| scholarly article | Q13442814 |
| P50 | author | Jeremy M. Brown | Q22102621 |
| Kathrin F. Stanger-Hall | Q37379754 | ||
| Emily Moriarty Lemmon | Q39357206 | ||
| Alan R. Lemmon | Q40417311 | ||
| P2860 | cites work | Heterotachy and long-branch attraction in phylogenetics | Q21283964 |
| MrBayes 3: Bayesian phylogenetic inference under mixed models | Q26778438 | ||
| Evolutionary trees from DNA sequences: A maximum likelihood approach | Q27860898 | ||
| Unravelling angiosperm genome evolution by phylogenetic analysis of chromosomal duplication events | Q28186749 | ||
| Molecular phylogenetics and the origins of placental mammals | Q28201892 | ||
| Phylogeny of North American fireflies (Coleoptera: Lampyridae): implications for the evolution of light signals | Q28237327 | ||
| Missing data and the design of phylogenetic analyses | Q28253408 | ||
| Phylogenies from molecular sequences: inference and reliability | Q28289703 | ||
| Morphological homoplasy, life history evolution, and historical biogeography of plethodontid salamanders inferred from complete mitochondrial genomes | Q28770124 | ||
| Maximum likelihood phylogenetic estimation from DNA sequences with variable rates over sites: approximate methods | Q29547744 | ||
| Seq-Gen: an application for the Monte Carlo simulation of DNA sequence evolution along phylogenetic trees | Q29614558 | ||
| Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites | Q29618512 | ||
| Phylogenomics of eukaryotes: impact of missing data on large alignments | Q29618583 | ||
| Predicting the evolution of human influenza A. | Q30011145 | ||
| AIDS. Origins of HIV. | Q30326943 | ||
| Fragmentary taxa, missing data, and ambiguity: mistaken assumptions and conclusions | Q30694585 | ||
| Does adding characters with missing data increase or decrease phylogenetic accuracy? | Q30698362 | ||
| Prospects for building the tree of life from large sequence databases | Q30772150 | ||
| Molecular phylogenetics of myliobatiform fishes (Chondrichthyes: Myliobatiformes), with comments on the effects of missing data on parsimony and likelihood. | Q30785624 | ||
| The importance of data partitioning and the utility of Bayes factors in Bayesian phylogenetics. | Q31120116 | ||
| MaxAlign: maximizing usable data in an alignment | Q31122829 | ||
| Missing data, incomplete taxa, and phylogenetic accuracy | Q33187728 | ||
| A simulation comparison of phylogeny algorithms under equal and unequal evolutionary rates | Q34329120 | ||
| Performance of maximum parsimony and likelihood phylogenetics when evolution is heterogeneous | Q34360850 | ||
| Overcredibility of molecular phylogenies obtained by Bayesian phylogenetics | Q34415633 | ||
| The supermatrix approach to systematics | Q36625725 | ||
| Evolution of chlorophyll and bacteriochlorophyll: the problem of invariant sites in sequence analysis | Q37705639 | ||
| Molecular phylogenetics and evolution of host plant use in the Neotropical rolled leaf 'hispine' beetle genus Cephaloleia (Chevrolat) (Chrysomelidae: Cassidinae). | Q38383927 | ||
| Should phylogenetic models be trying to "fit an elephant"? | Q38701562 | ||
| Polytomies and Bayesian phylogenetic inference | Q44089841 | ||
| Comparing bootstrap and posterior probability values in the four-taxon case | Q44246809 | ||
| Is there a star tree paradox? | Q47602128 | ||
| Among-site rate variation and phylogenetic analysis of 12S rRNA in sigmodontine rodents | Q48069583 | ||
| Exploring the Phylogenetic Structure of Ecological Communities: An Example for Rain Forest Trees. | Q51204015 | ||
| Phylogeny of the SARS coronavirus. | Q51641081 | ||
| Phylogenetic mixtures on a single tree can mimic a tree of another topology. | Q51905455 | ||
| Fair-balance paradox, star-tree paradox, and Bayesian phylogenetics. | Q51915433 | ||
| The Bayesian "star paradox" persists for long finite sequences. | Q51922382 | ||
| The importance of proper model assumption in bayesian phylogenetics. | Q51995935 | ||
| Branch-length prior influences Bayesian posterior probability of phylogeny. | Q52979681 | ||
| EXPERIMENTAL MOLECULAR EVOLUTION OF BACTERIOPHAGE T7. | Q53246126 | ||
| Heterotachy and tree building: a case study with plastids and eubacteria. | Q53892466 | ||
| Experimental Phylogenetics: Generation of a Known Phylogeny | Q54684327 | ||
| Comparison of models for nucleotide substitution used in maximum-likelihood phylogenetic estimation | Q57079033 | ||
| The Biasing Effect of Compositional Heterogeneity on Phylogenetic Estimates May be Underestimated | Q58468349 | ||
| Maximum likelihood estimation of the heterogeneity of substitution rate among nucleotide sites | Q72020725 | ||
| Likelihood, parsimony, and heterogeneous evolution | Q81474727 | ||
| P433 | issue | 1 | |
| P921 | main subject | phylogenetics | Q171184 |
| Bayesian inference | Q812535 | ||
| P304 | page(s) | 130-145 | |
| P577 | publication date | 2009-02-01 | |
| P1433 | published in | Systematic Biology | Q7663761 |
| P1476 | title | The effect of ambiguous data on phylogenetic estimates obtained by maximum likelihood and Bayesian inference | |
| P478 | volume | 58 |
| Q35909635 | A Phylogenomic Approach Based on PCR Target Enrichment and High Throughput Sequencing: Resolving the Diversity within the South American Species of Bartsia L. (Orobanchaceae) |
| Q28596153 | A Species-Level Phylogeny of Extant Snakes with Description of a New Colubrid Subfamily and Genus |
| Q24653659 | A class-wide phylogenetic assessment of Dothideomycetes |
| Q30846669 | A confounding effect of missing data on character conflict in maximum likelihood and Bayesian MCMC phylogenetic analyses |
| Q42740844 | A long PCR-based approach for DNA enrichment prior to next-generation sequencing for systematic studies |
| Q28730452 | A molecular phylogeny for the leaf-roller moths (Lepidoptera: Tortricidae) and its implications for classification and life history evolution |
| Q54534900 | A molecular phylogeny for the pyraloid moths (Lepidoptera: Pyraloidea) and its implications for higher-level classification |
| Q21089813 | A molecular phylogeny for yponomeutoidea (insecta, Lepidoptera, ditrysia) and its implications for classification, biogeography and the evolution of host plant use |
| Q54555167 | A morphological supermatrix-based phylogeny for the Neotropical fish superfamily Anostomoidea (Ostariophysi: Characiformes): phylogeny, missing data and homoplasy |
| Q39560215 | A multigenic perspective on phylogenetic relationships in the largest family of salamanders, the Plethodontidae. |
| Q34564581 | A multimarker phylogeography of crested newts (Triturus cristatus superspecies) reveals cryptic species |
| Q21694048 | A new genus of rodent from Wallacea (Rodentia: Muridae: Murinae: Rattini), and its implication for biogeography and Indo-Pacific Rattini systematics |
| Q28714203 | A phylogenomic approach to vertebrate phylogeny supports a turtle-archosaur affinity and a possible paraphyletic lissamphibia |
| Q21284044 | A phylogeny and molecular barcodes for Caenorhabditis, with numerous new species from rotting fruits |
| Q13416674 | A phylogeny and revised classification of Squamata, including 4161 species of lizards and snakes |
| Q52596290 | A phylotranscriptomic backbone of the orb-weaving spider family Araneidae (Arachnida, Araneae) supported by multiple methodological approaches. |
| Q92579676 | A proposed core genome scheme for analyses of the Salmonella genus |
| Q89792298 | A simple dynamic model explains the diversity of island birds worldwide |
| Q34113101 | A supermatrix-based molecular phylogeny of the family Drosophilidae |
| Q28715810 | A total-evidence approach to dating with fossils, applied to the early radiation of the hymenoptera |
| Q43615822 | A versatile and highly efficient toolkit including 102 nuclear markers for vertebrate phylogenomics, tested by resolving the higher level relationships of the caudata |
| Q34290442 | Accelerated speciation in colour-polymorphic birds |
| Q21145831 | Amazonian amphibian diversity is primarily derived from late Miocene Andean lineages |
| Q40489041 | An augmented supermatrix phylogeny of the avian family Picidae reveals uncertainty deep in the family tree. |
| Q28728212 | An estimation of Erinaceidae phylogeny: a combined analysis approach |
| Q33543555 | An expanded phylogeny of treefrogs (Hylidae) based on nuclear and mitochondrial sequence data |
| Q28715729 | An extreme case of plant-insect codiversification: figs and fig-pollinating wasps |
| Q110697138 | An ocean yet to be discovered: increasing systematic knowledge of Indo-Pacific Okenia Menke, 1830 (Nudibranchia:Goniodorididae) |
| Q58337704 | Anchored Hybrid Enrichment-Based Phylogenomics of Leafhoppers and Treehoppers (Hemiptera: Cicadomorpha: Membracoidea) |
| Q46854481 | Application of RAD-based phylogenetics to complex relationships among variously related taxa in a species flock |
| Q28683476 | Assessing phylogenetic relationships among galliformes: a multigene phylogeny with expanded taxon sampling in Phasianidae |
| Q42695619 | Assessing the utility of transcriptome data for inferring phylogenetic relationships among coleoid cephalopods |
| Q35001704 | BaCoCa--a heuristic software tool for the parallel assessment of sequence biases in hundreds of gene and taxon partitions |
| Q34597377 | Bayesian inference of phylogeny, morphology and range evolution reveals a complex evolutionary history in St. John's wort (Hypericum). |
| Q54490739 | Beyond the prolegomenon: a molecular phylogeny of the Australian camaenid land snail radiation |
| Q39218907 | Biogeography and divergent patterns of body size disparification in North American minnows |
| Q21089634 | Biogeography and taxonomy of extinct and endangered monk seals illuminated by ancient DNA and skull morphology |
| Q44547111 | Body plan convergence in the evolution of skates and rays (Chondrichthyes: Batoidea). |
| Q41637989 | Building the avian tree of life using a large-scale, sparse supermatrix |
| Q28743854 | Can deliberately incomplete gene sample augmentation improve a phylogeny estimate for the advanced moths and butterflies (Hexapoda: Lepidoptera)? |
| Q38367980 | Can quartet analyses combining maximum likelihood estimation and Hennigian logic overcome long branch attraction in phylogenomic sequence data? |
| Q28596652 | Cementing mussels to oysters in the pteriomorphian tree: a phylogenomic approach |
| Q36121800 | Chloroplast Genome Evolution in Actinidiaceae: clpP Loss, Heterogenous Divergence and Phylogenomic Practice |
| Q36293142 | Clock-dated phylogeny for 48% of the 700 species of Crotalaria (Fabaceae-Papilionoideae) resolves sections worldwide and implies conserved flower and leaf traits throughout its pantropical range |
| Q46258742 | Coevolution with pollinating resin midges led to resin-filled nurseries in the androecia, gynoecia and tepals of Kadsura (Schisandraceae). |
| Q110444671 | Combined phylogenetic analyses reveal interfamilial relationships and patterns of floral evolution in the eudicot order Fabales |
| Q28649864 | Concatabominations: identifying unstable taxa in morphological phylogenetics using a heuristic extension to safe taxonomic reduction |
| Q28601738 | Consequences of Secondary Calibrations on Divergence Time Estimates |
| Q39231113 | Construction of a Species-Level Tree of Life for the Insects and Utility in Taxonomic Profiling |
| Q92449339 | Cryptic species delineation in freshwater planarians of the genus Dugesia (Platyhelminthes, Tricladida): Extreme intraindividual genetic diversity, morphological stasis, and karyological variability |
| Q116673322 | DNA Barcodes Combined with Multilocus Data of Representative Taxa Can Generate Reliable Higher-Level Phylogenies |
| Q21131911 | Data concatenation, Bayesian concordance and coalescent-based analyses of the species tree for the rapid radiation of Triturus newts |
| Q42677698 | Delphinid systematics and biogeography with a focus on the current genus Lagenorhynchus: multiple pathways for antitropical and trans-oceanic radiation |
| Q51753765 | Differences between hard and soft phylogenetic data. |
| Q46894857 | Disparate parametric branch-support values from ambiguous characters |
| Q34182197 | Divergence time estimation using fossils as terminal taxa and the origins of Lissamphibia. |
| Q39199488 | Divergent maximum-likelihood-branch-support values for polytomies |
| Q34253766 | Diversification and biogeography of the Neotropical caviomorph lineage Octodontoidea (Rodentia: Hystricognathi). |
| Q36092060 | Diversification in vipers: Phylogenetic relationships, time of divergence and shifts in speciation rates |
| Q55881251 | Diversification of South American spiny rats (Echimyidae): a multigene phylogenetic approach |
| Q28690585 | Diversification rates have declined in the Malagasy herpetofauna |
| Q30892696 | Do missing data influence the accuracy of divergence-time estimation with BEAST? |
| Q88080156 | Dubious resolution and support from published sparse supermatrices: the importance of thorough tree searches |
| Q30991103 | EAPhy: A Flexible Tool for High-throughput Quality Filtering of Exon-alignments and Data Processing for Phylogenetic Methods |
| Q39035021 | ESA-UbiSite: accurate prediction of human ubiquitination sites by identifying a set of effective negatives |
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| Q91199419 | Effects of missing data and data type on phylotranscriptomic analysis of stony corals (Cnidaria: Anthozoa: Scleractinia) |
| Q30648515 | Effects of missing data on species tree estimation under the coalescent |
| Q30991264 | Effects of missing data on topological inference using a Total Evidence approach |
| Q46728961 | Employing Phylogenomics to Resolve the Relationships among Cnidarians, Ctenophores, Sponges, Placozoans, and Bilaterians |
| Q46846521 | Evaluating Summary Methods for Multilocus Species Tree Estimation in the Presence of Incomplete Lineage Sorting |
| Q111629653 | Evaluating character partitioning and molecular models in plastid phylogenomics at low taxonomic levels: A case study using Amphilophium (Bignonieae, Bignoniaceae) |
| Q31131999 | Evaluating the Impact of Genomic Data and Priors on Bayesian Estimates of the Angiosperm Evolutionary Timescale |
| Q30786867 | Evaluating topological conflict in centipede phylogeny using transcriptomic data sets |
| Q99708295 | Evidence of Absence Treated as Absence of Evidence: The Effects of Variation in the Number and Distribution of Gaps Treated as Missing Data on the Results of Standard Maximum Likelihood Analysis |
| Q57143783 | Evolution of floral traits and impact of reproductive mode on diversification in the phlox family (Polemoniaceae) |
| Q34512134 | Evolution. Who speaks with a forked tongue? |
| Q30914015 | Evolutionary origin of Ceratonova shasta and phylogeny of the marine myxosporean lineage |
| Q28743533 | Evolutionary relationships of the old world fruit bats (Chiroptera, Pteropodidae): another star phylogeny? |
| Q46285707 | Exon-based phylogenomics strengthens the phylogeny of Neotropical cichlids and identifies remaining conflicting clades (Cichliformes: Cichlidae: Cichlinae). |
| Q36161701 | Expanding anchored hybrid enrichment to resolve both deep and shallow relationships within the spider tree of life |
| Q58907801 | Exploring Diversification and Genome Size Evolution in Extant Gymnosperms through Phylogenetic Synthesis |
| Q28597241 | Exploring Phylogenetic Relationships within Myriapoda and the Effects of Matrix Composition and Occupancy on Phylogenomic Reconstruction |
| Q31027366 | Extracting phylogenetic signal and accounting for bias in whole-genome data sets supports the Ctenophora as sister to remaining Metazoa |
| Q50060470 | Filtering of target sequence capture individuals facilitates species tree construction in the plant subtribe Iochrominae (Solanaceae). |
| Q28681385 | Fossilization causes organisms to appear erroneously primitive by distorting evolutionary trees |
| Q43966677 | Fourteen nuclear genes provide phylogenetic resolution for difficult nodes in the turtle tree of life |
| Q46286600 | Fragmentary Gene Sequences Negatively Impact Gene Tree and Species Tree Reconstruction |
| Q34290887 | From Amazonia to the Atlantic forest: molecular phylogeny of Phyzelaphryninae frogs reveals unexpected diversity and a striking biogeographic pattern emphasizing conservation challenges |
| Q110668658 | Gene flow in phylogenomics: Sequence capture resolves species limits and biogeography of Afromontane forest endemic frogs from the Cameroon Highlands |
| Q58568763 | Gene-wise resampling outperforms site-wise resampling in phylogenetic coalescence analyses |
| Q27320123 | Genetic, ecological and morphological divergence between populations of the endangered Mexican Sheartail hummingbird (Doricha eliza). |
| Q28834248 | Genomic Characterization of a South American Phytophthora Hybrid Mandates Reassessment of the Geographic Origins of Phytophthora infestans |
| Q36177377 | Genotyping-by-sequencing provides the discriminating power to investigate the subspecies of Daucus carota (Apiaceae). |
| Q34520696 | Genus-level phylogeny of snakes reveals the origins of species richness in Sri Lanka. |
| Q104454515 | Higher-Level Phylogeny and Reclassification of Lampyridae (Coleoptera: Elateroidea) |
| Q28728486 | Highly incomplete taxa can rescue phylogenetic analyses from the negative impacts of limited taxon sampling |
| Q56997362 | Historical biogeography of a new antitropical clade of temperate freshwater fishes |
| Q30991088 | How Should Genes and Taxa be Sampled for Phylogenomic Analyses with Missing Data? An Empirical Study in Iguanian Lizards |
| Q56700488 | ITS phylogeny of Middle Asian geophilic Umbelliferae-Apioideae genera with comments on their morphology and utility of psbA-trnH sequences |
| Q41243559 | Identification of nuclear low-copy genes and their phylogenetic utility in rosids. |
| Q30559723 | Impact of missing data on phylogenies inferred from empirical phylogenomic data sets |
| Q40913324 | Impacts of Terraces on Phylogenetic Inference |
| Q39019250 | Implementing a cumulative supermatrix approach for a comprehensive phylogenetic study of the Teloschistales (Pezizomycotina, Ascomycota). |
| Q21284058 | Increased gene sampling strengthens support for higher-level groups within leaf-mining moths and relatives (Lepidoptera: Gracillariidae) |
| Q54530614 | Increased gene sampling yields robust support for higher-level clades within Bombycoidea (Lepidoptera) |
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| Q54677878 | Insect phylogenomics: new insights on the relationships of lower neopteran orders (Polyneoptera) |
| Q52738101 | Insect phylogenomics: results, problems and the impact of matrix composition. |
| Q40172520 | Integration of complete chloroplast genome sequences with small amplicon datasets improves phylogenetic resolution in Acacia. |
| Q36904221 | LS³: A Method for Improving Phylogenomic Inferences When Evolutionary Rates Are Heterogeneous among Taxa |
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| Q28706287 | Missing data and influential sites: choice of sites for phylogenetic analysis can be as important as taxon sampling and model choice |
| Q33857350 | Missing data in phylogenetic analysis: reconciling results from simulations and empirical data |
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| Q28934032 | Molecular systematics of teioid lizards (Teioidea/Gymnophthalmoidea: Squamata) based on the analysis of 48 loci under tree-alignment and similarity-alignment |
| Q26740127 | Multilocus inference of species trees and DNA barcoding |
| Q51148272 | Multilocus phylogenetic analysis of the first molecular data from the rare and monotypic Amarsipidae places the family within the Pelagia and highlights limitations of existing data sets in resolving pelagian interrelationships. |
| Q89720356 | Multilocus phylogeny and cryptic diversity of white-toothed shrews (Mammalia, Eulipotyphla, Crocidura) in China |
| Q34352674 | Multilocus phylogeny of the avian family Alaudidae (larks) reveals complex morphological evolution, non-monophyletic genera and hidden species diversity |
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| Q34385446 | New phylogenomic data support the monophyly of Lophophorata and an Ectoproct-Phoronid clade and indicate that Polyzoa and Kryptrochozoa are caused by systematic bias |
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| Q44459938 | Parallel tagged amplicon sequencing reveals major lineages and phylogenetic structure in the North American tiger salamander (Ambystoma tigrinum) species complex |
| Q51164805 | Phylodynamic applications in 21st century global infectious disease research. |
| Q44161169 | Phylogenetic analysis at deep timescales: unreliable gene trees, bypassed hidden support, and the coalescence/concatalescence conundrum |
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| Q28662139 | Phylogenetic position and subspecies divergence of the endangered New Zealand Dotterel (Charadrius obscurus) |
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| Q54534214 | Phylogenetic relationships of flesh flies in the subfamily Sarcophaginae based on three mtDNA fragments (Diptera: Sarcophagidae) |
| Q28647434 | Phylogenomic Analyses Indicate that Early Fungi Evolved Digesting Cell Walls of Algal Ancestors of Land Plants |
| Q36066323 | Phylogenomic analyses of large-scale nuclear genes provide new insights into the evolutionary relationships within the rosids |
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| Q36143716 | Phylogenomics of Lophotrochozoa with Consideration of Systematic Error. |
| Q89169838 | Phylogenomics resolves the deep phylogeny of seed plants and indicates partial convergent or homoplastic evolution between Gnetales and angiosperms |
| Q28750499 | Phylogenomics with incomplete taxon coverage: the limits to inference |
| Q33966732 | Phylogeny and temporal diversification of darters (Percidae: Etheostomatinae). |
| Q34048582 | Phylogeny of Celastraceae tribe Euonymeae inferred from morphological characters and nuclear and plastid genes. |
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| Q101632490 | Phylogeography of Middle American gophersnakes: mixed responses to biogeographical barriers across the Mexican Transition Zone |
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| Q34416122 | Platyzoan paraphyly based on phylogenomic data supports a noncoelomate ancestry of spiralia |
| Q54986973 | Practical considerations for plant phylogenomics. |
| Q57053111 | Pre-Pleistocene origin of an endangered habitat: links between vernal pools and aquaticOxalisin the Greater Cape Floristic Region of South Africa |
| Q31035127 | Prediction of missing sequences and branch lengths in phylogenomic data |
| Q28654446 | Prospects for building large timetrees using molecular data with incomplete gene coverage among species |
| Q44611790 | Quantification and relative severity of inflated branch-support values generated by alternative methods: an empirical example |
| Q28652860 | Quo vadis venomics? A roadmap to neglected venomous invertebrates |
| Q34069982 | Radical instability and spurious branch support by likelihood when applied to matrices with non-random distributions of missing data |
| Q33637375 | Range-wide phylogeographic structure of the vernal pool fairy shrimp (Branchinecta lynchi) |
| Q35467293 | Re-evaluating the phylogeny of Sipuncula through transcriptomics |
| Q38837676 | Recurrent breakdowns of mutualisms with ants in the neotropical ant-plant genus Cecropia (Urticaceae). |
| Q57276518 | Redescription of Szelepis Liu, 1981 (Placodermi, Arthrodira), from the Lower Devonian of China |
| Q34316204 | Relaxed phylogenetics and the palaeoptera problem: resolving deep ancestral splits in the insect phylogeny |
| Q24635078 | Reptilian-transcriptome v1.0, a glimpse in the brain transcriptome of five divergent Sauropsida lineages and the phylogenetic position of turtles |
| Q21092718 | Resolving difficult phylogenetic questions: why more sequences are not enough |
| Q90665157 | Resolving the rapid plant radiation of early diverging lineages in the tropical Zingiberales: Pushing the limits of genomic data |
| Q54576520 | Revision and phylogeny ofSyrphetodes(Coleoptera: Ulodidae): implications for biogeography, alpinization and conservation |
| Q39511514 | Sequence capture using RAD probes clarifies phylogenetic relationships and species boundaries in Primula sect. Auricula |
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| Q30842843 | Should genes with missing data be excluded from phylogenetic analyses? |
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| Q34119184 | Sparse supermatrices for phylogenetic inference: taxonomy, alignment, rogue taxa, and the phylogeny of living turtles |
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| Q28603676 | Spider phylogenomics: untangling the Spider Tree of Life |
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| Q98224875 | The Chloroplast Land Plant Phylogeny: Analyses Employing Better-Fitting Tree- and Site-Heterogeneous Composition Models |
| Q28606898 | The Gondwana Breakup and the History of the Atlantic and Indian Oceans Unveils Two New Clades for Early Neobatrachian Diversification |
| Q39593552 | The Identification of the Closest Living Relative(s) of Tetrapods: Phylogenomic Lessons for Resolving Short Ancient Internodes |
| Q31026927 | The Impact of Missing Data on Species Tree Estimation |
| Q39149590 | The changing face of the molecular evolutionary clock |
| Q33855238 | The devil in the details: interactions between the branch-length prior and likelihood model affect node support and branch lengths in the phylogeny of the Psoraceae |
| Q40107503 | The effects of subsampling gene trees on coalescent methods applied to ancient divergences |
| Q89576283 | The evolutionary history of the cellophane bee genus Colletes Latreille (Hymenoptera: Colletidae): Molecular phylogeny, biogeography and implications for a global infrageneric classification |
| Q29029370 | The impact of anchored phylogenomics and taxon sampling on phylogenetic inference in narrow-mouthed frogs (Anura, Microhylidae) |
| Q35653694 | The impact of taxon sampling on phylogenetic inference: a review of two decades of controversy |
| Q54521767 | The phylogeny and limits of Elateridae (Insecta, Coleoptera): is there a common tendency of click beetles to soft-bodiedness and neoteny? |
| Q28298259 | The phylogeny of advanced snakes (Colubroidea), with discovery of a new subfamily and comparison of support methods for likelihood trees |
| Q55007641 | The prevalence of terraced treescapes in analyses of phylogenetic data sets. |
| Q38389938 | The use of evolutionary approaches to understand single cell genomes |
| Q110444165 | Total evidence and sensitivity phylogenetic analyses of egg‐brooding frogs (Anura: Hemiphractidae) |
| Q28303530 | Toward a Tree-of-Life for the boas and pythons: multilocus species-level phylogeny with unprecedented taxon sampling |
| Q21284011 | Transitions between Andean and Amazonian centers of endemism in the radiation of some arboreal rodents |
| Q35139928 | Two mitochondrial genomes from the families Bethylidae and Mutillidae: independent rearrangement of protein-coding genes and higher-level phylogeny of the Hymenoptera. |
| Q46198301 | Ultraconserved elements anchor thousands of genetic markers spanning multiple evolutionary timescales |
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