On the public citation graph
Levels of Resistance to Pyrethroid among DistinctkdrAlleles inAedes aegyptiLaboratory Lines and Frequency ofkdrAlleles in 27 Natural Populations from Rio de Janeiro, Brazil
0 signed · 99 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.ibmb.2009.01.001openalex-snapshot
A novel amino acid substitution in a voltage-gated sodium channel is associated with knockdown resistance to permethrin in Aedes aegypti
inferredcites →https://doi.org/10.1016/j.ibmb.2010.09.005openalex-snapshot
A sodium channel mutation identified in Aedes aegypti selectively reduces cockroach sodium channel sensitivity to type I, but not type II pyrethroids
inferredcites →https://doi.org/10.1016/j.ibmb.2014.03.012openalex-snapshot
Molecular biology of insect sodium channels and pyrethroid resistance
inferredcites →https://doi.org/10.1017/s0950268800056788openalex-snapshot
Dengue epidemic in the state of Rio de Janeiro, Brazil, 1990–1: co-circulation of dengue 1 and dengue 2 serotypes
inferredcites →https://doi.org/10.1038/nature12060openalex-snapshot
The global distribution and burden of dengue
inferredcites →https://doi.org/10.1038/s41598-017-05186-3openalex-snapshot
Potential risk of re-emergence of urban transmission of Yellow Fever virus in Brazil facilitated by competent Aedes populations
inferredcites →https://doi.org/10.1046/j.1365-2915.2003.00412.xopenalex-snapshot
Pyrethroid and DDT cross‐resistance in Aedes aegypti is correlated with novel mutations in the voltage‐gated sodium channel gene
inferredcites →https://doi.org/10.1073/pnas.1305118110openalex-snapshot
Molecular evidence for dual pyrethroid-receptor sites on a mosquito sodium channel
inferredcites →https://doi.org/10.1073/pnas.1715788115openalex-snapshot
Field- and clinically derived estimates of Wolbachia -mediated blocking of dengue virus transmission potential in Aedes aegypti mosquitoes
inferredcites →https://doi.org/10.1093/emph/eot012openalex-snapshot
Evidence for gene duplication in the voltage-gated sodium channel gene of Aedes aegypti
inferredcites →https://doi.org/10.1093/jee/83.4.1151openalex-snapshot
Choosing the Optimal Diagnostic Dose for Monitoring Insecticide Resistance
inferredcites →https://doi.org/10.1098/rstb.1998.0319openalex-snapshot
Why are there so few resistance–associated mutations in insecticide target genes?
inferredcites →https://doi.org/10.1111/eva.12301openalex-snapshot
Contrasting genetic structure between mitochondrial and nuclear markers in the dengue fever mosquito from Rio de Janeiro: implications for vector control
inferredcites →https://doi.org/10.1111/imb.12206openalex-snapshot
Overcoming super‐knock down resistance ( super‐kdr ) mediated resistance: multi‐halogenated benzyl pyrethroids are more toxic to super‐kdr than kdr house flies
inferredcites →https://doi.org/10.1111/imb.12267openalex-snapshot
Diversity of knockdown resistance alleles in a single house fly population facilitates adaptation to pyrethroid insecticides
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00774.xopenalex-snapshot
A mutation in the voltage‐gated sodium channel gene associated with pyrethroid resistance in Latin American Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-3156.2009.02378.xopenalex-snapshot
Frequency of Val1016Ile mutation in the voltage‐gated sodium channel gene of Aedes aegypti Brazilian populations
inferredcites →https://doi.org/10.1111/mve.12241openalex-snapshot
Insecticide resistance, associated mechanisms and fitness aspects in two B razilian S tegomyia aegypti (= A edes aegypti ) populations
inferredcites →https://doi.org/10.1155/2016/8603263openalex-snapshot
Resistance Status to the Insecticides Temephos, Deltamethrin, and Diflubenzuron in BrazilianAedes aegyptiPopulations
inferredcites →https://doi.org/10.1186/1753-6561-8-s4-o11openalex-snapshot
Project Aedes transgenic population control in Juazeiro and Jacobina Bahia, Brazil
inferredcites →https://doi.org/10.1186/1756-3305-6-253openalex-snapshot
Detection of the V1016G mutation in the voltage-gated sodium channel gene of Aedes aegypti (Diptera: Culicidae) by allele-specific PCR assay, and its distribution and effect on deltamethrin resistance in Thailand
inferredcites →https://doi.org/10.1186/1756-3305-7-25openalex-snapshot
Distribution and dissemination of the Val1016Ile and Phe1534Cys Kdr mutations in Aedes aegypti Brazilian natural populations
inferredcites →https://doi.org/10.1186/s13071-015-0797-2openalex-snapshot
Contrasting patterns of insecticide resistance and knockdown resistance (kdr) in the dengue vectors Aedes aegypti and Aedes albopictus from Malaysia
inferredcites →https://doi.org/10.1186/s13071-016-1346-3openalex-snapshot
Spatial variation of insecticide resistance in the dengue vector Aedes aegypti presents unique vector control challenges
inferredcites →https://doi.org/10.1186/s13071-017-2096-6openalex-snapshot
Combined target site (kdr) mutations play a primary role in highly pyrethroid resistant phenotypes of Aedes aegypti from Saudi Arabia
inferredcites →https://doi.org/10.1371/journal.pntd.0000531openalex-snapshot
Recent Rapid Rise of a Permethrin Knock Down Resistance Allele in Aedes aegypti in México
inferredcites →https://doi.org/10.1371/journal.pntd.0002948openalex-snapshot
Mechanisms of Pyrethroid Resistance in the Dengue Mosquito Vector, Aedes aegypti: Target Site Insensitivity, Penetration, and Metabolism
inferredcites →https://doi.org/10.1371/journal.pntd.0004263openalex-snapshot
Coevolution of the Ile1,016 and Cys1,534 Mutations in the Voltage Gated Sodium Channel Gene of Aedes aegypti in Mexico
inferredcites →https://doi.org/10.1371/journal.pntd.0004780openalex-snapshot
Discovery of Point Mutations in the Voltage-Gated Sodium Channel from African Aedes aegypti Populations: Potential Phylogenetic Reasons for Gene Introgression
inferredcites →https://doi.org/10.1371/journal.pntd.0005625openalex-snapshot
Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans
inferredcites →https://doi.org/10.1371/journal.pntd.0005799openalex-snapshot
Insecticide resistance is mediated by multiple mechanisms in recently introduced Aedes aegypti from Madeira Island (Portugal)
inferredcites →https://doi.org/10.1371/journal.pntd.0006227openalex-snapshot
The impact of insecticide applications on the dynamics of resistance: The case of four Aedes aegypti populations from different Brazilian regions
inferredcites →https://doi.org/10.1371/journal.pone.0001243openalex-snapshot
Multiple Origins of Knockdown Resistance Mutations in the Afrotropical Mosquito Vector Anopheles gambiae
inferredcites →https://doi.org/10.1371/journal.pone.0031889openalex-snapshot
Effect of Insecticide Resistance on Development, Longevity and Reproduction of Field or Laboratory Selected Aedes aegypti Populations
inferredcites →https://doi.org/10.1371/journal.pone.0052761openalex-snapshot
Multiple Origins of kdr-type Resistance in the House Fly, Musca domestica
inferredcites →https://doi.org/10.1371/journal.pone.0060878openalex-snapshot
Assessing the Effects of Aedes aegypti kdr Mutations on Pyrethroid Resistance and Its Fitness Cost
inferredcites →https://doi.org/10.1590/0037-8682-0141-2014openalex-snapshot
Impact of insecticide resistance on the field control of Aedes aegypti in the State of São Paulo
inferredcites →https://doi.org/10.1590/s0074-02762001000700007openalex-snapshot
Dengue virus type 3 in Rio de Janeiro, Brazil
inferredcites →https://doi.org/10.1603/me10152openalex-snapshot
Early History of Laboratory Breeding of Aedes aegypti (Diptera: Culicidae) Focusing on the Origins and Use of Selected Strains
inferredcites →https://doi.org/10.3390/insects7040060openalex-snapshot
Sodium Channel Mutations and Pyrethroid Resistance in Aedes aegypti
inferredcites →https://doi.org/10.4269/ajtmh.2003.68.329openalex-snapshot
RESISTANCE OF AEDES AEGYPTI TO ORGANOPHOSPHATES IN SEVERAL MUNICIPALITIES IN THE STATE OF RIO DE JANEIRO AND ESPiRITO SANTO, BRAZIL
inferredcites →https://doi.org/10.4269/ajtmh.2009.81.108openalex-snapshot
Voltage-Gated Sodium Channel Polymorphism and Metabolic Resistance in Pyrethroid-Resistant Aedes aegypti from Brazil
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.6620/zs.2025.64-31zenodo-depositor-declared
Understanding the Global Dynamics of Pyrethroid Resistance-related kdr mutations in Aedes (Stegomyia) aegypti (Linnaeus, 1762) (Diptera: Culicidae).
inferred← citeshttps://doi.org/10.1002/arch.21686openalex-snapshot
Chronology of sodium channel mutations associated with pyrethroid resistance in Aedes aegypti
inferred← citeshttps://doi.org/10.1002/ps.6366openalex-snapshot
Mutations associated with pyrethroid resistance in Varroa mite, a parasite of honey bees, are widespread across the United States
inferred← citeshttps://doi.org/10.1002/ps.6679openalex-snapshot
On the use of inhibitors of 4‐hydroxyphenylpyruvate dioxygenase as a vector‐selective insecticide in the control of mosquitoes
inferred← citeshttps://doi.org/10.1002/ps.8495openalex-snapshot
The V410L kdr allele in the VGSC confers higher levels of field resistance to permethrin in urban mosquito populations of Aedes aegypti (L.)
inferred← citeshttps://doi.org/10.1016/j.actatropica.2018.12.021openalex-snapshot
Mechanisms of pyrethroid resistance in Aedes (Stegomyia) aegypti from Colombia
inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107946openalex-snapshot
Susceptibility to the larvicide pyriproxyfen and genotyping of kdr mutations in two Aedes aegypti populations from Maranhão State, Brazil
inferred← citeshttps://doi.org/10.1016/j.pestbp.2020.104652openalex-snapshot
Reduced neuronal sensitivity and susceptibility of the fall armyworm, Spodoptera frugiperda, to pyrethroids in the absence of known knockdown mutations
inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.105994openalex-snapshot
Glycine to valine substitution in the short intracellular linkers of domain II enhances I1011M-mediated sodium channel resistance to Type I pyrethroids, but not Type II pyrethroids
inferred← citeshttps://doi.org/10.1038/s41598-019-56766-4openalex-snapshot
Aedes aegypti insecticide resistance underlies the success (and failure) of Wolbachia population replacement
inferred← citeshttps://doi.org/10.1038/s41598-020-70029-7openalex-snapshot
Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018
inferred← citeshttps://doi.org/10.1038/s41598-021-83465-wopenalex-snapshot
Insecticide resistance and underlying targets-site and metabolic mechanisms in Aedes aegypti and Aedes albopictus from Lahore, Pakistan
inferred← citeshttps://doi.org/10.1038/s41598-023-44430-xopenalex-snapshot
Genetic structure and kdr mutations in Aedes aegypti populations along a road crossing the Amazon Forest in Amapá State, Brazil
inferred← citeshttps://doi.org/10.1038/s41598-025-08989-xopenalex-snapshot
High voltage-gated sodium channel gene diversity in Aedes albopictus across Brazil
inferred← citeshttps://doi.org/10.1038/s41598-026-74046-wopenalex-snapshot
Rapid and cost-effective screening of pyrethroid resistance markers in Musca domestica using RNAse H2 PCR
inferred← citeshttps://doi.org/10.1093/jisesa/iez054openalex-snapshot
Screening Aedes aegypti (Diptera: Culicidae) Populations From Pernambuco, Brazil for Resistance to Temephos, Diflubenzuron, and Cypermethrin and Characterization of Potential Resistance Mechanisms
inferred← citeshttps://doi.org/10.1093/jme/tjaa249openalex-snapshot
Effect of Larval Food Availability on Adult Aedes Aegypti (Diptera: Culicidae) Fitness and Susceptibility to Zika Infection
inferred← citeshttps://doi.org/10.1093/jme/tjad051openalex-snapshot
Persistent variation in insecticide resistance intensity in container breeding Aedes (Diptera: Culicidae) co-collected in Houston, TX
inferred← citeshttps://doi.org/10.1093/jme/tjz161openalex-snapshot
Action of Metarhizium brunneum (Hypocreales: Clavicipitaceae) Against Organophosphate- and Pyrethroid-Resistant Aedes aegypti (Diptera: Culicidae) and the Synergistic Effects of Phenylthiourea
inferred← citeshttps://doi.org/10.1093/jme/tjz241openalex-snapshot
Co-occurrence of kdr Mutations V1016I and F1534C and Its Association With Phenotypic Resistance to Pyrethroids in Aedes aegypti (Diptera: Culicidae) Populations From Costa Rica
inferred← citeshttps://doi.org/10.1101/2020.02.25.964270openalex-snapshot
The need to harmonize insecticide resistance testing: methodology, intensity concentrations and molecular mechanisms evaluated in Aedes aegypti populations in Central America and Hispaniola
inferred← citeshttps://doi.org/10.1101/2020.06.22.164483openalex-snapshot
Combination of kdr mutation and detoxification gene expression associated with high tolerance for permethrin in a resistant Aedes aegypti population
inferred← citeshttps://doi.org/10.1101/2022.08.26.505371openalex-snapshot
Multiplex high resolution melting PCR for simultaneous genotyping of pyrethroid-resistance associated mutations in Aedes aegypti. First report on kdr mutations in wild populations from Argentina
inferred← citeshttps://doi.org/10.1101/669747openalex-snapshot
On the use of inhibitors of 4-hydroxyphenylpyruvate dioxygenase as a vector-selective insecticide in the control of mosquitoes
inferred← citeshttps://doi.org/10.1111/eva.13269openalex-snapshot
Rapid evolution of knockdown resistance haplotypes in response to pyrethroid selection in Aedes aegypti
inferred← citeshttps://doi.org/10.1111/eva.70305openalex-snapshot
The Evolution of Knockdown Resistance: Genotypic and Phenotypic Insights Into Aedes aegypti Insecticide Resistance
inferred← citeshttps://doi.org/10.1128/spectrum.00128-24openalex-snapshot
Wolbachia strains w Mel and w AlbB differentially affect Aedes aegypti traits related to fecundity
inferred← citeshttps://doi.org/10.1136/bmjpo-2019-000469openalex-snapshot
Safety of azithromycin in paediatrics: a systematic review protocol
inferred← citeshttps://doi.org/10.1186/s12936-025-05385-8openalex-snapshot
First large-scale assessment of pyrethroid resistance in Anopheles darlingi (Diptera: Culicidae) in Brazil (2021-2024): a crucial step in informing decision-making in malaria control
inferred← citeshttps://doi.org/10.1186/s13071-020-04127-wopenalex-snapshot
Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State
inferred← citeshttps://doi.org/10.1186/s13071-020-04166-3openalex-snapshot
Insecticide resistance, fitness and susceptibility to Zika infection of an interbred Aedes aegypti population from Rio de Janeiro, Brazil
inferred← citeshttps://doi.org/10.1186/s13071-020-04503-6openalex-snapshot
Insecticide resistance status of Aedes aegypti in Bangladesh
inferred← citeshttps://doi.org/10.1186/s13071-023-05840-yopenalex-snapshot
First report on knockdown resistance mutations in wild populations of Aedes aegypti from Argentina determined by a novel multiplex high-resolution melting polymerase chain reaction method
inferred← citeshttps://doi.org/10.1186/s13071-023-06066-8openalex-snapshot
First report of kdr mutations in the voltage-gated sodium channel gene in the arbovirus vector, Aedes aegypti, from Nouakchott, Mauritania
inferred← citeshttps://doi.org/10.1186/s13071-025-06817-9openalex-snapshot
Global distribution and impact of knockdown resistance mutations in Aedes aegypti on pyrethroid resistance
inferred← citeshttps://doi.org/10.1186/s13071-026-07619-3openalex-snapshot
Insecticide susceptibility and knockdown resistance (Kdr) mutations (F1534C and V1016I) in Aedes aegypti populations from Dar es Salaam, Tanzania
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007023openalex-snapshot
Matching the genetics of released and local Aedes aegypti populations is critical to assure Wolbachia invasion
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007432openalex-snapshot
Molecular evidence of sequential evolution of DDT- and pyrethroid-resistant sodium channel in Aedes aegypti
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007439openalex-snapshot
Insecticide resistance levels and mechanisms in Aedes aegypti populations in and around Ouagadougou, Burkina Faso
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008219openalex-snapshot
Evolution of kdr haplotypes in worldwide populations of Aedes aegypti: Independent origins of the F1534C kdr mutation
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008492openalex-snapshot
Insecticide resistance and genetic structure of Aedes aegypti populations from Rio de Janeiro State, Brazil
inferred← citeshttps://doi.org/10.1371/journal.pntd.0009833openalex-snapshot
Kdr genotyping (V1016I, F1534C) of the Nav channel of Aedes aegypti (L.) mosquito populations in Harris County (Houston), Texas, USA, after Permanone 31–66 field tests and its influence on probability of survival
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010780openalex-snapshot
The role of voltage-gated sodium channel genotypes in pyrethroid resistance in Aedes aegypti in Taiwan
inferred← citeshttps://doi.org/10.1371/journal.pntd.0012768openalex-snapshot
First detection of the S989P+V1016G+D1763Y haplotype and expansion of voltage-gated sodium channel mutations in Aedes aegypti in Taiwan in 2016–2023
inferred← citeshttps://doi.org/10.1590/0074-02760190120openalex-snapshot
Liaisons dangereuses: cross-border gene flow and dispersal of insecticide resistance-associated genes in the mosquito Aedes aegypti from Brazil and French Guiana
inferred← citeshttps://doi.org/10.24072/pcjournal.497openalex-snapshot
A genomic duplication spanning multiple P450s contributes to insecticide resistance in the dengue mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.3389/fcimb.2026.1777964openalex-snapshot
F1534S kdr mutation drives the geographical heterogeneity of pyrethroid resistance in Aedes albopictus from Hangzhou, China
inferred← citeshttps://doi.org/10.3389/fgene.2022.867231openalex-snapshot
Genome-wide Association Study Reveals New Loci Associated With Pyrethroid Resistance in Aedes aegypti
inferred← citeshttps://doi.org/10.3389/fpubh.2023.1166007openalex-snapshot
Pyrethroid genetic resistance in the dengue vector (Aedes aegypti) in Posadas, Argentina
inferred← citeshttps://doi.org/10.3390/genes15081046openalex-snapshot
Impact of Long-Term Pyriproxyfen Exposure on the Genetic Structure and Diversity of Aedes aegypti and Aedes albopictus in Manaus, Amazonas, Brazil
inferred← citeshttps://doi.org/10.3390/insects12010071openalex-snapshot
Permethrin Resistance in Aedes aegypti Affects Aspects of Vectorial Capacity
inferred← citeshttps://doi.org/10.3390/insects15110863openalex-snapshot
Detection of the 1016Gly and 989Pro Knockdown Resistance Mutations in Florida, USA Aedes aegypti
inferred← citeshttps://doi.org/10.3390/insects16030254openalex-snapshot
Assessing Temperature-Dependent Deltamethrin Toxicity in Various kdr Genotypes of Aedes aegypti Mosquitoes
inferred← citeshttps://doi.org/10.3390/pathogens13060457openalex-snapshot
High Frequencies of kdr Mutation and Chikungunya Infection in Aedes aegypti Population from Minas Gerais, Brazil
inferred← citeshttps://doi.org/10.6084/m9.figshare.12344981openalex-snapshot
Additional file 1 of Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State
inferred← citeshttps://doi.org/10.6084/m9.figshare.26602603openalex-snapshot
Additional file 1 of First report on knockdown resistance mutations in wild populations of Aedes aegypti from Argentina determined by a novel multiplex high-resolution melting polymerase chain reaction method
inferred← citeshttps://doi.org/10.6084/m9.figshare.26602606openalex-snapshot
Additional file 2 of First report on knockdown resistance mutations in wild populations of Aedes aegypti from Argentina determined by a novel multiplex high-resolution melting polymerase chain reaction method
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.