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Asteraceae as a model system for evolutionary studies: from fossils to genomes
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Phylogenetic signatures of ecological divergence and leapfrog adaptive radiation in Espeletia
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Lineage‐specific vs. universal: A comparison of the Compositae1061 and Angiosperms353 enrichment panels in the sunflower family
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Temporal and palaeoclimatic context of the evolution of insular woodiness in the Canary Islands
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A draft genome provides hypotheses on drought tolerance in a keystone plant species in Western North America threatened by climate change
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A chromosome‐scale draft sequence of the Canada fleabane genome
inferredcites →https://doi.org/10.1002/tax.12235openalex-snapshot
The classification of the Compositae: A tribute to Vicki Ann Funk (1947–2019)
inferredcites →https://doi.org/10.1002/tax.12426openalex-snapshot
Photosynthesis metabolism in the Compositae: Current knowledge and future directions
inferredcites →https://doi.org/10.1002/tpg2.20095openalex-snapshot
Dynamic changes of genome sizes and gradual gain of cell‐specific distribution of C 4 enzymes during C 4 evolution in genus Flaveria
inferredcites →https://doi.org/10.1006/qres.1999.2065openalex-snapshot
Physiological Significance of Low Atmospheric CO2 for Plant–Climate Interactions
inferredcites →https://doi.org/10.1007/978-3-7091-1160-4_16openalex-snapshot
The Incidence of Polyploidy in Natural Plant Populations: Major Patterns and Evolutionary Processes
inferredcites →https://doi.org/10.1007/bf02857754openalex-snapshot
Capitula in the Asteridae: A widespread and varied phenomenon
inferredcites →https://doi.org/10.1007/bf02887192openalex-snapshot
Inflorescence and floral ontogeny in asteraceae: A synthesis of historical and current concepts
inferredcites →https://doi.org/10.1007/s00035-018-0208-3openalex-snapshot
The highest vascular plants on Earth
inferredcites →https://doi.org/10.1007/s00122-007-0605-2openalex-snapshot
Universal markers for comparative mapping and phylogenetic analysis in the Asteraceae (Compositae)
inferredcites →https://doi.org/10.1007/s00606-006-0451-8openalex-snapshot
Exceedingly high chromosome number in Strasburgeriaceae, a monotypic family endemic to New Caledonia
inferredcites →https://doi.org/10.1007/s00606-009-0185-5openalex-snapshot
New insights into the pollen morphology of the genus Mutisia (Asteraceae, Mutisieae)
inferredcites →https://doi.org/10.1007/s00606-009-0257-6openalex-snapshot
Echinate fossil pollen of Asteraceae from the Late Oligocene of Patagonia: an assessment of its botanical affinity
inferredcites →https://doi.org/10.1007/s00606-012-0618-4openalex-snapshot
Genome size and chromosome number in Echinops (Asteraceae, Cardueae) in the Aegean and Balkan regions: technical aspects of nuclear DNA amount assessment and genome evolution in a phylogenetic frame
inferredcites →https://doi.org/10.1007/s00606-013-0774-1openalex-snapshot
Pollen morphology and its taxonomic significance in the tribe Gochnatieae (Compositae, Gochnatioideae)
inferredcites →https://doi.org/10.1007/s11427-021-2033-2openalex-snapshot
Extensive sequence divergence between the reference genomes of Taraxacum kok-saghyz and Taraxacum mongolicum
inferredcites →https://doi.org/10.1007/s12229-010-9057-5openalex-snapshot
Paedomorphosis, Secondary Woodiness, and Insular Woodiness in Plants
inferredcites →https://doi.org/10.1007/s12892-020-00038-5openalex-snapshot
Improving productivity of steviol glycosides in Stevia rebaudiana via induced polyploidy
inferredcites →https://doi.org/10.1016/j.biombioe.2019.03.016openalex-snapshot
Towards high-biomass yielding bioenergy crop Silphium perfoliatum L.: phenotypic and genotypic evaluation of five cultivated populations
inferredcites →https://doi.org/10.1016/j.cretres.2004.02.002openalex-snapshot
Maastrichtian stratigraphy of Antarctica
inferredcites →https://doi.org/10.1016/j.cretres.2011.11.015openalex-snapshot
Sedimentary cycles, ammonite diversity and palaeoenvironmental changes in the Upper Cretaceous Marambio Group, Antarctica
inferredcites →https://doi.org/10.1016/j.cub.2011.12.027openalex-snapshot
Rapid, Repeated, and Clustered Loss of Duplicate Genes in Allopolyploid Plant Populations of Independent Origin
inferredcites →https://doi.org/10.1016/j.cub.2020.09.019openalex-snapshot
The Radiation of Darwin’s Giant Daisies in the Galápagos Islands
inferredcites →https://doi.org/10.1016/j.gene.2018.04.050openalex-snapshot
Contribution of transposable elements in the plant's genome
inferredcites →https://doi.org/10.1016/j.gloplacha.2021.103556openalex-snapshot
Role of climate and tectonism on the modernization of Patagonian floras: Evidence from the fossil record
inferredcites →https://doi.org/10.1016/j.molp.2018.03.015openalex-snapshot
The Genome of Artemisia annua Provides Insight into the Evolution of Asteraceae Family and Artemisinin Biosynthesis
inferredcites →https://doi.org/10.1016/j.molp.2018.10.003openalex-snapshot
The Chrysanthemum nankingense Genome Provides Insights into the Evolution and Diversification of Chrysanthemum Flowers and Medicinal Traits
inferredcites →https://doi.org/10.1016/j.palwor.2006.03.002openalex-snapshot
Correlation of pollen sequences in the Neogene palynofloristic regions of China
inferredcites →https://doi.org/10.1016/j.ppees.2013.07.003openalex-snapshot
Trans-oceanic dispersal and evolution of early composites (Asteraceae)
inferredcites →https://doi.org/10.1016/j.revpalbo.2006.07.010openalex-snapshot
Early history of Cainozoic Asteraceae along the Southern African west coast
inferredcites →https://doi.org/10.1016/j.revpalbo.2008.02.002openalex-snapshot
Fossil pollen grains of Asteraceae from the Miocene of Patagonia: Nassauviinae affinity
inferredcites →https://doi.org/10.1016/j.revpalbo.2009.03.001openalex-snapshot
Fossil pollen grains of Asteraceae from the Miocene of Patagonia: Barnadesioideae affinity
inferredcites →https://doi.org/10.1016/j.revpalbo.2010.02.004openalex-snapshot
Fossil pollen indicates an explosive radiation of basal Asteracean lineages and allied families during Oligocene and Miocene times in the Southern Hemisphere
inferredcites →https://doi.org/10.1016/j.revpalbo.2015.05.008openalex-snapshot
Evolutionary significance of exine ultrastructure in the subfamily Barnadesioideae (Asteraceae) in the light of molecular phylogenetics
inferredcites →https://doi.org/10.1016/j.ympev.2008.02.011openalex-snapshot
The value of sampling anomalous taxa in phylogenetic studies: Major clades of the Asteraceae revealed
inferredcites →https://doi.org/10.1016/j.ympev.2014.07.012openalex-snapshot
Resolution of deep nodes yields an improved backbone phylogeny and a new basal lineage to study early evolution of Asteraceae
inferredcites →https://doi.org/10.1016/j.ympev.2016.03.007openalex-snapshot
Macroevolutionary dynamics in the early diversification of Asteraceae
inferredcites →https://doi.org/10.1016/s0034-6667(02)00227-0openalex-snapshot
Proustia and Lophopappus (Asteraceae, Mutisieae): generic and subtribal relationships based on pollen morphology
inferredcites →https://doi.org/10.1016/s0034-6667(98)00049-9openalex-snapshot
Pollen morphology of the subfamily Barnadesioideae (Asteraceae) and its phylogenetic and taxonomic significance
inferredcites →https://doi.org/10.1016/s0037-0738(00)00159-7openalex-snapshot
A dolomitized diatomite in an Oligocene–Miocene deep-sea fan succession, Gonfolite Lombarda Group, Northern Italy
inferredcites →https://doi.org/10.1023/a:1011483901452openalex-snapshot
Diversity and abundance of vascular epiphytes: a comparison of secondary vegetation and primary montane rain forest in the Venezuelan Andes
inferredcites →https://doi.org/10.1038/nature22380openalex-snapshot
The sunflower genome provides insights into oil metabolism, flowering and Asterid evolution
inferredcites →https://doi.org/10.1038/ncomms14953openalex-snapshot
Genome assembly with in vitro proximity ligation data and whole-genome triplication in lettuce
inferredcites →https://doi.org/10.1038/s41438-017-0003-0openalex-snapshot
Genomic and transcriptomic alterations following intergeneric hybridization and polyploidization in the Chrysanthemum nankingense×Tanacetum vulgare hybrid and allopolyploid (Asteraceae)
inferredcites →https://doi.org/10.1038/s41467-019-13926-4openalex-snapshot
Mikania micrantha genome provides insights into the molecular mechanism of rapid growth
inferredcites →https://doi.org/10.1038/s41467-021-27897-yopenalex-snapshot
The rise of grasslands is linked to atmospheric CO2 decline in the late Palaeogene
inferredcites →https://doi.org/10.1038/s41477-020-00785-xopenalex-snapshot
Repeat-sequence turnover shifts fundamentally in species with large genomes
inferredcites →https://doi.org/10.1038/s41588-021-00831-0openalex-snapshot
Whole-genome resequencing of 445 Lactuca accessions reveals the domestication history of cultivated lettuce
inferredcites →https://doi.org/10.1038/s41598-019-54815-6openalex-snapshot
Draft genome of Tanacetum cinerariifolium, the natural source of mosquito coil
inferredcites →https://doi.org/10.1038/s42003-021-02704-yopenalex-snapshot
A chromosome-level genome sequence of Chrysanthemum seticuspe, a model species for hexaploid cultivated chrysanthemum
inferredcites →https://doi.org/10.1038/srep19427openalex-snapshot
The genome sequence of the outbreeding globe artichoke constructed de novo incorporating a phase-aware low-pass sequencing strategy of F1 progeny
inferredcites →https://doi.org/10.1073/pnas.1112041109openalex-snapshot
Extensive chromosomal variation in a recently formed natural allopolyploid species, Tragopogon miscellus (Asteraceae)
inferredcites →https://doi.org/10.1073/pnas.1423653112openalex-snapshot
Early evolution of the angiosperm clade Asteraceae in the Cretaceous of Antarctica
inferredcites →https://doi.org/10.1073/pnas.1903871116openalex-snapshot
A fully resolved backbone phylogeny reveals numerous dispersals and explosive diversifications throughout the history of Asteraceae
inferredcites →https://doi.org/10.1080/00087114.2013.829690openalex-snapshot
Genome size variation and evolution in the family Asteraceae
inferredcites →https://doi.org/10.1080/00173130150503795openalex-snapshot
Pollen of the Asteraceae from the Paleocene-Eocene of South Africa
inferredcites →https://doi.org/10.1080/00173130510010495openalex-snapshot
The unusual occurrence of tricolpate pollen within Mutisieae (Asteraceae)
inferredcites →https://doi.org/10.1080/00288306.2015.1086391openalex-snapshot
New Zealand Geological Timescale NZGT 2015/1
inferredcites →https://doi.org/10.1080/0035919x.2015.1072859openalex-snapshot
Shaping of modern southern African biomes: Neogene vegetation and climate changes
inferredcites →https://doi.org/10.1080/01916122.1999.9989528openalex-snapshot
Palynostratigraphy of the murray basin, inland Southeastern Australia
inferredcites →https://doi.org/10.1080/08912963.2020.1851686openalex-snapshot
Plant and invertebrate macrofossils from the Pipe Creek Sinkhole (Late Neogene), Grant County, Indiana
inferredcites →https://doi.org/10.1080/17550870802331904openalex-snapshot
The Arctic – an evolutionary freezer?
inferredcites →https://doi.org/10.1086/430055openalex-snapshot
Eocene Plant Diversity at Laguna del Hunco and Río Pichileufú, Patagonia, Argentina
inferredcites →https://doi.org/10.1086/593044openalex-snapshot
Correlated Evolution of Leaf Shape and Physiology in the Woody Sonchus Alliance (Asteraceae: Sonchinae) in Macaronesia
inferredcites →https://doi.org/10.1086/700581openalex-snapshot
The Role of Antarctica in Biogeographical Reconstruction: A Point of View
inferredcites →https://doi.org/10.1086/708386openalex-snapshot
Early Eocene Spore and Pollen Assemblages from the Laguna del Hunco Fossil Lake Beds, Patagonia, Argentina
inferredcites →https://doi.org/10.1086/713445openalex-snapshot
The Next Generation of Adaptive Radiation Studies in Plants
inferredcites →https://doi.org/10.1093/aob/mcr240openalex-snapshot
An extinct Eocene taxon of the daisy family (Asteraceae): evolutionary, ecological and biogeographical implications
inferredcites →https://doi.org/10.1093/aob/mcz183openalex-snapshot
Genome size variation at constant chromosome number is not correlated with repetitive DNA dynamism in Anacyclus (Asteraceae)
inferredcites →https://doi.org/10.1093/aobpla/plv081openalex-snapshot
250 years of hybridization between two biennial herb species without speciation
inferredcites →https://doi.org/10.1093/bfgp/elu004openalex-snapshot
Genomic variation in Helianthus: learning from the past and looking to the future
inferredcites →https://doi.org/10.1093/botlinnean/boaa058openalex-snapshot
The correlation of phylogenetics, elevation and ploidy on the incidence of apomixis in Asteraceae in the European Alps
inferredcites →https://doi.org/10.1093/database/baz098openalex-snapshot
Progress in the study of genome size evolution in Asteraceae: analysis of the last update
inferredcites →https://doi.org/10.1093/g3journal/jkab358openalex-snapshot
De novo whole-genome assembly of Chrysanthemum makinoi , a key wild chrysanthemum
inferredcites →https://doi.org/10.1093/g3journal/jkac122openalex-snapshot
A haploid pseudo-chromosome genome assembly for a keystone sagebrush species of western North American rangelands
inferredcites →https://doi.org/10.1093/gbe/evv230openalex-snapshot
Repetitive DNA and Plant Domestication: Variation in Copy Number and Proximity to Genes of LTR-Retrotransposons among Wild and Cultivated Sunflower (Helianthus annuus) Genotypes
inferredcites →https://doi.org/10.1093/gbe/evw251openalex-snapshot
The Evolution of Haploid Chromosome Numbers in the Sunflower Family
inferredcites →https://doi.org/10.1093/hr/uhab022openalex-snapshot
The Chrysanthemum lavandulifolium genome and the molecular mechanism underlying diverse capitulum types
inferredcites →https://doi.org/10.1093/jhered/esab077openalex-snapshot
A Genome forBidens hawaiensis: A Member of a Hexaploid Hawaiian Plant Adaptive Radiation
inferredcites →https://doi.org/10.1093/molbev/msw157openalex-snapshot
Multiple Polyploidization Events across Asteraceae with Two Nested Events in the Early History Revealed by Nuclear Phylogenomics
inferredcites →https://doi.org/10.1093/plcell/koaa015openalex-snapshot
Polyploidy: an evolutionary and ecological force in stressful times
inferredcites →https://doi.org/10.1093/sysbio/syy024openalex-snapshot
Dating the Species Network: Allopolyploidy and Repetitive DNA Evolution in American Daisies (Melampodium sect. Melampodium, Asteraceae)
inferredcites →https://doi.org/10.1098/rspb.2019.0099openalex-snapshot
Darwin review: angiosperm phylogeny and evolutionary radiations
inferredcites →https://doi.org/10.1104/pp.114.247668openalex-snapshot
De Novo Genome Assembly of the Economically Important Weed Horseweed Using Integrated Data from Multiple Sequencing Platforms
inferredcites →https://doi.org/10.1111/1365-2664.13656openalex-snapshot
Controlling invasive plant species in ecological restoration: A global review
inferredcites →https://doi.org/10.1111/1755-0998.12935openalex-snapshot
Application of CRISPR/Cas9 to Tragopogon (Asteraceae), an evolutionary model for the study of polyploidy
inferredcites →https://doi.org/10.1111/1755-0998.13257openalex-snapshot
High quality genome of Erigeron breviscapus provides a reference for herbal plants in Asteraceae
inferredcites →https://doi.org/10.1111/1755-0998.13547openalex-snapshot
The first high‐quality chromosomal genome assembly of a medicinal and edible plant Arctium lappa
inferredcites →https://doi.org/10.1111/boj.12357openalex-snapshot
Is post-polyploidization diploidization the key to the evolutionary success of angiosperms?
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00335.xopenalex-snapshot
Recent and recurrent polyploidy in Tragopogon (Asteraceae): cytogenetic, genomic and genetic comparisons
inferredcites →https://doi.org/10.1111/j.1095-8312.2006.00557.xopenalex-snapshot
An overview of the Cape geophytes
inferredcites →https://doi.org/10.1111/j.1095-8339.2004.00287.xopenalex-snapshot
On the origin and development of Artemisia (Asteraceae) in the geological past
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00270.xopenalex-snapshot
PARALLEL EVOLUTIONARY PATTERNS IN MULTIPLE LINEAGES OF ARCTIC ARTEMISIA L. (ASTERACEAE)
inferredcites →https://doi.org/10.1111/j.1601-5223.1969.tb02229.xopenalex-snapshot
CYTOGENETIC COMPARISON BETWEEN TWO KINDS OF CULTIVATED TARRAGON (ARTEMISIA DRACUNCULUS)
inferredcites →https://doi.org/10.1111/j.1744-7909.2005.00124.xopenalex-snapshot
Pollen Morphology of Eight Genera of the Subtribe Mutisiinae Less. Sensu Bremer (Compositae) from Asia
inferredcites →https://doi.org/10.1111/j.1759-6831.2010.00088.xopenalex-snapshot
Adding time-calibrated branch lengths to the Asteraceae supertree
inferredcites →https://doi.org/10.1111/jbi.13496openalex-snapshot
Big data for a large clade: Bioregionalization and ancestral range estimation in the daisy family (Asteraceae)
inferredcites →https://doi.org/10.1111/jipb.13078openalex-snapshot
Phylotranscriptomic insights into Asteraceae diversity, polyploidy, and morphological innovation
inferredcites →https://doi.org/10.1111/jse.12167openalex-snapshot
Using phylogenomics to resolve mega‐families: An example from Compositae
inferredcites →https://doi.org/10.1111/jse.12216openalex-snapshot
A comprehensive generic‐level phylogeny of the sunflower family: Implications for the systematics of Chinese Asteraceae
inferredcites →https://doi.org/10.1111/jse.12265openalex-snapshot
The Compositae Tree of Life in the age of phylogenomics
inferredcites →https://doi.org/10.1111/jse.12681openalex-snapshot
The importance of the Mexican taxa of Asteraceae in the family phylogeny
inferredcites →https://doi.org/10.1111/jse.12698openalex-snapshot
Phylogenomics of the hyperdiverse daisy tribes: Anthemideae, Astereae, Calenduleae, Gnaphalieae, and Senecioneae
inferredcites →https://doi.org/10.1111/jse.12704openalex-snapshot
Dispersal and adaptive radiation of Bidens (Compositae) across the remote archipelagoes of Polynesia
inferredcites →https://doi.org/10.1111/nph.13491openalex-snapshot
Nested radiations and the pulse of angiosperm diversification: increased diversification rates often follow whole genome duplications
inferredcites →https://doi.org/10.1111/nph.15797openalex-snapshot
Island woodiness underpins accelerated disparification in plant radiations
inferredcites →https://doi.org/10.1111/nph.15823openalex-snapshot
When flowering plants ruled Antarctica: evidence from Cretaceous pollen grains
inferredcites →https://doi.org/10.1111/nph.16434openalex-snapshot
Senecio as a model system for integrating studies of genotype, phenotype and fitness
inferredcites →https://doi.org/10.1111/nph.18024openalex-snapshot
Why does pollen morphology vary? Evolutionary dynamics and morphospace occupation in the largest angiosperm order (Asterales)
inferredcites →https://doi.org/10.1111/pbi.13586openalex-snapshot
The chromosome‐scale reference genome of safflower (Carthamus tinctorius) provides insights into linoleic acid and flavonoid biosynthesis
inferredcites →https://doi.org/10.1111/pce.13887openalex-snapshot
Angiosperms at the edge: Extremity, diversity, and phylogeny
inferredcites →https://doi.org/10.1111/tpj.13736openalex-snapshot
Spatial organization of silybin biosynthesis in milk thistle [Silybum marianum (L.) Gaertn]
inferredcites →https://doi.org/10.1111/tpj.15363openalex-snapshot
Genome downsizing after polyploidy: mechanisms, rates and selection pressures
inferredcites →https://doi.org/10.1126/science.1193108openalex-snapshot
Eocene Patagonia Fossils of the Daisy Family
inferredcites →https://doi.org/10.1126/science.231.4743.1278openalex-snapshot
Myrmecia pilosula , an Ant with Only One Pair of Chromosomes
inferredcites →https://doi.org/10.1186/1471-2229-13-219openalex-snapshot
Genome size expansion and the relationship between nuclear DNA content and spore size in the Asplenium monanthes fern complex (Aspleniaceae)
inferredcites →https://doi.org/10.1186/s12864-015-1830-8openalex-snapshot
Evolutionary transitions in the Asteraceae coincide with marked shifts in transposable element abundance
inferredcites →https://doi.org/10.1186/s12870-020-02742-4openalex-snapshot
Sequencing and analysis of gerbera daisy leaf transcriptomes reveal disease resistance and susceptibility genes differentially expressed and associated with powdery mildew resistance
inferredcites →https://doi.org/10.12688/f1000research.24396.1openalex-snapshot
The complete genome sequence of Stevia rebaudiana, the Sweetleaf
inferredcites →https://doi.org/10.12705/661.8openalex-snapshot
Cytogenetic insights into an oceanic island radiation: The dramatic evolution of pre‐existing traits in Cheirolophus (Asteraceae: Cardueae: Centaureinae)
inferredcites →https://doi.org/10.1371/journal.pone.0003353openalex-snapshot
Rapid Chromosome Evolution in Recently Formed Polyploids in Tragopogon (Asteraceae)
inferredcites →https://doi.org/10.1371/journal.pone.0069281openalex-snapshot
First Evidence for Wollemi Pine-type Pollen (Dilwynites: Araucariaceae) in South America
inferredcites →https://doi.org/10.1371/journal.pone.0253069openalex-snapshot
A global database of plant services for humankind
inferredcites →https://doi.org/10.1590/s0100-84042008000300018openalex-snapshot
Cypsela or achene? Refining terminology by considering anatomical and historical factors
inferredcites →https://doi.org/10.1600/0363644041744338openalex-snapshot
A Comparative Palynologic Study of Chaetanthera (Asteraceae, Mutisieae) and Allied Genera
inferredcites →https://doi.org/10.1600/036364414x683958openalex-snapshot
Independent Origins of Aquatic Eupatorieae (Asteraceae)
inferredcites →https://doi.org/10.2110/palo.2005.p05-131openalex-snapshot
Mangrove Forests and Marine Incursions in Neogene Amazonia (Lower Apaporis River, Colombia)
inferredcites →https://doi.org/10.2307/2395250openalex-snapshot
Studies in Neotropical Paleobotany. II. The Miocene Communities of Veracruz, Mexico
inferredcites →https://doi.org/10.2307/4135449openalex-snapshot
History and concepts of big plant genera
inferredcites →https://doi.org/10.2503/jjshs.38.343openalex-snapshot
The chromosome survey on the cultivated chrysanthemums, Chrysanthemum morifolium Ram
inferredcites →https://doi.org/10.25224/1097-993x-9.1.51openalex-snapshot
Mutisieae (Asteraceae) Pollen Ultrastructure Atlas
inferredcites →https://doi.org/10.26749/rstpp.128.1openalex-snapshot
K-Ar dated palynofloras in Tasmania 1: Early Oligocene, Proteacidites tuberculatus Zone sediments, Wilmot Dam, northwestern Tasmania
inferredcites →https://doi.org/10.3389/fgene.2020.00888openalex-snapshot
Transcriptome Dynamics of the Inflorescence in Reciprocally Formed Allopolyploid Tragopogon miscellus (Asteraceae)
inferredcites →https://doi.org/10.3389/fpls.2016.00247openalex-snapshot
Transcriptome Analysis of Gerbera hybrida Including in silico Confirmation of Defense Genes Found
inferredcites →https://doi.org/10.3389/fpls.2019.00676openalex-snapshot
Polyploidy in the Conifer Genus Juniperus: An Unexpectedly High Rate
inferredcites →https://doi.org/10.3389/fpls.2019.01102openalex-snapshot
Factors Affecting Targeted Sequencing of 353 Nuclear Genes From Herbarium Specimens Spanning the Diversity of Angiosperms
inferredcites →https://doi.org/10.3389/fpls.2020.00362openalex-snapshot
Differential Genome Size and Repetitive DNA Evolution in Diploid Species of Melampodium sect. Melampodium (Asteraceae)
inferredcites →https://doi.org/10.3389/fpls.2020.591053openalex-snapshot
Characterization and Dynamics of Repeatomes in Closely Related Species of Hieracium (Asteraceae) and Their Synthetic and Apomictic Hybrids
inferredcites →https://doi.org/10.3389/fpls.2021.669064openalex-snapshot
The Effects of Herbarium Specimen Characteristics on Short-Read NGS Sequencing Success in Nearly 8000 Specimens: Old, Degraded Samples Have Lower DNA Yields but Consistent Sequencing Success
inferredcites →https://doi.org/10.3390/genes9020088openalex-snapshot
Genome Size Diversity and Its Impact on the Evolution of Land Plants
inferredcites →https://doi.org/10.3390/plants10081492openalex-snapshot
Detecting Introgressed Populations in the Iberian Endemic Centaurea podospermifolia through Genome Size
inferredcites →https://doi.org/10.3390/plants10122699openalex-snapshot
Plastome Diversity and Phylogenomic Relationships in Asteraceae
inferredcites →https://doi.org/10.3390/plants11020182openalex-snapshot
Morphological and Genome-Wide Evidence of Homoploid Hybridisation in Urospermum (Asteraceae)
inferredcites →https://doi.org/10.3732/ajb.1400119openalex-snapshot
Doubling down on genomes: Polyploidy and crop plants
inferredcites →https://doi.org/10.3732/ajb.1600057openalex-snapshot
A reexamination of the North American Crepis agamic complex and comparison with the findings of Babcock and Stebbins’ classic biosystematic monograph
inferredcites →https://doi.org/10.3732/ajb.1600113openalex-snapshot
Most Compositae (Asteraceae) are descendants of a paleohexaploid and all share a paleotetraploid ancestor with the Calyceraceae
inferredcites →https://doi.org/10.3732/apps.1300085openalex-snapshot
A target enrichment method for gathering phylogenetic information from hundreds of loci: An example from the Compositae
inferredcites →https://doi.org/10.3767/blumea.2018.63.02.02openalex-snapshot
Palynotaxonomy of the genus Gladiopappus (Dicomeae, Asteraceae) with special emphasis on the exine ultrastructure and mesoapertures
inferredcites →https://doi.org/10.3897/neobiota.69.74121openalex-snapshot
Global costs of plant invasions must not be underestimated
inferredcites →https://doi.org/10.53875/capitulum.01.2.04openalex-snapshot
Understanding capitulum development: Gerbera hybrida inflorescence meristem as an experimental system
inferredcites →https://doi.org/10.5479/si.0081024x.89openalex-snapshot
Generic and subtribal classification of American Vernonieae
inferredcites →https://doi.org/10.6084/m9.figshare.12668570openalex-snapshot
InvaCost: Economic cost estimates associated with biological invasions worldwide.
inferredcites →https://doi.org/10.7208/chicago/9780226536705.001.0001openalex-snapshot
Plants of the World
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.675.2.1zenodo-depositor-declared
Roquea, a new genus of Lychnophorinae (Vernonieae, Asteraceae) from Brazil and its phylogenetic placement
inferred← citeshttps://doi.org/10.1002/aps3.70058openalex-snapshot
Ancient hybridization and phylogenetic discordance: Exploring evolutionary complexity in Asteraceae
inferred← citeshttps://doi.org/10.1002/ece3.72403openalex-snapshot
Spatial Phylogenetics Reveals Endemism Hotspots and Conservation Priorities in Chinese Asteraceae
inferred← citeshttps://doi.org/10.1002/fedr.70054openalex-snapshot
Three Replacement Names in Fossil Artemisia (Asteraceae: Asteroideae)
inferred← citeshttps://doi.org/10.1002/ppp3.70264openalex-snapshot
Hybridization patterns and research effort in Asteraceae, a megadiverse and economically important plant family
inferred← citeshttps://doi.org/10.1002/tax.70204openalex-snapshot
Taxonomic reassessment of Tolpis (Asteraceae) in the Azores and Madeira archipelagos with description of new species
inferred← citeshttps://doi.org/10.1002/tax.70245openalex-snapshot
Revisiting phylogenetics of Dahlia , Hidalgoa and allied genera (Coreopsideae, Asteraceae)
inferred← citeshttps://doi.org/10.1007/s00709-025-02119-0openalex-snapshot
Linking genome size to life form and community structure in a semi-natural landscape from Northeast India
inferred← citeshttps://doi.org/10.1007/s00709-025-02132-3openalex-snapshot
Shedding light on autonomous endosperm development
inferred← citeshttps://doi.org/10.1007/s10722-024-02094-0openalex-snapshot
Pollen morphology and variability among Indian cultivars of Chrysanthemum morifolium and comparative analysis with genera of the Asteraceae family
inferred← citeshttps://doi.org/10.1007/s11852-025-01155-5openalex-snapshot
Assessment of plant diversity in the sand dunes of Mounda, Kefalonia: a study of species frequency and coverage
inferred← citeshttps://doi.org/10.1007/s12229-023-09295-9openalex-snapshot
Reproductive Biology of Asteraceae on Oceanic Islands
inferred← citeshttps://doi.org/10.1016/j.flora.2026.152932openalex-snapshot
Xeromorphic leaf traits in southern South American Gochnatioideae (Asteraceae): An anatomical comparison
inferred← citeshttps://doi.org/10.1017/pab.2025.8openalex-snapshot
Which morphological traits can be used to reconstruct genome size in fossil plants? Assessing sporomorph size and stomatal guard cell length as paleo-genome size proxies
inferred← citeshttps://doi.org/10.1017/s0960258523000107openalex-snapshot
Seed dormancy in Asteraceae: a global vegetation zone and taxonomic/phylogenetic assessment
inferred← citeshttps://doi.org/10.1073/pnas.2426851123openalex-snapshot
Phylogenomic synteny reveals paleohexaploid-derived genomic blocks across Asteraceae
inferred← citeshttps://doi.org/10.1080/01916122.2024.2341321openalex-snapshot
Pollen morphology of Asteraceae from Garhwal Himalaya (Uttarakhand, India): part I
inferred← citeshttps://doi.org/10.1080/23818107.2026.2743227openalex-snapshot
Exploring the distribution range and conservation priority areas of the evolutionarily significant genus Schlechtendalia Less. (Barnadesioideae: Asteraceae)
inferred← citeshttps://doi.org/10.1086/724310openalex-snapshot
Diversification and Biogeography of North American Thistles (Cirsium: Carduoideae: Compositae): Drivers of a Rapid Continent-Wide Radiation
inferred← citeshttps://doi.org/10.1086/724311openalex-snapshot
Bidens wailele (Asteraceae: Coreopsideae): A New Critically Endangered Species from Kauai, Hawaiian Islands
inferred← citeshttps://doi.org/10.1086/724497openalex-snapshot
Pollen Evolution in the Genus Echinops (Cardueae, Asteraceae): Deciphering the Origin of Giant Pollen Grains
inferred← citeshttps://doi.org/10.1086/725046openalex-snapshot
The Use of Pollen Morphology to Disentangle the Origin, Early Evolution, and Diversification of the Asteraceae
inferred← citeshttps://doi.org/10.1093/aob/mcad099openalex-snapshot
Strategies of diaspore dispersal investment in Compositae: the case of the Andean highlands
inferred← citeshttps://doi.org/10.1093/botlinnean/boac055openalex-snapshot
Let’s pluck the daisy: dissection as a tool to explore the diversity of Asteraceae capitula
inferred← citeshttps://doi.org/10.1093/botlinnean/boad005openalex-snapshot
A focus on European plants: origins, hybridization and biogeography
inferred← citeshttps://doi.org/10.1093/botlinnean/boad030openalex-snapshot
Leaf morphology and anatomy of Schlechtendalia luzulifolia, a basal member of subfamily Barnadesioideae (Asteraceae)
inferred← citeshttps://doi.org/10.1093/botlinnean/boae079openalex-snapshot
Factors influencing the global invasion of the South American weedy species Praxelis clematidea (Asteraceae): a niche shift and modelling-based approach
inferred← citeshttps://doi.org/10.1093/botlinnean/boaf068openalex-snapshot
Morphology and anatomy of leaves in the succulent Duseniella patagonica (Barnadesioideae, Asteraceae) in relation to arid environments and saline soils of the Monte and Patagonia of Argentina
inferred← citeshttps://doi.org/10.1093/botlinnean/boag004openalex-snapshot
Impact of calibration points and molecular dating methods lead to different biogeographical scenarios in Vernonieae (Asteraceae)
inferred← citeshttps://doi.org/10.1093/sysbio/syag041openalex-snapshot
Phylogenomic Challenges in Polyploid-Rich Lineages: Insights from Paralog Processing and Reticulation Methods Using the Complex Genus Packera (Asteraceae: Senecioneae)
inferred← citeshttps://doi.org/10.1101/2023.07.19.549085openalex-snapshot
Compositae-ParaLoss-1272: Complementary sunflower specific probe-set reduces issues with paralogs in complex systems
inferred← citeshttps://doi.org/10.1101/2023.08.14.553290openalex-snapshot
From paralogy to hybridization: Investigating causes of underlying phylogenomic discordance using the complex genus Packera (Senecioneae; Asteraceae)
inferred← citeshttps://doi.org/10.1101/2025.01.08.631874openalex-snapshot
Phylogenomic synteny analysis tracks conserved ancient polyploid-derived triplicated genomic blocks across Asteraceae genomes
inferred← citeshttps://doi.org/10.1101/2025.09.19.677265openalex-snapshot
Trait-dependent diversification and spatio-ecological limits drive angiosperm diversity unevenness across the Canary Islands archipelago
inferred← citeshttps://doi.org/10.1111/jse.13118openalex-snapshot
A phylogenomic approach to disentangling the evolution of the large and diverse daisy tribe Anthemideae (Asteraceae)
inferred← citeshttps://doi.org/10.1111/nph.19590openalex-snapshot
Development and evolution of the Asteraceae capitulum
inferred← citeshttps://doi.org/10.1111/nph.20042openalex-snapshot
Diversity and functional differentiation of renewal buds in temperate herbaceous plants
inferred← citeshttps://doi.org/10.1186/s13717-025-00663-4openalex-snapshot
Physicochemical properties of soils drive floristic richness of pastures in eastern Democratic Republic of Congo
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.20003.1openalex-snapshot
The genome sequence of common fleabane, Pulicaria dysenterica (L.) Bernh. (Asteraceae)
inferred← citeshttps://doi.org/10.15560/20.4.1008openalex-snapshot
An updated checklist of the Asteraceae of Ñeembucú, Paraguay
inferred← citeshttps://doi.org/10.1590/0001-3765202620260017openalex-snapshot
New Generic Placements and Typifications for names in Chrysocoma (Asteraceae) Described in Vellozo’s Florae Fluminensis
inferred← citeshttps://doi.org/10.17129/botsci.3827openalex-snapshot
Beyond ornamentals: Ethnobotany of Mexican Dahlia (Asteraceae), the national flower of Mexico
inferred← citeshttps://doi.org/10.3389/fpls.2023.1198909openalex-snapshot
Phylogenomic analysis provides insights into MADS-box and TCP gene diversification and floral development of the Asteraceae, supported by de novo genome and transcriptome sequences from dandelion (Taraxacum officinale)
inferred← citeshttps://doi.org/10.3389/fpls.2024.1367132openalex-snapshot
Insights into comparative genomics, structural features, and phylogenetic relationship of species from Eurasian Aster and its related genera (Asteraceae: Astereae) based on complete chloroplast genome
inferred← citeshttps://doi.org/10.3389/fpls.2024.1393241openalex-snapshot
South America holds the greatest diversity of native daisies (Asteraceae) in the world: an updated catalogue supporting continental-scale conservation
inferred← citeshttps://doi.org/10.3390/d17020136openalex-snapshot
Nuclear Phylogenomics of Angiosperms and Evolutionary Implications
inferred← citeshttps://doi.org/10.48130/gcomm-0025-0019openalex-snapshot
Chloroplast phylogenomics reveals the maternal ancestry of cultivated chrysanthemums
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