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Phylogenetic analyses of “higher” Hamamelididae based on plastid sequence data
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1938.tb09239.xopenalex-snapshot
THE MORPHOLOGY OF THE FLOWERS OF THE JUGLANDACEAE. I. THE INFLORESCENCE
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THE MORPHOLOGY OF THE FLOWERS OF THE JUGLANDACEAE. II. THE PISTILLATE FLOWERS AND FRUIT
inferredcites →https://doi.org/10.1002/j.1537-2197.1941.tb11018.xopenalex-snapshot
STEM ANATOMY AND PHYLOGENY OF THE RHOIPTELEACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1980.tb07704.xopenalex-snapshot
CASTANEOID INFLORESCENCES FROM THE MIDDLE EOCENE OF TENNESSEE AND THE DIAGNOSTIC VALUE OF POLLEN (AT THE SUBFAMILY LEVEL) IN THE FAGACEAE
inferredcites →https://doi.org/10.1002/j.1537-2197.1981.tb12407.xopenalex-snapshot
PSEUDOFAGUS IDAHOENSIS, N. GEN. ET SP. (FAGACEAE) FROM THE MIOCENE CLARKIA FLORA OF IDAHO
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15061.xopenalex-snapshot
TRIGONOBALANUS (FAGACEAE): TAXONOMIC STATUS AND PHYLOGENETIC RELATIONSHIPS
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15062.xopenalex-snapshot
EARLIEST MEGAFOSSIL EVIDENCE OF FAGACEAE: PHYLOGENETIC AND BIOGEOGRAPHIC IMPLICATIONS
inferredcites →https://doi.org/10.1002/j.1537-2197.1989.tb15131.xopenalex-snapshot
EXTINCT TRANSITIONAL FAGACEAE FROM THE OLIGOCENE AND THEIR PHYLOGENETIC IMPLICATIONS
inferredcites →https://doi.org/10.1002/j.1537-2197.1995.tb11588.xopenalex-snapshot
A cladistic analysis of chloroplast DNA restriction site variation and morphology for the genera of the J uglandaceae
inferredcites →https://doi.org/10.1002/j.1537-2197.1996.tb13943.xopenalex-snapshot
The Evolution of Actinorhizal Symbioses: Evidence for Multiple Origins of the Symbiotic Association
inferredcites →https://doi.org/10.1007/978-0-585-23095-5_10openalex-snapshot
Comparison of Alternative Hypotheses for the Origin of the Angiosperms
inferredcites →https://doi.org/10.1007/978-3-642-39417-1openalex-snapshot
Flowering plants, Eudicots : Malpighiales
inferredcites →https://doi.org/10.1007/978-3-7091-7076-2_15openalex-snapshot
New Ideas About the Early Differentiation of Angiosperms
inferredcites →https://doi.org/10.1007/978-3-7091-7076-2_20openalex-snapshot
Evolutionary Trends in the Hamamelidales-Fagales-Group
inferredcites →https://doi.org/10.1007/bf00985904openalex-snapshot
Phylogenetic relationships of theJuglandaceae
inferredcites →https://doi.org/10.1007/bf02806171openalex-snapshot
Evolution and classification of flowering plants
inferredcites →https://doi.org/10.1007/bf02859135openalex-snapshot
Flowers and inflorescences of the “Amentiferae”
inferredcites →https://doi.org/10.1007/bf02860537openalex-snapshot
Fossil pollen records of extant angiosperms
inferredcites →https://doi.org/10.1007/bf02860849openalex-snapshot
Early cretaceous fossil evidence for angiosperm evolution
inferredcites →https://doi.org/10.1007/bf02861558openalex-snapshot
Outline of the classification of flowering plants (magnoliophyta)
inferredcites →https://doi.org/10.1016/0034-6667(83)90015-5openalex-snapshot
Upper Cretaceous (Senonian) floral structures of juglandalean affinity containing normapolles pollen
inferredcites →https://doi.org/10.1016/s0367-2530(17)32023-6openalex-snapshot
Development and Morphological Interpretation of the Cupule in Fagaceae
inferredcites →https://doi.org/10.1017/s0094837300015840openalex-snapshot
Phylogenies and angiosperm diversification
inferredcites →https://doi.org/10.1038/070598a0openalex-snapshot
The Classification of Flowering Plants
inferredcites →https://doi.org/10.1071/sb9930111openalex-snapshot
The evolutionary history of Nothofagus (Nothofagaceae)
inferredcites →https://doi.org/10.1071/sb9930441openalex-snapshot
Using Sequences of rbc L to Study Phylogeny and Biogeography of Nothofagus Species
inferredcites →https://doi.org/10.1073/pnas.82.11.3557openalex-snapshot
Tobacco chloroplast tRNA Lys (UUU) gene contains a 2.5-kilobase-pair intron: An open reading frame and a conserved boundary sequence in the intron
inferredcites →https://doi.org/10.1073/pnas.89.19.8986openalex-snapshot
Oldest fossil flowers of hamamelidaceous affinity, from the Late Cretaceous of New Jersey.
inferredcites →https://doi.org/10.1073/pnas.92.7.2647openalex-snapshot
Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms.
inferredcites →https://doi.org/10.1080/00378941.1920.10836114openalex-snapshot
Matériaux pour la flore de la Nouvelle-Calédonie
inferredcites →https://doi.org/10.1080/00378941.1940.10836426openalex-snapshot
Matériaux pour la flore de la Nouvelle-Calédonie. LVII. La présence d'une Myricacée
inferredcites →https://doi.org/10.1086/297231openalex-snapshot
Fagaceous Flowers, Fruits, and Cupules from the Campanian (Late Cretaceous) of Central Georgia, USA
inferredcites →https://doi.org/10.1086/335419openalex-snapshot
The Comparative Morphology of the Fagaceae I. The Genus Nothofagus
inferredcites →https://doi.org/10.1093/oxfordjournals.aob.a089518openalex-snapshot
The Structure of the Flower of Fagaceae, and its Bearing on the Affinities of the Group
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040343openalex-snapshot
A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040779openalex-snapshot
Complete congruence between morphological and rbcL-based molecular phylogenies in birches and related species (Betulaceae).
inferredcites →https://doi.org/10.1093/sysbio/43.4.467openalex-snapshot
Combining Data in Phylogenetic Systematics: An Empirical Approach Using Three Molecular Data Sets in the Solanaceae
inferredcites →https://doi.org/10.1111/j.1095-8339.1980.tb01661.xopenalex-snapshot
A revised system of classification of the angiosperms
inferredcites →https://doi.org/10.1111/j.1096-0031.1993.tb00217.xopenalex-snapshot
CLADISTICS: WHAT'S IN A WORD?
inferredcites →https://doi.org/10.1111/j.1469-8137.1964.tb07363.xopenalex-snapshot
THE INFLORESCENCE OF FAGUS AND CASTANEA, AND THE EVOLUTION OF THE CUPULES OF THE FAGACEAE
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb02497.xopenalex-snapshot
THE LIMITS OF AMINO ACID SEQUENCE DATA IN ANGIOSPERM PHYLOGENETIC RECONSTRUCTION
inferredcites →https://doi.org/10.1126/science.1523408openalex-snapshot
Carnivorous Plants: Phylogeny and Structural Evolution
inferredcites →https://doi.org/10.1139/g93-089openalex-snapshot
The rbcL gene sequence from chestnut indicates a slow rate of evolution in the Fagaceae
inferredcites →https://doi.org/10.2307/1222465openalex-snapshot
An Integrated System of Classification of Flowering Plants
inferredcites →https://doi.org/10.2307/2395267openalex-snapshot
The Bases of Angiosperm Phylogeny: Vegetative Morphology
inferredcites →https://doi.org/10.2307/2395271openalex-snapshot
The Bases of Angiosperm Phylogeny: Palynology
inferredcites →https://doi.org/10.2307/2399112openalex-snapshot
Evolution of the Fagaceae: The Implications of Foliar Features
inferredcites →https://doi.org/10.2307/2399117openalex-snapshot
Comparative Pollen Morphology and Its Relationship to Phylogeny of Pollen in the Hamamelidae
inferredcites →https://doi.org/10.2307/2399595openalex-snapshot
Wood and Bark Anatomy of Ticodendron: Comments on Relationships
inferredcites →https://doi.org/10.2307/2399596openalex-snapshot
The Leaf Architecture of Ticodendron and the Application of Foliar Characters in Discerning its Relationships
inferredcites →https://doi.org/10.2307/2399597openalex-snapshot
Sieve-Element Characters of Ticodendron
inferredcites →https://doi.org/10.2307/2399599openalex-snapshot
Pollen Morphology and the Systematic Relationships of Ticodendron incognitum
inferredcites →https://doi.org/10.2307/2399767openalex-snapshot
Rosidae and Their Relationships to Other Nonmagnoliid Dicotyledons: A Phylogenetic Analysis Using Morphological and Chemical Data
inferredcites →https://doi.org/10.2307/2399772openalex-snapshot
Phylogenetic Relationships of Dipsacales Based on rbcL Sequences
inferredcites →https://doi.org/10.2307/2399779openalex-snapshot
Phylogenetic Implications of rbcL Sequence Variation in the Asteraceae
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/10.2307/2399851openalex-snapshot
Phylogenetic Relationships Among Members of Saxifragaceae Sensu Lato Based on rbcL Sequence Data
inferredcites →https://doi.org/10.2307/2419533openalex-snapshot
Cladistic Analysis of Restriction Site Variation within the Chloroplast DNA Inverted Repeat Region of Selected Hamamelididae
inferredcites →https://doi.org/10.2307/2419717openalex-snapshot
Phylogenetic Analyses of Polemoniaceae Using Nucleotide Sequences of the Plastid Gene matK
inferredcites →https://doi.org/10.2307/2419719openalex-snapshot
Phylogenetic Affinities of Datiscaceae Based on an Analysis of Nucleotide Sequences from the Plastid rbcL Gene
inferredcites →https://doi.org/10.2307/2419806openalex-snapshot
A Phylogenetic Structure for the Monocotyledons, as Inferred from Chloroplast DNA Restriction Site Variation, and a Comparison of Measures of Clade Support
inferredcites →https://doi.org/10.2307/2446015openalex-snapshot
The structure and function of RuBisCO and their Implications for Systematic Studies
inferredcites →https://doi.org/10.2307/2446156openalex-snapshot
Systematics of Nothofagus (Nothofagaceae) based on rDNA spacer sequences (ITS): taxonomic congruence with morphology and plastid sequences
inferredcites →https://doi.org/10.2307/2805641openalex-snapshot
Patterns in the Evolution of Amentiferous Fruits
inferredcites →https://doi.org/10.2307/2806952openalex-snapshot
New Evidence for the Systematic Significance of Acylated Spermidines and Flavonoids in Pollen of Higher Hamamelidae
inferredcites →https://doi.org/10.2307/4108577openalex-snapshot
An Integrated System of Classification of Flowering Plants
inferredcites →https://doi.org/10.2307/4115792openalex-snapshot
On the Evolution of Cupules in the Fagaceae
inferredcites →https://doi.org/10.5642/aliso.19921302.08openalex-snapshot
An Updated Phylogenetic Classification of the Flowering Plants
inferredcites →https://doi.org/10.5962/bhl.part.27154openalex-snapshot
Results of the Archbold expeditions Papuan nothofagus
inferredcites →https://doi.org/10.5962/p.185922openalex-snapshot
Inflorescence Architecture and Evolution in the Fagaceae
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Revised circumscription of Nothofagus and recognition of the segregate genera Fuscospora, Lophozonia, and Trisyngyne (Nothofagaceae)
inferred← citeshttps://doi.org/10.3767/blumea.2024.69.01.01zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1006/mpev.1999.0614openalex-snapshot
Phylogeny, Biogeography, and Processes of Molecular Differentiation in Quercus Subgenus Quercus (Fagaceae)
inferred← citeshttps://doi.org/10.1006/mpev.2001.1029openalex-snapshot
A Molecular Phylogeny of Costaceae (Zingiberales)
inferred← citeshttps://doi.org/10.1007/978-1-319-15626-8_21openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-1-4020-9609-9_2openalex-snapshot
Class Magnoliopsida (Dicotyledons)
inferred← citeshttps://doi.org/10.1007/bf00538960openalex-snapshot
Possibility of grouping of Cyclobalanopsis species (Fagaceae) grown in Japan based on an analysis of several regions of chloroplast DNA
inferred← citeshttps://doi.org/10.1007/bf01089228openalex-snapshot
Phylogenetic relationships in the Hamamelidaceae: Evidence from the nucleotide sequences of the plastid genematK
inferred← citeshttps://doi.org/10.1007/bf01177723openalex-snapshot
Polymorphism analysis of Fagaceae and DNA-based identification ofFagus species grown in Japan based on therbcL gene
inferred← citeshttps://doi.org/10.1007/bf02869011openalex-snapshot
The classification and geography of the flowering plants: Dicotyledons of the class Angiospermae
inferred← citeshttps://doi.org/10.1007/pl00013885openalex-snapshot
Molecular Phylogeny of Magnolia (Magnoliaceae) Inferred from cpDNA Sequences and Evolutionary Divergence of the Floral Scents
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Comparative mapping between Quercus and Castanea using simple-sequence repeats (SSRs)
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Genetic diversity of steno endemic and critically endangered Monoon tirunelveliense (Annonaceae) from India as revealed by ISSRs
inferred← citeshttps://doi.org/10.1007/s00606-003-0018-xopenalex-snapshot
Phylogeny of Fagus L. (Fagaceae) based on morphological data
inferred← citeshttps://doi.org/10.1007/s00606-003-0113-zopenalex-snapshot
Phylogenetic relationships within the ?core? Laureae ( Litsea complex, Lauraceae) inferred from sequences of the chloroplast gene mat K and nuclear ribosomal DNA ITS regions
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Progress and problems in the assessment of flower morphology in higher-level systematics
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Further evidence for paraphyly of the Celtidaceae from the chloroplast gene mat K
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Reticulate hybridization of Alpinia (Zingiberaceae) in Taiwan
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Stone oak flowers are more likely generalist pollinated by insects rather than wind
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Evolution of rDNA FISH patterns in the Fagaceae
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Phylogenetic relationships and taxonomy of Grifola (Polyporales)
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New Zealand Eocene, Oligocene and Miocene Macrofossil and Pollen Records and Modern Plant Distributions in the Southern Hemisphere
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Comparative Flower and Inflorescence Organogenesis among Genera of Betulaceae: Implications for Phylogenetic Relationships
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Diversity and Classification of Flowering Plants: Eudicots
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Diversity and Classification of Flowering Plants: Eudicots
inferred← citeshttps://doi.org/10.1016/j.ode.2004.08.001openalex-snapshot
Phylogenetic analysis of the Malvadendrina clade (Malvaceae s.l.) based on plastid DNA sequences
inferred← citeshttps://doi.org/10.1016/j.phytochem.2005.08.001openalex-snapshot
Metabolic profiling and phylogenetic analysis of medicinal Zingiber species: Tools for authentication of ginger (Zingiber officinale Rosc.)
inferred← citeshttps://doi.org/10.1016/j.ppees.2014.03.001openalex-snapshot
Large-scale phylogenetic analyses reveal fagalean diversification promoted by the interplay of diaspores and environments in the Paleogene
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2008.08.001openalex-snapshot
Evolutionary significance of granular exine structure in the light of phylogenetic analyses
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Phylogeny of the Cucurbitales based on DNA sequences of nine loci from three genomes: Implications for morphological and sexual system evolution
inferred← citeshttps://doi.org/10.1016/j.ympev.2006.07.021openalex-snapshot
How should gaps be treated in parsimony? A comparison of approaches using simulation
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Rosales sister to Fabales: Towards resolving the rosid puzzle
inferred← citeshttps://doi.org/10.1016/j.ympev.2021.107232openalex-snapshot
Plastid phylogenomic analyses of Fagales reveal signatures of conflict and ancient chloroplast capture
inferred← citeshttps://doi.org/10.1016/s0034-6667(99)00008-1openalex-snapshot
Fossil flowers with Normapolles pollen from the Upper Cretaceous of southeastern North America
inferred← citeshttps://doi.org/10.1016/s0168-9525(03)00118-5openalex-snapshot
ITS2 is a double-edged tool for eukaryote evolutionary comparisons
inferred← citeshttps://doi.org/10.1016/s1055-7903(03)00028-9openalex-snapshot
Using matK sequence data to unravel the phylogeny of Casuarinaceae
inferred← citeshttps://doi.org/10.1034/j.1399-3054.2001.1120113.xopenalex-snapshot
Three MADS‐box genes similar toAPETALA1andFRUITFULLfrom silver birch (Betula pendula)
inferred← citeshttps://doi.org/10.1038/s41598-023-45879-6openalex-snapshot
Cyto-molecular characterization of rDNA and chromatin composition in the NOR-associated satellite in Chestnut (Castanea spp.)
inferred← citeshttps://doi.org/10.1043/0363-6445-26.3.670openalex-snapshot
Phylogenetics of Arethuseae (Orchidaceae) based on plastid matK and rbcL sequences
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Out of Africa: molecular phylogenetics and biogeography of Wolffiella (Lemnaceae)
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Phylogeography of the Southeast Asian stone oaks ( Lithocarpus )
inferred← citeshttps://doi.org/10.1071/bt05113openalex-snapshot
Genetic diversity of the rare Asian plant, Trigonobalanus doichangensis (Fagaceae)
inferred← citeshttps://doi.org/10.1071/bt19126openalex-snapshot
Fossil evidence for the evolution of the Casuarinaceae in response to low soil nutrients and a drying climate in Cenozoic Australia
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Relationships among felt scale insects (Hemiptera : Coccoidea : Eriococcidae) of southern beech, Nothofagus (Nothofagaceae), with the first descriptions of Australian species of the Nothofagus-feeding genus Madarococcus Hoy
inferred← citeshttps://doi.org/10.1071/sb15026openalex-snapshot
Why we should retain Nothofagus sensu lato
inferred← citeshttps://doi.org/10.1080/0028825x.2014.960946openalex-snapshot
Relationships, gene flow and species boundaries among New Zealand Fuscospora (Nothofagaceae: southern beech)
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Phylogeny of Extant and Fossil Juglandaceae Inferred from the Integration of Molecular and Morphological Data Sets
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Monoterpene emissions from threeNothofagusspecies in Patagonia, Argentina
inferred← citeshttps://doi.org/10.1086/297559openalex-snapshot
New Genus of Fossil Fagaceae from the Santonian (Late Cretaceous) of Central Georgia, U. S. A.
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Lower Species Richness in Dioecious Clades
inferred← citeshttps://doi.org/10.1086/314084openalex-snapshot
Phylogenetics of the Hamamelidae and Their Allies: Parsimony Analyses of Nucleotide Sequences of the Plastid GenerbcL
inferred← citeshttps://doi.org/10.1086/314090openalex-snapshot
Ontogeny and Diversity in Staminate Flowers ofNothofagus(Nothofagaceae)
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The Phylogenetic Affinities of Nothofagus (Nothofagaceae) Leaf Fossils based on Combined Molecular and Morphological Data
inferred← citeshttps://doi.org/10.1086/322949openalex-snapshot
Systematics of Fagaceae: Phylogenetic Tests of Reproductive Trait Evolution
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The Historical Biogeography of Fagaceae: Tracking the Tertiary History of Temperate and Subtropical Forests of the Northern Hemisphere
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Endressianthus, a New Normapolles‐Producing Plant Genus of Fagalean Affinity from the Late Cretaceous of Portugal
inferred← citeshttps://doi.org/10.1086/381920openalex-snapshot
Phylogenetic Relationships in Fagales Based on DNA Sequences from Three Genomes
inferred← citeshttps://doi.org/10.1086/596335openalex-snapshot
Permineralized Fagus Nuts from the Eocene of Vancouver Island, Canada
inferred← citeshttps://doi.org/10.1086/648993openalex-snapshot
A New Lineage‐Based Tribal Classification of the Family Caryophyllaceae
inferred← citeshttps://doi.org/10.1086/662135openalex-snapshot
Fruits of Ticodendraceae (Fagales) from the Eocene of Europe and North America
inferred← citeshttps://doi.org/10.1093/jisesa/iev118openalex-snapshot
New Gall Wasp Species Attacking Chestnut Trees:Dryocosmus zhuilin. sp. (Hymenoptera: Cynipidae) onCastanea henryifrom Southeastern China
inferred← citeshttps://doi.org/10.1093/sysbio/syr116openalex-snapshot
Testing the Impact of Calibration on Molecular Divergence Times Using a Fossil-Rich Group: The Case of Nothofagus (Fagales)
inferred← citeshttps://doi.org/10.1098/rspb.2001.1782openalex-snapshot
Evolution of the angiosperms: calibrating the family tree
inferred← citeshttps://doi.org/10.1098/rspb.2005.3219openalex-snapshot
Not so ancient: the extant crown group of Nothofagus represents a post-Gondwanan radiation
inferred← citeshttps://doi.org/10.1098/rspb.2012.0827openalex-snapshot
Parallel evolution of angiosperm colour signals: common evolutionary pressures linked to hymenopteran vision
inferred← citeshttps://doi.org/10.1098/rstb.2004.1526openalex-snapshot
Origins of the southeastern Australian vegetation
inferred← citeshttps://doi.org/10.1098/rstb.2004.1528openalex-snapshot
Radiation of the Australian flora: what can comparisons of molecular phylogenies across multiple taxa tell us about the evolution of diversity in present–day communities?
inferred← citeshttps://doi.org/10.1111/boj.12413openalex-snapshot
Comparative flower development ofJuglans regia,Cyclocarya paliurusandEngelhardia spicata: homology of floral envelopes in Juglandaceae
inferred← citeshttps://doi.org/10.1111/curt.12600openalex-snapshot
1119. Nothofagus alpina (Poepp. & Endl.) Oerst
inferred← citeshttps://doi.org/10.1111/curt.12603openalex-snapshot
The Southern Beeches: an introduction to the genus Nothofagus Blume
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Linking fine root traits to maximum potential growth rate among 11 mature temperate tree species
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2007.00670.xopenalex-snapshot
Karyomorphology of the endangered Trigonobalanus doichangensis (A. Camus) Forman (Fagaceae) and its taxonomic and biogeographical implications
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2008.00807.xopenalex-snapshot
Mode of pollen tube growth in pistils ofTicodendron incognitum(Ticodendraceae, Fagales) and the evolution of chalazogamy
inferred← citeshttps://doi.org/10.1111/j.1095-8339.2012.01217.xopenalex-snapshot
Fossil floral and fruit evidence for the evolution of unusual developmental characters in Fagales
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02139.xopenalex-snapshot
Ecological determinants of genetic diversity in an expanding population of the shrub Myrica cerifera
inferred← citeshttps://doi.org/10.1111/j.1756-1051.2008.00313.xopenalex-snapshot
Lithocarpus longzhouicus comb. nov. (Fagaceae) from China: based on morphological and molecular data
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2011.00116.xopenalex-snapshot
Molecular identification of species in Juglandaceae: A tiered method
inferred← citeshttps://doi.org/10.1111/j.1759-6831.2011.00179.xopenalex-snapshot
A new species of Zingiber (Zingiberaceae) from Taiwan, China, based on morphological and molecular data
inferred← citeshttps://doi.org/10.1111/j.2006.0030-1299.14418.xopenalex-snapshot
Is the composition of phytophagous insects and parasitic fungi among trees predictable?
inferred← citeshttps://doi.org/10.1111/jipb.70011openalex-snapshot
Genome duplications, genomic conflict, and rapid phenotypic evolution characterize the Cretaceous radiation of Fagales
inferred← citeshttps://doi.org/10.1111/tpj.16559openalex-snapshot
Testing the large genome constraint hypothesis in tropical rhizomatous herbs: life strategies, plant traits and habitat preferences in gingers
inferred← citeshttps://doi.org/10.1139/cjb-2013-0247openalex-snapshot
Cascadiacarpa exilissp. nov.: new fruits of Fagaceae from the Eocene of British Columbia
inferred← citeshttps://doi.org/10.1146/annurev.ecolsys.29.1.567openalex-snapshot
PHYLOGENY OF VASCULAR PLANTS
inferred← citeshttps://doi.org/10.11646/zootaxa.1796.1.1openalex-snapshot
A fully web-illustrated morphological phylogenetic study of relationships among oak gall wasps and their closest relatives (Hymenoptera: Cynipidae)
inferred← citeshttps://doi.org/10.1186/1471-2148-7-s2-s6openalex-snapshot
Unexpected presence of Fagus orientalis complex in Italy as inferred from 45,000-year-old DNA pollen samples from Venice lagoon
inferred← citeshttps://doi.org/10.1186/s12862-025-02435-2openalex-snapshot
Low population genetic structure in five Chilean Nothofagus species and high fluctuating asymmetry in Nothofagus pumilio x N. antarctica putative hybrids
inferred← citeshttps://doi.org/10.12657/denbio.086.005openalex-snapshot
Diversity, distribution, and threats of the Juglandaceae in Vietnam
inferred← citeshttps://doi.org/10.12705/644.10openalex-snapshot
Cupules and fruits of Lithocarpus (Fagaceae) from the Miocene of Yunnan, southwestern China
inferred← citeshttps://doi.org/10.12705/674.3openalex-snapshot
Sulettaria: A new ginger genus disjunct from Elettaria cardamomum
inferred← citeshttps://doi.org/10.1371/journal.pone.0183970openalex-snapshot
Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
inferred← citeshttps://doi.org/10.14258/pbssm.2019011openalex-snapshot
Молекулярная филогения Hamamelidaceae s.l. на основе анализа нуклеотидных последовательностей ITS ядерной и matK, trnL-F хлоропластной ДНК
inferred← citeshttps://doi.org/10.14288/1.0091394openalex-snapshot
Evolutionary consequences of dioecy in angiosperms : the effects of breeding system on speciation and extinction rates
inferred← citeshttps://doi.org/10.1534/genetics.105.048439openalex-snapshot
Comparison of Quantitative Trait Loci for Adaptive Traits Between Oak and Chestnut Based on an Expressed Sequence Tag Consensus Map
inferred← citeshttps://doi.org/10.1600/0363644053661850openalex-snapshot
Teasing Apart Molecular- Versus Fossil-based Error Estimates when Dating Phylogenetic Trees: A Case Study in the Birch Family (Betulaceae)
inferred← citeshttps://doi.org/10.1600/036364406775971688openalex-snapshot
Molecular Phylogeny of Conradina and Other Scrub Mints (Lamiaceae) from the Southeastern USA: Evidence for Hybridization in Pleistocene Refugia?
inferred← citeshttps://doi.org/10.1600/036364406777585900openalex-snapshot
Molecular Evidence Resolving the Systematic Position of Hectorella (Portulacaceae)
inferred← citeshttps://doi.org/10.1600/036364411x553216openalex-snapshot
The Phylogeny of Ayenia , Byttneria, and Rayleya (Malvaceae s. l.) and its Implications for the Evolution of Growth Forms
inferred← citeshttps://doi.org/10.1890/0012-9615(2000)070[0617:wgpcop]2.0.co;2openalex-snapshot
WHAT GOVERNS PROTEIN CONTENT OF POLLEN: POLLINATOR PREFERENCES, POLLEN–PISTIL INTERACTIONS, OR PHYLOGENY?
inferred← citeshttps://doi.org/10.1890/04-1036openalex-snapshot
MOLECULAR INDICATORS OF TREE MIGRATION CAPACITY UNDER RAPID CLIMATE CHANGE
inferred← citeshttps://doi.org/10.18942/apg.kj00004622912openalex-snapshot
Return from the lost: rediscovery of the presumed extinct "Leptosolena" (Zingiberaceae) in the Philippines and its phylogenetic placement in gingers
inferred← citeshttps://doi.org/10.20531/tfb.2018.46.1.03openalex-snapshot
Taxonomy of Boesenbergia parvula (Zingiberaceae) with new synonymy
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1361496/v1openalex-snapshot
Chloroplast Genome of Lithocarpus Dealbatus: Identification of Hotspots for Sequence Variability and Phylogeny Analysis in Quercoideae, a Sub-family of Fagaceae
inferred← citeshttps://doi.org/10.2307/2446156openalex-snapshot
Systematics of Nothofagus (Nothofagaceae) based on rDNA spacer sequences (ITS): taxonomic congruence with morphology and plastid sequences
inferred← citeshttps://doi.org/10.2307/25065582openalex-snapshot
Nuclear and plastid DNA sequences confirm the placement of the enigmatic Canacomyrica monticola in Myricaceae
inferred← citeshttps://doi.org/10.2307/25066014openalex-snapshot
Molecular phylogenetics and cupule evolution in Fagaceae as inferred from nuclear CRABS CLAW sequences
inferred← citeshttps://doi.org/10.2307/2656638openalex-snapshot
Phylogenetic systematics of the tribe Millettieae (Leguminosae) based on chloroplast trnK/matK sequences and its implications for evolutionary patterns in Papilionoideae
inferred← citeshttps://doi.org/10.2307/2656753openalex-snapshot
Anatomical and developmental study of petrified Quercus (Fagaceae) fruits from the Middle Miocene, Yakima Canyon, Washington, USA
inferred← citeshttps://doi.org/10.2307/2656775openalex-snapshot
Convergence and correlations among leaf size and function in seed plants: a comparative test using independent contrasts
inferred← citeshttps://doi.org/10.2307/2656895openalex-snapshot
Phylogeny and biogeography of Juglans (Juglandaceae) based on matK and ITS sequence data
inferred← citeshttps://doi.org/10.2307/2656981openalex-snapshot
Phylogeny and evolution of the Betulaceae as inferred from DNA sequences, morphology, and paleobotany
inferred← citeshttps://doi.org/10.26492/gbs72(1).2020-08openalex-snapshot
Nomenclatural changes in Zingiberaceae: Haplochorema is reduced to Boesenbergia
inferred← citeshttps://doi.org/10.3120/0024-9637-55.3.181openalex-snapshot
Phylogenetic Relationships and Taxonomic Status Of the Paleoendemic Fagaceae Of Western North America: Recognition Of A New Genus, Notholithocarpus
inferred← citeshttps://doi.org/10.3159/08-ra-036r.1openalex-snapshot
Natural history, distribution, phylogenetic relationships, and conservation of Central American black walnuts (Juglans sect. Rhysocaryon)1
inferred← citeshttps://doi.org/10.3389/fpls.2017.00816openalex-snapshot
Development of Chloroplast and Nuclear DNA Markers for Chinese Oaks (Quercus Subgenus Quercus) and Assessment of Their Utility as DNA Barcodes
inferred← citeshttps://doi.org/10.3389/fpls.2017.00968openalex-snapshot
The Complete Chloroplast Genome of Chinese Bayberry (Morella rubra, Myricaceae): Implications for Understanding the Evolution of Fagales
inferred← citeshttps://doi.org/10.3390/plants14010109openalex-snapshot
Response of Pedunculate Oak (Quercus robur L.) to Adverse Environmental Conditions in Genetic and Dendrochronological Studies
inferred← citeshttps://doi.org/10.34220/issn.2222-7962/2021.1/1openalex-snapshot
MODERN GENOSYSTEMATICS AND BIOLOGICAL FEATURES OF NATURALLY GROWING AND INTRODUCED SPECIES OF THE GENUS QUERCUS
inferred← citeshttps://doi.org/10.3732/ajb.1000404openalex-snapshot
Angiosperm phylogeny: 17 genes, 640 taxa
inferred← citeshttps://doi.org/10.3732/ajb.89.10.1682openalex-snapshot
The phylogeny and a new classification of the gingers (Zingiberaceae): evidence from molecular data
inferred← citeshttps://doi.org/10.3732/ajb.89.2.312openalex-snapshot
Phylogenetic relationships in the cactus family (Cactaceae) based on evidence from trn K / mat K and trn L‐trn F sequences
inferred← citeshttps://doi.org/10.3732/ajb.90.11.1567openalex-snapshot
A comparative flower and fruit anatomical study of Quercus acutissima, a biennial‐fruiting oak from the Cerris group (Fagaceae)
inferred← citeshttps://doi.org/10.3732/ajb.91.1.100openalex-snapshot
The phylogeny, evolution, and classification of the genus Globba and tribe Globbeae (Zingiberaceae): appendages do matter
inferred← citeshttps://doi.org/10.3732/ajb.91.10.1627openalex-snapshot
A survey of tricolpate (eudicot) phylogenetic relationships
inferred← citeshttps://doi.org/10.3732/ajb.91.11.1834openalex-snapshot
Phylogenetic relationships of Betula species (Betulaceae) based on nuclear ADH and chloroplast matK sequences
inferred← citeshttps://doi.org/10.3732/ajb.91.11.1846openalex-snapshot
A phylogeny of legumes (Leguminosae) based on analysis of the plastid mat K gene resolves many well‐supported subclades within the family
inferred← citeshttps://doi.org/10.3732/ajb.92.1.167openalex-snapshot
The molecular phylogeny of Alpinia (Zingiberaceae): a complex and polyphyletic genus of gingers
inferred← citeshttps://doi.org/10.3732/ajb.92.6.1006openalex-snapshot
Patterns of molecular and morphological differentiation in Fagus (Fagaceae): phylogenetic implications
inferred← citeshttps://doi.org/10.3732/ajb.92.7.1068openalex-snapshot
The evolution of unisexual flowers: morphological and functional convergence results from diverse developmental transitions
inferred← citeshttps://doi.org/10.3732/ajb.93.4.557openalex-snapshot
Beardia vancouverensis gen. et sp. nov. (Juglandaceae): permineralized fruits from the Eocene of British Columbia
inferred← citeshttps://doi.org/10.3732/ajb.94.3.351openalex-snapshot
Cascadiacarpa spinosa gen. et sp. nov. (Fagaceae): castaneoid fruits from the Eocene of Vancouver Island, Canada
inferred← citeshttps://doi.org/10.3897/jhr.41.7869openalex-snapshot
Nesting biology of an Oriental carpenter bee, Xylocopa (Biluna) nasalis Westwood, 1838, in Thailand (Hymenoptera, Apidae, Xylocopinae)
inferred← citeshttps://doi.org/10.4067/s0717-92002006000100001openalex-snapshot
El uso de marcadores genéticos en el género Nothofagus con especial referencia a raulí y roble
inferred← citeshttps://doi.org/10.5642/aliso.20022101.03openalex-snapshot
Wood and Bark Anatomy of Myricaceae: Relationships, Generic Definitions, and Ecological Interpretations
inferred← citeshttps://doi.org/10.5642/aliso.20062201.51openalex-snapshot
Phlogeny and Biogeography of the Prayer Plant Family
inferred← citeshttps://doi.org/10.5642/aliso.20153302.03openalex-snapshot
An Evolutionary Perspective on Human Cross-sensitivity to Tree Nut and Seed Allergens
inferred← citeshttps://doi.org/10.7287/peerj.7026v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The complete chloroplast genome of Fagus crenata (subgenus Fagus) and comparison with F. engleriana (subgenus Engleriana) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7026v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The complete chloroplast genome of Fagus crenata (subgenus Fagus) and comparison with F. engleriana (subgenus Engleriana) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7026v0.1/reviews/3openalex-snapshot
Peer Review #3 of "The complete chloroplast genome of Fagus crenata (subgenus Fagus) and comparison with F. engleriana (subgenus Engleriana) (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7026v0.2/reviews/3openalex-snapshot
Peer Review #3 of "The complete chloroplast genome of Fagus crenata (subgenus Fagus) and comparison with F. engleriana (subgenus Engleriana) (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.7026openalex-snapshot
The complete chloroplast genome of Fagus crenata (subgenus Fagus ) and comparison with F. engleriana (subgenus Engleriana )
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