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Malpighiales phylogenetics: Gaining ground on one of the most recalcitrant clades in the angiosperm tree of life

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Comparative Anatomy of the Young Stem, Node, and Leaf of Bonnetiaceae, Including Observations on a Foliar Endodermis

inferredcites →https://doi.org/10.1006/bojl.1998.0180openalex-snapshot

Gynoecium diversity and systematics of the paleoherbs

inferredcites →https://doi.org/10.1006/bojl.2000.0380openalex-snapshot

Angiosperm phylogeny inferred from 18S rDNA, rbcL, and atpB sequences

inferredcites →https://doi.org/10.1006/mpev.1998.0577openalex-snapshot

Phylogenetic Relationships of the Enigmatic Angiosperm Family Podostemaceae Inferred from 18S rDNA andrbcLSequence Data

inferredcites →https://doi.org/10.1007/978-3-540-32219-1openalex-snapshot

Flowering plants, Eudicots : Berberidopsidales, Buxales, Crossosomatales, Fabales p.p., Geraniales, Gunnerales, Myrtales p.p., Proteales, Saxifragales, Vitales, Zygophyllales, Clusiaceae Alliance, Passifloraceae Alliance, Dilleniaceae, Huaceae, Picramniaceae, Sabiaceae

inferredcites →https://doi.org/10.1007/978-3-540-32219-1_40openalex-snapshot

Podostemaceae

inferredcites →https://doi.org/10.1007/978-3-540-32219-1_8openalex-snapshot

Bonnetiaceae

inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot

Flowering plants, Eudicots : Malpighiales

inferredcites →https://doi.org/10.1007/978-3-662-07257-8_6openalex-snapshot

Celastraceae

inferredcites →https://doi.org/10.1007/bf00160257openalex-snapshot

Heterogeneity in the substitution process of amino acid sites of proteins coded for by mitochondrial DNA

inferredcites →https://doi.org/10.1007/bf00178250openalex-snapshot

High rates of nucleotide substitution in nuclear small-subunit (18S) rDNA from holoparasitic flowering plants

inferredcites →https://doi.org/10.1007/bf00983550openalex-snapshot

Comparative structure of ovules and seeds inRafflesiaceae

inferredcites →https://doi.org/10.1007/bf02668360openalex-snapshot

Amplification and sequencing of 16/18S rDNA from gel-purified total plant DNA

inferredcites →https://doi.org/10.1007/bf02858493openalex-snapshot

Index nominum familiarum plantarum vascularium

inferredcites →https://doi.org/10.1007/pl00013970openalex-snapshot

Ovules and Seeds in Subfamily Phyllanthoideae (Euphorbiaceae): Structure and Systematic Implications

inferredcites →https://doi.org/10.1007/s00239-004-2606-yopenalex-snapshot

Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron

inferredcites →https://doi.org/10.1007/s00239-004-5951-yopenalex-snapshot

Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron

inferredcites →https://doi.org/10.1007/s00438-004-1075-8openalex-snapshot

The complete nucleotide sequence and multipartite organization of the tobacco mitochondrial genome: comparative analysis of mitochondrial genomes in higher plants

inferredcites →https://doi.org/10.1007/s00606-006-0414-0openalex-snapshot

Female flowers and systematic position of Picrodendraceae (Euphorbiaceae s.l., Malpighiales)

inferredcites →https://doi.org/10.1007/s00606-006-0441-xopenalex-snapshot

The impact of extinct taxa on understanding the early evolution of Angiosperm clades: an example incorporating fossil reproductive structures of Saxifragales

inferredcites →https://doi.org/10.1007/s00606-006-0443-8openalex-snapshot

Floral structure and systematics in four orders of rosids, including a broad survey of floral mucilage cells

inferredcites →https://doi.org/10.1007/s00606-006-0444-7openalex-snapshot

First steps towards a floral structural characterization of the major rosid subclades

inferredcites →https://doi.org/10.1007/s00606-008-0099-7openalex-snapshot

Phylogeny of the eudicot order Malpighiales: analysis of a recalcitrant clade with sequences of the petD group II intron

inferredcites →https://doi.org/10.1007/s10265-002-0047-5openalex-snapshot

Ovules and seeds in Euphorbioideae (Euphorbiaceae): structure and systematic implications

inferredcites →https://doi.org/10.1007/s10265-003-0116-4openalex-snapshot

Ovules and seeds in Acalyphoideae (Euphorbiaceae): structure and systematic implications

inferredcites →https://doi.org/10.1007/s10265-006-0025-4openalex-snapshot

Phylogenetic analyses of Malpighiales using plastid and nuclear DNA sequences, with particular reference to the embryology of Euphorbiaceae sens. str.

inferredcites →https://doi.org/10.1007/s10265-007-0090-3openalex-snapshot

Molecular phylogenetic analysis of Euphorbiaceae sensu stricto based on plastid and nuclear DNA sequences and ovule and seed character evolution

inferredcites →https://doi.org/10.1007/s10265-008-0153-0openalex-snapshot

Molecular phylogenetic analysis of Violaceae (Malpighiales) based on plastid and nuclear DNA sequences

inferredcites →https://doi.org/10.1016/0034-6667(89)90014-6openalex-snapshot

New observations on the pollen of ctenolophon oliver (ctenolophonaceae), with remarks on the evolutionary history of the genus

inferredcites →https://doi.org/10.1016/j.cub.2008.08.046openalex-snapshot

Accelerated Rates of Floral Evolution at the Upper Size Limit for Flowers

inferredcites →https://doi.org/10.1016/j.cub.2008.10.011openalex-snapshot

Floral Evolution: Dramatic Size Change Was Recent and Rapid in the World's Largest Flowers

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The evolution of floral gigantism

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Sequencing and analysis of 14,842 expressed sequence tags of burma mangrove, Bruguiera gymnorrhiza

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Deciphering ancient rapid radiations

inferredcites →https://doi.org/10.1016/j.tree.2007.06.013openalex-snapshot

Estimating diversification rates from phylogenetic information

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Independence of alignment and tree search

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PRAP—computation of Bremer support for large data sets

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Should we be worried about long-branch attraction in real data sets? Investigations using metazoan 18S rDNA

inferredcites →https://doi.org/10.1016/j.ympev.2004.12.002openalex-snapshot

Molecular phylogenetics of Phyllanthaceae inferred from five genes (plastid atpB, matK, 3′ndhF, rbcL, and nuclear PHYC)

inferredcites →https://doi.org/10.1016/s0367-2530(17)32209-0openalex-snapshot

The Floral Nectaries of the Geraniales and their Systematic Implications.

inferredcites →https://doi.org/10.1023/a:1005860632601openalex-snapshot

Do nonasterid holoparasitic flowering plants have plastid genomes?

inferredcites →https://doi.org/10.1046/j.1095-8339.2002.00105.xopenalex-snapshot

Comparative floral structure and systematics in Oxalidales (Oxalidaceae, Connaraceae, Brunelliaceae, Cephalotaceae, Cunoniaceae, Elaeocarpaceae, Tremandraceae)

inferredcites →https://doi.org/10.1046/j.1095-8339.2003.t01-1-00158.xopenalex-snapshot

An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II

inferredcites →https://doi.org/10.1055/s-2001-12895openalex-snapshot

Infrafamilial Phylogeny of the Aquatic Angiosperm Podostemaceae Inferred from the Nucleotide Sequences of the matK Gene

inferredcites →https://doi.org/10.1055/s-2004-830462openalex-snapshot

ESTs from the Fibre‐Bearing Stem Tissues of Flax (Linum usitatissimum L.): Expression Analyses of Sequences Related to Cell Wall Development

inferredcites →https://doi.org/10.1071/sb03015openalex-snapshot

Use of nuclear genes for phylogeny reconstruction in plants

inferredcites →https://doi.org/10.1073/pnas.0305562101openalex-snapshot

Mitochondrial DNA sequences reveal the photosynthetic relatives of Rafflesia , the world's largest flower

inferredcites →https://doi.org/10.1073/pnas.042694899openalex-snapshot

Punctuated evolution of mitochondrial gene content: High and variable rates of mitochondrial gene loss and transfer to the nucleus during angiosperm evolution

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.0813376106openalex-snapshot

Rosid radiation and the rapid rise of angiosperm-dominated forests

inferredcites →https://doi.org/10.1073/pnas.212646199openalex-snapshot

Overcredibility of molecular phylogenies obtained by Bayesian phylogenetics

inferredcites →https://doi.org/10.1080/00173136509429138openalex-snapshot

Die Pollenmorphologie der Biovulaten Euphorbiaceae und ihre Bedeutung für die Taxonomie

inferredcites →https://doi.org/10.1080/106351501753462821openalex-snapshot

Phylogeny of Saxifragales (Angiosperms, Eudicots): Analysis of a Rapid, Ancient Radiation

inferredcites →https://doi.org/10.1080/10635150290069913openalex-snapshot

An Approximately Unbiased Test of Phylogenetic Tree Selection

inferredcites →https://doi.org/10.1080/10635150590945368openalex-snapshot

Hidden Likelihood Support in Genomic Data: Can Forty-Five Wrongs Make a Right?

inferredcites →https://doi.org/10.1080/10635150701294733openalex-snapshot

How Many Genes Should a Systematist Sample? Conflicting Insights from a Phylogenomic Matrix Characterized by Replicated Incongruence

inferredcites →https://doi.org/10.1080/10635150701397643openalex-snapshot

Detecting and Overcoming Systematic Errors in Genome-Scale Phylogenies

inferredcites →https://doi.org/10.1080/10635150801888871openalex-snapshot

Resolving an Ancient, Rapid Radiation in Saxifragales

inferredcites →https://doi.org/10.1086/329676openalex-snapshot

Anatomy of Dicotyledons

inferredcites →https://doi.org/10.1086/342521openalex-snapshot

Phylogeny of Clusiaceae Based onrbcL sequences

inferredcites →https://doi.org/10.1086/383337openalex-snapshot

High‐Latitude Tertiary Migrations of an Exclusively Tropical Clade: Evidence from Malpighiaceae

inferredcites →https://doi.org/10.1086/428296openalex-snapshot

Explosive Radiation of Malpighiales Supports a Mid‐Cretaceous Origin of Modern Tropical Rain Forests

inferredcites →https://doi.org/10.1086/431800openalex-snapshot

Phylogenetic Analyses of Basal Angiosperms Based on Nine Plastid, Mitochondrial, and Nuclear Genes

inferredcites →https://doi.org/10.1086/509586openalex-snapshot

Assessing Among‐Locus Variation in the Inference of Seed Plant Phylogeny

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Comparative Morphology and Molecular Systematics of African Podostemaceae‐Podostemoideae, with Emphasis on Dicraeanthus and Ledermanniella from Cameroon

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A 567‐Taxon Data Set for Angiosperms: The Challenges Posed by Bayesian Analyses of Large Data Sets

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Correlates of Diversification in the Plant Clade Dipsacales: Geographic Movement and Evolutionary Innovations

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The Endophytic System of Mediterranean Cytinus (Cytinaceae) Developing on Five Host Cistaceae Species

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MODELTEST: testing the model of DNA substitution.

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/17.8.754openalex-snapshot

MRBAYES: Bayesian inference of phylogenetic trees

inferredcites →https://doi.org/10.1093/bioinformatics/btg427openalex-snapshot

Parallel Metropolis coupled Markov chain Monte Carlo for Bayesian phylogenetic inference

inferredcites →https://doi.org/10.1093/genetics/142.3.1033openalex-snapshot

Synonymous Nucleotide Divergence: What Is “Saturation”?

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/msh014openalex-snapshot

How Meaningful Are Bayesian Support Values?

inferredcites →https://doi.org/10.1093/molbev/msi212openalex-snapshot

Maximum Likelihood Outperforms Maximum Parsimony Even When Evolutionary Rates Are Heterotachous

inferredcites →https://doi.org/10.1093/molbev/msj047openalex-snapshot

Origin and Evolution of the Chloroplast trnK (matK) Intron: A Model for Evolution of Group II Intron RNA Structures

inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025811openalex-snapshot

Bayesian phylogenetic inference using DNA sequences: a Markov Chain Monte Carlo Method

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025912openalex-snapshot

Evidence that the phytochrome gene family in black cottonwood has one PHYA locus and two PHYB loci but lacks members of the PHYC/F and PHYE subfamilies

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040082openalex-snapshot

Maximum-likelihood estimation of phylogeny from DNA sequences when substitution rates differ over sites.

inferredcites →https://doi.org/10.1093/sysbio/22.3.240openalex-snapshot

Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters

inferredcites →https://doi.org/10.1093/sysbio/38.1.7openalex-snapshot

A Concern for Evidence and a Phylogenetic Hypothesis of Relationships among Epicrates (Boidae, Serpentes)

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Combining Data in Phylogenetic Systematics: An Empirical Approach Using Three Molecular Data Sets in the Solanaceae

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Phylogenetics of Flowering Plants Based on Combined Analysis of Plastid atpB and rbcL Gene Sequences

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Evolution of the angiosperms: calibrating the family tree

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Gene transfer from a parasitic flowering plant to a fern

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A new look at the statistical model identification

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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV

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ABSOLUTE DIVERSIFICATION RATES IN ANGIOSPERM CLADES

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Molecular and morphological data reveal cryptic taxonomic diversity in the terrestrial slug complex Arion subfuscus/fuscus (Mollusca, Pulmonata, Arionidae) in continental north-west Europe

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Segregate families from the Euphorbiaceae

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Laticifers in Euphorbiaceae-a conspectus

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Comparative floral structure and systematics in Celastrales (Celastraceae, Parnassiaceae, Lepidobotryaceae)

inferredcites →https://doi.org/10.1111/j.1095-8339.2008.00803.xopenalex-snapshot

Comparative floral structure and systematics in Chrysobalanaceae s.l. (Chrysobalanaceae, Dichapetalaceae, Euphroniaceae, Trigoniaceae; Malpighiales)

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POLYMORPHIC TAXA, MISSING VALUES AND CLADISTIC ANALYSIS

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The Parsimony Ratchet, a New Method for Rapid Parsimony Analysis

inferredcites →https://doi.org/10.1111/j.1096-0031.2005.00059.xopenalex-snapshot

A review of long‐branch attraction

inferredcites →https://doi.org/10.1111/j.1365-2699.2007.01749.xopenalex-snapshot

Molecular dating of the ‘Gondwanan’ plant family Proteaceae is only partially congruent with the timing of the break‐up of Gondwana

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POLLEN MORPHOLOGY OF THE EUPHORBIACEAE WITH SPECIAL REFERENCE TO TAXONOMY

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CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://doi.org/10.1111/j.1931-0846.2007.tb00409.xopenalex-snapshot

The Fall Line: a Physiographic‐Forest Vegetation Boundary

inferredcites →https://doi.org/10.1126/science.1100671openalex-snapshot

Host-to-Parasite Gene Transfer in Flowering Plants: Phylogenetic Evidence from Malpighiales

inferredcites →https://doi.org/10.1126/science.1128691openalex-snapshot

The Genome of Black Cottonwood, Populus trichocarpa (Torr. & Gray)

inferredcites →https://doi.org/10.1126/science.1135260openalex-snapshot

Floral Gigantism in Rafflesiaceae

inferredcites →https://doi.org/10.1126/science.286.5441.947openalex-snapshot

The Root of Angiosperm Phylogeny Inferred from Duplicate Phytochrome Genes

inferredcites →https://doi.org/10.1146/annurev.ento.53.103106.093304openalex-snapshot

Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis

inferredcites →https://doi.org/10.1163/22941932-90000246openalex-snapshot

WOOD ANATOMY OF ACALYPHOIDEAE (EUPHORBIACEAE)

inferredcites →https://doi.org/10.1163/22941932-90001144openalex-snapshot

Wood Anatomy of Bhesa Sinica (Celastraceae)

inferredcites →https://doi.org/10.1186/1471-2148-4-40openalex-snapshot

Phylogenetic inference in Rafflesiales: the influence of rate heterogeneity and horizontal gene transfer

inferredcites →https://doi.org/10.1186/1471-2148-7-217openalex-snapshot

Mitochondrial matR sequences help to resolve deep phylogenetic relationships in rosids

inferredcites →https://doi.org/10.1186/1471-2148-7-248openalex-snapshot

Mitochondrial DNA suggests at least 11 origins of parasitism in angiosperms and reveals genomic chimerism in parasitic plants

inferredcites →https://doi.org/10.1371/journal.pbio.0030014openalex-snapshot

Relaxed Molecular Clock Provides Evidence for Long-Distance Dispersal of Nothofagus (Southern Beech)

inferredcites →https://doi.org/10.1600/036364405775097833openalex-snapshot

A Reinterpretation of the Staminate Flowers of Haptanthus

inferredcites →https://doi.org/10.1600/036364406775971778openalex-snapshot

Phylogeny and Delimitation of the Celastrales Inferred from Nuclear and Plastid Genes

inferredcites →https://doi.org/10.1614/0043-1745(2001)049[0590:rsocai]2.0.co;2openalex-snapshot

Random sequencing of cDNAs and identification of mRNAs

inferredcites →https://doi.org/10.1663/0006-8101(2005)071[0001:infpv]2.0.co;2openalex-snapshot

Index Nominum Familiarum Plantarum Vascularium

inferredcites →https://doi.org/10.2307/1221109openalex-snapshot

SIEVE‐ELEMENT PLASTIDS, PHLOEM PROTEIN, AND EVOLUTION OF FLOWERING PLANTS: III. MAGNOLIIDAE

inferredcites →https://doi.org/10.2307/1222465openalex-snapshot

An Integrated System of Classification of Flowering Plants

inferredcites →https://doi.org/10.2307/1222750openalex-snapshot

The Families and Genera of Vascular Plants. Vol. 2. Flowering Plants. Dicotyledons: Magnoliid, Hamamelid and Caryophyllid Families

inferredcites →https://doi.org/10.2307/1224719openalex-snapshot

Biogeography of Nothofagus supports the sequence of Gondwana break‐up

inferredcites →https://doi.org/10.2307/1292633openalex-snapshot

The Families of Flowering Plants

inferredcites →https://doi.org/10.2307/2399291openalex-snapshot

Sieve-Element Plastids and Systematic Relationships of Rhizophoraceae, Anisophylleaceae, and Allied Groups

inferredcites →https://doi.org/10.2307/2399846openalex-snapshot

Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL

inferredcites →https://doi.org/10.2307/2399877openalex-snapshot

The Utility of atpB Gene Sequences in Resolving Phylogenetic Relationships: Comparison with rbcL and 18S Ribosomal DNA Sequences in the Lardizabalaceae

inferredcites →https://doi.org/10.2307/2399909openalex-snapshot

Synopsis of the Genera and Suprageneric Taxa of Euphorbiaceae

inferredcites →https://doi.org/10.2307/2399952openalex-snapshot

Angiosperm Phylogeny Inferred from 18S Ribosomal DNA Sequences

inferredcites →https://doi.org/10.2307/2412304openalex-snapshot

Maximum Likelihood and Minimum-Steps Methods for Estimating Evolutionary Trees from Data on Discrete Characters

inferredcites →https://doi.org/10.2307/2419047openalex-snapshot

Haptanthus, a New Dicotyledonous Genus from Honduras

inferredcites →https://doi.org/10.2307/2419372openalex-snapshot

The Systematic Position of Euphronia, with Comments on the Position of Balanops: An Analysis Based on rbcL Sequence Data

inferredcites →https://doi.org/10.2307/2419571openalex-snapshot

Systematics of Plumbaginaceae Based upon Cladistic Analysis of rbcL Sequence Data

inferredcites →https://doi.org/10.2307/2421840openalex-snapshot

Anatomy of the Dicotyledons.

inferredcites →https://doi.org/10.2307/2446345openalex-snapshot

Fossil Clusiaceae from the Late Cretaceous (Turonian) of New Jersey and implications regarding the history of bee pollination

inferredcites →https://doi.org/10.2307/25065731openalex-snapshot

A linear sequence of Angiosperm Phylogeny Group II families

inferredcites →https://doi.org/10.2307/25065736openalex-snapshot

Monophyly and relationships of the enigmatic family Peridiscaceae

inferredcites →https://doi.org/10.2307/2656599openalex-snapshot

Systematic affinities of Rhizophoraceae and Anisophylleaceae, and intergeneric relationships within Rhizophoraceae, based on chloroplast DNA, nuclear ribosomal DNA, and morphology

inferredcites →https://doi.org/10.2307/2666142openalex-snapshot

The Evolution of Non-Coding Chloroplast DNA and Its Application in Plant Systematics

inferredcites →https://doi.org/10.2307/2666152openalex-snapshot

Relationships and Morphological Character Change among Genera of Celastraceae Sensu Lato (Including Hippocrateaceae)

inferredcites →https://doi.org/10.2307/2992003openalex-snapshot

A Combined Cladistic Analysis of Angiosperms Using rbcL and Non-Molecular Data Sets

inferredcites →https://doi.org/10.2307/2992015openalex-snapshot

An Ordinal Classification for the Families of Flowering Plants

inferredcites →https://doi.org/10.2307/2992093openalex-snapshot

Systematic Anatomy of Euphorbiaceae Subfamily Oldfieldioideae I. Overview

inferredcites →https://doi.org/10.2307/2992094openalex-snapshot

Phylogenetic Implications of Pollen Ultrastructure in the Oldfieldioideae (Euphorbiaceae)

inferredcites →https://doi.org/10.2307/2992104openalex-snapshot

Phytochemistry and Systematics of the Euphorbiaceae

inferredcites →https://doi.org/10.2307/2992432openalex-snapshot

A Concern for Evidence and a Phylogenetic Hypothesis of Relationships Among Epicrates (Boidae, Serpentes)

inferredcites →https://doi.org/10.2307/2997241openalex-snapshot

Floral Morphology and Anatomy of Bonnetiaceae

inferredcites →https://doi.org/10.2307/3558360openalex-snapshot

Phylogeny of Malpighiaceae: evidence from chloroplast ndhF and trnl‐F nucleotide sequences

inferredcites →https://doi.org/10.2307/3558361openalex-snapshot

Molecular systematics of Malpighiaceae: evidence from plastid rbcL and matK sequences

inferredcites →https://doi.org/10.2307/3647375openalex-snapshot

Rafflesia of the World

inferredcites →https://doi.org/10.2307/4109266openalex-snapshot

Plants of the Cambridge Expedition, 1947-1948: II. A New Order of Flowering Plants from the British Cameroons

inferredcites →https://doi.org/10.2307/4109268openalex-snapshot

Medusandra Richardsiana Brenan. Anatomy of the Leaf, Stem and Wood

inferredcites →https://doi.org/10.2307/4110825openalex-snapshot

When in Doubt, Put It in Flacourtiaceae: A Molecular Phylogenetic Analysis Based on Plastid rbcL DNA Sequences

inferredcites →https://doi.org/10.2307/4115596openalex-snapshot

A Note on the Taxonomic Position of the Genus Cyrillopsis Kuhlmann

inferredcites →https://doi.org/10.2307/4115630openalex-snapshot

Contributions to the Flora of Tropical America: LXIX. A New Genus of Peridiscaceae

inferredcites →https://doi.org/10.2307/4115632openalex-snapshot

Notes on the Systematic Anatomy of Whittonia and Peridiscus

inferredcites →https://doi.org/10.2307/4115644openalex-snapshot

Phylogeny of the Eudicots: A Nearly Complete Familial Analysis Based on rbcL Gene Sequences

inferredcites →https://doi.org/10.2307/4117362openalex-snapshot

Soyauxia, a Second Genus of Medusandraceae

inferredcites →https://doi.org/10.2307/4117844openalex-snapshot

Taxonomic Affinities of Medusagyne oppositifolia (Medusagynaceae)

inferredcites →https://doi.org/10.3732/ajb.89.10.1651openalex-snapshot

Group II introns as phylogenetic tools: structure, function, and evolutionary constraints

inferredcites →https://doi.org/10.3732/ajb.90.12.1758openalex-snapshot

Angiosperm phylogeny based on <011>mat K sequence information

inferredcites →https://doi.org/10.3732/ajb.90.3.461openalex-snapshot

Gunnerales are sister to other core eudicots: implications for the evolution of pentamery

inferredcites →https://doi.org/10.3732/ajb.91.11.1882openalex-snapshot

Molecular phylogenetic analysis of Phyllanthaceae (Phyllanthoideae pro parte, Euphorbiaceae sensu lato) using plastid RBCL DNA sequences

inferredcites →https://doi.org/10.3732/ajb.91.2.262openalex-snapshot

Elatinaceae are sister to Malpighiaceae; Peridiscaceae belong to Saxifragales

inferredcites →https://doi.org/10.3732/ajb.92.1.132openalex-snapshot

Molecular phylogenetics of Phyllanthaceae: evidence from plastid MATK and nuclear PHYC sequences

inferredcites →https://doi.org/10.3732/ajb.92.8.1397openalex-snapshot

Molecular phylogenetic analysis of uniovulate Euphorbiaceae (Euphorbiaceae sensu stricto) using plastid RBCL and TRNL‐F DNA sequences

inferredcites →https://doi.org/10.3732/ajb.94.8.1402openalex-snapshot

Expression of matK: functional and evolutionary implications

inferredcites →https://doi.org/10.3732/ajb.94.9.1439openalex-snapshot

Structural attributes of the hypogeous holoparasite Hydnora triceps Drège & Meyer (Hydnoraceae)

inferredcites →https://doi.org/10.7208/chicago/9780226441757.001.0001openalex-snapshot

Phylogeny and Evolution of the Angiosperms

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.166.3.2zenodo-depositor-declared

Acalypha subgenus Linostachys (Euphorbiaceae, Acalyphoideae): a global review

inferred← citeshttps://doi.org/10.11646/phytotaxa.181.4.1zenodo-depositor-declared

Synopsis of Euphorbia (Euphorbiaceae) in the state of São Paulo, Brazil

inferred← citeshttps://doi.org/10.11646/phytotaxa.221.3.6zenodo-depositor-declared

Kielmeyera ferruginosa (Calophyllaceae), a new species from the Atlantic Forest, southern Bahia, Brazil

inferred← citeshttps://doi.org/10.11646/phytotaxa.260.2.5zenodo-depositor-declared

Systematics of Irvingiaceae and Ixonanthaceae (Malpighiales): phylogenetic analysis based on three plastid DNA loci

inferred← citeshttps://doi.org/10.11646/phytotaxa.313.3.1zenodo-depositor-declared

A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence

inferred← citeshttps://doi.org/10.11646/phytotaxa.321.1.1zenodo-depositor-declared

The tribe Crotoneae (Euphorbiaceae, Crotonoideae) in the Chapada dos Veadeiros, Goiás, Brazil

inferred← citeshttps://doi.org/10.11646/phytotaxa.329.1.1zenodo-depositor-declared

Clusiaceae s.l. (Calophyllaceae, Clusiaceae s.s. and Hypericaceae) in the Viruá National Park, Roraima, Brazil

inferred← citeshttps://doi.org/10.11646/phytotaxa.349.2.4zenodo-depositor-declared

Rediscovery of Croton hadrianii (Euphorbiaceae), a well distributed but long-forgotten species in Brazilian Amazon

inferred← citeshttps://doi.org/10.11646/phytotaxa.539.3.1zenodo-depositor-declared

A new species of Acalypha (Euphorbiaceae) from Guerrero, Mexico

inferred← citeshttps://doi.org/10.11646/phytotaxa.649.2.5zenodo-depositor-declared

New species of Argythamnia (Euphorbiaceae) restricted to Seasonal Forest of Brazil, with morphological and phylogenetic support

inferred← citeshttps://doi.org/10.24823/ejb.2025.2058zenodo-depositor-declared

THE PUTRANJIVACEAE OF THE WORLD: A CROSS-REFERENCED CHECKLIST OF THE GENERA AND SPECIES

inferred← citeshttps://doi.org/10.1002/ajb2.1048openalex-snapshot

Plastid phylogenomic analysis of green plants: A billion years of evolutionary history

inferred← citeshttps://doi.org/10.1002/ajb2.1050openalex-snapshot

Character evolution and missing (morphological) data across Asteridae

inferred← citeshttps://doi.org/10.1002/ajb2.1350openalex-snapshot

First report of laticifers in lianas of Malpighiaceae and their phylogenetic implications

inferred← citeshttps://doi.org/10.1002/ajb2.16025openalex-snapshot

Incomplete lineage sorting and reticulate evolution mask species relationships in Brunelliaceae, an Andean family with rapid, recent diversification

inferred← citeshttps://doi.org/10.1002/ajb2.70201openalex-snapshot

The danger zone: The joint trap of incomplete lineage sorting and long‐branch attraction in resolving the Gondwanan origin of Rafflesiaceae and Apodanthaceae

inferred← citeshttps://doi.org/10.1002/ece3.4261openalex-snapshot

Plastome phylogeny and lineage diversification of Salicaceae with focus on poplars and willows

inferred← citeshttps://doi.org/10.1002/njb.04923openalex-snapshot

Terniopsis chanthaburiensis (Podostemaceae), a new record for China and its complete plastid genome

inferred← citeshttps://doi.org/10.1002/tax.12210openalex-snapshot

A lineage‐based infrageneric classification of Turnera (Turneraceae)

inferred← citeshttps://doi.org/10.1002/tax.13388openalex-snapshot

A nomenclatural review of Acalypha (Euphorbiaceae) of mainland Africa

inferred← citeshttps://doi.org/10.1002/tax.595014openalex-snapshot

Cladistic analysis of morphological characters in Hypericum (Hypericaceae)

inferred← citeshttps://doi.org/10.1002/tax.603013openalex-snapshot

A revised infrageneric classification and molecular phylogeny of New World Croton (Euphorbiaceae)

inferred← citeshttps://doi.org/10.1002/tax.612003openalex-snapshot

Phylogeny of the Turneraceae clade (Passifloraceae s.l.): Trans–Atlantic disjunctions and two new genera in Africa

inferred← citeshttps://doi.org/10.1007/7397_2016_24openalex-snapshot

Gourds: Bitter, Bottle, Wax, Snake, Sponge and Ridge

inferred← citeshttps://doi.org/10.1007/978-1-4419-5947-8_1openalex-snapshot

Phylogenetic Relationships of Saccharinae and Sorghinae

inferred← citeshttps://doi.org/10.1007/978-1-62703-221-6_5openalex-snapshot

Gene Expression Analysis of Aquatic Angiosperms Podostemaceae to Gain Insight into the Evolution of Their Enigmatic Morphology

inferred← citeshttps://doi.org/10.1007/978-3-030-82359-7_3openalex-snapshot

Relationships and Phylogeny

inferred← citeshttps://doi.org/10.1007/978-3-030-85239-9_101-1openalex-snapshot

Phyllanthaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-85239-9_24-1openalex-snapshot

Clusiaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-85239-9_58-1openalex-snapshot

Euphorbiaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-85239-9_58-2openalex-snapshot

Euphorbiaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-85239-9_99-1openalex-snapshot

Passifloraceae

inferred← citeshttps://doi.org/10.1007/978-3-030-93492-7_101openalex-snapshot

Phyllanthaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-93492-7_24openalex-snapshot

Clusiaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-93492-7_58openalex-snapshot

Euphorbiaceae

inferred← citeshttps://doi.org/10.1007/978-3-030-93492-7_99openalex-snapshot

Passifloraceae

inferred← citeshttps://doi.org/10.1007/978-3-642-38146-1_1openalex-snapshot

Introduction: The Parasitic Syndrome in Higher Plants

inferred← citeshttps://doi.org/10.1007/978-3-642-39417-1_1openalex-snapshot

Introduction to Malpighiales

inferred← citeshttps://doi.org/10.1007/978-3-642-39417-1_10openalex-snapshot

Euphorbiaceae

inferred← citeshttps://doi.org/10.1007/978-3-7091-1160-4_1openalex-snapshot

Angiosperm Phylogeny: A Framework for Studies of Genome Evolution

inferred← citeshttps://doi.org/10.1007/s00210-024-03350-xopenalex-snapshot

Properties and medical applications of the Euphorbiaceae family and their bioproducts: a patent review

inferred← citeshttps://doi.org/10.1007/s00299-017-2231-zopenalex-snapshot

The Linum usitatissimum L. plastome reveals atypical structural evolution, new editing sites, and the phylogenetic position of Linaceae within Malpighiales

inferred← citeshttps://doi.org/10.1007/s00425-020-03402-5openalex-snapshot

Rafflesia patma Blume flower organs: histology of the epidermis and vascular structures, and a search for stomata

inferred← citeshttps://doi.org/10.1007/s00425-022-04026-7openalex-snapshot

The first high-quality chromosome-level genome assembly of Phyllanthaceae (Phyllanthus cochinchinensis) provides insights into flavonoid biosynthesis

inferred← citeshttps://doi.org/10.1007/s00606-009-0214-4openalex-snapshot

How to get off the mismatch at the generic rank in African Podostemaceae?

inferred← citeshttps://doi.org/10.1007/s00606-010-0276-3openalex-snapshot

Placement of Kuhlmanniodendron Fiaschi & Groppo in Lindackerieae (Achariaceae, Malpighiales) confirmed by analyses of rbcL sequences, with notes on pollen morphology and wood anatomy

inferred← citeshttps://doi.org/10.1007/s00606-010-0356-4openalex-snapshot

Floral structure and palynology of Podostemum weddellianum (Podostemaceae: Malpighiales)

inferred← citeshttps://doi.org/10.1007/s00606-010-0388-9openalex-snapshot

Morphology, development and homologies of the perianth and floral nectaries in Croton and Astraea (Euphorbiaceae-Malpighiales)

inferred← citeshttps://doi.org/10.1007/s00606-011-0576-2openalex-snapshot

Progress and problems in the assessment of flower morphology in higher-level systematics

inferred← citeshttps://doi.org/10.1007/s00606-012-0629-1openalex-snapshot

Floral development of Phyllanthus chekiangensis (Phyllanthaceae), with special reference to androecium and gynoecium

inferred← citeshttps://doi.org/10.1007/s00606-013-0918-3openalex-snapshot

Comparative fruit development in some Euphorbiaceae and Phyllanthaceae

inferred← citeshttps://doi.org/10.1007/s00606-013-0977-5openalex-snapshot

Utility of low-copy nuclear markers in phylogenetic reconstruction of Hypericum L. (Hypericaceae)

inferred← citeshttps://doi.org/10.1007/s00606-014-1037-5openalex-snapshot

Foliar anatomy of neotropical Salicaceae: potentially useful characters for taxonomy

inferred← citeshttps://doi.org/10.1007/s00606-014-1191-9openalex-snapshot

Phenotypic differences are not explained by pre-zygotic reproductive barriers in sympatric varieties of the Humiria balsamifera complex (Humiriaceae)

inferred← citeshttps://doi.org/10.1007/s00606-016-1376-5openalex-snapshot

Evidence for diversification of Calophyllum L. (Calophyllaceae) in the Neogene Siwalik forests of eastern Himalaya

inferred← citeshttps://doi.org/10.1007/s00606-017-1453-4openalex-snapshot

Synopsis of Acalypha (Euphorbiaceae) of West Tropical Africa, including Cameroon, Chad, Equatorial Guinea, Gabon, and São Tomé and Príncipe

inferred← citeshttps://doi.org/10.1007/s00606-020-01711-6openalex-snapshot

Epidermal crystals in Acalypha (Euphorbiaceae, Acalyphoideae) as a new taxonomic trait of the genus

inferred← citeshttps://doi.org/10.1007/s00606-023-01872-0openalex-snapshot

Floral anatomy points to autogamy as a possible evolutionary path in Elatinaceae (Malpighiales)

inferred← citeshttps://doi.org/10.1007/s10265-010-0393-7openalex-snapshot

Embryology of the Irvingiaceae, a family with uncertain relationships among the Malpighiales

inferred← citeshttps://doi.org/10.1007/s10265-011-0472-4openalex-snapshot

Molecular phylogenetic analysis of Passifloraceae sensu lato (Malpighiales) based on plastid and nuclear DNA sequences

inferred← citeshttps://doi.org/10.1007/s10265-016-0801-8openalex-snapshot

Multidisciplinary studies of the diversity and evolution in river-weeds

inferred← citeshttps://doi.org/10.1007/s10265-017-0916-6openalex-snapshot

Embryology of Pera (Peraceae, Malpighiales): systematics and evolutionary implications

inferred← citeshttps://doi.org/10.1007/s10265-019-01113-xopenalex-snapshot

Expression pattern of CUC3 ortholog in Zeylanidium tailichenoides (Podostemaceae) infers organization of a unique distichous shoot in Podostemoideae

inferred← citeshttps://doi.org/10.1007/s10682-014-9742-7openalex-snapshot

The function of ant repellence by flowers: testing the “nectar protection” and “pollinator protection” hypotheses

inferred← citeshttps://doi.org/10.1007/s11101-018-9594-9openalex-snapshot

Mesua sp.: chemical aspects and pharmacological relevance of prenylated polyphenols

inferred← citeshttps://doi.org/10.1007/s11105-013-0568-1openalex-snapshot

Outlier Loci and Selection Signatures of Simple Sequence Repeats (SSRs) in Flax (Linum usitatissimum L.)

inferred← citeshttps://doi.org/10.1007/s11258-013-0185-yopenalex-snapshot

Phylogenetic and functional relationships in pastures and meadows from the North Adriatic Karst

inferred← citeshttps://doi.org/10.1007/s11284-017-1542-4openalex-snapshot

Nickel hyperaccumulation in Antidesma montis ‐ silam : from herbarium discovery to collection in the native habitat

inferred← citeshttps://doi.org/10.1007/s11284-018-1563-7openalex-snapshot

Foliar elemental profiles in the ultramafic flora of Kinabalu Park (Sabah, Malaysia)

inferred← citeshttps://doi.org/10.1007/s12224-020-09381-5openalex-snapshot

Chemosystematic implications based on metabolic profiling of the genus Byrsonima (Malpighiaceae)

inferred← citeshttps://doi.org/10.1007/s12228-012-9246-0openalex-snapshot

Two new species of Acalypha (Euphorbiaceae) from Bolivia

inferred← citeshttps://doi.org/10.1007/s12228-021-09675-8openalex-snapshot

A taxonomic revision of Ophiobotrys, Osmelia, and Pseudosmelia (Samydaceae/Salicaceae s.l.)

inferred← citeshttps://doi.org/10.1007/s12229-012-9106-3openalex-snapshot

The Immense Diversity of Floral Monosymmetry and Asymmetry Across Angiosperms

inferred← citeshttps://doi.org/10.1007/s12229-014-9136-0openalex-snapshot

The Bahamian Flora: Plant Exploration, Living Collections, and DNA – A Journey Started in 1963

inferred← citeshttps://doi.org/10.1007/s12229-020-09233-zopenalex-snapshot

Caryocaraceae Voigt (Malpighiales): a Synthesis Based on Science Mapping and Systematic Review

inferred← citeshttps://doi.org/10.1007/s13237-015-0146-zopenalex-snapshot

Micro-propagation of Hypericum gaitii Haines, an endangered medicinal plants : assessment of genetic fidelity

inferred← citeshttps://doi.org/10.1007/s40415-019-00543-0openalex-snapshot

Floral development in Hura crepitans (Euphorbiaceae): a bat-pollinated species with multicarpellate gynoecium

inferred← citeshttps://doi.org/10.1007/s40415-020-00657-wopenalex-snapshot

Genetic diversity and population structure of Croton urucurana Baill. (Euphorbiaceae) in Central Brazil by ISSR markers

inferred← citeshttps://doi.org/10.1007/s42535-025-01207-zopenalex-snapshot

Phytochemical composition and pharmaceutical activities of leaf essential oil and extracts of Hypericum gaitii Haines: a threatened medicinal plant of India

inferred← citeshttps://doi.org/10.1016/b978-0-12-374380-0.50008-7openalex-snapshot

Diversity and Classification of Flowering Plants: Eudicots

inferred← citeshttps://doi.org/10.1016/b978-0-12-812628-8.50008-0openalex-snapshot

Diversity and Classification of Flowering Plants: Eudicots

inferred← citeshttps://doi.org/10.1016/j.aquabot.2015.08.003openalex-snapshot

Historical biogeography of river-weeds (Podostemaceae)

inferred← citeshttps://doi.org/10.1016/j.aquabot.2020.103255openalex-snapshot

Culture of river-weed Terniopsis chanthaburiensis (Podostemaceae)

inferred← citeshttps://doi.org/10.1016/j.biocontrol.2010.11.014openalex-snapshot

The host range and impact of Bikasha collaris (Coleoptera: Chrysomelidae), a promising candidate agent for biological control of Chinese tallow, Triadica sebifera (Euphorbiaceae) in the United States

inferred← citeshttps://doi.org/10.1016/j.bse.2020.104218openalex-snapshot

Polyprenylated benzophenone derivatives from Clusia burle-marxii and their chemotaxonomic significance

inferred← citeshttps://doi.org/10.1016/j.bse.2021.104293openalex-snapshot

Chemical constituents isolated from Clusia criuva subsp. Criuva and their chemophenetics significance

inferred← citeshttps://doi.org/10.1016/j.cub.2008.10.011openalex-snapshot

Floral Evolution: Dramatic Size Change Was Recent and Rapid in the World's Largest Flowers

inferred← citeshttps://doi.org/10.1016/j.eujim.2018.10.011openalex-snapshot

Antibacterial activity of terpenoids isolated from Cnidoscolus quercifolius Pohl (Euphorbiaceae), a Brazilian medicinal plant from Caatinga biome

inferred← citeshttps://doi.org/10.1016/j.flora.2011.07.004openalex-snapshot

Phylogeny, traits, environment, and space in cerrado plant communities at Emas National Park (Brazil)

inferred← citeshttps://doi.org/10.1016/j.flora.2018.02.004openalex-snapshot

Ontogeny, structure and occurrence of interxylary cambia in Malpighiaceae

inferred← citeshttps://doi.org/10.1016/j.flora.2025.152858openalex-snapshot

Comparative leaf anatomy of Brazilian Manihot species (Euphorbiaceae): diversity, systematic value and ecological significance

inferred← citeshttps://doi.org/10.1016/j.flora.2026.152971openalex-snapshot

Endopachychalaza or vascularized inner integument? New data on the comparative anatomy and a review of Euphorbiaceae ovule vasculature

inferred← citeshttps://doi.org/10.1016/j.gexplo.2019.03.013openalex-snapshot

Herbarium X-ray fluorescence screening for nickel, cobalt and manganese hyperaccumulator plants in the flora of Sabah (Malaysia, Borneo Island)

inferred← citeshttps://doi.org/10.1016/j.phymed.2017.08.017openalex-snapshot

Phytochemical and pharmacological aspects of Cnidoscolus Pohl species: A systematic review

inferred← citeshttps://doi.org/10.1016/j.ppees.2011.11.004openalex-snapshot

The influence of fire on phylogenetic and functional structure of woody savannas: Moving from species to individuals

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2010.10.002openalex-snapshot

Euphorbiaceae: Acalyphoideae fossils from early Miocene New Zealand: Mallotus–Macaranga leaves, fruits, and inflorescence with in situ Nyssapollenites endobalteus pollen

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2012.03.016openalex-snapshot

A diverse charcoalified assemblage of Cretaceous (Santonian) angiosperm woods from Upatoi Creek, Georgia, USA. Part 1: Wood types with scalariform perforation plates

inferred← citeshttps://doi.org/10.1016/j.revpalbo.2015.12.007openalex-snapshot

Malloranga dentata (Euphorbiaceae: Acalyphoideae): A new fossil species from the Miocene of New Zealand

inferred← citeshttps://doi.org/10.1016/j.ympev.2010.08.005openalex-snapshot

Elucidating the evolutionary history of the Southeast Asian, holoparasitic, giant-flowered Rafflesiaceae: Pliocene vicariance, morphological convergence and character displacement

inferred← citeshttps://doi.org/10.1016/j.ympev.2011.12.022openalex-snapshot

Phylogenetics and the evolution of major structural characters in the giant genus Euphorbia L. (Euphorbiaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.08.022openalex-snapshot

Molecular phylogenetics and morphological evolution of St. John’s wort (Hypericum; Hypericaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2012.09.029openalex-snapshot

Application of the phylogenetic informativeness method to chloroplast markers: A test case of closely related species in tribe Hydrangeeae (Hydrangeaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2013.02.007openalex-snapshot

Bayesian inference of phylogeny, morphology and range evolution reveals a complex evolutionary history in St. John’s wort (Hypericum)

inferred← citeshttps://doi.org/10.1016/j.ympev.2014.05.018openalex-snapshot

Phylogenetics, ancestral state reconstruction, and a new infrafamilial classification of the pantropical Ochnaceae (Medusagynaceae, Ochnaceae s.str., Quiinaceae) based on five DNA regions

inferred← citeshttps://doi.org/10.1016/j.ympev.2014.11.011openalex-snapshot

Phylogeny, divergence times, and historical biogeography of the angiosperm family Saxifragaceae

inferred← citeshttps://doi.org/10.1016/j.ympev.2015.09.013openalex-snapshot

Biogeography of the Malagasy Celastraceae: Multiple independent origins followed by widespread dispersal of genera from Madagascar

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.2016.02.021openalex-snapshot

Biogeography and diversification of Brassicales: A 103 million year tale

inferred← citeshttps://doi.org/10.1016/j.ympev.2017.10.025openalex-snapshot

Why are there so many sedges? Sumatroscirpeae, a missing piece in the evolutionary puzzle of the giant genus Carex (Cyperaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.01.014openalex-snapshot

Phylogeny, historical biogeography, and diversification of angiosperm order Ericales suggest ancient Neotropical and East Asian connections

inferred← citeshttps://doi.org/10.1016/j.ympev.2018.01.023openalex-snapshot

Combining high-throughput sequencing and targeted loci data to infer the phylogeny of the “Adenocalymma-Neojobertia” clade (Bignonieae, Bignoniaceae)

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.02.005openalex-snapshot

Plastomes resolve generic limits within tribe Clusieae (Clusiaceae) and reveal the new genus Arawakia

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.04.015openalex-snapshot

A brainstorm on the systematics of Turnera (Turneraceae, Malpighiales) caused by insights from molecular phylogenetics and morphological evolution

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.106555openalex-snapshot

A phylogenetic and biogeographic study of Rafflesia (Rafflesiaceae) in the Philippines: Limited dispersal and high island endemism

inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106961openalex-snapshot

Phylogeny and biogeography of South American marsh pitcher plant genus Heliamphora (Sarraceniaceae) endemic to the Guiana Highlands

inferred← citeshttps://doi.org/10.1016/j.ympev.2020.106986openalex-snapshot

Extensive variation in nucleotide substitution rate and gene/intron loss in mitochondrial genomes of Pelargonium

inferred← citeshttps://doi.org/10.1016/j.ympev.2020.107041openalex-snapshot

Phylogeny, divergence times, and diversification in Calophyllaceae: Linking key characters and habitat changes to the evolution of Neotropical Calophylleae

inferred← citeshttps://doi.org/10.1038/ng.740openalex-snapshot

The genome of woodland strawberry (Fragaria vesca)

inferred← citeshttps://doi.org/10.1038/s41597-024-03681-7openalex-snapshot

Chromosome-level genome assembly and annotation of Flueggea virosa (Phyllanthaceae)

inferred← citeshttps://doi.org/10.1038/s41597-025-05230-2openalex-snapshot

A curated benchmark dataset for molecular identification based on genome skimming

inferred← citeshttps://doi.org/10.1038/s41598-018-20189-4openalex-snapshot

Chloroplast genomes of Byrsonima species (Malpighiaceae): comparative analysis and screening of high divergence sequences

inferred← citeshttps://doi.org/10.1038/s41598-021-99178-zopenalex-snapshot

Calophyllaceae plastomes, their structure and insights in relationships within the clusioids

inferred← citeshttps://doi.org/10.1038/s41598-022-23639-2openalex-snapshot

Characterization of the plastid genome of Cratoxylum species (Hypericaceae) and new insights into phylogenetic relationships

inferred← citeshttps://doi.org/10.1038/s42003-022-03003-wopenalex-snapshot

Elevated mutation rates underlie the evolution of the aquatic plant family Podostemaceae

inferred← citeshttps://doi.org/10.1039/d3np00039gopenalex-snapshot

The dichapetalins and dichapetalin-type compounds: structural diversity, bioactivity, and future research perspectives

inferred← citeshttps://doi.org/10.1073/pnas.0910155107openalex-snapshot

Floral symmetry genes and the origin and maintenance of zygomorphy in a plant-pollinator mutualism

inferred← citeshttps://doi.org/10.1073/pnas.1205818109openalex-snapshot

Phylogenomics and a posteriori data partitioning resolve the Cretaceous angiosperm radiation Malpighiales

inferred← citeshttps://doi.org/10.1073/pnas.1310356110openalex-snapshot

Developmental origins of the world’s largest flowers, Rafflesiaceae

inferred← citeshttps://doi.org/10.1073/pnas.1403157111openalex-snapshot

Long-term morphological stasis maintained by a plant–pollinator mutualism

inferred← citeshttps://doi.org/10.1080/00173134.2012.679310openalex-snapshot

Not a shrinking violet: Pollen morphology of Violaceae (Malpighiales)

inferred← citeshttps://doi.org/10.1080/00173134.2019.1594357openalex-snapshot

Origin and divergence of Afro-Indian Picrodendraceae: linking pollen morphology, dispersal modes, fossil records, molecular dating and paleogeography

inferred← citeshttps://doi.org/10.1080/01916122.2025.2601530openalex-snapshot

Pollen morphology and ancestral reconstruction provide new characters and evolutionary insights supporting the systematics of the tribes Adelieae, Caperonieae and Ditaxeae in Euphorbiaceae

inferred← citeshttps://doi.org/10.1080/08912963.2020.1870225openalex-snapshot

New records of fossil leaves from Abunã Basin, Upper Pleistocene, Rondônia, Brazil

inferred← citeshttps://doi.org/10.1080/09583157.2016.1243226openalex-snapshot

Life history and host range of Sauris nr. purpurotincta, an unsuitable biological control agent for Chinese tallowtree

inferred← citeshttps://doi.org/10.1080/11263504.2021.2020356openalex-snapshot

Intraspecific variability in yield and chemical composition of essential oil of the endemic species Hypericum gaitii from different natural habitats of Eastern India

inferred← citeshttps://doi.org/10.1080/14786419.2021.1982936openalex-snapshot

The Malaysian genus Calophyllum (Calophyllaceae): a review on its phytochemistry and pharmacological activities

inferred← citeshttps://doi.org/10.1080/23802359.2017.1390406openalex-snapshot

The complete plastome of tropical fruit Garcinia mangostana (Clusiaceae)

inferred← citeshttps://doi.org/10.1080/23802359.2019.1586493openalex-snapshot

The complete chloroplast genome sequence of Chinese tallow Triadica sebifera (Linnaeus) Small (Euphorbiaceae)

inferred← citeshttps://doi.org/10.1080/23802359.2023.2215350openalex-snapshot

The complete chloroplast genome of Calophyllum soulattri Burm. f. (Calophyllaceae)

inferred← citeshttps://doi.org/10.1080/23818107.2018.1458651openalex-snapshot

Implications and future prospects for evolutionary analyses of DNA in historical herbarium collections

inferred← citeshttps://doi.org/10.1086/651229openalex-snapshot

Phytogeographic History and Phylogeny of the Humiriaceae

inferred← citeshttps://doi.org/10.1086/658923openalex-snapshot

Phylogenetic Analysis of the Plastid Inverted Repeat for 244 Species: Insights into Deeper-Level Angiosperm Relationships from a Long, Slowly Evolving Sequence Region

inferred← citeshttps://doi.org/10.1086/661633openalex-snapshot

Comparative Structure and Development of Pollen and Tapetum in Malpighiales, With a Focus on the Parietal Clade

inferred← citeshttps://doi.org/10.1086/663163openalex-snapshot

Floral Structure ofGarcinia brasiliensisin Relation to Flower Biology and Evolution

inferred← citeshttps://doi.org/10.1086/667614openalex-snapshot

Pollen Evolution in the Clusioid Clade (Malpighiales)

inferred← citeshttps://doi.org/10.1086/670668openalex-snapshot

Combined Morphological and Molecular Phylogeny of the Clusioid Clade (Malpighiales) and the Placement of the Ancient Rosid MacrofossilPaleoclusia

inferred← citeshttps://doi.org/10.1086/671804openalex-snapshot

Evolution of Pollen and Tapetal Characters in Ochnaceae (Malpighiales)

inferred← citeshttps://doi.org/10.1086/676818openalex-snapshot

Phytogeographic History of the Humiriaceae (Part 2)

inferred← citeshttps://doi.org/10.1086/676984openalex-snapshot

Development of the Remarkable Pollen Apertures of the Jellyfish TreeMedusagyne oppositifolia(Ochnaceae, Malpighiales)

inferred← citeshttps://doi.org/10.1086/678086openalex-snapshot

Gynoecial Structure of Vitales and Implications for the Evolution of Placentation in the Rosids

inferred← citeshttps://doi.org/10.1086/683275openalex-snapshot

Paleoochna tiffneyigen. et sp. nov. (Ochnaceae) from the Late Paleocene Almont/Beicegel Creek Flora, North Dakota, USA

inferred← citeshttps://doi.org/10.1086/692989openalex-snapshot

Floral Development of the Endangered Genus Medusagyne (Medusagynaceae-Malpighiales): Spatial Constraints of Stamen and Carpel Increase

inferred← citeshttps://doi.org/10.1086/718830openalex-snapshot

Belenocarpa tertiara (Berry) gen. et comb. nov. (Euphorbiaceae): Fossil Fruits with Carunculate Seeds from the Oligocene of Peru

inferred← citeshttps://doi.org/10.1093/aob/mcaf148openalex-snapshot

Plastid phylogenomics of the parietal clade of Malpighiales: ancestral genome synteny and congruent signal across exons, introns and spacers in support of Salicaceae relationships

inferred← citeshttps://doi.org/10.1093/aob/mct056openalex-snapshot

Advances in the floral structural characterization of the major subclades of Malpighiales, one of the largest orders of flowering plants

inferred← citeshttps://doi.org/10.1093/botlinnean/box023openalex-snapshot

Molecular phylogenetic analyses of Euphorbiaceae tribe Epiprineae, with the description of a new genus, Tsaiodendron gen. nov., from south-western China

inferred← citeshttps://doi.org/10.1093/dnares/dsaf022openalex-snapshot

Chromosome-scale genome assembly of Sauvagesia rhodoleuca (Ochnaceae) provides insights into its genome evolution and demographic history

inferred← citeshttps://doi.org/10.1093/gbe/evw233openalex-snapshot

Loss of aTrans-Splicingnad1Intron from Geraniaceae and Transfer of the Maturase GenematRto the Nucleus inPelargonium

inferred← citeshttps://doi.org/10.1093/jpe/rtx044openalex-snapshot

Are the cerrado and the seasonal forest woody floras assembled by different processes despite their spatial proximity?

inferred← citeshttps://doi.org/10.1093/molbev/msu331openalex-snapshot

Coalescent Methods Are Robust to the Simultaneous Effects of Long Branches and Incomplete Lineage Sorting

inferred← citeshttps://doi.org/10.1093/pcp/pcad004openalex-snapshot

Dissecting the Biology ofRafflesiaSpecies: Current Progress and Future Directions Made Possible with High-Throughput Sequencing Data

inferred← citeshttps://doi.org/10.1093/sysbio/syaa083openalex-snapshot

The Perfect Storm: Gene Tree Estimation Error, Incomplete Lineage Sorting, and Ancient Gene Flow Explain the Most Recalcitrant Ancient Angiosperm Clade, Malpighiales

inferred← citeshttps://doi.org/10.1101/2022.12.23.521604openalex-snapshot

New mitochondrial genomes of leptosporangiate ferns allow modeling the mitogenomic inflation syndrome across all land plant lineages

inferred← citeshttps://doi.org/10.1101/208454openalex-snapshot

Reconstructing deep-time paleoclimate legacies unveil the demise and turnover of the ancient (boreo)tropical flora

inferred← citeshttps://doi.org/10.1105/tpc.109.073189openalex-snapshot

Expression ofSHOOT MERISTEMLESS,WUSCHEL, andASYMMETRIC LEAVES1Homologs in the Shoots of Podostemaceae: Implications for the Evolution of Novel Shoot Organogenesis

inferred← citeshttps://doi.org/10.1105/tpc.16.00398openalex-snapshot

The Reverse Transcriptase/RNA Maturase Protein MatR Is Required for the Splicing of Various Group II Introns in Brassicaceae Mitochondria

inferred← citeshttps://doi.org/10.1111/1755-0998.70173openalex-snapshot

Enrichment Probe Sets Combining Universal and Lineage‐Specific Targets Help Resolve Recalcitrant Lineages

inferred← citeshttps://doi.org/10.1111/boj.12008openalex-snapshot

Spatio-temporal history of the endemic genera of Madagascar

inferred← citeshttps://doi.org/10.1111/boj.12012openalex-snapshot

Multivariate analysis of morphological and anatomical characters ofCalophyllum(Calophyllaceae) in South America

inferred← citeshttps://doi.org/10.1111/boj.12048openalex-snapshot

Comparative floral structure and systematics of the clade of Lophopyxidaceae and Putranjivaceae (Malpighiales)

inferred← citeshttps://doi.org/10.1111/boj.12070openalex-snapshot

Rosids

inferred← citeshttps://doi.org/10.1111/boj.12285openalex-snapshot

Results from an online survey of family delimitation in angiosperms and ferns: recommendations to the Angiosperm Phylogeny Group for thorny problems in plant classification

inferred← citeshttps://doi.org/10.1111/boj.12385openalex-snapshot

An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV

inferred← citeshttps://doi.org/10.1111/boj.12432openalex-snapshot

Colleters inCasearia(Salicaceae): a new interpretation for the theoid teeth

inferred← citeshttps://doi.org/10.1111/cla.12507openalex-snapshot

Benefits of alignment quality‐control processing steps and an Angiosperms353 phylogenomics pipeline applied to the Celastrales

inferred← citeshttps://doi.org/10.1111/eea.12573openalex-snapshot

Quarantine host range of B ikasha collaris, a potential biological control agent of Chinese tallowtree ( T riadica sebifera) in North America

inferred← citeshttps://doi.org/10.1111/eea.12737openalex-snapshot

Quarantine host range and natural history of Gadirtha fusca, a potential biological control agent of Chinese tallowtree (Triadica sebifera) in North America

inferred← citeshttps://doi.org/10.1111/geb.12724openalex-snapshot

Reconstructing deep‐time palaeoclimate legacies in the clusioid Malpighiales unveils their role in the evolution and extinction of the boreotropical flora

inferred← citeshttps://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

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2009.01000.xopenalex-snapshot

The Linear Angiosperm Phylogeny Group (LAPG) III: a linear sequence of the families in APG III

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2010.01096.xopenalex-snapshot

Molecular phylogenetics of Linaceae with complete generic sampling and data from two plastid genes

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2011.01162.xopenalex-snapshot

Comparative floral structure and systematics in Rhizophoraceae, Erythroxylaceae and the potentially related Ctenolophonaceae, Linaceae, Irvingiaceae and Caryocaraceae (Malpighiales)

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01258.xopenalex-snapshot

Molecular phylogenetic analysis of Podostemaceae: implications for taxonomy of major groups

inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01299.xopenalex-snapshot

Comparative floral structure and systematics in Ochnaceaes.l.(Ochnaceae, Quiinaceae and Medusagynaceae; Malpighiales)

inferred← citeshttps://doi.org/10.1111/j.1096-0031.2010.00327.xopenalex-snapshot

Phylogenetic inference using non-redundant coding of dependent characters versus alternative approaches for protein-coding genes

inferred← citeshttps://doi.org/10.1111/j.1365-313x.2012.05093.xopenalex-snapshot

The genome of flax ( Linum usitatissimum ) assembled de novo from short shotgun sequence reads

inferred← citeshttps://doi.org/10.1111/j.1420-9101.2012.02494.xopenalex-snapshot

Evolutionary stasis in Euphorbiaceae pollen: selection and constraints

inferred← citeshttps://doi.org/10.1111/j.1525-142x.2011.00488.xopenalex-snapshot

Comparative anatomy of embryogenesis in three species of Podostemaceae and evolution of the loss of embryonic shoot and root meristems

inferred← citeshttps://doi.org/10.1111/j.1600-0706.2011.19513.xopenalex-snapshot

Trait diversity on the phylogeny of cerrado woody species

inferred← citeshttps://doi.org/10.1111/j.1759-6831.2010.00097.xopenalex-snapshot

Angiosperm phylogeny inferred from sequences of four mitochondrial genes

inferred← citeshttps://doi.org/10.1111/jipb.13609openalex-snapshot

Nuclear phylogenomics of angiosperms and insights into their relationships and evolution

inferred← citeshttps://doi.org/10.1111/jse.12211openalex-snapshot

Phylogeny of the Rosidae: A dense taxon sampling analysis

inferred← citeshttps://doi.org/10.1111/jse.12260openalex-snapshot

The big, the bad, and the beautiful: Biology of the world's largest flowers

inferred← citeshttps://doi.org/10.1111/njb.00850openalex-snapshot

Comparative wood anatomy of Indian Drypetes and Putranjiva (Putranjivaceae): systematic implications, identification and comments on the synonymy of D. sumatrana

inferred← citeshttps://doi.org/10.1111/njb.01009openalex-snapshot

Systematic wood anatomy of the subfamily Acalyphoideae s.l. (Euphorbiaceae) from India, with remarks on synonymy

inferred← citeshttps://doi.org/10.1111/nph.15357openalex-snapshot

Widespread ancient whole‐genome duplications in Malpighiales coincide with Eocene global climatic upheaval

inferred← citeshttps://doi.org/10.1111/syen.12569openalex-snapshot

A genome‐wide phylogeny and the diversification of genus Liriomyza (Diptera: Agromyzidae) inferred from anchored phylogenomics

inferred← citeshttps://doi.org/10.1111/tpj.16767openalex-snapshot

Haplotype‐resolved genomes of octoploid species in Phyllanthaceae family reveal a critical role for polyploidization and hybridization in speciation

inferred← citeshttps://doi.org/10.1139/cjb-2019-0103openalex-snapshot

New perspectives on secretory structures in Clusia (Clusiaceae – Clusiod clade): production of latex or resins?

inferred← citeshttps://doi.org/10.11606/d.11.2024.tde-08102024-165900openalex-snapshot

Dendrocronologia e dendroclimatologia de >i /i< (Schott) Poepp. Ex Baill., >i /i< Desf. e >i /i< Aubl provenientes do Cerrado do estado de São Paulo

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