On the public citation graph

Mechanisms of Recent Genome Size Variation in Flowering Plants

https://doi.org/10.1093/aob/mci008
0 signed · 636 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/j.1537-2197.1985.tb08425.xopenalex-snapshot
C-Band Heterochromatin and DNA Content in Zea mays
inferredcites →https://doi.org/10.1006/anbo.1998.0746openalex-snapshot
Evidence that a Recent Increase in Maize Genome Size was Caused by the Massive Amplification of Intergene Retrotransposons
inferredcites →https://doi.org/10.1006/anbo.1998.0783openalex-snapshot
Phylogenetic Analysis of DNA C-values provides Evidence for a Small Ancestral Genome Size in Flowering Plants
inferredcites →https://doi.org/10.1007/bf00485947openalex-snapshot
Genome size and the proportion of repeated nucleotide sequence DNA in plants
inferredcites →https://doi.org/10.1007/s10142-002-0055-5openalex-snapshot
Genomic sequencing reveals gene content, genomic organization, and recombination relationships in barley
inferredcites →https://doi.org/10.1016/0966-842x(96)10042-1openalex-snapshot
The contributions of retroelements to plant genome organization, function and evolution
inferredcites →https://doi.org/10.1016/j.tig.2003.09.010openalex-snapshot
Selfish DNA is maladaptive: evidence from the plant Red List
inferredcites →https://doi.org/10.1016/s1360-1385(99)01430-2openalex-snapshot
How plants make ends meet: DNA double-strand break repair
inferredcites →https://doi.org/10.1023/a:1006392424384openalex-snapshot
Genome evolution in polyploids
inferredcites →https://doi.org/10.1023/a:1016020030189openalex-snapshot
Feast and famine in plant genomes
inferredcites →https://doi.org/10.1023/a:1022324205661openalex-snapshot
Differences in the processing of DNA ends in Arabidopsis thaliana and tobacco: possible implications for genome evolution
inferredcites →https://doi.org/10.1038/1695openalex-snapshot
The paleontology of intergene retrotransposons of maize
inferredcites →https://doi.org/10.1038/35048692openalex-snapshot
Analysis of the genome sequence of the flowering plant Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/384346a0openalex-snapshot
High intrinsic rate of DNA loss in Drosophila
inferredcites →https://doi.org/10.1038/hdy.1985.112openalex-snapshot
Nuclear DNA content in the genera Zea and Sorghum. Intergeneric, interspecific and intraspecific variation
inferredcites →https://doi.org/10.1038/ng1063openalex-snapshot
Transcriptional activation of retrotransposons alters the expression of adjacent genes in wheat
inferredcites →https://doi.org/10.1073/pnas.132259199openalex-snapshot
Intraspecific violation of genetic colinearity and its implications in maize
inferredcites →https://doi.org/10.1073/pnas.1434476100openalex-snapshot
A complex history of rearrangement in an orthologous region of the maize, sorghum, and rice genomes
inferredcites →https://doi.org/10.1073/pnas.91.25.11792openalex-snapshot
Retrotransposons in the flanking regions of normal plant genes: a role for copia-like elements in the evolution of gene structure and expression.
inferredcites →https://doi.org/10.1073/pnas.94.13.6809openalex-snapshot
DNA sequence evidence for the segmental allotetraploid origin of maize
inferredcites →https://doi.org/10.1086/280745openalex-snapshot
Chromosome Homology in Races of Maize From Different Geographical Regions
inferredcites →https://doi.org/10.1093/aob/mci011openalex-snapshot
The Large Genome Constraint Hypothesis: Evolution, Ecology and Phenotype
inferredcites →https://doi.org/10.1093/aob/mci014openalex-snapshot
Evolution of DNA Amounts Across Land Plants (Embryophyta)
inferredcites →https://doi.org/10.1093/aob/mci015openalex-snapshot
Genome Evolution in the Genus Sorghum (Poaceae)
inferredcites →https://doi.org/10.1093/emboj/19.20.5562openalex-snapshot
Species‐specific double‐strand break repair and genome evolution in plants
inferredcites →https://doi.org/10.1093/genetics/10.2.117openalex-snapshot
THE EFFECTS OF UNEQUAL CROSSING OVER AT THE BAR LOCUS IN DROSOPHILA
inferredcites →https://doi.org/10.1093/genetics/34.5.524openalex-snapshot
NUMBERS AND DISTRIBUTION OF CHROMOSOME KNOBS IN UNITED STATES MAIZE
inferredcites →https://doi.org/10.1093/jhered/91.3.221openalex-snapshot
Pseudogene evolution and natural selection for a compact genome
inferredcites →https://doi.org/10.1098/rspb.1972.0042openalex-snapshot
Nuclear DNA content and minimum generation time in herbaceous plants
inferredcites →https://doi.org/10.1101/gr.10.7.908openalex-snapshot
A Contiguous 66-kb Barley DNA Sequence Provides Evidence for Reversible Genome Expansion
inferredcites →https://doi.org/10.1101/gr.132102openalex-snapshot
Genome Size Reduction through Illegitimate Recombination Counteracts Genome Expansion in Arabidopsis
inferredcites →https://doi.org/10.1101/gr.1466204openalex-snapshot
Analyses of LTR-Retrotransposon Structures Reveal Recent and Rapid Genomic DNA Loss in Rice
inferredcites →https://doi.org/10.1105/tpc.011023openalex-snapshot
Rapid Genome Divergence at Orthologous Low Molecular Weight Glutenin Loci of the A and Am Genomes of Wheat[W]
inferredcites →https://doi.org/10.1105/tpc.11.9.1769openalex-snapshot
Retrotransposon BARE-1 and Its Role in Genome Evolution in the Genus Hordeum
inferredcites →https://doi.org/10.1105/tpc.9.9.1509openalex-snapshot
Do Plants Have a One-Way Ticket to Genomic Obesity?
inferredcites →https://doi.org/10.1126/science.1061334openalex-snapshot
RNA Silencing in Plants--Defense and Counterdefense
inferredcites →https://doi.org/10.1126/science.1071402openalex-snapshot
Opening the Door to Comparative Plant Biology
inferredcites →https://doi.org/10.1126/science.134.3474.282openalex-snapshot
Correlation of Nuclear Volume and DNA Content with Higher Plant Tolerance to Chronic Radiation
inferredcites →https://doi.org/10.1126/science.274.5288.765openalex-snapshot
Nested Retrotransposons in the Intergenic Regions of the Maize Genome
inferredcites →https://doi.org/10.1126/science.287.5455.1060openalex-snapshot
Evidence for DNA Loss as a Determinant of Genome Size
inferredcites →https://doi.org/10.1126/science.6251544openalex-snapshot
The Origins of Gene Instability in Yeast
inferredcites →https://doi.org/10.1128/9781555818180.ch8openalex-snapshot
Illegitimate Recombination in Bacteria
inferredcites →https://doi.org/10.1146/annurev.genet.33.1.479openalex-snapshot
Plant Retrotransposons

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.265.3.4zenodo-depositor-declared
Taxonomic remarks on the genus Sternbergia L. (Amaryllidaceae) in Turkey based on leaf anatomy, karyosystematic analysis and nuclear DNA content
inferred← citeshttps://doi.org/10.24823/ejb.2022.1876zenodo-depositor-declared
EVOLUTIONARY PATTERNS OF GENOME SIZE AND CHROMOSOME NUMBER VARIATION IN BEGONIACEAE
inferred← citeshttps://doi.org/10.3897/phytokeys.234.108841zenodo-depositor-declared
Karyotype and genome size variation in Delphinium subg. Anthriscifolium (Ranunculaceae)
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026814openalex-snapshot
Genome Evolution in Plants
inferred← citeshttps://doi.org/10.1002/9781118305881.ch8openalex-snapshot
Comparative Evolutionary Genomics of Land Plants
inferred← citeshttps://doi.org/10.1002/9781118500156.ch10openalex-snapshot
Transposons, Genomic Shock, and Genome Evolution
inferred← citeshttps://doi.org/10.1002/9781118500156.ch6openalex-snapshot
Transposons in Plant Gene Regulation
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0493openalex-snapshot
Comparative Evolutionary Genomics of Land Plants
inferred← citeshttps://doi.org/10.1002/ajb2.1002openalex-snapshot
Adaptation in plant genomes: Bigger is different
inferred← citeshttps://doi.org/10.1002/ece3.70458openalex-snapshot
Comparison of the Distribution Patterns of Microsatellites Across the Genomes of Reptiles
inferred← citeshttps://doi.org/10.1002/ece3.7222openalex-snapshot
Which factors contribute most to genome size variation within angiosperms?
inferred← citeshttps://doi.org/10.1002/ece3.72438openalex-snapshot
Plant Genome Size Is Associated With Fine‐Scale Spatial Variation in Soil Depth, but Not Climatic Conditions, in the Grass Festuca ovina
inferred← citeshttps://doi.org/10.1002/ece3.73826openalex-snapshot
Chloroplast Genome Insights of Gleditsia japonica var. velutina and Evolutionary Implications for Variation and Phylogeny in Gleditsia
inferred← citeshttps://doi.org/10.1002/tax.603006openalex-snapshot
Phylogenetic relationships of Artemisia subg. Dracunculus (Asteraceae) based on ribosomal and chloroplast DNA sequences
inferred← citeshttps://doi.org/10.1002/tpg2.20027openalex-snapshot
Machine learning analyses of methylation profiles uncovers tissue‐specific gene expression patterns in wheat
inferred← citeshttps://doi.org/10.1007/7397_2016_20openalex-snapshot
Structural Genomics of Angiosperm Trees: Genome Duplications, Ploidy, and Repeat Sequences
inferred← citeshttps://doi.org/10.1007/978-0-387-72299-3_3openalex-snapshot
Legume Comparative Genomics
inferred← citeshttps://doi.org/10.1007/978-0-387-77489-3_17openalex-snapshot
Comparative Genomics in the Triticeae
inferred← citeshttps://doi.org/10.1007/978-0-387-77863-1_9openalex-snapshot
Maize Genome Structure and Evolution
inferred← citeshttps://doi.org/10.1007/978-1-4020-6295-7_8openalex-snapshot
Comparative Genomics of Cereals
inferred← citeshttps://doi.org/10.1007/978-1-4614-8087-7_13openalex-snapshot
Papaya Repeat Database
inferred← citeshttps://doi.org/10.1007/978-1-59745-569-5_22openalex-snapshot
Reduction and Possible Mechanisms of Evolution of the Bacterial Genomes
inferred← citeshttps://doi.org/10.1007/978-3-030-31005-9_7openalex-snapshot
Asymmetric Evolution of Transposable Elements in Brassica oleracea
inferred← citeshttps://doi.org/10.1007/978-3-031-26669-0_2openalex-snapshot
SINE Markers as a Powerful Tool for Assessing Genetic Diversity to Improve Potato
inferred← citeshttps://doi.org/10.1007/978-3-031-30175-9_3openalex-snapshot
Genome Structure of Triticeae Species
inferred← citeshttps://doi.org/10.1007/978-3-031-49193-1_21openalex-snapshot
Cabbage Can’t Always Be Transformed into Turnip: Decision Algorithms for Sorting by Symmetric Reversals
inferred← citeshttps://doi.org/10.1007/978-3-031-64601-0_11openalex-snapshot
Integration of Omics Tools for Enhancing Secondary Metabolite Content in Medicinal and Aromatic Plants
inferred← citeshttps://doi.org/10.1007/978-3-031-81995-7_7openalex-snapshot
Chromosomal Evolution
inferred← citeshttps://doi.org/10.1007/978-3-319-19932-0_5openalex-snapshot
Horizontal Transfers and the New Model of TE-Driven Genome Evolution in Eukaryotes
inferred← citeshttps://doi.org/10.1007/978-3-319-31703-8_1openalex-snapshot
Genome Analysis of Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-64198-0_11openalex-snapshot
Transposable Elements
inferred← citeshttps://doi.org/10.1007/978-3-319-66135-3_9openalex-snapshot
Repetitive Sequences in the Potato and Related Genomes
inferred← citeshttps://doi.org/10.1007/978-3-319-97427-9_4openalex-snapshot
Maize Transposable Element Dynamics
inferred← citeshttps://doi.org/10.1007/978-3-642-14228-4_7openalex-snapshot
Oryza
inferred← citeshttps://doi.org/10.1007/978-3-642-19454-2_12openalex-snapshot
Regulatory Roles of Novel Small RNAs from Pseudogenes
inferred← citeshttps://doi.org/10.1007/978-3-7091-1130-7_14openalex-snapshot
The Variation of Base Composition in Plant Genomes
inferred← citeshttps://doi.org/10.1007/978-3-7091-1160-4_13openalex-snapshot
Karyotype Diversity and Evolutionary Trends in Angiosperms
inferred← citeshttps://doi.org/10.1007/978-3-7091-1160-4_20openalex-snapshot
Genome Size and the Phenotype
inferred← citeshttps://doi.org/10.1007/978-90-481-2967-6_2openalex-snapshot
Comparative Genomics in Crop Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-1521-9_3openalex-snapshot
Genetic Mechanisms Enhancing Plant Biodiversity
inferred← citeshttps://doi.org/10.1007/978-981-15-7903-5_3openalex-snapshot
Biology
inferred← citeshttps://doi.org/10.1007/978-981-15-7903-5_5openalex-snapshot
Phylogeny, Classification, Biogeography, and Evolution
inferred← citeshttps://doi.org/10.1007/978-981-96-6871-7_2openalex-snapshot
Empowering Sugarcane Breeding with New Technologies
inferred← citeshttps://doi.org/10.1007/bf02806558openalex-snapshot
DNA ploidy levels and intraspecific DNA content variability in Romanian fescues (Festuca, Poaceae) measured in fresh and herbarium material
inferred← citeshttps://doi.org/10.1007/s00122-011-1607-7openalex-snapshot
High-throughput SNP discovery and genotyping in durum wheat (Triticum durum Desf.)
inferred← citeshttps://doi.org/10.1007/s00122-011-1626-4openalex-snapshot
Temporal dynamics in the evolution of the sunflower genome as revealed by sequencing and annotation of three large genomic regions
inferred← citeshttps://doi.org/10.1007/s00122-012-1825-7openalex-snapshot
Development and application of SINE-based markers for genotyping of potato varieties
inferred← citeshttps://doi.org/10.1007/s00239-004-0168-7openalex-snapshot
Variability, Recombination, and Mosaic Evolution of the Barley BARE-1 Retrotransposon
inferred← citeshttps://doi.org/10.1007/s00239-014-9663-7openalex-snapshot
Low Levels of LTR Retrotransposon Deletion by Ectopic Recombination in the Gigantic Genomes of Salamanders
inferred← citeshttps://doi.org/10.1007/s00300-016-2058-zopenalex-snapshot
Genome size comparison in Colobanthus quitensis populations show differences in species ploidy
inferred← citeshttps://doi.org/10.1007/s00300-020-02708-0openalex-snapshot
Nuclear DNA content estimations and nuclear development patterns in Antarctic macroalgae
inferred← citeshttps://doi.org/10.1007/s00425-019-03327-8openalex-snapshot
Characterization of Sicilian rosemary (Rosmarinus officinalis L.) germplasm through a multidisciplinary approach
inferred← citeshttps://doi.org/10.1007/s00425-021-03598-0openalex-snapshot
Large vs small genomes in Passiflora: the influence of the mobilome and the satellitome
inferred← citeshttps://doi.org/10.1007/s00438-005-0012-9openalex-snapshot
Updating of transposable element annotations from large wheat genomic sequences reveals diverse activities and gene associations
inferred← citeshttps://doi.org/10.1007/s00438-007-0226-0openalex-snapshot
Differential impact of retrotransposon populations on the genome of allotetraploid tobacco (Nicotiana tabacum)
inferred← citeshttps://doi.org/10.1007/s00438-007-0277-2openalex-snapshot
Structure of two melon regions reveals high microsynteny with sequenced plant species
inferred← citeshttps://doi.org/10.1007/s00438-011-0656-6openalex-snapshot
Matita, a new retroelement from peanut: characterization and evolutionary context in the light of the Arachis A–B genome divergence
inferred← citeshttps://doi.org/10.1007/s00438-014-0855-zopenalex-snapshot
Genomic localization of AtRE1 and AtRE2, copia-type retrotransposons, in natural variants of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00438-014-0973-7openalex-snapshot
Characterization of three active transposable elements recently inserted in three independent DFR-A alleles and one high-copy DNA transposon isolated from the Pink allele of the ANS gene in onion (Allium cepa L.)
inferred← citeshttps://doi.org/10.1007/s00438-015-1122-7openalex-snapshot
Genome-wide analysis of the IQD gene family in maize
inferred← citeshttps://doi.org/10.1007/s00438-016-1235-7openalex-snapshot
Partial sequencing reveals the transposable element composition of Coffea genomes and provides evidence for distinct evolutionary stories
inferred← citeshttps://doi.org/10.1007/s00606-008-0017-zopenalex-snapshot
The shrunken genome of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00606-010-0330-1openalex-snapshot
Genome size in Dipsacaceae and Morina longifolia (Morinaceae)
inferred← citeshttps://doi.org/10.1007/s00606-011-0489-0openalex-snapshot
Nuclear DNA content in the polyploid complex Turnera ulmifolia (Turnera L., Passifloraceae)
inferred← citeshttps://doi.org/10.1007/s00606-011-0534-zopenalex-snapshot
Genome size variation in Chenopodium quinoa (Chenopodiaceae)
inferred← citeshttps://doi.org/10.1007/s00606-011-0555-7openalex-snapshot
Molecular cytogenetics of Bellevalia (Hyacinthaceae) species occurring in Greece
inferred← citeshttps://doi.org/10.1007/s00606-012-0724-3openalex-snapshot
Genome size in Filago L. (Asteraceae, Gnaphalieae) and related genera: phylogenetic, evolutionary and ecological implications
inferred← citeshttps://doi.org/10.1007/s00606-016-1280-zopenalex-snapshot
Clues to the evolution of genome size and chromosome number in Tabebuia alliance (Bignoniaceae)
inferred← citeshttps://doi.org/10.1007/s00606-016-1385-4openalex-snapshot
Hybridization success is largely limited to homoploid Prunus hybrids: a multidisciplinary approach
inferred← citeshttps://doi.org/10.1007/s00606-018-1501-8openalex-snapshot
Small genome size variation across the range of European beech (Fagus sylvatica)
inferred← citeshttps://doi.org/10.1007/s00606-020-01650-2openalex-snapshot
Cytomolecular diversity of the subtribe Laeliinae (Epidendroidae, Orchidaceae) suggests no relationship between genome size and heterochromatin abundance
inferred← citeshttps://doi.org/10.1007/s00606-020-01670-yopenalex-snapshot
Genome size of Balkan flora: a database (GeSDaBaF) and C-values for 51 taxa of which 46 are novel
inferred← citeshttps://doi.org/10.1007/s00709-020-01576-zopenalex-snapshot
A phylogenetic analysis of Momordica (Cucurbitaceae) in India based on karyo-morphology, nuclear DNA content and rDNA ITS1–5.8S–ITS2 sequences
inferred← citeshttps://doi.org/10.1007/s10142-011-0237-0openalex-snapshot
Recent insertion of a 52-kb mitochondrial DNA segment in the wheat lineage
inferred← citeshttps://doi.org/10.1007/s10142-011-0258-8openalex-snapshot
Mutagenesis of barley malting quality QTLs with Ds transposons
inferred← citeshttps://doi.org/10.1007/s10265-014-0637-zopenalex-snapshot
DNA content in South American endemic species of Lathyrus
inferred← citeshttps://doi.org/10.1007/s10265-017-0987-4openalex-snapshot
A novel indicator of karyotype evolution in the tribe Leucocoryneae (Allioideae, Amaryllidaceae)
inferred← citeshttps://doi.org/10.1007/s10530-021-02557-wopenalex-snapshot
Genome size variation in Cactaceae and its relationship with invasiveness and seed traits
inferred← citeshttps://doi.org/10.1007/s10531-025-03062-5openalex-snapshot
Flow cytometry in conservation: detecting hybridization risks in threatened plant species
inferred← citeshttps://doi.org/10.1007/s10577-009-9109-zopenalex-snapshot
FIDEL—a retrovirus-like retrotransposon and its distinct evolutionary histories in the A- and B-genome components of cultivated peanut
inferred← citeshttps://doi.org/10.1007/s10577-011-9230-7openalex-snapshot
Bioinformatics and genomic analysis of transposable elements in eukaryotic genomes
inferred← citeshttps://doi.org/10.1007/s10577-014-9415-yopenalex-snapshot
DNA recombination in somatic plant cells: mechanisms and evolutionary consequences
inferred← citeshttps://doi.org/10.1007/s10709-006-7725-5openalex-snapshot
Morgane, a new LTR retrotransposon group, and its subfamilies in wheats
inferred← citeshttps://doi.org/10.1007/s10709-010-9449-9openalex-snapshot
Genomic screening in dioecious “yerba mate” tree (Ilex paraguariensis A. St. Hill., Aquifoliaceae) through representational difference analysis
inferred← citeshttps://doi.org/10.1007/s10709-015-9820-yopenalex-snapshot
First insight into divergence, representation and chromosome distribution of reverse transcriptase fragments from L1 retrotransposons in peanut and wild relative species
inferred← citeshttps://doi.org/10.1007/s10709-017-9964-zopenalex-snapshot
Transposable elements in the Anopheles funestus transcriptome
inferred← citeshttps://doi.org/10.1007/s10709-020-00094-3openalex-snapshot
Screening diversity and distribution of Copia retrotransposons reveals a specific amplification of BARE1 elements in genomes of the polyploid Hordeum murinum complex
inferred← citeshttps://doi.org/10.1007/s10722-008-9331-0openalex-snapshot
Measurement of nuclear DNA content of the genus Trifolium L. as a measure of genebank accession identity
inferred← citeshttps://doi.org/10.1007/s10722-011-9705-6openalex-snapshot
Ty1-Copia retrotransposons are heterogeneous, extremely high copy number and are major players in the genome organization and evolution of Agave tequilana
inferred← citeshttps://doi.org/10.1007/s10722-016-0448-2openalex-snapshot
Genome size estimations in Chrysanthemum and correlations with molecular phylogenies
inferred← citeshttps://doi.org/10.1007/s11032-009-9357-9openalex-snapshot
Utilization of next-generation sequencing platforms in plant genomics and genetic variant discovery
inferred← citeshttps://doi.org/10.1007/s11032-013-9997-7openalex-snapshot
Genome-wide single nucleotide polymorphism and Insertion-Deletion discovery through next-generation sequencing of reduced representation libraries in common bean
inferred← citeshttps://doi.org/10.1007/s11032-015-0346-xopenalex-snapshot
Identification and distribution of VERNALIZATION1 alleles in Chinese barley (Hordeum vulgare) germplasm
inferred← citeshttps://doi.org/10.1007/s11033-011-1112-8openalex-snapshot
Isolation of Ty1-copia retrotransposon in myrtle genome and development of S-SAP molecular marker
inferred← citeshttps://doi.org/10.1007/s11033-019-05179-7openalex-snapshot
GISH-based comparative genomic analysis in Urochloa P. Beauv.
inferred← citeshttps://doi.org/10.1007/s11103-024-01518-wopenalex-snapshot
Exploring the complexity of genome size reduction in angiosperms
inferred← citeshttps://doi.org/10.1007/s11104-013-1794-xopenalex-snapshot
Small genomes dominate in plants growing on serpentine soils in West Balkans, an exhaustive study of 8 habitats covering 308 taxa
inferred← citeshttps://doi.org/10.1007/s11295-011-0389-zopenalex-snapshot
Genome size and cytogenetic characterization of three Algerian Retama species
inferred← citeshttps://doi.org/10.1007/s11295-011-0421-3openalex-snapshot
A computational study of the dynamics of LTR retrotransposons in the Populus trichocarpa genome
inferred← citeshttps://doi.org/10.1007/s11295-011-0444-9openalex-snapshot
High synteny and colinearity among Eucalyptus genomes revealed by high-density comparative genetic mapping
inferred← citeshttps://doi.org/10.1007/s11295-013-0631-yopenalex-snapshot
Isolation, identification, and characterization of genomic LTR retrotransposon sequences from masson pine (Pinus massoniana)
inferred← citeshttps://doi.org/10.1007/s11295-017-1114-3openalex-snapshot
Genome-wide characterization and evolution analysis of long terminal repeat retroelements in moso bamboo (Phyllostachys edulis)
inferred← citeshttps://doi.org/10.1007/s11434-006-2049-5openalex-snapshot
Comparative analysis of A, B, C and D genomes in the genus Oryza with C 0 t-1 DNA of C genome
inferred← citeshttps://doi.org/10.1007/s11703-007-0041-8openalex-snapshot
Comparative analysis of genomes in Oryza sativa, O. officinalis and O. meyeriana with C 0 t-1 DNA and genomic DNA of cultivated rice
inferred← citeshttps://doi.org/10.1007/s11703-011-1092-4openalex-snapshot
Comparative karyotypic analysis of A and C genomes in the genus Oryza with C 0 t-1 DNA and RFLP
inferred← citeshttps://doi.org/10.1007/s11756-022-01176-7openalex-snapshot
High-efficiency organogenesis and evaluation of the regenerated plants by flow cytometry of a broad range of Saccharum spp. hybrids
inferred← citeshttps://doi.org/10.1007/s12033-009-9151-2openalex-snapshot
Genomic Subtraction Recovers Rye-Specific DNA Elements Enriched in the Rye Genome
inferred← citeshttps://doi.org/10.1007/s12033-018-0118-zopenalex-snapshot
Mutator-Based Transposon Display: A Genetic Tool for Evolutionary and Crop-Improvement Studies in Maize
inferred← citeshttps://doi.org/10.1007/s12042-008-9015-0openalex-snapshot
Genome-Wide Analysis of Repetitive Elements in Papaya
inferred← citeshttps://doi.org/10.1007/s12042-009-9029-2openalex-snapshot
Evolution of Genome size in Hawaiian Endemic Genus Schiedea (Caryophyllaceae)
inferred← citeshttps://doi.org/10.1007/s12224-013-9151-7openalex-snapshot
Substantial Genome Size Variation in Taraxacum stenocephalum (Asteraceae, Lactuceae)
inferred← citeshttps://doi.org/10.1007/s12284-008-9002-yopenalex-snapshot
Rapid and Differential Proliferation of the Ty3-Gypsy LTR Retrotransposon Atlantys in the Genus Oryza
inferred← citeshttps://doi.org/10.1007/s12284-008-9015-6openalex-snapshot
Grass Genomic Synteny Illuminates Plant Genome Function and Evolution
inferred← citeshttps://doi.org/10.1007/s12284-010-9054-7openalex-snapshot
Dynamic Oryza Genomes: Repetitive DNA Sequences as Genome Modeling Agents
inferred← citeshttps://doi.org/10.1007/s12298-018-0587-3openalex-snapshot
Estimation of nuclear DNA content and its variation among Indian Tea accessions by flow cytometry
inferred← citeshttps://doi.org/10.1007/s12374-009-9080-4openalex-snapshot
Evolutionary Process of the Genomic Sequence Around the 100 Map Unit of Chromosome 1 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s13237-011-0034-0openalex-snapshot
Image cytometric determination of nuclear and chromosomal DNA contents in Allium cepa L.
inferred← citeshttps://doi.org/10.1007/s13238-013-3037-6openalex-snapshot
Co-evolution of plant LTR-retrotransposons and their host genomes
inferred← citeshttps://doi.org/10.1007/s13258-011-0238-3openalex-snapshot
Genome-wide scan of the soybean genome using degenerate oligonucleotide primed PCR: an example for studying large complex genome structure
inferred← citeshttps://doi.org/10.1007/s13258-016-0398-2openalex-snapshot
Genetic diversity and structure analyses on the natural populations of diploids and triploids of tiger lily, Lilium lancifolium Thunb., from Korea, China, and Japan
inferred← citeshttps://doi.org/10.1007/s13258-017-0522-yopenalex-snapshot
The genomes and transposable elements in plants: are they friends or foes?
inferred← citeshttps://doi.org/10.1007/s13562-018-0457-7openalex-snapshot
Estimation of nuclear genome size and characterization of Ty1-copia like LTR retrotransposon in Mesua ferrea L.
inferred← citeshttps://doi.org/10.1007/s13580-023-00522-1openalex-snapshot
Comparative triple-color FISH mapping and genome size advances understanding of the cytogenetic diversity in wild Solanum species
inferred← citeshttps://doi.org/10.1007/s40415-016-0358-8openalex-snapshot
Genome size variation among and within Ophiopogoneae species by flow cytometric analysis
inferred← citeshttps://doi.org/10.1007/s40415-018-0449-9openalex-snapshot
Cytomolecular analysis of species in the Peltophorum clade (Caesalpinioideae, Leguminosae)
inferred← citeshttps://doi.org/10.1007/s40415-021-00714-yopenalex-snapshot
First report on genome size and ploidy determination of five indigenous coffee species using flow cytometry and stomatal analysis
inferred← citeshttps://doi.org/10.1007/s40415-021-00729-5openalex-snapshot
Chromosome numbers in Homalolepis Turcz. and their significance in Simaroubaceae evolution
inferred← citeshttps://doi.org/10.1016/b978-0-12-386033-0.00003-7openalex-snapshot
Strategies for Silencing and Escape
inferred← citeshttps://doi.org/10.1016/b978-0-12-397940-7.00003-3openalex-snapshot
Evolutionary and Adaptive Role of Transposable Elements in Fungal Genomes
inferred← citeshttps://doi.org/10.1016/b978-0-12-417163-3.00005-6openalex-snapshot
The First Monocot Genome Sequence
inferred← citeshttps://doi.org/10.1016/b978-0-12-818564-3.09988-1openalex-snapshot
Mutations
inferred← citeshttps://doi.org/10.1016/b978-012301463-4/50004-8openalex-snapshot
Genome Size Evolution in Plants
inferred← citeshttps://doi.org/10.1016/bs.abr.2018.09.001openalex-snapshot
Transposable Elements as Tool for Crop Improvement
inferred← citeshttps://doi.org/10.1016/j.ab.2020.113770openalex-snapshot
Impact of transposable elements on genome size variation between two closely related crustacean species
inferred← citeshttps://doi.org/10.1016/j.aquabot.2018.04.001openalex-snapshot
Karyomorphology and DNA quantification in the marine angiosperm Halophila stipulacea (Forsskål) Ascherson from Mediterranean and Red Seas
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2016.08.009openalex-snapshot
Putting DNA methylation in context: from genomes to gene expression in plants
inferred← citeshttps://doi.org/10.1016/j.bidere.2026.100108openalex-snapshot
Toward Genome-Aware Engineering of Pines: A Genome Architecture Perspective
inferred← citeshttps://doi.org/10.1016/j.biocon.2008.05.019openalex-snapshot
Molecular markers and a sequence deletion in intron 2 of the putative partial homologue of LEAFY reveal geographical structure to genetic diversity in the acutely threatened legume genus Clianthus
inferred← citeshttps://doi.org/10.1016/j.biosystems.2013.02.001openalex-snapshot
Patterns of nucleotide asymmetries in plant and animal genomes
inferred← citeshttps://doi.org/10.1016/j.bse.2021.104271openalex-snapshot
Ploidy differentiation and floral scent divergence in Buddleja macrostachya (Scrophulariaceae) complex
inferred← citeshttps://doi.org/10.1016/j.cpb.2020.100181openalex-snapshot
Antagonistic effects of whole-genome duplications and dysploidy on genome sizes in the pantropical monocot family Marantaceae: Consequences in the light of a new molecular phylogeny
inferred← citeshttps://doi.org/10.1016/j.crpv.2014.06.002openalex-snapshot
A new look at genome size, evolutionary duration and genetic variation in salamanders
inferred← citeshttps://doi.org/10.1016/j.crvi.2012.09.012openalex-snapshot
Estimation of nuclear genome size of the genus Mycetophylax Emery, 1913: Evidence of no whole-genome duplication in Neoattini
inferred← citeshttps://doi.org/10.1016/j.ejop.2023.125991openalex-snapshot
Genome size and GC content of myxomycetes
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2006.04.006openalex-snapshot
Genome size stability among five subspecies of Pinus nigra Arnold s.l.
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2007.07.017openalex-snapshot
Genome size variation and polyploidy in the resurrection plant genus Ramonda: Cytogeography of living fossils
inferred← citeshttps://doi.org/10.1016/j.gde.2005.09.010openalex-snapshot
Transposable elements, gene creation and genome rearrangement in flowering plants
inferred← citeshttps://doi.org/10.1016/j.gde.2007.08.010openalex-snapshot
Give-and-take: interactions between DNA transposons and their host plant genomes
inferred← citeshttps://doi.org/10.1016/j.gde.2015.11.003openalex-snapshot
Polyploidy and genome evolution in plants
inferred← citeshttps://doi.org/10.1016/j.gene.2008.01.009openalex-snapshot
Characterization, genomic organization and chromosomal distribution of Ty1-copia retrotransposons in species of Hypochaeris (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.gene.2012.07.042openalex-snapshot
The impact of transposable elements on eukaryotic genomes: From genome size increase to genetic adaptation to stressful environments
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148177openalex-snapshot
Plastid genomes provide insights into the phylogeny and chloroplast evolution of the paper daisy tribe Gnaphalieae (Asteraceae)
inferred← citeshttps://doi.org/10.1016/j.gpb.2016.06.003openalex-snapshot
Plant Proteins are Smaller Because They are Encoded by Fewer Exons than Animal Proteins
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e39140openalex-snapshot
Comprehensive analysis of computational approaches in plant transcription factors binding regions discovery
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.127132openalex-snapshot
The chromosome-level genome assembly of Fraxinus americana provides insights into the evolution of Oleaceae plants
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104574openalex-snapshot
Genome structure and evolutionary history of frankincense producing Boswellia sacra
inferred← citeshttps://doi.org/10.1016/j.jksuci.2021.11.012openalex-snapshot
Impact of Insertion Sequences and RNAs on Genomic Inversions in Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1016/j.jplph.2021.153365openalex-snapshot
Male gametophyte development in flowering plants: A story of quarantine and sacrifice
inferred← citeshttps://doi.org/10.1016/j.molp.2020.04.010openalex-snapshot
The Reference Genome of Tea Plant and Resequencing of 81 Diverse Accessions Provide Insights into Its Genome Evolution and Adaptation
inferred← citeshttps://doi.org/10.1016/j.pbi.2007.01.010openalex-snapshot
Patterns in grass genome evolution
inferred← citeshttps://doi.org/10.1016/j.plantsci.2008.03.015openalex-snapshot
Repeated big bangs and the expanding universe: Directionality in plant genome size evolution
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.12.004openalex-snapshot
New insights into the wheat chromosome 4D structure and virtual gene order, revealed by survey pyrosequencing
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.06.007openalex-snapshot
Loss of function of OsMADS3 via the insertion of a novel retrotransposon leads to recessive male sterility in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.sajb.2017.11.017openalex-snapshot
Nuclear DNA C-values are correlated with pollen size at tetraploid but not diploid level and linked to phylogenetic descent in Streptocarpus (Gesneriaceae)
inferred← citeshttps://doi.org/10.1016/j.sajb.2026.04.021openalex-snapshot
Quantifying the roles of environmental, seasonal, and genome size variation in the expression of medicinally valuable compounds in Helichrysum kraussii Sch. Bip
inferred← citeshttps://doi.org/10.1016/j.scienta.2015.12.025openalex-snapshot
The chromosomal distribution of repetitive DNA sequences in Chrysanthemum boreale revealed a characterization in its genome
inferred← citeshttps://doi.org/10.1016/j.scienta.2016.06.023openalex-snapshot
Nuclear DNA content variation within the genus Daucus (Apiaceae) determined by flow cytometry
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.108987openalex-snapshot
Determination of genome size and chromosome ploidy of selected taxa from Prunus armeniaca by flow cytometry
inferred← citeshttps://doi.org/10.1016/j.tig.2007.01.004openalex-snapshot
Plant centromere organization: a dynamic structure with conserved functions
inferred← citeshttps://doi.org/10.1016/j.tplants.2023.08.013openalex-snapshot
New whole-genome alignment tools are needed for tapping into plant diversity
inferred← citeshttps://doi.org/10.1016/j.tplants.2024.04.008openalex-snapshot
Can DNA methylation shape climate response in trees?
inferred← citeshttps://doi.org/10.1016/j.ygeno.2011.02.007openalex-snapshot
Comparative analysis of Gossypium and Vitis genomes indicates genome duplication specific to the Gossypium lineage
inferred← citeshttps://doi.org/10.1016/j.ympev.2026.108627openalex-snapshot
Genome size evolution in Helianthemum (Cistaceae): Dynamic genomes within a conserved chromosomal framework
inferred← citeshttps://doi.org/10.1016/s1671-2927(07)60143-6openalex-snapshot
Comparative Analysis of Genomes in Oryza sativa, O. officinalis, and O. meyeriana, with Ct-1 DNA and Genomic DNA of Cultivated Rice
inferred← citeshttps://doi.org/10.1016/s1672-6308(09)60016-0openalex-snapshot
Comparative Analysis on Genomes from Oryza alta and Oryza latifolia by Ct-1 DNA
inferred← citeshttps://doi.org/10.1017/s0016672306008020openalex-snapshot
Comparative gene mapping in Arabidopsis lyrata chromosomes 1 and 2 and the corresponding A. thaliana chromosome 1: recombination rates, rearrangements and centromere location
inferred← citeshttps://doi.org/10.1017/s1479262115000210openalex-snapshot
Sequence-related amplified polymorphism and inter-simple sequence repeat marker-based genetic diversity and nuclear DNA content variation in common vetch (Vicia sativaL.)
inferred← citeshttps://doi.org/10.1017/s1479262126100756openalex-snapshot
Assessment of genome size variation in palm germplasm revealed by flow cytometry
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c03001openalex-snapshot
Genomic Profiling: The Strengths and Limitations of Chloroplast Genome-Based Plant Variety Authentication
inferred← citeshttps://doi.org/10.1038/hdy.2012.99openalex-snapshot
The dynamics of LTR retrotransposon accumulation across 25 million years of panicoid grass evolution
inferred← citeshttps://doi.org/10.1038/nature12211openalex-snapshot
The Norway spruce genome sequence and conifer genome evolution
inferred← citeshttps://doi.org/10.1038/nature22011openalex-snapshot
Genomic innovation for crop improvement
inferred← citeshttps://doi.org/10.1038/ng.3517openalex-snapshot
The genome sequences of Arachis duranensis and Arachis ipaensis, the diploid ancestors of cultivated peanut
inferred← citeshttps://doi.org/10.1038/ng.807openalex-snapshot
The Arabidopsis lyrata genome sequence and the basis of rapid genome size change
inferred← citeshttps://doi.org/10.1038/ng1784openalex-snapshot
A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture
inferred← citeshttps://doi.org/10.1038/nrg1674openalex-snapshot
Synergy between sequence and size in Large-scale genomics
inferred← citeshttps://doi.org/10.1038/nrg1970openalex-snapshot
Recombination: an underappreciated factor in the evolution of plant genomes
inferred← citeshttps://doi.org/10.1038/nrg3374openalex-snapshot
How important are transposons for plant evolution?
inferred← citeshttps://doi.org/10.1038/s41438-019-0156-0openalex-snapshot
In the name of the rose: a roadmap for rose research in the genome era
inferred← citeshttps://doi.org/10.1038/s41598-017-01518-5openalex-snapshot
Inferring the evolutionary mechanism of the chloroplast genome size by comparing whole-chloroplast genome sequences in seed plants
inferred← citeshttps://doi.org/10.1038/s41598-019-41474-wopenalex-snapshot
Bromeliaceae subfamilies show divergent trends of genome size evolution
inferred← citeshttps://doi.org/10.1038/s41598-019-52840-zopenalex-snapshot
Expansion of LINEs and species-specific DNA repeats drives genome expansion in Asian Gypsy Moths
inferred← citeshttps://doi.org/10.1038/s42003-020-01593-xopenalex-snapshot
Coconut genome assembly enables evolutionary analysis of palms and highlights signaling pathways involved in salt tolerance
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800696openalex-snapshot
Does genome size in Dasypyrum villosum vary with fruit colour?
inferred← citeshttps://doi.org/10.1038/srep11636openalex-snapshot
Nitrogen limitation as a driver of genome size evolution in a group of karst plants
inferred← citeshttps://doi.org/10.1038/srep17644openalex-snapshot
Genome-wide Annotation and Comparative Analysis of Long Terminal Repeat Retrotransposons between Pear Species of P. bretschneideri and P. Communis
inferred← citeshttps://doi.org/10.1055/s-2005-865693openalex-snapshot
Nuclear DNA Content and Chromosome Number in Some Diploid and Tetraploid Centaurea (Asteraceae: Cardueae) from the Dalmatia Region
inferred← citeshttps://doi.org/10.1073/pnas.0403715101openalex-snapshot
Rapid recent growth and divergence of rice nuclear genomes
inferred← citeshttps://doi.org/10.1073/pnas.0509810102openalex-snapshot
Recombination, rearrangement, reshuffling, and divergence in a centromeric region of rice
inferred← citeshttps://doi.org/10.1073/pnas.0603080103openalex-snapshot
Remarkable variation in maize genome structure inferred from haplotype diversity at the bz locus
showing the first 200 of 593
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.