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Principles of Genome Evolution in the Drosophila melanogaster Species Group
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.950160410openalex-snapshot
Gross chromosome rearrangements mediated by transposable elements in Drosophila melanogaster
inferredcites →https://doi.org/10.1002/jez.1400170103openalex-snapshot
Chromosome studies in the Diptera. I. A preliminary survey of five different types of chromosome groups in the genus Drosophila
inferredcites →https://doi.org/10.1006/fgbi.2001.1296openalex-snapshot
Potential Role of Transposable Elements in the Rapid Reorganization of the Fusarium oxysporum Genome
inferredcites →https://doi.org/10.1006/mpev.1997.0438openalex-snapshot
Molecular and Chromosomal Phylogeny in theObscuraGroup ofDrosophilaInferred from Sequences of therp49Gene Region
inferredcites →https://doi.org/10.1007/bf00331251openalex-snapshot
Relationships within the melanogaster species subgroup of the genus Drosophila (Sophophora)
inferredcites →https://doi.org/10.1007/bf00333268openalex-snapshot
Mitotic recombination between dispersed but related rRNA genes of Schizosaccharomyces pombe generates a reciprocal translocation
inferredcites →https://doi.org/10.1007/bf01495434openalex-snapshot
Chromosomenmorphologie bei Drosophila melanogaster und Drosophila simulans und ihre genetische Bedeutung
inferredcites →https://doi.org/10.1007/bf02100081openalex-snapshot
Molecular evolution among someDrosophila species groups as indicated by two-dimensional electrophoresis
inferredcites →https://doi.org/10.1007/s00239-003-2510-xopenalex-snapshot
Molecular Phylogeny of the Drosophila melanogaster Species Subgroup
inferredcites →https://doi.org/10.1007/s004120050229openalex-snapshot
A framework physical map of Drosophila virilis based on P1 clones: applications in genome evolution
inferredcites →https://doi.org/10.1007/s004120100151openalex-snapshot
Whole arm inversions of chromosome 4 in Drosophila species
inferredcites →https://doi.org/10.1007/s00439-004-1120-zopenalex-snapshot
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
inferredcites →https://doi.org/10.1016/0035-9203(79)90036-1openalex-snapshot
Chromosomal differentiation and adaptation to human environments in the Anopheles gambiae complex
inferredcites →https://doi.org/10.1016/0047-2484(80)90077-9openalex-snapshot
Animal cytology and evolution
inferredcites →https://doi.org/10.1016/0168-9525(89)90039-5openalex-snapshot
Eukaryotic transposable elements and genome evolution
inferredcites →https://doi.org/10.1016/0168-9525(90)90257-7openalex-snapshot
Drosophila: a laboratory manual
inferredcites →https://doi.org/10.1016/j.tig.2004.09.005openalex-snapshot
Mammalian phylogenomics comes of age
inferredcites →https://doi.org/10.1016/j.tig.2005.09.009openalex-snapshot
Chromosome evolution in eukaryotes: a multi-kingdom perspective
inferredcites →https://doi.org/10.1016/j.ygeno.2004.07.009openalex-snapshot
Comparative sequence analysis of the Gdf6 locus reveals a duplicon-mediated chromosomal rearrangement in rodents and rapidly diverging coding and regulatory sequences
inferredcites →https://doi.org/10.1016/s0015-6264(78)80200-4openalex-snapshot
The Genetics and Biology of Drosophila
inferredcites →https://doi.org/10.1016/s0169-5347(01)02187-5openalex-snapshot
Chromosomal rearrangements and speciation
inferredcites →https://doi.org/10.1016/s0378-1119(98)00093-6openalex-snapshot
Do natural antisense transcripts make sense in eukaryotes?
inferredcites →https://doi.org/10.1023/a:1009206702214openalex-snapshot
Molecular organization of the Drosophila melanogaster Adh chromosomal region in D. replete and D. buzzatii, two distantly related species of the Drosophila subgenus
inferredcites →https://doi.org/10.1038/25126openalex-snapshot
Selective sweep of a newly evolved sperm-specific gene in Drosophila
inferredcites →https://doi.org/10.1038/316081a0openalex-snapshot
Spontaneous excision of a large composite transposable element of Drosophila melanogaster
inferredcites →https://doi.org/10.1038/35013058openalex-snapshot
Chromosomal evolution in Saccharomyces
inferredcites →https://doi.org/10.1038/365548a0openalex-snapshot
African and North American populations of Drosophila melanogaster are very different at the DNA level
inferredcites →https://doi.org/10.1038/384346a0openalex-snapshot
High intrinsic rate of DNA loss in Drosophila
inferredcites →https://doi.org/10.1038/hdy.1976.60openalex-snapshot
The Genetics and Biology of Drosophila
inferredcites →https://doi.org/10.1038/nature01216openalex-snapshot
Large clusters of co-expressed genes in the Drosophila genome
inferredcites →https://doi.org/10.1038/nature01418openalex-snapshot
Engineering evolution to study speciation in yeasts
inferredcites →https://doi.org/10.1038/nature01521openalex-snapshot
Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events
inferredcites →https://doi.org/10.1038/nature01644openalex-snapshot
Sequencing and comparison of yeast species to identify genes and regulatory elements
inferredcites →https://doi.org/10.1038/nrg1319openalex-snapshot
The evolutionary dynamics of eukaryotic gene order
inferredcites →https://doi.org/10.1038/nrg1895openalex-snapshot
Primate segmental duplications: crucibles of evolution, diversity and disease
inferredcites →https://doi.org/10.1038/sj.embor.7400123openalex-snapshot
Effects of reciprocal chromosomal translocations on the fitness of Saccharomyces cerevisiae
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/10.1073/pnas.0502702102openalex-snapshot
Genomic analysis of Drosophila chromosome underreplication reveals a link between replication control and transcriptional territories
inferredcites →https://doi.org/10.1073/pnas.0509683103openalex-snapshot
Breakpoint structure reveals the unique origin of an interspecific chromosomal inversion ( 2La ) in the Anopheles gambiae complex
inferredcites →https://doi.org/10.1073/pnas.1330369100openalex-snapshot
Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution
inferredcites →https://doi.org/10.1073/pnas.1432900100openalex-snapshot
Evolutionary genomics of inversions in Drosophila pseudoobscura : Evidence for epistasis
inferredcites →https://doi.org/10.1073/pnas.1932072100openalex-snapshot
Evolution's cauldron: Duplication, deletion, and rearrangement in the mouse and human genomes
inferredcites →https://doi.org/10.1073/pnas.22.7.448openalex-snapshot
Inversions in the Third Chromosome of Wild Races of Drosophila Pseudoobscura, and Their Use in the Study of the History of the Species
inferredcites →https://doi.org/10.1073/pnas.221274498openalex-snapshot
Chromosomal inversions and the reproductive isolation of species
inferredcites →https://doi.org/10.1073/pnas.7.8.235openalex-snapshot
A Case of Rearrangement of Genes in Drosophila
inferredcites →https://doi.org/10.1073/pnas.81.3.814openalex-snapshot
Lengths of chromosomal segments conserved since divergence of man and mouse.
inferredcites →https://doi.org/10.1073/pnas.91.8.3132openalex-snapshot
Isolation and analysis of the breakpoint sequences of chromosome inversion In(3L)Payne in Drosophila melanogaster.
inferredcites →https://doi.org/10.1073/pnas.95.21.12444openalex-snapshot
Cloning of inversion breakpoints in the Anopheles gambiae complex traces a transposable element at the inversion junction
inferredcites →https://doi.org/10.1074/jbc.275.15.11507openalex-snapshot
Post-transcriptional Regulation of Thyroid Hormone Receptor Expression by cis-Acting Sequences and a Naturally Occurring Antisense RNA
inferredcites →https://doi.org/10.1093/aibsbulletin/3.1.14-dopenalex-snapshot
Evolution in the Genus Drosophila
inferredcites →https://doi.org/10.1093/bioinformatics/18.3.492openalex-snapshot
GRIMM: genome rearrangements web server
inferredcites →https://doi.org/10.1093/genetics/113.2.287openalex-snapshot
DNA SEQUENCE COMPARISON AMONG CLOSELY RELATED DROSOPHILA SPECIES IN THE MULLERI COMPLEX
inferredcites →https://doi.org/10.1093/genetics/139.1.321openalex-snapshot
Molecular characterization of the breakpoints of an inversion fixed between Drosophila melanogaster and D. subobscura.
inferredcites →https://doi.org/10.1093/genetics/145.2.281openalex-snapshot
Chromosomal Homology and Molecular Organization of Muller's Elements D and E in the Drosophila repleta Species Group
inferredcites →https://doi.org/10.1093/genetics/147.1.223openalex-snapshot
Discordant Rates of Chromosome Evolution in the Drosophila virilis Species Group
inferredcites →https://doi.org/10.1093/genetics/153.3.1297openalex-snapshot
Unusual Haplotype Structure at the Proximal Breakpoint of In(2L)t in a Natural Population of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/genetics/161.3.1137openalex-snapshot
Chromosomal Elements Evolve at Different Rates in the Drosophila Genome
inferredcites →https://doi.org/10.1093/genetics/21.5.554openalex-snapshot
THE RELATIONS OF INVERSIONS IN THE X CHROMOSOME OF DROSOPHILA MELANOGASTER TO CROSSING OVER AND DISJUNCTION
inferredcites →https://doi.org/10.1093/genetics/24.2.234openalex-snapshot
A COMPARISON OF THE SALIVARY GLAND CHROMOSOMES OF DROSOPHILA MELANOGASTER AND D. SIMULANS
inferredcites →https://doi.org/10.1093/genetics/26.5.517openalex-snapshot
THE HOMOLOGIES OF THE CHROMOSOME ELEMENTS IN THE GENUS DROSOPHILA
inferredcites →https://doi.org/10.1093/genetics/48.9.1239openalex-snapshot
THE CHROMOSOMAL POLYMORPHISM OF DROSOPHILA BUSCKII IN NATURAL POPULATIONS
inferredcites →https://doi.org/10.1093/hmg/ddg223openalex-snapshot
Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements
inferredcites →https://doi.org/10.1093/jhered/esl065openalex-snapshot
Localization and Characterization of X Chromosome Inversion Breakpoints Separating Drosophila mojavensis and Drosophila arizonae
inferredcites →https://doi.org/10.1093/molbev/msg070openalex-snapshot
The Foldback-like Transposon Galileo Is Involved in the Generation of Two Different Natural Chromosomal Inversions of Drosophila buzzatii
inferredcites →https://doi.org/10.1093/molbev/msg236openalex-snapshot
Temporal Patterns of Fruit Fly (Drosophila) Evolution Revealed by Mutation Clocks
inferredcites →https://doi.org/10.1093/molbev/msi062openalex-snapshot
Clusters of Co-expressed Genes in Mammalian Genomes Are Conserved by Natural Selection
inferredcites →https://doi.org/10.1093/molbev/msi134openalex-snapshot
Genome Rearrangement Distances and Gene Order Phylogeny in γ-Proteobacteria
inferredcites →https://doi.org/10.1093/molbev/msi207openalex-snapshot
Inferring the Effects of Demography and Selection on Drosophila melanogaster Populations from a Chromosome-Wide Scan of DNA Variation
inferredcites →https://doi.org/10.1093/oso/9780195076912.001.0001openalex-snapshot
Progress and Prospects in Evolutionary Biology
inferredcites →https://doi.org/10.1093/oso/9780195138597.001.0001openalex-snapshot
The Role of Chromosomal Change in Plant Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a104022openalex-snapshot
SALIVARY CHROMOSOME MAPS
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a104629openalex-snapshot
STRUCTURE AND VARIATION OF THE CHROMOSOMES IN DROSOPHILA AZTECA
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a109571openalex-snapshot
Cladistic analysis of mosquito chromosome data (Anopheles (Cellia) Myzomyia)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025551openalex-snapshot
Molecular phylogeny and genome evolution in the Drosophila virilis species group: duplications of the alcohol dehydrogenase gene
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025883openalex-snapshot
Pseudogene Evolution in Drosophila Suggests a High Rate of DNA Loss
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040214openalex-snapshot
Molecular phylogeny and divergence times of drosophilid species.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040749openalex-snapshot
Phylogenetic reconstruction of the Drosophila obscura group, on the basis of mitochondrial DNA.
inferredcites →https://doi.org/10.1098/rspb.1976.0046openalex-snapshot
Relationships within the melanogaster species subgroup of the genus Drosophila ( Sophophora ) - II. Phylogenetic relationships between six species based upon polytene chromosome banding sequences
inferredcites →https://doi.org/10.1098/rspb.2000.1169openalex-snapshot
Evolutionary novelties in islands:Drosophila santomea, a newmelanogastersister species from São Tomé
inferredcites →https://doi.org/10.1098/rstb.1990.0015openalex-snapshot
DNA methylation and epigenetic inheritance
inferredcites →https://doi.org/10.1101/gr.10.4.577openalex-snapshot
PipMaker—A Web Server for Aligning Two Genomic DNA Sequences
inferredcites →https://doi.org/10.1101/gr.162901openalex-snapshot
How Malleable is the Eukaryotic Genome? Extreme Rate of Chromosomal Rearrangement in the GenusDrosophila
inferredcites →https://doi.org/10.1101/gr.172702openalex-snapshot
Fourfold Faster Rate of Genome Rearrangement in Nematodes Than in Drosophila
inferredcites →https://doi.org/10.1101/gr.181101openalex-snapshot
The Evolutionary Chromosome Translocation 4;19 in Gorilla gorilla is Associated with Microduplication of the Chromosome Fragment Syntenic to Sequences Surrounding the Human Proximal CMT1A-REP
inferredcites →https://doi.org/10.1101/gr.1975204openalex-snapshot
Reconstructing the Genomic Architecture of Ancestral Mammals: Lessons From Human, Mouse, and Rat Genomes
inferredcites →https://doi.org/10.1101/gr.2663304openalex-snapshot
Human, Mouse, and Rat Genome Large-Scale Rearrangements: Stability Versus Speciation
inferredcites →https://doi.org/10.1101/gr.3002305openalex-snapshot
Comparative architectures of mammalian and chicken genomes reveal highly variable rates of genomic rearrangements across different lineages
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/gr.436602openalex-snapshot
Molecular Characterization of a Chromosomal Rearrangement Involved in the Adaptive Evolution of Yeast Strains
inferredcites →https://doi.org/10.1101/gr.6049openalex-snapshot
Retroposed New Genes Out of the X in Drosophila
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00340.xopenalex-snapshot
LOW OCCURRENCE OF GENE TRANSPOSITION EVENTS DURING THE EVOLUTION OF THE GENUS DROSOPHILA
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb01155.xopenalex-snapshot
CHROMOSOMAL EVOLUTION OF ELEMENTS B AND C IN THE SOPHOPHORA SUBGENUS OF DROSOPHILA: EVOLUTIONARY RATE AND POLYMORPHISM
inferredcites →https://doi.org/10.1111/j.1574-6968.1999.tb13575.xopenalex-snapshot
BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences
inferredcites →https://doi.org/10.1126/science.1078170openalex-snapshot
Speciation Within Anopheles gambiae -- the Glass Is Half Full
inferredcites →https://doi.org/10.1126/science.1101312openalex-snapshot
A Gene Expression Map for the Euchromatic Genome of Drosophila melanogaster
inferredcites →https://doi.org/10.1126/science.1111387openalex-snapshot
Dynamics of Mammalian Chromosome Evolution Inferred from Multispecies Comparative Maps
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/10.1126/science.287.5461.2185openalex-snapshot
The Genome Sequence of Drosophila melanogaster
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/10.1159/000080806openalex-snapshot
Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans
inferredcites →https://doi.org/10.1159/000452856openalex-snapshot
Cellular Scaling Rules for the Brains of Marsupials: Not as “Primitive” as Expected
inferredcites →https://doi.org/10.1186/1471-2105-6-10openalex-snapshot
Modelling the correlation between the activities of adjacent genes in drosophila
inferredcites →https://doi.org/10.1186/1475-4924-1-5openalex-snapshot
Evidence for large domains of similarly expressed genes in the Drosophila genome
inferredcites →https://doi.org/10.1186/gb-2002-3-12-research0083openalex-snapshot
Annotation of the Drosophila melanogastereuchromatic genome: a systematic review
inferredcites →https://doi.org/10.1186/gb-2002-3-12-research0084openalex-snapshot
The transposable elements of the Drosophila melanogaster euchromatin: a genomics perspective
inferredcites →https://doi.org/10.1186/gb-2002-3-12-research0086openalex-snapshot
Assessing the impact of comparative genomic sequence data on the functional annotation of the Drosophilagenome
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-2003-5-1-r3openalex-snapshot
An integrated gene annotation and transcriptional profiling approach towards the full gene content of the Drosophila genome
inferredcites →https://doi.org/10.1186/gb-2004-5-4-r23openalex-snapshot
Hotspots of mammalian chromosomal evolution
inferredcites →https://doi.org/10.1186/gb-2004-5-6-r40openalex-snapshot
A survey of ovary-, testis-, and soma-biased gene expression in Drosophila melanogasteradults
inferredcites →https://doi.org/10.1186/gb-2006-7-11-r112openalex-snapshot
Recurrent insertion and duplication generate networks of transposable element sequences in the Drosophila melanogaster genome
inferredcites →https://doi.org/10.1186/gb-2006-7-7-r67openalex-snapshot
Fine scale structural variants distinguish the genomes of Drosophila melanogaster and D. pseudoobscura.
inferredcites →https://doi.org/10.1371/journal.pbio.0030285openalex-snapshot
Genomic Islands of Speciation in Anopheles gambiae
inferredcites →https://doi.org/10.1371/journal.pcbi.0010022openalex-snapshot
Combined Evidence Annotation of Transposable Elements in Genome Sequences
inferredcites →https://doi.org/10.1371/journal.pgen.0010056openalex-snapshot
Discovery of Human Inversion Polymorphisms by Comparative Analysis of Human and Chimpanzee DNA Sequence Assemblies
inferredcites →https://doi.org/10.1371/journal.pgen.0020032openalex-snapshot
Highly Variable Rates of Genome Rearrangements between Hemiascomycetous Yeast Lineages
inferredcites →https://doi.org/10.1534/genetics.104.033597openalex-snapshot
Multilocus Analysis of Introgression Between Two Sympatric Sister Species of Drosophila: Drosophila yakuba and D. santomea
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.105.054585openalex-snapshot
Rates and Patterns of Chromosomal Evolution in Drosophila pseudoobscura and D. miranda
inferredcites →https://doi.org/10.1590/s0100-84551997000400003openalex-snapshot
Chromosomal evolution and comparative gene mapping in the Drosophila repleta species group
inferredcites →https://doi.org/10.2307/1536631openalex-snapshot
SEQUENCE OF CORRESPONDING THIRD-CHROMOSOME GENES IN DROSOPHILA MELANOGASTER AND D. SIMULANS
inferredcites →https://doi.org/10.5281/zenodo.10742832openalex-snapshot
Genetics of the Evolutionary Process.
inferredcites →https://doi.org/10.5281/zenodo.10763570openalex-snapshot
Progress and Prospects in Evolutionary Biology. The Drosophila Model.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470015902.a0020738openalex-snapshot
Chromosomal Rearrangements in the Human and Chimpanzee Lineages
inferred← citeshttps://doi.org/10.1002/bies.200800182openalex-snapshot
The genome‐centric concept: resynthesis of evolutionary theory
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/10.1007/978-3-031-36911-7_6openalex-snapshot
Physical Mapping of Two Nested Fixed Inversions in the X Chromosome of the Malaria Mosquito Anopheles messeae
inferred← citeshttps://doi.org/10.1007/978-3-319-16483-0_42openalex-snapshot
Relation between Insertion Sequences and Genome Rearrangements in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1007/978-3-642-31316-5_3openalex-snapshot
Genome Mapping and Genomics in Drosophila
inferred← citeshttps://doi.org/10.1007/978-3-7091-1160-4_9openalex-snapshot
Mechanisms of Chromosome Rearrangements
inferred← citeshttps://doi.org/10.1007/978-4-431-55936-8_9openalex-snapshot
Genome Evolution: Helicobacter pylori as an Extreme Model
inferred← citeshttps://doi.org/10.1007/s00239-008-9071-yopenalex-snapshot
High Incidence of Interchromosomal Transpositions in the Evolutionary History of a Subset of Or Genes in Drosophila
inferred← citeshttps://doi.org/10.1007/s00335-014-9537-8openalex-snapshot
A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics
inferred← citeshttps://doi.org/10.1007/s00412-008-0201-5openalex-snapshot
Cloning and sequencing of the breakpoint regions of inversion 5g fixed in Drosophila buzzatii
inferred← citeshttps://doi.org/10.1007/s10340-025-01907-0openalex-snapshot
Adventively established Leptopilina japonica: a new opportunity for augmentative biocontrol of Drosophila suzukii
inferred← citeshttps://doi.org/10.1007/s10577-007-1207-1openalex-snapshot
Molecular mechanisms of chromosomal rearrangement during primate evolution
inferred← citeshttps://doi.org/10.1007/s10577-007-1208-0openalex-snapshot
Addressing chromosome evolution in the whole-genome sequence era
inferred← citeshttps://doi.org/10.1007/s10577-011-9195-6openalex-snapshot
Testing chromosomal phylogenies and inversion breakpoint reuse in Drosophila. The martensis cluster revisited
inferred← citeshttps://doi.org/10.1007/s10577-016-9549-1openalex-snapshot
Dense gene physical maps of the non-model species Drosophila subobscura
inferred← citeshttps://doi.org/10.1007/s10709-008-9296-0openalex-snapshot
Sequence signatures of a recent chromosomal rearrangement in Drosophila mojavensis
inferred← citeshttps://doi.org/10.1007/s10709-010-9495-3openalex-snapshot
Mitotic and polytene chromosomes analysis of the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.1007/s10709-012-9687-0openalex-snapshot
General survey of hAT transposon superfamily with highlight on hobo element in Drosophila
inferred← citeshttps://doi.org/10.1007/s10709-014-9791-4openalex-snapshot
Chromosomal evolution in the Drosophila cardini group (Diptera: Drosophilidae): photomaps and inversion analysis
inferred← citeshttps://doi.org/10.1007/s11033-011-1160-0openalex-snapshot
Molecular analysis of a ras-like nuclear (Ran) gene from Penaeus monodon and its expression at the different ovarian stages of development
inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00169-4openalex-snapshot
Genome Organization, Evolution of
inferred← citeshttps://doi.org/10.1016/b978-0-443-15750-9.00152-xopenalex-snapshot
Genome Organization, Evolution of
inferred← citeshttps://doi.org/10.1016/j.cell.2009.10.033openalex-snapshot
Little Effect of the tan Locus on Pigmentation in Female Hybrids between Drosophila santomea and D. melanogaster
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115644openalex-snapshot
How repeats rearrange chromosomes: The molecular basis of chromosomal inversions in deer mice
inferred← citeshttps://doi.org/10.1016/j.gene.2009.02.019openalex-snapshot
Repeat mediated gene duplication in the Drosophila pseudoobscura genome
inferred← citeshttps://doi.org/10.1016/j.gene.2015.08.001openalex-snapshot
Unique synteny and alternate splicing of the chitin synthases in closely related heliothine moths
inferred← citeshttps://doi.org/10.1016/j.ibmb.2010.03.001openalex-snapshot
What the loss of the hormone neuroparsin in the melanogaster subgroup of Drosophila can tell us about its function
inferred← citeshttps://doi.org/10.1016/j.meegid.2013.03.010openalex-snapshot
Cytogenetic analysis of Anopheles ovengensis revealed high structural divergence of chromosomes in the Anopheles nili group
inferred← citeshttps://doi.org/10.1016/j.tig.2009.08.002openalex-snapshot
The origins and impact of primate segmental duplications
inferred← citeshttps://doi.org/10.1038/hdy.2013.38openalex-snapshot
A sequential coalescent algorithm for chromosomal inversions
inferred← citeshttps://doi.org/10.1038/hdy.2015.4openalex-snapshot
A molecular perspective on a complex polymorphic inversion system with cytological evidence of multiply reused breakpoints
inferred← citeshttps://doi.org/10.1038/hdy.2016.63openalex-snapshot
Genetic dissection of intraspecific variation in a male-specific sexual trait in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/nature06341openalex-snapshot
Evolution of genes and genomes on the Drosophila phylogeny
inferred← citeshttps://doi.org/10.1038/ncomms2596openalex-snapshot
Whole-genome sequencing of Oryza brachyantha reveals mechanisms underlying Oryza genome evolution
inferred← citeshttps://doi.org/10.1038/ng.807openalex-snapshot
The Arabidopsis lyrata genome sequence and the basis of rapid genome size change
inferred← citeshttps://doi.org/10.1038/s41467-024-53079-7openalex-snapshot
The origin and maintenance of supergenes contributing to ecological adaptation in Atlantic herring
inferred← citeshttps://doi.org/10.1038/s41467-025-65870-1openalex-snapshot
Telomere-to-telomere genome assembly of the Dipteran Bactrocera dorsalis from a single individual
inferred← citeshttps://doi.org/10.1038/s41559-020-1156-zopenalex-snapshot
Deeply conserved synteny resolves early events in vertebrate evolution
inferred← citeshttps://doi.org/10.1038/s41598-017-05132-3openalex-snapshot
The chromosomes and the mitogenome of Ceratitis fasciventris (Diptera: Tephritidae): two genetic approaches towards the Ceratitis FAR species complex resolution
inferred← citeshttps://doi.org/10.1038/s41598-017-17650-1openalex-snapshot
Inversion evolutionary rates might limit the experimental identification of inversion breakpoints in non-model species
inferred← citeshttps://doi.org/10.1038/s41598-018-37121-5openalex-snapshot
The molecular characterization of fixed inversions breakpoints unveils the ancestral character of the Drosophila guanche chromosomal arrangements
inferred← citeshttps://doi.org/10.1038/s41598-019-53582-8openalex-snapshot
The molecular genealogy of sequential overlapping inversions implies both homologous chromosomes of a heterokaryotype in an inversion origin
inferred← citeshttps://doi.org/10.1038/s41598-020-68879-2openalex-snapshot
Adaptation of gene loci to heterochromatin in the course of Drosophila evolution is associated with insulator proteins
inferred← citeshttps://doi.org/10.1038/sj.hdy.6801046openalex-snapshot
Chromosomal evolution: Inversions: the chicken or the egg?
inferred← citeshttps://doi.org/10.1038/srep06076openalex-snapshot
Camello, a novel family of Histone Acetyltransferases that acetylate histone H4 and is essential for zebrafish development
inferred← citeshttps://doi.org/10.1038/srep30715openalex-snapshot
The origin of chromosomal inversions as a source of segmental duplications in the Sophophora subgenus of Drosophila
inferred← citeshttps://doi.org/10.1038/srep33828openalex-snapshot
Genetic and environmental influences on the germination of basidiospores in the Cryptococcus neoformans species complex
inferred← citeshttps://doi.org/10.1038/srep36248openalex-snapshot
Multiple and diverse structural changes affect the breakpoint regions of polymorphic inversions across the Drosophila genus
inferred← citeshttps://doi.org/10.1073/pnas.0712110105openalex-snapshot
The Foldback -like element Galileo belongs to the P superfamily of DNA transposons and is widespread within the Drosophila genus
inferred← citeshttps://doi.org/10.1080/23737867.2015.1040859openalex-snapshot
Modelling the evolution and expected lifetime of a deme’s principal gene sequence
inferred← citeshttps://doi.org/10.1089/cmb.2008.0076openalex-snapshot
Reconstructing Ancestral Autosomal Arrangements in the Anopheles gambiae Complex
inferred← citeshttps://doi.org/10.1089/cmb.2011.0086openalex-snapshot
Theory and Practice of Ultra-Perfection
inferred← citeshttps://doi.org/10.1093/bioinformatics/btad024openalex-snapshot
Evaluating impacts of syntenic block detection strategies on rearrangement phylogeny usingMycobacterium tuberculosisisolates
inferred← citeshttps://doi.org/10.1093/evolut/qpad027openalex-snapshot
The rate of chromosomal inversion fixation in plant genomes is highly variable
inferred← citeshttps://doi.org/10.1093/g3journal/jkad155openalex-snapshot
Demonstration of in vivo engineered tandem duplications of varying sizes using CRISPR and recombinases in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1093/g3journal/jkae176openalex-snapshot
Genomics of natural populations: gene conversion events reveal selected genes within the inversions of Drosophila pseudoobscura
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/evaf131openalex-snapshot
Chromosomal Inversions Mediated by Tandem Insertions of Transposable Elements
inferred← citeshttps://doi.org/10.1093/gbe/evaf225openalex-snapshot
Comparative Genomics of the Testacea Group of Drosophila Reveals Introgression and Variation in Chromosome Size and Structure
inferred← citeshttps://doi.org/10.1093/gbe/evp006openalex-snapshot
Footprints of Inversions at Present and Past Pseudoautosomal Boundaries in Human Sex Chromosomes
inferred← citeshttps://doi.org/10.1093/gbe/evq027openalex-snapshot
Evolution of a Bitter Taste Receptor Gene Cluster in a New World Sparrow
inferred← citeshttps://doi.org/10.1093/gbe/evr074openalex-snapshot
Evolutionary Patterns of Recently Emerged Animal Duplogs
inferred← citeshttps://doi.org/10.1093/gbe/evr081openalex-snapshot
Effects of Inversions on Within- and Between-Species Recombination and Divergence
inferred← citeshttps://doi.org/10.1093/gbe/evs034openalex-snapshot
Family Size and Turnover Rates among Several Classes of Small Non–Protein-Coding RNA Genes in Caenorhabditis Nematodes
inferred← citeshttps://doi.org/10.1093/gbe/evy239openalex-snapshot
Origin and Consequences of Chromosomal Inversions in thevirilisGroup ofDrosophila
inferred← citeshttps://doi.org/10.1093/genetics/177.3.1263openalex-snapshot
Drosophila Genomes by the Baker's Dozen
inferred← citeshttps://doi.org/10.1093/genetics/iyab062openalex-snapshot
Transposon-induced inversions activate gene expression in the maize pericarp
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/hmg/ddw415openalex-snapshot
Detailed analysis of inversions predicted between two human genomes: errors, real polymorphisms, and their origin and population distribution
inferred← citeshttps://doi.org/10.1093/jhered/esad018openalex-snapshot
Genome assemblies and comparison of two Neotropical spiral gingers: Costus pulverulentus and C. lasius
inferred← citeshttps://doi.org/10.1093/jhered/esr043openalex-snapshot
Haplotype-Based Genomic Sequencing of a Chromosomal Polymorphism in the White-Throated Sparrow (Zonotrichia albicollis)
inferred← citeshttps://doi.org/10.1093/jhered/esy057openalex-snapshot
Computational Sequence Analysis of Inversion Breakpoint Regions in the CactophilicDrosophila mojavensisLineage
inferred← citeshttps://doi.org/10.1093/molbev/msn101openalex-snapshot
Coexpression of Linked Genes in Mammalian Genomes Is Generally Disadvantageous
inferred← citeshttps://doi.org/10.1093/molbev/msq280openalex-snapshot
Recent and Recurrent Selective Sweeps of the Antiviral RNAi Gene Argonaute-2 in Three Species of Drosophila
inferred← citeshttps://doi.org/10.1093/molbev/mss067openalex-snapshot
Segmental Duplication, Microinversion, and Gene Loss Associated with a Complex Inversion Breakpoint Region in Drosophila
inferred← citeshttps://doi.org/10.1093/molbev/msu177openalex-snapshot
Characterization of the Breakpoints of a Polymorphic Inversion Complex Detects Strict and Broad Breakpoint Reuse at the Molecular Level
inferred← citeshttps://doi.org/10.1093/nar/gkag139openalex-snapshot
Transposable elements as drivers of genome evolution in Drosophila virilis
inferred← citeshttps://doi.org/10.1098/rsbm.2024.0036openalex-snapshot
Michael Ashburner. 23 May 1942—7 July 2023
inferred← citeshttps://doi.org/10.1098/rstb.2021.0206openalex-snapshot
The relevance of chromatin architecture to genome rearrangements in Drosophila
inferred← citeshttps://doi.org/10.1101/022244openalex-snapshot
Coevolution of male and female reproductive traits drive cascading reinforcement in Drosophila yakuba
inferred← citeshttps://doi.org/10.1101/2020.06.25.170522openalex-snapshot
rearrvisr : an R package to detect, classify, and visualize genome rearrangements
inferred← citeshttps://doi.org/10.1101/2021.06.01.446624openalex-snapshot
Molecular characterization of inversion breakpoints in the Drosophila nasuta species group
inferred← citeshttps://doi.org/10.1101/2022.02.18.481113openalex-snapshot
Evaluating Impacts of Syntenic Block Detection Strategies on Rearrangement Phylogeny Using M. tuberculosis Isolates
inferred← citeshttps://doi.org/10.1101/2022.08.31.506062openalex-snapshot
The rate of inversion fixation in plant genomes is highly variable
inferred← citeshttps://doi.org/10.1101/2023.10.23.562618openalex-snapshot
The origin and maintenance of supergenes contributing to ecological adaptation in Atlantic herring
inferred← citeshttps://doi.org/10.1101/2024.05.29.596518openalex-snapshot
How repeats rearrange chromosomes in deer mice
inferred← citeshttps://doi.org/10.1101/2024.06.17.599346openalex-snapshot
Analysis of 30 chromosome-level Drosophila genome assemblies reveals dynamic evolution of centromeric satellite repeats
inferred← citeshttps://doi.org/10.1101/2025.09.20.677491openalex-snapshot
Expansion of the DFR Gene Family in Fagopyrum
inferred← citeshttps://doi.org/10.1101/485334openalex-snapshot
Novitski’s Distal shift in Paracentric Inversion Evolution
inferred← citeshttps://doi.org/10.1101/802371openalex-snapshot
Insulator proteins contribute to expression of gene loci repositioned into heterochromatin in the course of Drosophila evolution
inferred← citeshttps://doi.org/10.1101/gr.086041.108openalex-snapshot
Sequencing human–gibbon breakpoints of synteny reveals mosaic new insertions at rearrangement sites
inferred← citeshttps://doi.org/10.1101/gr.097501.109openalex-snapshot
Comparative genomics of the fungal pathogens Candida dubliniensis and Candida albicans
inferred← citeshttps://doi.org/10.1101/gr.103713.109openalex-snapshot
Fragile regions and not functional constraints predominate in shaping gene organization in the genus Drosophila
inferred← citeshttps://doi.org/10.1101/gr.111252.110openalex-snapshot
Extensive recombination rate variation in the house mouse species complex inferred from genetic linkage maps
inferred← citeshttps://doi.org/10.1101/gr.117242.110openalex-snapshot
Copy number variation analysis in the great apes reveals species-specific patterns of structural variation
inferred← citeshttps://doi.org/10.1101/gr.263442.120openalex-snapshot
Evolution of genome structure in the Drosophila simulans species complex
inferred← citeshttps://doi.org/10.1105/tpc.108.062166openalex-snapshot
Chromosomal Phylogeny and Karyotype Evolution in x=7 Crucifer Species (Brassicaceae)
inferred← citeshttps://doi.org/10.1111/1744-7917.12034openalex-snapshot
Molecular cloning and characterization of a putative proline dehydrogenase gene in the Colorado potato beetle, Leptinotarsa decemlineata
inferred← citeshttps://doi.org/10.1111/brv.12213openalex-snapshot
Chromosomal polymorphism in mammals: an evolutionary perspective
inferred← citeshttps://doi.org/10.1111/evo.12372openalex-snapshot
GENE-DOSAGE EFFECTS ON FITNESS IN RECENT ADAPTIVE DUPLICATIONS:ace-1IN THE MOSQUITOCULEX PIPIENS
inferred← citeshttps://doi.org/10.1111/evo.13176openalex-snapshot
Chromosome inversions and ecological plasticity in the main African malaria mosquitoes
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2012.02550.xopenalex-snapshot
Fine‐scale genetic analysis of species‐specific female preference in Drosophila simulans
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2010.00414.xopenalex-snapshot
Catching the phylogenic history through the ontogenic hourglass: a phylogenomic analysis ofDrosophilabody segmentation genes
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2012.01731.xopenalex-snapshot
STRUCTURE AND POPULATION GENETICS OF THE BREAKPOINTS OF A POLYMORPHIC INVERSION INDROSOPHILA SUBOBSCURA
inferred← citeshttps://doi.org/10.1111/jeb.14242openalex-snapshot
How chromosomal inversions reorient the evolutionary process
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.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.14944openalex-snapshot
Chromosomal inversions associated with environmental adaptation in honeybees
inferred← citeshttps://doi.org/10.1111/mec.15907openalex-snapshot
Inversion breakpoints and the evolution of supergenes
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.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.70004openalex-snapshot
Genome Architecture and Speciation in Plants and Animals
inferred← citeshttps://doi.org/10.1111/tpj.13262openalex-snapshot
Molecular, genetic and evolutionary analysis of a paracentric inversion in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1134/s1022795410090255openalex-snapshot
Chromosome evolution in malaria mosquitoes
inferred← citeshttps://doi.org/10.1134/s1022795410100066openalex-snapshot
Location of genes in chromosomes: Random or not?
inferred← citeshttps://doi.org/10.1139/gen-2012-0074openalex-snapshot
Differential occurrence of chromosome inversion polymorphisms among Muller's elements in three species of thetripunctatagroup ofDrosophila, including a species with fast chromosomal evolution
inferred← citeshttps://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?
inferred← citeshttps://doi.org/10.1186/1471-2105-12-s9-s20openalex-snapshot
Genome dedoubling by DCJ and reversal
inferred← citeshttps://doi.org/10.1186/1471-2105-9-286openalex-snapshot
Precise detection of rearrangement breakpoints in mammalian chromosomes
inferred← citeshttps://doi.org/10.1186/1471-2148-11-91openalex-snapshot
Arm-specific dynamics of chromosome evolution in malaria mosquitoes
inferred← citeshttps://doi.org/10.1186/1471-2148-8-2openalex-snapshot
Coordinated evolution of co-expressed gene clusters in the Drosophila transcriptome
inferred← citeshttps://doi.org/10.1186/1471-2148-8-309openalex-snapshot
Chromosomal plasticity and evolutionary potential in the malaria vector Anopheles gambiae sensu stricto: insights from three decades of rare paracentric inversions
inferred← citeshttps://doi.org/10.1186/1471-2156-15-s2-s16openalex-snapshot
The Bactrocera dorsalis species complex: comparative cytogenetic analysis in support of Sterile Insect Technique applications
inferred← citeshttps://doi.org/10.1186/1471-2164-13-53openalex-snapshot
Gene alterations at Drosophila inversion breakpoints provide prima facie evidence for natural selection as an explanation for rapid chromosomal evolution
inferred← citeshttps://doi.org/10.1186/1471-2164-15-1060openalex-snapshot
Reconstruction of gross avian genome structure, organization and evolution suggests that the chicken lineage most closely resembles the dinosaur avian ancestor
inferred← citeshttps://doi.org/10.1186/1471-2164-9-384openalex-snapshot
The genomic distribution of intraspecific and interspecific sequence divergence of human segmental duplications relative to human/chimpanzee chromosomal rearrangements
inferred← citeshttps://doi.org/10.1186/gb-2008-9-12-r176openalex-snapshot
Selective maintenance of Drosophilatandemly arranged duplicated genes during evolution
inferred← citeshttps://doi.org/10.1186/gb-2008-9-6-r94openalex-snapshot
Chætognath transcriptome reveals ancestral and unique features among bilaterians
inferred← citeshttps://doi.org/10.1186/s12864-017-3655-0openalex-snapshot
Core-genome scaffold comparison reveals the prevalence that inversion events are associated with pairs of inverted repeats
inferred← citeshttps://doi.org/10.1186/s12864-018-4663-4openalex-snapshot
Partial-arm translocations in evolution of malaria mosquitoes revealed by high-coverage physical mapping of the Anopheles atroparvus genome
inferred← citeshttps://doi.org/10.1186/s12864-019-5590-8openalex-snapshot
Long-read based assembly and synteny analysis of a reference Drosophila subobscura genome reveals signatures of structural evolution driven by inversions recombination-suppression effects
inferred← citeshttps://doi.org/10.1186/s13059-014-0459-2openalex-snapshot
Genome analysis of a major urban malaria vector mosquito, Anopheles stephensi
inferred← citeshttps://doi.org/10.1186/s13059-025-03527-4openalex-snapshot
Analysis of 30 chromosome-level Drosophila genome assemblies reveals dynamic evolution of centromeric satellite repeats
inferred← citeshttps://doi.org/10.13140/2.1.2066.4649openalex-snapshot
Relation between Insertion Sequences and Genome Rearrangements in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1371/annotation/b1cace11-17ed-456e-b8a9-006c09125bd0openalex-snapshot
Correction: Population Genomics of Inversion Polymorphisms in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1371/journal.pbio.1000501openalex-snapshot
How and Why Chromosome Inversions Evolve
inferred← citeshttps://doi.org/10.1371/journal.pbio.1000552openalex-snapshot
Neighbourhood Continuity Is Not Required for Correct Testis Gene Expression in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1010647openalex-snapshot
Getting higher on rugged landscapes: Inversion mutations open access to fitter adaptive peaks in NK fitness landscapes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002364openalex-snapshot
Consequences of Eukaryotic Enhancer Architecture for Gene Expression Dynamics, Development, and Fitness
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003056openalex-snapshot
Population Genomics of Inversion Polymorphisms in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003567openalex-snapshot
Breakage-fusion-bridge Cycles and Large Insertions Contribute to the Rapid Evolution of Accessory Chromosomes in a Fungal Pathogen
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006212openalex-snapshot
Comparative Genomic Analyses Provide New Insights into the Evolutionary Dynamics of Heterochromatin in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008314openalex-snapshot
Chromosomal rearrangements as a source of new gene formation in Drosophila yakuba
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010087openalex-snapshot
Meiotic, genomic and evolutionary properties of crossover distribution in Drosophila yakuba
inferred← citeshttps://doi.org/10.1371/journal.pone.0005524openalex-snapshot
Chromosomal Rearrangements between Serotype A and D Strains in Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1371/journal.pone.0007883openalex-snapshot
The Transposon Galileo Generates Natural Chromosomal Inversions in Drosophila by Ectopic Recombination
inferred← citeshttps://doi.org/10.1371/journal.pone.0010592openalex-snapshot
Genome Landscape and Evolutionary Plasticity of Chromosomes in Malaria Mosquitoes
inferred← citeshttps://doi.org/10.1371/journal.pone.0064491openalex-snapshot
Females and Males Contribute in Opposite Ways to the Evolution of Gene Order in Drosophila
inferred← citeshttps://doi.org/10.1534/g3.113.008599openalex-snapshot
Rapid Degeneration of Noncoding DNA Regions SurroundingSlAP3X/YAfter Recombination Suppression in the Dioecious PlantSilene latifolia
inferred← citeshttps://doi.org/10.1534/g3.120.401559openalex-snapshot
Identification and Characterization of Breakpoints and Mutations onDrosophila melanogasterBalancer Chromosomes
inferred← citeshttps://doi.org/10.1534/g3.120.401727openalex-snapshot
Origins and Evolutionary Patterns of the1.688Satellite DNA Family inDrosophilaPhylogeny
inferred← citeshttps://doi.org/10.1534/genetics.107.086074openalex-snapshot
Polytene Chromosomal Maps of 11 Drosophila Species: The Order of Genomic Scaffolds Inferred From Genetic and Physical Maps
inferred← citeshttps://doi.org/10.1534/genetics.107.086108openalex-snapshot
Chromosomal Rearrangement Inferred From Comparisons of 12 Drosophila Genomes
inferred← citeshttps://doi.org/10.1534/genetics.111.130690openalex-snapshot
Massive Changes in Genome Architecture Accompany the Transition to Self-Fertility in the Filamentous FungusNeurospora tetrasperma
inferred← citeshttps://doi.org/10.1534/genetics.112.141622openalex-snapshot
Sequence-Based Detection and Breakpoint Assembly of Polymorphic Inversions
inferred← citeshttps://doi.org/10.1534/genetics.116.190389openalex-snapshot
Selection on Inversion Breakpoints Favors Proximity to Pairing Sensitive Sites in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1534/genetics.117.300583openalex-snapshot
Phylogeny of the Genus Drosophila
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.119.302385openalex-snapshot
Fine-Mapping Complex Inversion Breakpoints and Investigating Somatic Pairing in the Anopheles gambiae Species Complex Using Proximity-Ligation Sequencing
inferred← citeshttps://doi.org/10.1603/an10113openalex-snapshot
Analysis of Mitotic and Polytene Chromosomes and Photographic Polytene Chromosome Maps inBactrocera cucurbitae(Diptera: Tephritidae)
inferred← citeshttps://doi.org/10.17077/etd.76xs032sopenalex-snapshot
Geographically patterned variation in diapause and its relationship to other climate-associated phenotypes and genotypes of Drosophila americana
inferred← citeshttps://doi.org/10.21203/rs.3.rs-796229/v1openalex-snapshot
Sea anemone genomes reveal ancestral metazoan chromosomal macrosynteny
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/10.30707/lib2.1clarkopenalex-snapshot
Modelling the Evolution and Expected Lifetime of a Deme’s Principal Gene Sequence
inferred← citeshttps://doi.org/10.31274/td-20240329-352openalex-snapshot
Functional and structural impacts of Ac/Ds transposon system in maize
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/10.3389/fpls.2016.00304openalex-snapshot
Analyses of Old “Prokaryotic” Proteins Indicate Functional Diversification in Arabidopsis and Oryza sativa
inferred← citeshttps://doi.org/10.3389/fpls.2022.895437openalex-snapshot
Meiotic Chromosomal Abnormality Detected in a Heterozygote of Elymus nutans
inferred← citeshttps://doi.org/10.3390/genes12020175openalex-snapshot
Evolutionary Dynamics of the Pericentromeric Heterochromatin in Drosophila virilis and Related Species
inferred← citeshttps://doi.org/10.3390/insects14030222openalex-snapshot
Implications of the Niche Partitioning and Coexistence of Two Resident Parasitoids for Drosophila suzukii Management in Non-Crop Areas
inferred← citeshttps://doi.org/10.3390/insects15050312openalex-snapshot
Two Nested Inversions in the X Chromosome Differentiate the Dominant Malaria Vectors in Europe, Anopheles atroparvus and Anopheles messeae
inferred← citeshttps://doi.org/10.3390/insects16060586openalex-snapshot
Chromosomal Inversions in Chromosome U of Drosophila subobscura: A Story from Population Studies to Molecular Level
inferred← citeshttps://doi.org/10.37376/1571-000-027-008openalex-snapshot
الانقلابات الكروموسومية في العشائر الطبيعية لنوع Drosophila melanogaster بمنطقة البيضاء، الجبل الأخضر، ليبيا
inferred← citeshttps://doi.org/10.3897/zookeys.540.9857openalex-snapshot
Cytogenetic and symbiont analysis of five members of the B. dorsalis complex (Diptera, Tephritidae): no evidence of chromosomal or symbiont-based speciation events
inferred← citeshttps://doi.org/10.4161/fly.19423openalex-snapshot
The DAIBAM MITE element is involved in the origin of one fixed and two polymorphic Drosophila virilis phylad inversions
inferred← citeshttps://doi.org/10.4238/vol9-4gmr929openalex-snapshot
An interspecific QTL study of Drosophila wing size and shape variation to investigate the genetic basis of morphological differences
inferred← citeshttps://doi.org/10.48397/arriab.2020.20.068openalex-snapshot
ЭКСПРЕСС-МЕТОД МОЛЕКУЛЯРНОЙ ДИАГНОСТИКИ DROSOPHILA SIMULANS С ПОМОЩЬЮ ТРАДИЦИОННОЙ ПЦР
inferred← citeshttps://doi.org/10.48550/arxiv.1410.5415openalex-snapshot
Rearrangement Problems with Duplicated Genomic Markers
inferred← citeshttps://doi.org/10.5772/intechopen.73246openalex-snapshot
Drosophila Chromosomal Polymorphism: From Population Aspects to Origin Mechanisms of Inversions
inferred← citeshttps://doi.org/10.70675/335aaf0bz9f74z46cfzbdaezaa3b2ba7d16copenalex-snapshot
Lien entre les réarrangements chromosomiques et la structure de la chromatine chez la Drosophile
inferred← citeshttps://doi.org/10.70675/4303476fzea42z4d77zab40z685972eb85dcopenalex-snapshot
Weighted Genome Rearrangements
inferred← citeshttps://doi.org/10.70675/61afc6cbzaa0az44fdz82c6z534d4b753b8eopenalex-snapshot
Rearrangement Problems with duplicated genomic content
inferred← citeshttps://doi.org/10.70675/69479c04z83b5z4f98zbdefz33141a932dceopenalex-snapshot
Etude des mécanismes évolutifs perturbant l’organisation des gènes dans les génomes de vertébrés
inferred← citeshttps://doi.org/10.70675/738358caz5e8az4c8cza0c5z8eb894d1277eopenalex-snapshot
Influence de l’architecture génétique et des variations environnementales sur l’adaptation : la résistance aux insecticides chez les moustiques
inferred← citeshttps://doi.org/10.70675/77cd418cz1b0cz4dd0z9d8czf009e0fd8fafopenalex-snapshot
Investigating the Impact of Insertion Sequences on the Evolution of Prokaryotic Genomes
inferred← citeshttps://doi.org/10.70675/ad443f1azbcddz4496zb5bbze4348b3ff51eopenalex-snapshot
Evolution beyond substitutions : Computational modeling of the impact of chromosomal rearrangements on evolutionary dynamics
inferred← citeshttps://doi.org/10.70675/c571d613z737cz478fzb1e5zfd353254fc7copenalex-snapshot
Histoire naturelle des chaetognathes : une énigme zoologique à l'ère moléculaire
inferred← citeshttps://doi.org/10.70675/ef380bd2z14d5z4771za3e2z82b040f5da53openalex-snapshot
Impact phénotypique des réarrangements chromosomiques et évolution des génomes de levures
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