On the public citation graph
Genomics of natural populations: Evolutionary forces that establish and maintain gene arrangements in Drosophila pseudoobscura
0 signed · 189 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajmg.1320550207openalex-snapshot
Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases
inferredcites →https://doi.org/10.1007/bf00128015openalex-snapshot
Chromosome inversion polymorphisms in Drosophila melanogaster II. Geographic clines and climatic associations in Australasia, North America and Asia
inferredcites →https://doi.org/10.1007/bf00888760openalex-snapshot
Experimentelle Beitr�ge Zum Problem des Positiven Heterosiseffektes Bei der Strukturpolymorphen ArtDrosophila Subobscura
inferredcites →https://doi.org/10.1007/bf01245622openalex-snapshot
Linkage disequilibrium in finite populations
inferredcites →https://doi.org/10.1007/s00049-005-0331-7openalex-snapshot
Monoterpene chemodiversity of ponderosa pine in relation to herbivory and bark beetle colonization
inferredcites →https://doi.org/10.1007/s10709-014-9760-yopenalex-snapshot
Chromosomal polymorphism in two species of Hypancistrus (Siluriformes: Loricariidae): an integrative approach for understanding their biodiversity
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/j.molcel.2012.08.031openalex-snapshot
Gene Density, Transcription, and Insulators Contribute to the Partition of the Drosophila Genome into Physical Domains
inferredcites →https://doi.org/10.1017/s0016672300012684openalex-snapshot
Associative overdominance caused by linked detrimental mutations
inferredcites →https://doi.org/10.1017/s0016672300013343openalex-snapshot
Selection of new inversions in multi-locus genetic systems
inferredcites →https://doi.org/10.1017/s0016672300014634openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1017/s0016672302005955openalex-snapshot
Molecular population genetics of sequence length diversity in the Adh region of Drosophila pseudoobscura
inferredcites →https://doi.org/10.1017/s0016672308009579openalex-snapshot
The hitch-hiking effect of a favourable gene
inferredcites →https://doi.org/10.1038/hdy.2013.38openalex-snapshot
A sequential coalescent algorithm for chromosomal inversions
inferredcites →https://doi.org/10.1038/nature05260openalex-snapshot
Insights into social insects from the genome of the honeybee Apis mellifera
inferredcites →https://doi.org/10.1038/nature06784openalex-snapshot
The genome of the model beetle and pest Tribolium castaneum
inferredcites →https://doi.org/10.1038/nature09449openalex-snapshot
Higher rates of sex evolve in spatially heterogeneous environments
inferredcites →https://doi.org/10.1038/nature10811openalex-snapshot
The Drosophila melanogaster Genetic Reference Panel
inferredcites →https://doi.org/10.1038/nature13679openalex-snapshot
Gibbon genome and the fast karyotype evolution of small apes
inferredcites →https://doi.org/10.1038/nature17143openalex-snapshot
Sex speeds adaptation by altering the dynamics of molecular evolution
inferredcites →https://doi.org/10.1038/ng.2524openalex-snapshot
A heterozygous moth genome provides insights into herbivory and detoxification
inferredcites →https://doi.org/10.1038/ng.3241openalex-snapshot
A genetic mechanism for female-limited Batesian mimicry in Papilio butterfly
inferredcites →https://doi.org/10.1038/ng.3443openalex-snapshot
A supergene determines highly divergent male reproductive morphs in the ruff
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/ng1508openalex-snapshot
A common inversion under selection in Europeans
inferredcites →https://doi.org/10.1038/nprot.2008.211openalex-snapshot
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
inferredcites →https://doi.org/10.1038/nrg761openalex-snapshot
Resolving the paradox of sex and recombination
inferredcites →https://doi.org/10.1073/pnas.0404206101openalex-snapshot
Prospects for inferring very large phylogenies by using the neighbor-joining method
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.1516410112openalex-snapshot
Genome sequence of the Asian Tiger mosquito, Aedes albopictus , reveals insights into its biology, genetics, and evolution
inferredcites →https://doi.org/10.1073/pnas.1601232113openalex-snapshot
Rare recombination events generate sequence diversity among balancer chromosomes in Drosophila melanogaster
inferredcites →https://doi.org/10.1073/pnas.221274498openalex-snapshot
Chromosomal inversions and the reproductive isolation of species
inferredcites →https://doi.org/10.1073/pnas.59.2.398openalex-snapshot
A molecular approach to the study of genic heterozygosity in natural populations. 3. Direct evidence of coadaptation in gene arrangements of Drosophila.
inferredcites →https://doi.org/10.1073/pnas.88.1.305openalex-snapshot
Molecular evolution of inversions in Drosophila pseudoobscura: the amylase gene region.
inferredcites →https://doi.org/10.1073/pnas.88.22.10367openalex-snapshot
Four decades of inversion polymorphism in Drosophila pseudoobscura.
inferredcites →https://doi.org/10.1080/00031305.1998.10480559openalex-snapshot
Violin Plots: A Box Plot-Density Trace Synergism
inferredcites →https://doi.org/10.1086/284679openalex-snapshot
Long-Distance Migration of Drosophila. 2. Presence in Desolate Sites and Dispersal Near a Desert Oasis
inferredcites →https://doi.org/10.1086/427093openalex-snapshot
Temperature‐Related Genetic Changes in Laboratory Populations ofDrosophila subobscura: Evidence against Simple Climatic‐Based Explanations for Latitudinal Clines
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/chemse/bjv001openalex-snapshot
The Genetic Basis for Variation in Olfactory Behavior in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/gbe/evq001openalex-snapshot
Validation of Rearrangement Break Points Identified by Paired-End Sequencing in Natural Populations of Drosophila melanogaster
inferredcites →https://doi.org/10.1093/gbe/evt109openalex-snapshot
Complex Patterns of Local Adaptation in Teosinte
inferredcites →https://doi.org/10.1093/genetics/113.4.1057openalex-snapshot
ON THE DIVERGENCE OF ALLELES IN NESTED SUBSAMPLES FROM FINITE POPULATIONS
inferredcites →https://doi.org/10.1093/genetics/123.2.359openalex-snapshot
Distinguishing the forces controlling genetic variation at the Xdh locus in Drosophila pseudoobscura.
inferredcites →https://doi.org/10.1093/genetics/123.3.585openalex-snapshot
Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.
inferredcites →https://doi.org/10.1093/genetics/132.2.471openalex-snapshot
Estimates of gene flow in Drosophila pseudoobscura determined from nucleotide sequence analysis of the alcohol dehydrogenase region.
inferredcites →https://doi.org/10.1093/genetics/136.3.1105openalex-snapshot
Mitochondrial DNA variation and the evolution of Robertsonian chromosomal races of house mice, Mus domesticus.
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
inferredcites →https://doi.org/10.1093/genetics/153.1.251openalex-snapshot
Recombination Rate Predicts Inversion Size in Diptera
inferredcites →https://doi.org/10.1093/genetics/155.2.685openalex-snapshot
Effect of Inversion Polymorphism on the Neutral Nucleotide Variability of Linked Chromosomal Regions in Drosophila
inferredcites →https://doi.org/10.1093/genetics/156.1.155openalex-snapshot
Molecular Population Genetics of X -Linked Genes in Drosophila pseudoobscura
inferredcites →https://doi.org/10.1093/genetics/161.1.11openalex-snapshot
Distinguishing Between Selection and Population Expansion in an Experimental Lineage of Bacteriophage T7
inferredcites →https://doi.org/10.1093/genetics/165.1.287openalex-snapshot
A Method for Detecting Recent Selection in the Human Genome From Allele Age Estimates
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/23.1.28openalex-snapshot
INVERSIONS IN THE CHROMOSOMES OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/28.2.162openalex-snapshot
GENETICS OF NATURAL POPULATIONS IX. TEMPORAL CHANGES IN THE COMPOSITION OF POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/28.4.304openalex-snapshot
GENETICS OF NATURAL POPULATIONS. X. DISPERSION RATES IN DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/31.2.125openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XII. EXPERIMENTAL REPRODUCTION OF SOME OF THE CHANGES CAUSED BY NATURAL SELECTION IN CERTAIN POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/33.2.158openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XVI. ALTITUDINAL AND SEASONAL CHANGES PRODUCED BY NATURAL SELECTION IN CERTAIN POPULATIONS OF DROSOPHILA PSEUDOOBSCURA AND DROSOPHILA PERSIMILIS
inferredcites →https://doi.org/10.1093/genetics/33.6.588openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XVIII. EXPERIMENTS ON CHROMOSOMES OF DROSOPHILA PSEUDOOBSCURA FROM DIFFERENT GEOGRAPHIC REGIONS
inferredcites →https://doi.org/10.1093/genetics/35.3.288openalex-snapshot
GENETICS OF NATURAL POPULATIONS. XIX. ORIGIN OF HETEROSIS THROUGH NATURAL SELECTION IN POPULATIONS OF DROSOPHILA PSEUDOOBSCURA
inferredcites →https://doi.org/10.1093/genetics/36.3.267openalex-snapshot
NON-RANDOM DISJUNCTION IN DROSOPHILA
inferredcites →https://doi.org/10.1093/genetics/57.4.741openalex-snapshot
FREQUENCY CHANGES OF NEW INVERSIONS IN POPULATIONS UNDER MUTATION-SELECTION EQUILIBRIA
inferredcites →https://doi.org/10.1093/genetics/69.3.405openalex-snapshot
A MOLECULAR APPROACH TO THE STUDY OF GENIC HETEROZYGOSITY IN NATURAL POPULATIONS. V. FURTHER DIRECT EVIDENCE OF COADAPTATION IN INVERSIONS OF DROSOPHILA
inferredcites →https://doi.org/10.1093/genetics/75.1.199openalex-snapshot
THE AGE OF A NEUTRAL MUTANT PERSISTING IN A FINITE POPULATION
inferredcites →https://doi.org/10.1093/genetics/87.1.169openalex-snapshot
INVERSION CLINES IN POPULATIONS OF DROSOPHILA MELANOGASTER
inferredcites →https://doi.org/10.1093/genetics/98.4.833openalex-snapshot
CHROMOSOME INVERSION POLYMORPHISMS IN DROSOPHILA MELANOGASTER. I. LATITUDINAL CLINES AND ASSOCIATIONS BETWEEN INVERSIONS IN AUSTRALASIAN POPULATIONS
inferredcites →https://doi.org/10.1093/jhered/esh063openalex-snapshot
Centromere Dynamics and Chromosome Evolution in Marsupials
inferredcites →https://doi.org/10.1093/molbev/msp116openalex-snapshot
Large Gene Family Expansions and Adaptive Evolution for Odorant and Gustatory Receptors in the Pea Aphid, Acyrthosiphon pisum
inferredcites →https://doi.org/10.1093/molbev/msq248openalex-snapshot
Chromosomal Inversions, Natural Selection and Adaptation in the Malaria Vector Anopheles funestus
inferredcites →https://doi.org/10.1093/molbev/msr039openalex-snapshot
Evolutionary History of the Third Chromosome Gene Arrangements of Drosophila pseudoobscura Inferred from Inversion Breakpoints
inferredcites →https://doi.org/10.1093/molbev/mss067openalex-snapshot
Segmental Duplication, Microinversion, and Gene Loss Associated with a Complex Inversion Breakpoint Region in Drosophila
inferredcites →https://doi.org/10.1093/molbev/mst089openalex-snapshot
Genetic Signatures Reveal High-Altitude Adaptation in a Set of Ethiopian Populations
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://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
inferredcites →https://doi.org/10.1093/molbev/msw016openalex-snapshot
Genomic Evidence for Adaptive Inversion Clines inDrosophila melanogaster
inferredcites →https://doi.org/10.1093/nar/gkn923openalex-snapshot
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
inferredcites →https://doi.org/10.1093/nar/gku1099openalex-snapshot
FlyBase: introduction of the Drosophila melanogaster Release 6 reference genome assembly and large-scale migration of genome annotations
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a108793openalex-snapshot
Chromosomal and allozymic diagnosis of three species of Drosophila
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040454openalex-snapshot
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
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/10.1111/1467-9868.00346openalex-snapshot
A Direct Approach to False Discovery Rates
inferredcites →https://doi.org/10.1111/brv.12213openalex-snapshot
Chromosomal polymorphism in mammals: an evolutionary perspective
inferredcites →https://doi.org/10.1111/evo.13176openalex-snapshot
Chromosome inversions and ecological plasticity in the main African malaria mosquitoes
inferredcites →https://doi.org/10.1111/gbb.12252openalex-snapshot
Genes located in a chromosomal inversion are correlated with territorial song in white‐throated sparrows
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00591.xopenalex-snapshot
EVOLUTIONARY PACE OF CHROMOSOMAL POLYMORPHISM IN COLONIZING POPULATIONS OF DROSOPHILA SUBOBSCURA: AN EVOLUTIONARY TIME SERIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01509.xopenalex-snapshot
QTL MAPPING REVEALS A STRIKING COINCIDENCE IN THE POSITIONS OF GENOMIC REGIONS ASSOCIATED WITH ADAPTIVE VARIATION IN BODY SIZE IN PARALLEL CLINES OF DROSOPHILA MELANOGASTER ON DIFFERENT CONTINENTS
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01537.xopenalex-snapshot
ACCUMULATING POSTZYGOTIC ISOLATION GENES IN PARAPATRY: A NEW TWIST ON CHROMOSOMAL SPECIATION
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02445.xopenalex-snapshot
The latitudinal cline in the In(3R)Payne inversion polymorphism has shifted in the last 20 years in Australian Drosophila melanogaster populations
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02683.xopenalex-snapshot
Molecular evidence for glacial refugia of mountain plants in the European Alps
inferredcites →https://doi.org/10.1111/j.1558-5646.1967.tb03423.xopenalex-snapshot
SELECTION AND INVERSION POLYMORPHISM IN EXPERIMENTAL POPULATIONS OFDROSOPHILA PSEUDOOBSCURAINITIATED WITH THE CHROMOSOMAL CONSTITUTIONS OF NATURAL POPULATIONS
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.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb03962.xopenalex-snapshot
INVERSION LENGTH AND BREAKPOINT DISTRIBUTION IN THEDROSOPHILA BUZZATIISPECIES COMPLEX: IS INVERSION LENGTH A SELECTED TRAIT?
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00435.xopenalex-snapshot
CLINAL DISTRIBUTION OF A CHROMOSOMAL REARRANGEMENT: A PRECURSOR TO CHROMOSOMAL SPECIATION?
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.1558-5646.2012.01731.xopenalex-snapshot
STRUCTURE AND POPULATION GENETICS OF THE BREAKPOINTS OF A POLYMORPHIC INVERSION INDROSOPHILA SUBOBSCURA
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.12856openalex-snapshot
Tracking changes in chromosomal arrangements and their genetic content during adaptation
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/10.1126/science.1077769openalex-snapshot
A Polytene Chromosome Analysis of the Anopheles gambiae Species Complex
inferredcites →https://doi.org/10.1126/science.1138878openalex-snapshot
Genome Sequence of Aedes aegypti , a Major Arbovirus Vector
inferredcites →https://doi.org/10.1126/science.1190371openalex-snapshot
Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude
inferredcites →https://doi.org/10.1126/science.1258524openalex-snapshot
Extensive introgression in a malaria vector species complex revealed by phylogenomics
inferredcites →https://doi.org/10.1128/aem.00670-14openalex-snapshot
Gene Discovery for Enzymes Involved in Limonene Modification or Utilization by the Mountain Pine Beetle-Associated Pathogen Grosmannia clavigera
inferredcites →https://doi.org/10.1139/g98-159openalex-snapshot
Chromosome evolution in kangaroos (Marsupialia: Macropodidae): Cross species chromosome painting between the tammar wallaby and rock wallaby spp. with the 2n = 22 ancestral macropodid karyotype
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.ge.01.120167.000443openalex-snapshot
NONRANDOM DISJUNCTION IN DROSOPHILA
inferredcites →https://doi.org/10.1159/000323416openalex-snapshot
Chromosomal Polymorphisms in African Vlei Rats, Otomys irroratus (Muridae: Otomyini), Detected by Banding Techniques and Chromosome Painting: Inversions, Centromeric Shifts and Diploid Number Variation
inferredcites →https://doi.org/10.1186/1471-2156-12-1openalex-snapshot
Conservation genetics and phylogeography of endangered and endemic shrub Tetraena mongolica (Zygophyllaceae) in Inner Mongolia, China
inferredcites →https://doi.org/10.1186/1471-2156-12-60openalex-snapshot
A genetic linkage map and comparative mapping of the prairie vole (Microtus ochrogaster) genome
inferredcites →https://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
inferredcites →https://doi.org/10.1186/1479-7364-1-4-274openalex-snapshot
The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs
inferredcites →https://doi.org/10.1186/gb-2014-15-1-r1openalex-snapshot
Dynamic regulation of genome-wide pre-mRNA splicing and stress tolerance by the Sm-like protein LSm5 in Arabidopsis
inferredcites →https://doi.org/10.1186/gb-2014-15-3-r43openalex-snapshot
The genome and life-stage specific transcriptomes of Globodera pallidaelucidate key aspects of plant parasitism by a cyst nematode
inferredcites →https://doi.org/10.1186/s13059-014-0466-3openalex-snapshot
Genome of the house fly, Musca domestica L., a global vector of diseases with adaptations to a septic environment
inferredcites →https://doi.org/10.1214/aos/1074290335openalex-snapshot
The positive false discovery rate: a Bayesian interpretation and the q-value
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.1000313openalex-snapshot
Genome Sequence of the Pea Aphid Acyrthosiphon pisum
inferredcites →https://doi.org/10.1371/journal.pbio.1001317openalex-snapshot
The Evolution of Sex Is Favoured During Adaptation to New Environments
inferredcites →https://doi.org/10.1371/journal.pbio.1001422openalex-snapshot
Recombination Modulates How Selection Affects Linked Sites in Drosophila
inferredcites →https://doi.org/10.1534/g3.114.014860openalex-snapshot
Evidence for Stabilizing Selection on Codon Usage in Chromosomal Rearrangements ofDrosophila pseudoobscura
inferredcites →https://doi.org/10.1534/genetics.105.041947openalex-snapshot
Mechanisms of Genetic Exchange Within the Chromosomal Inversions of Drosophila pseudoobscura
inferredcites →https://doi.org/10.1534/genetics.105.047985openalex-snapshot
Chromosome Inversions, Local Adaptation and Speciation
inferredcites →https://doi.org/10.1534/genetics.105.053173openalex-snapshot
Patterns of Diversity and Linkage Disequilibrium Within the Cosmopolitan Inversion In(3R)Payne in Drosophila melanogaster Are Indicative of Coadaptation
inferredcites →https://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
inferredcites →https://doi.org/10.1534/genetics.107.086108openalex-snapshot
Chromosomal Rearrangement Inferred From Comparisons of 12 Drosophila Genomes
inferredcites →https://doi.org/10.1534/genetics.108.089409openalex-snapshot
Correlation-Based Inference for Linkage Disequilibrium With Multiple Alleles
inferredcites →https://doi.org/10.1534/genetics.110.123059openalex-snapshot
Genomic Differentiation Between Temperate and Tropical Australian Populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.111.137794openalex-snapshot
Ecological Genomics of Anopheles gambiae Along a Latitudinal Cline: A Population-Resequencing Approach
inferredcites →https://doi.org/10.1534/genetics.112.141622openalex-snapshot
Sequence-Based Detection and Breakpoint Assembly of Polymorphic Inversions
inferredcites →https://doi.org/10.1534/genetics.112.142018openalex-snapshot
Genomic Variation in Natural Populations ofDrosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.115.183566openalex-snapshot
A Segregating Inversion Generates Fitness Variation in Yellow Monkeyflower (Mimulus guttatus)
inferredcites →https://doi.org/10.1534/genetics.116.190389openalex-snapshot
Selection on Inversion Breakpoints Favors Proximity to Pairing Sensitive Sites in Drosophila melanogaster
inferredcites →https://doi.org/10.1534/genetics.116.191429openalex-snapshot
Genomics of Natural Populations: How Differentially Expressed Genes Shape the Evolution of Chromosomal Inversions in Drosophila pseudoobscura
inferredcites →https://doi.org/10.1554/02-577openalex-snapshot
EVOLUTIONARY PACE OF CHROMOSOMAL POLYMORPHISM IN COLONIZING POPULATIONS OF DROSOPHILA SUBOBSCURA: AN EVOLUTIONARY TIME SERIES
inferredcites →https://doi.org/10.1673/031.010.14141openalex-snapshot
Geographic Patterns of Inversion Polymorphism in the Second Chromosome of the CactophilicDrosophila buzzatiifrom Northeastern Argentina
inferredcites →https://doi.org/10.2298/gensr1503959sopenalex-snapshot
Four decades of inversion polymorphism in Drosophila pseudoobscura from Mexico
inferredcites →https://doi.org/10.2307/1942552openalex-snapshot
Proximal Causes of Natal Dispersal in Belding's Ground Squirrels (Spermophilus Beldingi)
inferredcites →https://doi.org/10.2307/2406763openalex-snapshot
Selection and Inversion Polymorphism in Experimental Populations of Drosophila pseudoobscura Initiated with the Chromosomal Constitutions of Natural Populations
inferredcites →https://doi.org/10.2307/2411044openalex-snapshot
Inversion Length and Breakpoint Distribution in the Drosophila buzzatii Species Complex: Is Inversion Length a Selected Trait?
inferredcites →https://doi.org/10.48550/arxiv.1207.3907openalex-snapshot
Haplotype-based variant detection from short-read sequencing
inferredcites →https://doi.org/10.5281/zenodo.10742696openalex-snapshot
Chromosomal races in Drosophila pseudoobscura and Drosophila persimilis.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ece3.71846openalex-snapshot
Genomic Landscape of High‐Altitude Adaptation in East African Mountain Honey Bees ( Apis mellifera )
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/10.1007/978-1-0716-0199-0_15openalex-snapshot
Population Genomics on the Fly: Recent Advances in Drosophila
inferred← citeshttps://doi.org/10.1007/s00412-020-00731-yopenalex-snapshot
Eight million years of maintained heterozygosity in chromosome homologs of cercopithecine monkeys
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.cois.2018.11.002openalex-snapshot
Evolutionary insights from large scale resequencing datasets in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.cois.2024.101280openalex-snapshot
Chromosomal inversions and their impact on insect evolution
inferred← citeshttps://doi.org/10.1016/j.tree.2018.04.002openalex-snapshot
Eco-Evolutionary Genomics of Chromosomal Inversions
inferred← citeshttps://doi.org/10.1017/s0007485324000579openalex-snapshot
Making sense of chromosome polymorphisms in two leptysmine grasshoppers
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/s41598-017-17650-1openalex-snapshot
Inversion evolutionary rates might limit the experimental identification of inversion breakpoints in non-model species
inferred← citeshttps://doi.org/10.1093/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/g3journal/jkag210openalex-snapshot
A population genomic resource for 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/evae263openalex-snapshot
Complex Genomic Landscape of Inversion Polymorphism in Europe's Most Destructive Forest Pest
inferred← citeshttps://doi.org/10.1093/gbe/evy239openalex-snapshot
Origin and Consequences of Chromosomal Inversions in thevirilisGroup ofDrosophila
inferred← citeshttps://doi.org/10.1093/icb/icaf040openalex-snapshot
Roles and Future Opportunities for Genomic Architecture in Understanding Repeated Evolution
inferred← citeshttps://doi.org/10.1093/iob/obac008openalex-snapshot
Does the Pachytene Checkpoint, a Feature of Meiosis, Filter Out Mistakes in Double-Strand DNA Break Repair and as a side-Effect Strongly Promote Adaptive Speciation?
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/jhered/esy057openalex-snapshot
Computational Sequence Analysis of Inversion Breakpoint Regions in the CactophilicDrosophila mojavensisLineage
inferred← citeshttps://doi.org/10.1093/molbev/msad118openalex-snapshot
An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation
inferred← citeshttps://doi.org/10.1098/rstb.2021.0206openalex-snapshot
The relevance of chromatin architecture to genome rearrangements in Drosophila
inferred← citeshttps://doi.org/10.1101/2025.05.02.651970openalex-snapshot
Evolutionary Influences on Local Patterns of Genetic Relatedness
inferred← citeshttps://doi.org/10.1101/504126openalex-snapshot
Extensive recombination suppression and chromosome-wide differentiation of a segregation distorter in Drosophila
inferred← citeshttps://doi.org/10.1111/1365-2656.13711openalex-snapshot
Understanding climate change response in the age of genomics
inferred← citeshttps://doi.org/10.1111/evo.14278openalex-snapshot
Inversions shape the divergence of Drosophila pseudoobscura and Drosophila persimilis on multiple timescales
inferred← citeshttps://doi.org/10.1111/jeb.14242openalex-snapshot
How chromosomal inversions reorient the evolutionary process
inferred← citeshttps://doi.org/10.1111/mec.14804openalex-snapshot
Dissecting the role of a large chromosomal inversion in life history divergence throughout the Mimulus guttatus species complex
inferred← citeshttps://doi.org/10.1111/mec.14921openalex-snapshot
Pervasive gene conversion in chromosomal inversion heterozygotes
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.16305openalex-snapshot
Stable inversion clines in a grasshopper species group despite complex geographical history
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/10.1371/journal.pbio.3003043openalex-snapshot
Incomplete recombination suppression fuels extensive haplotype diversity in a butterfly colour pattern supergene
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007526openalex-snapshot
Ancestral polymorphisms explain the role of chromosomal inversions in speciation
inferred← citeshttps://doi.org/10.1534/g3.119.400445openalex-snapshot
In Silico Karyotyping of Chromosomally Polymorphic Malaria Mosquitoes in the Anopheles gambiae Complex
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.120.303460openalex-snapshot
Extensive Recombination Suppression and Epistatic Selection Causes Chromosome-Wide Differentiation of a Selfish Sex Chromosome in Drosophila pseudoobscura
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/genes11020165openalex-snapshot
Chromosome and Genome Divergence between the Cryptic Eurasian Malaria Vector-Species Anopheles messeae and Anopheles daciae
inferred← citeshttps://doi.org/10.64898/2026.04.06.716560openalex-snapshot
Drosophila pseudoobscura third chromosome inversion arrangements have temperature-dependent and sex-specific effects on life history traits
inferred← citeshttps://doi.org/10.7554/elife.78981openalex-snapshot
Epistatic selection on a selfish Segregation Distorter supergene – drive, recombination, and genetic load
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.