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Accelerated Rate of Molecular Evolution for Vittarioid Ferns is Strong and Not Driven by Selection
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471650129.dob0522openalex-snapshot
PAUP * [Phylogenetic Analysis Using Parsimony (and Other Methods)]
inferredcites →https://doi.org/10.1002/j.1537-2197.1974.tb06040.xopenalex-snapshot
GEMMIFEROUS FERN GAMETOPHYTES—VITTARIACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1992.tb14613.xopenalex-snapshot
MATERNAL INHERITANCE OF THE CHLOROPLAST AND MITOCHONDRIAL GENOMES IN CHEILANTHOID FERNS
inferredcites →https://doi.org/10.1002/tax.562008openalex-snapshot
Phylogenetic relationships among Pteridaceae, including Brazilian species, inferred from rbcL sequences
inferredcites →https://doi.org/10.1002/tax.562009openalex-snapshot
First insights in the phylogeny of Asian cheilanthoid ferns based on sequences of two chloroplast markers
inferredcites →https://doi.org/10.1002/tax.573005openalex-snapshot
Toward a monophyletic Notholaena (Pteridaceae): resolving patterns of evolutionary convergence in xeric‐adapted ferns
inferredcites →https://doi.org/10.1002/tax.605004openalex-snapshot
Evidence for radiations of cheilanthoid ferns in the Greater Cape Floristic Region
inferredcites →https://doi.org/10.1006/mpev.1994.1040openalex-snapshot
Metabolic Rate, Generation Time, and the Rate of Molecular Evolution in Birds
inferredcites →https://doi.org/10.1006/mpev.1996.0012openalex-snapshot
Rates of Nucleotide Substitution in Primates and Rodents and the Generation–Time Effect Hypothesis
inferredcites →https://doi.org/10.1006/mpev.1996.0395openalex-snapshot
Phylogenetic Relationships of the Liverworts (Hepaticae), a Basal Embryophyte Lineage, Inferred from Nucleotide Sequence Data of the Chloroplast GenerbcL
inferredcites →https://doi.org/10.1006/mpev.2000.0782openalex-snapshot
Variation in Modes and Rates of Evolution in Nuclear and Mitochondrial Ribosomal DNA in the Mushroom Genus Amanita (Agaricales, Basidiomycota): Phylogenetic Implications
inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot
Flowering plants, Eudicots : Malpighiales
inferredcites →https://doi.org/10.1007/bf00040696openalex-snapshot
Molecular characterization of a novel, nuclear-encoded, NAD+-dependent glyceraldehyde-3-phosphate dehydrogenase in plastids of the gymnosperm Pinus sylvestris L.
inferredcites →https://doi.org/10.1007/bf00161167openalex-snapshot
Relative rates of nucleotide substitution at the rbcl locus of monocotyledonous plants
inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot
A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences
inferredcites →https://doi.org/10.1007/bf02100204openalex-snapshot
Rates of synonymous substitution in plant nuclear genes
inferredcites →https://doi.org/10.1007/bf02202109openalex-snapshot
Determinants of rate variation in mammalian DNA sequence evolution
inferredcites →https://doi.org/10.1007/pl00006320openalex-snapshot
Synonymous and nonsynonymous rate variation in nuclear genes of mammals
inferredcites →https://doi.org/10.1007/s001220100741openalex-snapshot
PCR-mediated recombination in amplification products derived from polyploid cotton
inferredcites →https://doi.org/10.1007/s00239-002-2441-yopenalex-snapshot
Origin, Evolution, and Metabolic Role of a Novel Glycolytic GAPDH Enzyme Recruited by Land Plant Plastids
inferredcites →https://doi.org/10.1007/s00239-004-2597-8openalex-snapshot
A Maximum Likelihood Method for Detecting Functional Divergence at Individual Codon Sites, with Application to Gene Family Evolution
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Phylogenetic relationships of Chinese Adiantum based on five plastid markers
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Responses to environmental stresses in woody plants: key to survive and longevity
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Among-site rate variation and its impact on phylogenetic analyses
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Evolutionary Divergence and Convergence in Proteins
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Watching the clock: Studying variation in rates of molecular evolution between species
inferredcites →https://doi.org/10.1016/j.ympev.2003.09.018openalex-snapshot
Unraveling the phylogeny of polygrammoid ferns (Polypodiaceae and Grammitidaceae): exploring aspects of the diversification of epiphytic plants
inferredcites →https://doi.org/10.1016/j.ympev.2005.04.008openalex-snapshot
Incongruence between primary sequence data and the distribution of a mitochondrial atp1 group II intron among ferns and horsetails
inferredcites →https://doi.org/10.1016/j.ympev.2007.04.011openalex-snapshot
A molecular phylogeny of the fern family Pteridaceae: Assessing overall relationships and the affinities of previously unsampled genera
inferredcites →https://doi.org/10.1016/j.ympev.2008.07.010openalex-snapshot
Rates of nucleotide substitution in Cornaceae (Cornales)—Pattern of variation and underlying causal factors
inferredcites →https://doi.org/10.1016/j.ympev.2012.06.003openalex-snapshot
Concordance analysis in mitogenomic phylogenetics
inferredcites →https://doi.org/10.1016/s1055-7903(03)00215-xopenalex-snapshot
Slow algae, fast fungi: exceptionally high nucleotide substitution rate differences between lichenized fungi Omphalina and their symbiotic green algae Coccomyxa
inferredcites →https://doi.org/10.1023/a:1006319803002openalex-snapshot
Examining rates and patterns of nucleotide substitution in plants
inferredcites →https://doi.org/10.1038/337283a0openalex-snapshot
Mutation rates differ among regions of the mammalian genome
inferredcites →https://doi.org/10.1038/ncomms2836openalex-snapshot
Taller plants have lower rates of molecular evolution
inferredcites →https://doi.org/10.1038/ncomms3929openalex-snapshot
Correction: Corrigendum: Endogenous fructose production and metabolism in the liver contributes to the development of metabolic syndrome
inferredcites →https://doi.org/10.1038/nrg2158openalex-snapshot
Mutation rate variation in multicellular eukaryotes: causes and consequences
inferredcites →https://doi.org/10.1046/j.1095-8312.2003.00186.xopenalex-snapshot
Evolution in the slow lane: molecular rates of evolution in sexual and asexual ostracods (Crustacea: Ostracoda)
inferredcites →https://doi.org/10.1071/sb09047openalex-snapshot
Phylogeny and generic taxonomy of the New Zealand Pteridaceae ferns from chloroplast rbcL DNA sequences
inferredcites →https://doi.org/10.1073/pnas.032087199openalex-snapshot
Rate heterogeneity among lineages of tracheophytes: Integration of molecular and fossil data and evidence for molecular living fossils
inferredcites →https://doi.org/10.1073/pnas.0408302101openalex-snapshot
Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants
inferredcites →https://doi.org/10.1073/pnas.0510251103openalex-snapshot
There is no universal molecular clock for invertebrates, but rate variation does not scale with body size
inferredcites →https://doi.org/10.1073/pnas.0703359104openalex-snapshot
Metabolic rate does not calibrate the molecular clock
inferredcites →https://doi.org/10.1073/pnas.0705658104openalex-snapshot
Life-history traits drive the evolutionary rates of mammalian coding and noncoding genomic elements
inferredcites →https://doi.org/10.1073/pnas.0811136106openalex-snapshot
Evidence for a Cenozoic radiation of ferns in an angiosperm-dominated canopy
inferredcites →https://doi.org/10.1073/pnas.84.24.9054openalex-snapshot
Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.
inferredcites →https://doi.org/10.1073/pnas.89.16.7844openalex-snapshot
Extensive variation in evolutionary rate of rbcL gene sequences among seed plants.
inferredcites →https://doi.org/10.1073/pnas.94.11.5722openalex-snapshot
Molecular evolution of angiosperm mitochondrial introns and exons
inferredcites →https://doi.org/10.1073/pnas.94.21.11422openalex-snapshot
Accelerated evolution as a consequence of transitions to mutualism
inferredcites →https://doi.org/10.1080/106351501753462876openalex-snapshot
A Likelihood Approach to Estimating Phylogeny from Discrete Morphological Character Data
inferredcites →https://doi.org/10.1080/10635150490522278openalex-snapshot
Explosive Radiations and the Reliability of Molecular Clocks: Island Endemic Radiations as a Test Case
inferredcites →https://doi.org/10.1080/10635150500433722openalex-snapshot
Computing Bayes Factors Using Thermodynamic Integration
inferredcites →https://doi.org/10.1080/10635150590946808openalex-snapshot
Partitioned Bayesian Analyses, Partition Choice, and the Phylogenetic Relationships of Scincid Lizards
inferredcites →https://doi.org/10.1080/10635150600755438openalex-snapshot
Reconciling Extreme Branch Length Differences: Decoupling Time and Rate through the Evolutionary History of Filmy Ferns
inferredcites →https://doi.org/10.1080/10635150600865567openalex-snapshot
Detecting the Node-Density Artifact in Phylogeny Reconstruction
inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot
A Rapid Bootstrap Algorithm for the RAxML Web Servers
inferredcites →https://doi.org/10.1086/376817openalex-snapshot
Phylogenetic Relationships and Evolution of Extant Horsetails,Equisetum, Based on Chloroplast DNA Sequence Data (rbcLandtrnL‐F)
inferredcites →https://doi.org/10.1093/bioinformatics/19.2.301openalex-snapshot
r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/bioinformatics/btl175openalex-snapshot
BAli-Phy: simultaneous Bayesian inference of alignment and phylogeny
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/biomet/76.2.297openalex-snapshot
Regression and Time Series Model Selection in Small Samples
inferredcites →https://doi.org/10.1093/genetics/132.1.269openalex-snapshot
Testing for equality of evolutionary rates.
inferredcites →https://doi.org/10.1093/genetics/146.1.393openalex-snapshot
Comparing Patterns of Nucleotide Substitution Rates Among Chloroplast Loci Using the Relative Ratio Test
inferredcites →https://doi.org/10.1093/genetics/148.3.929openalex-snapshot
Likelihood Models for Detecting Positively Selected Amino Acid Sites and Applications to the HIV-1 Envelope Gene
inferredcites →https://doi.org/10.1093/genetics/155.1.431openalex-snapshot
Codon-Substitution Models for Heterogeneous Selection Pressure at Amino Acid Sites
inferredcites →https://doi.org/10.1093/molbev/msg167openalex-snapshot
Increased Rates of Sequence Evolution in Endosymbiotic Bacteria and Fungi with Small Effective Population Sizes
inferredcites →https://doi.org/10.1093/molbev/msg176openalex-snapshot
Rates of Gene Rearrangement and Nucleotide Substitution Are Correlated in the Mitochondrial Genomes of Insects
inferredcites →https://doi.org/10.1093/molbev/msh081openalex-snapshot
Phylogeny and Comparative Substitution Rates of Frogs Inferred from Sequences of Three Nuclear Genes
inferredcites →https://doi.org/10.1093/molbev/msi097openalex-snapshot
Bayes Empirical Bayes Inference of Amino Acid Sites Under Positive Selection
inferredcites →https://doi.org/10.1093/molbev/msi133openalex-snapshot
Sociality and the Rate of Molecular Evolution
inferredcites →https://doi.org/10.1093/molbev/msj021openalex-snapshot
Choosing Appropriate Substitution Models for the Phylogenetic Analysis of Protein-Coding Sequences
inferredcites →https://doi.org/10.1093/molbev/msj024openalex-snapshot
Bayesian Estimation of Species Divergence Times Under a Molecular Clock Using Multiple Fossil Calibrations with Soft Bounds
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/msm248openalex-snapshot
Strong Variations of Mitochondrial Mutation Rate across Mammals--the Longevity Hypothesis
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/molbev/msp071openalex-snapshot
Strong Evidence for Lineage and Sequence Specificity of Substitution Rates and Patterns in Drosophila
inferredcites →https://doi.org/10.1093/molbev/msp300openalex-snapshot
Accelerated Mutation Accumulation in Asexual Lineages of a Freshwater Snail
inferredcites →https://doi.org/10.1093/molbev/msq224openalex-snapshot
Choosing among Partition Models in Bayesian Phylogenetics
inferredcites →https://doi.org/10.1093/molbev/msq244openalex-snapshot
A Phylogenetic Model for Investigating Correlated Evolution of Substitution Rates and Continuous Phenotypic Characters
inferredcites →https://doi.org/10.1093/molbev/msq263openalex-snapshot
A Likelihood Method for Detecting Trait-Dependent Shifts in the Rate of Molecular Evolution
inferredcites →https://doi.org/10.1093/molbev/mss020openalex-snapshot
PartitionFinder: Combined Selection of Partitioning Schemes and Substitution Models for Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/molbev/mss084openalex-snapshot
Improving the Accuracy of Demographic and Molecular Clock Model Comparison While Accommodating Phylogenetic Uncertainty
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003974openalex-snapshot
Estimating Absolute Rates of Molecular Evolution and Divergence Times: A Penalized Likelihood Approach
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004007openalex-snapshot
A Novel Use of Equilibrium Frequencies in Models of Sequence Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004083openalex-snapshot
Molecular Clocks in Reptiles: Life History Influences Rate of Molecular Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004148openalex-snapshot
Codon-Substitution Models for Detecting Molecular Adaptation at Individual Sites Along Specific Lineages
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025781openalex-snapshot
Correlated rates of synonymous site evolution across plant genomes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025957openalex-snapshot
Likelihood ratio tests for detecting positive selection and application to primate lysozyme evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026389openalex-snapshot
Estimation of Primate Speciation Dates Using Local Molecular Clocks
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a039989openalex-snapshot
Molecular phylogenies in angiosperm evolution.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040153openalex-snapshot
A codon-based model of nucleotide substitution for protein-coding DNA sequences.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040617openalex-snapshot
Correcting parsimonious trees for unseen nucleotide substitutions: the effect of dense branching as exemplified by ribonuclease.
inferredcites →https://doi.org/10.1093/sysbio/49.2.369openalex-snapshot
Gaps as Characters in Sequence-Based Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/sysbio/syp072openalex-snapshot
Relaxed Molecular Clocks, the Bias–Variance Trade-off, and the Quality of Phylogenetic Inference
inferredcites →https://doi.org/10.1093/sysbio/syq085openalex-snapshot
Improving Marginal Likelihood Estimation for Bayesian Phylogenetic Model Selection
inferredcites →https://doi.org/10.1093/sysbio/sys001openalex-snapshot
Overcoming Deep Roots, Fast Rates, and Short Internodes to Resolve the Ancient Rapid Radiation of Eupolypod II Ferns
inferredcites →https://doi.org/10.1098/rsbl.2009.0136openalex-snapshot
Why do species vary in their rate of molecular evolution?
inferredcites →https://doi.org/10.1098/rspb.2004.2849openalex-snapshot
Environmental energy and evolutionary rates in flowering plants
inferredcites →https://doi.org/10.1098/rspb.2005.3217openalex-snapshot
Population size and molecular evolution on islands
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
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TESTING THE RELATIONSHIP BETWEEN MORPHOLOGICAL AND MOLECULAR RATES OF CHANGE ALONG PHYLOGENIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb01404.xopenalex-snapshot
ACCELERATED MOLECULAR EVOLUTION IN HALOPHILIC CRUSTACEANS
inferredcites →https://doi.org/10.1111/j.1438-8677.1999.tb00249.xopenalex-snapshot
Phylogenetic Information in the Mitochondrial nad5 Gene of Pteridophytes: RNA Editing and Intron Sequences
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00188.xopenalex-snapshot
THE LIKELIHOOD NODE DENSITY EFFECT AND CONSEQUENCES FOR EVOLUTIONARY STUDIES OF MOLECULAR RATES
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01000.xopenalex-snapshot
ABRUPT DECELERATION OF MOLECULAR EVOLUTION LINKED TO THE ORIGIN OF ARBORESCENCE IN FERNS
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01160.xopenalex-snapshot
THE LOCAL-CLOCK PERMUTATION TEST: A SIMPLE TEST TO COMPARE RATES OF MOLECULAR EVOLUTION ON PHYLOGENETIC TREES
inferredcites →https://doi.org/10.1126/science.1129647openalex-snapshot
Large Punctuational Contribution of Speciation to Evolutionary Divergence at the Molecular Level
inferredcites →https://doi.org/10.1126/science.1163197openalex-snapshot
Rates of Molecular Evolution Are Linked to Life History in Flowering Plants
inferredcites →https://doi.org/10.1126/science.147.3653.68openalex-snapshot
Evolving Genes and Proteins
inferredcites →https://doi.org/10.1126/science.158.3805.1200openalex-snapshot
Immunological Time Scale for Hominid Evolution
inferredcites →https://doi.org/10.11646/phytotaxa.7.1.7openalex-snapshot
The new fern genus Calciphilopteris (Pteridaceae)
inferredcites →https://doi.org/10.1177/117693430700300008openalex-snapshot
Fast Genes and Slow Clades: Comparative Rates of Molecular Evolution in Mammals
inferredcites →https://doi.org/10.1186/1471-2148-5-73openalex-snapshot
Multiple major increases and decreases in mitochondrial substitution rates in the plant family Geraniaceae
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1186/1471-2148-7-40openalex-snapshot
Incorporating indel information into phylogeny estimation for rapidly emerging pathogens
inferredcites →https://doi.org/10.1186/1471-2148-8-130openalex-snapshot
The complete plastid genome sequence of Welwitschia mirabilis: an unusually compact plastome with accelerated divergence rates
inferredcites →https://doi.org/10.1186/1471-2148-8-257openalex-snapshot
Accelerated evolutionary rates in tropical and oceanic parmelioid lichens (Ascomycota)
inferredcites →https://doi.org/10.1186/1471-2148-8-53openalex-snapshot
Correlates of substitution rate variation in mammalian protein-coding sequences
inferredcites →https://doi.org/10.1186/1741-7007-8-1openalex-snapshot
THOC5/FMIP, an mRNA export TREX complex protein, is essential for hematopoietic primitive cell survival in vivo
inferredcites →https://doi.org/10.1186/1741-7007-8-114openalex-snapshot
Bayesian random local clocks, or one rate to rule them all
inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot
Relaxed Phylogenetics and Dating with Confidence
inferredcites →https://doi.org/10.1371/journal.pone.0026597openalex-snapshot
rbcL and matK Earn Two Thumbs Up as the Core DNA Barcode for Ferns
inferredcites →https://doi.org/10.1371/journal.pone.0076957openalex-snapshot
Transcriptome-Mining for Single-Copy Nuclear Markers in Ferns
inferredcites →https://doi.org/10.1534/genetics.104.031153openalex-snapshot
Accuracy and Power of Statistical Methods for Detecting Adaptive Evolution in Protein Coding Sequences and for Identifying Positively Selected Sites
inferredcites →https://doi.org/10.1600/036364407782250616openalex-snapshot
Investigating the Monophyly of Pellaea (Pteridaceae) in the Context of a Phylogenetic Analysis of Cheilanthoid Ferns
inferredcites →https://doi.org/10.1600/036364408783887410openalex-snapshot
Phylogenetic Placement of Rheopteris and the Polyphyly of Monogramma (Pteridaceae s.l.): Evidence from rbcL Sequence Data
inferredcites →https://doi.org/10.1600/036364408786500127openalex-snapshot
The Utility of Nuclear gapCp in Resolving Polyploid Fern Origins
inferredcites →https://doi.org/10.1600/036364413x666787openalex-snapshot
A Plastid Phylogeny of the Cosmopolitan Fern Family Cystopteridaceae (Polypodiopsida)
inferredcites →https://doi.org/10.2307/1547811openalex-snapshot
Phylogeny of the Vittariaceae: Convergent Simplification Leads to a Polyphyletic Vittaria
inferredcites →https://doi.org/10.2307/1547814openalex-snapshot
Phylogeny and Generic Circumscriptions of Cheilanthoid Ferns (Pteridaceae: Cheilanthoideae) Inferred from rbcL Nucleotide Sequences
inferredcites →https://doi.org/10.2307/2419824openalex-snapshot
A Revised Circumscription of the Genera of the Fern Family Vittariaceae
inferredcites →https://doi.org/10.2307/2446141openalex-snapshot
Evaluation of atpB nucleotide sequences for phylogenetic studies of ferns and other pteridophytes
inferredcites →https://doi.org/10.2307/2446640openalex-snapshot
The tortoise and the hare: choosing between noncoding plastome and nuclear Adh sequences for phylogeny reconstruction in a recently diverged plant group
inferredcites →https://doi.org/10.2307/25065407openalex-snapshot
The Families and Genera of Vascular Plants
inferredcites →https://doi.org/10.2307/25065684openalex-snapshot
Plastid atpA data provide improved support for deep relationships among ferns
inferredcites →https://doi.org/10.2307/25065903openalex-snapshot
Fern phylogeny inferred from 400 leptosporangiate species and three plastid genes
inferredcites →https://doi.org/10.2307/3802723openalex-snapshot
Model Selection and Multimodel Inference: A Practical Information-Theoretic Approach
inferredcites →https://doi.org/10.3732/ajb.1100125openalex-snapshot
Biogeographic disjunction between eastern Asia and North America in the Adiantum pedatum complex (Pteridaceae)
inferredcites →https://doi.org/10.3732/ajb.1200049openalex-snapshot
Unique expression of a sporophytic character on the gametophytes of notholaenid ferns (Pteridaceae)
inferredcites →https://doi.org/10.3732/ajb.91.10.1582openalex-snapshot
Phylogeny and evolution of ferns (monilophytes) with a focus on the early leptosporangiate divergences
inferredcites →https://doi.org/10.3852/10-120openalex-snapshot
Align or not to align? Resolving species complexes within theCaloplaca saxicolagroup as a case study
inferredcites →https://doi.org/10.5642/aliso.19981702.04openalex-snapshot
Cheilanthoid Ferns (Pteridaceae: Cheilanthoideae) in the Southwestern United States and Adjacent Mexico-A Molecular Phylogenetic Reassessment of Generic Lines
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Prodromus of a fern flora for Bolivia. XXVII. Pteridaceae
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The third opinion on fern phylogenetics with novel insights into their mitogenome evolution
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Organellomic data sets confirm a cryptic consensus on (unrooted) land‐plant relationships and provide new insights into bryophyte molecular evolution
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Target sequence capture of nuclear‐encoded genes for phylogenetic analysis in ferns
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Taxonomy and spore morphology of genus Adiantum (Vittarioideae; Pteridaceae) from Pakistan
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Taxonomy and spore morphology of selected taxa of Cheilanthoideae and Pteridoideae (Pteridaceae) from Pakistan
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A phylogenetically informed generic reclassification of the hemionitid ferns (Pteridaceae: Cheilanthoideae)
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Evolution and Classification of Ferns and Lycophytes
inferred← citeshttps://doi.org/10.1007/978-981-16-6170-9_4openalex-snapshot
Plastogenomics Provides a Tool to Study Phylogenetic Interrelationships of Monilophytes: A Review
inferred← citeshttps://doi.org/10.1007/s11104-015-2484-7openalex-snapshot
Root morphology, histology and chemistry of nine fern species (pteridophyta) in a temperate forest
inferred← citeshttps://doi.org/10.1007/s13127-018-0366-6openalex-snapshot
Further progress towards the delimitation of Cheilanthes (Cheilanthoideae, Pteridaceae), with emphasis on South American species
inferred← citeshttps://doi.org/10.1016/b978-0-12-813012-4.00012-7openalex-snapshot
A Comprehensive Assessment of the Fossil Record of Liverworts in Amber
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.04.014openalex-snapshot
A review of molecular-clock calibrations and substitution rates in liverworts, mosses, and hornworts, and a timeframe for a taxonomically cleaned-up genus Nothoceros
inferred← citeshttps://doi.org/10.1016/j.ympev.2014.07.005openalex-snapshot
Exploring new dating approaches for parasites: The worldwide Apodanthaceae (Cucurbitales) as an example
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.05.008openalex-snapshot
Horsetails are the sister group to all other monilophytes and Marattiales are sister to leptosporangiate ferns
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.08.011openalex-snapshot
Rearrangement and evolution of mitochondrial genomes in parrots
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.02.018openalex-snapshot
A well-sampled phylogenetic analysis of the polystichoid ferns (Dryopteridaceae) suggests a complex biogeographical history involving both boreotropical migrations and recent transoceanic dispersals
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.09.003openalex-snapshot
A 4000-species dataset provides new insight into the evolution of ferns
inferred← citeshttps://doi.org/10.1016/j.ympev.2024.108253openalex-snapshot
Phylogenomics of Paragymnopteris (Cheilanthoideae, Pteridaceae): Insights from plastome, mitochondrial, and nuclear datasets
inferred← citeshttps://doi.org/10.1016/j.ympev.2025.108454openalex-snapshot
Widespread incongruence in the phylogenomics of the ancient land plant lineage, Selaginellaceae (lycophytes)
inferred← citeshttps://doi.org/10.1038/s42003-023-04659-8openalex-snapshot
Rickettsial DNA and a trans-splicing rRNA group I intron in the unorthodox mitogenome of the fern Haplopteris ensiformis
inferred← citeshttps://doi.org/10.1071/sb18011openalex-snapshot
Classification and typification of Australian lycophytes and ferns based on Pteridophyte Phylogeny Group classification PPG I
inferred← citeshttps://doi.org/10.1086/679662openalex-snapshot
Natural Hybridization between Genera That Diverged from Each Other Approximately 60 Million Years Ago
inferred← citeshttps://doi.org/10.1086/724824openalex-snapshot
Life without a Sporophyte: The Origin and Genomic Consequences of Asexual Reproduction in a Gametophyte-Only Fern
inferred← citeshttps://doi.org/10.1093/botlinnean/box001openalex-snapshot
A systematic study of East Asian vittarioid ferns (Pteridaceae: Vittarioideae)
inferred← citeshttps://doi.org/10.1093/gbe/evu087openalex-snapshot
Two New Fern Chloroplasts and Decelerated Evolution Linked to the Long Generation Time in Tree Ferns
inferred← citeshttps://doi.org/10.1093/gbe/evw167openalex-snapshot
Genes Translocated into the Plastid Inverted Repeat Show Decelerated Substitution Rates and Elevated GC Content
inferred← citeshttps://doi.org/10.1093/gbe/evw173openalex-snapshot
Convergent Evolution of Fern-Specific Mitochondrial Group II Intron atp1i361g2 and Its Ancient Source Paralogue rps3i249g2 and Independent Losses of Intron and RNA Editing among Pteridaceae
inferred← citeshttps://doi.org/10.1093/gbe/evy189openalex-snapshot
Mobile Elements Shape Plastome Evolution in Ferns
inferred← citeshttps://doi.org/10.1093/sysbio/syab020openalex-snapshot
Inferring the Total-Evidence Timescale of Marattialean Fern Evolution in the Face of Model Sensitivity
inferred← citeshttps://doi.org/10.1105/tpc.15.00157openalex-snapshot
Horsetails Are Ancient Polyploids: Evidence from Equisetum giganteum
inferred← citeshttps://doi.org/10.1111/cla.12419openalex-snapshot
Exploring the phylogeny of the marattialean ferns
inferred← citeshttps://doi.org/10.1111/jbi.13119openalex-snapshot
Phylogenetic biogeography reveals the timing and source areas of the Adiantum species (Pteridaceae) in the West Indies, with a special focus on Cuba
inferred← citeshttps://doi.org/10.1111/jbi.15169openalex-snapshot
Was the Dry Diagonal of South America a Barrier for Dispersing Pteridaceae (Polypodiopsida) Species Between the Brazilian Atlantic Forest and Amazon Forest?
inferred← citeshttps://doi.org/10.1111/jse.12229openalex-snapshot
A community‐derived classification for extant lycophytes and ferns
inferred← citeshttps://doi.org/10.1111/jse.12514openalex-snapshot
Heinrichsia cheilanthoides gen. et sp. nov., a fossil fern in the family Pteridaceae (Polypodiales) from the Cretaceous amber forests of Myanmar
inferred← citeshttps://doi.org/10.1111/nph.14111openalex-snapshot
Next‐generation polyploid phylogenetics: rapid resolution of hybrid polyploid complexes using PacBio single‐molecule sequencing
inferred← citeshttps://doi.org/10.1111/nph.20433openalex-snapshot
Population genomics of the gametophyte‐only fern Vittaria appalachiana provides insights into clonal plant evolution
inferred← citeshttps://doi.org/10.1111/nph.70244openalex-snapshot
Comparative phylogenetic analyses of RNA editing in fern plastomes suggest possible adaptive innovations
inferred← citeshttps://doi.org/10.1186/s12864-016-3034-2openalex-snapshot
Transcriptome sequencing reveals genome-wide variation in molecular evolutionary rate among ferns
inferred← citeshttps://doi.org/10.1186/s12870-017-1199-8openalex-snapshot
Negative correlation between rates of molecular evolution and flowering cycles in temperate woody bamboos revealed by plastid phylogenomics
inferred← citeshttps://doi.org/10.12705/635.32openalex-snapshot
Low‐copy nuclear data confirm rampant allopolyploidy in the Cystopteridaceae (Polypodiales)
inferred← citeshttps://doi.org/10.12705/654.2openalex-snapshot
A revised generic classification of vittarioid ferns (Pteridaceae) based on molecular, micromorphological, and geographic data
inferred← citeshttps://doi.org/10.12705/656.1openalex-snapshot
Phylogeny and relationships of the neotropical Adiantum raddianum group (Pteridaceae)
inferred← citeshttps://doi.org/10.12705/673.3openalex-snapshot
A worldwide phylogeny of Adiantum (Pteridaceae) reveals remarkable convergent evolution in leaf blade architecture
inferred← citeshttps://doi.org/10.1371/journal.pone.0076957openalex-snapshot
Transcriptome-Mining for Single-Copy Nuclear Markers in Ferns
inferred← citeshttps://doi.org/10.1371/journal.pone.0104933openalex-snapshot
Infrageneric Phylogeny and Temporal Divergence of Sorghum (Andropogoneae, Poaceae) Based on Low-Copy Nuclear and Plastid Sequences
inferred← citeshttps://doi.org/10.1371/journal.pone.0160611openalex-snapshot
Applying DNA Barcodes to Identify Closely Related Species of Ferns: A Case Study of the Chinese Adiantum (Pteridaceae)
inferred← citeshttps://doi.org/10.14203/reinwardtia.v14i1.409openalex-snapshot
MOLECULAR PHYLOGENY OF MAIDENHAIR FERN GENUS ADIANTUM (PTERIDACEAE) FROM LESSER SUNDA ISLANDS INDONESIA BASED ON RBCL AND TRNL-F
inferred← citeshttps://doi.org/10.1590/2175-7860202172003openalex-snapshot
Lytoneuron (Pteridaceae) no estado do Rio de Janeiro, Brasil
inferred← citeshttps://doi.org/10.1600/036364416x690660openalex-snapshot
Maidenhair Ferns, Adiantum, are Indeed Monophyletic and Sister to Shoestring Ferns, Vittarioids (Pteridaceae)
inferred← citeshttps://doi.org/10.1600/036364418x697166openalex-snapshot
Microsorum × tohieaense (Polypodiaceae), a New Hybrid Fern from French Polynesia, with Implications for the Taxonomy of Microsorum
inferred← citeshttps://doi.org/10.1600/036364421x16231782047280openalex-snapshot
Cheilanthes ecuadorensis: A New Species of Cheilanthes s. s. (Pteridaceae) from Northern South America
inferred← citeshttps://doi.org/10.1640/0002-8444-107.2.84openalex-snapshot
Four New Species of Adiantum (Pteridaceae) from the Guianas
inferred← citeshttps://doi.org/10.18475/cjos.v51i2.a13openalex-snapshot
DNA Barcoding of Adiantum (Pteridaceae: Vittarioideae) in Puerto Rico
inferred← citeshttps://doi.org/10.2139/ssrn.4884258openalex-snapshot
Phylogenomics of Paragymnopteris S.L. (Cheilanthoideae, Pteridaceae) with the Segeration of Sericopteris Gen. Nov
inferred← citeshttps://doi.org/10.21608/bfszu.2023.213984.1277openalex-snapshot
Adiantum pedatum as anticancer, anti-oxidant and anti-inflammatory agent
inferred← citeshttps://doi.org/10.21826/2446-82312023v78e2023021openalex-snapshot
O gênero Adiantum (Pteridaceae) no Estado do Paraná, Brasil
inferred← citeshttps://doi.org/10.3372/wi.47.47307openalex-snapshot
Novelties inAdiantum(Pteridaceae) from South America
inferred← citeshttps://doi.org/10.3389/fpls.2022.882441openalex-snapshot
Phylotranscriptomics Illuminates the Placement of Whole Genome Duplications and Gene Retention in Ferns
inferred← citeshttps://doi.org/10.3732/ajb.1500089openalex-snapshot
The evolutionary history of ferns inferred from 25 low‐copy nuclear genes
inferred← citeshttps://doi.org/10.5194/fr-20-147-2017openalex-snapshot
Problems related to the taxonomic placement of incompletely preserved amber fossils: transfer of the Paleogene liverwort Cylindrocolea dimorpha (Cephaloziellaceae) to the extant Odontoschisma sect. Iwatsukia (Cephaloziaceae)
inferred← citeshttps://doi.org/10.7717/peerj.9937openalex-snapshot
Morphological and anatomical adaptations to dry, shady environments in Adiantum reniforme var. sinense (Pteridaceae)
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