On the public citation graph

Global, asynchronous partial sweeps at multiple insecticide resistance genes in Aedes mosquitoes

https://doi.org/10.1101/2024.04.09.588653
0 signed · 79 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/arch.21428openalex-snapshot
Carbonic anhydrase II confers resistance to deltamethrin in Culex pipiens pallens
inferredcites →https://doi.org/10.1002/ece3.5198openalex-snapshot
Wolbachia pipientis occurs in Aedes aegypti populations in New Mexico and Florida, USA
inferredcites →https://doi.org/10.1002/ps.5538openalex-snapshot
Origin of resistance to pyrethroids in the redlegged earth mite (Halotydeus destructor) in Australia: repeated local evolution and migration
inferredcites →https://doi.org/10.1006/pest.1993.1001openalex-snapshot
Action of Esterase B1 on Chlorpyrifos in Organophosphate-Resistant Culex Mosquitos
inferredcites →https://doi.org/10.1007/s11356-022-21362-zopenalex-snapshot
Biomarker development for neonicotinoid exposure in soil under interaction with the synergist piperonyl butoxide in Folsomia candida
inferredcites →https://doi.org/10.1016/j.abb.2005.03.021openalex-snapshot
Serine proteinase over-expression in relation to deltamethrin resistance in Culex pipiens pallens
inferredcites →https://doi.org/10.1016/j.ajhg.2015.11.020openalex-snapshot
Genotype Imputation with Millions of Reference Samples
inferredcites →https://doi.org/10.1016/j.ibmb.2008.08.007openalex-snapshot
P450 reductase and cytochrome b5 interactions with cytochrome P450: Effects on house fly CYP6A1 catalysis
inferredcites →https://doi.org/10.1016/j.ibmb.2010.12.005openalex-snapshot
The role of the Aedes aegypti Epsilon glutathione transferases in conferring resistance to DDT and pyrethroid insecticides
inferredcites →https://doi.org/10.1016/j.micinf.2009.05.005openalex-snapshot
Aedes albopictus, an arbovirus vector: From the darkness to the light
inferredcites →https://doi.org/10.1016/j.pestbp.2016.03.005openalex-snapshot
Pyrethroid resistance in Aedes aegypti and Aedes albopictus: Important mosquito vectors of human diseases
inferredcites →https://doi.org/10.1016/j.pestbp.2019.10.002openalex-snapshot
Polymorphisms in GSTE2 is associated with temephos resistance in Aedes aegypti
inferredcites →https://doi.org/10.1016/j.pt.2021.05.002openalex-snapshot
Improving mosquito control strategies with population genomics
inferredcites →https://doi.org/10.1016/j.tree.2012.08.024openalex-snapshot
Founder takes all: density-dependent processes structure biodiversity
inferredcites →https://doi.org/10.1016/s0025-326x(02)00131-5openalex-snapshot
Chlorohydrocarbon pesticides in the Australian marine environment after banning in the period from the 1970s to 1980s
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1038/23685openalex-snapshot
Tracking the evolution of insecticide resistance in the mosquito Culex pipiens
inferredcites →https://doi.org/10.1038/nature08365openalex-snapshot
Reconstructing Indian population history
inferredcites →https://doi.org/10.1038/nature12060openalex-snapshot
The global distribution and burden of dengue
inferredcites →https://doi.org/10.1038/ncomms5105openalex-snapshot
Mesoporous silicon sponge as an anti-pulverization structure for high-performance lithium-ion battery anodes
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/s41467-022-32316-xopenalex-snapshot
Repeated genetic adaptation to altitude in two tropical butterflies
inferredcites →https://doi.org/10.1038/s41586-018-0692-zopenalex-snapshot
Improved reference genome of Aedes aegypti informs arbovirus vector control
inferredcites →https://doi.org/10.1038/s41598-019-56766-4openalex-snapshot
Aedes aegypti insecticide resistance underlies the success (and failure) of Wolbachia population replacement
inferredcites →https://doi.org/10.1042/bst025526sopenalex-snapshot
Amplification of a xanthine dehydrogenase gene is associated with insecticide resistance in the common house mosquito Culex quinquefasciatus
inferredcites →https://doi.org/10.1046/j.1365-2915.2000.00222.xopenalex-snapshot
Resistance to dieldrin + fipronil assorts with chromosome inversion 2La in the malaria vector Anopheles gambiae
inferredcites →https://doi.org/10.1073/pnas.0508391103openalex-snapshot
Global traffic and disease vector dispersal
inferredcites →https://doi.org/10.1074/jbc.271.33.20187openalex-snapshot
Identification of a Drosophila melanogaster Glutamate-gated Chloride Channel Sensitive to the Antiparasitic Agent Avermectin
inferredcites →https://doi.org/10.1083/jcb.200109026openalex-snapshot
Ankyrin-G coordinates assembly of the spectrin-based membrane skeleton, voltage-gated sodium channels, and L1 CAMs at Purkinje neuron initial segments
inferredcites →https://doi.org/10.1093/bioinformatics/bts606openalex-snapshot
A high-performance computing toolset for relatedness and principal component analysis of SNP data
inferredcites →https://doi.org/10.1093/biosci/biy119openalex-snapshot
Recent History of Aedes aegypti : Vector Genomics and Epidemiology Records
inferredcites →https://doi.org/10.1093/biosci/biz005openalex-snapshot
Letter to the Editor
inferredcites →https://doi.org/10.1093/gigascience/giab008openalex-snapshot
Twelve years of SAMtools and BCFtools
inferredcites →https://doi.org/10.1093/jme/tjad015openalex-snapshot
A Globally Distributed Insecticide Resistance Allele Confers a Fitness Cost in the Absence of Insecticide in Aedes aegypti (Diptera: Culicidae), the Yellow Fever Mosquito
inferredcites →https://doi.org/10.1093/jme/tjae005openalex-snapshot
Diversity and distribution of sodium channel mutations in Aedes albopictus (Diptera: Culicidae)
inferredcites →https://doi.org/10.1093/jme/tjx145openalex-snapshot
Pyrethroid Susceptibility Has Been Maintained in the Dengue Vector, Aedes aegypti (Diptera: Culicidae), in Queensland, Australia
inferredcites →https://doi.org/10.1093/molbev/msad072openalex-snapshot
Strong Positive Selection in Aedes aegypti and the Rapid Evolution of Insecticide Resistance
inferredcites →https://doi.org/10.1093/molbev/msy023openalex-snapshot
RADpainter and fineRADstructure: Population Inference from RADseq Data
inferredcites →https://doi.org/10.1097/00001756-200008210-00018openalex-snapshot
Co-existence in DUM neurones of two GluCl channels that differ in their picrotoxin sensitivity
inferredcites →https://doi.org/10.1098/rstb.2012.0429openalex-snapshot
Role of cytochrome P450s in insecticide resistance: impact on the control of mosquito-borne diseases and use of insecticides on Earth
inferredcites →https://doi.org/10.1101/gr.245795.118openalex-snapshot
Whole-genome sequencing reveals high complexity of copy number variation at insecticide resistance loci in malaria mosquitoes
inferredcites →https://doi.org/10.1111/1755-0998.12369openalex-snapshot
Linkage disequilibrium network analysis ( LD na) gives a global view of chromosomal inversions, local adaptation and geographic structure
inferredcites →https://doi.org/10.1111/1755-0998.12995openalex-snapshot
Minor allele frequency thresholds strongly affect population structure inference with genomic data sets
inferredcites →https://doi.org/10.1111/1755-0998.13366openalex-snapshot
LEA 3: Factor models in population genetics and ecological genomics with R
inferredcites →https://doi.org/10.1111/eva.12787openalex-snapshot
Tracking genetic invasions: Genome‐wide single nucleotide polymorphisms reveal the source of pyrethroid‐resistant Aedes aegypti (yellow fever mosquito) incursions at international ports
inferredcites →https://doi.org/10.1111/j.0269-283x.2004.00513.xopenalex-snapshot
Critical review of the vector status of Aedes albopictus
inferredcites →https://doi.org/10.1111/mec.15253openalex-snapshot
Stacks 2: Analytical methods for paired‐end sequencing improve RADseq‐based population genomics
inferredcites →https://doi.org/10.1111/mec.15430openalex-snapshot
Heterogeneous genetic invasions of three insecticide resistance mutations in Indo‐Pacific populations of Aedes aegypti (L.)
inferredcites →https://doi.org/10.1111/mec.15645openalex-snapshot
A 6.5‐kb intergenic structural variation enhances P450‐mediated resistance to pyrethroids in malaria vectors lowering bed net efficacy
inferredcites →https://doi.org/10.1126/sciadv.abq7345openalex-snapshot
Discovery of super–insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations
inferredcites →https://doi.org/10.1146/annurev-genet-111212-133526openalex-snapshot
Detecting Natural Selection in Genomic Data
inferredcites →https://doi.org/10.1186/1741-7007-7-47openalex-snapshot
Evidence for inhibition of cholinesterases in insect and mammalian nervous systems by the insect repellent deet
inferredcites →https://doi.org/10.1186/1756-3305-6-315openalex-snapshot
Patterns of phenoloxidase activity in insecticide resistant and susceptible mosquitoes differ between laboratory-selected and wild-caught individuals
inferredcites →https://doi.org/10.1186/gb-2014-15-2-r27openalex-snapshot
A single mutation in the GSTe2 gene allows tracking of metabolically based insecticide resistance in a major malaria vector
inferredcites →https://doi.org/10.1186/s12936-019-2705-2openalex-snapshot
UDP-glycosyltransferase genes and their association and mutations associated with pyrethroid resistance in Anopheles sinensis (Diptera: Culicidae)
inferredcites →https://doi.org/10.1186/s13071-019-3585-6openalex-snapshot
Insecticide resistance status of Aedes aegypti and Aedes albopictus mosquitoes in Papua New Guinea
inferredcites →https://doi.org/10.1371/journal.pbio.2000618openalex-snapshot
The ace-1 Locus Is Amplified in All Resistant Anopheles gambiae Mosquitoes: Fitness Consequences of Homogeneous and Heterogeneous Duplications
inferredcites →https://doi.org/10.1371/journal.pbio.3001190openalex-snapshot
Peroxiredoxin alleviates the fitness costs of imidacloprid resistance in an insect pest of rice
inferredcites →https://doi.org/10.1371/journal.pgen.1000686openalex-snapshot
A Genealogical Interpretation of Principal Components Analysis
inferredcites →https://doi.org/10.1371/journal.pgen.1002967openalex-snapshot
Inference of Population Splits and Mixtures from Genome-Wide Allele Frequency Data
inferredcites →https://doi.org/10.1371/journal.pgen.1006539openalex-snapshot
Genomic Footprints of Selective Sweeps from Metabolic Resistance to Pyrethroids in African Malaria Vectors Are Driven by Scale up of Insecticide-Based Vector Control
inferredcites →https://doi.org/10.1371/journal.pgen.1008822openalex-snapshot
An Africa-wide genomic evolution of insecticide resistance in the malaria vector Anopheles funestus involves selective sweeps, copy number variations, gene conversion and transposons
inferredcites →https://doi.org/10.1371/journal.pntd.0004374openalex-snapshot
Genetic Diversity and Phylogeny of Aedes aegypti, the Main Arbovirus Vector in the Pacific
inferredcites →https://doi.org/10.1371/journal.pntd.0005546openalex-snapshot
Tiger on the prowl: Invasion history and spatio-temporal genetic structure of the Asian tiger mosquito Aedes albopictus (Skuse 1894) in the Indo-Pacific
inferredcites →https://doi.org/10.1371/journal.pntd.0005653openalex-snapshot
Tracking the return of Aedes aegypti to Brazil, the major vector of the dengue, chikungunya and Zika viruses
inferredcites →https://doi.org/10.1371/journal.pntd.0006933openalex-snapshot
CYP-mediated permethrin resistance in Aedes aegypti and evidence for trans-regulation
inferredcites →https://doi.org/10.1371/journal.pntd.0008154openalex-snapshot
Evidence for both sequential mutations and recombination in the evolution of kdr alleles in Aedes aegypti
inferredcites →https://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
inferredcites →https://doi.org/10.1371/journal.pntd.0008463openalex-snapshot
Population genomics of two invasive mosquitoes (Aedes aegypti and Aedes albopictus) from the Indo-Pacific
inferredcites →https://doi.org/10.1371/journal.pone.0037135openalex-snapshot
Double Digest RADseq: An Inexpensive Method for De Novo SNP Discovery and Genotyping in Model and Non-Model Species
inferredcites →https://doi.org/10.1371/journal.pone.0151049openalex-snapshot
The Role of Oxidative Stress in the Longevity and Insecticide Resistance Phenotype of the Major Malaria Vectors Anopheles arabiensis and Anopheles funestus
inferredcites →https://doi.org/10.1371/journal.pone.0211497openalex-snapshot
Vgsc-interacting proteins are genetically associated with pyrethroid resistance in Aedes aegypti
inferredcites →https://doi.org/10.1534/genetics.115.183913openalex-snapshot
Admixture, Population Structure, and F -Statistics
inferredcites →https://doi.org/10.1603/033.046.0411openalex-snapshot
Permethrin Induces Overexpression of Cytochrome c Oxidase Subunit 3 in Aedes aegypti
inferredcites →https://doi.org/10.3390/insects12020167openalex-snapshot
A Linkage-Based Genome Assembly for the Mosquito Aedes albopictus and Identification of Chromosomal Regions Affecting Diapause
inferredcites →https://doi.org/10.4137/ijis.s18029openalex-snapshot
Insecticides and Bio-insecticides Modulate the Glutathione-related Antioxidant Defense System of Cowpea Storage Bruchid (Callosobruchus maculatus)
inferredcites →https://doi.org/10.5897/ajb2009.000-9218openalex-snapshot
Insecticide resistance and glutathione S-transferases in mosquitoes: A review
inferredcites →https://doi.org/10.7554/elife.08347openalex-snapshot
The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus
inferredcites →https://doi.org/10.7883/yoken.64.217openalex-snapshot
First Detection of a Putative Knockdown Resistance Gene in Major Mosquito Vector, Aedes albopictus
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.