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A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales)

https://doi.org/10.3114/sim0019
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What this work says

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

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New Genes for Phylogenetic Studies of Lichenized Fungi: Glyceraldehyde-3-Phosphate Dehydrogenase and Beta-Tubulin Genes
inferredcites →https://doi.org/10.1007/s10267-009-0487-zopenalex-snapshot
Phylogenetic analyses of Japanese species of Phyllosticta sensu stricto
inferredcites →https://doi.org/10.1007/s13225-011-0117-xopenalex-snapshot
Pleosporales
inferredcites →https://doi.org/10.1007/s13225-011-0140-yopenalex-snapshot
Phyllosticta species associated with citrus diseases in China
inferredcites →https://doi.org/10.1007/s13225-011-0145-6openalex-snapshot
Capnodiaceae
inferredcites →https://doi.org/10.1007/s13225-011-0146-5openalex-snapshot
Phyllosticta—an overview of current status of species recognition
inferredcites →https://doi.org/10.1007/s13225-012-0182-9openalex-snapshot
Phyllosticta species associated with freckle disease of banana
inferredcites →https://doi.org/10.1007/s13225-012-0207-4openalex-snapshot
Towards a natural classification of Botryosphaeriales
inferredcites →https://doi.org/10.1007/s13225-013-0235-8openalex-snapshot
Phyllosticta capitalensis, a widespread endophyte of plants
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PCR protocols — A guide to methods and applications
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AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
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Molecular phylogeny of Phoma and allied anamorph genera: Towards a reclassification of the Phoma complex
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Sphaeropsis sapinea and Botryosphaeria dothidea endophytic in Pinus spp. and Eucalyptus spp. in South Africa
inferredcites →https://doi.org/10.1016/s0254-6299(15)30597-4openalex-snapshot
Microfungi associated with Podocarpus leaf litter in South Africa
inferredcites →https://doi.org/10.1016/s0953-7562(09)81181-7openalex-snapshot
Mycosphaerella parkii and Phyllosticta eucalyptorum, two new species from Eucalyptus leaves in Brazil
inferredcites →https://doi.org/10.1038/138384a0openalex-snapshot
British Stem- and Leaf-Fungi (Coelomycetes)
inferredcites →https://doi.org/10.1071/ap05082openalex-snapshot
Hosts, species and genotypes: opinions versus data
inferredcites →https://doi.org/10.1071/ap07079openalex-snapshot
Preinfection behaviour ofPhyllosticta musarumon banana leaves
inferredcites →https://doi.org/10.1073/pnas.95.5.2044openalex-snapshot
Multiple evolutionary origins of the fungus causing Panama disease of banana: Concordant evidence from nuclear and mitochondrial gene genealogies
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Studies on Some Fungi from North-Western Wyoming. II. Fungi Imperfecti
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Some Amerosporous Ascomycetes on Ericaceae and Empetraceae
inferredcites →https://doi.org/10.1080/00275514.1982.12021470openalex-snapshot
Taxonomy of Phyllosticta Vaccinii (Coelomycetes) and a New Name for the True Anamorph of Botryosphaeria Vaccinii (Dothideales, Dothioraceae)
inferredcites →https://doi.org/10.1080/00275514.1995.12026524openalex-snapshot
Phylogenetic relationships in Ganoderma inferred from the internal transcribed spacers and 25S ribosomal DNA sequences
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A Method for Designing Primer Sets for Speciation Studies in Filamentous Ascomycetes
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A multigene phylogeny of the Dothideomycetes using four nuclear loci
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/sysbio/42.2.182openalex-snapshot
An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis
inferredcites →https://doi.org/10.1094/phyto.2002.92.5.464openalex-snapshot
Nonpathogenic Isolates of the Citrus Black Spot Fungus, Guignardia citricarpa, Identified as a Cosmopolitan Endophyte of Woody Plants, G. mangiferae (Phyllosticta capitalensis)
inferredcites →https://doi.org/10.1111/j.1364-3703.2011.00768.xopenalex-snapshot
One fungus, one name promotes progressive plant pathology
inferredcites →https://doi.org/10.1111/j.1439-0507.1998.tb00321.xopenalex-snapshot
Molecular diagnostics of clinical strains of filamentous Basidiomycetes
inferredcites →https://doi.org/10.1128/jb.172.8.4238-4246.1990openalex-snapshot
Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species
inferredcites →https://doi.org/10.1139/b79-158openalex-snapshot
Observations on Mucosetospora (Coelomycetes)
inferredcites →https://doi.org/10.1139/b86-230openalex-snapshot
Discochora yuccae sp. nov. with Phyllosticta and Leptodothiorella synanamorphs
inferredcites →https://doi.org/10.1139/b89-410openalex-snapshot
Species of Phyllosticta on conifers
inferredcites →https://doi.org/10.2307/1216075openalex-snapshot
REPORT OF THE COMMITTEE FOR FUNGI AND LICHENS 1964–1969
inferredcites →https://doi.org/10.2307/2992540openalex-snapshot
An Empirical Test of Bootstrapping as a Method for Assessing Confidence in Phylogenetic Analysis
inferredcites →https://doi.org/10.2307/3755769openalex-snapshot
Die Gattungen der amerosporen Pyrenomyceten
inferredcites →https://doi.org/10.2307/3758189openalex-snapshot
Studies in Phyllosticta I
inferredcites →https://doi.org/10.2307/3760908openalex-snapshot
Phylogenetic Relationships in Ganoderma Inferred from the Internal Transcribed Spacers and 25S Ribosomal DNA Sequences
inferredcites →https://doi.org/10.2307/3762016openalex-snapshot
Characterization of Diversity in Colletotrichum acutatum sensu lato by Sequence Analysis of Two Gene Introns, mtDNA and Intron RFLPs, and Mating Compatibility
inferredcites →https://doi.org/10.2307/3792629openalex-snapshot
Taxonomy of Phyllosticta vaccinii (Coelomycetes) and a New Name for the True Anamorph of Botryosphaeria vaccinii (Dothideales, Dothioraceae)
inferredcites →https://doi.org/10.3114/sim.2010.65.01openalex-snapshot
Highlights of the Didymellaceae: A polyphasic approach to characterise Phoma and related pleosporalean genera
inferredcites →https://doi.org/10.3114/sim.2011.68.11openalex-snapshot
Two new pathogenic ascomycetes in Guignardia and Rosenscheldiella on New Zealand's pygmy mistletoes (Korthalsella: Viscaceae)
inferredcites →https://doi.org/10.3114/sim.55.1.235openalex-snapshot
Phylogenetic lineages in the Botryosphaeriaceae
inferredcites →https://doi.org/10.3114/sim0004openalex-snapshot
Redisposition of phoma-like anamorphs in Pleosporales
inferredcites →https://doi.org/10.3114/sim0005openalex-snapshot
Phylogenetic lineages in Pseudocercospora
inferredcites →https://doi.org/10.3114/sim0012openalex-snapshot
Species concepts in Cercospora: spotting the weeds among the roses
inferredcites →https://doi.org/10.3114/sim0014openalex-snapshot
Colletotrichum – current status and future directions
inferredcites →https://doi.org/10.3114/sim0020openalex-snapshot
Phylogenetic lineages in the Botryosphaeriales: a systematic and evolutionary framework
inferredcites →https://doi.org/10.3767/003158508x340742openalex-snapshot
Resolving the phylogenetic and taxonomic status of dark-spored teleomorph genera in the Botryosphaeriaceae
inferredcites →https://doi.org/10.3767/003158510x548668openalex-snapshot
A case for re-inventory of Australia's plant pathogens
inferredcites →https://doi.org/10.3767/003158511x569169openalex-snapshot
Endophytic and pathogenic Phyllosticta species, with reference to those associated with Citrus Black Spot
inferredcites →https://doi.org/10.3767/003158512x645334openalex-snapshot
Polyphasic characterisation of three new Phyllosticta spp.
inferredcites →https://doi.org/10.3767/003158512x652633openalex-snapshot
Fungal Planet description sheets: 107–127
inferredcites →https://doi.org/10.3852/09-240openalex-snapshot
Systematic reappraisal of species in Phoma section Paraphoma , Pyrenochaeta and Pleurophoma
inferredcites →https://doi.org/10.3852/11-242openalex-snapshot
Molecular, proteomic and morphological characterization of the ascomycete Guignardia bidwellii, agent of grape black rot: a polyphasic approach to fungal identification
inferredcites →https://doi.org/10.3852/12-392openalex-snapshot
Typification and phylogenetic study of Phyllosticta ampelicida and P. vaccinii
inferredcites →https://doi.org/10.3852/mycologia.98.6.1041openalex-snapshot
A multigene phylogeny of the Dothideomycetes using four nuclear loci
inferredcites →https://doi.org/10.5169/seals-821061openalex-snapshot
Die Gattungen der amerosporen Pyrenomyceten
inferredcites →https://doi.org/10.5281/zenodo.16197769openalex-snapshot
Preliminary studies on the Dothideales in temperate North America
inferredcites →https://doi.org/10.5281/zenodo.16289189openalex-snapshot
Sur la dénomination botanique (Guignardia bidwellii) du black-rot
inferredcites →https://doi.org/10.5598/imafungus.2011.02.01.14openalex-snapshot
The Amsterdam Declaration on Fungal Nomenclature

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.188.3.2zenodo-depositor-declared
Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China
inferred← citeshttps://doi.org/10.11646/phytotaxa.202.2.1zenodo-depositor-declared
Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae
inferred← citeshttps://doi.org/10.11646/phytotaxa.653.1.2zenodo-depositor-declared
Morphological and multi-gene phylogenetic analyses of two new species of Phyllosticta (Phyllostictaceae, Botryosphaeriales) from Southwestern China
inferred← citeshttps://doi.org/10.11646/phytotaxa.678.3.1zenodo-depositor-declared
Phyllosticta cangshanensis sp. nov., an endophytic fungus from Rhododendron decorum in Cangshan Mountain, Yunnan Province, China
inferred← citeshttps://doi.org/10.3897/imafungus.16.168055zenodo-depositor-declared
Molecular and morphological characterization of four new Phyllosticta species (Botryosphaeriales, Phyllostictaceae): Genomic insights into evolutionary dynamics and metabolic adaptation
inferred← citeshttps://doi.org/10.3897/mycokeys.102.112815zenodo-depositor-declared
Morphology and multigene phylogeny reveal three new species of Distoseptispora (Distoseptisporales, Distoseptisporaceae) on palms (Arecaceae) from peatswamp areas in southern Thailand
inferred← citeshttps://doi.org/10.3897/mycokeys.106.122890zenodo-depositor-declared
New species and records of Botryosphaeriales (Dothideomycetes) associated with tree dieback in Beijing, China
inferred← citeshttps://doi.org/10.3897/mycokeys.118.153609zenodo-depositor-declared
Morphological and phylogenetic analysis reveal three new species Phyllosticta (Phyllostictaceae, Botryosphaeriales) in China
inferred← citeshttps://doi.org/10.1002/cbdv.202100314openalex-snapshot
Neuroprotective Activities of Constituents from Phyllosticta capitalensis, an Endophyte Fungus of Loropetalum chinense var. rubrum
inferred← citeshttps://doi.org/10.1007/978-3-030-35512-8_30-1openalex-snapshot
Diseases of Taro and Malanga
inferred← citeshttps://doi.org/10.1007/s00253-020-10880-wopenalex-snapshot
New multiplex conventional PCR and quadruplex real-time PCR assays for one-tube detection of Phyllosticta citricarpa, Elsinoë fawcettii, Elsinoë australis, and Pseudocercospora angolensis in Citrus: development and validation
inferred← citeshttps://doi.org/10.1007/s00284-026-04863-9openalex-snapshot
Effects of Host Taxonomic Relatedness on Colonisation Rates and Community Patterns of Foliar Endophytic Fungi in Zingiberaceae
inferred← citeshttps://doi.org/10.1007/s10343-025-01151-7openalex-snapshot
Morpho-molecular Characterization of Phyllosticta capitalensis, Causing Leaf Spot of Curry Leaf from West Bengal, India
inferred← citeshttps://doi.org/10.1007/s10658-016-1005-8openalex-snapshot
MAT gene idiomorphs suggest a heterothallic sexual cycle in the citrus pathogen Phyllosticta citricarpa
inferred← citeshttps://doi.org/10.1007/s10658-021-02453-yopenalex-snapshot
Polyphasic identification and MAT1-2 isolates of Phyllosticta citricarpa in Cuba
inferred← citeshttps://doi.org/10.1007/s10658-025-03057-6openalex-snapshot
Occurrence of Phyllosticta citricarpa and Phyllosticta citriasiana in EU imported Citrus spp. and its impact on diagnostics of citrus black spot on fruits
inferred← citeshttps://doi.org/10.1007/s11557-019-01532-zopenalex-snapshot
Botryosphaerialean fungi causing canker and dieback of tree hosts from Mount Yudu in China
inferred← citeshttps://doi.org/10.1007/s13225-013-0263-4openalex-snapshot
Families of Dothideomycetes
inferred← citeshttps://doi.org/10.1007/s13225-014-0279-4openalex-snapshot
Species of Lasiodiplodia associated with papaya stem-end rot in Brazil
inferred← citeshttps://doi.org/10.1007/s13225-014-0298-1openalex-snapshot
One stop shop: backbones trees for important phytopathogenic genera: I (2014)
inferred← citeshttps://doi.org/10.1007/s13225-014-0303-8openalex-snapshot
Dothideales
inferred← citeshttps://doi.org/10.1007/s13225-014-0309-2openalex-snapshot
Naming and outline of Dothideomycetes–2014 including proposals for the protection or suppression of generic names
inferred← citeshttps://doi.org/10.1007/s13225-015-0346-5openalex-snapshot
Fungal diversity notes 111–252—taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-016-0360-2openalex-snapshot
Taxonomy and phylogeny of dematiaceous coelomycetes
inferred← citeshttps://doi.org/10.1007/s13225-016-0368-7openalex-snapshot
Microfungi on Tectona grandis (teak) in Northern Thailand
inferred← citeshttps://doi.org/10.1007/s13225-016-0373-xopenalex-snapshot
Fungal diversity notes 367–490: taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-017-0378-0openalex-snapshot
Fungal diversity notes 491–602: taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-017-0386-0openalex-snapshot
Notes for genera: Ascomycota
inferred← citeshttps://doi.org/10.1007/s13225-018-0415-7openalex-snapshot
Thailand’s amazing diversity: up to 96% of fungi in northern Thailand may be novel
inferred← citeshttps://doi.org/10.1007/s13225-018-0416-6openalex-snapshot
Families in Botryosphaeriales: a phylogenetic, morphological and evolutionary perspective
inferred← citeshttps://doi.org/10.1007/s13225-019-00418-5openalex-snapshot
One stop shop II: taxonomic update with molecular phylogeny for important phytopathogenic genera: 26–50 (2019)
inferred← citeshttps://doi.org/10.1007/s13225-020-00439-5openalex-snapshot
Fungal diversity notes 1151–1276: taxonomic and phylogenetic contributions on genera and species of fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-020-00440-yopenalex-snapshot
Taxonomy and phylogeny of hyaline-spored coelomycetes
inferred← citeshttps://doi.org/10.1007/s13225-020-00462-6openalex-snapshot
Refined families of Dothideomycetes: orders and families incertae sedis in Dothideomycetes
inferred← citeshttps://doi.org/10.1007/s13225-021-00484-8openalex-snapshot
What is a species in fungal plant pathogens?
inferred← citeshttps://doi.org/10.1007/s13225-021-00485-7openalex-snapshot
Species concepts of Dothideomycetes: classification, phylogenetic inconsistencies and taxonomic standardization
inferred← citeshttps://doi.org/10.1007/s13225-022-00501-4openalex-snapshot
The numbers of fungi: are the most speciose genera truly diverse?
inferred← citeshttps://doi.org/10.1007/s13225-022-00513-0openalex-snapshot
Fungal diversity notes 1512–1610: taxonomic and phylogenetic contributions on genera and species of fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-023-00524-5openalex-snapshot
Ascomycetes from karst landscapes of Guizhou Province, China
inferred← citeshttps://doi.org/10.1007/s13225-024-00536-9openalex-snapshot
Current insights into palm fungi with emphasis on taxonomy and phylogeny
inferred← citeshttps://doi.org/10.1007/s13225-025-00554-1openalex-snapshot
A worldwide checklist and morpho-molecular systematics of fungi associated with pteridophytes
inferred← citeshttps://doi.org/10.1007/s13225-025-00562-1openalex-snapshot
Taxonomy, phylogeny, diversity and host preference of leaf litter inhabiting microfungi across six host species in northern Thailand
inferred← citeshttps://doi.org/10.1007/s13313-014-0284-9openalex-snapshot
Botryosphaeriaceae associated with diseases of mango (Mangifera indica)
inferred← citeshttps://doi.org/10.1007/s13313-019-00628-0openalex-snapshot
Phyllosticta capitalensis and P. paracapitalensis are endophytic fungi that show potential to inhibit pathogenic P. citricarpa on citrus
inferred← citeshttps://doi.org/10.1007/s13314-017-0263-4openalex-snapshot
Phyllosticta capitalensis causes black spot on persimmon (Diospyros kaki) fruit in Taiwan
inferred← citeshttps://doi.org/10.1007/s42770-019-00221-zopenalex-snapshot
Tibouchina granulosa (Vell.) Cogn (Melastomataceae) as source of endophytic fungi: isolation, identification, and antiprotozoal activity of metabolites from Phyllosticta capitalensis
inferred← citeshttps://doi.org/10.1016/j.cropro.2025.107436openalex-snapshot
First report of Phyllosticta capitalensis causing black leaf spot on Camellia oleifera in Hunan, China
inferred← citeshttps://doi.org/10.1016/j.fbr.2021.09.002openalex-snapshot
Next-generation sequencing provides important insights into the biology and evolution of the Botryosphaeriaceae
inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103444openalex-snapshot
Mating-type locus rearrangements and shifts in thallism states in Citrus-associated Phyllosticta species
inferred← citeshttps://doi.org/10.1016/j.fgb.2022.103727openalex-snapshot
Discerning the global phylogeographic distribution of Phyllosticta citricarpa by means of whole genome sequencing
inferred← citeshttps://doi.org/10.1016/j.fgb.2024.103925openalex-snapshot
Phyllosticta paracitricarpa is synonymous with the EU quarantine fungus P. citricarpa based on phylogenomic analyses
inferred← citeshttps://doi.org/10.1016/j.funbio.2014.08.006openalex-snapshot
Polyphasic characterization of four new plant pathogenic Phyllosticta species from China, Japan, and the United States
inferred← citeshttps://doi.org/10.1016/j.funbio.2015.06.003openalex-snapshot
The rise of Ramularia from the Mycosphaerella labyrinth
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.04.005openalex-snapshot
The new family Septorioideaceae, within the Botryosphaeriales and Septorioides strobi as a new species associated with needle defoliation of Pinus strobus in the United States
inferred← citeshttps://doi.org/10.1016/j.funbio.2016.11.001openalex-snapshot
Families, genera, and species of Botryosphaeriales
inferred← citeshttps://doi.org/10.1016/j.funbio.2017.02.002openalex-snapshot
Diversity in the Botryosphaeriales: Looking back, looking forward
inferred← citeshttps://doi.org/10.1016/j.funbio.2021.05.003openalex-snapshot
Carbon utilization and growth-inhibition of citrus-colonizing Phyllosticta species
inferred← citeshttps://doi.org/10.1016/j.microb.2026.100688openalex-snapshot
Endophytic Phyllosticta diversity in mangroves and its antimicrobial potential: Dominance of P. capitalensis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113918openalex-snapshot
Meroterpenoids with divers' rings systems from Phyllosticta capitalensis and their anti-inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.simyco.2015.10.002openalex-snapshot
Revision of the Massarineae ( Pleosporales , Dothideomycetes )
inferred← citeshttps://doi.org/10.1016/j.simyco.2017.05.003openalex-snapshot
First report of Phyllosticta citricarpa and description of two new species, P. paracapitalensis and P. paracitricarpa , from citrus in Europe
inferred← citeshttps://doi.org/10.1016/j.simyco.2018.04.002openalex-snapshot
Genera of phytopathogenic fungi: GOPHY 2
inferred← citeshttps://doi.org/10.1016/j.simyco.2019.08.001openalex-snapshot
Foliar pathogens of eucalypts
inferred← citeshttps://doi.org/10.1038/s41598-017-09157-6openalex-snapshot
Phytotoxic dioxolanones are potential virulence factors in the infection process of Guignardia bidwellii
inferred← citeshttps://doi.org/10.1038/s41598-025-86508-8openalex-snapshot
Study of endophytic fungi of Ipomoea pes-caprae reveals the superiority of in situ plant conservation over ex situ conservation from a mycological view
inferred← citeshttps://doi.org/10.1079/cabicompendium.120352openalex-snapshot
Phyllosticta citrimaxima
inferred← citeshttps://doi.org/10.1079/cabicompendium.26154openalex-snapshot
Guignardia citricarpa (citrus black spot)
inferred← citeshttps://doi.org/10.1080/12298093.2022.2038843openalex-snapshot
Two New Species and Three New Records of Ascomycetes in Korea
inferred← citeshttps://doi.org/10.1080/21501203.2023.2225552openalex-snapshot
Four new species of Phyllosticta from China based on morphological and phylogenetic characterization
inferred← citeshttps://doi.org/10.1093/g3journal/jkac061openalex-snapshot
Enemy or ally: a genomic approach to elucidate the lifestyle of Phyllosticta citrichinaensis
inferred← citeshttps://doi.org/10.1094/pdis-01-22-0164-pdnopenalex-snapshot
First Report of Leaf Spot Caused by Phyllosticta capitalensis on Illicium difengpi in China
inferred← citeshttps://doi.org/10.1094/pdis-04-25-0738-pdnopenalex-snapshot
First Report of Brown Leaf Spot Disease on Dendrobium denneanum Caused by Phyllosticta capitalensis in China
inferred← citeshttps://doi.org/10.1094/pdis-06-19-1232-pdnopenalex-snapshot
First Report of Leaf Spot on Oil Palm Caused by Phyllosticta capitalensis in Malaysia
inferred← citeshttps://doi.org/10.1094/pdis-07-22-1687-pdnopenalex-snapshot
First Report of Leaf Spot Caused by Phyllosticta capitalensis on Alpinia oxyphylla in China
inferred← citeshttps://doi.org/10.1094/pdis-07-25-1366-pdnopenalex-snapshot
First Report of Phyllosticta capitalensis Causing Leaf Blight on Quercus acutissima in China
inferred← citeshttps://doi.org/10.1094/pdis-08-23-1669-pdnopenalex-snapshot
First Report of Phyllosticta capitalensis Causing Leaf Spot in Hymenocallis littoralis in China
inferred← citeshttps://doi.org/10.1094/pdis-09-17-1374-pdnopenalex-snapshot
First Report of Citrus Black Spot Caused by Phyllosticta citricarpa in Angola
inferred← citeshttps://doi.org/10.1094/pdis-10-23-2155-pdnopenalex-snapshot
First Report of Leaf Spot on Asparagus cochinchinensis Caused by Phyllosticta citrichinaensis in China
inferred← citeshttps://doi.org/10.1094/pdis-11-19-2490-pdnopenalex-snapshot
First Report of Castor Dark Leaf Spot Caused by Phyllosticta capitalensis in Zhanjiang, China
inferred← citeshttps://doi.org/10.1094/pdis-11-22-2722-pdnopenalex-snapshot
First Report of Leaf Blotch Caused by Phyllosticta capitalensis on Daphne odora in China
inferred← citeshttps://doi.org/10.1094/phyto-05-20-0157-ropenalex-snapshot
Quantification of Colletotrichum fioriniae in Orchards and Deciduous Forests Indicates It Is Primarily a Leaf Endophyte
inferred← citeshttps://doi.org/10.1094/phyto-08-16-0292-ropenalex-snapshot
A Global Perspective on the Population Structure and Reproductive System ofPhyllosticta citricarpa
inferred← citeshttps://doi.org/10.1094/phyto-12-18-0451-ropenalex-snapshot
Genetic Diversity and Population Structure ofPhyllosticta citriasianain China
inferred← citeshttps://doi.org/10.1101/2020.04.14.040725openalex-snapshot
Mating-type locus rearrangement leads to shift from homothallism to heterothallism in Citrus -associated Phyllosticta species
inferred← citeshttps://doi.org/10.1111/efp.12630openalex-snapshot
Taxonomical re‐examination of the genus Phyllosticta —Parasitic fungi on Cupressaceae trees in Japan
inferred← citeshttps://doi.org/10.1111/epp.12555openalex-snapshot
Species‐specific real‐time PCR for diagnosis of Phyllosticta citricarpa on Citrus species
inferred← citeshttps://doi.org/10.1111/jph.13292openalex-snapshot
Geographic distribution, prevalence, and incidence of citrus black spot caused by Phyllosticta citricarpa in Tunisia
inferred← citeshttps://doi.org/10.1111/mpp.12861openalex-snapshot
Phyllosticta citricarpa and sister species of global importance to Citrus
inferred← citeshttps://doi.org/10.1111/nph.16709openalex-snapshot
Species diversity of fungal endophytes across a stress gradient for plants
inferred← citeshttps://doi.org/10.1111/plb.13598openalex-snapshot
Searching new targets for the control of Black Rot: following the role of host factors modulating the infection process of Phyllosticta ampelicida
inferred← citeshttps://doi.org/10.1111/ppa.13430openalex-snapshot
“Phytopathological strolls” in the dual context of COVID‐19 lockdown and IYPH2020: Transforming constraints into an opportunity for public education about plant pathogens
inferred← citeshttps://doi.org/10.1111/ppa.70094openalex-snapshot
Revealing Pathogens and Disease‐Associated Ascomycetes in Post‐Harvest Citrus and Psidium Fruits in Markets in Northern Thailand
inferred← citeshttps://doi.org/10.1146/annurev-phyto-080614-120245openalex-snapshot
Identifying and Naming Plant-Pathogenic Fungi: Past, Present, and Future
inferred← citeshttps://doi.org/10.1186/s12864-019-5911-yopenalex-snapshot
Comparative genome analysis of Phyllosticta citricarpa and Phyllosticta capitalensis, two fungi species that share the same host
inferred← citeshttps://doi.org/10.1264/jsme2.me18075openalex-snapshot
Diversity of Endophytic Fungi of the Coastal Plant Vitex rotundifolia in Taiwan
inferred← citeshttps://doi.org/10.14601/phytopathol_mediterr-16230openalex-snapshot
Trail of decryption of molecular research on Botryosphaeriaceae in woody plants
inferred← citeshttps://doi.org/10.15287/afr.2023.2492openalex-snapshot
A review of Botryosphaeriales in Venezuela with special reference to woody plants
inferred← citeshttps://doi.org/10.17102/sherubdoenme.16.2023.05openalex-snapshot
Study of Fungal Diseases of Ornamental Plants of Sherubtse College Campus, Kanglung
inferred← citeshttps://doi.org/10.24843/jbiounud.2024.v28.i02.p04openalex-snapshot
Identifikasi jamur endofit dari tumbuhan Sonneratia alba J. E. Smith dan potensi antagonisnya terhadap jamur Alternaria alternata (Fr.) Keissler
inferred← citeshttps://doi.org/10.2903/j.efsa.2014.3557openalex-snapshot
Scientific Opinion on the risk of Phyllosticta citricarpa (Guignardia citricarpa) for the EU territory with identification and evaluation of risk reduction options
inferred← citeshttps://doi.org/10.2903/sp.efsa.2025.en-9322openalex-snapshot
Phyllosticta citricarpa Pest Report to support ranking of EU candidate priority pests
inferred← citeshttps://doi.org/10.3114/fuse.2023.11.03openalex-snapshot
Phyllosticta rizhaoensis sp. nov. causing leaf blight of Ophiopogon japonicus in China
inferred← citeshttps://doi.org/10.3114/sim0020openalex-snapshot
Phylogenetic lineages in the Botryosphaeriales: a systematic and evolutionary framework
inferred← citeshttps://doi.org/10.3114/sim0021openalex-snapshot
The Botryosphaeriaceae: genera and species known from culture
inferred← citeshttps://doi.org/10.33619/2414-2948/110/26openalex-snapshot
Leaf Blotch of Horse Chestnut (Review)
inferred← citeshttps://doi.org/10.33687/phytopath.013.01.4712openalex-snapshot
Inventory, and Dissemination of Citrus Fungal Diseases in Benin
inferred← citeshttps://doi.org/10.3390/agriculture9120247openalex-snapshot
Endophytic Fungi of Citrus Plants
inferred← citeshttps://doi.org/10.3390/genes15010111openalex-snapshot
The Mitogenomic Characterization and Phylogenetic Analysis of the Plant Pathogen Phyllosticta yuccae
inferred← citeshttps://doi.org/10.3390/jof10010007openalex-snapshot
Morphological and Phylogenetic Analyses Reveal Three New Species of Phyllosticta (Botryosphaeriales, Phyllostictaceae) in China
inferred← citeshttps://doi.org/10.3390/jof4020042openalex-snapshot
Endophytic Mycoflora and Their Bioactive Compounds from Azadirachta Indica: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/jof7110893openalex-snapshot
Occurrence and Morpho-Molecular Identification of Botryosphaeriales Species from Guizhou Province, China
inferred← citeshttps://doi.org/10.3390/jof9020184openalex-snapshot
Re-Evaluating Botryosphaeriales: Ancestral State Reconstructions of Selected Characters and Evolution of Nutritional Modes
inferred← citeshttps://doi.org/10.3390/jof9040449openalex-snapshot
Clonal Expansion in Multiple Phyllosticta Species Causing Citrus Black Spot or Similar Symptoms in China
inferred← citeshttps://doi.org/10.37208/tgn27408openalex-snapshot
Daniel Alexander Boyd 1855-1928: a formidable amateur Scottish mycologist
inferred← citeshttps://doi.org/10.3767/003158514x685680openalex-snapshot
Fungal Planet description sheets: 281–319
inferred← citeshttps://doi.org/10.3767/003158515x685841openalex-snapshot
Caulicolous Botryosphaeriales from Thailand
inferred← citeshttps://doi.org/10.3767/003158515x690269openalex-snapshot
Fungal Planet description sheets: 371–399
inferred← citeshttps://doi.org/10.3767/003158516x694499openalex-snapshot
Fungal Planet description sheets: 469-557
inferred← citeshttps://doi.org/10.3767/persoonia.2019.42.11openalex-snapshot
Fungal Planet description sheets: 868–950
inferred← citeshttps://doi.org/10.3767/persoonia.2021.46.03openalex-snapshot
Evaluating species in Botryosphaeriales
inferred← citeshttps://doi.org/10.3897/mycokeys.32.23670openalex-snapshot
Identification of endophytic fungi from leaves of Pandanaceae based on their morphotypes and DNA sequence data from southern Thailand
inferred← citeshttps://doi.org/10.3897/mycokeys.33.23670openalex-snapshot
Identification of endophytic fungi from leaves of Pandanaceae based on their morphotypes and DNA sequence data from southern Thailand
inferred← citeshttps://doi.org/10.3897/mycokeys.73.54054openalex-snapshot
Neodactylariales, Neodactylariaceae (Dothideomycetes, Ascomycota): new order and family, with a new species from China
inferred← citeshttps://doi.org/10.3897/mycokeys.91.84803openalex-snapshot
Morphological and phylogenetic analyses reveal two new species and a new record of Phyllosticta (Botryosphaeriales, Phyllostictaceae) from Hainan, China
inferred← citeshttps://doi.org/10.3897/mycokeys.95.100414openalex-snapshot
Multi-gene phylogeny and morphology of two new Phyllosticta (Phyllostictaceae, Botryosphaeriales) species from China
inferred← citeshttps://doi.org/10.47371/mycosci.2022.12.004openalex-snapshot
Taxonomic re-examination of Japanese isolates of the genus Lasiodiplodia
inferred← citeshttps://doi.org/10.47371/mycosci.2025.07.006openalex-snapshot
ITS phylogeny reveals a wide host range and a high genetic diversity of endophytic Phyllosticta capitalensis in Indonesia
inferred← citeshttps://doi.org/10.5252/cryptogamie-mycologie2020v41a7openalex-snapshot
First Report of the Sexual Morph of Pseudofusicoccum adansoniae Pavlic, T.I.Burgess & M.J.Wingf. on Para Rubber
inferred← citeshttps://doi.org/10.5598/imafungus.2015.06.02.14openalex-snapshot
Recommended names for pleomorphic genera in Dothideomycetes
inferred← citeshttps://doi.org/10.5943/ajom/5/1/9openalex-snapshot
Checklist of ascomycetes recorded on eucalypts in Brazil (1976 2022)
inferred← citeshttps://doi.org/10.5943/cream/13/1/1openalex-snapshot
Bambusicolous fungi in Guangdong, China: establishing Apiospora magnispora sp. nov. (Apiosporaceae, Amphisphaeriales) based on morphological and molecular evidence
inferred← citeshttps://doi.org/10.5943/mycosphere/13/1/12openalex-snapshot
Morphology, phylogeny, host association and geography of fungi associated with plants of Annonaceae, Apocynaceae and Magnoliaceae
inferred← citeshttps://doi.org/10.5943/mycosphere/13/1/3openalex-snapshot
Mycosphere notes 345–386
inferred← citeshttps://doi.org/10.5943/mycosphere/13/1/6openalex-snapshot
Ten important forest fungal pathogens: a review on their emergence and biology
inferred← citeshttps://doi.org/10.5943/mycosphere/14/1/2openalex-snapshot
Morphology and multigene phylogeny reveal ten novel taxa in Ascomycota from terrestrial palm substrates (Arecaceae) in Thailand
inferred← citeshttps://doi.org/10.5943/mycosphere/7/11/3openalex-snapshot
Perspectives into the value of genera, families and orders in classification
inferred← citeshttps://doi.org/10.5943/mycosphere/8/10/11openalex-snapshot
Can ITS sequence data identify fungal endophytes from cultures? A case study from Rhizophora apiculata
inferred← citeshttps://doi.org/10.5943/mycosphere/si/1b/13openalex-snapshot
Botryosphaeriaceae: Current status of genera and species
inferred← citeshttps://doi.org/10.5943/mycosphere/si/1b/3openalex-snapshot
Mycosphere Essays 5: Is it important to name species of Botryosphaeriaceae?
inferred← citeshttps://doi.org/10.5943/sif/6/1/5openalex-snapshot
New host and geographic records of five pleosporalean hyphomycetes associated with Musa spp. (Banana)
inferred← citeshttps://doi.org/10.7717/peerj.16354openalex-snapshot
Harnessing the power of comparative genomics to support the distinction of sister species within Phyllosticta and development of highly specific detection of Phyllosticta citricarpa causing citrus black spot by real-time PCR
inferred← citeshttps://doi.org/10.7872/crym/v36.iss4.2015.419openalex-snapshot
The GenusMurispora
inferred← citeshttps://doi.org/10.9734/arrb/2024/v39i62087openalex-snapshot
Isolation, Identification and Characterization of Phyllosticta citricarpa Causing Citrus Black Spot Disease in Benin
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