On the public citation graph
Karyotype Diversification and Chromosome Rearrangements in Squamate Reptiles
0 signed · 109 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bies.200800182openalex-snapshot
The genome‐centric concept: resynthesis of evolutionary theory
inferredcites →https://doi.org/10.1007/bf00285830openalex-snapshot
Multiple sex-chromosomes in the common Indian Krait, Bungarus caeruleus Schneider
inferredcites →https://doi.org/10.1007/s00412-016-0585-6openalex-snapshot
New insights into sex chromosome evolution in anole lizards (Reptilia, Dactyloidae)
inferredcites →https://doi.org/10.1007/s10577-014-9403-2openalex-snapshot
Multiple sex chromosomes in the light of female meiotic drive in amniote vertebrates
inferredcites →https://doi.org/10.1007/s10709-006-9133-2openalex-snapshot
Banding patterns and chromosomal evolution in five species of neotropical Teiinae lizards (Squamata: Teiidae)
inferredcites →https://doi.org/10.1016/j.biosystems.2023.105016openalex-snapshot
Karyotype as code of codes: An inheritance platform to shape the pattern and scale of evolution
inferredcites →https://doi.org/10.1016/j.celrep.2022.111237openalex-snapshot
Single-chromosome fission yeast models reveal the configuration robustness of a functional genome
inferredcites →https://doi.org/10.1016/j.crvi.2008.07.010openalex-snapshot
The molecular evolutionary tree of lizards, snakes, and amphisbaenians
inferredcites →https://doi.org/10.1016/j.jcz.2017.04.006openalex-snapshot
When can chromosomes drive speciation? The peculiar case of the Malagasy tomato frogs (genus Dyscophus)
inferredcites →https://doi.org/10.1016/j.tree.2009.12.004openalex-snapshot
Evolutionary stasis: the stable chromosomes of birds
inferredcites →https://doi.org/10.1016/j.ympev.2015.10.009openalex-snapshot
Combining phylogenomic and supermatrix approaches, and a time-calibrated phylogeny for squamate reptiles (lizards and snakes) based on 52 genes and 4162 species
inferredcites →https://doi.org/10.1016/j.zool.2018.01.005openalex-snapshot
Cold-blooded in the Ice Age: “refugia within refugia”, inter-and intraspecific biogeographic diversification of European whipsnakes (Squamata, Colubridae, Hierophis)
inferredcites →https://doi.org/10.1016/s0169-5347(01)02187-5openalex-snapshot
Chromosomal rearrangements and speciation
inferredcites →https://doi.org/10.1017/s0016672300014051openalex-snapshot
Sex differences in fitness and selection for centric fusions between sex-chromosomes and autosomes
inferredcites →https://doi.org/10.1023/a:1009218628942openalex-snapshot
Chromosomal Polymorphisms Due to Supernumerary Chromosomes and Pericentric Inversions in the Eyelidless Microteiid Lizard Nothobachia Ablephara (Squamata, Gymnophthalmidae)
inferredcites →https://doi.org/10.1023/a:1009219126909openalex-snapshot
Supernumerary Chromosome Variation, Heteromorphic Sex Chromosomes and Banding Patterns in Microteiid Lizards of the Genus Micrablepharus (Squamata, Gymnophthalmidae)
inferredcites →https://doi.org/10.1038/hdy.2013.143openalex-snapshot
Comparative linkage maps suggest that fission, not polyploidy, underlies near-doubling of chromosome number within monkeyflowers (Mimulus; Phrymaceae)
inferredcites →https://doi.org/10.1038/nature10390openalex-snapshot
The genome of the green anole lizard and a comparative analysis with birds and mammals
inferredcites →https://doi.org/10.1038/s41437-018-0179-6openalex-snapshot
Conserved sex chromosomes and karyotype evolution in monitor lizards (Varanidae)
inferredcites →https://doi.org/10.1038/s41467-022-33319-4openalex-snapshot
Early stages of sympatric homoploid hybrid speciation in crater lake cichlid fishes
inferredcites →https://doi.org/10.1038/s41467-023-43012-9openalex-snapshot
Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs
inferredcites →https://doi.org/10.1038/s41559-022-01980-zopenalex-snapshot
Chromosome fusions repatterned recombination rate and facilitated reproductive isolation during Pristionchus nematode speciation
inferredcites →https://doi.org/10.1038/sj.hdy.6800697openalex-snapshot
Steps in the evolution of heteromorphic sex chromosomes
inferredcites →https://doi.org/10.1046/j.1525-142x.2000.00045.xopenalex-snapshot
Macroevolution is more than repeated rounds of microevolution
inferredcites →https://doi.org/10.1073/pnas.0605274103openalex-snapshot
Evidence for different origin of sex chromosomes in snakes, birds, and mammals and step-wise differentiation of snake sex chromosomes
inferredcites →https://doi.org/10.1073/pnas.0605578104openalex-snapshot
Chromosome-wide linkage disequilibrium as a consequence of meiotic drive
inferredcites →https://doi.org/10.1073/pnas.1701658114openalex-snapshot
Evolutionary strata on young mating-type chromosomes despite the lack of sexual antagonism
inferredcites →https://doi.org/10.1073/pnas.1730757100openalex-snapshot
Allopatric genetic origins for sympatric host-plant shifts and race formation in Rhagoletis
inferredcites →https://doi.org/10.1073/pnas.2112494118openalex-snapshot
Microchromosomes are building blocks of bird, reptile, and mammal chromosomes
inferredcites →https://doi.org/10.1073/pnas.221274498openalex-snapshot
Chromosomal inversions and the reproductive isolation of species
inferredcites →https://doi.org/10.1073/pnas.74.9.3942openalex-snapshot
Rapid speciation and chromosomal evolution in mammals.
inferredcites →https://doi.org/10.1080/00087114.1991.10797199openalex-snapshot
Description of the chromosomes of three lizard species belonging to the genusMabuya(Scincidae, Reptilia)
inferredcites →https://doi.org/10.1080/11250007709430179openalex-snapshot
Chromosomal Rearrangement, Reproductive Isolation and Speciation in Mammals. The Case ofMus Musculus
inferredcites →https://doi.org/10.1080/24750263.2023.2180547openalex-snapshot
Comparative cytogenetics of Hemorrhois hippocrepis and Malpolon monspessulanus highlights divergent karyotypes in Colubridae and Psammophiidae (Squamata: Serpentes)
inferredcites →https://doi.org/10.1093/evolut/qpad097openalex-snapshot
Microchromosome fusions underpin convergent evolution of chameleon karyotypes
inferredcites →https://doi.org/10.1093/g3journal/jkab036openalex-snapshot
Characterization of a pericentric inversion in plateau fence lizards ( Sceloporus tristichus ): evidence from chromosome-scale genomes
inferredcites →https://doi.org/10.1093/gbe/evab068openalex-snapshot
Chromosomal Inversion Polymorphisms in Two Sympatric Ascidian Lineages
inferredcites →https://doi.org/10.1093/genetics/134.2.487openalex-snapshot
The fertility effects of pericentric inversions in Drosophila melanogaster.
inferredcites →https://doi.org/10.1093/icb/icn049openalex-snapshot
Trends in the evolution of reptilian chromosomes
inferredcites →https://doi.org/10.1093/jhered/esad023openalex-snapshot
A lizard is never late: Squamate genomics as a recent catalyst for understanding sex chromosome and microchromosome evolution
inferredcites →https://doi.org/10.1093/jhered/esw053openalex-snapshot
Origin of Amniote Sex Chromosomes: An Ancestral Super-Sex Chromosome, or Common Requirements?
inferredcites →https://doi.org/10.1093/molbev/msab185openalex-snapshot
Chromosome Fusion Affects Genetic Diversity and Evolutionary Turnover of Functional Loci but Consistently Depends on Chromosome Size
inferredcites →https://doi.org/10.1093/molbev/msab212openalex-snapshot
Two Reference-Quality Sea Snake Genomes Reveal Their Divergent Evolution of Adaptive Traits and Venom Systems
inferredcites →https://doi.org/10.1093/molbev/msad043openalex-snapshot
Chromosome Fissions and Fusions Act as Barriers to Gene Flow between Brenthis Fritillary Butterflies
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111452openalex-snapshot
An Extraordinarily Low Diploid Chromosome Number in the Reptile Gonatodes taniae (Squamata, Gekkonidae)
inferredcites →https://doi.org/10.1093/sysbio/syz062openalex-snapshot
Interrogating Genomic-Scale Data for Squamata (Lizards, Snakes, and Amphisbaenians) Shows no Support for Key Traditional Morphological Relationships
inferredcites →https://doi.org/10.1093/zoolinnean/zlad153openalex-snapshot
Karyotype stasis but species-specific repetitive DNA patterns in Anguis lizards (Squamata: Anguidae), in the evolutionary framework of Anguiformes
inferredcites →https://doi.org/10.1098/rspb.1999.0603openalex-snapshot
Inbreeding, heterozygote advantage and the evolution of neo–X and neo–Y sex chromosomes
inferredcites →https://doi.org/10.1098/rstb.2019.0539openalex-snapshot
Speciation through chromosomal fusion and fission in Lepidoptera
inferredcites →https://doi.org/10.1098/rstb.2020.0099openalex-snapshot
Whole-chromosome fusions in the karyotype evolution of Sceloporus (Iguania, Reptilia) are more frequent in sex chromosomes than autosomes
inferredcites →https://doi.org/10.1101/gr.152660.112openalex-snapshot
Extensive chromosomal reshuffling drives evolution of virulence in an asexual pathogen
inferredcites →https://doi.org/10.1111/cla.12407openalex-snapshot
A species‐level total evidence phylogeny of the microteiid lizard family Alopoglossidae (Squamata: Gymnophthalmoidea)
inferredcites →https://doi.org/10.1111/ele.12728openalex-snapshot
Fast life history traits promote invasion success in amphibians and reptiles
inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01770.xopenalex-snapshot
Evidence for Gondwanan vicariance in an ancient clade of gecko lizards
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03194.xopenalex-snapshot
Hybridization between multiple fence lizard lineages in an ecotone: locally discordant variation in mitochondrial DNA, chromosomes, and morphology
inferredcites →https://doi.org/10.1111/jzo.12355openalex-snapshot
Non‐random accumulation of LINE1‐like sequences on differentiated snake W chromosomes
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.1249884openalex-snapshot
Fossilized Nuclei and Chromosomes Reveal 180 Million Years of Genomic Stasis in Royal Ferns
inferredcites →https://doi.org/10.1159/000130037openalex-snapshot
Cytotaxonomy and chromosomal evolution in Serpentes
inferredcites →https://doi.org/10.1159/000295789openalex-snapshot
Cytogenetics and Molecular Data in Snakes: A Phylogenetic Approach
inferredcites →https://doi.org/10.1159/000495974openalex-snapshot
Understanding the Evolution of Reptile Chromosomes through Applications of Combined Cytogenetics and Genomics Approaches
inferredcites →https://doi.org/10.1159/000497304openalex-snapshot
Isolation and Characterization of Interspersed Repeated Sequences in the Common Lizard, Zootoca vivipara, and Their Conservation in Squamata
inferredcites →https://doi.org/10.1186/1471-2148-13-93openalex-snapshot
A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes
inferredcites →https://doi.org/10.1186/1471-2148-14-40openalex-snapshot
The role of chromosome variation in the speciation of the red brocket deer complex: the study of reproductive isolation in females
inferredcites →https://doi.org/10.1186/1810-522x-52-60openalex-snapshot
Pattern of chromosomal changes in ‘beta’ Anolis (Norops group) (Squamata: Polychrotidae) depicted by an ancestral state analysis
inferredcites →https://doi.org/10.1186/s12862-016-0628-xopenalex-snapshot
Phylogenomics of a rapid radiation: is chromosomal evolution linked to increased diversification in north american spiny lizards (Genus Sceloporus)?
inferredcites →https://doi.org/10.1186/s12862-017-1044-6openalex-snapshot
Lack of satellite DNA species-specific homogenization and relationship to chromosomal rearrangements in monitor lizards (Varanidae, Squamata)
inferredcites →https://doi.org/10.1186/s12864-016-2774-3openalex-snapshot
Anchoring genome sequence to chromosomes of the central bearded dragon (Pogona vitticeps) enables reconstruction of ancestral squamate macrochromosomes and identifies sequence content of the Z chromosome
inferredcites →https://doi.org/10.13128/a_h-8437openalex-snapshot
First karyological analysis of the endemic Malagasy phantom gecko Matoatoa brevipes (Squamata: Gekkonidae)
inferredcites →https://doi.org/10.1371/journal.pone.0053027openalex-snapshot
Inference of the Protokaryotypes of Amniotes and Tetrapods and the Evolutionary Processes of Microchromosomes from Comparative Gene Mapping
inferredcites →https://doi.org/10.1371/journal.pone.0132380openalex-snapshot
Comparative Chromosome Painting and NOR Distribution Suggest a Complex Hybrid Origin of Triploid Lepidodactylus lugubris (Gekkonidae)
inferredcites →https://doi.org/10.1371/journal.pone.0134829openalex-snapshot
Karyotype Reorganization in the Hokou Gecko (Gekko hokouensis, Gekkonidae): The Process of Microchromosome Disappearance in Gekkota
inferredcites →https://doi.org/10.1371/journal.pone.0160274openalex-snapshot
Is the Karyotype of Neotropical Boid Snakes Really Conserved? Cytotaxonomy, Chromosomal Rearrangements and Karyotype Organization in the Boidae Family
inferredcites →https://doi.org/10.1371/journal.pone.0161070openalex-snapshot
A Species-Level Phylogeny of Extant Snakes with Description of a New Colubrid Subfamily and Genus
inferredcites →https://doi.org/10.1534/genetics.105.047985openalex-snapshot
Chromosome Inversions, Local Adaptation and Speciation
inferredcites →https://doi.org/10.1590/0001-3765201820170374openalex-snapshot
Comparative cytogenetic analysis in Erythrolamprus snakes (Serpentes: Dipsadidae) from Argentina
inferredcites →https://doi.org/10.2307/1441645openalex-snapshot
Chromosomes and the Systematics of the Family Teiidae (Sauria, Reptilia)
inferredcites →https://doi.org/10.3389/fgene.2014.00295openalex-snapshot
Assessing when chromosomal rearrangements affect the dynamics of speciation: implications from computer simulations
inferredcites →https://doi.org/10.3389/fgene.2017.00010openalex-snapshot
Chromosomal Speciation in the Genomics Era: Disentangling Phylogenetic Evolution of Rock-wallabies
inferredcites →https://doi.org/10.3389/fgene.2019.01082openalex-snapshot
What Is Karyotype Coding and Why Is Genomic Topology Important for Cancer and Evolution?
inferredcites →https://doi.org/10.3389/fgene.2020.00948openalex-snapshot
Partial Amniote Sex Chromosomal Linkage Homologies Shared on Snake W Sex Chromosomes Support the Ancestral Super-Sex Chromosome Evolution in Amniotes
inferredcites →https://doi.org/10.3389/fgene.2020.583827openalex-snapshot
Incomplete Sterility of Chromosomal Hybrids: Implications for Karyotype Evolution and Homoploid Hybrid Speciation
inferredcites →https://doi.org/10.3389/fmars.2019.00628openalex-snapshot
Overview on Karyotype Stasis in Atlantic Grunts (Eupercaria, Haemulidae) and the Evolutionary Extensions for Other Marine Fish Groups
inferredcites →https://doi.org/10.3390/ani12162054openalex-snapshot
First Insights on the Karyotype Diversification of the Endemic Malagasy Leaf-Toed Geckos (Squamata: Gekkonidae: Uroplatus)
inferredcites →https://doi.org/10.3390/ani13132068openalex-snapshot
Chromosome Diversity and Evolution of the Endemic Malagasy Velvet Geckos of the Genus Blaesodactylus (Reptilia, Gekkonidae)
inferredcites →https://doi.org/10.3390/cells10092182openalex-snapshot
Why Do Some Vertebrates Have Microchromosomes?
inferredcites →https://doi.org/10.3390/cells9102268openalex-snapshot
Revisiting the Karyotype Evolution of Neotropical Boid Snakes: A Puzzle Mediated by Chromosomal Fissions
inferredcites →https://doi.org/10.3390/genes12091341openalex-snapshot
Lizards as Model Organisms of Sex Chromosome Evolution: What We Really Know from a Systematic Distribution of Available Data?
inferredcites →https://doi.org/10.3390/genes14010178openalex-snapshot
Cytogenetic Analysis of Seven Species of Gekkonid and Phyllodactylid Geckos
inferredcites →https://doi.org/10.3390/genes14071387openalex-snapshot
The State of Squamate Genomics: Past, Present, and Future of Genome Research in the Most Speciose Terrestrial Vertebrate Order
inferredcites →https://doi.org/10.3390/genes8120382openalex-snapshot
Evolution of Karyotypes in Chameleons
inferredcites →https://doi.org/10.3390/genes9050239openalex-snapshot
Did Lizards Follow Unique Pathways in Sex Chromosome Evolution?
inferredcites →https://doi.org/10.3390/life14020181openalex-snapshot
First Cytogenetic Analysis of Hemidactylus mercatorius Gray, 1842 Provides Insights on Interspecific Chromosomal Diversification in the Genus Hemidactylus (Squamata: Gekkonidae)
inferredcites →https://doi.org/10.3897/compcytogen.v7i3.5398openalex-snapshot
Karyological evidence for diversification of Italian slow worm populations (Squamata, Anguidae)
inferredcites →https://doi.org/10.3897/compcytogen.v9i4.5371openalex-snapshot
Cytogenetic analyses of five amazon lizard species of the subfamilies Teiinae and Tupinambinae and review of karyotyped diversity the family Teiidae
inferredcites →https://doi.org/10.4238/gmr18701openalex-snapshot
Research Article The unusual high number of chromosomes signals rare multiple fission events in the Polynemidae (Carangaria, Teleostei)
inferredcites →https://doi.org/10.7554/elife.02630openalex-snapshot
Genome rearrangements and pervasive meiotic drive cause hybrid infertility in fission yeast
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/compcytogen.19.165160zenodo-depositor-declared
Comparative cytogenetics among populations of two Bothriurus species (Scorpiones, Bothriuridae)
inferred← citeshttps://doi.org/10.1093/g3journal/jkaf302openalex-snapshot
Telomere-to-telomere reference genome of the common five-lined skink, Plestiodon fasciatus (Squamata: Scincidae)
inferred← citeshttps://doi.org/10.1134/s1022795425701455openalex-snapshot
Immunocytological Identification of Nucleoli in Spermatocytes of Three Viper Species of the Genus Vipera
inferred← citeshttps://doi.org/10.1186/s12915-026-02540-8openalex-snapshot
Chromosomal rearrangements and segmental deletions contribute to gene loss in squamates
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011772openalex-snapshot
Recombination plasticity in response to temperature variation in reptiles
inferred← citeshttps://doi.org/10.3390/ani14111708openalex-snapshot
Comparative Cytogenetics of the Malagasy Ground Geckos of the Paroedura bastardi and Paroedura picta Species Groups
inferred← citeshttps://doi.org/10.3390/ani14192818openalex-snapshot
New Insights on Chromosome Diversification in Malagasy Chameleons
inferred← citeshttps://doi.org/10.3390/ani15020168openalex-snapshot
Sex Determination in Reptiles: A Review
inferred← citeshttps://doi.org/10.3390/biology14111601openalex-snapshot
Towards a Research Programme Aiming at Causes and Consequences of Reticulate Evolution
inferred← citeshttps://doi.org/10.3390/ijms26104540openalex-snapshot
Evolution of ZW Sex Chromosomes in Ptyas Snakes (Reptilia, Colubridae): New Insights from a Molecular Cytogenetic Perspective
inferred← citeshttps://doi.org/10.64898/2026.05.21.726861openalex-snapshot
Genomic Architecture, Differentiation, and Adaptation in Three Large Falcons
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.