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Resolving ancient radiations: can complete plastid gene sets elucidate deep relationships among the tropical gingers (Zingiberales)?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1991.tb14485.xopenalex-snapshot
HOMEOSIS IN THE FLOWERS OF THE ZINGIBERALES
inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot
Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences
inferredcites →https://doi.org/10.1007/978-3-642-61663-1openalex-snapshot
The Families of the Monocotyledons
inferredcites →https://doi.org/10.1007/s12229-012-9111-6openalex-snapshot
Homoplasy, Pollination, and Emerging Complexity During the Evolution of Floral Development in the Tropical Gingers (Zingiberales)
inferredcites →https://doi.org/10.1016/0031-9422(80)85004-7openalex-snapshot
Deviations from michaelis-menten behaviour of plant glutamate dehydrogenase with ammonium as variable substrate
inferredcites →https://doi.org/10.1016/j.tree.2007.01.012openalex-snapshot
Deciphering ancient rapid radiations
inferredcites →https://doi.org/10.1016/j.ympev.2010.03.003openalex-snapshot
Phylogenetic relationships within Orchidaceae based on a low-copy nuclear coding gene, Xdh: Congruence with organellar and nuclear ribosomal DNA results
inferredcites →https://doi.org/10.1016/j.ympev.2011.06.003openalex-snapshot
Spurious 99% bootstrap and jackknife support for unsupported clades
inferredcites →https://doi.org/10.1016/s0076-6879(05)95039-8openalex-snapshot
Maximum-Likelihood Methods for Phylogeny Estimation
inferredcites →https://doi.org/10.1016/s1055-7903(02)00326-3openalex-snapshot
An index of substitution saturation and its application
inferredcites →https://doi.org/10.1017/cbo9781139002950.015openalex-snapshot
Contrasting patterns of support among plastid genes and genomes for major clades of the monocotyledons
inferredcites →https://doi.org/10.1038/nature06614openalex-snapshot
Broad phylogenomic sampling improves resolution of the animal tree of life
inferredcites →https://doi.org/10.1073/pnas.0708072104openalex-snapshot
Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms
inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
inferredcites →https://doi.org/10.1073/pnas.0907801107openalex-snapshot
Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots
inferredcites →https://doi.org/10.1073/pnas.1205818109openalex-snapshot
Phylogenomics and a posteriori data partitioning resolve the Cretaceous angiosperm radiation Malpighiales
inferredcites →https://doi.org/10.1080/106351501753462885openalex-snapshot
Unraveling the Evolutionary Radiation of the Families of the Zingiberales Using Morphological and Molecular Evidence
inferredcites →https://doi.org/10.1080/10635150290102339openalex-snapshot
Increased Taxon Sampling Greatly Reduces Phylogenetic Error
inferredcites →https://doi.org/10.1080/10635150290102429openalex-snapshot
Identifiability of Parameters in MCMC Bayesian Inference of Phylogeny
inferredcites →https://doi.org/10.1080/10635150390132911openalex-snapshot
Is Sparse Taxon Sampling a Problem for Phylogenetic Inference?
inferredcites →https://doi.org/10.1080/10635150490423520openalex-snapshot
The Importance of Proper Model Assumption in Bayesian Phylogenetics
inferredcites →https://doi.org/10.1080/10635150490468675openalex-snapshot
A Phylogenetic Mixture Model for Detecting Pattern-Heterogeneity in Gene Sequence or Character-State Data
inferredcites →https://doi.org/10.1080/10635150701884640openalex-snapshot
Taxon Sampling Affects Inferences of Macroevolutionary Processes from Phylogenetic Trees
inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot
A Rapid Bootstrap Algorithm for the RAxML Web Servers
inferredcites →https://doi.org/10.1086/297218openalex-snapshot
Upper Cretaceous Zingiberalean Fruits with in Situ Seeds from Southeastern Coahuila, Mexico
inferredcites →https://doi.org/10.1093/aobpla/plt009openalex-snapshot
Tracking the development of the petaloid fertile stamen in Canna indica: insights into the origin of androecial petaloidy in the Zingiberales
inferredcites →https://doi.org/10.1093/bioinformatics/17.12.1246openalex-snapshot
CONSEL: for assessing the confidence of phylogenetic tree selection
inferredcites →https://doi.org/10.1093/bioinformatics/bth352openalex-snapshot
Automatic annotation of organellar genomes with DOGMA
inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp666openalex-snapshot
Tablet—next generation sequence assembly visualization
inferredcites →https://doi.org/10.1093/jhered/92.4.371openalex-snapshot
DAMBE: Software Package for Data Analysis in Molecular Biology and Evolution
inferredcites →https://doi.org/10.1093/molbev/msj030openalex-snapshot
Application of Phylogenetic Networks in Evolutionary Studies
inferredcites →https://doi.org/10.1093/molbev/msl137openalex-snapshot
Lack of Resolution in the Animal Phylogeny: Closely Spaced Cladogeneses or Undetected Systematic Errors?
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
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/gkn502openalex-snapshot
Multiplex sequencing of plant chloroplast genomes using Solexa sequencing-by-synthesis technology
inferredcites →https://doi.org/10.1093/oso/9780198545040.001.0001openalex-snapshot
Anatomy Of The Monocotyledons
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026201openalex-snapshot
Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference
inferredcites →https://doi.org/10.1093/sysbio/syp021openalex-snapshot
Complete Generic-Level Phylogenetic Analyses of Palms (Arecaceae) with Comparisons of Supertree and Supermatrix Approaches
inferredcites →https://doi.org/10.1101/gr.074492.107openalex-snapshot
Velvet: Algorithms for de novo short read assembly using de Bruijn graphs
inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot
Creating the CIPRES Science Gateway for inference of large phylogenetic trees
inferredcites →https://doi.org/10.1111/j.1095-8339.2004.00345.xopenalex-snapshot
The age of major monocot groups inferred from 800+rbcL sequences
inferredcites →https://doi.org/10.1111/j.1095-8339.2009.00996.xopenalex-snapshot
An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III
inferredcites →https://doi.org/10.1111/j.1096-0031.1996.tb00196.xopenalex-snapshot
PARSIMONY JACKKNIFING OUTPERFORMS NEIGHBOR‐JOINING
inferredcites →https://doi.org/10.1111/j.1096-0031.2003.tb00376.xopenalex-snapshot
Improvements to resampling measures of group support
inferredcites →https://doi.org/10.1111/j.1096-0031.2008.00217.xopenalex-snapshot
TNT, a free program for phylogenetic analysis
inferredcites →https://doi.org/10.1111/j.1096-0031.2010.00304.xopenalex-snapshot
Branch support via resampling: an empirical study
inferredcites →https://doi.org/10.1111/j.1096-0031.2010.00329.xopenalex-snapshot
SequenceMatrix: concatenation software for the fast assembly of multi-gene datasets with character set and codon information
inferredcites →https://doi.org/10.1111/j.1096-0031.2012.00418.xopenalex-snapshot
Plastid genomes and deep relationships among the commelinid monocot angiosperms
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01032.xopenalex-snapshot
Evolution of zygomorphy in monocot flowers: iterative patterns and developmental constraints
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03279.xopenalex-snapshot
Evidence for the involvement of GLOBOSA‐like gene duplications and expression divergence in the evolution of floral morphology in the Zingiberales
inferredcites →https://doi.org/10.1111/j.1558-5646.1962.tb03211.xopenalex-snapshot
PHYLOGENY OF THE SCITAMINEAE-MORPHOLOGICAL AND ANATOMICAL CONSIDERATIONS
inferredcites →https://doi.org/10.1186/1471-2148-12-100openalex-snapshot
Separating the wheat from the chaff: mitigating the effects of noise in a plastome phylogenomic data set from Pinus L. (Pinaceae)
inferredcites →https://doi.org/10.1186/1741-7007-7-84openalex-snapshot
Increasing phylogenetic resolution at low taxonomic levels using massively parallel sequencing of chloroplast genomes
inferredcites →https://doi.org/10.1371/journal.pbio.1000602openalex-snapshot
Resolving Difficult Phylogenetic Questions: Why More Sequences Are Not Enough
inferredcites →https://doi.org/10.1371/journal.pone.0022594openalex-snapshot
MACSE: Multiple Alignment of Coding SEquences Accounting for Frameshifts and Stop Codons
inferredcites →https://doi.org/10.1600/0363644041744365openalex-snapshot
A Phylogeny of the Monocots, as Inferred from rbcL and atpA Sequence Variation, and a Comparison of Methods for Calculating Jackknife and Bootstrap Values
inferredcites →https://doi.org/10.1600/036364408783887366openalex-snapshot
Monocots: Comparative Biology and Evolution (Excluding Poales)
inferredcites →https://doi.org/10.2307/2399669openalex-snapshot
The Phylogeny and Classification of the Zingiberales
inferredcites →https://doi.org/10.2307/2399850openalex-snapshot
Phylogenetic Analysis of the Zingiberales Based on rbcL Sequences
inferredcites →https://doi.org/10.3417/2010023openalex-snapshot
Assembling the Tree of the Monocotyledons: Plastome Sequence Phylogeny and Evolution of Poales 1
inferredcites →https://doi.org/10.3732/ajb.0800060openalex-snapshot
Angiosperm diversification through time
inferredcites →https://doi.org/10.3732/ajb.0800305openalex-snapshot
Early floral development of Heliconia latispatha (Heliconiaceae), a key taxon for understanding the evolution of flower development in the Zingiberales
inferredcites →https://doi.org/10.3732/ajb.1000246openalex-snapshot
Changes in expression pattern of the teosinte branched1‐like genes in the Zingiberales provide a mechanism for evolutionary shifts in symmetry across the order
inferredcites →https://doi.org/10.3732/ajb.1000404openalex-snapshot
Angiosperm phylogeny: 17 genes, 640 taxa
inferredcites →https://doi.org/10.3732/ajb.1100468openalex-snapshot
Phylogeny of the Asparagales based on three plastid and two mitochondrial genes
inferredcites →https://doi.org/10.3732/ajb.1100491openalex-snapshot
Quality and quantity of data recovered from massively parallel sequencing: Examples in Asparagales and Poaceae
inferredcites →https://doi.org/10.3732/ajb.1200256openalex-snapshot
The plastid genome of the mycoheterotrophic Corallorhiza striata (Orchidaceae) is in the relatively early stages of degradation
inferredcites →https://doi.org/10.3732/ajb.89.10.1682openalex-snapshot
The phylogeny and a new classification of the gingers (Zingiberaceae): evidence from molecular data
inferredcites →https://doi.org/10.3732/ajb.91.1.149openalex-snapshot
An expanded plastid DNA phylogeny of Orchidaceae and analysis of jackknife branch support strategy
inferredcites →https://doi.org/10.3732/ajb.91.10.1614openalex-snapshot
The origin and diversification of angiosperms
inferredcites →https://doi.org/10.3732/ajb.92.4.613openalex-snapshot
An overview of the phylogenetic relationships within Epidendroideae inferred from multiple DNA regions and recircumscription of Epidendreae and Arethuseae (Orchidaceae)
inferredcites →https://doi.org/10.3732/apps.1200497openalex-snapshot
A targeted enrichment strategy for massively parallel sequencing of angiosperm plastid genomes
inferredcites →https://doi.org/10.5642/aliso.20062201.02openalex-snapshot
Robust Inference of Monocot Deep Phylogeny Using an Expanded Multigene Plastid Data Set
inferredcites →https://doi.org/10.5642/aliso.20062201.06openalex-snapshot
Multigene Analyses of Monocot Relationships
inferredcites →https://doi.org/10.5642/aliso.20062201.49openalex-snapshot
The Evolutionary and Biogeographic Origin and Diversification of the Tropical Monocot Order Zingiberales
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4066.3.1zenodo-depositor-declared
Observations on the biology of Afrotropical Hesperiidae (Lepidoptera). Part 9. Hesperiinae incertae sedis: Zingiberales feeders, genera of unknown biology and an overview of the Hesperiinae incertae sedis
inferred← citeshttps://doi.org/10.1002/ajb2.1178openalex-snapshot
Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi‐gene analyses, and a functional model for the origin of monocots
inferred← citeshttps://doi.org/10.1002/ajb2.70153openalex-snapshot
Phylogenomics, ecomorphological evolution, and historical biogeography in Deuterocohnia (Bromeliaceae: Pitcairnioideae)
inferred← citeshttps://doi.org/10.1002/jez.b.22724openalex-snapshot
Change of Fate and Staminodial Laminarity as Potential Agents of Floral Diversification in the Zingiberales
inferred← citeshttps://doi.org/10.1007/978-981-15-7903-5_5openalex-snapshot
Phylogeny, Classification, Biogeography, and Evolution
inferred← citeshttps://doi.org/10.1007/s00606-015-1274-2openalex-snapshot
Development of SSR markers from Musa balbisiana for genetic diversity analysis among Thai bananas
inferred← citeshttps://doi.org/10.1007/s00606-019-01610-5openalex-snapshot
Why the monophyly of Nymphaeaceae currently remains indeterminate: an assessment based on gene-wise plastid phylogenomics
inferred← citeshttps://doi.org/10.1007/s10722-021-01260-yopenalex-snapshot
Organelle DNA sequence data provide new insights into the maternal and paternal lineages of Musa species germplasms
inferred← citeshttps://doi.org/10.1007/s10722-024-01872-0openalex-snapshot
Comparative analysis of the chloroplast genomes in abaca (Musa textilis Née) cultivars reveals low chloroplast genome variation
inferred← citeshttps://doi.org/10.1007/s10722-025-02675-7openalex-snapshot
The complete chloroplast genome of Curcuma cochinchinensis Gagnep, 1907 (Zingiberaceae): insights into phylogeny and comparative genomics
inferred← citeshttps://doi.org/10.1007/s11295-017-1124-1openalex-snapshot
Plastomes of Mimosoideae: structural and size variation, sequence divergence, and phylogenetic implication
inferred← citeshttps://doi.org/10.1007/s12229-021-09253-3openalex-snapshot
From the Machete to the Microscope: Dennis Stevenson, Plant Morphologist
inferred← citeshttps://doi.org/10.1016/b978-0-12-814232-5.00001-0openalex-snapshot
Genomics and Evolution of Medicinal Plants
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.11.014openalex-snapshot
Molecular Evolution of Plastid Genomes in Parasitic Flowering Plants
inferred← citeshttps://doi.org/10.1016/j.bse.2016.03.013openalex-snapshot
Phylogenetic and ancestral area reconstruction of Zingiberales from plastid genomes
inferred← citeshttps://doi.org/10.1016/j.gene.2022.146732openalex-snapshot
Diverse function of the PISTILLATA, APETALA 3, and AGAMOUS-like MADS-box genes involved in the floral development in Alpinia hainanensis (Zingiberaceae)
inferred← citeshttps://doi.org/10.1016/j.pld.2019.04.003openalex-snapshot
Evaluation of rapid molecular diagnostics for differentiating medicinal Kaempferia species from its adulterants
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.07.020openalex-snapshot
Phylogenetic signal detection from an ancient rapid radiation: Effects of noise reduction, long-branch attraction, and model selection in crown clade Apocynaceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.10.003openalex-snapshot
Utilizing next-generation sequencing to resolve the backbone of the Core Goodeniaceae and inform future taxonomic and floral form studies
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.12.015openalex-snapshot
Nuclear phylogenomics of the palm subfamily Arecoideae (Arecaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.12.001openalex-snapshot
The phylogeny of Heliconia (Heliconiaceae) and the evolution of floral presentation
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.07.001openalex-snapshot
Plastome organization, genome-based phylogeny and evolution of plastid genes in Podophylloideae (Berberidaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.07.020openalex-snapshot
Resolving the rapid plant radiation of early diverging lineages in the tropical Zingiberales: Pushing the limits of genomic data
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106601openalex-snapshot
Plastid phylogenomics and biogeographic analysis support a trans-Tethyan origin and rapid early radiation of Cornales in the Mid-Cretaceous
inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106658openalex-snapshot
Multilocus data reveal deep phylogenetic relationships and intercontinental biogeography of the Eurasian-North American genus Corylus (Betulaceae)
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107664openalex-snapshot
Next-generation sequencing data show rapid radiation and several long-distance dispersal events in early Costaceae
inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108325openalex-snapshot
Phylogenomic conflict analyses of plastid and mitochondrial genomes of Impatiens (Balsaminaceae) reveal its complex evolutionary history
inferred← citeshttps://doi.org/10.1038/s41477-019-0468-yopenalex-snapshot
Fossil evidence of core monocots in the Early Cretaceous
inferred← citeshttps://doi.org/10.1086/709296openalex-snapshot
Inflorescence and Flower Development in Orchidantha chinensis T. L. Wu (Lowiaceae; Zingiberales): Similarities to Inflorescence Structure in the Strelitziaceae
inferred← citeshttps://doi.org/10.1086/710083openalex-snapshot
The Chloroplast Genome of Salvia : Genomic Characterization and Phylogenetic Analysis
inferred← citeshttps://doi.org/10.1086/711474openalex-snapshot
Fossil Fruits and Seeds of Zingiberales from the Late Cretaceous–Early Cenozoic Deccan Intertrappean Beds of India
inferred← citeshttps://doi.org/10.1093/aob/mcaa024openalex-snapshot
Insights into phylogeny, age and evolution of Allium (Amaryllidaceae) based on the whole plastome sequences
inferred← citeshttps://doi.org/10.1093/aob/mcaa201openalex-snapshot
Plastome phylogenomics ofCephalotaxus(Cephalotaxaceae) and allied genera
inferred← citeshttps://doi.org/10.1093/aob/mcw060openalex-snapshot
Sequencing of whole plastid genomes and nuclear ribosomal DNA ofDiospyrosspecies (Ebenaceae) endemic to New Caledonia: many species, little divergence
inferred← citeshttps://doi.org/10.1093/aob/mcw086openalex-snapshot
Organellar phylogenomics of an emerging model system: Sphagnum (peatmoss)
inferred← citeshttps://doi.org/10.1093/aobpla/plv046openalex-snapshot
Plastid phylogenomics of the cool-season grass subfamily: clarification of relationships among early-diverging tribes
inferred← citeshttps://doi.org/10.1093/botlinnean/boaa052openalex-snapshot
Rapid diversification rates in Amazonian Chrysobalanaceae inferred from plastid genome phylogenetics
inferred← citeshttps://doi.org/10.1093/botlinnean/boac064openalex-snapshot
Molecular phylogenetics of Maranta (Marantaceae: Zingiberales): non-monophyly and support for a wider circumscription
inferred← citeshttps://doi.org/10.1093/botlinnean/boy081openalex-snapshot
Systematics and evolution of the Old World Ebenaceae, a review with emphasis on the large genusDiospyrosand its radiation in New Caledonia
inferred← citeshttps://doi.org/10.1093/jxb/erab484openalex-snapshot
MADS-box transcription factors determine the duration of temporary winter dormancy in closely related evergreen and deciduousIrisspp.
inferred← citeshttps://doi.org/10.1093/sysbio/syx050openalex-snapshot
Resolving Rapid Radiations within Angiosperm Families Using Anchored Phylogenomics
inferred← citeshttps://doi.org/10.1101/110296openalex-snapshot
Resolving Rapid Radiations Within Angiosperm Families Using Anchored Phylogenomics
inferred← citeshttps://doi.org/10.1111/1755-0998.12626openalex-snapshot
Strategies for complete plastid genome sequencing
inferred← citeshttps://doi.org/10.1111/boj.12399openalex-snapshot
An introduction to plant phylogenomics with a focus on palms
inferred← citeshttps://doi.org/10.1111/cla.12133openalex-snapshot
Plastid phylogenomics and molecular evolution of Alismatales
inferred← citeshttps://doi.org/10.1111/cla.12153openalex-snapshot
Phylogenomics and historical biogeography of the monocot order Liliales: out of Australia and through Antarctica
inferred← citeshttps://doi.org/10.1111/jse.12522openalex-snapshot
Chloroplast phylogenomic data support Eocene amphi‐Pacific early radiation for the Asian Palmate core Araliaceae
inferred← citeshttps://doi.org/10.1111/jse.12526openalex-snapshot
Revisiting the phylogeny of Dipsacales: New insights from phylogenomic analyses of complete plastomic sequences
inferred← citeshttps://doi.org/10.1111/nph.13617openalex-snapshot
Plastid genomes reveal support for deep phylogenetic relationships and extensive rate variation among palms and other commelinid monocots
inferred← citeshttps://doi.org/10.1111/nph.14461openalex-snapshot
Diversification of Rosaceae since the Late Cretaceous based on plastid phylogenomics
inferred← citeshttps://doi.org/10.1111/nph.70080openalex-snapshot
Well‐resolved phylogeny supports repeated evolution of keel flowers as a synergistic contributor to papilionoid legume diversification
inferred← citeshttps://doi.org/10.1186/s12862-021-01827-4openalex-snapshot
Plastome structure and phylogenetic relationships of Styracaceae (Ericales)
inferred← citeshttps://doi.org/10.1186/s12862-025-02396-6openalex-snapshot
Plastome phylogenomics of the diverse neotropical orchid genus Lepanthes with emphasis on subgenus Marsipanthes (Pleurothallidinae: Orchidaceae)
inferred← citeshttps://doi.org/10.1186/s12864-023-09680-zopenalex-snapshot
The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae
inferred← citeshttps://doi.org/10.1186/s12864-024-09996-4openalex-snapshot
Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.1186/s12870-019-1879-7openalex-snapshot
Chloroplast phylogenomic analysis provides insights into the evolution of the largest eukaryotic genome holder, Paris japonica (Melanthiaceae)
inferred← citeshttps://doi.org/10.1186/s12870-019-2147-6openalex-snapshot
Plastome phylogenomics, biogeography, and clade diversification of Paris (Melanthiaceae)
inferred← citeshttps://doi.org/10.1186/s12870-022-03577-xopenalex-snapshot
Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.1186/s12870-023-04183-1openalex-snapshot
Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.1186/s12870-025-08072-7openalex-snapshot
Chloroplast genomes provide new insights into the phylogeny and evolution of the genus Hibiscus L.
inferred← citeshttps://doi.org/10.1186/s13059-016-1004-2openalex-snapshot
Chloroplast genomes: diversity, evolution, and applications in genetic engineering
inferred← citeshttps://doi.org/10.1186/s13227-020-00157-8openalex-snapshot
Can the anatomy of abnormal flowers elucidate relationships of the androecial members in the ginger (Zingiberaceae)?
inferred← citeshttps://doi.org/10.1371/journal.pone.0218817openalex-snapshot
The complete chloroplast genome sequence of Alpinia oxyphylla Miq. and comparison analysis within the Zingiberaceae family
inferred← citeshttps://doi.org/10.20944/preprints201905.0002.v1openalex-snapshot
Why the Monophyly of Nymphaeaceae Currently Remains Indeterminate: An Assessment Based on Gene-Wise Plastid Phylogenomics
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2487518/v1openalex-snapshot
Comparison of chloroplast genomes of Calypsoinae species (Orchidaceae) living on different lifeforms
inferred← citeshttps://doi.org/10.21203/rs.3.rs-403712/v1openalex-snapshot
Comparative and Phylogenetic Analyses of Complete Plastomes of Aucuba (Garryaceae)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-55283/v1openalex-snapshot
Plastome Structure and Phylogenetic Relationships of Styracaceae (Ericales)
inferred← citeshttps://doi.org/10.21203/rs.3.rs-55283/v2openalex-snapshot
Plastome Structure and Phylogenetic Relationships of Styracaceae (Ericales)
inferred← citeshttps://doi.org/10.22541/au.170666257.77947781/v1openalex-snapshot
Peculiar winter dormancy processes of perennial monocots represented by rhizomatous irises with distinct durations
inferred← citeshttps://doi.org/10.3109/19401736.2015.1079836openalex-snapshot
The complete chloroplast genome sequence of Curcuma flaviflora ( Curcuma )
inferred← citeshttps://doi.org/10.3389/fevo.2020.00133openalex-snapshot
Floral Development Reveals the Existence of a Fifth Staminode on the Labellum of Basal Globbeae
inferred← citeshttps://doi.org/10.3389/fevo.2021.794977openalex-snapshot
Whence Came These Plants Most Foul? Phylogenomics and Biogeography of Lowiaceae (Zingiberales)
inferred← citeshttps://doi.org/10.3389/fgene.2020.542017openalex-snapshot
Transit From Autotrophism to Heterotrophism: Sequence Variation and Evolution of Chloroplast Genomes in Orobanchaceae Species
inferred← citeshttps://doi.org/10.3389/fpls.2017.01536openalex-snapshot
Comparative and Phylogenetic Analyses of the Complete Chloroplast Genomes of Three Arcto-Tertiary Relicts: Camptotheca acuminata, Davidia involucrata, and Nyssa sinensis
inferred← citeshttps://doi.org/10.3389/fpls.2021.662715openalex-snapshot
Highly Diverse Shrub Willows (Salix L.) Share Highly Similar Plastomes
inferred← citeshttps://doi.org/10.3389/fpls.2021.699226openalex-snapshot
Phylogeny, Age, and Evolution of Tribe Lilieae (Liliaceae) Based on Whole Plastid Genomes
inferred← citeshttps://doi.org/10.3389/fpls.2022.876779openalex-snapshot
Phylogenomic resolution of order- and family-level monocot relationships using 602 single-copy nuclear genes and 1375 BUSCO genes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1160446openalex-snapshot
Evolutionary differences in gene loss and pseudogenization among mycoheterotrophic orchids in the tribe Vanilleae (subfamily Vanilloideae)
inferred← citeshttps://doi.org/10.3389/fpls.2024.1535549openalex-snapshot
Unveiling the conserved nature of Heliconia chloroplast genomes: insights from the assembly and analysis of four complete chloroplast genomes
inferred← citeshttps://doi.org/10.3390/genes15121577openalex-snapshot
Revealing the Dynamic History of Parasitic Plant Plastomes via Structural Characterization, Comparative Analysis, and Phylogenomics
inferred← citeshttps://doi.org/10.3390/ijms241915031openalex-snapshot
Comparative Chloroplast Genomics of 21 Species in Zingiberales with Implications for Their Phylogenetic Relationships and Molecular Dating
inferred← citeshttps://doi.org/10.3390/ijms252011137openalex-snapshot
Assessing Genetic Diversity in Endangered Plant Orchidantha chinensis: Chloroplast Genome Assembly and Simple Sequence Repeat Marker-Based Evaluation
inferred← citeshttps://doi.org/10.3390/plants11192512openalex-snapshot
Correlation between Inflorescence Architecture and Floral Asymmetry—Evidence from Aberrant Flowers in Canna L. (Cannaceae)
inferred← citeshttps://doi.org/10.3417/2014014openalex-snapshot
Evolution of Angiosperm Pollen. 3. Monocots1
inferred← citeshttps://doi.org/10.3732/ajb.1700025openalex-snapshot
The East Asian origin of the giant lobelias
inferred← citeshttps://doi.org/10.3732/apps.1400085openalex-snapshot
Plastid primers for angiosperm phylogenetics and phylogeography
inferred← citeshttps://doi.org/10.3835/plantgenome2015.09.0089openalex-snapshot
Complete Chloroplast Genome Sequence of Musa balbisiana Corroborates Structural Heterogeneity of Inverted Repeats in Wild Progenitors of Cultivated Bananas and Plantains
inferred← citeshttps://doi.org/10.4137/ebo.s22448openalex-snapshot
Phylotranscriptomic Analysis Based on Coalescence was Less Influenced by the Evolving Rates and the Number of Genes: A Case Study in Ericales
inferred← citeshttps://doi.org/10.4137/ebo.s31326openalex-snapshot
Genomics and Evolution in Traditional Medicinal Plants: Road to a Healthier Life
inferred← citeshttps://doi.org/10.6084/m9.figshare.14700482openalex-snapshot
Additional file 6 of Plastome structure and phylogenetic relationships of Styracaceae (Ericales)
inferred← citeshttps://doi.org/10.6084/m9.figshare.14700485openalex-snapshot
Additional file 7 of Plastome structure and phylogenetic relationships of Styracaceae (Ericales)
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588947openalex-snapshot
Additional file 10 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588950openalex-snapshot
Additional file 1 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588956openalex-snapshot
Additional file 2 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588962openalex-snapshot
Additional file 3 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588965openalex-snapshot
Additional file 4 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588968openalex-snapshot
Additional file 5 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588974openalex-snapshot
Additional file 6 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588980openalex-snapshot
Additional file 7 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588986openalex-snapshot
Additional file 8 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.19588992openalex-snapshot
Additional file 9 of Plastome structure, phylogenomics and evolution of plastid genes in Swertia (Gentianaceae) in the Qing-Tibetan Plateau
inferred← citeshttps://doi.org/10.6084/m9.figshare.24202491openalex-snapshot
Additional file 1 of The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae
inferred← citeshttps://doi.org/10.6084/m9.figshare.24202494openalex-snapshot
Additional file 2 of The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae
inferred← citeshttps://doi.org/10.6084/m9.figshare.24202497openalex-snapshot
Additional file 3 of The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae
inferred← citeshttps://doi.org/10.6084/m9.figshare.24202500openalex-snapshot
Additional file 4 of The complete chloroplast genome of Diplodiscus trichospermus and phylogenetic position of Brownlowioideae within Malvaceae
inferred← citeshttps://doi.org/10.6084/m9.figshare.25017854openalex-snapshot
Additional file 1 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.25017942openalex-snapshot
Additional file 2 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578283openalex-snapshot
Additional file 1 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578286openalex-snapshot
Additional file 2 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578289openalex-snapshot
Additional file 3 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578292openalex-snapshot
Additional file 4 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578295openalex-snapshot
Additional file 5 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26578298openalex-snapshot
Additional file 6 of Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668737openalex-snapshot
Additional file 3 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668740openalex-snapshot
Additional file 4 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668743openalex-snapshot
Additional file 5 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668746openalex-snapshot
Additional file 6 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668749openalex-snapshot
Additional file 7 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668752openalex-snapshot
Additional file 8 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668755openalex-snapshot
Additional file 9 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668758openalex-snapshot
Additional file 10 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668761openalex-snapshot
Additional file 11 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.6084/m9.figshare.26668764openalex-snapshot
Additional file 12 of Thirteen complete chloroplast genomes of the costaceae family: insights into genome structure, selective pressure and phylogenetic relationships
inferred← citeshttps://doi.org/10.64898/2026.01.16.699981openalex-snapshot
Gene tree conflict between genomic and functional partitions impacts phylogenetic inference in Zygophylloideae
inferred← citeshttps://doi.org/10.7287/peerj.1584v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Revisiting the Zingiberales: using multiplexed exon capture to resolve ancient and recent phylogenetic splits in a charismatic plant lineage (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.1584v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Revisiting the Zingiberales: using multiplexed exon capture to resolve ancient and recent phylogenetic splits in a charismatic plant lineage (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.1584v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Revisiting the Zingiberales: using multiplexed exon capture to resolve ancient and recent phylogenetic splits in a charismatic plant lineage (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.1584openalex-snapshot
Revisiting the Zingiberales: using multiplexed exon capture to resolve ancient and recent phylogenetic splits in a charismatic plant lineage
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.