On the public citation graph

Genomic evidence for role of inversion 3 RP of Drosophila melanogaster in facilitating climate change adaptation

0 signed · 105 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.
Claim with ORCID
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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferreduses_data →https://doi.org/10.5281/zenodo.10723540zenodo-depositor-declared
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/s10709-006-7375-7openalex-snapshot
The association between inversion In(3R)Payne and clinally varying traits in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s10709-006-9010-zopenalex-snapshot
Climatic selection on genes and traits after a 100 year-old invasion: a critical look at the temperate-tropical clines in Drosophila melanogaster from eastern Australia
inferredcites →https://doi.org/10.1016/j.ajhg.2009.01.005openalex-snapshot
A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
inferredcites →https://doi.org/10.1017/s0016672301004955openalex-snapshot
Inversion polymorphisms and nucleotide variability in Drosophila
inferredcites →https://doi.org/10.1038/75556openalex-snapshot
Gene Ontology: tool for the unification of biology
inferredcites →https://doi.org/10.1038/hdy.2013.38openalex-snapshot
A sequential coalescent algorithm for chromosomal inversions
inferredcites →https://doi.org/10.1038/nature10341openalex-snapshot
Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry
inferredcites →https://doi.org/10.1046/j.1420-9101.2003.00560.xopenalex-snapshot
Latitudinal countergradient variation in the common frog ( Rana temporaria ) development rates – evidence for local adaptation
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00380.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.1432900100openalex-snapshot
Evolutionary genomics of inversions in Drosophila pseudoobscura : Evidence for epistasis
inferredcites →https://doi.org/10.1093/bioinformatics/bth457openalex-snapshot
Haploview: analysis and visualization of LD and haplotype maps
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/bioinformatics/btr330openalex-snapshot
The variant call format and VCFtools
inferredcites →https://doi.org/10.1093/bioinformatics/bts315openalex-snapshot
Gowinda: unbiased analysis of gene set enrichment for genome-wide association studies
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
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/165.2.667openalex-snapshot
Testing for Asymmetrical Gene Flow in a Drosophila melanogaster Body-Size Cline
inferredcites →https://doi.org/10.1093/genetics/91.3.581openalex-snapshot
SELECTION ON RECOMBINATION IN CLINES
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/nar/gks1024openalex-snapshot
FlyBase: improvements to the bibliography
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.631202openalex-snapshot
Interrogating a High-Density SNP Map for Signatures of Natural Selection
inferredcites →https://doi.org/10.1111/j.1365-2583.2012.01149.xopenalex-snapshot
A proline repeat polymorphism of the Frost gene of Drosophila melanogaster showing clinal variation but not associated with cold resistance
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.2012.05731.xopenalex-snapshot
Genome‐wide patterns of latitudinal differentiation among populations of D rosophila melanogaster from N orth A merica
inferredcites →https://doi.org/10.1111/j.1420-9101.2010.02136.xopenalex-snapshot
Recombination and selection in the maintenance of the adaptive value of inversions
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00835.xopenalex-snapshot
CLINAL PATTERNS OF CHROMOSOMAL INVERSION POLYMORPHISMS INDROSOPHILA SUBOBSCURAARE PARTLY ASSOCIATED WITH THERMAL PREFERENCES AND HEAT STRESS RESISTANCE
inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01836.xopenalex-snapshot
REPRODUCTIVE ISOLATION AND LOCAL ADAPTATION QUANTIFIED FOR A CHROMOSOME INVERSION IN A MALARIA MOSQUITO
inferredcites →https://doi.org/10.1111/mec.12276openalex-snapshot
RAD seq underestimates diversity and introduces genealogical biases due to nonrandom haplotype sampling
inferredcites →https://doi.org/10.1111/mec.12360openalex-snapshot
Estimation of population allele frequencies from next‐generation sequencing data: pool‐versus individual‐based genotyping
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/10.1126/science.1080600openalex-snapshot
Chromosomal Speciation and Molecular Divergence--Accelerated Evolution in Rearranged Chromosomes
inferredcites →https://doi.org/10.1126/science.1109523openalex-snapshot
A Rapid Shift in a Classic Clinal Pattern in Drosophila Reflecting Climate Change
inferredcites →https://doi.org/10.1126/science.287.5461.2185openalex-snapshot
The Genome Sequence of Drosophila melanogaster
inferredcites →https://doi.org/10.1136/jmg.8.4.545-bopenalex-snapshot
Genetics of the Evolutionary Process
inferredcites →https://doi.org/10.1146/annurev.ecolsys.39.110707.173532openalex-snapshot
Revisiting the Impact of Inversions in Evolution: From Population Genetic Markers to Drivers of Adaptive Shifts and Speciation?
inferredcites →https://doi.org/10.1186/1471-2148-13-100openalex-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/10.1371/journal.pbio.1000313openalex-snapshot
Genome Sequence of the Pea Aphid Acyrthosiphon pisum
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.pgen.0030217openalex-snapshot
Localization of Candidate Regions Maintaining a Common Polymorphic Inversion (2La) in Anopheles gambiae
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.pone.0037135openalex-snapshot
Double Digest RADseq: An Inexpensive Method for De Novo SNP Discovery and Genotyping in Model and Non-Model Species
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.105.041947openalex-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.106.057562openalex-snapshot
A Nonself Recognition Gene Complex inNeurospora crassa
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.114.161463openalex-snapshot
Parallel Geographic Variation in Drosophila melanogaster
inferredcites →https://doi.org/10.4161/fly.19695openalex-snapshot
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff

What points at this work

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

inferred← citeshttps://doi.org/10.1002/ece3.2995openalex-snapshot
Bioclimatic transect networks: Powerful observatories of ecological change
inferred← citeshttps://doi.org/10.1002/ece3.70443openalex-snapshot
Long‐Term Maintenance of Complex Chromosomal Inversion Polymorphism in Drosophila mediopunctata
inferred← citeshttps://doi.org/10.1002/ece3.7428openalex-snapshot
An endangered flightless grasshopper with strong genetic structure maintains population genetic variation despite extensive habitat loss
inferred← citeshttps://doi.org/10.1002/ps.5700openalex-snapshot
Climate change and the genetics of insecticide resistance
inferred← citeshttps://doi.org/10.1007/13836_2019_69openalex-snapshot
Population Genomics and Wildlife Adaptation in the Face of Climate Change
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/s10682-021-10111-2openalex-snapshot
Bucking the trend of pollinator decline: the population genetics of a range expanding bumblebee
inferred← citeshttps://doi.org/10.1007/s10709-018-0035-xopenalex-snapshot
Climatic adaptation of chromosomal inversions in Drosophila subobscura
inferred← citeshttps://doi.org/10.1016/j.tig.2015.05.006openalex-snapshot
Revisiting classic clines in Drosophila melanogaster in the age of genomics
inferred← citeshttps://doi.org/10.1016/j.tig.2017.03.003openalex-snapshot
Variation in Recombination Rate: Adaptive or Not?
inferred← citeshttps://doi.org/10.1016/j.tree.2018.04.002openalex-snapshot
Eco-Evolutionary Genomics of Chromosomal Inversions
inferred← citeshttps://doi.org/10.1016/s2095-3119(18)62042-8openalex-snapshot
Adaptation of Drosophila species to climate change — A literature review since 2003
inferred← citeshttps://doi.org/10.1038/s41559-019-0837-yopenalex-snapshot
The spread of resistance to imidacloprid is restricted by thermotolerance in natural populations of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/s41598-020-79720-1openalex-snapshot
Demographic analyses of a new sample of haploid genomes from a Swedish population of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1038/srep23754openalex-snapshot
Inversions and adaptation to the plant toxin ouabain shape DNA sequence variation within and between chromosomal inversions of Drosophila subobscura.
inferred← citeshttps://doi.org/10.1073/pnas.1806760115openalex-snapshot
Systems genetic analysis of inversion polymorphisms in the malaria mosquito Anopheles gambiae
inferred← citeshttps://doi.org/10.1073/pnas.2513080122openalex-snapshot
Ancestral and local adaptation contribute to dispersal out of the Qinghai–Tibet Plateau in a bumblebee
inferred← citeshttps://doi.org/10.1093/bioinformatics/btz498openalex-snapshot
Estimation of population genetic parameters using an EM algorithm and sequence data from experimental evolution populations
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/evw057openalex-snapshot
“Islands of Divergence” in the Atlantic Cod Genome Represent Polymorphic Chromosomal Rearrangements
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/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/msad118openalex-snapshot
An Ancestral Balanced Inversion Polymorphism Confers Global Adaptation
inferred← citeshttps://doi.org/10.1093/molbev/msw016openalex-snapshot
Genomic Evidence for Adaptive Inversion Clines inDrosophila melanogaster
inferred← citeshttps://doi.org/10.1101/053371openalex-snapshot
Range Overlap Drives Chromosome Inversion Fixation in Passerine Birds
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/10.1101/2025.07.01.662526openalex-snapshot
Selection inference in a complex genomic landscape: the impact of polymorphic inversions
inferred← citeshttps://doi.org/10.1101/313759openalex-snapshot
Genomic analysis of European Drosophila melanogaster populations reveals longitudinal structure, continent-wide selection, and previously unknown DNA viruses
inferred← citeshttps://doi.org/10.1111/brv.12709openalex-snapshot
Eco‐genetics of desiccation resistance in Drosophila
inferred← citeshttps://doi.org/10.1111/ens.12398openalex-snapshot
Global warming and chromosomal inversion adaptation in isolated islands:Drosophila subobscurapopulations from Madeira
inferred← citeshttps://doi.org/10.1111/gcb.16512openalex-snapshot
Rapid adaptation in a fast‐changing world: Emerging insights from insect genomics
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/jeb.13310openalex-snapshot
An inversion supergene in Drosophila underpins latitudinal clines in survival traits
inferred← citeshttps://doi.org/10.1111/mec.14051openalex-snapshot
Genetic architecture and balancing selection: the life and death of differentiated variants
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.16305openalex-snapshot
Stable inversion clines in a grasshopper species group despite complex geographical history
inferred← citeshttps://doi.org/10.1111/mec.16752openalex-snapshot
Genomic profiling of climate adaptation in Aedes aegypti along an altitudinal gradient in Nepal indicates nongradual expansion of the disease vector
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.17708openalex-snapshot
The Evolution of Locally Adaptive Chromosome Inversions in Mimulus guttatus
inferred← citeshttps://doi.org/10.1186/s12862-018-1178-1openalex-snapshot
Patterns of geographic variation of thermal adapted candidate genes in Drosophila subobscura sex chromosome arrangements
inferred← citeshttps://doi.org/10.1186/s12862-020-01629-0openalex-snapshot
Analysis of structural variants in four African cichlids highlights an association with developmental and immune related genes
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/10.1590/0074-02760150470openalex-snapshot
Anopheles darlingi polytene chromosomes: revised maps including newly described inversions and evidence for population structure in Manaus
inferred← citeshttps://doi.org/10.3389/fphys.2018.00822openalex-snapshot
Enhancing Ebony? Common Associations With a cis-Regulatory Haplotype for Drosophila melanogaster Thoracic Pigmentation in a Japanese Population and Australian Populations
inferred← citeshttps://doi.org/10.3390/insects14070596openalex-snapshot
The Adaptive Value of Chromosomal Inversions and Climatic Change—Studies on the Natural Populations of Drosophila subobscura from the Balkans
inferred← citeshttps://doi.org/10.5038/1827-806x.52.1.2446openalex-snapshot
Why the delay in recognizing terrestrial obligate cave species in the tropics?
inferred← citeshttps://doi.org/10.5772/intechopen.73246openalex-snapshot
Drosophila Chromosomal Polymorphism: From Population Aspects to Origin Mechanisms of Inversions
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.