On the public citation graph

Fragaria mitogenomes evolve rapidly in structure but slowly in sequence and incur frequent multinucleotide mutations mediated by microinversions

https://doi.org/10.1111/nph.18334
0 signed · 182 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/10.1002/9781119312994.apr0544openalex-snapshot
Mitochondrial DNA Repair and Genome Evolution
inferredcites →https://doi.org/10.1002/tax.574004openalex-snapshot
Phylogeny and evolutionary patterns in Nymphaeales: integrating genes, genomes and morphology
inferredcites →https://doi.org/10.1007/978-3-7091-1130-7_9openalex-snapshot
Plant Mitochondrial Genome Diversity: The Genomics Revolution
inferredcites →https://doi.org/10.1007/bf02103617openalex-snapshot
Nucleotide sequences of the 5.8S rRNA gene and internal transcribed spacer regions in carrot and broad bean ribosomal DNA
inferredcites →https://doi.org/10.1007/bf02111281openalex-snapshot
DNA turnover and the molecular clock
inferredcites →https://doi.org/10.1007/bf02143500openalex-snapshot
Plant mitochondrial DNA evolved rapidly in structure, but slowly in sequence
inferredcites →https://doi.org/10.1007/s00239-010-9346-yopenalex-snapshot
Testing for Selection on Synonymous Sites in Plant Mitochondrial DNA: The Role of Codon Bias and RNA Editing
inferredcites →https://doi.org/10.1007/s00239-015-9704-xopenalex-snapshot
Are Synonymous Substitutions in Flowering Plant Mitochondria Neutral?
inferredcites →https://doi.org/10.1007/s00239-017-9792-xopenalex-snapshot
Plastome-Wide Nucleotide Substitution Rates Reveal Accelerated Rates in Papilionoideae and Correlations with Genome Features Across Legume Subfamilies
inferredcites →https://doi.org/10.1007/s002940050130openalex-snapshot
Hairpins create minute inversions in non-coding regions of chloroplast DNA
inferredcites →https://doi.org/10.1007/s00438-004-1058-9openalex-snapshot
The cytoplasmic male-sterile type and normal type mitochondrial genomes of sugar beet share the same complement of genes of known function but differ in the content of expressed ORFs
inferredcites →https://doi.org/10.1007/s00606-009-0210-8openalex-snapshot
Mutational dynamics and phylogenetic utility of noncoding chloroplast DNA
inferredcites →https://doi.org/10.1007/s10592-005-9073-xopenalex-snapshot
Development and characterization of polymorphic microsatellite loci in endangered fern Adiantum reniforme var. sinense
inferredcites →https://doi.org/10.1007/s11103-011-9762-4openalex-snapshot
The evolution of the plastid chromosome in land plants: gene content, gene order, gene function
inferredcites →https://doi.org/10.1016/b978-0-08-057430-1.50016-0openalex-snapshot
HOMOLOGY IN MOLECULAR BIOLOGY
inferredcites →https://doi.org/10.1016/bs.abr.2017.11.013openalex-snapshot
Structural Diversity Among Plastid Genomes of Land Plants
inferredcites →https://doi.org/10.1016/j.cub.2011.05.013openalex-snapshot
Pervasive Multinucleotide Mutational Events in Eukaryotes
inferredcites →https://doi.org/10.1016/j.mito.2007.10.006openalex-snapshot
Angiosperm mitochondrial genomes and mutations
inferredcites →https://doi.org/10.1016/j.ympev.2008.09.009openalex-snapshot
Relative rates of synonymous substitutions in the mitochondrial, chloroplast and nuclear genomes of seed plants
inferredcites →https://doi.org/10.1016/s1016-8478(23)13143-8openalex-snapshot
Widespread Occurrence of Small Inversions in the Chloroplast Genomes of Land Plants
inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1038/s41467-018-07641-9openalex-snapshot
High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries
inferredcites →https://doi.org/10.1038/s41588-019-0356-4openalex-snapshot
Origin and evolution of the octoploid strawberry genome
inferredcites →https://doi.org/10.1038/s41598-020-71473-1openalex-snapshot
Nucleotide substitution rates of diatom plastid encoded protein genes are positively correlated with genome architecture
inferredcites →https://doi.org/10.1073/pnas.0408302101openalex-snapshot
Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants
inferredcites →https://doi.org/10.1073/pnas.1421397112openalex-snapshot
The massive mitochondrial genome of the angiosperm Silene noctiflora is evolving by gain or loss of entire chromosomes
inferredcites →https://doi.org/10.1073/pnas.1422049112openalex-snapshot
Mitochondrial and plastid genome architecture: Reoccurring themes, but significant differences at the extremes
inferredcites →https://doi.org/10.1073/pnas.1504491112openalex-snapshot
Miniaturized mitogenome of the parasitic plant Viscum scurruloideum is extremely divergent and dynamic and has lost all nad genes
inferredcites →https://doi.org/10.1073/pnas.2001998117openalex-snapshot
MSH1 is required for maintenance of the low mutation rates in plant mitochondrial and plastid genomes
inferredcites →https://doi.org/10.1073/pnas.2105431118openalex-snapshot
Evolutionary history and pan-genome dynamics of strawberry ( Fragaria spp.)
inferredcites →https://doi.org/10.1073/pnas.84.24.9054openalex-snapshot
Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.
inferredcites →https://doi.org/10.1093/bioinformatics/18.3.492openalex-snapshot
GRIMM: genome rearrangements web server
inferredcites →https://doi.org/10.1093/bioinformatics/bti079openalex-snapshot
HyPhy: hypothesis testing using phylogenies
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btq033openalex-snapshot
BEDTools: a flexible suite of utilities for comparing genomic features
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/btv383openalex-snapshot
Bandage: interactive visualization of de novo genome assemblies
inferredcites →https://doi.org/10.1093/dnares/11.4.247openalex-snapshot
Complete Chloroplast Genome Sequences from Korean Ginseng (Panax schinseng Nees) and Comparative Analysis of Sequence Evolution among 17 Vascular Plants
inferredcites →https://doi.org/10.1093/dnares/dsl012openalex-snapshot
Pattern and Rate of Indel Evolution Inferred from Whole Chloroplast Intergenic Regions in Sugarcane, Maize and Rice
inferredcites →https://doi.org/10.1093/gbe/evaa012openalex-snapshot
Can Green Algal Plastid Genome Size Be Explained by DNA Repair Mechanisms?
inferredcites →https://doi.org/10.1093/gbe/evr042openalex-snapshot
Structural and Content Diversity of Mitochondrial Genome in Beet: A Comparative Genomic Analysis
inferredcites →https://doi.org/10.1093/gbe/evt069openalex-snapshot
Plant Mitochondrial Genome Evolution Can Be Explained by DNA Repair Mechanisms
inferredcites →https://doi.org/10.1093/gbe/evu115openalex-snapshot
Genes and Junk in Plant Mitochondria—Repair Mechanisms and Selection
inferredcites →https://doi.org/10.1093/gbe/evu253openalex-snapshot
History of Plastid DNA Insertions Reveals Weak Deletion and AT Mutation Biases in Angiosperm Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/gbe/evu261openalex-snapshot
Evolutionary Origins and Dynamics of Octoploid Strawberry Subgenomes Revealed by Dense Targeted Capture Linkage Maps
inferredcites →https://doi.org/10.1093/gbe/evv069openalex-snapshot
Mutation Rates in Plastid Genomes: They Are Lower than You Might Think
inferredcites →https://doi.org/10.1093/gbe/evw195openalex-snapshot
Animal Mitochondrial DNA as We Do Not Know It: mt-Genome Organization and Evolution in Nonbilaterian Lineages
inferredcites →https://doi.org/10.1093/gbe/evx214openalex-snapshot
A New Perspective on Polyploid Fragaria (Strawberry) Genome Composition Based on Large-Scale, Multi-Locus Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/gbe/evz263openalex-snapshot
The Mitogenome of Norway Spruce and a Reappraisal of Mitochondrial Recombination in Plants
inferredcites →https://doi.org/10.1093/molbev/msaa238openalex-snapshot
Tracing the Diploid Ancestry of the Cultivated Octoploid Strawberry
inferredcites →https://doi.org/10.1093/molbev/msg163openalex-snapshot
Molecular Evolution of Insertions and Deletion in the Chloroplast Genome of Silene
inferredcites →https://doi.org/10.1093/molbev/msg190openalex-snapshot
Patterns and Relative Rates of Nucleotide and Insertion/Deletion Evolution at Six Chloroplast Intergenic Regions in New World Species of the Lecythidaceae
inferredcites →https://doi.org/10.1093/molbev/msn074openalex-snapshot
Parallel Rate Heterogeneity in Chloroplast and Mitochondrial Genomes of Brazil Nut Trees (Lecythidaceae) Is Consistent with Lineage Effects
inferredcites →https://doi.org/10.1093/molbev/msp063openalex-snapshot
Variation in the Ratio of Nucleotide Substitution and Indel Rates across Genomes in Mammals and Bacteria
inferredcites →https://doi.org/10.1093/molbev/msq029openalex-snapshot
Insights into the Evolution of Mitochondrial Genome Size from Complete Sequences of Citrullus lanatus and Cucurbita pepo (Cucurbitaceae)
inferredcites →https://doi.org/10.1093/molbev/msu079openalex-snapshot
Unprecedented Heterogeneity in the Synonymous Substitution Rate within a Plant Genome
inferredcites →https://doi.org/10.1093/molbev/msw024openalex-snapshot
GinkgoandWelwitschiaMitogenomes Reveal Extreme Contrasts in Gymnosperm Mitochondrial Evolution
inferredcites →https://doi.org/10.1093/molbev/msw242openalex-snapshot
Evolution of Rosaceae Fruit Types Based on Nuclear Phylogeny in the Context of Geological Times and Genome Duplication
inferredcites →https://doi.org/10.1093/molbev/msx093openalex-snapshot
Evolution of Rosaceae Fruit Types Based on Nuclear Phylogeny in the Context of Geological Times and Genome Duplication
inferredcites →https://doi.org/10.1093/molbev/msy096openalex-snapshot
MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms
inferredcites →https://doi.org/10.1093/molbev/msy176openalex-snapshot
High and Variable Rates of Repeat-Mediated Mitochondrial Genome Rearrangement in a Genus of Plants
inferredcites →https://doi.org/10.1093/molbev/msz108openalex-snapshot
Molecular Evolution in Large Steps—Codon Substitutions under Positive Selection
inferredcites →https://doi.org/10.1093/nar/25.5.955openalex-snapshot
tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic Sequence
inferredcites →https://doi.org/10.1093/nar/27.8.1767openalex-snapshot
Animal mitochondrial genomes
inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot
MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform
inferredcites →https://doi.org/10.1093/nar/gkg795openalex-snapshot
The complete nucleotide sequence and RNA editing content of the mitochondrial genome of rapeseed (Brassica napus L.): comparative analysis of the mitochondrial genomes of rapeseed and Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkx744openalex-snapshot
Plant organellar DNA polymerases are replicative and translesion DNA synthesis polymerases
inferredcites →https://doi.org/10.1093/oso/9780195135848.001.0001openalex-snapshot
Molecular Evolution and Phylogenetics
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025693openalex-snapshot
Deep-level diagnostic value of the rDNA-ITS region
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025860openalex-snapshot
Association between chloroplast and mitochondrial lineages in oaks
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/sysbio/syq010openalex-snapshot
New Algorithms and Methods to Estimate Maximum-Likelihood Phylogenies: Assessing the Performance of PhyML 3.0
inferredcites →https://doi.org/10.1104/pp.111.190231openalex-snapshot
A Reevaluation of Rice Mitochondrial Evolution Based on the Complete Sequence of Male-Fertile and Male-Sterile Mitochondrial Genomes
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03195.xopenalex-snapshot
Recombination and the maintenance of plant organelle genome stability
inferredcites →https://doi.org/10.1111/mec.13742openalex-snapshot
The mutational hazard hypothesis of organelle genome evolution: 10 years on
inferredcites →https://doi.org/10.1111/nph.12395openalex-snapshot
One ring to rule them all? Genome sequencing provides new insights into the ‘master circle’ model of plant mitochondrial DNA structure
inferredcites →https://doi.org/10.1111/nph.14135openalex-snapshot
Complete mitochondrial genomes from the ferns Ophioglossum californicum and Psilotum nudum are highly repetitive with the largest organellar introns
inferredcites →https://doi.org/10.1111/nph.16753openalex-snapshot
Episodic and guanine–cytosine‐biased bursts of intragenomic and interspecific synonymous divergence in Ajugoideae (Lamiaceae) mitogenomes
inferredcites →https://doi.org/10.1111/pbi.12141openalex-snapshot
Highly rearranged and size‐variable chloroplast genomes in conifers II clade (cupressophytes): evolution towards shorter intergenic spacers
inferredcites →https://doi.org/10.1126/science.287.5456.1283openalex-snapshot
Evidence for a High Frequency of Simultaneous Double-Nucleotide Substitutions
inferredcites →https://doi.org/10.1186/1471-2148-6-13openalex-snapshot
Adaptive evolution of chloroplast genome structure inferred using a parametric bootstrap approach
inferredcites →https://doi.org/10.1186/1471-2148-7-135openalex-snapshot
Extensive variation in synonymous substitution rates in mitochondrial genes of seed plants
inferredcites →https://doi.org/10.1186/1741-7007-11-29openalex-snapshot
The “fossilized” mitochondrial genome of Liriodendron tulipifera: ancestral gene content and order, ancestral editing sites, and extraordinarily low mutation rate
inferredcites →https://doi.org/10.1186/1741-7007-9-61openalex-snapshot
The intriguing evolutionary dynamics of plant mitochondrial DNA
inferredcites →https://doi.org/10.1186/s12870-021-03202-3openalex-snapshot
Extensive genomic rearrangements mediated by repetitive sequences in plastomes of Medicago and its relatives
inferredcites →https://doi.org/10.1371/journal.pbio.1001241openalex-snapshot
Rapid Evolution of Enormous, Multichromosomal Genomes in Flowering Plant Mitochondria with Exceptionally High Mutation Rates
inferredcites →https://doi.org/10.1371/journal.pgen.1008373openalex-snapshot
The alternative reality of plant mitochondrial DNA: One ring does not rule them all
inferredcites →https://doi.org/10.1371/journal.pone.0011147openalex-snapshot
progressiveMauve: Multiple Genome Alignment with Gene Gain, Loss and Rearrangement
inferredcites →https://doi.org/10.1371/journal.pone.0112963openalex-snapshot
Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement
inferredcites →https://doi.org/10.1371/journal.pone.0224622openalex-snapshot
Characterization of 20 complete plastomes from the tribe Laureae (Lauraceae) and distribution of small inversions
inferredcites →https://doi.org/10.1534/g3.118.200948openalex-snapshot
Repeats of Unusual Size in Plant Mitochondrial Genomes: Identification, Incidence and Evolution
inferredcites →https://doi.org/10.1534/g3.119.401023openalex-snapshot
The Tempo and Mode of Angiosperm Mitochondrial Genome Divergence Inferred from Intraspecific Variation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1534/genetics.107.073312openalex-snapshot
Comparisons Among Two Fertile and Three Male-Sterile Mitochondrial Genomes of Maize
inferredcites →https://doi.org/10.1534/genetics.118.301721openalex-snapshot
Fine-Grained Analysis of Spontaneous Mutation Spectrum and Frequency in Arabidopsis thaliana
inferredcites →https://doi.org/10.17660/actahortic.2009.842.1openalex-snapshot
STRAWBERRY BIOGEOGRAPHY, GENETICS AND SYSTEMATICS
inferredcites →https://doi.org/10.17660/actahortic.2017.1156.5openalex-snapshot
TheFragariaspecies native to China and their geographical distribution
inferredcites →https://doi.org/10.2307/2399846openalex-snapshot
Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL
inferredcites →https://doi.org/10.2307/2399880openalex-snapshot
The its Region of Nuclear Ribosomal DNA: A Valuable Source of Evidence on Angiosperm Phylogeny
inferredcites →https://doi.org/10.3389/fgene.2020.00257openalex-snapshot
Comparative Analysis of the Mitochondrial Genomes of Nicotiana tabacum: Hints Toward the Key Factors Closely Related to the Cytoplasmic Male Sterility Mechanism
inferredcites →https://doi.org/10.3732/ajb.1400140openalex-snapshot
Fragaria: A genus with deep historical roots and ripe for evolutionary and ecological insights
inferredcites →https://doi.org/10.3732/ajb.1500026openalex-snapshot
Comparison of nuclear, plastid, and mitochondrial phylogenies and the origin of wild octoploid strawberry species
inferredcites →https://doi.org/10.3732/ajb.1600453openalex-snapshot
Recombination‐dependent replication and gene conversion homogenize repeat sequences and diversify plastid genome structure

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4757412openalex-extracted
Phylogenomics of the Bupleurum in East Asia: Species Distribution Patterns and Diversification
inferred← citeshttps://doi.org/10.1007/s00299-023-03102-wopenalex-snapshot
Remarkable mitochondrial genome heterogeneity in Meniocus linifolius (Brassicaceae)
inferred← citeshttps://doi.org/10.1007/s00425-025-04629-wopenalex-snapshot
The Taihangia mitogenome provides new insights into its adaptation and organelle genome evolution in Rosaceae
inferred← citeshttps://doi.org/10.1007/s00425-025-04860-5openalex-snapshot
Complete mitochondrial genome assembly and structural feature analysis of Thinopyrum elongatum (Poaceae)
inferred← citeshttps://doi.org/10.1007/s00425-026-05071-2openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genome of Viola philippica (Malpighiales, Violaceae)
inferred← citeshttps://doi.org/10.1007/s11105-026-01723-5openalex-snapshot
Past, Present and Future of Rice Breeding: From Domestication to Genomics
inferred← citeshttps://doi.org/10.1016/j.indcrop.2023.117712openalex-snapshot
Comparative chloroplast genome analyses provide new insights into phylogeny of Taraxacum and molecular markers for distinguishing rubber producing dandelions from their weedy relatives in China
inferred← citeshttps://doi.org/10.1016/j.indcrop.2026.124291openalex-snapshot
Mitochondrial genome architecture and evolutionary characteristics of cliff-endemic Opisthopappus in Asteraceae
inferred← citeshttps://doi.org/10.1016/j.pld.2026.08.003openalex-snapshot
Mitogenome structural diversification accompanied by rapid repeat-family turnover: A comparative organellar perspective from Salvia
inferred← citeshttps://doi.org/10.1016/j.postharvbio.2025.114099openalex-snapshot
A novel mitochondrial pyruvate dehydrogenase E1α subunit gene links carbon flow and redox signaling to enhance postharvest disease resistance in strawberry
inferred← citeshttps://doi.org/10.1016/j.ympev.2023.107956openalex-snapshot
Phylogenomic conflict analyses of the plastid and mitochondrial genomes via deep genome skimming highlight their independent evolutionary histories: A case study in the cinquefoil genus Potentilla sensu lato (Potentilleae, Rosaceae)
inferred← citeshttps://doi.org/10.1038/s41598-025-86411-2openalex-snapshot
De novo assembly of the complete mitochondrial genomes of two Camellia-oil tree species reveals their multibranch conformation and evolutionary relationships
inferred← citeshttps://doi.org/10.1038/s42003-025-08418-9openalex-snapshot
Evolution of mitochondrial RNA editing sites and stop codon-lacking transcripts in angiosperms
inferred← citeshttps://doi.org/10.1073/pnas.2502814122openalex-snapshot
Homoploid hybridization adds clarity to the origins of octoploid strawberries
inferred← citeshttps://doi.org/10.1080/23802359.2024.2429655openalex-snapshot
The complete mitochondrial genome of Rosa laevigata Michx. (Rosaceae), an edible and medicinal plant
inferred← citeshttps://doi.org/10.1093/gbe/evad041openalex-snapshot
De novoAssembly and Comparative Analyses of Mitochondrial Genomes in Piperales
inferred← citeshttps://doi.org/10.1093/gbe/evad155openalex-snapshot
The Mitochondrial Genome of the Holoparasitic PlantThonningia sanguineaProvides Insights into the Evolution of the Multichromosomal Structure
inferred← citeshttps://doi.org/10.1093/molbev/msad049openalex-snapshot
Recombination Variation Shapes Phylogeny and Introgression in Wild Diploid Strawberries
inferred← citeshttps://doi.org/10.1093/molbev/msaf082openalex-snapshot
Unequally Abundant Chromosomes and Unusual Collections of Transferred Sequences Characterize Mitochondrial Genomes of Gastrodia (Orchidaceae), One of the Largest Mycoheterotrophic Plant Genera
inferred← citeshttps://doi.org/10.1093/plcell/koad314openalex-snapshot
Genomic signatures of strawberry domestication and diversification
inferred← citeshttps://doi.org/10.1101/2023.07.12.548723openalex-snapshot
Genomic signatures of strawberry domestication and breeding
inferred← citeshttps://doi.org/10.1101/2024.09.12.612680openalex-snapshot
Homoploid Hybridization Resolves the Origin of Octoploid Strawberries
inferred← citeshttps://doi.org/10.1101/2025.01.11.632530openalex-snapshot
The structure of mitochondrial genomes is associated with geography in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1111/1755-0998.70025openalex-snapshot
Test Species Discrimination in Codonopsis (Campanulaceae) Using Genome Skimming Data
inferred← citeshttps://doi.org/10.1111/jse.13189openalex-snapshot
Phylogenomics of the Bupleurum in East Asia: Insights into distribution patterns and diversification
inferred← citeshttps://doi.org/10.1186/s12864-024-10818-wopenalex-snapshot
Complete mitochondrial genome assembly of Juglans regia unveiled its molecular characteristics, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.1186/s12864-024-10985-wopenalex-snapshot
The complete mitochondrial genome assembly of Capsicum pubescens reveals key evolutionary characteristics of mitochondrial genes of two Capsicum subspecies
inferred← citeshttps://doi.org/10.1186/s12864-024-11086-4openalex-snapshot
Comprehensive analysis of the first complete mitogenome and plastome of a traditional Chinese medicine Viola diffusa
inferred← citeshttps://doi.org/10.1186/s12864-025-11440-0openalex-snapshot
A near-complete genome assembly of Fragaria iinumae
inferred← citeshttps://doi.org/10.1186/s12864-025-11540-xopenalex-snapshot
The first complete mitochondrial genome of Curcuma amarissima (Zingiberaceae): insights into multi-branch structure, codon usage, and phylogenetic evolution
inferred← citeshttps://doi.org/10.1186/s12864-026-12646-6openalex-snapshot
The complete mitochondrial genome of Prinsepia uniflora (Rosaceae): De novo assembly, characterization, and phylogenetic analysis
inferred← citeshttps://doi.org/10.1186/s12870-023-04529-9openalex-snapshot
Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.1186/s12870-024-04978-wopenalex-snapshot
De novo assembly of the complete mitochondrial genome of pepino (Solanum muricatum) using PacBio HiFi sequencing: insights into structure, phylogenetic implications, and RNA editing
inferred← citeshttps://doi.org/10.1186/s12870-025-06461-6openalex-snapshot
Mitochondrial genome assembly of the Chinese endemic species of Camellia luteoflora and revealing its repetitive sequence mediated recombination, codon preferences and MTPTs
inferred← citeshttps://doi.org/10.1186/s12870-025-07506-6openalex-snapshot
Pan-mitogenome in Dipterocarpoideae: mitochondrial plastid DNAs and repeats shape the dynamic evolution of mitogenomes
inferred← citeshttps://doi.org/10.1186/s12870-025-07650-zopenalex-snapshot
Assembly and comparative analysis of chromosomal mitochondrial genomes in multiple Medicago species
inferred← citeshttps://doi.org/10.1186/s12870-026-08260-zopenalex-snapshot
Comparative analysis of complete mitogenomes of two ornamental plants Chimonanthus salicifolius and Chimonanthus praecox in the family Calycanthaceae
inferred← citeshttps://doi.org/10.1186/s12870-026-08314-2openalex-snapshot
De novo assembly of the first mitochondrial genome in Benincasa reveals structural dynamics and evolutionary insights in Cucurbitaceae
inferred← citeshttps://doi.org/10.1186/s12870-026-09074-9openalex-snapshot
The mitochondrial genome of the soil pH-indicator plant Hydrangea macrophylla provides insights into mitogenome variation and evolution in superasterids
inferred← citeshttps://doi.org/10.1186/s12870-026-09085-6openalex-snapshot
Characterization of the mitochondrial genome of the aquatic vegetable Eleocharis dulcis (Burm. f.) Trin. ex Hensch.: the first representative of genus Eleocharis with evolutionary insights in Cyperaceae
inferred← citeshttps://doi.org/10.1186/s12870-026-09180-8openalex-snapshot
Comparative analysis of the complete multi-chromosomal mitogenome of Anoectochilus emeiensis (Orchidaceae)
inferred← citeshttps://doi.org/10.1186/s12870-026-09339-3openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genome of Polygonatum odoratum (Yuzhu), a medicine-food homologous plant
inferred← citeshttps://doi.org/10.1186/s12915-025-02115-zopenalex-snapshot
Evolutionary dynamics of mitochondrial genomes and intracellular transfers among diploid and allopolyploid cotton species
inferred← citeshttps://doi.org/10.1186/s13100-024-00336-7openalex-snapshot
Analysis of pericentromere composition and structure elucidated the history of the Hieracium alpinum L. genome, revealing waves of transposable elements insertions
inferred← citeshttps://doi.org/10.21203/rs.3.rs-5409755/v1openalex-snapshot
Assembly of the complete mitochondrial genome of Prinsepia uniflora (Rosaceae): Insights into genomic characterization and phylogenetic analysis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9546695/v1openalex-snapshot
Organelle genome assembly and analysis of Euonymus chloranthoides, insights into an endemic and endangered species
inferred← citeshttps://doi.org/10.3389/fpls.2023.1132551openalex-snapshot
Assembly and analysis of the first complete mitochondrial genome of Punica granatum and the gene transfer from chloroplast genome
inferred← citeshttps://doi.org/10.3389/fpls.2023.1166420openalex-snapshot
Comprehensive analysis of the complete mitochondrial genomes of three Coptis species (C. chinensis, C. deltoidea and C. omeiensis): the important medicinal plants in China
inferred← citeshttps://doi.org/10.3389/fpls.2023.1301164openalex-snapshot
Complete mitochondrial genome of Syzygium samarangense reveals genomic recombination, gene transfer, and RNA editing events
inferred← citeshttps://doi.org/10.3389/fpls.2024.1429545openalex-snapshot
Comparative analysis of the mitochondrial genomes of four Dendrobium species (Orchidaceae) reveals heterogeneity in structure, synteny, intercellular gene transfer, and RNA editing
inferred← citeshttps://doi.org/10.3389/fpls.2024.1442178openalex-snapshot
Comparison of organelle genomes between endangered mangrove plant Dolichandrone spathacea to terrestrial relative provides insights into its origin and adaptative evolution
inferred← citeshttps://doi.org/10.3389/fpls.2024.1469267openalex-snapshot
Mitochondrial genome insights into the spatio-temporal distribution and genetic diversity of Dendrobium hancockii Rolfe (Orchidaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2025.1546449openalex-snapshot
Unraveling the mitochondrial genome of the medicinal Chinese motherwort (Leonurus japonicus, Lamiaceae): structural dynamics, organelle-to-nuclear gene transfer, and evolutionary implications
inferred← citeshttps://doi.org/10.3389/fpls.2025.1619267openalex-snapshot
Complete plastome and mitogenome assembly of endangered tree Karpatiosorbus bristoliensis reveals phylogenetic architecture for Sorbus sensu lato (Rosaceae)
inferred← citeshttps://doi.org/10.3389/fpls.2025.1684062openalex-snapshot
Unveiling the complete organelle genomes of Gypsophila vaccaria: de novo assembly and evolutionary insights into a medicinally important species
inferred← citeshttps://doi.org/10.3389/fpls.2026.1701753openalex-snapshot
Assembly and comparative analysis of the complete multichromosomal mitochondrial genome of an endangered orchid species, Calanthe sieboldii
inferred← citeshttps://doi.org/10.3389/fpls.2026.1906069openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genomes of Pyrus calleryana Decne. and Pyrus betulifolia Bunge
inferred← citeshttps://doi.org/10.3389/fpls.2026.1921030openalex-snapshot
The complete mitochondrial genome of Hemiboea subcapitata (Gesneriaceae) and comparative analysis across Lamiales
inferred← citeshttps://doi.org/10.3390/biom14080912openalex-snapshot
Morphological Structure Identification, Comparative Mitochondrial Genomics and Population Genetic Analysis toward Exploring Interspecific Variations and Phylogenetic Implications of Malus baccata ‘ZA’ and Other Species
inferred← citeshttps://doi.org/10.3390/genes14040864openalex-snapshot
The Evolution of Mitochondrial Genomes between Two Cymbidium Sister Species: Dozens of Circular Chromosomes and the Maintenance and Deterioration of Genome Synteny
inferred← citeshttps://doi.org/10.3390/genes16101241openalex-snapshot
Comparative Analysis of Araceae Mitochondrial Genomes: Implications for Adaptation to Ecological Transitions in Plants
inferred← citeshttps://doi.org/10.3390/genes17091103openalex-snapshot
The Cucurbita ficifolia Mitochondrial Genome: Repeat-Rich Architecture, Plastid Homology, and Synteny Turnover Across Cucurbitaceae
inferred← citeshttps://doi.org/10.3390/horticulturae11030225openalex-snapshot
Mitochondrial Genomes of Hibiscus Reveal Structural Heterogeneity and Phylogenetic Relationships
inferred← citeshttps://doi.org/10.3390/life13112114openalex-snapshot
Complete Mitochondrial Genome Assembly of an Upland Wild Rice Species, Oryza granulata and Comparative Mitochondrial Genomic Analyses of the Genus Oryza
inferred← citeshttps://doi.org/10.48130/gcomm-0024-0003openalex-snapshot
Rethinking the mutation hypotheses of plant organellar DNA
inferred← citeshttps://doi.org/10.48130/gcomm-0025-0018openalex-snapshot
Mitochondrial genomes of four Dendrobium species (Orchidaceae): a comprehensive analysis of structural diversity, synteny, and plastid-derived sequences
inferred← citeshttps://doi.org/10.48130/gcomm-0026-0003openalex-snapshot
Rapid turnover of mitogenomic repeats and congruent phylogenomic signal among Digitalideae genomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.24499311openalex-snapshot
Additional file 1 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.24499482openalex-snapshot
Additional file 2 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.25749990openalex-snapshot
Additional file 1 of De novo assembly of the complete mitochondrial genome of pepino (Solanum muricatum) using PacBio HiFi sequencing: insights into structure, phylogenetic implications, and RNA editing
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635740openalex-snapshot
Additional file 3 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635743openalex-snapshot
Additional file 4 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635746openalex-snapshot
Additional file 5 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635749openalex-snapshot
Additional file 6 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635752openalex-snapshot
Additional file 7 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635755openalex-snapshot
Additional file 8 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635758openalex-snapshot
Additional file 9 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635761openalex-snapshot
Additional file 10 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.6084/m9.figshare.26635764openalex-snapshot
Additional file 11 of Complete mitogenome assembly of Selenicereus monacanthus revealed its molecular features, genome evolution, and phylogenetic implications
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.