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Redisposition of phoma-like anamorphs in Pleosporales

https://doi.org/10.3114/sim0004
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Outgoing claims: the papers this work cites, builds on, or argues with.

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World-Wide Importance of Phoma Stem Canker (Leptosphaeria maculans and L. biglobosa) on Oilseed Rape (Brassica napus)
inferredcites →https://doi.org/10.1007/s13225-011-0117-xopenalex-snapshot
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inferredcites →https://doi.org/10.1016/0031-9422(94)00759-mopenalex-snapshot
Phomaligin a and other yellow pigments in Phoma lingam and P. wasabiae
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PCR protocols — A guide to methods and applications
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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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First record of Colletogloeopsis zuluense comb. nov., causing a stem canker of Eucalyptus in China
inferredcites →https://doi.org/10.1016/j.mycres.2007.08.014openalex-snapshot
The polyphyletic nature of Pleosporales: an example from Massariosphaeria based on rDNA and RBP2 gene phylogenies
inferredcites →https://doi.org/10.1016/j.mycres.2009.01.002openalex-snapshot
Molecular phylogeny of Phoma and allied anamorph genera: Towards a reclassification of the Phoma complex
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Studies on British pyrenomycetes
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Studies on British pyrenomycetes
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Species of Phoma Isolated from marine soils in India
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Notes on Phoma
inferredcites →https://doi.org/10.1016/s0007-1536(85)80080-2openalex-snapshot
Notes on Phoma 2
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inferredcites →https://doi.org/10.1017/s0953756203008554openalex-snapshot
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inferredcites →https://doi.org/10.1046/j.1365-3059.2001.00546.xopenalex-snapshot
Epidemiology and management of Leptosphaeria maculans (phoma stem canker) on oilseed rape in Australia, Canada and Europe
inferredcites →https://doi.org/10.1046/j.1365-3059.2002.00689.xopenalex-snapshot
Colonization of winter oilseed rape tissues by A/Tox + and B/Tox 0 Leptosphaeria maculans (phoma stem canker) in France and England
inferredcites →https://doi.org/10.1079/9780851997438.0000openalex-snapshot
Phoma identification manual. Differentiation of specific and infra-specific taxa in culture
inferredcites →https://doi.org/10.1080/00275514.1957.12024619openalex-snapshot
An Undescribed Species of Pyrenochaeta on Soybean
inferredcites →https://doi.org/10.1080/00275514.1999.12061051openalex-snapshot
A Method for Designing Primer Sets for Speciation Studies in Filamentous Ascomycetes
inferredcites →https://doi.org/10.1080/15572536.2003.11833191openalex-snapshot
Molecular Phylogeny of Leptosphaeria and Phaeosphaeria
inferredcites →https://doi.org/10.1093/bioinformatics/12.4.357openalex-snapshot
Tree View: An application to display phylogenetic trees on personal computers
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MRBAYES: Bayesian inference of phylogenetic trees
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Phaeohyphomycotic Cutaneous Disease Caused by Pleurophoma in a Cardiac Transplant Patient
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Loculoascomycete origins and evolution of filamentous ascomycete morphology based on 18S rRNA gene sequence data
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Genetic and Morphological Evidence that Phoma sclerotioides, Causal Agent of Brown Root Rot of Alfalfa, Is Composed of a Species Complex
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Occurrence of a New Subclade of Leptosphaeria biglobosa in Western Australia
inferredcites →https://doi.org/10.1111/j.1439-0507.1998.tb00321.xopenalex-snapshot
Molecular diagnostics of clinical strains of filamentous Basidiomycetes
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Are Melanomma pulvis-pyrius and Trematosphaeria pertusa congeneric?
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A Nomenclator of Leptosphaeria V. Cesati & G. de Notaris
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(1408‐1411) Proposals to conserve the names of four species of Fungi (Phomabetae, Helminthosporium avenae, Pyrenophora avenae, and Pleospora triticirepentis) against competing earlier synonyms
inferredcites →https://doi.org/10.2307/3755822openalex-snapshot
Etudes Taxonomiques sur les Pleosporacees
inferredcites →https://doi.org/10.2307/3756425openalex-snapshot
A World Monograph of the Genus Pleospora and Its Segregates
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Saccharicola, a New Genus for Two Leptosphaeria Species on Sugar Cane
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inferredcites →https://doi.org/10.3114/sim.2009.64.04openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2009.64.05openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2010.65.01openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2010.66.01openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2010.66.02openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2010.66.03openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2011.68.04openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.2011.68.05openalex-snapshot
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inferredcites →https://doi.org/10.3114/sim.55.1.235openalex-snapshot
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inferredcites →https://doi.org/10.3767/003158508x286842openalex-snapshot
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inferredcites →https://doi.org/10.3767/003158508x340742openalex-snapshot
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inferredcites →https://doi.org/10.3767/003158509x427808openalex-snapshot
Multiple Didymella teleomorphs are linked to the Phoma clematidina morphotype
inferredcites →https://doi.org/10.3767/003158509x479487openalex-snapshot
Unravelling Mycosphaerella: do you believe in genera?
inferredcites →https://doi.org/10.3852/08-071openalex-snapshot
Pleosporaspecies withStemphyliumanamorphs: a four locus phylogeny resolves new lineages yet does not distinguish among species in thePleospora herbarumclade
inferredcites →https://doi.org/10.3852/08-199openalex-snapshot
DNA phylogeny reveals polyphyly ofPhomasectionPeyronellaeaand multiple taxonomic novelties
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/mycologia.98.4.571openalex-snapshot
The family Pleosporaceae: intergeneric relationships and phylogenetic perspectives based on sequence analyses of partial 28S rDNA
inferredcites →https://doi.org/10.3929/ethz-a-000096214openalex-snapshot
Die schweizerischen Arten der Gattung Leptosphaeria und ihrer Verwandten
inferredcites →https://doi.org/10.5598/imafungus.2011.02.01.14openalex-snapshot
The Amsterdam Declaration on Fungal Nomenclature
inferredcites →https://doi.org/10.5962/p.415376openalex-snapshot
Contributions towards a monograph of Phoma (Coelomycetes) - V. Subdivision of the genus in sections
inferredcites →https://doi.org/10.5962/p.415814openalex-snapshot
Reexamination of species of Leptosphaeria on Asteraceous hosts

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Crassiparies yunnanensis sp. nov. (Neohendersoniaceae, Pleosporales) from dead twigs of Coffea arabica in China
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inferred← citeshttps://doi.org/10.11646/phytotaxa.568.2.2zenodo-depositor-declared
Microfungi associated with ornamental palms: Byssosphaeria phoenicis sp. nov. (Melanommataceae) and Pseudocoleophoma rhapidis sp. nov. (Dictyosporiaceae) from south China
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inferred← citeshttps://doi.org/10.11646/phytotaxa.663.3.2zenodo-depositor-declared
Stemphylium persianum sp. nov., (Pleosporales, Ascomycota) from Iran
inferred← citeshttps://doi.org/10.11646/phytotaxa.663.4.2zenodo-depositor-declared
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Hongkongmyces wuhanensis sp. nov. from freshwater habitats in Wuhan, China
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inferred← citeshttps://doi.org/10.3897/mycokeys.100.109423zenodo-depositor-declared
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Melanomma populicola Crous & R. K. Schumach
inferred← citeshttps://doi.org/10.1002/9781683670438.mcm0124openalex-snapshot
Fusarium and Other Opportunistic Hyaline Fungi
inferred← citeshttps://doi.org/10.1002/9781683670438.mcm0129openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781683674849.mcm0124openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781683674849.mcm0129openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ps.70643openalex-snapshot
Temporal dynamics of co‐inoculation of Leptosphaeria maculans and Leptosphaeria biglobosa determine interspecific competition and disease development on oilseed rape
inferred← citeshttps://doi.org/10.1002/ps.71339openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ps.7275openalex-snapshot
Leptosphaeria biglobosa inhibits the production of sirodesmin PL by L. maculans
inferred← citeshttps://doi.org/10.1002/ps.7401openalex-snapshot
Large‐scale population survey of Leptosphaeria maculans in France highlights both on‐going breakdowns and potentially effective resistance genes in oilseed rape
inferred← citeshttps://doi.org/10.1002/ps.7432openalex-snapshot
Leptosphaeria maculans isolates with variations in AvrLm1 and AvrLm4 effector genes induce differences in defence responses but not in resistance phenotypes in cultivars carrying the Rlm7 gene
inferred← citeshttps://doi.org/10.1002/ps.7799openalex-snapshot
Co‐inoculation timing affects the interspecific interactions between phoma stem canker pathogens Leptosphaeria maculans and Leptosphaeria biglobosa
inferred← citeshttps://doi.org/10.1002/ps.8926openalex-snapshot
Decreased DMI sensitivity of Plenodomus biglobosus (phoma of oilseed rape) associated with CYP51 substitution G476S
inferred← citeshttps://doi.org/10.1007/978-3-030-81218-8_1openalex-snapshot
The Genus Phoma: What We Know and What We Need to Know?
inferred← citeshttps://doi.org/10.1007/978-3-030-81218-8_18openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-030-81218-8_2openalex-snapshot
Taxonomical Evaluation of Phoma: History of Classification, Current Status and Future Directions
inferred← citeshttps://doi.org/10.1007/978-3-030-81218-8_8openalex-snapshot
Major Plant Diseases Caused by Phoma sensu lato Species and Their Integrated Management Strategies
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inferred← citeshttps://doi.org/10.1007/978-94-017-9020-8_12openalex-snapshot
Diagnosis of Plant Pathogens and Implications for Plant Quarantine: A Risk Assessment Perspective
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inferred← citeshttps://doi.org/10.1007/s00284-023-03238-8openalex-snapshot
Two Novel Species of Mesophoma gen. nov. from China
inferred← citeshttps://doi.org/10.1007/s00606-016-1350-2openalex-snapshot
Biatriospora (Ascomycota: Pleosporales) is an ecologically diverse genus including facultative marine fungi and endophytes with biotechnological potential
inferred← citeshttps://doi.org/10.1007/s10327-013-0480-4openalex-snapshot
Brown root rot of Russell prairie gentian caused by Subplenodomus drobnjacensis
inferred← citeshttps://doi.org/10.1007/s10327-021-01042-5openalex-snapshot
Foot rot disease of sweet potato in Japan caused by Diaporthe destruens: first report, pathogenicity and taxonomy
inferred← citeshttps://doi.org/10.1007/s10343-026-01418-7openalex-snapshot
First Report and Morpho-Molecular Characterization of Boeremia Exigua Causing Leaf Spot of Mungbean (Vigna Radiata (L.) Wilczek)
inferred← citeshttps://doi.org/10.1007/s10482-017-0966-8openalex-snapshot
Characterization of fungi causing lesion blight on Papaver dubium in Iran
inferred← citeshttps://doi.org/10.1007/s10658-021-02428-zopenalex-snapshot
Detection of the Phoma pathogens Plenodomus biglobosus subclades ‘brassicae’ and ‘canadensis’ on wasabi, and ‘canadensis’ in Europe
inferred← citeshttps://doi.org/10.1007/s10658-022-02498-7openalex-snapshot
Comparing the effectiveness of R genes in a 2-year canola–wheat rotation against Leptosphaeria maculans, the causal agent of blackleg disease in Brassica species
inferred← citeshttps://doi.org/10.1007/s11046-012-9608-xopenalex-snapshot
Molecular Identification of Melanised Non-Sporulating Moulds: A Useful Tool for Studying the Epidemiology of Phaeohyphomycosis
inferred← citeshttps://doi.org/10.1007/s11046-019-00379-yopenalex-snapshot
Long-Term Carriage of Medicopsis romeroi, an Agent of Black-Grain Mycetoma, Presenting as Phaeohyphomycosis in a Renal Transplant Patient
inferred← citeshttps://doi.org/10.1007/s11557-012-0887-xopenalex-snapshot
Description of Gibellulopsis chrysanthemi sp. nov. from leaves of garland chrysanthemum
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/s11557-017-1305-1openalex-snapshot
Biodiversity and chemotaxonomy of Preussia isolates from the Iberian Peninsula
inferred← citeshttps://doi.org/10.1007/s11557-017-1360-7openalex-snapshot
Allophoma hayatii sp. nov., an undescribed pathogenic fungus causing dieback of Lantana camara in Iran
inferred← citeshttps://doi.org/10.1007/s11557-019-01535-wopenalex-snapshot
Phylogenetic placement of Leptosphaeria polylepidis, a pathogen of Andean endemic Polylepis tarapacana, and its newly discovered mycoparasite Sajamaea mycophila gen. et sp. nov.
inferred← citeshttps://doi.org/10.1007/s11557-019-01546-7openalex-snapshot
In vitro inferred interactions of selected entomopathogenic fungi from Taiwan and eggs of Meloidogyne graminicola
inferred← citeshttps://doi.org/10.1007/s11557-020-01586-4openalex-snapshot
Prunus trees in Germany—a hideout of unknown fungi?
inferred← citeshttps://doi.org/10.1007/s11557-020-01623-2openalex-snapshot
Do mangrove habitats serve as a reservoir for Medicopsis romeroi, a clinically important fungus
inferred← citeshttps://doi.org/10.1007/s11557-020-01633-0openalex-snapshot
Two new species and a new record of Nigrograna (Nigrogranaceae, Pleosporales) from China and Thailand
inferred← citeshttps://doi.org/10.1007/s11557-022-01800-5openalex-snapshot
New species of the family Didymellaceae in Iran
inferred← citeshttps://doi.org/10.1007/s11557-022-01827-8openalex-snapshot
Pyrenochaeta fraxinina as colonizer of ash and sycamore petioles, its morphology, ecology, and phylogenetic connections
inferred← citeshttps://doi.org/10.1007/s11557-023-01888-3openalex-snapshot
Groenewaldia (Lentitheciaceae), a new corticolous fungal genus from India
inferred← citeshttps://doi.org/10.1007/s11557-025-02043-wopenalex-snapshot
Nigrograna andamanica sp. nov. from mangroves of Andaman Islands, India and keys for delineation of different species of Nigrograna
inferred← citeshttps://doi.org/10.1007/s11557-025-02050-xopenalex-snapshot
Four saprobic species associated with Mahonia in Guizhou Province, China
inferred← citeshttps://doi.org/10.1007/s11557-025-02077-0openalex-snapshot
Paraphoma rubrobrunnea sp. nov. and Paraphoma cirsii sp. nov. from Cirsium species and biological characterization of their phytotoxins
inferred← citeshttps://doi.org/10.1007/s11557-026-02125-3openalex-snapshot
New species of Epicoccum from Quercus brantii in Iran
inferred← citeshttps://doi.org/10.1007/s12223-023-01066-8openalex-snapshot
Taxonomic analysis reveals host preference of rare fungi in endophytes of Vitis vinifera from the Czech Republic
inferred← citeshttps://doi.org/10.1007/s12281-013-0139-9openalex-snapshot
Coelomycete Fungi in the Clinical Lab
inferred← citeshttps://doi.org/10.1007/s13225-013-0235-8openalex-snapshot
Phyllosticta capitalensis, a widespread endophyte of plants
inferred← citeshttps://doi.org/10.1007/s13225-013-0263-4openalex-snapshot
Families of Dothideomycetes
inferred← citeshttps://doi.org/10.1007/s13225-014-0305-6openalex-snapshot
A molecular phylogenetic reappraisal of the Didymosphaeriaceae (= Montagnulaceae)
inferred← citeshttps://doi.org/10.1007/s13225-014-0308-3openalex-snapshot
Revision of Phaeosphaeriaceae
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/s13225-015-0323-zopenalex-snapshot
Towards a natural classification and backbone tree for Pleosporaceae
inferred← citeshttps://doi.org/10.1007/s13225-015-0324-yopenalex-snapshot
Fungal diversity notes 1–110: taxonomic and phylogenetic contributions to fungal species
inferred← citeshttps://doi.org/10.1007/s13225-015-0339-4openalex-snapshot
Classification of marine Ascomycota, Basidiomycota, Blastocladiomycota and Chytridiomycota
inferred← citeshttps://doi.org/10.1007/s13225-015-0345-6openalex-snapshot
Phylogenetic insights resolve Dacampiaceae (Pleosporales) as polyphyletic: Didymocyrtis (Pleosporales, Phaeosphaeriaceae) with Phoma-like anamorphs resurrected and segregated from Polycoccum (Trypetheliales, Polycoccaceae fam. nov.)
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/s13225-015-0349-2openalex-snapshot
Revision and phylogeny of Leptosphaeriaceae
inferred← citeshttps://doi.org/10.1007/s13225-015-0350-9openalex-snapshot
Phylogenetic relationships and morphological reappraisal of Melanommataceae (Pleosporales)
inferred← citeshttps://doi.org/10.1007/s13225-015-0352-7openalex-snapshot
Towards a natural classification of Astrosphaeriella-like species; introducing Astrosphaeriellaceae and Pseudoastrosphaeriellaceae fam. nov. and Astrosphaeriellopsis, gen. nov.
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/s13225-016-0371-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/s13225-017-0391-3openalex-snapshot
Fungal diversity notes 603–708: taxonomic and phylogenetic notes on genera and species
inferred← citeshttps://doi.org/10.1007/s13225-017-0393-1openalex-snapshot
Towards a natural classification of Ophiobolus and ophiobolus-like taxa; introducing three novel genera Ophiobolopsis, Paraophiobolus and Pseudoophiobolus in Phaeosphaeriaceae (Pleosporales)
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/s13225-020-00439-5openalex-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/s13225-020-00444-8openalex-snapshot
Taxonomic and phylogenetic contributions to fungi associated with the invasive weed Chromolaena odorata (Siam weed)
inferred← citeshttps://doi.org/10.1007/s13225-020-00448-4openalex-snapshot
Microfungi associated with Clematis (Ranunculaceae) with an integrated approach to delimiting species boundaries
inferred← citeshttps://doi.org/10.1007/s13225-020-00463-5openalex-snapshot
Freshwater Dothideomycetes
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/s13225-021-00489-3openalex-snapshot
Fungal diversity notes 1387–1511: taxonomic and phylogenetic contributions on genera and species of fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-022-00502-3openalex-snapshot
The numbers of fungi: contributions from traditional taxonomic studies and challenges of metabarcoding
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/s13225-023-00529-0openalex-snapshot
Fungal diversity notes 1717–1817: taxonomic and phylogenetic contributions on genera and species of fungal taxa
inferred← citeshttps://doi.org/10.1007/s13225-024-00549-4openalex-snapshot
Micro-fungi in southern China and northern Thailand: emphasis on medicinal plants
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/s13225-025-00566-xopenalex-snapshot
Taxonomy and systematics of micro-fungi associated with Coffea in southern China and northern Thailand
inferred← citeshttps://doi.org/10.1007/s13313-012-0161-3openalex-snapshot
Stagonosporopsis spp. associated with ray blight disease of Asteraceae
inferred← citeshttps://doi.org/10.1007/s40858-017-0200-2openalex-snapshot
Phoma destructiva causing blight of tomato plants: a new fungal threat for tomato plantations in Brazil?
inferred← citeshttps://doi.org/10.1007/s40858-022-00491-3openalex-snapshot
Xenodidymella iranica sp. nov. and new hosts of X. glycyrrhizicola in Iran
inferred← citeshttps://doi.org/10.1007/s41348-023-00720-0openalex-snapshot
Phylogenetic analysis of Plenodomus lingam and Plenodomus biglobosus isolates in Hungary
inferred← citeshttps://doi.org/10.1007/s42161-018-0003-4openalex-snapshot
Molecular characterization of Boeremia strasseri the causal agent of black stems and rhizomes rot of peppermint
inferred← citeshttps://doi.org/10.1007/s42161-022-01068-4openalex-snapshot
Paraconiothyrium fuckelii, Diaporthe eres and Neocosmospora parceramosa causing cane blight of red raspberry in Northern Italy
inferred← citeshttps://doi.org/10.1007/s42161-023-01543-6openalex-snapshot
Green solutions and new technologies for sustainable management of fungus and oomycete diseases in the citrus fruit supply chain
inferred← citeshttps://doi.org/10.1016/j.biopha.2021.111958openalex-snapshot
Phloroglucinol prevents albumin glycation as well as diminishes ROS production, glycooxidative damage, nitrosative stress and inflammation in hepatocytes treated with high glucose
inferred← citeshttps://doi.org/10.1016/j.cropro.2024.106825openalex-snapshot
A portable fluorescence-based recombinase polymerase amplification assay for the detection of mal secco disease by Plenodomus tracheiphilus
inferred← citeshttps://doi.org/10.1016/j.cropro.2024.106889openalex-snapshot
Neocamarosporium betae causing leaf spot and stem necrosis disease on Chenopodium quinoa in Shanxi Province, China
inferred← citeshttps://doi.org/10.1016/j.funbio.2018.10.007openalex-snapshot
Occurrence of Phoma Sacc. in the phyllosphere of Neogene Siwalik forest of Arunachal sub-Himalaya and its palaeoecological implications
inferred← citeshttps://doi.org/10.1016/j.funbio.2019.02.001openalex-snapshot
Diversity of coelomycetous fungi in human infections: A 10-y experience of two European reference centres
inferred← citeshttps://doi.org/10.1016/j.funeco.2014.08.010openalex-snapshot
How many fungi make sclerotia?
inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100962openalex-snapshot
Fairy rings harbor distinct soil fungal communities and high fungal diversity in a montane grassland
inferred← citeshttps://doi.org/10.1016/j.idc.2024.11.005openalex-snapshot
Fungal Nomenclature
inferred← citeshttps://doi.org/10.1016/j.ijid.2020.04.028openalex-snapshot
Medicopsis romeroi nodular subcutaneous infection in a kidney transplant recipient
inferred← citeshttps://doi.org/10.1016/j.jdcr.2016.03.015openalex-snapshot
Cutaneous phaeohyphomycosis caused by Biatriospora mackinnonii in a renal transplant recipient
inferred← citeshttps://doi.org/10.1016/j.jprot.2020.103878openalex-snapshot
Proteome of the fungus Phoma macdonaldii, the causal agent of black stem of sunflower
inferred← citeshttps://doi.org/10.1016/j.ocsci.2023.02.001openalex-snapshot
First report of Leptosphaeria sclerotioides on Brassica napus in Northwestern China
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.2015.10.003openalex-snapshot
Resolving the Phoma enigma
inferred← citeshttps://doi.org/10.1016/j.simyco.2016.09.002openalex-snapshot
Hidden diversity in Thyridaria and a new circumscription of the Thyridariaceae
inferred← citeshttps://doi.org/10.1016/j.simyco.2016.11.008openalex-snapshot
Wood staining fungi revealed taxonomic novelties in Pezizomycotina: New order Superstratomycetales and new species Cyanodermella oleoligni
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.2017.06.001openalex-snapshot
Stemphylium revisited
inferred← citeshttps://doi.org/10.1016/j.simyco.2017.07.002openalex-snapshot
Pseudodidymellaceaefam. nov.: Phylogenetic affiliations of mycopappus-like genera inDothideomycetes
inferred← citeshttps://doi.org/10.1016/j.simyco.2017.08.001openalex-snapshot
Phylogenetic revision of Camarosporium ( Pleosporineae , Dothideomycetes ) and allied genera
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.2017.11.003openalex-snapshot
Coelomycetous Dothideomycetes with emphasis on the families Cucurbitariaceae and Didymellaceae
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/10.1016/j.simyco.2020.05.001openalex-snapshot
The phoma-like dilemma
inferred← citeshttps://doi.org/10.1016/j.soilbio.2026.110129openalex-snapshot
Rapid assembly and functional differentiation of the soil surface microbiome in temperate agricultural soil
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c09049openalex-snapshot
Multiomics Reveals Mechanisms of Alternaria oxytropis Inhibiting Pathogenic Fungi in Oxytropis ochrocephala
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00641openalex-snapshot
Campafungins: Inhibitors of Candida albicans and Cryptococcus neoformans Hyphal Growth
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00305openalex-snapshot
(±)-Nigronetides A−D and Nigronetides E−H, Complex Polyketides Produced by the Marine-Derived Fungus Nigrograna sp. M13
inferred← citeshttps://doi.org/10.1021/np500577vopenalex-snapshot
MDN-0104, an Antiplasmodial Betaine Lipid from Heterospora chenopodii
inferred← citeshttps://doi.org/10.1038/ja.2016.70openalex-snapshot
Paraphaeosphaeride D and berkleasmin F, new circumventors of arbekacin resistance in MRSA, produced by Paraphaeosphaeria sp. TR-022
inferred← citeshttps://doi.org/10.1042/bj20140268openalex-snapshot
Polyglycine hydrolases secreted by Pleosporineae fungi that target the linker region of plant class IV chitinases
inferred← citeshttps://doi.org/10.1063/5.0148440openalex-snapshot
Interaction of a promising bacterial antagonist strain 11-1 Bacillus sp. with the phoma rot pathogen Plenodomus lindquistii
inferred← citeshttps://doi.org/10.1071/cp15221openalex-snapshot
Blackleg disease of canola in Australia
inferred← citeshttps://doi.org/10.1071/cp16308openalex-snapshot
Analysis of Leptosphaeria species complex causing phoma leaf spot and stem canker of winter oilseed rape (Brassica napus) in the Czech Republic
inferred← citeshttps://doi.org/10.1079/cabicompendium.17687openalex-snapshot
Coniothyrium glycines (red leaf blotch)
inferred← citeshttps://doi.org/10.1080/00275514.2017.1387432openalex-snapshot
Brevicollum , a new genus in Neohendersoniaceae, Pleosporales
inferred← citeshttps://doi.org/10.1080/00275514.2024.2367470openalex-snapshot
Reappraisal of Didymella macrostoma causing white tip disease of Canada thistle as a new species, Didymella baileyae , sp. nov., and bioactivity of its major metabolites
inferred← citeshttps://doi.org/10.1080/00275514.2024.2383114openalex-snapshot
Phylogenetic analyses show the Select Agent Coniothyrium glycines represents a single species that has significant morphological and genetic variation
inferred← citeshttps://doi.org/10.1080/00275514.2025.2497588openalex-snapshot
Didymellaceae species associated with Convolvulaceae plants, with description of three new species
inferred← citeshttps://doi.org/10.1080/00275514.2025.2602414openalex-snapshot
Pleoscrubiaceae, a new family in Pleosporales (Dothideomycetes) from the Florida scrub ecosystem
inferred← citeshttps://doi.org/10.1080/00275514.2026.2677228openalex-snapshot
Phylogenomic analysis supports the transfer of Coniothyrium glycines , a soybean pathogen and USDA Select Agent, to the genus Aristastoma
inferred← citeshttps://doi.org/10.1080/0028825x.2023.2258583openalex-snapshot
Two new species and a new host record of Pleosporales (Dothideomycetes) from palm ( Arecaceae ) in Guangdong Province, China
inferred← citeshttps://doi.org/10.1080/0028825x.2023.2272957openalex-snapshot
Sexual morph of Allophoma tropica and Didymella coffeae-arabicae ( Didymellaceae , Pleosporales , Dothidiomycetes ), including novel host records from leaf litter in Thailand
inferred← citeshttps://doi.org/10.1080/07060661.2019.1620337openalex-snapshot
A real-time PCR assay for detection of light leaf spot onBrassicacrops in the Pacific Northwest of the USA
inferred← citeshttps://doi.org/10.1080/07060661.2026.2702309openalex-snapshot
Polyphasic characterization, pathogenicity and host range of Neocamarosporium betae causing quinoa stem rot in Saskatchewan, Canada
inferred← citeshttps://doi.org/10.1080/1040841x.2021.1933898openalex-snapshot
The genus Paraconiothyrium : species concepts, biological functions, and secondary metabolites
inferred← citeshttps://doi.org/10.1080/12298093.2024.2426840openalex-snapshot
Descriptions of 19 Unrecorded Species Belonging to Sordariomycetes in Korea
inferred← citeshttps://doi.org/10.1080/12298093.2026.2632471openalex-snapshot
Querciphoma phyllanthi-emblicae , a Novel Leaf Endophyte in Amla ( Phyllanthus emblica L.) from Yunnan, China
inferred← citeshttps://doi.org/10.1080/21501203.2015.1027507openalex-snapshot
Synopsis of Phyllosticta in China
inferred← citeshttps://doi.org/10.1080/21501203.2019.1700025openalex-snapshot
Molecular data reveals a new holomorphic marine fungus, Halobyssothecium estuariae , and the asexual morph of Keissleriella phragmiticola
inferred← citeshttps://doi.org/10.1080/26895293.2020.1835740openalex-snapshot
Molecular identification of fungal pathogens associated with leaf spot disease of date palms (Phoenix dactylifera)
inferred← citeshttps://doi.org/10.1093/ofid/ofac559openalex-snapshot
Fungal Nomenclature: Managing Change is the Name of the Game
inferred← citeshttps://doi.org/10.1093/ofid/ofw106openalex-snapshot
Ten-Year Experience of Cutaneous and/or Subcutaneous Infections Due to Coelomycetes in France
inferred← citeshttps://doi.org/10.1094/pdis-03-21-0665-reopenalex-snapshot
Black Leg and Chlorotic Leaf Spot Occurrence on Brassicaceae Crop and Weed Hosts
inferred← citeshttps://doi.org/10.1094/pdis-04-23-0645-reopenalex-snapshot
Characterization and Pathogenicity of Fungal Species Associated with Dieback of Apple Trees in Northern Italy
inferred← citeshttps://doi.org/10.1094/pdis-05-18-0905-reopenalex-snapshot
Applications of Next-Generation Sequencing for Large-Scale Pathogen Diagnoses in Soybean
inferred← citeshttps://doi.org/10.1094/pdis-05-21-1017-reopenalex-snapshot
Evaluation of Soybean Entries in the Pan-African Trials for Response to Coniothyrium glycines, the Cause of Red Leaf Blotch
inferred← citeshttps://doi.org/10.1094/pdis-09-16-1373-reopenalex-snapshot
Development of an Inoculation Technique and the Evaluation of Soybean Genotypes for Resistance to Coniothyrium glycines
inferred← citeshttps://doi.org/10.1094/pdis-09-18-1675-reopenalex-snapshot
Genetic Diversity and Differentiation in Phoma betae Populations on Table Beet in New York and Washington States
inferred← citeshttps://doi.org/10.1094/pdis-09-19-2042-reopenalex-snapshot
Identification, Pathogenicity, and Fungicide Sensitivity of Ascochyta caulina (Teleomorph: Neocamarosporium calvescens) Associated with Black Stem on Quinoa in China
inferred← citeshttps://doi.org/10.1094/pdis-10-14-0998-reopenalex-snapshot
Influence of Harvest Timing, Fungicides, and Beet necrotic yellow vein virus on Sugar Beet Storage
inferred← citeshttps://doi.org/10.1094/pdis-10-24-2201-sropenalex-snapshot
Characterization of Didymellaceae Leaf Spot Associated with Elymus Plants in the Tibetan Plateau of China
inferred← citeshttps://doi.org/10.1094/pdis-11-21-2506-reopenalex-snapshot
Control of Phoma Leaf Spot and Root Decay of Table Beet in New York
inferred← citeshttps://doi.org/10.1094/phyto-06-19-0195-ropenalex-snapshot
Spatial and Temporal Dynamics of Mal Secco Disease Spread in Lemon Orchards in Israel
inferred← citeshttps://doi.org/10.1094/phyto-11-19-0412-ropenalex-snapshot
Detection of Cercospora beticola and Phoma betae on Table Beet Seed using Quantitative PCR
inferred← citeshttps://doi.org/10.1094/phyto-11-20-0512-peropenalex-snapshot
Names of Phytopathogenic Fungi: A Practical Guide
inferred← citeshttps://doi.org/10.1094/phytofr-10-22-0113-aopenalex-snapshot
Genome Sequence Resources for Five Isolates of Coniothyrium glycines, Causal Pathogen of Red Leaf Blotch of Soybeans
inferred← citeshttps://doi.org/10.1094/phytofr-11-24-0128-fiopenalex-snapshot
Integrating In Silico and In Vitro Approaches for Detecting Coniothyrium glycines in High-Throughput Sequencing (HTS) Datasets Using EDNA-MiFi
inferred← citeshttps://doi.org/10.1097/ico.0000000000002676openalex-snapshot
A Case of Black Fungal Keratitis Caused by Biatriospora mackinnonii
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