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The transmission and effects of Wolbachia bacteria in parasitoids
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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 Centrosome and Its Mode of Inheritance: The Reduction of the Centrosome during Gametogenesis and Its Restoration during Fertilization
inferredcites →https://doi.org/10.1006/jipa.1997.4739openalex-snapshot
Screening Mollusks forWolbachiaInfection
inferredcites →https://doi.org/10.1007/978-1-4684-1402-8_14openalex-snapshot
Sex Determination and Sex Ratio Patterns in Parasitic Hymenoptera
inferredcites →https://doi.org/10.1007/bf00053306openalex-snapshot
Wolbachia: intracellular manipulators of mite reproduction
inferredcites →https://doi.org/10.1007/bf00260866openalex-snapshot
The generation of transplasmic Drosophila simulans by cytoplasmic injection Effects of segregation and selection on the perpetuation of mitochondrial DNA heteroplasmy
inferredcites →https://doi.org/10.1007/bf00330961openalex-snapshot
Genetics of mitochondria in Drosophila: mtDNA inheritance in heteroplasmic strains of D. mauritiana
inferredcites →https://doi.org/10.1007/bf01854097openalex-snapshot
An analysis of non-reciprocal cross incompatibility in Mormoniella vitripennis (Walker)
inferredcites →https://doi.org/10.1007/bf01928904openalex-snapshot
Microorganism-associated variation in host infestation efficiency in a parasitoid wasp,Trichogramma bourarachae (Hymenoptera: Trichogrammatidae)
inferredcites →https://doi.org/10.1007/s002849900270openalex-snapshot
Distribution of Parthenogenesis-Inducing Symbionts in Ovaries and Eggs of Aphytis (Hymenoptera: Aphelinidae)
inferredcites →https://doi.org/10.1016/0022-2011(89)90137-7openalex-snapshot
Ultrastructural evidence of Wolbachia rickettsiales in Drosophila simulans and their relationships with unidirectional cross-incompatibility
inferredcites →https://doi.org/10.1016/0166-6851(95)02494-8openalex-snapshot
Molecular evidence for a close relative of the arthropod endosymbiont Wolbachia in a filarial worm
inferredcites →https://doi.org/10.1016/0168-9525(91)90457-2openalex-snapshot
Mitosis in the Drosophila embryo — in and out of control
inferredcites →https://doi.org/10.1016/0169-5347(95)90011-xopenalex-snapshot
Sex determination and population biology in the hymenoptera
inferredcites →https://doi.org/10.1016/0923-2508(96)80284-1openalex-snapshot
Phylogenetic analysis of the genus Rickettsia by 16S rDNA sequencing
inferredcites →https://doi.org/10.1016/s0022-5320(80)90135-5openalex-snapshot
The ultrastructure and symbiotic relationships of Wolbachia of mosquitoes of the Aedes scutellaris group
inferredcites →https://doi.org/10.1017/cbo9780511721946.013openalex-snapshot
Mating systems of parasitoid wasps
inferredcites →https://doi.org/10.1017/s0016672300031529openalex-snapshot
Evidence for aWolbachiasymbiont inDrosophila melanogaster
inferredcites →https://doi.org/10.1017/s0031182000084997openalex-snapshot
Wolbachiaas a possible means of driving genes into populations
inferredcites →https://doi.org/10.1038/283071a0openalex-snapshot
Cytoplasmic incompatibility in natural populations of a mosquito, Culex pipiens L.
inferredcites →https://doi.org/10.1038/346558a0openalex-snapshot
Microorganisms associated with chromosome destruction and reproductive isolation between two insect species
inferredcites →https://doi.org/10.1038/348178a0openalex-snapshot
Bidirectional incompatibility between conspecific populations of Drosophila simulans
inferredcites →https://doi.org/10.1038/36017openalex-snapshot
Rescuing Wolbachia have been overlooked
inferredcites →https://doi.org/10.1038/361066a0openalex-snapshot
Molecular identification of microorganisms associated with parthenogenesis
inferredcites →https://doi.org/10.1038/367453a0openalex-snapshot
Replacement of the natural Wolbachia symbiont of Drosophila simulans with a mosquito counterpart
inferredcites →https://doi.org/10.1038/373072a0openalex-snapshot
Increased male fertility in Tribolium confusum beetles after infection with the intracellular parasite Wolbachia
inferredcites →https://doi.org/10.1038/hdy.1993.157openalex-snapshot
Sex determination in the Hymenoptera: a review of models and evidence
inferredcites →https://doi.org/10.1038/hdy.1994.139openalex-snapshot
Cytogenetics of microbe-associated parthenogenesis and its consequences for gene flow in Trichogramma wasps
inferredcites →https://doi.org/10.1038/hdy.1994.48openalex-snapshot
Properties of Drosophila simulans strains experimentally infected by different clones of the bacterium Wolbachia
inferredcites →https://doi.org/10.1038/hdy.1996.73openalex-snapshot
Asexuality cured: the relations and differences between sexual and asexual Apoanagyrus diversicornis
inferredcites →https://doi.org/10.1038/hdy.1997.121openalex-snapshot
Wolbachia and cytoplasmic incompatibility in the spider mites Tetranychus urticae and T. turkestani
inferredcites →https://doi.org/10.1038/hdy.1997.207openalex-snapshot
Nonrandom partition of mitochondria in heteroplasmic Drosophila
inferredcites →https://doi.org/10.1038/sj.hdy.6883850openalex-snapshot
Distribution of Wolbachia among the guild associated with the parthenogenetic gall wasp Diplolepis rosae
inferredcites →https://doi.org/10.1038/sj.hdy.6883910openalex-snapshot
Female-biased sex ratio in the Asian corn borer, Ostrinia furnacalis: evidence for the occurrence of feminizing bacteria in an insect
inferredcites →https://doi.org/10.1046/j.1365-2583.1998.740393.xopenalex-snapshot
Phylogenetic analysis of parthenogenesis‐inducing Wolbachia in the genus Aphytis (Hymenoptera: Aphelinidae)
inferredcites →https://doi.org/10.1046/j.1365-2583.1999.810067.xopenalex-snapshot
Phylogenetic status of a fecundity‐enhancing Wolbachia that does not induce thelytoky in Trichogramma
inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00467.xopenalex-snapshot
Wolbachia in two insect host–parasitoid communities
inferredcites →https://doi.org/10.1046/j.1420-9101.1995.8020249.xopenalex-snapshot
Success and failure of horizontal transfers of feminizing Wolbachia endosymbionts in woodlice
inferredcites →https://doi.org/10.1073/pnas.93.7.2873openalex-snapshot
Accelerated evolution and Muller's rachet in endosymbiotic bacteria.
inferredcites →https://doi.org/10.1073/pnas.94.20.10792openalex-snapshot
Wolbachia , normally a symbiont of Drosophila , can be virulent, causing degeneration and early death
inferredcites →https://doi.org/10.1086/285172openalex-snapshot
The Paternal-Sex-Ratio Chromosome of Nasonia
inferredcites →https://doi.org/10.1093/aesa/83.3.475openalex-snapshot
Taxonomic Status of Thelytokous Forms of Trichogramma (Hymenoptera: Trichogrammatidae)
inferredcites →https://doi.org/10.1093/genetics/132.3.713openalex-snapshot
Dynamics of cytoplasmic incompatibility and mtDNA variation in natural Drosophila simulans populations.
inferredcites →https://doi.org/10.1093/genetics/135.2.565openalex-snapshot
Cytoplasmic incompatibility and bacterial density in Nasonia vitripennis.
inferredcites →https://doi.org/10.1093/genetics/140.4.1307openalex-snapshot
Wolbachia infections and the expression of cytoplasmic incompatibility in Drosophila sechellia and D. mauritiana.
inferredcites →https://doi.org/10.1093/genetics/140.4.1319openalex-snapshot
Cytoplasmic incompatibility in Drosophila simulans: dynamics and parameter estimates from natural populations.
inferredcites →https://doi.org/10.1093/genetics/143.2.961openalex-snapshot
Single and Double Infections with Wolbachia in the Parasitic Wasp Nasonia vitripennis Effects on Compatibility
inferredcites →https://doi.org/10.1093/genetics/144.3.1063openalex-snapshot
Wolbachia Infection and Cytoplasmic Incompatibility in Drosophila Species
inferredcites →https://doi.org/10.1093/genetics/148.1.221openalex-snapshot
Population Dynamics of the Wolbachia Infection Causing Cytoplasmic Incompatibility in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/148.4.1833openalex-snapshot
Effects of A and B Wolbachia and Host Genotype on Interspecies Cytoplasmic Incompatibility in Nasonia
inferredcites →https://doi.org/10.1093/genetics/28.5.365openalex-snapshot
MULTIPLE ALLELES IN COMPLEMENTARY SEX DETERMINATION OF HABROBRACON
inferredcites →https://doi.org/10.1093/genetics/39.1.4openalex-snapshot
PARTHENOGENESIS IN DROSOPHILA
inferredcites →https://doi.org/10.1093/oso/9780198502944.001.0001openalex-snapshot
The Major Transitions in Evolution
inferredcites →https://doi.org/10.1093/oso/9780198577867.003.0001openalex-snapshot
The evolution of heritable symbionts
inferredcites →https://doi.org/10.1093/oso/9780198577867.003.0002openalex-snapshot
Cytoplasmic incompatibility in insects
inferredcites →https://doi.org/10.1093/oso/9780198577867.003.0006openalex-snapshot
The potential application of inherited symbiont systems to pest control
inferredcites →https://doi.org/10.1098/rspb.1992.0023openalex-snapshot
Molecular identification ofWolbachia, the agent of cytoplasmic incompatibility inDrosophila simulans, and variability in relation with host mitochondrial types
inferredcites →https://doi.org/10.1098/rspb.1995.0117openalex-snapshot
Evolution and phylogeny of Wolbachia : reproductive parasites of arthropods
inferredcites →https://doi.org/10.1098/rspb.1995.0154openalex-snapshot
Wolbachia superinfections and the expression of cytoplasmic incompatibility
inferredcites →https://doi.org/10.1098/rspb.1995.0196openalex-snapshot
Distribution ofWolbachiaamong neotropical arthropods
inferredcites →https://doi.org/10.1098/rspb.1997.0052openalex-snapshot
Horizontal transmission of parthenogenesis–inducing microbes in Trichogramma wasps
inferredcites →https://doi.org/10.1098/rspb.1998.0324openalex-snapshot
Phylogeny and PCR–based classification of Wolbachia strains using wsp gene sequences
inferredcites →https://doi.org/10.1098/rspb.1998.0401openalex-snapshot
Wolbachia–induced thelytoky in the rose gallwasp Diplolepis spinosissimae (Giraud) (Hymenoptera: Cynipidae), and its consequences on the genetic structure of its host
inferredcites →https://doi.org/10.1098/rspb.1998.0402openalex-snapshot
Evidence for widespread Wolbachia infection in isopod crustaceans: molecular identification and host feminization
inferredcites →https://doi.org/10.1098/rspb.1998.0455openalex-snapshot
Successful horizontal transfer of Wolbachia symbionts between Trichogramma wasps
inferredcites →https://doi.org/10.1101/sqb.1959.024.01.017openalex-snapshot
SPECIATION IN MOSQUITOES: Speciation by Cytoplasmic Isolation in the Culex Pipiens-Complex
inferredcites →https://doi.org/10.1111/j.1365-2583.1993.tb00074.xopenalex-snapshot
Phylogeny of cytoplasmic incompatibility microorganisms in the parasitoid wasp genus Nasonia (Hymenoptera: Pteromalidae) based on 16S ribosomal DNA sequences
inferredcites →https://doi.org/10.1111/j.1365-2583.1993.tb00113.xopenalex-snapshot
Genetic transformation and phylogeny of bacterial symbionts from tsetse
inferredcites →https://doi.org/10.1111/j.1365-2583.1995.tb00023.xopenalex-snapshot
Parthenogenesis‐inducing microorganisms in Aphytis (Hymenoptera: Aphelinidae)
inferredcites →https://doi.org/10.1111/j.1365-2915.1992.tb00608.xopenalex-snapshot
Crossing type variability associated with cytoplasmic incompatibility in Australian populations of the mosquito Culex quinquefasciatus Say
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb02192.xopenalex-snapshot
EVOLUTION OF INCOMPATIBILITY‐INDUCING MICROBES AND THEIR HOSTS
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02399.xopenalex-snapshot
WOLBACHIAINFECTION INDROSOPHILA SIMULANS: DOES THE FEMALE HOST BEAR A PHYSIOLOGICAL COST?
inferredcites →https://doi.org/10.1111/j.1570-7458.1993.tb01667.xopenalex-snapshot
Influence of microbe‐associated parthenogenesis on the fecundity of Trichogramma deion and T. pretiosum
inferredcites →https://doi.org/10.1126/science.156.3774.477openalex-snapshot
Extraordinary Sex Ratios
inferredcites →https://doi.org/10.1126/science.8511587openalex-snapshot
Interspecific and Intraspecific Horizontal Transfer of Wolbachia in Drosophila
inferredcites →https://doi.org/10.1128/jb.180.9.2373-2378.1998openalex-snapshot
Cloning and Characterization of a Gene Encoding the Major Surface Protein of the Bacterial EndosymbiontWolbachia pipientis
inferredcites →https://doi.org/10.1242/jcs.107.3.673openalex-snapshot
The distribution of cytoplasmic bacteria in the early Drosophila embryo is mediated by astral microtubules
inferredcites →https://doi.org/10.2108/zsj.14.701openalex-snapshot
groE-Homologous Operon of Wolbachia, an Intracellular Symbiont of Arthropods: A New Approach for Their Phylogeny
inferredcites →https://doi.org/10.5860/choice.36-1561openalex-snapshot
Influential passengers: inherited microorganisms and arthropod reproduction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.5852/ejt.2019.550zenodo-depositor-declared
Review of the Swedish species of Ophion (Hymenoptera: Ichneumonidae: Ophioninae), with the description of 18 new species and an illustrated key to Swedish species
inferred← citeshttps://doi.org/10.1002/9780470696200.ch12openalex-snapshot
Parasitoid Sex Ratios and Biological Control
inferred← citeshttps://doi.org/10.1002/evl3.30openalex-snapshot
Evolution and comparative ecology of parthenogenesis in haplodiploid arthropods
inferred← citeshttps://doi.org/10.1007/s00203-025-04289-0openalex-snapshot
Unveiling the diversity of gut microbes in green lacewings (Chrysopidae: Neuroptera) and their role as protagonist in nutrition
inferred← citeshttps://doi.org/10.1007/s00248-006-9036-xopenalex-snapshot
Closely Related Wolbachia Strains within the Pumpkin Arthropod Community and the Potential for Horizontal Transmission via the Plant
inferred← citeshttps://doi.org/10.1007/s00248-013-0198-zopenalex-snapshot
Diversity of Wolbachia in Natural Populations of Spider Mites (genus Tetranychus): Evidence for Complex Infection History and Disequilibrium Distribution
inferred← citeshttps://doi.org/10.1007/s00248-017-0971-5openalex-snapshot
Relative Abundance and Strain Diversity in the Bacterial Endosymbiont Community of a Sap-Feeding Insect Across Its Native and Introduced Geographic Range
inferred← citeshttps://doi.org/10.1007/s00284-026-04728-1openalex-snapshot
Metagenomic Exploration of the Bacteriome Reveals Natural Wolbachia Infections in Yellow Fever Mosquito Aedes aegypti and Asian Tiger Mosquito Aedes albopictus
inferred← citeshttps://doi.org/10.1007/s11756-022-01184-7openalex-snapshot
Interrupted hibernation of the gall-inducer affects its parasitoids – a case study on some gall communities of Diplolepis rosae (Hymenoptera: Cynipidae) in Bulgaria
inferred← citeshttps://doi.org/10.1007/s11829-019-09684-1openalex-snapshot
Affect of food provisioning on survival and reproductive success of the olive fruit fly parasitoid, Psyttalia lounsburyi, in the field
inferred← citeshttps://doi.org/10.1016/b978-0-12-415874-0.00004-4openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-415874-0.00010-xopenalex-snapshot
Sex Determination in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-815230-0.00004-2openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-815230-0.00010-8openalex-snapshot
Sex Determination in Insects
inferred← citeshttps://doi.org/10.1016/b978-012357031-4/50023-6openalex-snapshot
Genetic Systems, Genome Evolution, and Genetic Control of Embryonic Development in Insects
inferred← citeshttps://doi.org/10.1016/b978-012357031-4/50029-7openalex-snapshot
Sex Determination in Insects
inferred← citeshttps://doi.org/10.1016/j.aspen.2011.08.004openalex-snapshot
Molecular characterization of Iranian Trichogrammatids (Hymenoptera: Trichogrammatidae) and their Wolbachia endosymbiont
inferred← citeshttps://doi.org/10.1016/j.baae.2018.05.014openalex-snapshot
Biased parasitoid sex ratios: Wolbachia, functional traits, local and landscape effects
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2004.07.004openalex-snapshot
Reproductive compatibility and genetic variation between two strains of Aphelinus albipodus (Hymenoptera: Aphelinidae), a parasitoid of the soybean aphid, Aphis glycines (Homoptera: Aphididae)
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2004.12.012openalex-snapshot
Microbial diversity in the predatory mite Metaseiulus occidentalis (Acari: Phytoseiidae) and its prey, Tetranychus urticae (Acari: Tetranychidae)
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2017.02.004openalex-snapshot
Symbiont-conferred resistance to parasitoids in aphids – Challenges for biological control
inferred← citeshttps://doi.org/10.1016/j.rsci.2016.06.003openalex-snapshot
Influence of Temperature on Symbiotic Bacterium Composition in Successive Generations of Egg Parasitoid, Anagrus nilaparvatae
inferred← citeshttps://doi.org/10.1016/s0168-9525(00)02085-0openalex-snapshot
Influential passengers come of age 1st International Wolbachia Conference, Orthodox Academy, Kolymbari, Crete, Greece, 7–12 June 2000
inferred← citeshttps://doi.org/10.1038/hdy.2009.2openalex-snapshot
Outbreeding and possibly inbreeding depression in a pollinating fig wasp with a mixed mating system
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800063openalex-snapshot
Infection polymorphism and cytoplasmic incompatibility in Hymenoptera-Wolbachia associations
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00185.xopenalex-snapshot
Microorganisms and parthenogenesis
inferred← citeshttps://doi.org/10.1046/j.1365-2583.2000.00199.xopenalex-snapshot
Microsatellite frequency and size variation in the parthenogenetic parasitic wasp Venturia canescens (Gravenhorst) (Hymenoptera: Ichneumonidae)
inferred← citeshttps://doi.org/10.1046/j.1365-2583.2000.00203.xopenalex-snapshot
Long PCR improves Wolbachia DNA amplification: wsp sequences found in 76% of sixty‐three arthropod species
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2000.00836.xopenalex-snapshot
Molecular evidence for multiple infections of a new subgroup ofWolbachiain the European raspberry beetleByturus tomentosus
inferred← citeshttps://doi.org/10.1046/j.1420-9101.2000.00203.xopenalex-snapshot
Complementary sex determination in the genus Diadegma (Hymenoptera: Ichneumonidae)
inferred← citeshttps://doi.org/10.1046/j.1570-7458.2000.00693.xopenalex-snapshot
Wolbachia‐induced parthenogenesis in the egg parasitoid Telenomus nawai
inferred← citeshttps://doi.org/10.1046/j.1570-7458.2001.00821.xopenalex-snapshot
Antibiotic curing of parthenogenesis in Eretmocerus mundus (Australian parthenogenic form)
inferred← citeshttps://doi.org/10.1051/apido:2002048openalex-snapshot
Wolbachia is present in Apis mellifera capensis, A. m. scutellata, and their hybrid in Southern Africa
inferred← citeshttps://doi.org/10.1093/biolinnean/blaf010openalex-snapshot
Endosymbionts in agriculturally important parasitoid wasps from Australia
inferred← citeshttps://doi.org/10.1093/biolinnean/blx157openalex-snapshot
Wolbachia infections in Australian ichneumonid parasitoid wasps (Hymenoptera: Ichneumonidae): evidence for adherence to the global equilibrium hypothesis
inferred← citeshttps://doi.org/10.1093/molbev/msg082openalex-snapshot
High Levels of Multiple Wolbachia Infection and Recombination in the Ant Formica exsecta
inferred← citeshttps://doi.org/10.1093/plankt/fbh145openalex-snapshot
No evidence of Wolbachia among Great Lakes area populations of Daphnia pulex (Crustacea: Cladocera)
inferred← citeshttps://doi.org/10.1098/rspb.2001.1628openalex-snapshot
Wolbachia–mediated parthenogenesis in the predatory thripsFranklinothrips vespiformis(Thysanoptera: Insecta)
inferred← citeshttps://doi.org/10.1098/rspb.2003.2640openalex-snapshot
Natural interspecific and intraspecific horizontal transfer of parthenogenesis–inducingWolbachiainTrichogrammawasps
inferred← citeshttps://doi.org/10.1098/rspb.2004.2956openalex-snapshot
Convergent incidences ofWolbachiainfection in fig wasp communities from two continents
inferred← citeshttps://doi.org/10.1111/1462-2920.15833openalex-snapshot
Wolbachia in scale insects: a distinct pattern of infection frequencies and potential transfer routes via ant associates
inferred← citeshttps://doi.org/10.1111/brv.12663openalex-snapshot
Wolbachiahost shifts: routes, mechanisms, constraints and evolutionary consequences
inferred← citeshttps://doi.org/10.1111/eea.12293openalex-snapshot
Does W olbachiainfection affect decision‐making in a parasitic wasp?
inferred← citeshttps://doi.org/10.1111/eea.12477openalex-snapshot
No evidence of parthenogenesis‐inducing bacteria involved in T hripoctenus javae thelytoky: an unusual finding in C halcidoidea
inferred← citeshttps://doi.org/10.1111/ens.12264openalex-snapshot
Prevalence and evolutionary history of endosymbiont Wolbachia (Rickettsiales: Anaplasmataceae) in parasitoids (Hymenoptera: Braconidae) associated with Bactrocera fruit flies (Diptera: Tephritidae) infesting carambola
inferred← citeshttps://doi.org/10.1111/j.0307-6946.2005.00715.xopenalex-snapshot
Horizontal transmission of Wolbachia in a Drosophila community
inferred← citeshttps://doi.org/10.1111/j.0962-1075.2004.00492.xopenalex-snapshot
Distribution and prevalence of Wolbachia in Japanese populations of Lepidoptera
inferred← citeshttps://doi.org/10.1111/j.1365-2311.2009.01141.xopenalex-snapshot
Rapid genetic changes in natural insect populations
inferred← citeshttps://doi.org/10.1111/j.1461-9563.2008.00369.xopenalex-snapshot
Effects and implications of antibiotic treatment on Wolbachia ‐infected vine weevil (Coleoptera: Curculionidae)
inferred← citeshttps://doi.org/10.1111/j.1570-7458.2010.00974.xopenalex-snapshot
Occurrence ofWolbachiain central European weevils: correlations with host systematics, ecology, and biology
inferred← citeshttps://doi.org/10.1111/mec.16883openalex-snapshot
Host phylogeny and ecological associations best explain Wolbachia host shifts in scale insects
inferred← citeshttps://doi.org/10.1111/zoj.12380openalex-snapshot
Wolbachiaendosymbionts distort DNA barcoding in the parasitoid wasp genusDiplazon(Hymenoptera: Ichneumonidae)
inferred← citeshttps://doi.org/10.1139/g02-112openalex-snapshot
The cytogenetics of thelytoky in a predominantly asexual parasitoid wasp with covert sex
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.32.081501.114132openalex-snapshot
Male-Killing, Nematode Infections, Bacteriophage Infection, and Virulence of Cytoplasmic Bacteria in the GenusWolbachia
inferred← citeshttps://doi.org/10.1146/annurev.ento.47.091201.145247openalex-snapshot
The Population Biology of Oak Gall Wasps (Hymenoptera: Cynipidae)
inferred← citeshttps://doi.org/10.1146/annurev.ento.48.091801.112703openalex-snapshot
T HE E VOLUTION OF A LTERNATIVE G ENETIC S YSTEMS IN I NSECTS
inferred← citeshttps://doi.org/10.1159/000356508openalex-snapshot
Thelytoky and Sex Determination in the Hymenoptera: Mutual Constraints
inferred← citeshttps://doi.org/10.1163/156854201x00017openalex-snapshot
Single-Locus Complementary Sex Determination in the Ichneumonid Venturia Canescens (Gravenhorst) (Hymenoptera)
inferred← citeshttps://doi.org/10.1186/1742-9994-3-1openalex-snapshot
Single locus complementary sex determination in Hymenoptera: an "unintelligent" design?
inferred← citeshttps://doi.org/10.1186/s13071-021-04937-6openalex-snapshot
Wolbachia prevalence in the vector species Culex pipiens and Culex torrentium in a Sindbis virus-endemic region of Sweden
inferred← citeshttps://doi.org/10.1303/aez.2009.535openalex-snapshot
Parental genetic traits in offspring from inter-specific crosses between introduced and indigenous Diadegma Foerster (Hymenoptera: Ichneumonidae): Possible effects on conservation genetics
inferred← citeshttps://doi.org/10.14411/eje.2012.022openalex-snapshot
Wolbachia infection in Trissolcus species (Hymenoptera: Scelionidae)
inferred← citeshttps://doi.org/10.14411/eje.2013.014openalex-snapshot
Occurrence of arrhenotoky and thelytoky in a parasitic wasp Venturia canescens (Hymenoptera: Ichneumonidae): Effect of endosymbionts or existence of two distinct reproductive modes?
inferred← citeshttps://doi.org/10.1534/genetics.167.1.243openalex-snapshot
Whole-Genome Scan in Thelytokous-Laying Workers of the Cape Honeybee (Apis mellifera capensis): Central Fusion, Reduced Recombination Rates and Centromere Mapping Using Half-Tetrad Analysis
inferred← citeshttps://doi.org/10.1590/s1415-47572012000600013openalex-snapshot
First record of Wolbachia in South American terrestrial isopods: prevalence and diversity in two species of Balloniscus (Crustacea, Oniscidea)
inferred← citeshttps://doi.org/10.1590/s1519-566x2008000600002openalex-snapshot
Wolbachia in two populations of Melittobia digitata Dahms (Hymenoptera: Eulophidae)
inferred← citeshttps://doi.org/10.3126/ijls.v5i1.5230openalex-snapshot
Absence of Wolbachia in the workers of Asian honeybee, Apis cerana indica
inferred← citeshttps://doi.org/10.3389/fpubh.2016.00043openalex-snapshot
Risk Associated with the Release of Wolbachia-Infected Aedes aegypti Mosquitoes into the Environment in an Effort to Control Dengue
inferred← citeshttps://doi.org/10.3390/biology13030151openalex-snapshot
Wolbachia Interactions with Diverse Insect Hosts: From Reproductive Modulations to Sustainable Pest Management Strategies
inferred← citeshttps://doi.org/10.4236/aim.2025.152007openalex-snapshot
Quantitative Risk Assessment of a Potential Release of Aedes aegypti Carrying Wolbachia Strains for Dengue Control in Burkina Faso
inferred← citeshttps://doi.org/10.5281/zenodo.16012135openalex-snapshot
Gynandromorphism In Pollinating Fig Wasps (Hymenoptera : Agaonidae)
inferred← citeshttps://doi.org/10.70675/49fb02b4z5688z4356za72bzb0258f4cc852openalex-snapshot
Étude des stratégies de mouvement chez les parasitoïdes du genre Trichogramma : apports des techniques d’analyse d’images automatiques
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