavior, and movement in free‐ranging snakes
inferred← citeshttps://doi.org/10.1002/jez.2442openalex-snapshot
Long‐term monitoring of two snake species reveals immune–endocrine interactions and the importance of ecological context
inferred← citeshttps://doi.org/10.1002/jez.70061openalex-snapshot
Ophidiomycosis Prevalence and Disease Ecology in a Natrix tessellata (Laurenti, 1768) Population From Northern Italy
inferred← citeshttps://doi.org/10.1002/jwmg.21345openalex-snapshot
Estimation of Ophidiomyces prevalence to evaluate snake fungal disease risk
inferred← citeshttps://doi.org/10.1007/978-3-031-50531-7_4openalex-snapshot
Disease Ecology in Terrestrial Reptiles from Latin America: A Call for Research
inferred← citeshttps://doi.org/10.1007/s10344-022-01612-8openalex-snapshot
Ophidiomyces ophidiicola detection and infection: a global review on a potential threat to the world’s snake populations
inferred← citeshttps://doi.org/10.1007/s10393-018-1384-8openalex-snapshot
Field Diagnostics and Seasonality of Ophidiomyces ophiodiicola in Wild Snake Populations
inferred← citeshttps://doi.org/10.1016/j.cbpa.2022.111162openalex-snapshot
Physiological effects of capture and short-term captivity in an invasive snake species, the Burmese python (Python bivittatus) in Florida
inferred← citeshttps://doi.org/10.1016/j.dci.2018.03.002openalex-snapshot
Antibacterial properties of plasma from the prairie rattlesnake (Crotalus viridis)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.177478openalex-snapshot
Gene expression provides mechanistic insights into a viral disease in seabirds
inferred← citeshttps://doi.org/10.1016/j.ygcen.2018.05.027openalex-snapshot
Seasonal testosterone and corticosterone patterns in relation to body condition and reproduction in a subtropical pitviper, Sistrurus miliarius
inferred← citeshttps://doi.org/10.1016/j.ygcen.2020.113416openalex-snapshot
The relationship between steroid hormones and seasonal reproductive events in free-living female Pygmy Rattlesnakes, Sistrurus miliarius
inferred← citeshttps://doi.org/10.1016/j.ygcen.2023.114295openalex-snapshot
Ophidiomycosis is associated with alterations in the acute glycemic and glucocorticoid stress response in a free-living snake species
inferred← citeshttps://doi.org/10.1038/s41586-024-07582-yopenalex-snapshot
Hotspot shelters stimulate frog resistance to chytridiomycosis
inferred← citeshttps://doi.org/10.1038/s41598-022-07042-5openalex-snapshot
Host microbiome responses to the Snake Fungal Disease pathogen (Ophidiomyces ophidiicola) are driven by changes in microbial richness
inferred← citeshttps://doi.org/10.1038/s41598-022-16664-8openalex-snapshot
Comparative host–pathogen associations of Snake Fungal Disease in sympatric species of water snakes (Nerodia)
inferred← citeshttps://doi.org/10.1038/s41598-024-54568-xopenalex-snapshot
Effects of ophidiomycosis on movement, survival, and reproduction of eastern foxsnakes (Pantherophis vulpinus)
inferred← citeshttps://doi.org/10.1038/s41598-025-21190-4openalex-snapshot
An emergent disease reduces survival of mature female eastern diamondback rattlesnakes (Crotalus adamanteus), a key demographic for a slow-lived species
inferred← citeshttps://doi.org/10.1038/s42003-024-06092-xopenalex-snapshot
Contribution of host species and pathogen clade to snake fungal disease hotspots in Europe
inferred← citeshttps://doi.org/10.1093/jhered/esag080openalex-snapshot
Population genetics, trait mapping and fungal pathogen surveillance using untargeted sequencing in timber rattlesnakes ( Crotalus horridus)
inferred← citeshttps://doi.org/10.1111/brv.12927openalex-snapshot
Habitat split as a driver of disease in amphibians
inferred← citeshttps://doi.org/10.1111/cobi.14411openalex-snapshot
Effects of snake fungal disease (ophidiomycosis) on the skin microbiome across two major experimental scales
inferred← citeshttps://doi.org/10.1111/jzo.12628openalex-snapshot
Seasonal sex steroids indicate reproductive costs associated with snake fungal disease
inferred← citeshttps://doi.org/10.1111/jzo.13024openalex-snapshot
Ophidiomycosis is related to seasonal patterns of reproduction, ecdysis, and thermoregulatory behavior in a free‐living snake species
inferred← citeshttps://doi.org/10.1111/mec.17210openalex-snapshot
Genetic mechanisms and biological processes underlying host response to ophidiomycosis (snake fungal disease) inferred from tissue‐specific transcriptome analyses
inferred← citeshttps://doi.org/10.1128/mmbr.00128-25openalex-snapshot
The microbiome in reptile health, disease, and ecology
inferred← citeshttps://doi.org/10.1177/0300985820953423openalex-snapshot
Ophidiomycosis in Red Cornsnakes ( Pantherophis guttatus ): Potential Roles of Brumation and Temperature on Pathogenesis and Transmission
inferred← citeshttps://doi.org/10.1242/jeb.225185openalex-snapshot
The metabolic response to an immune challenge in a viviparous snake, Sistrurus miliarius
inferred← citeshttps://doi.org/10.1242/jeb.247962openalex-snapshot
Glucocorticoid and glycemic responses to immune challenge in a viviparous snake afflicted with an emerging mycosis
inferred← citeshttps://doi.org/10.1371/journal.pone.0218351openalex-snapshot
Ophidiomycosis prevalence in Georgia’s Eastern Indigo Snake (Drymarchon couperi) populations
inferred← citeshttps://doi.org/10.1371/journal.pone.0240415openalex-snapshot
Ophidiomycosis, an emerging fungal disease of snakes: Targeted surveillance on military lands and detection in the western US and Puerto Rico
inferred← citeshttps://doi.org/10.1371/journal.pone.0289641openalex-snapshot
Environmental temperature influences ophidiomycosis progression and survival in experimentally challenged prairie rattlesnakes (Crotalus viridis)
inferred← citeshttps://doi.org/10.1638/2017-0112r.1openalex-snapshot
DETECTION OFOPHIDIOMYCES OPHIODIICOLAIN TWO CAPTIVE BOCOURT WATER SNAKES (SUBSESSOR BOCOURTI) AND ONE CAPTIVE PUEBLAN MILK SNAKE (LAMPROPELTIS TRIANGULUM CAMPBELLI)
inferred← citeshttps://doi.org/10.1638/2018-0143openalex-snapshot
HOST FACTORS AND TESTING MODALITY AGREEMENT ASSOCIATED WITH OPHIDIOMYCES INFECTION IN A FREE-RANGING SNAKE POPULATION IN SOUTHEAST OHIO, USA
inferred← citeshttps://doi.org/10.1638/2018-0198openalex-snapshot
POSTNATAL MORTALITY IN NEONATE RATTLESNAKES ASSOCIATED WITH OPHIDIOMYCES OPHIODIICOLA
inferred← citeshttps://doi.org/10.1638/2020-0213openalex-snapshot
RETROSPECTIVE REVIEW OF OPHIDIOMYCOSIS (OPHIDIOMYCES OPHIODIICOLA) AT THE SMITHSONIAN'S NATIONAL ZOOLOGICAL PARK (1983–2017)
inferred← citeshttps://doi.org/10.1643/h2025015openalex-snapshot
Long-Term Demographics Link Transmitter Removal to Declines in Prevalence of Ophidiomyces and Clinical Signs of Ophidiomycosis in a Threatened Pitviper Population
inferred← citeshttps://doi.org/10.1655/herp-2025-004openalex-snapshot
Communal Overwintering is Positively Associated with Ophidiomyces ophiodiicola Infection Load within a Southeastern Population of Timber Rattlesnakes (Crotalus horridus)
inferred← citeshttps://doi.org/10.1670/18-147openalex-snapshot
Interactive Effects of Food Supplementation and Snake Fungal Disease on Pregnant Pygmy Rattlesnakes and Their Offspring
inferred← citeshttps://doi.org/10.3389/famrs.2026.1812456openalex-snapshot
Methods for examining immune and skin microbiome associations with dermatomycoses in reptiles: a review
inferred← citeshttps://doi.org/10.3389/fvets.2026.1754420openalex-snapshot
Health assessment and multipathogen surveillance of free-ranging snakes in the southeastern United States
inferred← citeshttps://doi.org/10.3390/ani13040744openalex-snapshot
Past, Present, and Future of Naturally Occurring Antimicrobials Related to Snake Venoms
inferred← citeshttps://doi.org/10.3390/jof10020125openalex-snapshot
Snake Fungal Disease in Free-Ranging Northern Pine Snakes (Pituophis melanoleucus melanoleucus) in New Jersey: Lesions, Severity of Sores and Investigator’s Perceptions
inferred← citeshttps://doi.org/10.3390/pathogens12030429openalex-snapshot
Major Emerging Fungal Diseases of Reptiles and Amphibians
inferred← citeshttps://doi.org/10.5818/jhms-d-23-00025openalex-snapshot
Ophidiomycosis in Wild Dice Snakes (Natrix tessellata) in Germany
inferred← citeshttps://doi.org/10.5818/jhms-s-20-00008openalex-snapshot
Hematology of Wild Lake Erie Watersnakes (Nerodia sipedon insularum) with Natural Ophidiomycosis
inferred← citeshttps://doi.org/10.5818/jhms-s-20-00018openalex-snapshot
Detection of Ophidiomyces ophidiicola in a Wild Burmese Python (Python bivittatus) in Hong Kong SAR, China
inferred← citeshttps://doi.org/10.7589/2017-05-109openalex-snapshot
Tracking Outcomes of Snake Fungal Disease in Free-ranging Pygmy Rattlesnakes (Sistrurus miliarius)
inferred← citeshttps://doi.org/10.7589/2018-04-100openalex-snapshot
Snake Fungal Disease in Colubridae Snakes in Connecticut, USA in 2015 and 2017
inferred← citeshttps://doi.org/10.7589/jwd-d-20-00123openalex-snapshot
USING MULTIVARIATE ANALYSES TO EXPLORE DISEASE PROGRESSION OF FINCH MYCOPLASMOSIS
inferred← citeshttps://doi.org/10.7589/jwd-d-21-00100openalex-snapshot
INNATE IMMUNE FUNCTION IN LAKE ERIE WATERSNAKES (NERODIA SIPEDON INSULARUM) WITH OPHIDIOMYCOSIS
inferred← citeshttps://doi.org/10.7589/jwd-d-21-00111openalex-snapshot
EPIDEMIOLOGY OF OPHIDIOMYCOSIS IN LAKE ERIE WATERSNAKES (NERODIA SIPEDON INSULARUM)
inferred← citeshttps://doi.org/10.7589/jwd-d-21-00116openalex-snapshot
REPEATED SAMPLING OF WILD INDIVIDUALS REVEALS OPHIDIOMYCES OPHIDIICOLA INFECTION DYNAMICS IN A PENNSYLVANIA SNAKE ASSEMBLAGE
inferred← citeshttps://doi.org/10.7589/jwd-d-21-00134openalex-snapshot
SEASONAL AND INTERSPECIFIC VARIATION IN THE PREVALENCE OF OPHIDIOMYCES OPHIDIICOLA AND OPHIDIOMYCOSIS IN A COMMUNITY OF FREE-RANGING SNAKES
inferred← citeshttps://doi.org/10.7589/jwd-d-24-00081openalex-snapshot
APPARENT OPHIDIOMYCOSIS ALTERS EASTERN COPPERHEAD (AGKISTRODON CONTORTRIX) BEHAVIOR AND HABITAT USE
inferred← citeshttps://doi.org/10.7589/jwd-d-25-00027openalex-snapshot
DETECTION OF OPHIDIOMYCES OPHIDIICOLA IN SAMPLES FROM FREE-RANGING SNAKES IN GERMANY, 2021–22
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