On the public citation graph

Phylogenetic lineages in the Botryosphaeriales: a systematic and evolutionary framework

https://doi.org/10.3114/sim0020
0 signed · 347 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1006/lich.1999.0220openalex-snapshot
Pcr Primers for the Amplification of Mitochondrial Small Subunit Ribosomal DNA of Lichen-forming Ascomycetes
inferredcites →https://doi.org/10.1007/bf02464320openalex-snapshot
Fungal endophytes of Proteaceae, with particular emphasis on Botryosphaeria proteae
inferredcites →https://doi.org/10.1007/s10342-010-0424-xopenalex-snapshot
Diversity and pathogenicity of Botryosphaeriaceae on declining Ostrya carpinifolia in Slovenia and Italy following extreme weather conditions
inferredcites →https://doi.org/10.1007/s11046-005-0256-2openalex-snapshot
Morphology and phylogeny of Botryosphaeria dothidea causing fruit rot of olives
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
inferredcites →https://doi.org/10.1007/s13313-011-0060-zopenalex-snapshot
Distribution of Diplodia pinea and its genotypic diversity within asymptomatic Pinus patula trees
inferredcites →https://doi.org/10.1016/0169-5347(96)10006-9openalex-snapshot
Combining data in phylogenetic analysis
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.fbr.2010.03.001openalex-snapshot
Dating the molecular clock in fungi – how close are we?
inferredcites →https://doi.org/10.1016/j.fgb.2012.12.004openalex-snapshot
Phylogenetic analyses of RPB1 and RPB2 support a middle Cretaceous origin for a clade comprising all agriculturally and medically important fusaria
inferredcites →https://doi.org/10.1016/j.funbio.2011.04.002openalex-snapshot
Rock-inhabiting fungi originated during periods of dry climate in the late Devonian and middle Triassic
inferredcites →https://doi.org/10.1016/j.mycres.2007.03.004openalex-snapshot
A higher-level phylogenetic classification of the Fungi
inferredcites →https://doi.org/10.1016/j.mycres.2008.11.010openalex-snapshot
Botryosphaeriaceae from tuart (Eucalyptus gomphocephala) woodland, including descriptions of four new species
inferredcites →https://doi.org/10.1016/j.revpalbo.2013.07.002openalex-snapshot
Amber fossils of sooty moulds
inferredcites →https://doi.org/10.1016/j.ympev.2008.12.017openalex-snapshot
Multiple gene genealogies and phenotypic data reveal cryptic species of the Botryosphaeriaceae: A case study on the Neofusicoccum parvum/N. ribis complex
inferredcites →https://doi.org/10.1016/j.ympev.2011.04.026openalex-snapshot
Use of the Genealogical Sorting Index (GSI) to delineate species boundaries in the Neofusicoccum parvum–Neofusicoccum ribis species complex
inferredcites →https://doi.org/10.1016/s0007-1536(75)80036-2openalex-snapshot
Redisposition and descriptions of some Amphisphaeria species and a note on Macrovalsaria
inferredcites →https://doi.org/10.1017/s0953756205003989openalex-snapshot
Botryosphaeria species from Eucalyptus in Australia are pleoanamorphic, producing Dichomera synanamorphs in culture
inferredcites →https://doi.org/10.1038/nature05110openalex-snapshot
Reconstructing the early evolution of Fungi using a six-gene phylogeny
inferredcites →https://doi.org/10.1051/forest:2006040openalex-snapshot
Interactive effects of drought and pathogens in forest trees
inferredcites →https://doi.org/10.1071/ap09085openalex-snapshot
The opportunistic pathogen,Neofusicoccum australe, is responsible for crown dieback of peppermint (Agonis flexuosa) in Western Australia
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.0900906106openalex-snapshot
Plants with double genomes might have had a better chance to survive the Cretaceous–Tertiary extinction event
inferredcites →https://doi.org/10.1080/15572536.2006.11832614openalex-snapshot
Dating divergences in the Fungal Tree of Life: review and new analyses
inferredcites →https://doi.org/10.1080/15572536.2006.11832632openalex-snapshot
A multigene phylogeny of the Dothideomycetes using four nuclear loci
inferredcites →https://doi.org/10.1093/bib/bbn013openalex-snapshot
Recent developments in the MAFFT multiple sequence alignment program
inferredcites →https://doi.org/10.1093/molbev/mss075openalex-snapshot
Bayesian Phylogenetics with BEAUti and the BEAST 1.7
inferredcites →https://doi.org/10.1093/nar/gki352openalex-snapshot
PHYML Online--a web server for fast maximum likelihood-based phylogenetic inference
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025813openalex-snapshot
Can three incongruence tests predict when data should be combined?
inferredcites →https://doi.org/10.1093/sysbio/42.3.384openalex-snapshot
Partitioning and Combining Data in Phylogenetic Analysis
inferredcites →https://doi.org/10.1093/sysbio/44.4.570openalex-snapshot
Constructing a Significance Test for Incongruence
inferredcites →https://doi.org/10.1094/pd-75-0761openalex-snapshot
Biology and Control ofSphaeropsis sapineaonPinusSpecies in South Africa
inferredcites →https://doi.org/10.1111/ddi.12030openalex-snapshot
The challenge of understanding the origin, pathways and extent of fungal invasions: global populations of the Neofusicoccum parvum–N. ribis species complex
inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
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.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
inferredcites →https://doi.org/10.1128/aem.61.4.1323-1330.1995openalex-snapshot
Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes
inferredcites →https://doi.org/10.1186/1471-2105-4-6openalex-snapshot
GapCoder automates the use of indel characters in phylogenetic analysis
inferredcites →https://doi.org/10.1196/annals.1438.005openalex-snapshot
Origin and Early Evolution of Angiosperms
inferredcites →https://doi.org/10.2307/3759946openalex-snapshot
Westcott's Plant Disease Handbook
inferredcites →https://doi.org/10.2307/3761737openalex-snapshot
Relationships among Botryosphaeria Species and Associated Anamorphic Fungi Inferred from the Analyses of ITS and 5.8S rDNA Sequences
inferredcites →https://doi.org/10.2307/3761991openalex-snapshot
Combined Multiple Gene Genealogies and Phenotypic Characters Differentiate Several Species Previously Identified as Botryosphaeria dothidea
inferredcites →https://doi.org/10.2307/3762040openalex-snapshot
Circumscription of Botryosphaeria Species Associated with Proteaceae Based on Morphology and DNA Sequence Data
inferredcites →https://doi.org/10.3114/sim.2009.64.01openalex-snapshot
A class-wide phylogenetic assessment of Dothideomycetes
inferredcites →https://doi.org/10.3114/sim.55.1.235openalex-snapshot
Phylogenetic lineages in the Botryosphaeriaceae
inferredcites →https://doi.org/10.3114/sim0019openalex-snapshot
A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales)
inferredcites →https://doi.org/10.3114/sim0021openalex-snapshot
The Botryosphaeriaceae: genera and species known from culture
inferredcites →https://doi.org/10.3732/ajb.0900346openalex-snapshot
The age and diversification of the angiosperms re‐revisited
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/10.3767/003158508x372387openalex-snapshot
Species of Botryosphaeriaceae occurring on Proteaceae
inferredcites →https://doi.org/10.3767/003158508x380612openalex-snapshot
Foliicolous microfungi occurring on Encephalartos
inferredcites →https://doi.org/10.3767/003158509x467552openalex-snapshot
Barriopsis iraniana and Phaeobotryon cupressi: two new species of the Botryosphaeriaceae from trees in Iran
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/10.3767/003158512x658766openalex-snapshot
Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towards a monograph of the genus Kellermania
inferredcites →https://doi.org/10.3767/003158514x684780openalex-snapshot
Confronting the constraints of morphological taxonomy in the Botryosphaeriales
inferredcites →https://doi.org/10.3852/08-193openalex-snapshot
Molecular and phenotypic characterization of three phylogenetic species discovered within theNeofusicoccum parvum/N. ribiscomplex
inferredcites →https://doi.org/10.3852/mycologia.97.2.513openalex-snapshot
Two new species of Botryosphaeria with brown, 1-septate ascospores and Dothiorella anamorphs
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/10.5598/imafungus.2011.02.01.14openalex-snapshot
The Amsterdam Declaration on Fungal Nomenclature
inferredcites →https://doi.org/10.5860/choice.46-1250openalex-snapshot
Westcott's plant disease handbook

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.176.1.10zenodo-depositor-declared
Barriopsis tectonae sp. nov. a new species of Botryosphaeriaceae from Tectona grandis (teak) in Thailand
inferred← citeshttps://doi.org/10.11646/phytotaxa.183.1.2zenodo-depositor-declared
Camarosporium sensu stricto in Pleosporinae, Pleosporales with two new species
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.205.2.2zenodo-depositor-declared
Multigene phylogeny and morphology reveal Phaeobotryon rhois sp. nov. (Botryosphaeriales, Ascomycota)
inferred← citeshttps://doi.org/10.11646/phytotaxa.233.1.1zenodo-depositor-declared
Botryosphaeriaceae associated with Tectona grandis (teak) in Northern Thailand
inferred← citeshttps://doi.org/10.11646/phytotaxa.319.3.3zenodo-depositor-declared
Helicosporium luteosporum sp. nov. and Acanthohelicospora aurea (Tubeufiaceae, Tubeufiales) from terrestrial habitats
inferred← citeshttps://doi.org/10.11646/phytotaxa.333.2.5zenodo-depositor-declared
Spissiomyces endophytica (Dothideomycetes, Ascomycota), a new endophytic fungus from Thailand
inferred← citeshttps://doi.org/10.11646/phytotaxa.348.2.1zenodo-depositor-declared
Studies of botryosphaerialean fungi associated with canker and dieback of tree hosts in Dongling Mountain of China
inferred← citeshttps://doi.org/10.11646/phytotaxa.494.2.2zenodo-depositor-declared
Three new host records of endophytic Neofusicoccum species reported from Dendrobium orchid
inferred← citeshttps://doi.org/10.11646/phytotaxa.508.2.3zenodo-depositor-declared
Morpho-phylogenetic evidence reveals Lasiodiplodia chiangraiensis sp. nov. (Botryosphaeriaceae) associated with woody hosts in northern Thailand
inferred← citeshttps://doi.org/10.11646/phytotaxa.514.2.2zenodo-depositor-declared
Diplodia parva sp. nov., a novel species of the family Botryosphaeriaceae isolated from soil in Korea
inferred← citeshttps://doi.org/10.11646/phytotaxa.525.3.3zenodo-depositor-declared
Molecular phylogeny of Aplosporella abexaminans: a novel species revealing the second report of sexual-asexual connection in Aplosporellaceae (Botryosphaeriales) from India
inferred← citeshttps://doi.org/10.11646/phytotaxa.530.1.2zenodo-depositor-declared
New species, Parahelicomyces yunnanensis sp. nov. and Tubeufia nigroseptum sp. nov. from freshwater habitats in Yunnan, China
inferred← citeshttps://doi.org/10.11646/phytotaxa.564.1.2zenodo-depositor-declared
Two new species of Botryosphaeriaceae (Botryosphaeriales) and new host/geographical records
inferred← citeshttps://doi.org/10.11646/phytotaxa.583.3.1zenodo-depositor-declared
Interesting Botryosphaeria (Botryosphaeriaceae) associated with Magnolia species in Thailand: Additions of two new host records with their lifestyles
inferred← citeshttps://doi.org/10.11646/phytotaxa.627.1.1zenodo-depositor-declared
Botryosphaeriaceae on palms—a new species of Neodeightonia, N. chamaeropicola, and new records from diseased foliage of ornamental palms in Portugal
inferred← citeshttps://doi.org/10.3897/imafungus.16.147543zenodo-depositor-declared
Cryptic host-associated differentiation and diversity: unravelling the evolutionary dynamics of the plant pathogen Lasiodiplodia
inferred← citeshttps://doi.org/10.3897/imafungus.16.173033zenodo-depositor-declared
Pleurophragmium parvisporum (Ascomycota): One name, seven stories – a case highlighting the need for verification of strains from public culture collections
inferred← citeshttps://doi.org/10.3897/imafungus.17.176189zenodo-depositor-declared
Standardised sporulation methods for Diplodia, Lasiodiplodia and Neofusicoccum
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.130.183564zenodo-depositor-declared
Taxonomic novelties of Dothiorella and additions to Botryosphaeriaceae from Yunnan, China
inferred← citeshttps://doi.org/10.5252/cryptogamie-mycologie2020v41a7zenodo-depositor-declared
First Report of the Sexual Morph of Pseudofusicoccum adansoniae Pavlic, T.I.Burgess & M.J.Wingf. on Para Rubber
inferred← citeshttps://doi.org/10.1007/978-3-031-09293-0_8openalex-snapshot
Genomic Designing for Biotic Stress Resistance in Mulberry
inferred← citeshttps://doi.org/10.1007/978-3-031-81770-0_3openalex-snapshot
Botryosphaeria
inferred← citeshttps://doi.org/10.1007/978-3-319-29137-6_2openalex-snapshot
Recent Changes in Fungal Nomenclature and Their Impact on Naming of Microfungi
inferred← citeshttps://doi.org/10.1007/978-3-319-55804-2_15openalex-snapshot
Translating Endophyte Research to Applications: Prospects and Challenges
inferred← citeshttps://doi.org/10.1007/978-3-662-46011-5_6openalex-snapshot
6 Pezizomycotina: Dothideomycetes and Arthoniomycetes
inferred← citeshttps://doi.org/10.1007/s00203-024-04018-zopenalex-snapshot
Emergence of Lasiodiplodia theobromae induced leaf necrosis in tea (Camellia sinensis [L.] O. Kuntze) from India
inferred← citeshttps://doi.org/10.1007/s00253-020-10395-4openalex-snapshot
Fast and reliable molecular methods to detect fungal pathogens in woody plants
inferred← citeshttps://doi.org/10.1007/s00284-024-03954-9openalex-snapshot
Development of a Multiplex PCR Assay to Detect Neofusicoccum parvum and Botryosphaeria dothidea in Walnut
inferred← citeshttps://doi.org/10.1007/s10327-024-01187-zopenalex-snapshot
Lasiodiplodia species isolated from Theobroma cacao in the Philippines and their pathogenicity
inferred← citeshttps://doi.org/10.1007/s10342-017-1075-yopenalex-snapshot
Symptoms and fungi associated with elm trees decline in Iran
inferred← citeshttps://doi.org/10.1007/s10342-019-01200-7openalex-snapshot
Diversity and pathogenicity of Botryosphaeriaceae species on forest trees in the north of Iran
inferred← citeshttps://doi.org/10.1007/s10482-016-0659-8openalex-snapshot
Botryosphaeriaceae associated with the die-back of ornamental trees in the Western Balkans
inferred← citeshttps://doi.org/10.1007/s10658-016-0949-zopenalex-snapshot
Botryosphariaceae species associated with stem canker, die-back and fruit rot on apple in Uruguay
inferred← citeshttps://doi.org/10.1007/s10658-018-01640-8openalex-snapshot
Identification and characterization of Diplodia mutila, D. seriata, Phacidiopycnis washingtonensis and Phacidium lacerum obtained from apple (Malus x domestica) fruit rot in Maule Region, Chile
inferred← citeshttps://doi.org/10.1007/s10658-020-01945-7openalex-snapshot
Characterization of apple cultivar susceptibility to Neofusicoccum parvum Brazilian strains
inferred← citeshttps://doi.org/10.1007/s10658-020-01996-wopenalex-snapshot
Fungal pathogens associated with branch and trunk cankers of nut crops in Iran
inferred← citeshttps://doi.org/10.1007/s10658-021-02210-1openalex-snapshot
Virulence tests of Neofusicoccum parvum, Lasiodiplodia theobromae, and Phytophthora palmivora on Theobroma cacao
inferred← citeshttps://doi.org/10.1007/s10658-023-02743-7openalex-snapshot
Barberry (Berberis vulgaris L.) as an alternative host of grapevine fungal trunk pathogens
inferred← citeshttps://doi.org/10.1007/s10658-024-02847-8openalex-snapshot
Anthracnose and similar symptoms on mango leaves are caused by several other pathogenic fungi, including Colletotrichum spp.
inferred← citeshttps://doi.org/10.1007/s11046-021-00545-1openalex-snapshot
Genotyping and In Vitro Antifungal Susceptibility Profile of Neoscytalidium Species Isolates from Respiratory Tract
inferred← citeshttps://doi.org/10.1007/s11046-025-00964-4openalex-snapshot
A Systematic Review on the Emerging Fungal Pathogen Neoscytalidium Causing Infections Worldwide
inferred← citeshttps://doi.org/10.1007/s11557-016-1254-0openalex-snapshot
Bezerromycetales and Wiesneriomycetales ord. nov. (class Dothideomycetes), with two novel genera to accommodate endophytic fungi from Brazilian cactus
inferred← citeshttps://doi.org/10.1007/s11557-017-1270-8openalex-snapshot
The Genera of Fungi—G3: Aleurocystis, Blastacervulus, Clypeophysalospora, Licrostroma, Neohendersonia and Spumatoria
inferred← citeshttps://doi.org/10.1007/s11557-017-1280-6openalex-snapshot
Four new species of Tubeufia (Tubeufiaceae, Tubeufiales) from Thailand
inferred← citeshttps://doi.org/10.1007/s11557-017-1336-7openalex-snapshot
Molecular taxonomy of five species of microfungi on Alnus spp. from Italy
inferred← citeshttps://doi.org/10.1007/s11557-017-1365-2openalex-snapshot
Phylogenetic characterization of two novel Kamalomyces species in Tubeufiaceae (Tubeufiales)
inferred← citeshttps://doi.org/10.1007/s11557-017-1366-1openalex-snapshot
Multi-gene phylogenetic analyses reveals Neohelicosporium gen. nov. and five new species of helicosporous hyphomycetes from aquatic habitats
inferred← citeshttps://doi.org/10.1007/s11557-018-1423-4openalex-snapshot
Pileospora piceae gen. et sp. nov. (Septorioideaceae, Botryosphaeriales) from Picea rubens
inferred← citeshttps://doi.org/10.1007/s11557-018-1428-zopenalex-snapshot
Parastagonosporella fallopiae gen. et sp. nov. (Phaeosphaeriaceae) on Fallopia convolvulus from Iran
inferred← citeshttps://doi.org/10.1007/s11557-019-01480-8openalex-snapshot
Kevinhydea brevistipitata gen. et sp. nov. and Helicoma hydei sp. nov., (Tubeufiaceae) from decaying wood habitats
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/s11829-021-09853-1openalex-snapshot
Investigating gall midges (Asphondylia), associated microfungi and parasitoids in some chenopod plant hosts (Amaranthaceae) in south-eastern Australia
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/s13225-016-0366-9openalex-snapshot
Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-016-0367-8openalex-snapshot
Bambusicolous fungi
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/s13225-016-0371-zopenalex-snapshot
Microfungi on Tamarix
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/s13225-017-0389-xopenalex-snapshot
DISCOMYCETES: the apothecial representatives of the phylum Ascomycota
inferred← citeshttps://doi.org/10.1007/s13225-018-0408-6openalex-snapshot
Fungal diversity notes 840–928: micro-fungi associated with Pandanaceae
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/s13225-019-00421-wopenalex-snapshot
Fungal diversity notes 929–1035: taxonomic and phylogenetic contributions on genera and species of fungi
inferred← citeshttps://doi.org/10.1007/s13225-019-00429-2openalex-snapshot
Fungal diversity notes 1036–1150: taxonomic and phylogenetic contributions on genera and species of fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-019-00433-6openalex-snapshot
One stop shop III: taxonomic update with molecular phylogeny for important phytopathogenic genera: 51–75 (2019)
inferred← citeshttps://doi.org/10.1007/s13225-020-00440-yopenalex-snapshot
Taxonomy and phylogeny of hyaline-spored coelomycetes
inferred← citeshttps://doi.org/10.1007/s13225-020-00444-8openalex-snapshot
Taxonomic and phylogenetic contributions to fungi associated with the invasive weed Chromolaena odorata (Siam weed)
inferred← citeshttps://doi.org/10.1007/s13225-020-00461-7openalex-snapshot
Fungal diversity notes 1277–1386: taxonomic and phylogenetic contributions to fungal taxa
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/s13225-021-00474-wopenalex-snapshot
Taxonomic and phylogenetic contributions to Celtis formosana, Ficus ampelas, F. septica, Macaranga tanarius and Morus australis leaf litter inhabiting microfungi
inferred← citeshttps://doi.org/10.1007/s13225-021-00489-3openalex-snapshot
Fungal diversity notes 1387–1511: taxonomic and phylogenetic contributions on genera and species of fungal taxa
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/s13225-023-00522-7openalex-snapshot
Taxonomic monograph of epifoliar fungi
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/s13225-025-00562-1openalex-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/s13225-025-00564-zopenalex-snapshot
Taxonomy and phylogeny of lignicolous freshwater fungi from plateau lakes in Yunnan Province, China
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/s13313-014-0332-5openalex-snapshot
Dothiorella and Spencermartinsia, new species and records from grapevines in Australia
inferred← citeshttps://doi.org/10.1007/s13313-015-0367-2openalex-snapshot
Re-classification of the causal agent of white grain disorder on wheat as three separate species of Eutiarosporella
inferred← citeshttps://doi.org/10.1007/s13313-017-0516-xopenalex-snapshot
Diversity of tree-infecting Botryosphaeriales on native and non-native trees in South Africa and Namibia
inferred← citeshttps://doi.org/10.1007/s13313-018-0559-7openalex-snapshot
Australian cultures of Botryosphaeriaceae held in Queensland and Victoria plant pathology herbaria revisited
inferred← citeshttps://doi.org/10.1007/s13313-021-00797-xopenalex-snapshot
Botryosphaeriaceae species involved in crown and root rot of English ivy (Hedera helix L.)
inferred← citeshttps://doi.org/10.1007/s13314-024-00555-0openalex-snapshot
First report of Botryosphaeria dothidea causing fruit rot on Choerospondias axillaris in China
inferred← citeshttps://doi.org/10.1007/s40725-024-00236-2openalex-snapshot
The Pine Pathogen Diplodia sapinea: Expanding Frontiers
inferred← citeshttps://doi.org/10.1007/s41348-022-00591-xopenalex-snapshot
Occurrence of twig blight and branch dieback of walnut caused by Botryosphaeriaceae species in Turkey
inferred← citeshttps://doi.org/10.1007/s42161-020-00598-zopenalex-snapshot
Characterization and pathogenicity of fungal trunk pathogens associated with declining of neem (Azadirachta indica A. Juss) trees in Iran
inferred← citeshttps://doi.org/10.1016/b978-0-323-91872-5.00010-7openalex-snapshot
World of fungi and fungal ecosystems
inferred← citeshttps://doi.org/10.1016/b978-0-443-18694-3.00019-5openalex-snapshot
Dynamics of diseases and insect pests of cashew tree
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2019.04.015openalex-snapshot
An emerging problem affecting apple production: Neofusicoccum parvum. Aureobasidium pullulans L1 and L8 strains as an alternative control strategy
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.2018.03.003openalex-snapshot
Evolution of the mating types and mating strategies in prominent genera in the Botryosphaeriaceae
inferred← citeshttps://doi.org/10.1016/j.foreco.2017.06.044openalex-snapshot
Predicting current and future disease outbreaks of Diplodia sapinea shoot blight in Italy: species distribution models as a tool for forest management planning
inferred← citeshttps://doi.org/10.1016/j.funbio.2014.09.001openalex-snapshot
Phylogeny of ambrosia beetle symbionts in the genus Raffaelea
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.2016.09.005openalex-snapshot
Botryosphaeriaceae species associated with dieback and canker disease of bay laurel in northern California with the description of Dothiorella californica sp. nov.
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.2019.07.001openalex-snapshot
Botryosphaeriaceae associated with Acacia heterophylla (La Réunion) and Acacia koa (Hawaii)
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101552openalex-snapshot
Mango Microcosm: Unveiling the species diversity and pathogenic potential of fungi isolated from mango (Mangifera indica) in northern Thailand
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2022.104921openalex-snapshot
Survey and identification of coinfecting Botryosphaeriales causing stem canker diseases of Eucalyptus camaldulensis in Ethiopia
inferred← citeshttps://doi.org/10.1016/j.pmpp.2024.102445openalex-snapshot
Phytopathological investigations of collar rot of chia (Salvia hispanica L.) caused by Macrophomina phaseolina – A new host record from India
inferred← citeshttps://doi.org/10.1016/j.pmpp.2024.102474openalex-snapshot
Phylogeny, pathogenicity, and fungicide sensitivity of Botryosphaeriaceae fungi associated with Persian lime dieback in Sinaloa, Mexico
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102709openalex-snapshot
Detection of fungal trunk pathogens from wood tissues and pruning wood debris of olive trees in Iran
inferred← citeshttps://doi.org/10.1016/j.pmpp.2026.103506openalex-snapshot
Fungal species associated with trunk diseases of Russian olive (Elaeagnus angustifolia L.), a widely used windbreak and ornamental landscape tree in Iran
inferred← citeshttps://doi.org/10.1016/j.ram.2015.03.003openalex-snapshot
Caracterización morfológica y molecular de aislados de Macrophomina phaseolina asociados a caña de azúcar en México
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.2017.04.002openalex-snapshot
Genera of phytopathogenic fungi: GOPHY 1
inferred← citeshttps://doi.org/10.1016/j.simyco.2017.11.002openalex-snapshot
A preliminary account of the Cucurbitariaceae
inferred← citeshttps://doi.org/10.1016/j.simyco.2019.08.001openalex-snapshot
Foliar pathogens of eucalypts
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.01.009openalex-snapshot
Phytopathogen emergence in the genomics era
inferred← citeshttps://doi.org/10.1016/j.ufug.2017.04.009openalex-snapshot
Diversity, phylogeny and pathogenicity of Botryosphaeriaceae on non-native Eucalyptus grown in an urban environment: A case study
inferred← citeshttps://doi.org/10.1016/j.ufug.2022.127573openalex-snapshot
Sooty canker, a destructive disease of banyan (Ficus benghalensis L.) trees in landscapes of Kish Island (Iran)
inferred← citeshttps://doi.org/10.1016/j.ympev.2015.01.008openalex-snapshot
Phylogenetic analyses of eurotiomycetous endophytes reveal their close affinities to Chaetothyriales, Eurotiales, and a new order – Phaeomoniellales
inferred← citeshttps://doi.org/10.1038/s41598-022-13057-9openalex-snapshot
Lasiodiplodia theobromae as a causal pathogen of leaf blight, stem canker, and pod rot of Theobroma cacao in Malaysia
inferred← citeshttps://doi.org/10.1038/s41598-023-42534-yopenalex-snapshot
Morphological, pathogenic and genetic diversity in Diplodia seriata associated with black rot canker of apple in India
inferred← citeshttps://doi.org/10.1079/cabicompendium.9630openalex-snapshot
Diplodia seriata (grapevine trunk disease)
inferred← citeshttps://doi.org/10.1080/00275514.2020.1837566openalex-snapshot
Two new species and one new record of Xenosporium with ellipsoidal or ovoid conidia from Taiwan
inferred← citeshttps://doi.org/10.1080/07060661.2019.1569559openalex-snapshot
Lasiodiplodia theobromae and L. pseudotheobromae causing leaf necrosis on Camellia sinensis in Fujian Province, China
inferred← citeshttps://doi.org/10.1080/07060661.2026.2652368openalex-snapshot
Botryosphaeriaceae in woody hosts: detection, epidemiology, and integrated management strategies
inferred← citeshttps://doi.org/10.1080/10549811.2019.1673182openalex-snapshot
Susceptibility of Eucalyptus hybrid clones to Botryosphaeria canker in Uganda
inferred← citeshttps://doi.org/10.1080/15592324.2016.1197470openalex-snapshot
Tracking ancestral lineages and recent expansions of NBS-LRR genes in angiosperms
inferred← citeshttps://doi.org/10.1093/forestry/cpaf014openalex-snapshot
Identification, pathogenicity, and fungicide screening of Neofusicoccum parvum, causal agent of a new branch blight disease on Fujian cypress (Fokienia hodginsii)
inferred← citeshttps://doi.org/10.1093/mmy/myw034openalex-snapshot
Cutaneous murine model of infection caused by Neoscytalidium dimidiatum: a preliminary study of an emerging human pathogen
inferred← citeshttps://doi.org/10.1094/pbiomes-01-20-0004-ropenalex-snapshot
A Richer Community of Botryosphaeriaceae Within a Less Diverse Community of Fungal Endophytes in Grapevines than in Adjacent Forest Trees Revealed by a Mixed Metabarcoding Strategy
inferred← citeshttps://doi.org/10.1094/pbiomes-4-3openalex-snapshot
Full Issue PDF
inferred← citeshttps://doi.org/10.1094/pdis-01-20-0064-pdnopenalex-snapshot
Kellermania macrospora Causes Leaf Dieback of Yucca filifera in Queretaro, Mexico
inferred← citeshttps://doi.org/10.1094/pdis-02-25-0441-reopenalex-snapshot
Re-Evaluating the Etiology of Citrus “Dothiorella Gummosis” in Italy
inferred← citeshttps://doi.org/10.1094/pdis-03-16-0362-reopenalex-snapshot
Identification, Distribution, and Pathogenicity of Diatrypaceae and Botryosphaeriaceae Associated with Citrus Branch Canker in the Southern California Desert
inferred← citeshttps://doi.org/10.1094/pdis-03-19-0622-feopenalex-snapshot
Ecology and Epidemiology of Diseases of Nut Crops and Olives Caused by Botryosphaeriaceae Fungi in California and Spain
inferred← citeshttps://doi.org/10.1094/pdis-04-24-0831-reopenalex-snapshot
Characterization, Phylogenetic Analyses, and Pathogenicity of Eutiarosporella dactylidis on Sorghum in China
inferred← citeshttps://doi.org/10.1094/pdis-05-20-0977-reopenalex-snapshot
Morphological and Phylogenetic Resolution of Diplodia corticola and D. quercivora , Emerging Canker Pathogens of Oak ( Quercus spp.), in the United States
inferred← citeshttps://doi.org/10.1094/pdis-06-18-1036-reopenalex-snapshot
Phylogeny, Distribution, and Pathogenicity of Lasiodiplodia Species Associated With Cankers and Dieback Symptoms of Persian Lime in Mexico
inferred← citeshttps://doi.org/10.1094/pdis-07-14-0727-reopenalex-snapshot
Identification of Botryosphaeriaceae Species Causing Kiwifruit Rot in Sichuan Province, China
inferred← citeshttps://doi.org/10.1094/pdis-07-22-1519-pdnopenalex-snapshot
First Report of Neofusicoccum ribis Causing Stem Blight and Dieback of Blueberry (Vaccinium corymbosum) in Michigan
inferred← citeshttps://doi.org/10.1094/pdis-07-24-1404-sropenalex-snapshot
Identifying the Distribution and Causal Pathogens of Blueberry Stem Blight Disease in Alabama and Nearby States
inferred← citeshttps://doi.org/10.1094/pdis-07-25-1494-reopenalex-snapshot
Etiology and Epidemiology of Branch Dieback and Fruit Blight and Necrosis of English Walnut in France
inferred← citeshttps://doi.org/10.1094/pdis-09-15-0994-pdnopenalex-snapshot
First Report of Diplodia corticola Causing Decline of Red Oak (Quercus rubra) Trees in Maine
inferred← citeshttps://doi.org/10.1094/pdis-12-17-1967-reopenalex-snapshot
Neoscytalidium dimidiatum Causing Canker, Shoot Blight and Fruit Rot of Almond in California
inferred← citeshttps://doi.org/10.1094/phyto-07-21-0304-ropenalex-snapshot
Diversity of Botryosphaeriaceae and Diaporthe Species Associated with Postharvest Apple Fruit Decay in Serbia
inferred← citeshttps://doi.org/10.1094/phyto-11-21-0487-ropenalex-snapshot
The Effect of Temperature and Moisture on Colonization of Apple Fruit and Branches by Botryosphaeria dothidea
inferred← citeshttps://doi.org/10.1094/phyto-12-20-0551-ropenalex-snapshot
Progression of Symptoms Caused byBotryosphaeria dothideaon Apple Branches
inferred← citeshttps://doi.org/10.1104/pp.15.01487openalex-snapshot
Large-Scale Analyses of Angiosperm Nucleotide-Binding Site-Leucine-Rich Repeat Genes Reveal Three Anciently Diverged Classes with Distinct Evolutionary Patterns
inferred← citeshttps://doi.org/10.1111/efp.12109openalex-snapshot
Diplodia sapinea: the main fungal species involved in the colonization of pine shoots in Italy
inferred← citeshttps://doi.org/10.1111/efp.12410openalex-snapshot
Host specificity of co‐infecting Botryosphaeriaceae on ornamental and forest trees in the Western Balkans
inferred← citeshttps://doi.org/10.1111/efp.12824openalex-snapshot
Fungal pathogens associated with twig canker of shrub species in Tunisia: Considering the effect of the factors correlated
inferred← citeshttps://doi.org/10.1111/efp.70077openalex-snapshot
Diversity, Distribution and Host Range of Botryosphaeriaceae in China
inferred← citeshttps://doi.org/10.1111/jam.14828openalex-snapshot
Identification of Botryosphaeriaceae associated with stem‐end rot of mango ( Mangifera indica L.) in Malaysia
inferred← citeshttps://doi.org/10.1111/jph.13078openalex-snapshot
Diversity of Botryosphaeriaceae species causing stem canker and fruit rot in olive trees in Uruguay
inferred← citeshttps://doi.org/10.1111/lam.13293openalex-snapshot
A new collar rot disease of cowpea ( Vigna unguiculata ) caused by Aplosporella hesperidica in India
inferred← citeshttps://doi.org/10.1111/mpp.12495openalex-snapshot
Botryosphaeria dothidea : a latent pathogen of global importance to woody plant health
inferred← citeshttps://doi.org/10.1111/myc.12849openalex-snapshot
Identification and biofilm development by a new fungal keratitis aetiologic agent
inferred← citeshttps://doi.org/10.1111/ppa.12296openalex-snapshot
Intraspecific variation in Diplodia seriata isolates occurring on grapevines in Spain
inferred← citeshttps://doi.org/10.1111/ppa.12565openalex-snapshot
Diversity of genus Lasiodiplodia associated with perennial tropical fruit plants in northeastern Brazil
inferred← citeshttps://doi.org/10.1111/ppa.13060openalex-snapshot
Botryosphaeriaceae species causing dieback on Annonaceae in Brazil
inferred← citeshttps://doi.org/10.1111/ppa.13895openalex-snapshot
Botryosphaeria dothidea causes stem canker of Idesia polycarpa in China
inferred← citeshttps://doi.org/10.1139/cjm-2014-0134openalex-snapshot
Botryosphaeriales fungi produce extracellular enzymes with biotechnological potential
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/s12864-021-07902-wopenalex-snapshot
Increased abundance of secreted hydrolytic enzymes and secondary metabolite gene clusters define the genomes of latent plant pathogens in the Botryosphaeriaceae
inferred← citeshttps://doi.org/10.1186/s43008-020-00043-xopenalex-snapshot
Variation in Botryosphaeriaceae from Eucalyptus plantations in YunNan Province in southwestern China across a climatic gradient
inferred← citeshttps://doi.org/10.1371/journal.pone.0232448openalex-snapshot
Lasiodiplodia mitidjana sp. nov. and other Botryosphaeriaceae species causing branch canker and dieback of Citrus sinensis in Algeria
inferred← citeshttps://doi.org/10.14601/phytopathol_mediterr-13736openalex-snapshot
Genetic diversity in Macrophomina phaseolina, the causal agent of charcoal rot
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/10.14692/jfi.17.2.58-66openalex-snapshot
Keragaman Morfologi dan Molekuler Lasiodiplodia theobromae dari Tanaman Jeruk, Kakao, Karet, Manggis, dan Pisang
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/10.16955/bitkorb.646134openalex-snapshot
Türkiye’nin güneyinde asmada Botryosphaeria geriye ölüm hastalığına neden olan fungusların filogenetik ayrımı ve patojenisiteleri
inferred← citeshttps://doi.org/10.17221/82/2022-ppsopenalex-snapshot
Morphological and molecular characterization of Neoscytalidium isolates that cause canker and dieback in Eucalyptus and Chinaberry trees in Iraq
inferred← citeshttps://doi.org/10.17268/sci.agropecu.2021.068openalex-snapshot
Lasiodiplodiatheobromae(Pat.) Griffon & Maubl [(syn.) Botryodiplodia theobromae Pat] in the cocoa crop: symptoms, biological cycle,and strategies management
inferred← citeshttps://doi.org/10.17520/biods.2016314openalex-snapshot
Systematics and species diversity of botryosphaeriaceous fungi
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2851628/v1openalex-snapshot
Epityfication of Perisporiopsis struthanthi and Perisporiopsis lantanae, and the taxonomic implications for Perisporiopsidaceae, Perisporiopsis and Setophoma
inferred← citeshttps://doi.org/10.2174/2211550105666160504130322openalex-snapshot
Biological Control Through Fungal Endophytes: Gaps In Knowledge Hindering Success
inferred← citeshttps://doi.org/10.2298/pif2501001mopenalex-snapshot
Botryosphaeriaceae fungi on apple fruit - identification and sensitivity to fungicides and essential oils in vitro
inferred← citeshttps://doi.org/10.23902/trkjnat.863506openalex-snapshot
MOLECULAR IDENTIFICATION OF Diplodia seriata De Not. CAUSING DIEBACK EFFECT ON GRAPEVINES AND EVALUATION OF in vitro EFFICACY OF FIVE DIFFERENT SYNTHETIC FUNGICIDES AGAINST THIS DISEASE
inferred← citeshttps://doi.org/10.2903/j.efsa.2023.7737openalex-snapshot
Pest categorisation of Lasiodiplodia pseudotheobromae
inferred← citeshttps://doi.org/10.2903/j.efsa.2023.8001openalex-snapshot
Pest categorisation of Neoscytalidium dimidiatum
inferred← citeshttps://doi.org/10.2903/j.efsa.2023.8070openalex-snapshot
Pest categorisation of Diplodia bulgarica
inferred← citeshttps://doi.org/10.29133/yyutbd.964030openalex-snapshot
Identification and Pathogenicity of Neoscytalidium novaehollandiae, the Agent of Canker and Dieback in Almonds and In Vitro Activities of Some Fungicides
inferred← citeshttps://doi.org/10.29312/remexca.v12i3.2640openalex-snapshot
Reporte de Lasiodiplodia theobromae (Pat.) Griffon y Maubl. en árboles cítricos de Tamaulipas
inferred← citeshttps://doi.org/10.29312/remexca.v15i5.3745openalex-snapshot
Botryosphaeriaceae en el cultivo de aguacate
inferred← citeshttps://doi.org/10.3114/sim.2024.108.01openalex-snapshot
What are the 100 most cited fungal genera?
inferred← citeshttps://doi.org/10.3114/sim0019openalex-snapshot
A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales)
inferred← citeshttps://doi.org/10.3114/sim0021openalex-snapshot
The Botryosphaeriaceae: genera and species known from culture
inferred← citeshttps://doi.org/10.33687/phytopath.010.01.3447openalex-snapshot
Botryosphaeria Tree Fungal Pathogens and Their Diversity
inferred← citeshttps://doi.org/10.3389/fgene.2023.1103969openalex-snapshot
Population genomic analysis reveals geographic structure and climatic diversification for Macrophomina phaseolina isolated from soybean and dry bean across the United States, Puerto Rico, and Colombia
inferred← citeshttps://doi.org/10.3389/fmicb.2022.866085openalex-snapshot
Xylella fastidiosa Infection Reshapes Microbial Composition and Network Associations in the Xylem of Almond Trees
inferred← citeshttps://doi.org/10.3390/agriculture10100488openalex-snapshot
The Thin Line between Pathogenicity and Endophytism: The Case of Lasiodiplodia theobromae
inferred← citeshttps://doi.org/10.3390/agronomy12102553openalex-snapshot
Disease-Causing Agents in Cashew: A Review in a Tropical Cash Crop
inferred← citeshttps://doi.org/10.3390/f12030313openalex-snapshot
What Do We Know about Botryosphaeriaceae? An Overview of a Worldwide Cured Dataset
inferred← citeshttps://doi.org/10.3390/f12060695openalex-snapshot
Botryosphaeria Dothidea and Neofusicoccum Yunnanense Causing Canker and Die-Back of Sequoiadendron Giganteum in Croatia
inferred← citeshttps://doi.org/10.3390/f14050864openalex-snapshot
Species Diversity of Phaeobotryon Associated with Tree Canker and Dieback Diseases in Xinjiang, China
inferred← citeshttps://doi.org/10.3390/f8100367openalex-snapshot
Pine Nuts: A Review of Recent Sanitary Conditions and Market Development
showing the first 200 of 284
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.