On the public citation graph
Parallel effects of the inversion In(3R)Payne on body size across the North American and Australian clines in Drosophila melanogaster
0 signed · 135 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/bies.20584openalex-snapshot
Size and shape: the developmental regulation of static allometry in insects
inferredcites →https://doi.org/10.1002/dvdy.24255openalex-snapshot
Making quantitative morphological variation from basic developmental processes: Where are we? The case of the Drosophila wing
inferredcites →https://doi.org/10.1007/bf00128015openalex-snapshot
Chromosome inversion polymorphisms in Drosophila melanogaster II. Geographic clines and climatic associations in Australasia, North America and Asia
inferredcites →https://doi.org/10.1007/bf01990682openalex-snapshot
Evolution in a cosmopolitan species: Genetic latitudinal clines inDrosophila melanogaster wild populations
inferredcites →https://doi.org/10.1007/bf02715819openalex-snapshot
Latitudinal clines inDrosophila melanogaster: Body size, allozyme frequencies, inversion frequencies, and the insulin-signalling pathway
inferredcites →https://doi.org/10.1007/bf02715842openalex-snapshot
Homogeneity of common cosmopolitan inversion frequencies in Southeast AsianDrosophila melanogaster
inferredcites →https://doi.org/10.1007/s10709-005-2375-6openalex-snapshot
Analysis of two components of flight using recombinant inbred lines of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10709-006-7375-7openalex-snapshot
The association between inversion In(3R)Payne and clinally varying traits in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10709-006-9010-zopenalex-snapshot
Climatic selection on genes and traits after a 100 year-old invasion: a critical look at the temperate-tropical clines in Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1007/s11692-009-9061-zopenalex-snapshot
Inferring the Nature of Allometry from Geometric Data
inferredcites →https://doi.org/10.1007/s11692-012-9159-6openalex-snapshot
The Measurement of Local Variation in Shape
inferredcites →https://doi.org/10.1007/s11692-013-9235-6openalex-snapshot
Latitudinal Variation in Starvation Resistance is Explained by Lipid Content in Natural Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0168-9525(88)90098-4openalex-snapshot
Genetic variation of Drosophila melanogaster natural populations
inferredcites →https://doi.org/10.1016/j.cub.2006.12.031openalex-snapshot
Drosophila melanogaster's history as a human commensal
inferredcites →https://doi.org/10.1016/j.tig.2015.05.006openalex-snapshot
Revisiting classic clines in Drosophila melanogaster in the age of genomics
inferredcites →https://doi.org/10.1016/j.tree.2004.06.013openalex-snapshot
Chromosomal inversion polymorphisms and adaptation
inferredcites →https://doi.org/10.1016/j.ygcen.2014.11.021openalex-snapshot
Insulin/IGF signaling and its regulation in Drosophila
inferredcites →https://doi.org/10.1016/j.ymeth.2014.02.034openalex-snapshot
Methods for studying metabolism in Drosophila
inferredcites →https://doi.org/10.1016/s0960-9822(01)00068-9openalex-snapshot
An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control
inferredcites →https://doi.org/10.1016/s0962-8924(02)00042-9openalex-snapshot
Insulin/IGF and target of rapamycin signaling: a TOR de force in growth control
inferredcites →https://doi.org/10.1017/s0016672301005407openalex-snapshot
Chromosomal inversion polymorphism in Afrotropical populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1023/b:gene.0000017639.62427.8bopenalex-snapshot
Comparative Analysis of Morphological Traits Among Drosophila Melanogaster and D. Simulans: Genetic Variability, Clines and Phenotypic Plasticity
inferredcites →https://doi.org/10.1038/39362openalex-snapshot
Daughters against dpp modulates dpp organizing activity in Drosophila wing development
inferredcites →https://doi.org/10.1038/hdy.1976.60openalex-snapshot
The Genetics and Biology of Drosophila
inferredcites →https://doi.org/10.1038/hdy.1994.68openalex-snapshot
Variation in wing length in Eurasian natural populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/nature09670openalex-snapshot
Climate change and evolutionary adaptation
inferredcites →https://doi.org/10.1038/nrg1989openalex-snapshot
How flies get their size: genetics meets physiology
inferredcites →https://doi.org/10.1038/nrg3522openalex-snapshot
Ecological genomics of local adaptation
inferredcites →https://doi.org/10.1038/sj.hdy.6800121openalex-snapshot
Quantitative genetic analysis of natural variation in body size in Drosophila melanogaster
inferredcites →https://doi.org/10.1038/sj.hdy.6800220openalex-snapshot
Thermal tolerance trade-offs associated with the right arm of chromosome 3 and marked by the hsr-omega gene in Drosophila melanogaster
inferredcites →https://doi.org/10.1046/j.1365-2540.1999.00649.xopenalex-snapshot
Desiccation and starvation resistance in Drosophila: patterns of variation at the species, population and intrapopulation levels
inferredcites →https://doi.org/10.1046/j.1365-2540.2000.00677.xopenalex-snapshot
Cellular basis of wing size variation in Drosophila melanogaster: a comparison of latitudinal clines on two continents
inferredcites →https://doi.org/10.1046/j.1365-2540.2001.00779.xopenalex-snapshot
The contrasting genetic architecture of wing size and shape in Drosophila melanogaster
inferredcites →https://doi.org/10.1046/j.1420-9101.1995.8030315.xopenalex-snapshot
Thermal evolution of rate of larval development in Drosophila melanogaster in laboratory and field populations
inferredcites →https://doi.org/10.1046/j.1420-9101.1999.00029.xopenalex-snapshot
Latitudinal variation in wild populations of Drosophila melanogaster: heritabilities and reaction norms
inferredcites →https://doi.org/10.1046/j.1420-9101.2003.00560.xopenalex-snapshot
Latitudinal countergradient variation in the common frog ( Rana temporaria ) development rates – evidence for local adaptation
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00367.xopenalex-snapshot
Opposing clines for high and low temperature resistance in Drosophila melanogaster
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00380.xopenalex-snapshot
Dissecting adaptive clinal variation: markers, inversions and size/stress associations in Drosophila melanogaster from a central field population
inferredcites →https://doi.org/10.1046/j.1525-142x.2000.00041.xopenalex-snapshot
Adaptation and constraint in the evolution of Drosophila melanogaster wing shape
inferredcites →https://doi.org/10.1073/pnas.0805485105openalex-snapshot
An amino acid polymorphism in the couch potato gene forms the basis for climatic adaptation in Drosophila melanogaster
inferredcites →https://doi.org/10.1086/432265openalex-snapshot
The Evolutionary Genetics of Canalization
inferredcites →https://doi.org/10.1093/clinchem/29.3.538openalex-snapshot
A peroxidase-coupled method for the colorimetric determination of serum triglycerides.
inferredcites →https://doi.org/10.1093/genetics/117.4.727openalex-snapshot
Heritability of Two Morphological Characters Within and Among Natural Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/140.2.659openalex-snapshot
Cellular basis and developmental timing in a size cline of Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/genetics/143.4.1615openalex-snapshot
Response of Two Heat Shock Genes to Selection for Knockdown Heat Resistance in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/146.3.881openalex-snapshot
Genetic and Environmental Responses to Temperature of Drosophila melanogaster From a Latitudinal Cline
inferredcites →https://doi.org/10.1093/genetics/158.1.319openalex-snapshot
Nonclinality of Molecular Variation Implicates Selection in Maintaining a Morphological Cline of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/87.1.169openalex-snapshot
INVERSION CLINES IN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/95.1.211openalex-snapshot
CHROMOSOME STUDIES IN WILD POPULATIONS OF DROSOPHILA MELANOGASTER. II. RELATIONSHIP OF INVERSION FREQUENCIES TO LATITUDE, SEASON, WING-LOADING AND FLIGHT ACTIVITY
inferredcites →https://doi.org/10.1093/genetics/98.4.833openalex-snapshot
CHROMOSOME INVERSION POLYMORPHISMS IN DROSOPHILA MELANOGASTER. I. LATITUDINAL CLINES AND ASSOCIATIONS BETWEEN INVERSIONS IN AUSTRALASIAN POPULATIONS
inferredcites →https://doi.org/10.1093/molbev/msr064openalex-snapshot
Molecular Basis of Adaptive Shift in Body Size in Drosophila melanogaster: Functional and Sequence Analyses of the Dca Gene
inferredcites →https://doi.org/10.1093/molbev/msw016openalex-snapshot
Genomic Evidence for Adaptive Inversion Clines inDrosophila melanogaster
inferredcites →https://doi.org/10.1111/evo.12351openalex-snapshot
SIMILARITIES AND DIFFERENCES IN ALTITUDINAL VERSUS LATITUDINAL VARIATION FOR MORPHOLOGICAL TRAITS INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/evo.12546openalex-snapshot
A highly pleiotropic amino acid polymorphism in the Drosophila insulin receptor contributes to life-history adaptation
inferredcites →https://doi.org/10.1111/j.0014-3820.2000.tb00726.xopenalex-snapshot
STARVATION RESISTANCE AND ADULT BODY COMPOSITION IN A LATITUDINAL CLINE OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00623.xopenalex-snapshot
CHILL-COMA TOLERANCE, A MAJOR CLIMATIC ADAPTATION AMONG DROSOPHILA SPECIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01418.xopenalex-snapshot
GEOGRAPHIC VARIATION FOR WING SHAPE IN DROSOPHILA SERRATA
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01509.xopenalex-snapshot
QTL MAPPING REVEALS A STRIKING COINCIDENCE IN THE POSITIONS OF GENOMIC REGIONS ASSOCIATED WITH ADAPTIVE VARIATION IN BODY SIZE IN PARALLEL CLINES OF DROSOPHILA MELANOGASTER ON DIFFERENT CONTINENTS
inferredcites →https://doi.org/10.1111/j.0014-3820.2005.tb01821.xopenalex-snapshot
GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE‐HISTORY TRAITS, AND CLIMATIC ADAPTATION INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.0022-1112.2004.00433.xopenalex-snapshot
Phylogeographic relationships within the Mediterranean turbot inferred by mitochondrial DNA haplotype variation
inferredcites →https://doi.org/10.1111/j.0269-8463.2004.00904.xopenalex-snapshot
Cold adaptation in geographical populations of Drosophila melanogaster : phenotypic plasticity is more important than genetic variability
inferredcites →https://doi.org/10.1111/j.1095-8312.1989.tb02098.xopenalex-snapshot
An integrated approach to environmental stress tolerance and life-history variation: desiccation tolerance in Drosophila
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02445.xopenalex-snapshot
The latitudinal cline in the In(3R)Payne inversion polymorphism has shifted in the last 20 years in Australian Drosophila melanogaster populations
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04509.xopenalex-snapshot
A clinally varying promoter polymorphism associated with adaptive variation in wing size inDrosophila
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05089.xopenalex-snapshot
The molecular genetics of clinal variation: a case study of ebony and thoracic trident pigmentation in Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1111/j.1365-294x.2011.05260.xopenalex-snapshot
Divergent enhancer haplotype of ebony on inversion In(3R)Payne associated with pigmentation variation in a tropical population of Drosophila melanogaster
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05731.xopenalex-snapshot
Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica
inferredcites →https://doi.org/10.1111/j.1558-5646.1978.tb04617.xopenalex-snapshot
GEOGRAPHIC VARIATION, SPECIATION, AND CLINES
inferredcites →https://doi.org/10.1111/j.1558-5646.1994.tb05311.xopenalex-snapshot
EVOLUTION AND DEVELOPMENT OF BODY SIZE AND CELL SIZE INDROSOPHILA MELANOGASTERIN RESPONSE TO TEMPERATURE
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02454.xopenalex-snapshot
BERGMANN'S RULE IN ECTOTHERMS: IS IT ADAPTIVE?
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb02017.xopenalex-snapshot
LATITUDINAL VARIATION OF WING:THORAX SIZE RATIO AND WING-ASPECT RATIO INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00351.xopenalex-snapshot
REPRODUCTIVE DIAPAUSE AND LIFE-HISTORY CLINES IN NORTH AMERICAN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/jeb.12607openalex-snapshot
Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub‐Saharan Africa
inferredcites →https://doi.org/10.1111/mec.12594openalex-snapshot
Inference of chromosomal inversion dynamics from P ool‐ S eq data in natural and laboratory populations of D rosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.13137openalex-snapshot
Population genomic analysis uncovers African and European admixture in Drosophila melanogaster populations from the south‐eastern United States and Caribbean Islands
inferredcites →https://doi.org/10.1111/mec.13161openalex-snapshot
Genomic evidence for role of inversion 3 RP of Drosophila melanogaster in facilitating climate change adaptation
inferredcites →https://doi.org/10.1111/mec.13455openalex-snapshot
Secondary contact and local adaptation contribute to genome‐wide patterns of clinal variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.13534openalex-snapshot
Genomics of clinal variation in Drosophila: disentangling the interactions of selection and demography
inferredcites →https://doi.org/10.1126/science.1109523openalex-snapshot
A Rapid Shift in a Classic Clinal Pattern in Drosophila Reflecting Climate Change
inferredcites →https://doi.org/10.1126/science.179.4070.243openalex-snapshot
Gene Flow and Population Differentiation
inferredcites →https://doi.org/10.1126/science.284.5422.1954openalex-snapshot
Wing Rotation and the Aerodynamic Basis of Insect Flight
inferredcites →https://doi.org/10.1139/g91-094openalex-snapshot
Genetic differentiation and inversion clines in Indian natural populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1146/annurev.cellbio.23.090506.123606openalex-snapshot
Wing Vein Patterning in Drosophila and the Analysis of Intercellular Signaling
inferredcites →https://doi.org/10.1146/annurev.ecolsys.39.110707.173532openalex-snapshot
Revisiting the Impact of Inversions in Evolution: From Population Genetic Markers to Drivers of Adaptive Shifts and Speciation?
inferredcites →https://doi.org/10.1186/1297-9686-17-2-211openalex-snapshot
Thoracic trident pigmentation in Drosophila melanogaster: Differentiation of geographical populations
inferredcites →https://doi.org/10.1186/1297-9686-25-6-517openalex-snapshot
Phenotypic and genetic variability of morphometrical traits in natural populations of Drosophila melanogaster and D simulans. I. Geographic variations
inferredcites →https://doi.org/10.1186/1297-9686-29-5-601openalex-snapshot
Thoracic trident pigmentation in Drosophila melanogaster: latitudinal and altitudinal clines in Indian populations
inferredcites →https://doi.org/10.1266/jjg.54.69openalex-snapshot
Inversion polymorphisms in Japanese natural populations of Drosophila melanogaster.
inferredcites →https://doi.org/10.1371/journal.pgen.1002314openalex-snapshot
Developmental Stability: A Major Role for Cyclin G in Drosophila melanogaster
inferredcites →https://doi.org/10.1371/journal.pgen.1004775openalex-snapshot
Genomic Evidence of Rapid and Stable Adaptive Oscillations over Seasonal Time Scales in Drosophila
inferredcites →https://doi.org/10.1371/journal.pone.0001987openalex-snapshot
Functional Significance of Allelic Variation at methuselah, an Aging Gene in Drosophila
inferredcites →https://doi.org/10.1534/genetics.104.038810openalex-snapshot
The Structure and Population Genetics of the Breakpoints Associated With the Cosmopolitan Chromosomal Inversion In(3R)Payne in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.107.074336openalex-snapshot
Mapping Regions Within Cosmopolitan Inversion In(3R)Payne Associated With Natural Variation in Body Size in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.110.123059openalex-snapshot
Genomic Differentiation Between Temperate and Tropical Australian Populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.112.141622openalex-snapshot
Sequence-Based Detection and Breakpoint Assembly of Polymorphic Inversions
inferredcites →https://doi.org/10.1534/genetics.114.161463openalex-snapshot
Parallel Geographic Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.1554/0014-3820(2001)055[1063:cctamc]2.0.co;2openalex-snapshot
CHILL-COMA TOLERANCE, A MAJOR CLIMATIC ADAPTATION AMONG DROSOPHILA SPECIES
inferredcites →https://doi.org/10.2307/1270020openalex-snapshot
Statistical Power Analysis for the Behavioral Sciences
inferredcites →https://doi.org/10.25911/5d6e489737ebeopenalex-snapshot
Chromosome inversion polymorphisms in Drosophila Melanogaster
inferredcites →https://doi.org/10.3389/fendo.2012.00049openalex-snapshot
Integrating Body and Organ Size in Drosophila: Recent Advances and Outstanding Problems
inferredcites →https://doi.org/10.4161/cib.29240openalex-snapshot
The roles of juvenile hormone, insulin/target of rapamycin, and ecydsone signaling in regulating body size inDrosophila
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/evl3.227openalex-snapshot
Genetic variation for adaptive traits is associated with polymorphic inversions in Littorina saxatilis
inferred← citeshttps://doi.org/10.1007/978-1-0716-4583-3_7openalex-snapshot
The Influence of Chromosomal Inversions on Genetic Variation and Clinal Patterns in Genomic Data of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.tplants.2017.03.001openalex-snapshot
Evolutionary Transcriptomics and Proteomics: Insight into Plant Adaptation
inferred← citeshttps://doi.org/10.1038/s41437-025-00780-yopenalex-snapshot
Multiple forms of balancing selection maintain inversion polymorphism
inferred← citeshttps://doi.org/10.1038/s41437-025-00784-8openalex-snapshot
Experimental test of the fitness effects of divergent marine–freshwater chromosomal inversions in stickleback under different salinity conditions
inferred← citeshttps://doi.org/10.1093/evlett/qraf014openalex-snapshot
Continent-wide differentiation of fitness traits and patterns of climate adaptation among European populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/gbe/evaa103openalex-snapshot
Fine-Scale Position Effects Shape the Distribution of Inversion Breakpoints in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/gbe/evae024openalex-snapshot
Chromosomal Inversions and the Demography of Speciation in Drosophila montana and Drosophila flavomontana
inferred← citeshttps://doi.org/10.1093/molbev/msaa120openalex-snapshot
Genomic Analysis of European Drosophila melanogaster Populations Reveals Longitudinal Structure, Continent-Wide Selection, and Previously Unknown DNA Viruses
inferred← citeshttps://doi.org/10.1093/molbev/msac223openalex-snapshot
Patterns of Population Structure and Introgression Among Recently Differentiated Drosophila melanogaster Populations
inferred← citeshttps://doi.org/10.1093/molbev/msad118openalex-snapshot
An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation
inferred← citeshttps://doi.org/10.1093/molbev/msaf132openalex-snapshot
Footprints of Worldwide Adaptation in Structured Populations of Drosophila melanogaster Through the Expanded DEST 2.0 Genomic Resource
inferred← citeshttps://doi.org/10.1093/molbev/msaf209openalex-snapshot
A Balanced Inversion Polymorphism Exhibits a Dominance Reversal at the Gene Expression Level that Depends on Developmental Context
inferred← citeshttps://doi.org/10.1101/068205openalex-snapshot
Chromosome arm specific patterns of polymorphism associated with chromosomal inversions in the major African malaria vector, Anopheles funestus
inferred← citeshttps://doi.org/10.1101/2024.02.08.579525openalex-snapshot
Polygenic architecture of adaptation to a high-altitude environment for Drosophila melanogaster wing shape and size
inferred← citeshttps://doi.org/10.1101/2024.11.10.622744openalex-snapshot
Footprints of worldwide adaptation in structured populations of D. melanogaster through the expanded DEST 2.0 genomic resource
inferred← citeshttps://doi.org/10.1101/313759openalex-snapshot
Genomic analysis of European Drosophila melanogaster populations reveals longitudinal structure, continent-wide selection, and previously unknown DNA viruses
inferred← citeshttps://doi.org/10.1111/evo.13517openalex-snapshot
Geographic clines in wing morphology relate to colonization history in New World but not Old World populations of yellow dung flies
inferred← citeshttps://doi.org/10.1111/evo.13759openalex-snapshot
A clinal polymorphism in the insulin signaling transcription factor foxo contributes to life‐history adaptation in Drosophila *
inferred← citeshttps://doi.org/10.1111/evo.14602openalex-snapshot
Genetic architecture of repeated phenotypic divergence in Littorina saxatilis ecotype evolution
inferred← citeshttps://doi.org/10.1111/jeb.13310openalex-snapshot
An inversion supergene in Drosophila underpins latitudinal clines in survival traits
inferred← citeshttps://doi.org/10.1111/jeb.14242openalex-snapshot
How chromosomal inversions reorient the evolutionary process
inferred← citeshttps://doi.org/10.1111/jzs.12327openalex-snapshot
Exaggerated male forelegs are not more differentiated than wing morphology in two widespread sister species of black scavenger flies
inferred← citeshttps://doi.org/10.1111/mec.14335openalex-snapshot
Chromosome arm‐specific patterns of polymorphism associated with chromosomal inversions in the major African malaria vector, Anopheles funestus
inferred← citeshttps://doi.org/10.1111/mec.14381openalex-snapshot
Genomics of natural populations: Evolutionary forces that establish and maintain gene arrangements in Drosophila pseudoobscura
inferred← citeshttps://doi.org/10.1111/mec.14871openalex-snapshot
The adaptive significance of chromosomal inversion polymorphisms inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1111/mec.17062openalex-snapshot
Ecology, the pace‐of‐life, epistatic selection and the maintenance of genetic variation in life‐history genes
inferred← citeshttps://doi.org/10.11606/d.41.2025.tde-13062025-173146openalex-snapshot
Acompanhando a evolução de clinas genômicas em Drosophila melanogaster por meio de amostragens históricas
inferred← citeshttps://doi.org/10.1371/journal.pgen.1012012openalex-snapshot
Cosmopolitan inversions have a major impact on trait variation and the power of different GWAS approaches to identify associations
inferred← citeshttps://doi.org/10.1534/genetics.118.301084openalex-snapshot
Muller “Elements” in Drosophila : How the Search for the Genetic Basis for Speciation Led to the Birth of Comparative Genomics
inferred← citeshttps://doi.org/10.1534/genetics.119.300160openalex-snapshot
Life-History Evolution and the Genetics of Fitness Components in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2023-0348openalex-snapshot
Clinal variation in natural populations of Drosophila melanogaster: An old debate about natural selection and neutral processes
inferred← citeshttps://doi.org/10.70675/22847453z7110z4c06za4f2zc6e29efaccc6openalex-snapshot
Origins and impacts of chromosomal inversions in the evolution and adaptation of pearl millet
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.