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The adaptive significance of chromosomal inversion polymorphisms inDrosophila melanogaster

https://doi.org/10.1111/mec.14871
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Mitotic recombination between dispersed but related rRNA genes of Schizosaccharomyces pombe generates a reciprocal translocation
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Latitudinal clines inDrosophila melanogaster: Body size, allozyme frequencies, inversion frequencies, and the insulin-signalling pathway
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Segmental duplication associated with the human-specific inversion of chromosome�18: a further example of the impact of segmental duplications on karyotype and genome evolution in primates
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The association between inversion In(3R)Payne and clinally varying traits in Drosophila melanogaster
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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
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Animal cytology and evolution
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Matrix inversions for chromosomal inversions: A method to construct summary statistics in complex coalescent models
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Chromosomal inversion polymorphisms and adaptation
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Eco-Evolutionary Genomics of Chromosomal Inversions
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The Genetics and Biology of Drosophila
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Chromosomal rearrangements and speciation
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Selection of new inversions in multi-locus genetic systems
inferredcites →https://doi.org/10.1017/s0016672300014919openalex-snapshot
Inversion polymorphism in a two-locus genetic system
inferredcites →https://doi.org/10.1017/s0016672301004955openalex-snapshot
Inversion polymorphisms and nucleotide variability in Drosophila
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Chromosomal inversion polymorphism in Afrotropical populations of Drosophila melanogaster
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Mitotic and Polytene Chromosomes: Comparisons Between Drosophila Melanogaster and Drosophila Simulans
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A further study of fitness of chromosomally polymorphic and monomorphic populations of Drosophila pseudoobscura
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The Genetics and Biology of Drosophila
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Gene flow and gene flux shape evolutionary patterns of variation in Drosophila subobscura
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A sequential coalescent algorithm for chromosomal inversions
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Population genetics from 1966 to 2016
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Sequencing and comparison of yeast species to identify genes and regulatory elements
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The Drosophila melanogaster Genetic Reference Panel
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Next-generation DNA sequencing
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A common inversion under selection in Europeans
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Inversion evolutionary rates might limit the experimental identification of inversion breakpoints in non-model species
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Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism
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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/10.1038/srep36248openalex-snapshot
Multiple and diverse structural changes affect the breakpoint regions of polymorphic inversions across the Drosophila genus
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Synapsis and recombination in inversion heterozygotes
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Latitudinal countergradient variation in the common frog ( Rana temporaria ) development rates – evidence for local adaptation
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Opposing clines for high and low temperature resistance in Drosophila melanogaster
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Seasonally fluctuating selection can maintain polymorphism at many loci via segregation lift
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Linked genetic variation and not genome structure causes widespread differential expression associated with chromosomal inversions
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Chromosomal inversions and the reproductive isolation of species
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Concerning the Origin of the Polytene Chromosomes of Diptera
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Genetic Factors Affecting the Strength of Linkage in Drosophila
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The Suppression of Crossing Over in Inversion Heterozygotes of Drosophila Pseudoobscura
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SELECTION FOR GEOTAXIS IN MONOMORPHIC AND POLYMORPHIC POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
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A Case of Rearrangement of Genes in Drosophila
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Temporal Frequency Changes of Enzyme and Chromosomal Polymorphisms in Natural Populations of Drosophila
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Four decades of inversion polymorphism in Drosophila pseudoobscura.
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Gene conversion is involved in the transfer of genetic information between naturally occurring inversions of Drosophila.
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Isolation and analysis of the breakpoint sequences of chromosome inversion In(3L)Payne in Drosophila melanogaster.
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Genetic Equilibrium When More Than One Ecological Niche is Available
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Chromosomal Influences on Life-History Variation Along an Altitudinal Transect in Drosophila robusta
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Human inversions and their functional consequences
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Effects of Inversions on Within- and Between-Species Recombination and Divergence
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BALANCING SELECTION, INVERSION POLYMORPHISM AND ADAPTATION IN DDT-RESISTANT POPULATIONS OF DROSOPHILA MELANOGASTER
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ASSOCIATION OF CHROMOSOME AND ENZYME POLYMORPHISMS IN NATURAL AND CAGE POPULATIONS OF DROSOPHILA MELANOGASTER
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Heritability of Two Morphological Characters Within and Among Natural Populations of Drosophila melanogaster
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The rosy region of Drosophila melanogaster and Drosophila simulans. I. Contrasting levels of naturally occurring DNA restriction map variation and divergence.
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Changes in relative fitness with temperature among second chromosome arrangements in Drosophila melanogaster.
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Molecular variation of Adh and P6 genes in an African population of Drosophila melanogaster and its relation to chromosomal inversions.
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Time-Series Analysis of Seasonal Changes of the O Inversion Polymorphism of Drosophila subobscura
inferredcites →https://doi.org/10.1093/genetics/144.4.1565openalex-snapshot
Contrasting Histories of Three Gene Regions Associated With In(3L)Payne of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/146.2.695openalex-snapshot
Recombination and Gene Flux Caused by Gene Conversion and Crossing Over in Inversion Heterokaryotypes
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Multiple Origins of Cytologically Identical Chromosome Inversions in the Anopheles gambiae Complex
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Unusual Haplotype Structure at the Proximal Breakpoint of In(2L)t in a Natural Population of Drosophila melanogaster
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Effect of Inversion Polymorphism on the Neutral Nucleotide Variability of Linked Chromosomal Regions in Drosophila
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THE EFFECT OF AUTOSOMAL INVERSIONS ON CROSSING OVER IN THE X-CHROMOSOME OF DROSOPHILA MELANOGASTER
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SALIVARY ANALYSIS OF INVERSION-3R-PAYNE IN THE "VENATION" STOCK OF DROSOPHILA MELANOGASTER
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INVERSIONS IN THE CHROMOSOMES OF DROSOPHILA PSEUDOOBSCURA
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GENETICS OF NATURAL POPULATIONS IX. TEMPORAL CHANGES IN THE COMPOSITION OF POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
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GENETICS OF NATURAL POPULATIONS. X. DISPERSION RATES IN DROSOPHILA PSEUDOOBSCURA
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STUDIES ON THE EFFECT OF X CHROMOSOME INVERSIONS ON CROSSING OVER IN THE THIRD CHROMOSOME OF DROSOPHILA MELANOGASTER
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GENETICS OF NATURAL POPULATIONS. XII. EXPERIMENTAL REPRODUCTION OF SOME OF THE CHANGES CAUSED BY NATURAL SELECTION IN CERTAIN POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
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GENETICS OF NATURAL POPULATIONS. XVIII. EXPERIMENTS ON CHROMOSOMES OF DROSOPHILA PSEUDOOBSCURA FROM DIFFERENT GEOGRAPHIC REGIONS
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GENE CONVERSION AND TRANSFER OF GENETIC INFORMATION WITHIN THE INVERTED REGION OF INVERSION HETEROZYGOTES
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CHROMOSOME STUDIES IN WILD POPULATIONS OF D. MELANOGASTER
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THE GENETIC STRUCTURE OF NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER XIII. FURTHER STUDIES ON LINKAGE DISEQUILIBRIUM
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INVERSION CLINES IN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/88.3.515openalex-snapshot
INVERSIONS FAIL TO ACCOUNT FOR ALLOZYME CLINES
inferredcites →https://doi.org/10.1093/genetics/9.4.327openalex-snapshot
CROSSOVER MODIFIERS IN THE THIRD CHROMOSOME OF DROSOPHILA MELANOGASTER
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CHROMOSOME STUDIES IN WILD POPULATIONS OF DROSOPHILA MELANOGASTER. II. RELATIONSHIP OF INVERSION FREQUENCIES TO LATITUDE, SEASON, WING-LOADING AND FLIGHT ACTIVITY
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CHROMOSOME INVERSION POLYMORPHISMS IN DROSOPHILA MELANOGASTER. I. LATITUDINAL CLINES AND ASSOCIATIONS BETWEEN INVERSIONS IN AUSTRALASIAN POPULATIONS
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The Evolution of Genome Structure by Natural and Sexual Selection
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Molecular Basis of Adaptive Shift in Body Size in Drosophila melanogaster: Functional and Sequence Analyses of the Dca Gene
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Genomic Evidence for Adaptive Inversion Clines inDrosophila melanogaster
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Parallel Evolution of Cold Tolerance Within Drosophila melanogaster
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Neutral Variation in the Context of Selection
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Progress and Prospects in Evolutionary Biology
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Drosophila
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SALIVARY CHROMOSOME MAPS
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Chromosome Inversions and Frequency of Extra Bristles in Natural Populations of Drosophila melanogaster
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Further Evidence for Latitudinal Inversion Clines in Natural Populations of Drosophila melanogaster from India
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Pigmentation and fitness trade-offs through the lens of artificial selection
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Genetic organization in higher organisms
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Relationships within the melanogaster species subgroup of the genus Drosophila ( Sophophora ). I. Inversion polymorphisms in Drosophila melanogaster and Drosophila simulans
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Models of the evolution of some genetic systems
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Coalescent patterns for chromosomal inversions in divergent populations
inferredcites →https://doi.org/10.1098/rstb.2017.0423openalex-snapshot
Local adaptation and the evolution of inversions on sex chromosomes and autosomes
inferredcites →https://doi.org/10.1101/337543openalex-snapshot
Broad geographic sampling reveals predictable, pervasive, and strong seasonal adaptation in Drosophila
inferredcites →https://doi.org/10.1101/gr.126037.111openalex-snapshot
The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism
inferredcites →https://doi.org/10.1101/gr.171546.113openalex-snapshot
Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines
inferredcites →https://doi.org/10.1101/gr.3059305openalex-snapshot
Comparative genome sequencing of Drosophila pseudoobscura : Chromosomal, gene, and cis -element evolution
inferredcites →https://doi.org/10.1101/gr.3732505openalex-snapshot
Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16
inferredcites →https://doi.org/10.1101/pdb.prot4708openalex-snapshot
Dissection of Larval Salivary Glands and Polytene Chromosome Preparation: Figure 1.
inferredcites →https://doi.org/10.1101/pdb.prot5389openalex-snapshot
Preparation and Orcein Staining of Mitotic Chromosomes from Drosophila Larval Brain
inferredcites →https://doi.org/10.1101/sqb.1955.020.01.003openalex-snapshot
A REVIEW OF SOME FUNDAMENTAL CONCEPTS AND PROBLEMS OF POPULATION GENETICS
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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/evo.13144openalex-snapshot
Adaptive patterns of phenotypic plasticity in laboratory and field environments in Drosophila melanogaster
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LATITUDINAL VARIATION FOR TWO ENZYME LOCI AND AN INVERSION POLYMORPHISM INDROSOPHILA MELANOGASTERFROM CENTRAL AND SOUTH AMERICA
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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
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ACCUMULATING POSTZYGOTIC ISOLATION GENES IN PARAPATRY: A NEW TWIST ON CHROMOSOMAL SPECIATION
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GENETIC VARIANCE FOR DIAPAUSE EXPRESSION AND ASSOCIATED LIFE HISTORIES IN DROSOPHILA MELANOGASTER
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GEOGRAPHIC VARIATION IN DIAPAUSE INCIDENCE, LIFE‐HISTORY TRAITS, AND CLIMATIC ADAPTATION INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00505.xopenalex-snapshot
ENVIRONMENTAL HETEROGENEITY AND THE MAINTENANCE OF GENETIC VARIATION FOR REPRODUCTIVE DIAPAUSE IN DROSOPHILA MELANOGASTER
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Phylogeographic relationships within the Mediterranean turbot inferred by mitochondrial DNA haplotype variation
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Relative importance of plastic vs genetic factors in adaptive differentiation: geographical variation for stress resistance in Drosophila melanogaster from eastern Australia
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The latitudinal cline in the In(3R)Payne inversion polymorphism has shifted in the last 20 years in Australian Drosophila melanogaster populations
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The genetic basis of adaptive pigmentation variation in Drosophila melanogaster
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Identification of a candidate adaptive polymorphism forDrosophilalife history by parallel independent clines on two continents
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A clinally varying promoter polymorphism associated with adaptive variation in wing size inDrosophila
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Divergent enhancer haplotype of ebony on inversion In(3R)Payne associated with pigmentation variation in a tropical population of Drosophila melanogaster
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Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica
inferredcites →https://doi.org/10.1111/j.1399-0004.1980.tb00121.xopenalex-snapshot
Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication‐deletion of chromosome 9 and gene dosage effect for adenylate kinase‐1
inferredcites →https://doi.org/10.1111/j.1558-5646.1973.tb00694.xopenalex-snapshot
FERTILITY GENES IN NATURAL POPULATIONS OFDROSOPHILA MELANOGASTER.III. SUPERIORITY OF INVERSION HETEROZYGOTES
inferredcites →https://doi.org/10.1111/j.1558-5646.1973.tb00705.xopenalex-snapshot
FREQUENCY-DEPENDENT SELECTION AT THE PAYNE INVERSION INDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.1975.tb00851.xopenalex-snapshot
THE GENETIC BASIS OF EVOLUTIONARY CHANGE
inferredcites →https://doi.org/10.1111/j.1558-5646.1976.tb00887.xopenalex-snapshot
GENETIC CHANGES IN NATURAL POPULATIONS OFDROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb00347.xopenalex-snapshot
THE EXPECTED FIXATION RATE OF CHROMOSOMAL INVERSIONS
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb00348.xopenalex-snapshot
EVOLUTIONARY CHANGE OF THE CHROMOSOMAL POLYMORPHISM IN DROSOPHILA MELANOGASTER POPULATIONS
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb05176.xopenalex-snapshot
THE ASSOCIATION BETWEEN THE POLYMORPHISMS AT THEAdhANDαGpdhLOCI AND THEIn(2L)tINVERSION INDROSOPHILA MELANOGASTERIN RELATION TO TEMPERATURE
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/j.1558-5646.2008.00504.xopenalex-snapshot
SELECTION IN HETEROGENEOUS ENVIRONMENTS MAINTAINS THE GENE ARRANGEMENT POLYMORPHISM OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1111/j.1601-5223.1966.tb02023.xopenalex-snapshot
THE INTERCHROMOSOMAL EFFECT OF INVERSIONS ON CROSSING-OVER IN RELATION TO NON HOMOLOGOUS PAIRING IN DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1111/j.1601-5223.1986.tb00521.xopenalex-snapshot
Whole mount electron microscopic maps of Drosophila melanogaster polytene chromosomes
inferredcites →https://doi.org/10.1111/j.1755-0998.2011.03024.xopenalex-snapshot
Field guide to next‐generation DNA sequencers
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/jeb.12690openalex-snapshot
Seasonal variation in life history traits in two Drosophila species
inferredcites →https://doi.org/10.1111/jeb.12847openalex-snapshot
Parallel effects of the inversion In(3R)Payne on body size across the North American and Australian clines in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/jeb.13310openalex-snapshot
An inversion supergene in Drosophila underpins latitudinal clines in survival traits
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.12685openalex-snapshot
Pool and conquer: new tricks for (c)old problems
inferredcites →https://doi.org/10.1111/mec.12719openalex-snapshot
Fine‐mapping natural alleles: quantitative complementation to the rescue
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.13226openalex-snapshot
Detecting balancing selection in genomes: limits and prospects
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/10.1111/mec.14781openalex-snapshot
Pleiotropic effects of regulatory variation in tan result in correlation of two pigmentation traits in Drosophila melanogaster
inferredcites →https://doi.org/10.1111/mec.14923openalex-snapshot
How chromosomal rearrangements shape adaptation and speciation: Case studies in Drosophila pseudoobscura and its sibling species Drosophila persimilis
inferredcites →https://doi.org/10.1126/science.1077769openalex-snapshot
A Polytene Chromosome Analysis of the Anopheles gambiae Species Complex
inferredcites →https://doi.org/10.1126/science.1131002openalex-snapshot
Global Genetic Change Tracks Global Climate Warming in Drosophila subobscura
inferredcites →https://doi.org/10.1126/science.179.4070.243openalex-snapshot
Gene Flow and Population Differentiation
inferredcites →https://doi.org/10.1126/science.285.5426.415openalex-snapshot
Generation of a Widespread Drosophila Inversion by a Transposable Element
inferredcites →https://doi.org/10.1128/jb.180.18.4834-4842.1998openalex-snapshot
A Natural Large Chromosomal Inversion in Lactococcus lactis Is Mediated by Homologous Recombination between Two Insertion Sequences
inferredcites →https://doi.org/10.1136/jmg.8.4.545-bopenalex-snapshot
Genetics of the Evolutionary Process
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.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/10.1146/annurev.es.07.110176.000245openalex-snapshot
Genetic Polymorphism in Heterogeneous Environments
inferredcites →https://doi.org/10.1146/annurev.genet.30.1.261openalex-snapshot
POPULATION GENETIC PERSPECTIVES ON THE EVOLUTION OF RECOMBINATION
inferredcites →https://doi.org/10.1186/1297-9686-22-1-47openalex-snapshot
Seasonal fluctuations of cosmopolitan inversion frequencies in a natural population of Drosophila melanogaster
inferredcites →https://doi.org/10.1186/1471-2148-13-100openalex-snapshot
Patterns of genetic variation across inversions: geographic variation in the In(2L)t inversion in populations of Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1186/gb-2003-4-8-r50openalex-snapshot
Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster
inferredcites →https://doi.org/10.1186/gb-2009-10-3-r32openalex-snapshot
Evaluation of next generation sequencing platforms for population targeted sequencing studies
inferredcites →https://doi.org/10.1186/gm132openalex-snapshot
Inversion variants in the human genome: role in disease and genome architecture
inferredcites →https://doi.org/10.1186/s12862-014-0179-yopenalex-snapshot
Pigmentation in Drosophila melanogaster reaches its maximum in Ethiopia and correlates most strongly with ultra-violet radiation in sub-Saharan Africa
inferredcites →https://doi.org/10.1266/jjg.44.171openalex-snapshot
FREQUENCY OF DELETERIOUS CHROMOSOMES AND ALLELISM BETWEEN LETHAL GENES IN JAPANESE NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1266/jjg.54.69openalex-snapshot
Inversion polymorphisms in Japanese natural populations of Drosophila melanogaster.
inferredcites →https://doi.org/10.1266/jjg.54.83openalex-snapshot
The fate of polymorphic inversions of Drosophila melanogaster transferred to laboratory conditions.
inferredcites →https://doi.org/10.1266/jjg.69.105openalex-snapshot
On the category of naturally occurring inversions of Drosophila melanogaster.
inferredcites →https://doi.org/10.1371/journal.pbio.0050152openalex-snapshot
Principles of Genome Evolution in the Drosophila melanogaster Species Group
inferredcites →https://doi.org/10.1371/journal.pbio.1000500openalex-snapshot
A Widespread Chromosomal Inversion Polymorphism Contributes to a Major Life-History Transition, Local Adaptation, and Reproductive Isolation
inferredcites →https://doi.org/10.1371/journal.pbio.1000501openalex-snapshot
How and Why Chromosome Inversions Evolve
inferredcites →https://doi.org/10.1371/journal.pgen.1003056openalex-snapshot
Population Genomics of Inversion Polymorphisms 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/10.1534/g3.117.1133openalex-snapshot
The Effect of Common Inversion Polymorphisms In(2L)t and In(3R)Mo on Patterns of Transcriptional Variation in Drosophila melanogaster
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Contributions to Trachelyopterus (Siluriformes: Auchenipteridae) species diagnosis by cytotaxonomic autapomorphies: from U2 snRNA chromosome polymorphism to rDNA and histone gene synteny
inferred← citeshttps://doi.org/10.1002/9780470015902.a0028745openalex-snapshot
How Selection Acts on Chromosomal Inversions
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029007openalex-snapshot
Inversions and Evolution
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/10.1007/s10709-021-00125-7openalex-snapshot
Adaptation of Drosophila subobscura chromosomal inversions to climatic variables: the Balkan natural population of Avala
inferred← citeshttps://doi.org/10.1007/s10709-025-00232-9openalex-snapshot
Temporal and habitat adaptations in Drosophila subobscura populations: changes in chromosomal inversions
inferred← citeshttps://doi.org/10.1007/s12041-021-01295-1openalex-snapshot
Genetic structuring of Drosophila bipectinata in Indian natural populations based on the distribution of cosmopolitan inversions
inferred← citeshttps://doi.org/10.1007/s12041-022-01387-6openalex-snapshot
Long-term changes in the inversion chromosomal polymorphism: Drosophila subobscura population from Rasht (north of Iran)
inferred← citeshttps://doi.org/10.1016/b978-0-323-95424-2.00021-2openalex-snapshot
Insects in the cold
inferred← citeshttps://doi.org/10.1016/j.cub.2019.11.032openalex-snapshot
An Ancient and Eroded Social Supergene Is Widespread across Formica Ants
inferred← citeshttps://doi.org/10.1016/j.egg.2024.100272openalex-snapshot
Microsatellite polymorphism based genetic variation in two sympatric species of Drosophila: D. bipectinata and D. malerkotliana
inferred← citeshttps://doi.org/10.1016/j.isci.2025.112809openalex-snapshot
Evolution of temperature preference behaviour among Drosophila larvae
inferred← citeshttps://doi.org/10.1016/j.tig.2023.02.004openalex-snapshot
Fluctuating selection and the determinants of genetic variation
inferred← citeshttps://doi.org/10.1016/j.tree.2018.12.005openalex-snapshot
Evolving Inversions
inferred← citeshttps://doi.org/10.1016/j.tree.2025.08.004openalex-snapshot
Beyond supergenes: the diverse roles of inversions in trait evolution
inferred← citeshttps://doi.org/10.1017/s0007485321000699openalex-snapshot
Spatial population structure: patterns of adaptation in populations of the water hyacinth grasshopper Cornops aquaticum (Bruner 1906)
inferred← citeshttps://doi.org/10.1017/s0007485324000579openalex-snapshot
Making sense of chromosome polymorphisms in two leptysmine grasshoppers
inferred← citeshttps://doi.org/10.1038/s41437-024-00707-zopenalex-snapshot
Multiple karyotype differences between populations of the Hoplias malabaricus (Teleostei; Characiformes), a species complex in the gray area of the speciation process
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/10.1038/s41437-025-00808-3openalex-snapshot
Parallel clines of chromosomal inversion frequencies in seaweed flies are associated with thermal variation
inferred← citeshttps://doi.org/10.1038/s41437-026-00832-xopenalex-snapshot
Structural variation in context: mechanisms, functions and selection regimes across the tree of life
inferred← citeshttps://doi.org/10.1038/s41477-023-01361-9openalex-snapshot
Recurrent neo-sex chromosome evolution in kiwifruit
inferred← citeshttps://doi.org/10.1038/s41559-022-01890-0openalex-snapshot
Chromosomal inversion polymorphisms shape the genomic landscape of deer mice
inferred← citeshttps://doi.org/10.1038/s41559-024-02593-4openalex-snapshot
Inversions contribute disproportionately to parallel genomic divergence in dune sunflowers
inferred← citeshttps://doi.org/10.1038/s41559-025-02751-2openalex-snapshot
Haploblocks contribute to parallel climate adaptation following global invasion of a cosmopolitan plant
inferred← citeshttps://doi.org/10.1038/s41598-020-69719-zopenalex-snapshot
Multiple loci linked to inversions are associated with eye size variation in species of the Drosophila virilis phylad
inferred← citeshttps://doi.org/10.1073/pnas.2409943121openalex-snapshot
Fitness consequences of structural variation inferred from a House Finch pangenome
inferred← citeshttps://doi.org/10.1086/726012openalex-snapshot
Revisiting the Role of Genetic Variation in Adaptation
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/g3journal/jkag043openalex-snapshot
Manual validation finds ultra-long-read sequencing best enables faithful, population-level structural variant calling in Drosophila melanogaster euchromatin with nanopore
inferred← citeshttps://doi.org/10.1093/gbe/evad183openalex-snapshot
Evolution, Inheritance, and Strata Formation of the W Chromosome in Duck (Anas platyrhynchos)
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/gbe/evae263openalex-snapshot
Complex Genomic Landscape of Inversion Polymorphism in Europe's Most Destructive Forest Pest
inferred← citeshttps://doi.org/10.1093/gbe/evaf205openalex-snapshot
Large Inversion Polymorphisms are Widespread in North American Songbirds
inferred← citeshttps://doi.org/10.1093/genetics/iyad116openalex-snapshot
The effects of inversion polymorphisms on patterns of neutral genetic diversity
inferred← citeshttps://doi.org/10.1093/genetics/iyad158openalex-snapshot
Female meiotic drive shapes the distribution of rare inversion polymorphisms in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/genetics/iyad207openalex-snapshot
A cosmopolitan inversion facilitates seasonal adaptation in overwintering Drosophila
inferred← citeshttps://doi.org/10.1093/genetics/iyad218openalex-snapshot
The fitness consequences of genetic divergence between polymorphic gene arrangements
inferred← citeshttps://doi.org/10.1093/jeb/voaf142openalex-snapshot
Comparative studies on genetic differentiation between two closely related species of Drosophila, D. bipectinata and D. malerkotliana
inferred← citeshttps://doi.org/10.1093/jhered/esaa020openalex-snapshot
Consequences of Single-Locus and Tightly Linked Genomic Architectures for Evolutionary Responses to Environmental Change
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/msab061openalex-snapshot
The Genomic Architecture of Adaptation to Larval Malnutrition Points to a Trade-off with Adult Starvation Resistance in Drosophila
inferred← citeshttps://doi.org/10.1093/molbev/msab143openalex-snapshot
Locally Adaptive Inversions Modulate Genetic Variation at Different Geographic Scales in a Seaweed Fly
inferred← citeshttps://doi.org/10.1093/molbev/msab259openalex-snapshot
Drosophila Evolution over Space and Time (DEST): A New Population Genomics Resource
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/msae044openalex-snapshot
Rapid and Repeated Climate Adaptation Involving Chromosome Inversions following Invasion of an Insect
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/10.1098/rstb.2020.0507openalex-snapshot
Supergenes on steroids
inferred← citeshttps://doi.org/10.1098/rstb.2021.0199openalex-snapshot
Mutation accumulation opposes polymorphism: supergenes and the curious case of balanced lethals
inferred← citeshttps://doi.org/10.1098/rstb.2021.0203openalex-snapshot
Inversions and parallel evolution
inferred← citeshttps://doi.org/10.1101/2020.10.23.352732openalex-snapshot
Florida Drosophila melanogaster genomes sampled 13 years apart show increases in warm-associated SNP alleles
inferred← citeshttps://doi.org/10.1101/2021.11.27.470204openalex-snapshot
Supergene degeneration opposes polymorphism: The curious case of balanced lethals
inferred← citeshttps://doi.org/10.1101/2022.07.16.500113openalex-snapshot
Genomic islands of divergence between Drosophila yakuba subspecies predominantly overlap with chromosomal inversions
inferred← citeshttps://doi.org/10.1101/2022.09.10.507406openalex-snapshot
Tropical High-Altitude Insects Show Limited Capacity to Handle High Temperatures
inferred← citeshttps://doi.org/10.1101/2023.12.06.570460openalex-snapshot
The evolutionary dynamics of locally adaptive chromosome inversions in Mimulus guttatus
inferred← citeshttps://doi.org/10.1101/2024.04.17.589934openalex-snapshot
Transposable elements in a cold-tolerant fly species, Drosophila montana : a link to adaptation to the harsh cold environments
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/10.1101/2025.04.21.649836openalex-snapshot
Computer Simulations and Analyses of Coupling Among Reproductive Barriers in Late-Stage Sympatric Speciation
inferred← citeshttps://doi.org/10.1101/2025.04.21.649852openalex-snapshot
Manual validation finds only ultra-long long-read sequencing enables faithful, population-level structural variant calling in Drosophila melanogaster euchromatin
inferred← citeshttps://doi.org/10.1101/2025.06.12.659260openalex-snapshot
Disentangling the role of chromosome inversions in the structure of flat oyster ( Ostrea edulis ): origin, adaptation and phylogeography
inferred← citeshttps://doi.org/10.1101/2025.06.22.660940openalex-snapshot
Expansion of chromosome F heterochromatin in parthenogenetic Drosophila mercatorum
inferred← citeshttps://doi.org/10.1101/2025.08.30.673289openalex-snapshot
Genomic signatures of adaptation across a landscape of crickets exposed to an introduced parasitoid
inferred← citeshttps://doi.org/10.1101/2025.09.10.675386openalex-snapshot
Shifting balancing selection on a chromosomal inversion in island populations
inferred← citeshttps://doi.org/10.1101/2025.11.28.691231openalex-snapshot
Gene flow erodes spatial genomic clines while selection preserves adaptive loci over hundreds of generations
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/10.1101/337543openalex-snapshot
Broad geographic sampling reveals predictable, pervasive, and strong seasonal adaptation in Drosophila
inferred← citeshttps://doi.org/10.1111/ens.12582openalex-snapshot
New insights on the chromosomal inversion thermal adaptation in insects: American populations of Drosophila subobscura
inferred← citeshttps://doi.org/10.1111/evo.14300openalex-snapshot
Clinal and seasonal changes are correlated in Drosophila melanogaster natural populations
inferred← citeshttps://doi.org/10.1111/jeb.14242openalex-snapshot
How chromosomal inversions reorient the evolutionary process
inferred← citeshttps://doi.org/10.1111/mec.14923openalex-snapshot
How chromosomal rearrangements shape adaptation and speciation: Case studies in Drosophila pseudoobscura and its sibling species Drosophila persimilis
inferred← citeshttps://doi.org/10.1111/mec.15066openalex-snapshot
Going beyond SNPs: The role of structural genomic variants in adaptive evolution and species diversification
inferred← citeshttps://doi.org/10.1111/mec.15328openalex-snapshot
Editorial 2020
inferred← citeshttps://doi.org/10.1111/mec.15500openalex-snapshot
Making the most of population genomic data to understand the importance of chromosomal inversions for adaptation and speciation
inferred← citeshttps://doi.org/10.1111/mec.15783openalex-snapshot
Temperature, rainfall and wind variables underlie environmental adaptation in natural populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1111/mec.16026openalex-snapshot
On the fixation or nonfixation of inversions under epistatic selection
inferred← citeshttps://doi.org/10.1111/mec.16091openalex-snapshot
Natural selection and the distribution of chromosomal inversion lengths
inferred← citeshttps://doi.org/10.1111/mec.16305openalex-snapshot
Stable inversion clines in a grasshopper species group despite complex geographical history
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/10.1111/mec.17160openalex-snapshot
Chromosomal inversion polymorphisms are widespread across the species ranges of rough periwinkles ( Littorina saxatilis and L. arcana )
inferred← citeshttps://doi.org/10.1111/mec.17362openalex-snapshot
Limited genomic signatures of population collapse in the critically endangered black abalone ( Haliotis cracherodii )
inferred← citeshttps://doi.org/10.1111/mec.17627openalex-snapshot
Genomic Islands of Divergence Between Drosophila yakuba Subspecies are Predominantly Driven by Chromosomal Inversions and the Recombination Landscape
inferred← citeshttps://doi.org/10.1111/mec.17708openalex-snapshot
The Evolution of Locally Adaptive Chromosome Inversions in Mimulus guttatus
inferred← citeshttps://doi.org/10.1111/mec.17776openalex-snapshot
Putting Structural Variants Into Practice: The Role of Chromosomal Inversions in the Management of Marine Environments
inferred← citeshttps://doi.org/10.1111/mec.70250openalex-snapshot
Demographic History Inferred From an Inversion‐Rich Spruce Bark Beetle Genome
inferred← citeshttps://doi.org/10.1111/mec.70344openalex-snapshot
When South Meets North: A Joint Contact Zone Coinciding With Environmental Gradients in Three Boreal Tree Species
inferred← citeshttps://doi.org/10.1111/pbi.13938openalex-snapshot
Time‐ordering japonica/geng genomes analysis indicates the importance of large structural variants in rice breeding
inferred← citeshttps://doi.org/10.1111/tpj.15381openalex-snapshot
Reconstruction of ancestral karyotype illuminates chromosome evolution in the genus Cucumis
inferred← citeshttps://doi.org/10.1126/sciadv.aed1906openalex-snapshot
Genomic signatures of adaptation across a landscape of crickets following the introduction of a parasitoid fly
inferred← citeshttps://doi.org/10.1126/science.abg0718openalex-snapshot
A chromosomal inversion contributes to divergence in multiple traits between deer mouse ecotypes
inferred← citeshttps://doi.org/10.1126/science.abj7484openalex-snapshot
Direct observation of adaptive tracking on ecological time scales in Drosophila
inferred← citeshttps://doi.org/10.1126/science.adp3745openalex-snapshot
Adaptation repeatedly uses complex structural genomic variation
inferred← citeshttps://doi.org/10.1126/science.adp5936openalex-snapshot
A single gene orchestrates androgen variation underlying male mating morphs in ruffs
inferred← citeshttps://doi.org/10.1186/s13071-023-06014-6openalex-snapshot
A novel tetra-primer ARMS-PCR approach for the molecular karyotyping of chromosomal inversion 2Ru in the main malaria vectors Anopheles gambiae and Anopheles coluzzii
inferred← citeshttps://doi.org/10.1186/s13100-024-00328-7openalex-snapshot
Transposable elements in Drosophila montana from harsh cold environments
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003254openalex-snapshot
The evolution of separate sexes in waterhemp is associated with surprising chromosomal diversity and complexity
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/10.14411/eje.2025.040openalex-snapshot
Evolutionary rate of adaptive chromosomal inversions in Drosophila subobscura (Diptera: Drosophilidae) in response to global warming
inferred← citeshttps://doi.org/10.1534/g3.120.401285openalex-snapshot
Genomics of Clinal Local Adaptation in Pinus sylvestris Under Continuous Environmental and Spatial Genetic Setting
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-2023-0116openalex-snapshot
Chromosomal Radiation: A model to explain karyotypic diversity in cryptic species
inferred← citeshttps://doi.org/10.22541/au.161474567.72404976/v1openalex-snapshot
On the Fixation or Non-Fixation of Adaptive Inversions
inferred← citeshttps://doi.org/10.22541/au.169446672.24240496/v1openalex-snapshot
Chromosomal inversion polymorphisms are widespread across the species ranges of rough periwinkles (Littorina saxatilis and L. arcana) Running title: Widespread inversions in Littorina
inferred← citeshttps://doi.org/10.3389/fevo.2022.986925openalex-snapshot
Temporal and biting dynamics of the chromosomal inversion 2La in the malaria vectors Anopheles gambiae and Anopheles coluzzii in Bangui, Central African Republic
inferred← citeshttps://doi.org/10.3389/fevo.2025.1562456openalex-snapshot
Preface: the paradox of generalism, a philosophical perspective
inferred← citeshttps://doi.org/10.3389/fgene.2020.565836openalex-snapshot
The Cyclically Seasonal Drosophila subobscura Inversion O7 Originated From Fragile Genomic Sites and Relocated Immunity and Metabolic Genes
inferred← citeshttps://doi.org/10.3390/genes11030270openalex-snapshot
Chromosomal Differentiation in Genetically Isolated Populations of the Marsh-Specialist Crocidura suaveolens (Mammalia: Soricidae)
inferred← citeshttps://doi.org/10.3390/genes13071129openalex-snapshot
The Relative Power of Structural Genomic Variation versus SNPs in Explaining the Quantitative Trait Growth in the Marine Teleost Chrysophrys auratus
inferred← citeshttps://doi.org/10.3390/life13061333openalex-snapshot
Population History Shapes Responses to Different Temperature Regimes in Drosophila subobscura
inferred← citeshttps://doi.org/10.37398/jsr.2020.640112openalex-snapshot
Non-random Distribution of Heterozygous Inversions in a Natural Population of Drosophila malerkotliana
inferred← citeshttps://doi.org/10.6084/m9.figshare.26633031openalex-snapshot
Additional file 1 of A novel tetra-primer ARMS-PCR approach for the molecular karyotyping of chromosomal inversion 2Ru in the main malaria vectors Anopheles gambiae and Anopheles coluzzii
inferred← citeshttps://doi.org/10.64898/2026.01.20.700628openalex-snapshot
Evidence of Adaptation in Structural Variants among Wild Populations of the purple sea urchin, Strongylocentrotus purpuratus
inferred← citeshttps://doi.org/10.64898/2026.03.01.708907openalex-snapshot
The distribution of fitness effects of new mutations in regulatory regions of the D. melanogaster genome
inferred← citeshttps://doi.org/10.64898/2026.04.02.716010openalex-snapshot
Adaptive coupling of chromosomal inversions with multilocus ecological, mating-bias, and hybrid-incompatibility genotypes facilitates sympatric speciation
inferred← citeshttps://doi.org/10.70675/22847453z7110z4c06za4f2zc6e29efaccc6openalex-snapshot
Origins and impacts of chromosomal inversions in the evolution and adaptation of pearl millet
inferred← citeshttps://doi.org/10.7554/elife.67577openalex-snapshot
Broad geographic sampling reveals the shared basis and environmental correlates of seasonal adaptation in Drosophila
inferred← citeshttps://doi.org/10.7554/elife.93338openalex-snapshot
The potential of inversions to accumulate balanced sexual antagonism is supported by simulations and Drosophila experiments
inferred← citeshttps://doi.org/10.7554/elife.93338.1openalex-snapshot
Inversions Can Accumulate Balanced Sexual Antagonism: Evidence from Simulations and Drosophila Experiments
inferred← citeshttps://doi.org/10.7554/elife.93338.2openalex-snapshot
Inversions Can Accumulate Balanced Sexual Antagonism: Evidence from Simulations and Drosophila Experiments
inferred← citeshttps://doi.org/10.7554/elife.93338.3openalex-snapshot
Inversions Can Accumulate Balanced Sexual Antagonism: Evidence from Simulations and Drosophila Experiments
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