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Host heterogeneity dominates West Nile virus transmission

https://doi.org/10.1098/rspb.2006.3575
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The Population Dynamics of Infectious Diseases: Theory and Applications
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Infectious diseases of humans
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Should we expect population thresholds for wildlife disease?
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West Nile Virus: Epidemiology and Ecology in North America
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Fruit bats as reservoirs of Ebola virus
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Estimated risk of West Nile virus transmission through blood transfusion during an epidemic in Queens, New York City
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Westward Ho? — The Spread of West Nile Virus
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The ecology of infectious disease: Effects of host diversity and community composition on Lyme disease risk
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Heterogeneities in the transmission of infectious agents: Implications for the design of control programs
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Population Dynamics of Pathogens with Multiple Host Species
inferredcites →https://doi.org/10.1089/153036604773083013openalex-snapshot
Host Feeding Patterns of Established and Potential Mosquito Vectors of West Nile Virus in the Eastern United States
inferredcites →https://doi.org/10.1089/vbz.2004.4.360openalex-snapshot
Epidemiology of West Nile Virus in Connecticut: A Five-Year Analysis of Mosquito Data 1999–2003
inferredcites →https://doi.org/10.1097/00001432-200110000-00004openalex-snapshot
West Nile virus in the western hemisphere
inferredcites →https://doi.org/10.1098/rspb.2005.3284openalex-snapshot
Avian diversity and West Nile virus: testing associations between biodiversity and infectious disease risk
inferredcites →https://doi.org/10.1099/0022-1317-70-1-37openalex-snapshot
Antigenic Relationships between Flaviviruses as Determined by Cross-neutralization Tests with Polyclonal Antisera
inferredcites →https://doi.org/10.1111/j.0906-7590.2004.03708.xopenalex-snapshot
Geographic locale and relative dominance patterns among North American passerine communities
inferredcites →https://doi.org/10.1126/science.1060638openalex-snapshot
Modeling Household Transmission of American Trypanosomiasis
inferredcites →https://doi.org/10.1126/science.1086925openalex-snapshot
Modeling the SARS Epidemic
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Bats Are Natural Reservoirs of SARS-Like Coronaviruses
inferredcites →https://doi.org/10.1128/jcm.41.8.3661-3667.2003openalex-snapshot
Virus Detection Protocols for West Nile Virus in Vertebrate and Mosquito Specimens
inferredcites →https://doi.org/10.1371/journal.pbio.0040082openalex-snapshot
West Nile Virus Epidemics in North America Are Driven by Shifts in Mosquito Feeding Behavior
inferredcites →https://doi.org/10.1603/0022-2585-39.5.777openalex-snapshot
Host-Feeding Habits ofCulexand Other Mosquitoes (Diptera: Culicidae) in the Borough of Queens in New York City, with Characters and Techniques for Identification ofCulexMosquitoes
inferredcites →https://doi.org/10.1603/0022-2585-40.2.215openalex-snapshot
Identification of Mosquito Bloodmeals Using Polymerase Chain Reaction (PCR) With Order-Specific Primers
inferredcites →https://doi.org/10.1603/0022-2585-40.6.968openalex-snapshot
Experimental Infection of California Birds with Western Equine Encephalomyelitis and St. Louis Encephalitis Viruses
inferredcites →https://doi.org/10.1641/0006-3568(2004)054[0393:wnvaw]2.0.co;2openalex-snapshot
West Nile Virus and Wildlife
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[0609:batdei]2.0.co;2openalex-snapshot
BIODIVERSITY AND THE DILUTION EFFECT IN DISEASE ECOLOGY
inferredcites →https://doi.org/10.1890/02-3125openalex-snapshot
COMMUNITY DISASSEMBLY, BIODIVERSITY LOSS, AND THE EROSION OF AN ECOSYSTEM SERVICE
inferredcites →https://doi.org/10.2173/bna.amerob.02openalex-snapshot
American Robin (Turdus migratorius)
inferredcites →https://doi.org/10.2307/2404917openalex-snapshot
Shifting Host Choices of the Vector of Chagas Disease, Triatoma Infestans, in Relation to the Availability of Host in Houses in North-West Argentina
inferredcites →https://doi.org/10.3201/eid0704.010403openalex-snapshot
Serologic Evidence for West Nile Virus Infection in Birds in the New York City Vicinity During an Outbreak in 1999
inferredcites →https://doi.org/10.3201/eid0704.010415openalex-snapshot
West Nile Virus Infection in Birds and Mosquitoes, New York State, 2000
inferredcites →https://doi.org/10.3201/eid0704.017403openalex-snapshot
Serologic Evidence for West Nile Virus Infection in Birds in the New York City Vicinity During an Outbreak in 1999
inferredcites →https://doi.org/10.3201/eid0704.017415openalex-snapshot
West Nile Virus Infection in Birds and Mosquitoes, New York State, 2000
inferredcites →https://doi.org/10.3201/eid0809.020152openalex-snapshot
Detection by Enzyme-Linked Immunosorbent Assay of Antibodies toWest Nile virusin Birds
inferredcites →https://doi.org/10.3201/eid0812.010317openalex-snapshot
Identifying Reservoirs of Infection: A Conceptual and Practical Challenge
inferredcites →https://doi.org/10.3201/eid0903.020628openalex-snapshot
Experimental Infection of North American Birds with the New York 1999 Strain of West Nile Virus
inferredcites →https://doi.org/10.3201/eid1008.040077openalex-snapshot
West Nile Virus in California
inferredcites →https://doi.org/10.3201/eid1103.040364openalex-snapshot
West Nile Virus Risk Assessment and the Bridge Vector Paradigm
inferredcites →https://doi.org/10.3201/eid1203.051004openalex-snapshot
Host Feeding Patterns ofCulexMosquitoes and West Nile Virus Transmission, Northeastern United States
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Development of a Species-Diagnostic Polymerase Chain Reaction Assay for the Identification of Culex Vectors of St. Louis Encephalitis Virus Based on Interspecies Sequence Variation in Ribosomal DNA Spacers
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Eastern equine encephalitis virus in birds: relative competence of European starlings (Sturnus vulgaris).
inferredcites →https://doi.org/10.4269/ajtmh.2003.69.641openalex-snapshot
AVIAN HOST PREFERENCE BY VECTORS OF EASTERN EQUINE ENCEPHALOMYELITIS VIRUS
inferredcites →https://doi.org/10.4269/ajtmh.2004.70.566openalex-snapshot
PATTERNS OF WEST NILE VIRUS INFECTION IN OHIO BLUE JAYS: IMPLICATIONS FOR INITIATION OF THE ANNUAL CYCLE
inferredcites →https://doi.org/10.4269/ajtmh.2005.73.1031openalex-snapshot
AVIAN HOSTS FOR WEST NILE VIRUS IN ST. TAMMANY PARISH, LOUISIANA, 2002
inferredcites →https://doi.org/10.7326/0003-4819-117-2-174_4openalex-snapshot
Infectious Diseases of Humans: Dynamics and Control

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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A Novel Temperature-Dependent Mathematical Model of West Nile Virus Transmission Dynamics to Predict the Impacts of Vector-Host Interactions and Vector Management on R0
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Comparative Usutu and West Nile virus transmission potential by local Culex pipiens mosquitoes in north-western Europe
inferred← citeshttps://doi.org/10.1016/j.onehlt.2023.100550openalex-snapshot
Trypanosomes infection, endosymbionts, and host preferences in tsetse flies (Glossina spp.) collected from Akagera park region, Rwanda: A correlational xenomonitoring study
inferred← citeshttps://doi.org/10.1016/j.onehlt.2025.101041openalex-snapshot
Patterns of West Nile virus vector co-occurrence and spatial overlap with human cases across Europe
inferred← citeshttps://doi.org/10.1016/j.onehlt.2026.101326openalex-snapshot
The ecology of biting: buzzing through the main ecological, environmental and biological drivers of mosquito-borne diseases
inferred← citeshttps://doi.org/10.1016/j.onehlt.2026.101571openalex-snapshot
Life-history traits associated to West Nile virus seroprevalence in wild birds: Lessons from the recent outbreaks in Spain
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2010.10.013openalex-snapshot
Simulation of the seasonal cycles of bird, equine and human West Nile virus cases
inferred← citeshttps://doi.org/10.1016/j.pt.2010.06.007openalex-snapshot
New perspectives in tracing vector-borne interaction networks
inferred← citeshttps://doi.org/10.1016/j.pt.2014.11.002openalex-snapshot
Fur or feather? Feeding preferences of species of Culicoides biting midges in Europe
inferred← citeshttps://doi.org/10.1016/j.pt.2015.05.002openalex-snapshot
The context of host competence: a role for plasticity in host–parasite dynamics
inferred← citeshttps://doi.org/10.1016/j.pt.2016.01.001openalex-snapshot
Coupled Heterogeneities and Their Impact on Parasite Transmission and Control
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.180308openalex-snapshot
Toward ecological forecasting of West Nile virus in Florida: Insights from two decades of sentinel chicken surveillance
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.181098openalex-snapshot
Infection and host-feeding patterns of West Nile virus vectors varies by urban greenspace composition
inferred← citeshttps://doi.org/10.1016/j.tim.2009.07.006openalex-snapshot
Bacteriophages as model organisms for virus emergence research
inferred← citeshttps://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot
The ecology and impact of chytridiomycosis: an emerging disease of amphibians
inferred← citeshttps://doi.org/10.1016/j.tree.2014.03.002openalex-snapshot
Assembling evidence for identifying reservoirs of infection
inferred← citeshttps://doi.org/10.1016/j.trstmh.2006.11.007openalex-snapshot
Amplification due to spatial clustering in an individual-based model of mosquito–avian arbovirus transmission
inferred← citeshttps://doi.org/10.1016/j.virol.2007.12.040openalex-snapshot
Fine-scale genetic variation and evolution of West Nile Virus in a transmission “hot spot” in suburban Chicago, USA
inferred← citeshttps://doi.org/10.1016/j.virol.2014.07.009openalex-snapshot
A positively selected mutation in the WNV 2K peptide confers resistance to superinfection exclusion in vivo
inferred← citeshttps://doi.org/10.1016/s0140-6736(12)61151-9openalex-snapshot
Drivers, dynamics, and control of emerging vector-borne zoonotic diseases
inferred← citeshttps://doi.org/10.1017/9781316479964.013openalex-snapshot
Mycoplasma ovipneumoniaein bighorn sheep: from exploration to action
inferred← citeshttps://doi.org/10.1017/s0031182012000200openalex-snapshot
Pangloss revisited: a critique of the dilution effect and the biodiversity-buffers-disease paradigm
inferred← citeshttps://doi.org/10.1017/s0031182015001183openalex-snapshot
Plasmodium prevalence across avian host species is positively associated with exposure to mosquito vectors
inferred← citeshttps://doi.org/10.1017/s0031182016000536openalex-snapshot
The diversity–disease relationship: evidence for and criticisms of the dilution effect
inferred← citeshttps://doi.org/10.1017/s003118201700035xopenalex-snapshot
Avian malaria, ecological host traits and mosquito abundance in southeastern Amazonia
inferred← citeshttps://doi.org/10.1017/s0031182020000943openalex-snapshot
Towards a mechanistic understanding of competence: a missing link in diversity–disease research
inferred← citeshttps://doi.org/10.1017/s0950268816002739openalex-snapshot
Epidemic host community contribution to mosquito-borne disease transmission: Ross River virus
inferred← citeshttps://doi.org/10.1029/2022gh000747openalex-snapshot
Patterns of West Nile Virus in the Northeastern United States Using Negative Binomial and Mechanistic Trait‐Based Models
inferred← citeshttps://doi.org/10.1029/2024gh001194openalex-snapshot
Seasonal Bird Migration Could Explain Regional Synchronicity and Amplification in Human West Nile Virus Case Numbers
inferred← citeshttps://doi.org/10.1038/emi.2017.82openalex-snapshot
Vector competence of European mosquitoes for West Nile virus
inferred← citeshttps://doi.org/10.1038/nature05829openalex-snapshot
West Nile virus emergence and large-scale declines of North American bird populations
inferred← citeshttps://doi.org/10.1038/ncomms13604openalex-snapshot
Anthropogenic impacts on mosquito populations in North America over the past century
inferred← citeshttps://doi.org/10.1038/ncomms14592openalex-snapshot
Ensemble forecast of human West Nile virus cases and mosquito infection rates
inferred← citeshttps://doi.org/10.1038/ncomms2730openalex-snapshot
Identifying sources of tick blood meals using unidentified tandem mass spectral libraries
inferred← citeshttps://doi.org/10.1038/s41467-026-68927-xopenalex-snapshot
Variation in pathogen load and the pathogen load–infectiousness relationship broaden avian malaria’s distribution
inferred← citeshttps://doi.org/10.1038/s41597-026-07648-8openalex-snapshot
A global database of West Nile virus host prevalence and competence
inferred← citeshttps://doi.org/10.1038/s41598-018-24133-4openalex-snapshot
Overwintering of West Nile virus in a bird community with a communal crow roost
inferred← citeshttps://doi.org/10.1038/s41598-019-43246-yopenalex-snapshot
Long-term surveillance defines spatial and temporal patterns implicating Culex tarsalis as the primary vector of West Nile virus
inferred← citeshttps://doi.org/10.1038/s41598-024-73820-yopenalex-snapshot
Mosquito bloodmeals can be used to determine vertebrate diversity, host preference, and pathogen exposure in humans and wildlife
inferred← citeshttps://doi.org/10.1038/s41598-025-97367-8openalex-snapshot
Host and environmental factors drive prevalence of the pathogen Batrachochytrium dendrobatidis in Central African amphibians
inferred← citeshttps://doi.org/10.1038/s42003-020-1032-zopenalex-snapshot
A systemic approach to assess the potential and risks of wildlife culling for infectious disease control
inferred← citeshttps://doi.org/10.1038/srep01519openalex-snapshot
Aedes Taeniorhynchus Vectorial Capacity Informs A Pre-Emptive Assessment Of West Nile Virus Establishment In Galápagos
inferred← citeshttps://doi.org/10.1039/c0em00046aopenalex-snapshot
Environmental monitoring to enhance comprehension and control of infectious diseases
inferred← citeshttps://doi.org/10.1051/mmnp/201712205openalex-snapshot
A Seasonal Model for West Nile Virus
inferred← citeshttps://doi.org/10.1051/vetres/2009026openalex-snapshot
Changing patterns of West Nile virus transmission: altered vector competence and host susceptibility
inferred← citeshttps://doi.org/10.1073/pnas.1310557110openalex-snapshot
Host and parasite diversity jointly control disease risk in complex communities
inferred← citeshttps://doi.org/10.1073/pnas.1416356111openalex-snapshot
Species formation by host shifting in avian malaria parasites
inferred← citeshttps://doi.org/10.1073/pnas.1807106115openalex-snapshot
Species diversity concurrently dilutes and amplifies transmission in a zoonotic host–pathogen system through competing mechanisms
inferred← citeshttps://doi.org/10.1073/pnas.2122851119openalex-snapshot
Wildlife susceptibility to infectious diseases at global scales
inferred← citeshttps://doi.org/10.1080/17513758.2023.2293780openalex-snapshot
A stochastic multi-host model for West Nile virus transmission
inferred← citeshttps://doi.org/10.1080/20477724.2025.2538838openalex-snapshot
New enemies: contribution of C ulex perexiguus in the transmission dynamic of West Nile virus
inferred← citeshttps://doi.org/10.1080/22221751.2022.2134055openalex-snapshot
A One Health view of the West Nile virus outbreak in Andalusia (Spain) in 2020
inferred← citeshttps://doi.org/10.1080/22221751.2024.2348510openalex-snapshot
Warm winters are associated to more intense West Nile virus circulation in southern Spain
inferred← citeshttps://doi.org/10.1080/23744235.2023.2288614openalex-snapshot
Implications of migratory and exotic birds and the mosquito community on West Nile virus transmission
inferred← citeshttps://doi.org/10.1086/668591openalex-snapshot
The Impact of Community Organization on Vector-Borne Pathogens
inferred← citeshttps://doi.org/10.1086/676854openalex-snapshot
Why Is Living Fast Dangerous? Disentangling the Roles of Resistance and Tolerance of Disease
inferred← citeshttps://doi.org/10.1086/682069openalex-snapshot
Host Genotype and Coinfection Modify the Relationship of within and between Host Transmission
inferred← citeshttps://doi.org/10.1086/683173openalex-snapshot
Are All Hosts Created Equal? Partitioning Host Species Contributions to Parasite Persistence in Multihost Communities
inferred← citeshttps://doi.org/10.1086/704182openalex-snapshot
Can Community Structure Causally Determine Dynamics of Constituent Species? A Test Using a Host-Parasite Community
inferred← citeshttps://doi.org/10.1086/736501openalex-snapshot
Temporal Patterns, Behavioral Drivers, and Physiological Correlates of West Nile Virus Exposure in American Robins (Turdus migratorius)
inferred← citeshttps://doi.org/10.1088/0034-4885/77/2/026602openalex-snapshot
Dynamics of infectious diseases
inferred← citeshttps://doi.org/10.1089/vbz.2006.0560openalex-snapshot
Mosquito Landing Rates on Nesting American Robins ( Turdus migratorius )
inferred← citeshttps://doi.org/10.1089/vbz.2006.0602openalex-snapshot
Host Choice and West Nile Virus Infection Rates in Blood-Fed Mosquitoes, Including Members of the Culex pipiens Complex, from Memphis and Shelby County, Tennessee, 2002–2003
inferred← citeshttps://doi.org/10.1089/vbz.2006.0646openalex-snapshot
Bird Movement Predicts Buggy Creek Virus Infection in Insect Vectors
inferred← citeshttps://doi.org/10.1089/vbz.2007.0123openalex-snapshot
Rapid Amplification of West Nile Virus: The Role of Hatch-Year Birds
inferred← citeshttps://doi.org/10.1089/vbz.2007.0200openalex-snapshot
Prevalence of West Nile Virus Neutralizing Antibodies in Spain Is Related to the Behavior of Migratory Birds
inferred← citeshttps://doi.org/10.1089/vbz.2008.0124openalex-snapshot
Dryland Salinity and the Ecology of Ross River Virus: The Ecological Underpinnings of the Potential for Transmission
inferred← citeshttps://doi.org/10.1089/vbz.2008.0146openalex-snapshot
Genetic Variation Associated with Mammalian Feeding in Culex pipiens from a West Nile Virus Epidemic Region in Chicago, Illinois
inferred← citeshttps://doi.org/10.1089/vbz.2009.0029openalex-snapshot
DNA Vaccination of American Robins ( Turdus migratorius ) Against West Nile Virus
inferred← citeshttps://doi.org/10.1089/vbz.2009.0232openalex-snapshot
Incidence of West Nile Virus in Birds Arriving in Wildlife Rehabilitation Centers in Southern Spain
inferred← citeshttps://doi.org/10.1089/vbz.2011.0609openalex-snapshot
Avian Hosts of West Nile Virus in Puerto Rico
inferred← citeshttps://doi.org/10.1089/vbz.2011.0902openalex-snapshot
Implications of Spatial Patterns of Roosting and Movements of American Robins for West Nile Virus Transmission
inferred← citeshttps://doi.org/10.1089/vbz.2013.1342openalex-snapshot
Limited Spillover to Humans from West Nile Virus Viremic Birds in Atlanta, Georgia
inferred← citeshttps://doi.org/10.1089/vbz.2013.1501openalex-snapshot
Reproductive Biology and Susceptibility of Florida Culex coronator to Infection with West Nile Virus
inferred← citeshttps://doi.org/10.1089/vbz.2013.1536openalex-snapshot
Diverse Host Feeding on Nesting Birds May Limit Early-Season West Nile Virus Amplification
inferred← citeshttps://doi.org/10.1089/vbz.2017.2124openalex-snapshot
Culex Flavivirus During West Nile Virus Epidemic and Interepidemic Years in Chicago, United States
inferred← citeshttps://doi.org/10.1089/vbz.2018.2366openalex-snapshot
Influence of Demography, Land Use, and Urban Form on West Nile Virus Risk and Human West Nile Virus Incidence in Ottawa, Canada
inferred← citeshttps://doi.org/10.1089/vbz.2018.2381openalex-snapshot
Feeding Success and Host Selection by Culex quinquefasciatus Say Mosquitoes in Experimental Trials
inferred← citeshttps://doi.org/10.1089/vbz.2018.2387openalex-snapshot
Reviewing the Potential Vectors and Hosts of African Swine Fever Virus Transmission in the United States
inferred← citeshttps://doi.org/10.1089/vbz.2019.2585openalex-snapshot
Associations Between Ross River Virus Infection in Humans and Vector-Vertebrate Community Ecology in Brisbane, Australia
inferred← citeshttps://doi.org/10.1089/vbz.2020.2648openalex-snapshot
Species Traits and Hotspots Associated with Ross River Virus Infection in Nonhuman Vertebrates in South East Queensland
inferred← citeshttps://doi.org/10.1089/vbz.2020.2739openalex-snapshot
Characterization and Host-Feeding Patterns of Culex pipiens s.l. Taxa in a West Nile Virus-Endemic Area in Southeastern Romania
inferred← citeshttps://doi.org/10.1089/vbz.2021.0069openalex-snapshot
Host Associations of Culex pipiens : A Two-Year Analysis of Bloodmeal Sources and Implications for Arboviral Transmission in Southeastern Virginia
inferred← citeshttps://doi.org/10.1093/aesa/saab011openalex-snapshot
Human–Mosquito Contact: A Missing Link in Our Understanding of Mosquito-Borne Disease Transmission Dynamics
inferred← citeshttps://doi.org/10.1093/aje/kwt046openalex-snapshot
Predicting Human West Nile Virus Infections With Mosquito Surveillance Data
inferred← citeshttps://doi.org/10.1093/beheco/arm043openalex-snapshot
Avian defensive behavior and blood-feeding success of the West Nile vector mosquito, Culex pipiens
inferred← citeshttps://doi.org/10.1093/femsle/fnx050openalex-snapshot
Escherichia coli, cattle and the propagation of disease
inferred← citeshttps://doi.org/10.1093/femsmc/xtac018openalex-snapshot
Bacterial–viral interactions: a factor that facilitates transmission heterogeneities
inferred← citeshttps://doi.org/10.1093/icb/icaf077openalex-snapshot
Advancing Theory Underlying Diversity-Disease Relationships: Competence in the Context of Life History, Demography, and Disease
inferred← citeshttps://doi.org/10.1093/icb/icw064openalex-snapshot
Host Competence: An Organismal Trait to Integrate Immunology and Epidemiology
inferred← citeshttps://doi.org/10.1093/icb/icy080openalex-snapshot
Dim light at night: physiological effects and ecological consequences for infectious disease
inferred← citeshttps://doi.org/10.1093/ilar/ilx020openalex-snapshot
Toward an Ecological Framework for Assessing Reservoirs of Vector-Borne Pathogens: Wildlife Reservoirs of Trypanosoma cruzi across the Southern United States
inferred← citeshttps://doi.org/10.1093/jme/tjaa109openalex-snapshot
Surveillance of Culicine Mosquitoes in Six Villages of Taita-Taveta County, Kenya, With Host Determinations From Blood-Fed Females
inferred← citeshttps://doi.org/10.1093/jme/tjaa262openalex-snapshot
Higher West Nile Virus Infection in Aedes albopictus (Diptera: Culicidae) and Culex (Diptera: Culicidae) Mosquitoes From Lower Income Neighborhoods in Urban Baltimore, MD
inferred← citeshttps://doi.org/10.1093/jme/tjaf068openalex-snapshot
Exploring factors affecting the reintroduction and amplification of West Nile virus in heterogeneous landscapes in Canada, using a cellular automata approach
inferred← citeshttps://doi.org/10.1093/jme/tjaf105openalex-snapshot
Mosquitoes in small urban spaces: identification of blood meals and flight distances of engorged females in the southern Great Plains of the United States
inferred← citeshttps://doi.org/10.1093/jme/tjx078openalex-snapshot
Abundance and Bloodfeeding Patterns of Mosquitoes (Diptera: Culicidae) in an Oak Woodland on the Eastern Slope of the Northern Coast Range of California
inferred← citeshttps://doi.org/10.1093/jme/tjz146openalex-snapshot
West Nile Virus Mosquito Vectors in North America
inferred← citeshttps://doi.org/10.1093/jme/tjz149openalex-snapshot
Impact of West Nile Virus on Bird Populations: Limited Lasting Effects, Evidence for Recovery, and Gaps in Our Understanding of Impacts on Ecosystems
inferred← citeshttps://doi.org/10.1093/jme/tjz151openalex-snapshot
Introduction, Spread, and Establishment of West Nile Virus in the Americas
inferred← citeshttps://doi.org/10.1093/jmedent/45.1.125openalex-snapshot
Culex pipiens(Diptera: Culicidae): A Bridge Vector of West Nile Virus to Humans
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