On the public citation graph
The biogeography and population genetics of neotropical vector species
0 signed · 162 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known work and none has been retracted — and get a dated CiteStamped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/10.1006/mpev.2000.0863openalex-snapshot
Speciation and Population Structure in the Morphospecies Lutzomyia longipalpis (Lutz & Neiva) as Derived from the Mitochondrial ND4 Gene
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/bf02027726openalex-snapshot
9-Methylgermacrene-B; proposed structure for novel homosesquiterpene from the sex pheromone glands ofLutzomyia longipalpis (Diptera: Psychodidae) from Lapinha, Brazil
inferredcites →https://doi.org/10.1007/bf02029550openalex-snapshot
3-Methyl-α-himachalene: Proposed structure for novel homosesquiterpene sex pheromone ofLutzomyia longipalpis (diptera: Psychodidae) from Jacobina, Brazil
inferredcites →https://doi.org/10.1007/bf02399823openalex-snapshot
Genetic evidence for the existence of cryptic species in theAnopheles albitarsis complex in Brazil: Allozymes and mitochondrial DNA restriction fragment length polymorphisms
inferredcites →https://doi.org/10.1007/s00239-004-2586-yopenalex-snapshot
Genetic Divergence in the cacophony IVS6 Intron Among Five BrazilianPopulations of Lutzomyia longipalpis
inferredcites →https://doi.org/10.1007/s10709-005-1399-2openalex-snapshot
Diversity of Boll Weevil Populations in South America: A Phylogeographic Approach
inferredcites →https://doi.org/10.1016/0035-9203(83)90154-2openalex-snapshot
Leishmaniasis in Brazil. XIX: Visceral leishmaniasis in the Amazon Region, and the presence of Lutzomyia longipalpis+ on the Island of Marajo, Para State
inferredcites →https://doi.org/10.1016/0035-9203(93)90054-topenalex-snapshot
Isozymic data question the specific status of some blood-sucking bugs of the genus Rhodnius, vectors of Chagas disease
inferredcites →https://doi.org/10.1016/b978-012498315-1/50017-0openalex-snapshot
Phylogeographic Studies of North American Birds
inferredcites →https://doi.org/10.1016/b978-012510451-7/50007-4openalex-snapshot
TRUE BUGS ( Hemiptera )
inferredcites →https://doi.org/10.1016/j.palaeo.2006.01.020openalex-snapshot
The Pan-Amazonian Ucayali Peneplain, late Neogene sedimentation in Amazonia, and the birth of the modern Amazon River system
inferredcites →https://doi.org/10.1016/j.yqres.2004.10.001openalex-snapshot
New geological framework for Western Amazonia (Brazil) and implications for biogeography and evolution
inferredcites →https://doi.org/10.1016/s0003-3472(05)80549-4openalex-snapshot
Communication among phlebotomine sandflies: a field study of domesticated Lutzomyia longipalpis populations in Amazonian Brazil
inferredcites →https://doi.org/10.1016/s0012-8252(98)00027-0openalex-snapshot
Neogene and Quaternary development of the neotropical rain forest: the forest refugia hypothesis, and a literature overview
inferredcites →https://doi.org/10.1016/s0031-0182(02)00255-9openalex-snapshot
Influence of biotic and abiotic environment on dental size and shape evolution in a Late Miocene lineage of murine rodents (Teruel Basin, Spain)
inferredcites →https://doi.org/10.1016/s0031-0182(96)00096-xopenalex-snapshot
Plus ça change — a model for stasis and evolution in different environments
inferredcites →https://doi.org/10.1016/s0277-3791(99)00059-1openalex-snapshot
Amazonian and neotropical plant communities on glacial time-scales: The failure of the aridity and refuge hypotheses
inferredcites →https://doi.org/10.1016/s0895-9811(01)00008-6openalex-snapshot
Late Cenozoic sedimentary evolution in northeastern Pará, Brazil, within the context of sea level changes
inferredcites →https://doi.org/10.1016/s1567-1348(02)00087-4openalex-snapshot
Phylogeography of the neotropical sand fly Lutzomyia longipalpis inferred from mitochondrial DNA sequences
inferredcites →https://doi.org/10.1038/sj.hdy.6800805openalex-snapshot
Molecular population genetics of the malaria vector Anopheles darlingi in Central and South America
inferredcites →https://doi.org/10.1038/sj.hdy.6800913openalex-snapshot
Erratum: Molecular population genetics of the malaria vector Anopheles darlingi in central and South America
inferredcites →https://doi.org/10.1046/j.1365-2583.2002.00340.xopenalex-snapshot
The period gene and genetic differentiation between three Brazilian populations of Lutzomyia longipalpis
inferredcites →https://doi.org/10.1046/j.1365-2915.1999.00139.xopenalex-snapshot
Metaphase karyotypes and G‐banding in sandflies of the Lutzomyia longipalpis complex
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01802.xopenalex-snapshot
Molecular phylogeography of the Amazonian Chagas disease vectors Rhodnius prolixus and R. robustus
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01871.xopenalex-snapshot
Genetic identification of two sibling species ofLutzomyia longipalpis(Diptera: Psychodidae) that produce distinct male sex pheromones in Sobral, Ceará State, Brazil
inferredcites →https://doi.org/10.1073/pnas.1434337100openalex-snapshot
Semipermeable species boundaries between Anopheles gambiae and Anopheles arabiensis : Evidence from multilocus DNA sequence variation
inferredcites →https://doi.org/10.1073/pnas.230136397openalex-snapshot
Riverine barriers and the geographic distribution of Amazonian species
inferredcites →https://doi.org/10.1073/pnas.91.14.6491openalex-snapshot
Rapid morphological radiation and convergence among races of the butterfly Heliconius erato inferred from patterns of mitochondrial DNA evolution.
inferredcites →https://doi.org/10.1080/00034983.1989.11812389openalex-snapshot
Capture-recapture studies with the South American malaria vector Anopheles darlingi , Root
inferredcites →https://doi.org/10.1080/00034983.1996.11813079openalex-snapshot
Comparison of the sex-pheromone components ofLutzomyia longipalpis(Diptera: Psychodidae) from areas of visceral and atypical cutaneous leishmaniasis in Honduras and Costa Rica
inferredcites →https://doi.org/10.1080/10635150500234674openalex-snapshot
Between Two Extremes: Mitochondrial DNA is neither the Panacea nor the Nemesis of Phylogenetic and Taxonomic Inference
inferredcites →https://doi.org/10.1093/bib/5.2.150openalex-snapshot
MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment
inferredcites →https://doi.org/10.1093/jmedent/30.2.427openalex-snapshot
Dispersal of the Sand Fly Lutzomyia longipalpis (Diptera: Psychodidae) at an Endemic Focus of Visceral Leishmaniasis in Colombia
inferredcites →https://doi.org/10.1093/jmedent/32.5.697openalex-snapshot
Diagnosis by Random Amplified Polymorphic DNA Polymerase Chain Reaction of Four Cryptic Species Related to Anopheles (Nyssorhynchus) albitarsis (Diptera: Culicidae) from Paraguay, Argentina, and Brazil
inferredcites →https://doi.org/10.1093/jmedent/34.5.499openalex-snapshot
Ecoregional Classification of Malaria Vectors in the Neotropics
inferredcites →https://doi.org/10.1093/jmedent/36.5.631openalex-snapshot
Analysis of ITS2 DNA Sequences from Brazilian Anopheles darlingi (Diptera: Culicidae)
inferredcites →https://doi.org/10.1093/oso/9780195109009.003.0015openalex-snapshot
Rivers, Refuges, and Ridges: The Geography of Speciation of Amazonian Mammals
inferredcites →https://doi.org/10.1093/oso/9780198540618.001.0001openalex-snapshot
An Outline of Phanerozoic Biogeography
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004224openalex-snapshot
Molecular Divergence in the period Gene Between Two Putative Sympatric Species of the Lutzomyia longipalpis Complex
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026377openalex-snapshot
Population Structure and Population History of Anopheles dirus Mosquitoes in Southeast Asia
inferredcites →https://doi.org/10.1098/rspb.1974.0082openalex-snapshot
Quaternary refugia in tropical America: evidence from race formation in Heliconius butterflies
inferredcites →https://doi.org/10.1098/rspb.2002.2032openalex-snapshot
Not as the crow flies: a historical explanation for circuitous migration in Swainson's thrush (Catharus ustulatus)
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01460.xopenalex-snapshot
THE PHYLOGEOGRAPHY OF AMAZONIA REVISITED: NEW EVIDENCE FROM RIODINID BUTTERFLIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01709.xopenalex-snapshot
HISTORICAL DIVERSIFICATION OF A TERRA-FIRME FOREST BIRD SUPERSPECIES: A PHYLOGEOGRAPHIC PERSPECTIVE ON THE ROLE OF DIFFERENT HYPOTHESES OF AMAZONIAN DIVERSIFICATION
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01161.xopenalex-snapshot
DIVERGENT TIMING AND PATTERNS OF SPECIES ACCUMULATION IN LOWLAND AND HIGHLAND NEOTROPICAL BIRDS
inferredcites →https://doi.org/10.1111/j.1095-8312.1999.tb01160.xopenalex-snapshot
Post-glacial re-colonization of European biota
inferredcites →https://doi.org/10.1111/j.1365-2915.1992.tb00032.xopenalex-snapshot
Isozyme variability and differentiation between Rhodnius prolixus, R.robustus and R.pictipes , vectors of Chagas disease in Venezuela
inferredcites →https://doi.org/10.1111/j.1365-2915.1997.tb00428.xopenalex-snapshot
Isozymic and metric variation in the Lutzomyia longipalpis complex
inferredcites →https://doi.org/10.1111/j.1365-2915.2005.00594.xopenalex-snapshot
Analysis of the sex pheromone extract of individual male Lutzomyia longipalpis sandflies from six regions in Brazil
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02374.xopenalex-snapshot
Long‐distance gene flow and cross‐Andean dispersal of lowland rainforest bees (Apidae: Euglossini) revealed by comparative mitochondrial DNA phylogeography
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03061.xopenalex-snapshot
Comparative phylogeography of unglaciated eastern North America
inferredcites →https://doi.org/10.1126/science.165.3889.131openalex-snapshot
Speciation in Amazonian Forest Birds
inferredcites →https://doi.org/10.1126/science.269.5222.361openalex-snapshot
Biological Implications of the Middle Miocene Amazon Seaway
inferredcites →https://doi.org/10.1126/science.269.5222.386openalex-snapshot
Late Miocene Tidal Deposits in the Amazonian Foreland Basin
inferredcites →https://doi.org/10.1136/bmj.326.7404.1444openalex-snapshot
American trypanosomiasis (Chagas' disease) and the role of molecular epidemiology in guiding control strategies
inferredcites →https://doi.org/10.1146/annurev.ecolsys.31.1.533openalex-snapshot
Diversification of Rainforest Faunas: An Integrated Molecular Approach
inferredcites →https://doi.org/10.1146/annurev.es.18.110187.002421openalex-snapshot
INTRASPECIFIC PHYLOGEOGRAPHY: The Mitochondrial DNA Bridge Between Population Genetics and Systematics
inferredcites →https://doi.org/10.1206/0003-0090(2000)244<0001:motrja>2.0.co;2openalex-snapshot
MAMMALS OF THE RIO JURUÁ AND THE EVOLUTIONARY AND ECOLOGICAL DIVERSIFICATION OF AMAZONIA
inferredcites →https://doi.org/10.1590/1809-43921976064473openalex-snapshot
Cytogenetically distinguishable sympatric and allopatric populations of the mosquito Anopheles albitarsis
inferredcites →https://doi.org/10.1590/1809-43921982122353openalex-snapshot
Biologia de Anofelinos amazônicos. V. Polimorfismo cromossômico de Anopheles darlingi Root (Diptera, Culicidae)
inferredcites →https://doi.org/10.1590/1809-43921988183143openalex-snapshot
A proposed Pleistocene/Holocene lake in the Amazon basin and its significance to Amazonian geology and biogeography
inferredcites →https://doi.org/10.1590/s0001-37652005000300007openalex-snapshot
Molecular research and the control of Chagas disease vectors
inferredcites →https://doi.org/10.1590/s0034-89101980000300002openalex-snapshot
Biogeografia, origem e distribuição da domiciliação de triatomíneos no Brasil
inferredcites →https://doi.org/10.1590/s0034-89102002000100012openalex-snapshot
Intra-population plasticity of Anopheles darlingi's (Diptera, Culicidae) biting activity patterns in the state of Amapá, Brazil
inferredcites →https://doi.org/10.1590/s0034-89102006000700004openalex-snapshot
Biogeografia, origem e distribuição da domiciliação de triatomíneos no Brasil
inferredcites →https://doi.org/10.1590/s0037-86821991000100003openalex-snapshot
Biting behavior of Anopheles mosquitoes in Costa Marques, Rondonia, Brazil
inferredcites →https://doi.org/10.1590/s0074-02761983000300005openalex-snapshot
Reproductive isolation between different forms of Lutzomyia longipalpis (Lutz & Neiva), (Diptera: Psychodidae), the vector of Leishmania donovani chagasi Cunha & Chagas and its significance to kala-azar distribution in South America
inferredcites →https://doi.org/10.1590/s0074-02761995000600013openalex-snapshot
Identification of species related to Anopheles (Nyssorhynchus) albitarsis by random amplified polymorphic DNA-Polymerase chain reaction (Diptera: Culicidae)
inferredcites →https://doi.org/10.1590/s0074-02761996000400001openalex-snapshot
Biological variation in Anopheles darlingi root
inferredcites →https://doi.org/10.1590/s0074-02762000000300005openalex-snapshot
Studies on populations of Lutzomyia longipalpis (Lutz & Neiva, 1912) (Diptera: Psychodidae: Phlebotominae) in Brazil
inferredcites →https://doi.org/10.1590/s0074-02762002000300032openalex-snapshot
Medical and Veterinary Entomology
inferredcites →https://doi.org/10.1590/s0074-02762005000500009openalex-snapshot
Identification of Anopheles (Nyssorhynchus) albitarsis complex species (Diptera: Culicidae) using rDNA internal transcribed spacer 2-based polymerase chain reaction primes
inferredcites →https://doi.org/10.1590/s0074-02762005000800001openalex-snapshot
Lutzomyia longipalpis and the eco-epidemiology of American visceral leishmaniasis, with particular reference to Brazil: a review
inferredcites →https://doi.org/10.1590/s0074-02762006000200008openalex-snapshot
The importance of Anopheles albitarsis E and An. darlingi in human malaria transmission in Boa Vista, state of Roraima, Brazil
inferredcites →https://doi.org/10.1590/s0074-02762007005000045openalex-snapshot
Population genetic structure of the major malaria vector Anopheles darlingi (Diptera: Culicidae) from the Brazilian Amazon, using microsatellite markers
inferredcites →https://doi.org/10.1603/0013-8746(2002)095[0740:gdapol]2.0.co;2openalex-snapshot
Genetic Differentiation among Populations of Lutzomyia longipalpis (Diptera: Psychodidae) in Central and South America
inferredcites →https://doi.org/10.1603/0013-8746(2005)098[0908:csitan]2.0.co;2openalex-snapshot
Cryptic Species in the Anopheles (Nyssorhynchus) albitarsis (Diptera: Culicidae) Complex: Incongruence Between Random Amplified Polymorphic DNA-Polymerase Chain Reaction Identification and Analysis of Mitochondrial DNA COI Gene Sequences
inferredcites →https://doi.org/10.1603/0022-2585-40.5.615openalex-snapshot
The Taxonomic Status of Genetically Divergent Populations ofLutzomyia longipalpis(Diptera: Psychodidae) Based on the Distribution of Mitochondrial and Isozyme Variation
inferredcites →https://doi.org/10.1603/0022-2585-41.5.888openalex-snapshot
Analysis of Reproductive Isolation Between Sibling SpeciesAnopheles albitarsissensu stricto andAnopheles deaneorum, Two Malaria Vectors Belonging to the Albitarsis Complex (Diptera: Culicidae)
inferredcites →https://doi.org/10.1603/0022-2585-41.5.906openalex-snapshot
Analysis of the Copulatory Courtship Songs ofLutzomyia longipalpisin Six Populations from Brazil
inferredcites →https://doi.org/10.21236/ada285737openalex-snapshot
Guide to the Identification and Geographic Distribution of Lutzomyia Sand Flies in Mexico, the West Indies, Central and South America (Diptera:Psychodidae)
inferredcites →https://doi.org/10.2307/1222013openalex-snapshot
Biological Diversification in the Tropics
inferredcites →https://doi.org/10.2307/1381862openalex-snapshot
Mammals as a Key to Evolutionary Theory
inferredcites →https://doi.org/10.2307/2666185openalex-snapshot
The History of Neotropical Vegetation: New Developments and Status
inferredcites →https://doi.org/10.2307/40168278openalex-snapshot
Historical Biogeography and Patterns of Differentiation within the South American Avifauna: Areas of Endemism
inferredcites →https://doi.org/10.2987/8756-971x(2005)21[182:baabso]2.0.co;2openalex-snapshot
BITING ACTIVITY AND BREEDING SITES OF ANOPHELES SPECIES IN THE MUNICIPALITY VILLAVICENCIO, META, COLOMBIA
inferredcites →https://doi.org/10.3201/eid0303.970305openalex-snapshot
DDT, Global Strategies, and a Malaria Control Crisis in South America
inferredcites →https://doi.org/10.4269/ajtmh.1988.38.223openalex-snapshot
Malaria Studies and Control in Brazil
inferredcites →https://doi.org/10.4269/ajtmh.1991.44.598openalex-snapshot
Comparative Susceptibility of Anopheline Mosquitoes to Plasmodium Falciparum in Rondonia, Brazil
inferredcites →https://doi.org/10.4269/ajtmh.1991.45.463openalex-snapshot
Comparative Susceptibility of Anopheline Mosquitoes in Rondonia, Brazil to Infection by Plasmodium Vivax
inferredcites →https://doi.org/10.4269/ajtmh.1993.48.839openalex-snapshot
Lutzomyia longipalpis is a Species Complex: Genetic Divergence and Interspecific Hybrid Sterility among Three Populations
inferredcites →https://doi.org/10.4269/ajtmh.1998.59.893openalex-snapshot
Genetic variability in biochemical characters of Brazilian field populations of the Leishmania vector, Lutzomyia longipalpis (Diptera: Psychodidae).
inferredcites →https://doi.org/10.4269/ajtmh.1999.60.364openalex-snapshot
Population structure of the primary malaria vector in South America, Anopheles darlingi, using isozyme, random amplified polymorphic DNA, internal transcribed spacer 2, and morphologic markers.
inferredcites →https://doi.org/10.4269/ajtmh.1999.60.377openalex-snapshot
Mitochondrial DNA sequence variation among triatomine vectors of Chagas' disease.
inferredcites →https://doi.org/10.4269/ajtmh.1999.61.1004openalex-snapshot
Occurrence of sibling species of Lutzomyia longipalpis (Diptera: Psychodidae) in Venezuela: first evidence from reproductively isolated sympatric populations.
inferredcites →https://doi.org/10.4269/ajtmh.2000.62.460openalex-snapshot
Phylogeny and molecular taxonomy of the Rhodniini derived from mitochondrial and nuclear DNA sequences.
inferredcites →https://doi.org/10.4269/ajtmh.2002.66.18openalex-snapshot
Emergence of a new neotropical malaria vector facilitated by human migration and changes in land use.
inferredcites →https://doi.org/10.4269/ajtmh.2003.69.386openalex-snapshot
MITOCHONDRIAL CYTOCHROME B VARIATION IN POPULATIONS OF THE VISCERAL LEISHMANIASIS VECTOR LUTZOMYIA LONGIPALPIS ACROSS EASTERN BRAZIL
inferredcites →https://doi.org/10.4269/ajtmh.2005.73.734openalex-snapshot
MALE SEX PHEROMONES AND THE PHYLOGEOGRAPHIC STRUCTURE OF THE LUTZOMYIA LONGIPALPIS SPECIES COMPLEX (DIPTERA: PSYCHODIDAE) FROM BRAZIL AND VENEZUELA
inferredcites →https://doi.org/10.4269/ajtmh.2006.74.798openalex-snapshot
POPULATION STRUCTURE OF THE MALARIA VECTOR ANOPHELES DARLINGI IN A MALARIA-ENDEMIC REGION OF EASTERN AMAZONIAN BRAZIL
inferredcites →https://doi.org/10.4269/ajtmh.2007.76.1113openalex-snapshot
A NEWLY RECOGNIZED SPECIES IN THE ANOPHELES (NYSSORHYNCHUS) ALBITARSIS COMPLEX (DIPTERA: CULICIDAE) FROM PUERTO CARRENO, COLOMBIA
inferredcites →https://doi.org/10.4269/ajtmh.2007.76.461openalex-snapshot
MALARIA VECTOR INCRIMINATION IN THREE RURAL RIVERINE VILLAGES IN THE BRAZILIAN AMAZON
inferredcites →https://doi.org/10.5860/choice.35-1515openalex-snapshot
Avian molecular evolution and systematics
inferredcites →https://doi.org/10.5860/choice.37-5647openalex-snapshot
Phylogeography: the history and formation of species
inferredcites →https://doi.org/10.5962/bhl.title.56497openalex-snapshot
The distribution of bird-life in Colombia; a contribution to a biological survey of South America
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4949.3.1zenodo-depositor-declared
Multi-character taxonomic review, systematics, and biogeography of the Black-capped/Tawny-bellied Screech Owl (Megascops atricapilla-M. watsonii) complex (Aves: Strigidae)
inferred← citeshttps://doi.org/10.1002/9781118148594.ch32openalex-snapshot
Malaria in the Brazilian Amazon
inferred← citeshttps://doi.org/10.1007/s12237-026-01688-4openalex-snapshot
Mitochondrial Spatial Diversity in a Keystone Salt Marsh Mussel Geukensia demissa
inferred← citeshttps://doi.org/10.1007/s13744-017-0488-0openalex-snapshot
Genetic Differentiation of Colombian Populations of Anopheles darlingi Root (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1016/bs.apar.2017.12.002openalex-snapshot
Evolution, Systematics, and Biogeography of the Triatominae, Vectors of Chagas Disease
inferred← citeshttps://doi.org/10.1016/j.actatropica.2008.06.005openalex-snapshot
Ecology, evolution, and the long-term surveillance of vector-borne Chagas disease: A multi-scale appraisal of the tribe Rhodniini (Triatominae)
inferred← citeshttps://doi.org/10.1016/j.actatropica.2010.03.002openalex-snapshot
Research needs for Chagas disease prevention
inferred← citeshttps://doi.org/10.1016/j.actatropica.2020.105607openalex-snapshot
Niche divergence and paleo-distributions of Lutzomyia longipalpis mitochondrial haplogroups (Diptera: Psychodidae)
inferred← citeshttps://doi.org/10.1016/j.actatropica.2021.105983openalex-snapshot
DNA barcoding of Lutzomyia longipalpis species complex (Diptera: Psychodidae), suggests the existence of 8 candidate species
inferred← citeshttps://doi.org/10.1016/j.meegid.2013.02.004openalex-snapshot
Genetic structure and divergence in populations of Lutzomyia cruciata, a phlebotomine sand fly (Diptera: Psychodidae) vector of Leishmania mexicana in southeastern Mexico
inferred← citeshttps://doi.org/10.1016/j.meegid.2016.08.019openalex-snapshot
Population dynamics of Anopheles nuneztovari in Colombia
inferred← citeshttps://doi.org/10.1016/j.meegid.2018.06.018openalex-snapshot
Discrimination of Anopheles species of the Arribalzagia Series in Colombia using a multilocus approach
inferred← citeshttps://doi.org/10.1016/j.pt.2007.10.003openalex-snapshot
The Lutzomyia longipalpis species complex: does population sub-structure matter to Leishmania transmission?
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.01.003openalex-snapshot
Analysis of the evolutionary forces shaping mitochondrial genomes of a Neotropical malaria vector complex
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.08.017openalex-snapshot
Evolutionary history and identification of conservation units in the giant otter, Pteronura brasiliensis
inferred← citeshttps://doi.org/10.1038/hdy.2008.123openalex-snapshot
During the reign of frogs and toads
inferred← citeshttps://doi.org/10.1038/hdy.2008.45openalex-snapshot
Forest-obligate Sabethes mosquitoes suggest palaeoecological perturbations
inferred← citeshttps://doi.org/10.1038/s41598-017-06313-wopenalex-snapshot
After infection with Leishmania infantum, Golden Hamsters (Mesocricetus auratus) become more attractive to female sand flies (Lutzomyia longipalpis)
inferred← citeshttps://doi.org/10.1051/parasite/2008153252openalex-snapshot
Sandfly pheromones: Their biology and potential for use in control programs
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaf006openalex-snapshot
Molecular species delimitation and historical biogeography among species of the genus Partamona (Hymenoptera: Apidae: Meliponini), with emphasis on the Eastern group from South America
inferred← citeshttps://doi.org/10.1111/j.1095-8312.2009.01226.xopenalex-snapshot
Spatial expansion and population structure of the neotropical malaria vector, Anopheles darlingi (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1111/j.1365-2915.2007.00703.xopenalex-snapshot
Evidence for late Pleistocene population expansion of the malarial mosquitoes, Anopheles arabiensis and Anopheles gambiae in Nigeria
inferred← citeshttps://doi.org/10.1111/j.1365-2915.2008.00731.xopenalex-snapshot
Population analysis using the nuclear white gene detects Pliocene/Pleistocene lineage divergence within Anopheles nuneztovari in South America
inferred← citeshttps://doi.org/10.1111/j.1744-7917.2010.01378.xopenalex-snapshot
Radiation of the Oriental phlebotomine sand flies (Diptera: Psychodidae)
inferred← citeshttps://doi.org/10.1111/mve.12326openalex-snapshot
Inferring distributional shifts of epidemiologically important North and Central American sandflies from Pleistocene to future scenarios
inferred← citeshttps://doi.org/10.1111/mve.12695openalex-snapshot
High climatic ancestral affinity between the lineages of the Leishmania vector Psathyromyia shannoni sensu stricto (Diptera: Phlebotominae)
inferred← citeshttps://doi.org/10.1111/zsc.12398openalex-snapshot
A complex biogeographic history of diversification in Neotropical lancehead pitvipers (Serpentes, Viperidae)
inferred← citeshttps://doi.org/10.1186/1471-2148-10-91openalex-snapshot
Estimation of divergence time between two sibling species of the Anopheles (Kerteszia) cruziicomplex using a multilocus approach
inferred← citeshttps://doi.org/10.1186/1471-2148-13-207openalex-snapshot
Evidence for the occurrence of two sympatric sibling species within the Anopheles (Kerteszia) cruzii complex in southeast Brazil and the detection of asymmetric introgression between them using a multilocus analysis
inferred← citeshttps://doi.org/10.1186/1475-2875-9-127openalex-snapshot
Complete mtDNA genomes of Anopheles darlingi and an approach to anopheline divergence time
inferred← citeshttps://doi.org/10.1186/1756-3305-1-16openalex-snapshot
Lutzomyia longipalpis s.l. in Brazil and the impact of the Sao Francisco River in the speciation of this sand fly vector
inferred← citeshttps://doi.org/10.1186/1756-3305-5-249openalex-snapshot
Evidence for genetic differentiation at the microgeographic scale in Phlebotomus papatasi populations from Sudan
inferred← citeshttps://doi.org/10.1186/1756-3305-6-47openalex-snapshot
Phylogeography of the neotropical Anopheles triannulatus complex (Diptera: Culicidae) supports deep structure and complex patterns
inferred← citeshttps://doi.org/10.1186/1756-3305-7-423openalex-snapshot
Demographic history and population structure of Anopheles pseudopunctipennis in Argentina based on the mitochondrial COI gene
inferred← citeshttps://doi.org/10.1186/s12936-015-1037-0openalex-snapshot
Larval habitat characterization of Anopheles darlingi from its northernmost geographical distribution in Chiapas, Mexico
inferred← citeshttps://doi.org/10.1371/journal.pntd.0000365openalex-snapshot
Molecular and Behavioral Differentiation among Brazilian Populations of Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae)
inferred← citeshttps://doi.org/10.1371/journal.pntd.0003266openalex-snapshot
Phylogeny and Niche Conservatism in North and Central American Triatomine Bugs (Hemiptera: Reduviidae: Triatominae), Vectors of Chagas' Disease
inferred← citeshttps://doi.org/10.1371/journal.pntd.0003364openalex-snapshot
Population Genetics of Two Key Mosquito Vectors of Rift Valley Fever Virus Reveals New Insights into the Changing Disease Outbreak Patterns in Kenya
inferred← citeshttps://doi.org/10.1371/journal.pntd.0006614openalex-snapshot
Genetic diversity, phylogeography and molecular clock of the Lutzomyia longipalpis complex (Diptera: Psychodidae)
inferred← citeshttps://doi.org/10.1371/journal.pone.0193591openalex-snapshot
Molecular taxonomy and evolutionary relationships in the Oswaldoi-Konderi complex (Anophelinae: Anopheles: Nyssorhynchus) from the Brazilian Amazon region
inferred← citeshttps://doi.org/10.1371/journal.pone.0253230openalex-snapshot
Updating the bionomy and geographical distribution of Anopheles (Nyssorhynchus) albitarsis F: A vector of malaria parasites in northern South America
inferred← citeshttps://doi.org/10.1590/0037-8682-0701-2021openalex-snapshot
Phylogenetic relationships of the supercontig of sodium channel subunit I (NaV) in 17 species of Anopheles (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1590/s0074-02762012000300016openalex-snapshot
A morphologically distinct Phlebotomus argentipes population from active cutaneous leishmaniasis foci in central Sri Lanka
inferred← citeshttps://doi.org/10.1603/me10153openalex-snapshot
Genetic Structure and Demographic History of New World Screwworm Across Its Current Geographic Range
inferred← citeshttps://doi.org/10.1603/me11256openalex-snapshot
Molecular Markers Reveal Infestation Dynamics of the Bed Bug (Hemiptera: Cimicidae) Within Apartment Buildings
inferred← citeshttps://doi.org/10.17533/udea.hm.10875openalex-snapshot
confirmación molecular de especie en especímenes Anopheles recolectados en el corregimiento de Juan José,Puerto Libertador, Córdoba, colombia
inferred← citeshttps://doi.org/10.4269/ajtmh.12-0203openalex-snapshot
Ecological Suitability and Spatial Distribution of Five Anopheles Species in Amazonian Brazil
inferred← citeshttps://doi.org/10.4269/ajtmh.2009.81.223openalex-snapshot
Very Low Levels of Genetic Variation in Natural Peridomestic Populations of the Chagas Disease Vector Triatoma sordida (Hemiptera: Reduviidae) in Southeastern Brazil
inferred← citeshttps://doi.org/10.4269/ajtmh.2010.09-0381openalex-snapshot
Microgeographic Genetic Variation of the Malaria Vector Anopheles darlingi Root (Diptera: Culicidae) from Córdoba and Antioquia, Colombia
inferred← citeshttps://doi.org/10.4269/ajtmh.2010.09-0423openalex-snapshot
Evidence for Pleistocene Population Divergence and Expansion of Anopheles albimanus in Southern Central America
inferred← citeshttps://doi.org/10.47749/t/unicamp.2011.794056openalex-snapshot
Análise filogeográfica da mosca da bicheira, Cochliomyia hominivorax
inferred← citeshttps://doi.org/10.5772/55217openalex-snapshot
Phylogeography, Vectors and Transmission in Latin America
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.