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A phylogenetic study of the tribe Antirrhineae: Genome duplications and long‐distance dispersals from the Old World to the New World
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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/fedr.19430520103openalex-snapshot
Zur Gliederung der Antirrhineae
inferredcites →https://doi.org/10.1007/bf00037152openalex-snapshot
Universal primers for amplification of three non-coding regions of chloroplast DNA
inferredcites →https://doi.org/10.1007/bf00985047openalex-snapshot
Phylogeny of the tribe Antirrhineae (Scrophulariaceae) based on morphological andndhF sequence data
inferredcites →https://doi.org/10.1007/bf00987959openalex-snapshot
Chloroplastrps16 intron phylogeny of the tribeSileneae (Caryophyllaceae)
inferredcites →https://doi.org/10.1007/s00606-004-0216-1openalex-snapshot
Molecular evidence for naturalness of genera in the tribe Antirrhineae (Scrophulariaceae) and three independent evolutionary lineages from the New World and the Old
inferredcites →https://doi.org/10.1007/s10592-005-9073-xopenalex-snapshot
Development and characterization of polymorphic microsatellite loci in endangered fern Adiantum reniforme var. sinense
inferredcites →https://doi.org/10.1016/1055-7903(92)90030-kopenalex-snapshot
Phylogenetic utility of the internal transcribed spacers of nuclear ribosomal DNA in plants: An example from the compositae
inferredcites →https://doi.org/10.1016/j.jtbi.2008.04.005openalex-snapshot
The conditioned reconstructed process
inferredcites →https://doi.org/10.1016/j.ppees.2015.07.003openalex-snapshot
Bees and evolution of occluded corollas in snapdragons and relatives (Antirrhineae)
inferredcites →https://doi.org/10.1016/j.tree.2004.07.002openalex-snapshot
Bayesian inference of character evolution
inferredcites →https://doi.org/10.1016/j.tree.2005.07.008openalex-snapshot
Genome duplication and the origin of angiosperms
inferredcites →https://doi.org/10.1016/j.ympev.2015.03.008openalex-snapshot
RASP (Reconstruct Ancestral State in Phylogenies): A tool for historical biogeography
inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot
jModelTest 2: more models, new heuristics and parallel computing
inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00070.xopenalex-snapshot
Phylogenetic relationships within Plantago (Plantaginaceae): evidence from nuclear ribosomal ITS and plastid trnL-F sequence data
inferredcites →https://doi.org/10.1046/j.1365-2699.2001.00525.xopenalex-snapshot
Endemism, species selection and the origin and distribution of the vascular plant flora of New Zealand
inferredcites →https://doi.org/10.1073/pnas.0811575106openalex-snapshot
The frequency of polyploid speciation in vascular plants
inferredcites →https://doi.org/10.1080/07352689309701903openalex-snapshot
Molecular Data and the Dynamic Nature of Polyploidy
inferredcites →https://doi.org/10.1080/10635150290102302openalex-snapshot
The Utility of the Incongruence Length Difference Test
inferredcites →https://doi.org/10.1080/10635150390235485openalex-snapshot
Reliability of Bayesian Posterior Probabilities and Bootstrap Frequencies in Phylogenetics
inferredcites →https://doi.org/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150701883881openalex-snapshot
Maximum Likelihood Inference of Geographic Range Evolution by Dispersal, Local Extinction, and Cladogenesis
inferredcites →https://doi.org/10.1086/280872openalex-snapshot
The Significance of Polyploidy in Plant Evolution
inferredcites →https://doi.org/10.1086/421067openalex-snapshot
Ancient Vicariance or Recent Long‐Distance Dispersal? Inferences about Phylogeny and South American–African Disjunctions in Rapateaceae and Bromeliaceae Based onndhF Sequence Data
inferredcites →https://doi.org/10.1086/499251openalex-snapshot
Polyploidy and Diversification: A Phylogenetic Investigation in Rosaceae
inferredcites →https://doi.org/10.1086/668790openalex-snapshot
A Phylogeny of Toadflaxes ( Linaria Mill.) Based on Nuclear Internal Transcribed Spacer Sequences: Systematic and Evolutionary Consequences
inferredcites →https://doi.org/10.1093/aob/mcu047openalex-snapshot
Does polyploidy facilitate long-distance dispersal?
inferredcites →https://doi.org/10.1093/bioinformatics/btm226openalex-snapshot
Multiple alignment by aligning alignments
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/molbev/msg042openalex-snapshot
Comparison of Bayesian and Maximum Likelihood Bootstrap Measures of Phylogenetic Reliability
inferredcites →https://doi.org/10.1093/molbev/msi121openalex-snapshot
More Genes or More Taxa? The Relative Contribution of Gene Number and Taxon Number to Phylogenetic Accuracy
inferredcites →https://doi.org/10.1093/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
inferredcites →https://doi.org/10.1093/molbev/msu122openalex-snapshot
ChromEvol: Assessing the Pattern of Chromosome Number Evolution and the Inference of Polyploidy along a Phylogeny
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004098openalex-snapshot
When Does the Incongruence Length Difference Test Fail?
inferredcites →https://doi.org/10.1093/sysbio/46.1.195openalex-snapshot
Dispersal-Vicariance Analysis: A New Approach to the Quantification of Historical Biogeography
inferredcites →https://doi.org/10.1093/sysbio/syp083openalex-snapshot
Probabilistic Models of Chromosome Number Evolution and the Inference of Polyploidy
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/1755-0998.12185openalex-snapshot
Discriminating plants using the DNA barcode rbc L b: an appraisal based on a large data set
inferredcites →https://doi.org/10.1111/j.1095-8312.2004.00337.xopenalex-snapshot
Polyploidy in arctic plants
inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
inferredcites →https://doi.org/10.1111/j.1096-0031.2011.00375.xopenalex-snapshot
Misleading results of likelihood‐based phylogenetic analyses in the presence of missing data
inferredcites →https://doi.org/10.1111/jbi.12253openalex-snapshot
Testing the biogeographical congruence of palaeofloras using molecular phylogenetics: snapdragons and the Madrean–Tethyan flora
inferredcites →https://doi.org/10.1111/nph.13191openalex-snapshot
The Chromosome Counts Database ( CCDB ) – a community resource of plant chromosome numbers
inferredcites →https://doi.org/10.1126/science.1207205openalex-snapshot
Recently Formed Polyploid Plants Diversify at Lower Rates
inferredcites →https://doi.org/10.1139/cjb-2012-0177openalex-snapshot
Origin, elevation, and evolutionary success of hybrids and polyploids in British Columbia, Canada
inferredcites →https://doi.org/10.1186/1471-2148-13-221openalex-snapshot
Looking for trees in the forest: summary tree from posterior samples
inferredcites →https://doi.org/10.1186/1741-7007-9-55openalex-snapshot
The taming of an impossible child: a standardized all-in approach to the phylogeny of Hymenoptera using public database sequences
inferredcites →https://doi.org/10.1214/aos/1176344136openalex-snapshot
Estimating the Dimension of a Model
inferredcites →https://doi.org/10.1371/journal.pone.0022234openalex-snapshot
Historical Isolation versus Recent Long-Distance Connections between Europe and Africa in Bifid Toadflaxes (Linaria sect. Versicolores)
inferredcites →https://doi.org/10.1371/journal.pone.0085266openalex-snapshot
Karyotypic Changes through Dysploidy Persist Longer over Evolutionary Time than Polyploid Changes
inferredcites →https://doi.org/10.2307/2395021openalex-snapshot
Angiosperm Biogeography and Past Continental Movements
inferredcites →https://doi.org/10.3732/ajb.0900346openalex-snapshot
The age and diversification of the angiosperms re‐revisited
inferredcites →https://doi.org/10.3732/ajb.92.2.297openalex-snapshot
Piecing together the “new” Plantaginaceae
inferredcites →https://doi.org/10.5169/seals-65859openalex-snapshot
Polyploidy and the distribution of the arctic-alpine flora : new evidence and a new approach
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.298.3.1zenodo-depositor-declared
Gadoria (Antirrhineae, Plantaginaceae): A new genus, endemic from Sierra de Gádor, Almería, Spain
inferred← citeshttps://doi.org/10.3897/natureconservation.64.177895zenodo-depositor-declared
Advances in the recovery of Galvezia leucantha subsp. leucantha (Plantaginaceae): restoring a critically endangered species on northern Isabela Island, Galápagos
inferred← citeshttps://doi.org/10.1002/tax.70230openalex-snapshot
All pieces together now? A phylogenomic analysis and tribe‐level classification of the heterogeneous family Plantaginaceae
inferred← citeshttps://doi.org/10.1007/s11101-021-09774-0openalex-snapshot
Iridoid glycosides of the tribe Antirrhineae
inferred← citeshttps://doi.org/10.1007/s11829-017-9525-5openalex-snapshot
Pollen and stamen mimicry: the alpine flora as a case study
inferred← citeshttps://doi.org/10.1016/j.cub.2020.01.060openalex-snapshot
Shared Mutations in a Novel Glutaredoxin Repressor of Multicellular Trichome Fate Underlie Parallel Evolution of Antirrhinum Species
inferred← citeshttps://doi.org/10.1016/j.ppees.2017.04.001openalex-snapshot
Diversification rates in Antirrhineae (Plantaginaceae): The contribution of range shifts and pollination modes
inferred← citeshttps://doi.org/10.1038/s41598-025-22748-yopenalex-snapshot
RETRACTED ARTICLE: Comparative plastome analysis of Schweinfurthia papilionacea and Schweinfurthia imbricata clarifying their taxonomic position in Lamiales
inferred← citeshttps://doi.org/10.1101/518183openalex-snapshot
Loss of a glutaredoxin gene underlies parallel evolution of trichome pattern in Antirrhinum
inferred← citeshttps://doi.org/10.1111/1755-0998.12927openalex-snapshot
OneTwoTree: An online tool for phylogeny reconstruction
inferred← citeshttps://doi.org/10.1111/brv.12696openalex-snapshot
The G alápagos I slands: biogeographic patterns and geology
inferred← citeshttps://doi.org/10.1111/jbi.13939openalex-snapshot
Out of the Mediterranean Region: Worldwide biogeography of snapdragons and relatives (tribe Antirrhineae, Plantaginaceae)
inferred← citeshttps://doi.org/10.1111/nph.15654openalex-snapshot
Macroevolutionary dynamics of nectar spurs, a key evolutionary innovation
inferred← citeshttps://doi.org/10.11648/j.plant.20251303.13openalex-snapshot
J. L. Reveal’s Revelance Re-revealed: Addenda to Newly Required Infrafamilial Ranks in Selected Families
inferred← citeshttps://doi.org/10.1186/s13007-020-00683-5openalex-snapshot
Rapid, high efficiency virus-mediated mutant complementation and gene silencing in Antirrhinum
inferred← citeshttps://doi.org/10.1186/s13227-021-00187-wopenalex-snapshot
A CYC–RAD–DIV–DRIF interaction likely pre-dates the origin of floral monosymmetry in Lamiales
inferred← citeshttps://doi.org/10.3389/fpls.2020.00514openalex-snapshot
Chromosomal Evolution and Apomixis in the Cruciferous Tribe Boechereae
inferred← citeshttps://doi.org/10.34971/1c6n-5e71openalex-snapshot
Nuttallanthus canadensis (L.) D.A. Sutton (Plantaginaceae), une nouvelle espèce exogène pour la flore française
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