On the public citation graph

Nuclear and Mitochondrial DNA Comparisons Reveal Extreme Rate Variation in the Molecular Clock

0 signed · 317 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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.

inferredcites →https://doi.org/10.1002/ajpa.1330270504openalex-snapshot
Primate evolution: Evidence from the fossil record, comparative morphology, and molecular biology
inferredcites →https://doi.org/10.1007/bf00293186openalex-snapshot
Single copy DNA and structural gene sequence relationships among four sea urchin species
inferredcites →https://doi.org/10.1007/bf01731580openalex-snapshot
Evolution of sea urchin non-repetitive DNA
inferredcites →https://doi.org/10.1007/bf01734101openalex-snapshot
Mitochondrial DNA sequences of primates: Tempo and mode of evolution
inferredcites →https://doi.org/10.1007/bf02100221openalex-snapshot
Molecular clock of silent substitution: At least six-fold preponderance of silent changes in mitochondrial genes over those in nuclear genes
inferredcites →https://doi.org/10.1007/bf02100996openalex-snapshot
Mitochondrial DNA evolution in themelanogaster species subgroup ofDrosophila
inferredcites →https://doi.org/10.1007/bf02101980openalex-snapshot
The phylogeny of the hominoid primates, as indicated by DNA-DNA hybridization
inferredcites →https://doi.org/10.1016/0012-1606(72)90051-6openalex-snapshot
Evolution of mitochondrial DNA sequences in Xenopus
inferredcites →https://doi.org/10.1016/0092-8674(78)90044-2openalex-snapshot
The single-copy DNA sequence polymorphism of the sea urchin strongylocentrotus purpuratus
inferredcites →https://doi.org/10.1038/297541a0openalex-snapshot
The relationships of Sivapithecus and Ramapithecus and the evolution of the orang-utan
inferredcites →https://doi.org/10.1073/pnas.76.4.1967openalex-snapshot
Rapid evolution of animal mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.77.6.3605openalex-snapshot
Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis.
inferredcites →https://doi.org/10.1073/pnas.78.4.2432openalex-snapshot
Evolutionary tree for apes and humans based on cleavage maps of mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.80.15.4614openalex-snapshot
Comparison of sea urchin and human mtDNA: evolutionary rearrangement.
inferredcites →https://doi.org/10.1073/pnas.83.23.9090openalex-snapshot
Rates of nucleotide substitution in Drosophila mitochondrial DNA and nuclear DNA are similar.
inferredcites →https://doi.org/10.1093/genetics/104.4.699openalex-snapshot
LENGTH MUTATIONS IN HUMAN MITOCHONDRIAL DNA
inferredcites →https://doi.org/10.1093/genetics/105.1.207openalex-snapshot
MAXIMUM LIKELIHOOD ESTIMATION OF THE NUMBER OF NUCLEOTIDE SUBSTITUTIONS FROM RESTRICTION SITES DATA
inferredcites →https://doi.org/10.1093/nar/4.5.1257openalex-snapshot
Estimation of DNA sequence divergence from comparison of restriction endonuclease digests
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040333openalex-snapshot
Methods for computing the standard errors of branching points in an evolutionary tree and their application to molecular data from humans and apes.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040391openalex-snapshot
Temporal scaling of molecular evolution in primates and other mammals.
inferredcites →https://doi.org/10.1111/j.1432-0436.1978.tb00939.xopenalex-snapshot
The Evolution of Nonrepetitive DNA in Sea Urchins* *Submitted by M. M. Harpold to the Department of Biology, Tulane University in partial fulfillment of the requirements for the doctor of philosophy degree
inferredcites →https://doi.org/10.1111/j.1749-6632.1981.tb46515.xopenalex-snapshot
MECHANISMS OF EVOLUTION IN ANIMAL MITOCHONDRIAL DNA
inferredcites →https://doi.org/10.1126/science.200.4346.1183openalex-snapshot
Response : Do Albumin Clocks Run on Time?
inferredcites →https://doi.org/10.1126/science.3082006openalex-snapshot
Rates of DNA Sequence Evolution Differ Between Taxonomic Groups

What points at this work

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

inferred← citeshttps://doi.org/10.26028/cybium/2020-442-004zenodo-depositor-declared
A new species of Sicyopterus (Teleostei: Gobioidei: Sicydiinae) from Papua New Guinea
inferred← citeshttps://doi.org/10.26028/cybium/2023-011zenodo-depositor-declared
Stenogobius (Teleostei: Gobioidei) from the Indian-Pacific island rivers
inferred← citeshttps://doi.org/10.1002/9781118496411.ch2openalex-snapshot
DNA, Genomes and Genetic Variation
inferred← citeshttps://doi.org/10.1002/ajpa.1330300506openalex-snapshot
Nucleic acid evidence bearing on hominoid relationships
inferred← citeshttps://doi.org/10.1002/ajpa.1330300510openalex-snapshot
Genetics and history of sub-Saharan Africa
inferred← citeshttps://doi.org/10.1002/jsfa.10793openalex-snapshot
Development of duplex real‐time polymerase chain reaction for simultaneous detection of oilfish‑ and escolar‐derived components
inferred← citeshttps://doi.org/10.1002/jsfa.11507openalex-snapshot
The development of genus‐specific and species‐specific real‐time PCR assays for the authentication of P atagonian toothfish and A ntarctic toothfish in commercial seafood products
inferred← citeshttps://doi.org/10.1006/fstl.2000.0630openalex-snapshot
PCR-RFLP Analysis of Mitochondrial DNA: Differentiation of Fish Species
inferred← citeshttps://doi.org/10.1006/jasc.2001.0693openalex-snapshot
Re-examination of Ancient DNA in Texas Rock Paintings
inferred← citeshttps://doi.org/10.1006/mpev.2000.0885openalex-snapshot
Recombination among Multiple Mitochondrial Pseudogenes from a Passerine Genus
inferred← citeshttps://doi.org/10.1006/mpev.2000.0902openalex-snapshot
A Molecular Biogeographic Analysis of the Relationship between North American Melanoploid Grasshoppers and Their Eurasian and South American Relatives
inferred← citeshttps://doi.org/10.1006/mpev.2001.0962openalex-snapshot
Retrieval of Four Adaptive Lineages in Duiker Antelope: Evidence from Mitochondrial DNA Sequences and Fluorescence in Situ Hybridization
inferred← citeshttps://doi.org/10.1007/3-540-45784-4_22openalex-snapshot
Estimating the Deviation from a Molecular Clock
inferred← citeshttps://doi.org/10.1007/978-1-4020-5614-7_1257openalex-snapshot
Genetic Susceptibility
inferred← citeshttps://doi.org/10.1007/978-3-031-28624-7_1openalex-snapshot
Philosophy of Science
inferred← citeshttps://doi.org/10.1007/978-3-031-28624-7_11openalex-snapshot
Metabolic/Endocrine Disorders
inferred← citeshttps://doi.org/10.1007/978-3-031-28624-7_5openalex-snapshot
Critical Thinking Identifies Misconceptions and False Trails
inferred← citeshttps://doi.org/10.1007/978-3-0348-7527-1_24openalex-snapshot
Developing model systems for molecular biogeography: Vicariance and interchange in marine invertebrates
inferred← citeshttps://doi.org/10.1007/978-3-0348-7527-1_29openalex-snapshot
Diversity within diversity: Molecular approaches to studying microbial interactions with insects
inferred← citeshttps://doi.org/10.1007/978-3-319-07623-2_3openalex-snapshot
A Preliminary Transcriptomic Study of Galaxiid Fishes Reveals a Larval Glycoprotein Gene Under Strong Positive Selection
inferred← citeshttps://doi.org/10.1007/978-3-642-59884-5_17openalex-snapshot
The Control of Ageing and Mitochondria
inferred← citeshttps://doi.org/10.1007/978-3-642-72236-3_3openalex-snapshot
Origin and Phylogeny of Metazoans as Reconstructed with rDNA Sequences
inferred← citeshttps://doi.org/10.1007/978-3-642-78650-1_13openalex-snapshot
Literaturverzeichnis
inferred← citeshttps://doi.org/10.1007/978-3-642-83962-7_3openalex-snapshot
Variation at the DNA Level: Something for Everyone
inferred← citeshttps://doi.org/10.1007/978-3-642-83962-7_4openalex-snapshot
Molecular Systematics at the Species Boundary: Exploiting Conserved and Variable Regions of the Mitochondrial Genome of Animals via Direct Sequencing from Amplified DNA
inferred← citeshttps://doi.org/10.1007/978-3-662-06303-3_4openalex-snapshot
Molecular Evolution
inferred← citeshttps://doi.org/10.1007/978-94-011-1606-0_71openalex-snapshot
Hierarchal gene trees and molecular phylogeny of the Rotifera: use of the Polymerase Chain Reaction (PCR) to dissect ecological and evolutionary patterns
inferred← citeshttps://doi.org/10.1007/978-94-011-2052-4_19openalex-snapshot
Molecular approaches to the study of evolution and phylogeny of the Nemertina
inferred← citeshttps://doi.org/10.1007/978-94-011-3092-9_4openalex-snapshot
Molecular and cytological investigations
inferred← citeshttps://doi.org/10.1007/bf00013373openalex-snapshot
Molecular approaches to the study of evolution and phylogeny of the Nemertina
inferred← citeshttps://doi.org/10.1007/bf00025884openalex-snapshot
Hierarchal gene trees and molecular phylogeny of the Rotifera: use of the Polymerase Chain Reaction (PCR) to dissect ecological and evolutionary patterns
inferred← citeshttps://doi.org/10.1007/bf00160483openalex-snapshot
Tempo and mode of mitochondrial DNA evolution in vertebrates at the amino acid sequence level: Rapid evolution in warm-blooded vertebrates
inferred← citeshttps://doi.org/10.1007/bf00173152openalex-snapshot
Faster evolutionary rates in endosymbiotic bacteria than in cospeciating insect hosts
inferred← citeshttps://doi.org/10.1007/bf00173173openalex-snapshot
The sequence, organization, and evolution of the Locusta migratoria mitochondrial genome
inferred← citeshttps://doi.org/10.1007/bf00173176openalex-snapshot
Increased genetic diversity in mitochondrial genes is correlated with the evolution of parasitism in the Hymenoptera
inferred← citeshttps://doi.org/10.1007/bf00176090openalex-snapshot
The cytochrome b region in the mitochondrial DNA of the ant Tetraponera rufoniger: Sequence divergence in hymenoptera may be associated with nucleotide content
inferred← citeshttps://doi.org/10.1007/bf00178250openalex-snapshot
High rates of nucleotide substitution in nuclear small-subunit (18S) rDNA from holoparasitic flowering plants
inferred← citeshttps://doi.org/10.1007/bf00182393openalex-snapshot
Three patterns of mitochondrial DNA nucleotide divergence in the meadow vole, Microtus pennsylvanicus
inferred← citeshttps://doi.org/10.1007/bf00310808openalex-snapshot
Multi-copy nuclear pseudogenes of mitochondrial DNA reveal recent acute genetic changes in the human genome
inferred← citeshttps://doi.org/10.1007/bf00349391openalex-snapshot
Molecular and morphometric variation in European populations of the articulate brachiopod Terebratulina retusa
inferred← citeshttps://doi.org/10.1007/bf00566059openalex-snapshot
T4 phage evolution data in terms of a time-dependent Topal-Fresco mechanism
inferred← citeshttps://doi.org/10.1007/bf01647289openalex-snapshot
Comparative studies of avian DNA by restriction fragment length polymorphism analysis: Convenient procedures based on blood samples from live birds
inferred← citeshttps://doi.org/10.1007/bf02099730openalex-snapshot
Synonymous nucleotide substitution rates of β-tubulin and histone genes conform to high overall genomic rates in rodents but not in sea urchins
inferred← citeshttps://doi.org/10.1007/bf02100116openalex-snapshot
Rates of molecular evolution and the fraction of nucleotide positions free to vary
inferred← citeshttps://doi.org/10.1007/bf02103430openalex-snapshot
Mitochondrial DNA evolution in theDrosophila nasuta subgroup of species
inferred← citeshttps://doi.org/10.1007/bf02109480openalex-snapshot
Mitochondrial DNA evolution in primates: Transition rate has been extremely low in the lemur
inferred← citeshttps://doi.org/10.1007/bf02111280openalex-snapshot
On the molecular evolutionary clock
inferred← citeshttps://doi.org/10.1007/bf02111281openalex-snapshot
DNA turnover and the molecular clock
inferred← citeshttps://doi.org/10.1007/bf02111283openalex-snapshot
Evolution in bacteria: Evidence for a universal substitution rate in cellular genomes
inferred← citeshttps://doi.org/10.1007/bf02111289openalex-snapshot
Tempo and mode of sequence evolution in mitochondrial DNA of HawaiianDrosophila
inferred← citeshttps://doi.org/10.1007/pl00006321openalex-snapshot
Mitochondrial DNA of the coral sarcophyton glaucum contains a gene for a homologue of bacterial muts: A possible case of gene transfer from the nucleus to the mitochondrion
inferred← citeshttps://doi.org/10.1007/pl00006336openalex-snapshot
The Molecular Clock Runs at Different Rates Among Closely Related Members of a Gene Family
inferred← citeshttps://doi.org/10.1007/s00239-003-2513-7openalex-snapshot
Relative Rates of Nucleotide Substitution in Frogs
inferred← citeshttps://doi.org/10.1007/s002390010132openalex-snapshot
The Rates of Molecular Evolution in Rodent and Primate Mitochondrial DNA
inferred← citeshttps://doi.org/10.1007/s00338-007-0248-4openalex-snapshot
DNA barcoding as a tool for coral reef conservation
inferred← citeshttps://doi.org/10.1007/s00606-015-1269-zopenalex-snapshot
Mode and tempo of sequence and floral evolution within the Anserineae
inferred← citeshttps://doi.org/10.1007/s10528-015-9668-yopenalex-snapshot
Mitochondrial DNA-Based Analyses of Relatedness Among Turkeys, Meleagris gallopavo
inferred← citeshttps://doi.org/10.1016/0020-7519(96)82612-9openalex-snapshot
Molecular genetic approaches to parasite identification: their value in diagnostic parasitology and systematics
inferred← citeshttps://doi.org/10.1016/0022-2836(88)90452-4openalex-snapshot
Nucleotide sequence and gene organization of sea urchin mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/0040-5809(90)90012-kopenalex-snapshot
Towards a unified Theory of Molecular Evolution (TME)
inferred← citeshttps://doi.org/10.1016/0169-5347(89)90006-2openalex-snapshot
Animal mitochondrial DNA as a genetic marker in population and evolutionary biology
inferred← citeshttps://doi.org/10.1016/0169-5347(94)90176-7openalex-snapshot
Thermal habit, metabolic rate and the evolution of mitochondrial DNA
inferred← citeshttps://doi.org/10.1016/0303-2647(88)90011-1openalex-snapshot
Ribosomal RNA and the major lines of evolution: a perspective
inferred← citeshttps://doi.org/10.1016/0378-1119(87)90281-2openalex-snapshot
Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase
inferred← citeshttps://doi.org/10.1016/0378-1119(94)90065-5openalex-snapshot
Evolutionary trail of the mitochondrial genome as based on human 16S rDNA pseudogenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-152517-0.50008-6openalex-snapshot
Mitochondrial Myopathies: Genetic Aspects
inferred← citeshttps://doi.org/10.1016/b978-0-12-480553-8.50025-0openalex-snapshot
Bibliography
inferred← citeshttps://doi.org/10.1016/b978-012361160-4/50074-8openalex-snapshot
References
inferred← citeshttps://doi.org/10.1016/b978-012417540-2/50009-9openalex-snapshot
Fish Biogeography and Molecular Clocks: Perspectives from the Panamanian Isthmus
inferred← citeshttps://doi.org/10.1016/b978-012498315-1/50002-9openalex-snapshot
Molecular Evolution of the Mitochondrial Genome
inferred← citeshttps://doi.org/10.1016/j.foodcont.2005.01.001openalex-snapshot
Species identification in salted products of red snappers by semi-nested PCR–RFLP based on the mitochondrial 12S rRNA gene sequence
inferred← citeshttps://doi.org/10.1016/j.foodcont.2005.01.011openalex-snapshot
Species identification in salted products of red snappers by semi-nested PCR-RFLP based on the mitochondrial 12S rRNA gene sequence
inferred← citeshttps://doi.org/10.1016/j.foodcont.2005.11.002openalex-snapshot
Using the PCR–RFLP method to identify the species of different processed products of billfish meats
inferred← citeshttps://doi.org/10.1016/j.gde.2023.102053openalex-snapshot
When and why are mitochondria paternally inherited?
inferred← citeshttps://doi.org/10.1016/j.gene.2011.09.009openalex-snapshot
Evaluation of the 16S and 12S rRNA genes as universal markers for the identification of commercial fish species in South Africa
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148954openalex-snapshot
Characterization of the complete mitochondrial genomes of four tarantulas (Arachnida: Theraphosidae) with phylogenetic analysis
inferred← citeshttps://doi.org/10.1016/j.lwt.2018.04.031openalex-snapshot
Purification procedures meaningfully influence DNA quantification in milk
inferred← citeshttps://doi.org/10.1016/j.marenvres.2025.107450openalex-snapshot
Assessing the efficiency of COI primers in eDNA metabarcoding for marine metazoan biodiversity
inferred← citeshttps://doi.org/10.1016/j.meegid.2010.04.008openalex-snapshot
Phylogenetic inference of Indian malaria vectors from multilocus DNA sequences
inferred← citeshttps://doi.org/10.1016/j.meegid.2017.10.008openalex-snapshot
Inter-individual and intragenomic variations in the ITS region of Clonorchis sinensis (Trematoda: Opisthorchiidae) from Russia and Vietnam
inferred← citeshttps://doi.org/10.1016/j.ympev.2003.10.013openalex-snapshot
Molecular phylogenetics and biogeography of transisthmian and amphi-Atlantic needlefishes (Belonidae: Strongylura and Tylosurus): perspectives on New World marine speciation
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.12.015openalex-snapshot
Reconstructing the phylogenetic relationships of the earth’s most diverse clade of freshwater fishes—order Cypriniformes (Actinopterygii: Ostariophysi): A case study using multiple nuclear loci and the mitochondrial genome
inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106754openalex-snapshot
A taxonomic conundrum: Characterizing a cryptic radiation of Asian gracile skinks (Squamata: Scincidae: Riopa) in Myanmar
inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108448openalex-snapshot
Hidden diversity in the driest desert on Earth: genomics unveils cryptic diversity in an ancient South American gecko lineage (Phyllodactylidae, Garthia)
inferred← citeshttps://doi.org/10.1016/s0022-5193(05)80297-8openalex-snapshot
Koinophilia groups sexual creatures into species, promotes stasis, and stabilizes social behaviour
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)62066-5openalex-snapshot
Animal Mitochondrial DNA: Structure and Evolution
inferred← citeshttps://doi.org/10.1016/s0166-6851(98)00102-9openalex-snapshot
The mitochondrial genome of Onchocerca volvulus: Sequence, structure and phylogenetic analysis
inferred← citeshttps://doi.org/10.1016/s0169-5347(00)89195-8openalex-snapshot
Is mitochondrial DNA a strictly neutral marker?
inferred← citeshttps://doi.org/10.1016/s0304-3975(99)00028-6openalex-snapshot
A few logs suffice to build (almost) all trees: Part II
inferred← citeshttps://doi.org/10.1016/s0305-1978(00)00027-2openalex-snapshot
Genetic divergence between three sea urchin species of the genus Strongylocentrotus from the Sea of Japan
inferred← citeshttps://doi.org/10.1016/s1383-5742(98)00003-9openalex-snapshot
Monitoring for induced heritable mutations in natural populations: application of minisatellite DNA screening
inferred← citeshttps://doi.org/10.1016/s1568-1637(02)00015-6openalex-snapshot
Aging is a deprivation syndrome driven by a germ–soma conflict
inferred← citeshttps://doi.org/10.1017/s0031182003004359openalex-snapshot
Echinococcus granulosus strain typing in North Africa: comparison of eight nuclear and mitochondrial DNA fragments
inferred← citeshttps://doi.org/10.1017/s0953756298006339openalex-snapshot
Intraspecific polymorphism in Metarhizium anisopliae var. anisopliae revealed by analysis of rRNA gene complex and mtDNA RFLPs
inferred← citeshttps://doi.org/10.1021/jf034525xopenalex-snapshot
Applying DNA Techniques to the Identification of the Species of Dressed Toasted Eel Products
inferred← citeshttps://doi.org/10.1021/jf9808426openalex-snapshot
PCR−RFLP Analysis of Mitochondrial DNA: A Reliable Method for Species Identification
inferred← citeshttps://doi.org/10.1038/325013a0openalex-snapshot
Out of the garden of Eden
inferred← citeshttps://doi.org/10.1038/329270a0openalex-snapshot
Conformational mutations in human mitochondrial DNA
inferred← citeshttps://doi.org/10.1038/329853a0openalex-snapshot
Duplication and remoulding of tRNA genes during the evolutionary rearrangement of mitochondrial genomes
inferred← citeshttps://doi.org/10.1038/332206a0openalex-snapshot
One source not many
inferred← citeshttps://doi.org/10.1038/s41598-023-34059-1openalex-snapshot
Mito-nuclear discordance within Anthozoa, with notes on unique properties of their mitochondrial genomes
inferred← citeshttps://doi.org/10.1038/s41598-025-23191-9openalex-snapshot
Post-bottleneck increase in mitochondrial DNA diversity in Yaku sika deer (Cervus nippon yakushimae) on Yakushima Island, Japan
inferred← citeshttps://doi.org/10.1038/s41598-025-24574-8openalex-snapshot
De novo genome assembly, inversion detection, and worldwide adaptation on the invasive species Styela plicata
inferred← citeshttps://doi.org/10.1038/s41598-025-25890-9openalex-snapshot
Three distinct genetic lineages of Trichonephila clavata based on mitochondrial COI and genome-wide SNPs on the Korean Peninsula
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1996.00074.xopenalex-snapshot
Phylogenetic relationships and introgression patterns between incipient parapatric species of Italian brown trout (Salmo trutta L. complex)
inferred← citeshttps://doi.org/10.1046/j.1365-294x.1996.00115.xopenalex-snapshot
Genetic exchange and recombination in populations of the root‐infecting fungus Armillaria gallica
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2002.01652.xopenalex-snapshot
Slow mitochondrial DNA sequence evolution in the Anthozoa (Cnidaria)
inferred← citeshttps://doi.org/10.1046/j.1525-142x.2003.03043.xopenalex-snapshot
Phylogeny and development of marine model species: strongylocentrotid sea urchins
inferred← citeshttps://doi.org/10.1051/apido:2006021openalex-snapshot
Molecular markers as a tool for population and evolutionary studies of stingless bees
inferred← citeshttps://doi.org/10.1051/gse:19940713openalex-snapshot
Diversité et gestion génétique de la truite commune : apport de l'étude du polymorphisme des locus protéiques et microsatellites
inferred← citeshttps://doi.org/10.1071/bi9880327openalex-snapshot
Are Megabats Flying Primates? Contrary Evidence from a Mitochondrial DNA Sequence
inferred← citeshttps://doi.org/10.1071/mf9900835openalex-snapshot
Mitochondrial DNA and marine stock assessment: A review
inferred← citeshttps://doi.org/10.1073/pnas.83.23.9090openalex-snapshot
Rates of nucleotide substitution in Drosophila mitochondrial DNA and nuclear DNA are similar.
inferred← citeshttps://doi.org/10.1073/pnas.84.20.7183openalex-snapshot
Tandem duplications in animal mitochondrial DNAs: variation in incidence and gene content among lizards.
inferred← citeshttps://doi.org/10.1073/pnas.85.8.2658openalex-snapshot
Sequence analyses of herpesviral enzymes suggest an ancient origin for human sexual behavior.
inferred← citeshttps://doi.org/10.1073/pnas.86.16.6196openalex-snapshot
Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers.
inferred← citeshttps://doi.org/10.1073/pnas.87.5.1772openalex-snapshot
Large sequence divergence among mitochondrial DNA genotypes within populations of eastern African black-backed jackals.
inferred← citeshttps://doi.org/10.1073/pnas.90.7.2734openalex-snapshot
Rate variation of protein and mitochondrial DNA evolution as revealed by sea urchins separated by the isthmus of Panama.
inferred← citeshttps://doi.org/10.1073/pnas.90.9.4087openalex-snapshot
Body size, metabolic rate, generation time, and the molecular clock.
inferred← citeshttps://doi.org/10.1073/pnas.93.19.10274openalex-snapshot
Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL.
inferred← citeshttps://doi.org/10.1073/pnas.93.22.12137openalex-snapshot
Multilocus DNA fingerprinting reveals high rate of heritable genetic mutation in herring gulls nesting in an industrialized urban site.
inferred← citeshttps://doi.org/10.1073/pnas.93.26.15239openalex-snapshot
Multiple independent transpositions of mitochondrial DNA control region sequences to the nucleus
inferred← citeshttps://doi.org/10.1080/00218839.2022.2093576openalex-snapshot
Morphometric and genetic analyses show differentiation of the widely distributed stingless bee Nannotrigona perilampoides (Hymenoptera: Meliponini) across geographic regions in Mexico
inferred← citeshttps://doi.org/10.1080/00275514.1988.12025569openalex-snapshot
Estimation of Relatedness Between Phytophthora Species by Analysis of Mitochondrial DNA
inferred← citeshttps://doi.org/10.1080/10495398.2024.2397682openalex-snapshot
Sequencing and characterization of complete mitogenome DNA of worldwide turkey ( Meleagris gallopavo ) populations
inferred← citeshttps://doi.org/10.1080/11250009209386643openalex-snapshot
Structural and molecular approaches to the phylogeny of Amphibia
inferred← citeshttps://doi.org/10.1080/14772000.2012.666293openalex-snapshot
Molecular systematics of the genusSonora(Squamata: Colubridae) in central and western Mexico
inferred← citeshttps://doi.org/10.1080/17451000.2019.1601226openalex-snapshot
Mitochondrial gene rearrangement and phylogenetic relationships in the Amphilepidida and Ophiacanthida (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.1086/509046openalex-snapshot
The Sorry State of F2 Hybrids: Consequences of Rapid Mitochondrial DNA Evolution in Allopatric Populations
inferred← citeshttps://doi.org/10.1093/biolinnean/blaa109openalex-snapshot
Genetic diversity ofCalliphora vicina(Diptera: Calliphoridae) in the Iberian Peninsula based oncox1, 16S and ITS2 sequences
inferred← citeshttps://doi.org/10.1093/genetics/120.2.485openalex-snapshot
Evidence for non-neutrality of mitochondrial DNA haplotypes in Drosophila pseudoobscura.
inferred← citeshttps://doi.org/10.1093/genetics/121.3.551openalex-snapshot
Molecular population genetics of mtDNA size variation in crickets.
inferred← citeshttps://doi.org/10.1093/genetics/123.2.399openalex-snapshot
Mitochondrial and nuclear gene dynamics of introduced populations of Lepomis macrochirus.
inferred← citeshttps://doi.org/10.1093/genetics/124.2.397openalex-snapshot
A genetic discontinuity in a continuously distributed species: mitochondrial DNA in the American oyster, Crassostrea virginica.
inferred← citeshttps://doi.org/10.1093/genetics/128.2.269openalex-snapshot
Mode and tempo of molecular evolution in the nematode caenorhabditis: cytochrome oxidase II and calmodulin sequences.
inferred← citeshttps://doi.org/10.1093/genetics/135.4.1197openalex-snapshot
A method for calibrating molecular clocks and its application to animal mitochondrial DNA.
inferred← citeshttps://doi.org/10.1093/jhered/89.5.459openalex-snapshot
Species identification using genetic tools: the value of nuclear and mitochondrial gene sequences in whale conservation
inferred← citeshttps://doi.org/10.1093/jisesa/ieae008openalex-snapshot
Application of noninvasive sampling technique in mitochondrial genome intraspecific phylogeny of the endangered butterfly, Teinopalpus aureus (Lepidoptera: Papilionidae)
inferred← citeshttps://doi.org/10.1093/jme/tjaf124openalex-snapshot
A review and updated checklist of the Anopheles mosquitoes (Diptera: Culicidae: Anophelinae) of Thailand
inferred← citeshttps://doi.org/10.1093/molbev/msg125openalex-snapshot
Molecular Phylogenies and Divergence Times of Sea Urchin Species of Strongylocentrotidae, Echinoida
inferred← citeshttps://doi.org/10.1093/molbev/msg136openalex-snapshot
Assessing the Phylogenetic Utility of Four Mitochondrial Genes and a Nuclear Intron in the Asian Pit Viper Genus, Trimeresurus: Separate, Simultaneous, and Conditional Data Combination Analyses
inferred← citeshttps://doi.org/10.1093/molbev/msh031openalex-snapshot
Evolution of Interacting Proteins in the Mitochondrial Electron Transport System in a Marine Copepod
inferred← citeshttps://doi.org/10.1093/molbev/msh081openalex-snapshot
Phylogeny and Comparative Substitution Rates of Frogs Inferred from Sequences of Three Nuclear Genes
inferred← citeshttps://doi.org/10.1093/molbev/msx197openalex-snapshot
Large Variation in the Ratio of Mitochondrial to Nuclear Mutation Rate across Animals: Implications for Genetic Diversity and the Use of Mitochondrial DNA as a Molecular Marker
inferred← citeshttps://doi.org/10.1093/nar/16.1.327openalex-snapshot
Phylogenetic relationships and altered genome structures amongTetrahymenamitochondrial DNAs
inferred← citeshttps://doi.org/10.1093/nar/17.18.7325openalex-snapshot
Rapid segregation of heteroplasmic bovine mitodiondria
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003787openalex-snapshot
Mitochondrial Versus Nuclear Gene Sequences in Deep-Level Mammalian Phylogeny Reconstruction
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a003837openalex-snapshot
Multimeric Hemoglobin of the Australian Brine Shrimp Parartemia
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025612openalex-snapshot
Numerous transposed sequences of mitochondrial cytochrome oxidase I-II in aphids of the genus Sitobion (Hemiptera: Aphididae)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025781openalex-snapshot
Correlated rates of synonymous site evolution across plant genomes
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a025902openalex-snapshot
The molecular evolution of sperm bindin in six species of sea urchins (Echinoida: Strongylocentrotidae)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026189openalex-snapshot
Substitution rates of organelle and nuclear genes in sharks: implicating metabolic rate (again)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040131openalex-snapshot
Comparative evolutionary analysis of rDNA ITS regions in Drosophila.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040462openalex-snapshot
Systematics and Mitochondrial Genome Evolution of Australian Rosellas (Aves: Platycercidae)
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040464openalex-snapshot
Analysis of nucleotide substitutions of mitochondrial DNAs in Drosophila melanogaster and its sibling species.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040477openalex-snapshot
Mitochondrial DNA polymorphism in three Antillean island populations of the fruit bat, Artibeus jamaicensis.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040504openalex-snapshot
Current versus historical population sizes in vertebrate species with high gene flow: a comparison based on mitochondrial DNA lineages and inbreeding theory for neutral mutations.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040526openalex-snapshot
Mitochondrial DNA evolution in the Drosophila obscura group.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040553openalex-snapshot
The CO-I and CO-II region of honeybee mitochondrial DNA: evidence for variation in insect mitochondrial evolutionary rates.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040642openalex-snapshot
Strong reproductive isolation between closely related tropical sea urchins (genus Echinometra).
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040651openalex-snapshot
Molecular distance and divergence time in carnivores and primates.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040662openalex-snapshot
Evolution of the cetacean mitochondrial D-loop region.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040735openalex-snapshot
Mitochondrial DNA evolution at a turtle's pace: evidence for low genetic variability and reduced microevolutionary rate in the Testudines.
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a040778openalex-snapshot
Sequence evolution in mitochondrial ribosomal and ND-1 genes in lepidoptera: implications for phylogenetic analyses.
inferred← citeshttps://doi.org/10.1093/sysbio/38.2.126openalex-snapshot
Allozymes, Mitochondrial DNA, and Levels of Phylogenetic Resolution among Four Minnow Species (Notropis: Cyprinidae)
inferred← citeshttps://doi.org/10.1093/sysbio/46.1.126openalex-snapshot
Mitochondrial DNA Rates and Biogeography in European Newts (Genus Euproctus)
inferred← citeshttps://doi.org/10.1093/zoolinnean/zly047openalex-snapshot
Phylogeny and biogeography of the endemic Hemidactylus geckos of the Indian subregion suggest multiple dispersals from Peninsular India to Sri Lanka
inferred← citeshttps://doi.org/10.1098/rstb.1995.0085openalex-snapshot
Comparing patterns of evolution: larval and adult life history stages and ribosomal RNA of post-Palaeozoic echinoids
inferred← citeshttps://doi.org/10.1099/vir.0.80650-0openalex-snapshot
Utility of JC polyomavirus in tracing the pattern of human migrations dating to prehistoric times
inferred← citeshttps://doi.org/10.1111/1471-0307.12446openalex-snapshot
Changes in physicochemical properties and DNA quality of milk as affected by different heat treatments
inferred← citeshttps://doi.org/10.1111/j.0300-3256.2004.00166.xopenalex-snapshot
Non‐monophyly of the avian genus Seicercus (Aves: Sylviidae) revealed by mitochondrial DNA
inferred← citeshttps://doi.org/10.1111/j.1365-2621.2004.tb17847.xopenalex-snapshot
Application of DNA Technique for Identifying the Species of Different Processed Products of Swordfish Meat
inferred← citeshttps://doi.org/10.1111/j.1365-294x.1994.tb00057.xopenalex-snapshot
A molecular analysis of relationships and biogeography within a species complex of Holarctic fish (genus Osmerus )
inferred← citeshttps://doi.org/10.1111/j.1365-294x.1994.tb00068.xopenalex-snapshot
Genetic variation of microsatellite loci in a bottlenecked species: the northern hairy‐nosed wombat Lasiorhinus krefftii
inferred← citeshttps://doi.org/10.1111/j.1365-294x.1996.tb00308.xopenalex-snapshot
Phylogenetic relationships and introgression patterns between incipient parapatric species of Italian brown trout (Salmo trutta L. complex)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2005.02723.xopenalex-snapshot
Historical colonization and demography of the Mediterranean damselfish, Chromis chromis
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2007.03572.xopenalex-snapshot
Differential gene flow of mitochondrial and nuclear DNA markers among chromosomal races of Australian morabine grasshoppers (Vandiemenella, viatica species group)
inferred← citeshttps://doi.org/10.1111/j.1463-6409.2010.00436.xopenalex-snapshot
Nuclear and mitochondrial phylogenies provide evidence for four species of Eurasian badgers (Carnivora)
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1992.tb04340.xopenalex-snapshot
Mitochondrial DNA variation and phylogenetic relationships of Jasus spp. (Decapoda: Palinuridae)
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1989.tb01338.xopenalex-snapshot
Molecular clocks, molecular phylogenies and the origin of phyla
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1987.tb05872.xopenalex-snapshot
GEOGRAPHIC POPULATION STRUCTURE AND SPECIES DIFFERENCES IN MITOCHONDRIAL DNA OF MOUTHBROODING MARINE CATFISHES (ARIIDAE) AND DEMERSAL SPAWNING TOADFISHES (BATRACHOIDIDAE)
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1988.tb04124.xopenalex-snapshot
DNA Evolution
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1989.tb02568.xopenalex-snapshot
GENE TREES AND ORGANISMAL HISTORIES: A PHYLOGENETIC APPROACH TO POPULATION BIOLOGY
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1989.tb04209.xopenalex-snapshot
MITOCHONDRIAL-DNA VARIATION IN THE CRESTED NEWT SUPERSPECIES: LIMITED CYTOPLASMIC GENE FLOW AMONG SPECIES
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1989.tb04229.xopenalex-snapshot
PHYLOGENETIC RELATIONSHIPS AND MOLECULAR VARIABILITY WITHIN AND AMONG SIX CHROMOSOME RACES OF SCELOPORUS GRAMMICUS (SAURIA, IGUANIDAE), BASED ON NUCLEAR AND MITOCHONDRIAL MARKERS
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1989.tb04257.xopenalex-snapshot
REPRODUCTIVE ISOLATION AND INTROGRESSION BETWEEN NOTROPIS CORNUTUS AND NOTROPIS CHRYSOCEPHALUS (FAMILY CYPRINIDAE): COMPARISON OF MORPHOLOGY, ALLOZYMES, AND MITOCHONDRIAL DNA
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1990.tb03826.xopenalex-snapshot
DIFFERING LEVELS OF AMONG‐POPULATION DIVERGENCE IN THE MITOCHONDRIAL DNA OF PERIODICAL CICADAS RELATED TO HISTORICAL BIOGEOGRAPHY
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1990.tb05208.xopenalex-snapshot
MITOCHONDRIAL DNA DIVERSITY IN THE SEA URCHINS STRONGYLOCENTROTUS PURPURATUS AND S. DROEBACHIENSIS
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1991.tb02688.xopenalex-snapshot
POPULATION BIOLOGY OF THE TRANS‐ARCTIC EXCHANGE: MtDNA SEQUENCE SIMILARITY BETWEEN PACIFIC AND ATLANTIC SEA URCHINS
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1992.tb01125.xopenalex-snapshot
POPULATION GENETIC CONSEQUENCES OF DEVELOPMENTAL EVOLUTION IN SEA URCHINS (GENUS HELIOCIDARIS )
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1993.tb02122.xopenalex-snapshot
MITOCHONDRIAL DNA INGASTEROSTEUSAND PLEISTOCENE GLACIAL REFUGIUM ON THE QUEEN CHARLOTTE ISLANDS, BRITISH COLUMBIA
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1994.tb02223.xopenalex-snapshot
INTRASPECIFIC MOLECULAR PHYLOGENY IN THE YELLOW WARBLER (DENDROICA PETECHIA), AND IMPLICATIONS FOR AVIAN BIOGEOGRAPHY IN THE WEST INDIES
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1996.tb03617.xopenalex-snapshot
EVOLUTIONARY HISTORY OF NORTHERN HEMISPHERE NUCELLA (GASTROPODA, MURICIDAE): MOLECULAR, MORPHOLOGICAL, ECOLOGICAL, AND PALEONTOLOGICAL EVIDENCE
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1998.tb01655.xopenalex-snapshot
EVOLUTIONARY ASSOCIATIONS OF BROOD PARASITIC FINCHES (VIDUA) AND THEIR HOST SPECIES: ANALYSES OF MITOCHONDRIAL DNA RESTRICTION SITES
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1998.tb02246.xopenalex-snapshot
TESTS OF PHYLOGEOGRAPHIC MODELS WITH NUCLEAR AND MITOCHONDRIAL DNA SEQUENCE VARIATION IN THE STONE CRABS, MENIPPE ADINA AND MENIPPE MERCENARIA
inferred← citeshttps://doi.org/10.1111/j.1748-7692.1993.tb00439.xopenalex-snapshot
POPULATION STRUCTURE OF THE BOTTLENOSE DOLPHIN (TURSIOPS TRUNCATUS) AS DETERMINED BY RESTRICTION ENDONUCLEASE ANALYSIS OF MITOCHONDRIAL DNA
inferred← citeshttps://doi.org/10.1111/zsc.70076openalex-snapshot
On the Origin of the Tingidae (Insecta, Heteroptera)
inferred← citeshttps://doi.org/10.1126/science.1672472openalex-snapshot
Heteroplasmy Suggests Limited Biparental Inheritance of Mytilus Mitochondrial DNA
inferred← citeshttps://doi.org/10.1128/aem.59.12.4283-4288.1993openalex-snapshot
Identification of Molecular Variants in Mitochondrial DNAs of Members of the Genera Beauveria, Verticillium, Paecilomyces, Tolypocladium , and Metarhizium
inferred← citeshttps://doi.org/10.1134/s1063074019060051openalex-snapshot
The Transposons of the Sea Urchin Strongylocentrotus intermedius Agassiz, 1863: In Silico Versus In Vitro
showing the first 200 of 293 · page through all 293
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.