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Population structure of the invasive forest pathogen H ymenoscyphus pseudoalbidus
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Invasion history and demographic pattern of C ryphonectria hypovirus 1 across E uropean populations of the chestnut blight fungus
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Systematics of Fraxinus (Oleaceae) and evolution of dioecy
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Species diversity and drivers of spread of alien fungi (sensu lato) in Europe with a particular focus on France
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Combining field epidemiological information and genetic data to comprehensively reconstruct the invasion history and the microevolution of the sudden oak death agent Phytophthora ramorum (Stramenopila: Oomycetes) in California
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Genetic variability of Chalara fraxinea, dieback cause of European ash (Fraxinus excelsior L.)
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Hymenoscyphus albidoides sp. nov. and H. pseudoalbidus from China
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STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method
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European ash (Fraxinus excelsior) dieback – A conservation biology challenge
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International plant trade associated risks: Laissez-faire or novel solutions
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Reproductive mode and life cycle of the ash dieback pathogen Hymenoscyphus pseudoalbidus
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Population structure of Hymenoscyphus pseudoalbidus and its genetic relationship to Hymenoscyphus albidus
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Molecular evidence for recent founder populations and human-mediated migration in the barley scald pathogen Rhynchosporium secalis
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Revealing cryptic spatial patterns in genetic variability by a new multivariate method
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Recent range expansion and agricultural landscape heterogeneity have only minimal effect on the spatial genetic structure of the plant pathogenic fungus Mycosphaerella fijiensis
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Epidemiological patterns at multiple spatial scales: an 11‐year study of a Triphragmium ulmariae– Filipendula ulmaria metapopulation
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spag e d i: a versatile computer program to analyse spatial genetic structure at the individual or population levels
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Responding to diseases caused by exotic tree pathogens.
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Intercontinental population structure of the chestnut blight fungus, Cryphonectria parasitica
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RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
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adegenet : a R package for the multivariate analysis of genetic markers
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ADZE: a rarefaction approach for counting alleles private to combinations of populations
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GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research—an update
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Description and Power Analysis of Two Tests for Detecting Recent Population Bottlenecks From Allele Frequency Data
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Genetic Differentiation and Estimation of Gene Flow from F -Statistics Under Isolation by Distance
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Inference of Population Structure Using Multilocus Genotype Data
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MULTILOCUS STRUCTURE OF NATURAL POPULATIONS OF HORDEUM SPONTANEUM
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Distortion of allele frequency distributions provides a test for recent population bottlenecks
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The Fate of Mutations Surfing on the Wave of a Range Expansion
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Microsatellite Null Alleles and Estimation of Population Differentiation
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MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
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Hypovirus Virulence and Vegetative Incompatibility in Populations of the Chestnut Blight Fungus
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Sequence and Simple-Sequence Repeat Analyses of the Fungal PathogenSeiridium cardinaleIndicate California Is the Most Likely Source of the Cypress Canker Epidemic for the Mediterranean Region
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Strong Genetic Differentiation Between North American and European Populations of Phytophthora alni subsp. uniformis
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The Population Genetics of Fungi: Tools and Techniques
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Natural infection of F raxinus excelsior seeds by C halara fraxinea
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AFLP analyses of C alifornia and M editerranean populations of S eiridium cardinale provide insights on its origin, biology and spread pathways
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On the longevity of H ymenoscyphus pseudoalbidus in petioles of F raxinus excelsior
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ENVIRONMENTAL CORRELATES OF POPULATION DIFFERENTIATION IN ATLANTIC HERRING
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Secrets of the subterranean pathosystem of Armillaria
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Ash dieback: pathogen spread and diurnal patterns of ascospore dispersal, with special emphasis on Norway*
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Contrasting patterns of nuclear microsatellite genetic structure of Fraxinus mandshurica var. japonica between northern and southern populations in Japan
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02209.xopenalex-snapshot
A simple method for the calculation of microsatellite genotype distances irrespective of ploidy level
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Genetic variation in eastern North American and putatively introduced populations of Ceratocystis fimbriata f. platani
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FAST‐TRACK: Integrating QTL mapping and genome scans towards the characterization of candidate loci under parallel selection in the lake whitefish (Coregonus clupeaformis)
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02568.xopenalex-snapshot
Streams over mountains: influence of riparian connectivity on gene flow in the Pacific jumping mouse ( Zapus trinotatus )
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02728.xopenalex-snapshot
Selective acquisition of novel mating type and vegetative incompatibility genes via interspecies gene transfer in the globally invading eukaryote Ophiostoma novo‐ulmi
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.02908.xopenalex-snapshot
Refugia, differentiation and postglacial migration in arctic‐alpine Eurasia, exemplified by the mountain avens ( Dryas octopetala L.)
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03067.xopenalex-snapshot
Site‐specific genetic divergence in parallel hybrid zones suggests nonallopatric evolution of reproductive barriers
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03538.xopenalex-snapshot
Founding events in species invasions: genetic variation, adaptive evolution, and the role of multiple introductions
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04089.xopenalex-snapshot
Ancient isolation and independent evolution of the three clonal lineages of the exotic sudden oak death pathogen Phytophthora ramorum
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04773.xopenalex-snapshot
Reconstructing routes of invasion using genetic data: why, how and so what?
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05556.xopenalex-snapshot
Disentangling the genetic origins of a plant pathogen during disease spread using an original molecular epidemiology approach
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05575.xopenalex-snapshot
The chestnut blight fungus world tour: successive introduction events from diverse origins in an invasive plant fungal pathogen
inferredcites →https://doi.org/10.1111/j.1365-3059.2012.02621.xopenalex-snapshot
Long‐distance dispersal and its influence on adaptation to host resistance in a heterogeneous landscape
inferredcites →https://doi.org/10.1111/j.1365-3059.2012.02665.xopenalex-snapshot
Genetic structure of populations of Rhizoctonia solani AG‐4 from five provinces in Iran
inferredcites →https://doi.org/10.1111/j.1420-9101.2012.02495.xopenalex-snapshot
Sex, outcrossing and mating types: unsolved questions in fungi and beyond
inferredcites →https://doi.org/10.1111/j.1439-0329.2010.00645.xopenalex-snapshot
Cryptic speciation in Hymenoscyphus albidus
inferredcites →https://doi.org/10.1111/j.1439-0329.2011.00751.xopenalex-snapshot
A molecular toolkit for population genetic investigations of the ash dieback pathogen Hymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1111/j.1461-0248.2012.01817.xopenalex-snapshot
Eight questions about invasions and ecosystem functioning
inferredcites →https://doi.org/10.1111/j.1469-185x.2010.00123.xopenalex-snapshot
Plant health and global change – some implications for landscape management
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04364.xopenalex-snapshot
Biogeographical patterns and determinants of invasion by forest pathogens in Europe
inferredcites →https://doi.org/10.1111/j.1471-8286.2005.01155.xopenalex-snapshot
genalex 6: genetic analysis in Excel. Population genetic software for teaching and research
inferredcites →https://doi.org/10.1111/j.1558-5646.1975.tb00807.xopenalex-snapshot
THE BOTTLENECK EFFECT AND GENETIC VARIABILITY IN POPULATIONS
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ANALYZING TABLES OF STATISTICAL TESTS
inferredcites →https://doi.org/10.1111/j.1755-0998.2008.02336.xopenalex-snapshot
Development and characterization of novel, polymorphic microsatellite markers for oat crown rust, Puccinia coronata
inferredcites →https://doi.org/10.1111/j.1755-0998.2009.02757.xopenalex-snapshot
Microsatellite size homoplasies and null alleles do not affect species diagnosis and population genetic analysis in a fungal species complex
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Spatial Contact Models for Ecological and Epidemic Spread
inferredcites →https://doi.org/10.1111/jph.12173openalex-snapshot
Genetic Variability of H ymenoscyphus pseudoalbidus on Ash Leaf Rachises in Leaf Litter of Forest Stands in P oland
inferredcites →https://doi.org/10.1111/mec.12452openalex-snapshot
Population genetic analyses provide insights on the introduction pathway and spread patterns of the North American forest pathogen Heterobasidion irregulare in Italy
inferredcites →https://doi.org/10.1111/mec.12631openalex-snapshot
Fungal evolutionary genomics provides insight into the mechanisms of adaptive divergence in eukaryotes
inferredcites →https://doi.org/10.1111/mpp.12071openalex-snapshot
Chaperones of the endoplasmic reticulum are required for Ve1 ‐mediated resistance to V erticillium
inferredcites →https://doi.org/10.1111/mpp.12073openalex-snapshot
H ymenoscyphus pseudoalbidus , the causal agent of E uropean ash dieback
inferredcites →https://doi.org/10.1111/nph.12415openalex-snapshot
Integrative invasion science: model systems, multi‐site studies, focused meta‐analysis and invasion syndromes
inferredcites →https://doi.org/10.1111/ppa.12196openalex-snapshot
The ash dieback crisis: genetic variation in resistance can prove a long‐term solution
inferredcites →https://doi.org/10.1126/science.1072678openalex-snapshot
Aerial Dispersal of Pathogens on the Global and Continental Scales and Its Impact on Plant Disease
inferredcites →https://doi.org/10.1126/science.1235773openalex-snapshot
The Consequence of Tree Pests and Diseases for Ecosystem Services
inferredcites →https://doi.org/10.1128/aem.64.8.2988-2994.1998openalex-snapshot
Genetics of Vegetative Incompatibility in Cryphonectria parasitica
inferredcites →https://doi.org/10.1139/b95-261openalex-snapshot
Population biology of the chestnut blight fungus,Cryphonectria parasitica
inferredcites →https://doi.org/10.1146/annurev-phyto-072910-095246openalex-snapshot
Evolution and Population Genetics of Exotic and Re-Emerging Pathogens: Novel Tools and Approaches
inferredcites →https://doi.org/10.1146/annurev-phyto-082712-102225openalex-snapshot
Biology, Epidemiology, and Control of Heterobasidion Species Worldwide
inferredcites →https://doi.org/10.1146/annurev.ecolsys.39.110707.173414openalex-snapshot
Genetic Consequences of Range Expansions
inferredcites →https://doi.org/10.1146/annurev.py.32.090194.003053openalex-snapshot
BIOLOGICAL CONTROL OF CHESTNUT BLIGHT IN EUROPE
inferredcites →https://doi.org/10.1177/117693430500100003openalex-snapshot
Arlequin (version 3.0): An integrated software package for population genetics data analysis
inferredcites →https://doi.org/10.2307/3760921openalex-snapshot
Intercontinental Population Structure of the Chestnut Blight Fungus, Cryphonectria parasitica
inferredcites →https://doi.org/10.3897/neobiota.14.3435openalex-snapshot
Support for major hypotheses in invasion biology is uneven and declining
inferredcites →https://doi.org/10.5248/122.25openalex-snapshot
Hymenoscyphus pseudoalbidus, the correct name for Lambertella albida reported from Japan
inferredcites →https://doi.org/10.5424/817openalex-snapshot
Molecular analysis of evolutionary changes in populations of Ophiostma novo-ulmi
inferredcites →https://doi.org/10.5897/jaerd12.055openalex-snapshot
Dieback of ash (Fraxinus excelsior and Fraxinus angustifolia) in Eastern Austria: Disease development on monitoring plots from 2007 to 2010
inferredcites →https://doi.org/10.5897/jaerd12.057openalex-snapshot
Ash dieback associated with Hymenoscyphus pseudoalbidus in forest nurseries in Austria
inferredcites →https://doi.org/10.7717/peerj.281openalex-snapshot
Poppr : an R package for genetic analysis of populations with clonal, partially clonal, and/or sexual reproduction
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/mycokeys.115.143994zenodo-depositor-declared
Three new species of Dicephalospora (Leotiomycetes, Helotiales) from Northern Thailand and Southwestern China
inferred← citeshttps://doi.org/10.1002/ece3.5239openalex-snapshot
Multiple introductions and population structure during the rapid expansion of the invasive Sahara mustard (Brassica tournefortii)
inferred← citeshttps://doi.org/10.1002/ece3.71513openalex-snapshot
Evolution of Thermal Plasticity in Hymenoscyphus fraxineus During Ash Dieback Expansion in Europe
inferred← citeshttps://doi.org/10.1002/ndr2.12054openalex-snapshot
First report of Hymenoscyphus fraxineus causing ash dieback in Spain
inferred← citeshttps://doi.org/10.1007/978-1-0716-2517-0_7openalex-snapshot
Invasive Alien Plant Pathogens: The Need of New Detection Methods
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Genome Evolution in Fungal Plant Pathogens: From Populations to Kingdom-Wide Dynamics
inferred← citeshttps://doi.org/10.1007/978-3-319-89833-9_11openalex-snapshot
Dieback of European Ash: What Can We Learn from the Microbial Community and Species-Specific Traits of Endophytic Fungi Associated with Ash?
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Forest Health in a Changing World
inferred← citeshttps://doi.org/10.1007/s00253-023-12480-wopenalex-snapshot
Applying molecular and genetic methods to trees and their fungal communities
inferred← citeshttps://doi.org/10.1007/s10342-016-1009-0openalex-snapshot
The susceptibility of Asian, European and North American Fraxinus species to the ash dieback pathogen Hymenoscyphus fraxineus reflects their phylogenetic history
inferred← citeshttps://doi.org/10.1007/s10530-015-0911-6openalex-snapshot
Genetic population structure of the invasive ash dieback pathogen Hymenoscyphus fraxineus in its expanding range
inferred← citeshttps://doi.org/10.1007/s10530-021-02716-zopenalex-snapshot
Expansion of Ash Dieback towards the scattered Fraxinus excelsior range of the Italian peninsula
inferred← citeshttps://doi.org/10.1007/s10530-023-03057-9openalex-snapshot
Evidence of a component Allee effect for an invasive pathogen: Hymenoscyphus fraxineus, the ash dieback agent
inferred← citeshttps://doi.org/10.1007/s10531-015-1019-0openalex-snapshot
Tree pests and diseases: the threat to biodiversity and the delivery of ecosystem services
inferred← citeshttps://doi.org/10.1007/s10531-019-01760-5openalex-snapshot
Soil microbiome: a key player for conservation of soil health under changing climate
inferred← citeshttps://doi.org/10.1007/s10531-019-01890-wopenalex-snapshot
Impact of Fraxinus excelsior dieback on biota of ash-associated lichen epiphytes at the landscape and community level
inferred← citeshttps://doi.org/10.1007/s10841-025-00647-xopenalex-snapshot
The genetic structure of the ash obligate moth prays fraxinella suggests that it is not affected by current habitat fragmentation
inferred← citeshttps://doi.org/10.1007/s10886-025-01678-zopenalex-snapshot
Constitutive Metabolite Profiling of European and Asian Fraxinus with Varying Susceptibility to Ash Dieback
inferred← citeshttps://doi.org/10.1007/s11557-015-1035-1openalex-snapshot
Hymenoscyphus fraxineus and two new Hymenoscyphus species identified in Korea
inferred← citeshttps://doi.org/10.1007/s11557-015-1041-3openalex-snapshot
Hymenoscyphus linearis sp. nov: another close relative of the ash dieback pathogen H. fraxineus
inferred← citeshttps://doi.org/10.1007/s11557-016-1209-5openalex-snapshot
The earliest samples of Hymenoscyphus albidus vs. H. fraxineus in Estonian mycological herbaria
inferred← citeshttps://doi.org/10.1007/s11557-020-01567-7openalex-snapshot
Phylogenetic revision of Petrakia and Seifertia (Melanommataceae, Pleosporales): new and rediscovered species from Europe and North America
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“Rädda Asken”: A scientific perspective on Sweden’s efforts to conserve Ash Fraxinus excelsior since 2013
inferred← citeshttps://doi.org/10.1007/s13595-015-0487-4openalex-snapshot
An evolutionary ecology perspective to address forest pathology challenges of today and tomorrow
inferred← citeshttps://doi.org/10.1007/s41348-022-00670-zopenalex-snapshot
FraxForFuture—research on European ash dieback in Germany
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The fungal predominance in stem collar necroses of Fraxinus excelsior: a study on Hymenoscyphus fraxineus multilocus genotypes
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Population dynamics of forest tree pathogens
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Genomic patterns and the evolutionary origin of an invasive fungal pathogen (Hymenoscyphus fraxineus) in Europe
inferred← citeshttps://doi.org/10.1016/j.fgb.2015.12.013openalex-snapshot
MAT – gene structure and mating behavior of Hymenoscyphus fraxineus and Hymenoscyphus albidus
inferred← citeshttps://doi.org/10.1016/j.foreco.2018.10.018openalex-snapshot
Is the introduction of novel exotic forest tree species a rational response to rapid environmental change? – A British perspective
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Development of a multiplex PCR assay to discriminate native Hymenoscyphus albidus and introduced Hymenoscyphus fraxineus in Britain and assess their distribution
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Insights into the pathways of spread and potential origins of Dothistroma septosporum in Britain
inferred← citeshttps://doi.org/10.1016/j.funeco.2019.03.009openalex-snapshot
Recombination and local population structure of the root endophytic fungus Glutinomyces brunneus based on microsatellite analyses
inferred← citeshttps://doi.org/10.1016/j.meegid.2014.09.001openalex-snapshot
Detection and genetic characterisation of a novel mycovirus in Hymenoscyphus fraxineus, the causal agent of ash dieback
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The life cycle of Hymenoscyphus fraxineus on Manchurian ash, Fraxinus mandshurica, in Japan
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WITHDRAWN: Systematics, ecology, and application of Helotiales: Recent progress and future perspectives for research with special emphasis activities within Japan
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Forestry stakeholders' perspectives on the prospects for restoring European ash in Sweden
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Phytopathogen emergence in the genomics era
inferred← citeshttps://doi.org/10.1016/j.virusres.2022.198901openalex-snapshot
Novel RNA viruses from the native range of Hymenoscyphus fraxineus, the causal fungal agent of ash dieback
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Genetic signatures of variation in population size in a native fungal pathogen after the recent massive plantation of its host tree
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The ash dieback invasion of Europe was founded by two genetically divergent individuals
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Friend or foe? Biological and ecological traits of the European ash dieback pathogen Hymenoscyphus fraxineus in its native environment
inferred← citeshttps://doi.org/10.1038/srep34638openalex-snapshot
A role for the asexual spores in infection of Fraxinus excelsior by the ash-dieback fungus Hymenoscyphus fraxineus
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A Threat to Holocene Resurgence Is a Threat to Livability
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Hymenoscyphus fraxineus mitovirus 1 naturally disperses through the airborne inoculum of its host, Hymenoscyphus fraxineus , in the Czech Republic
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Hymenoscyphus fraxineus vs. Hymenoscyphus albidus – A comparative light microscopic study on the causal agent of European ash dieback and related foliicolous, stroma-forming species
inferred← citeshttps://doi.org/10.1093/biosci/biac108openalex-snapshot
Approaches to Forecasting Damage by Invasive Forest Insects and Pathogens: A Cross-Assessment
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Current understanding and future prospects for ash dieback disease with a focus on Britain
inferred← citeshttps://doi.org/10.1093/forestry/cpaf038openalex-snapshot
Resistance and tolerance mechanisms of common ash ( Fraxinus excelsior ) against the ash dieback pathogen Hymenoscyphus fraxineus : latest advances and knowledge gaps
inferred← citeshttps://doi.org/10.1094/phyto-07-17-0252-ropenalex-snapshot
Changes inCryphonectria parasiticaPopulations Affect Natural Biological Control of Chestnut Blight
inferred← citeshttps://doi.org/10.1094/phyto-09-20-0405-ropenalex-snapshot
Temporal and Spatial Genetic Population Structure of Cryphonectria parasitica and Its Associated Hypovirus Across an Invasive Range of Chestnut Blight in Europe
inferred← citeshttps://doi.org/10.1094/phyto-09-23-0346-kcopenalex-snapshot
Possible Biological Control of Ash Dieback Using the Mycoparasite Hymenoscyphus Fraxineus Mitovirus 2
inferred← citeshttps://doi.org/10.1094/phyto-10-15-0271-ropenalex-snapshot
Genetic Analyses Suggest Separate Introductions of the Pine Pathogen Lecanosticta acicola Into Europe
inferred← citeshttps://doi.org/10.1094/phyto-10-24-0329-fiopenalex-snapshot
Population Genomic Analysis of Two Independent Clonal Invasions of the Sudden Oak Death Pathogen into One Forest
inferred← citeshttps://doi.org/10.1101/154492openalex-snapshot
“Genome-wide population diversity in Hymenoscyphus fraxineus points to an eastern Russian origin of European Ash dieback”
inferred← citeshttps://doi.org/10.1101/2022.10.17.512473openalex-snapshot
Evidences of a component Allee effect for an invasive pathogen: Hymenoscyphus fraxineus , the ash dieback agent
inferred← citeshttps://doi.org/10.1101/2023.03.03.530786openalex-snapshot
Possible biological control of ash dieback using the parasitic Hymenoscyphus fraxineus mitovirus 2?
inferred← citeshttps://doi.org/10.1111/1365-2745.12566openalex-snapshot
Biological Flora of the British Isles:Fraxinus excelsior
inferred← citeshttps://doi.org/10.1111/1365-2745.13383openalex-snapshot
Landscape epidemiology of ash dieback
inferred← citeshttps://doi.org/10.1111/1462-2920.13801openalex-snapshot
A distinct and genetically diverse lineage of the hybrid fungal pathogen Verticillium longisporum population causes stem striping in British oilseed rape
inferred← citeshttps://doi.org/10.1111/ecog.02855openalex-snapshot
Invasion of the Hawaiian Islands by a parasite infecting imperiled stream fishes
inferred← citeshttps://doi.org/10.1111/efp.12179openalex-snapshot
Genetic variation in dieback resistance in Fraxinus excelsior confirmed by progeny inoculation assay
inferred← citeshttps://doi.org/10.1111/efp.12182openalex-snapshot
Pathogenicity of Hymenoscyphus fraxineus and Hymenoscyphus albidus towards Fraxinus mandshurica var. japonica
inferred← citeshttps://doi.org/10.1111/efp.12185openalex-snapshot
Local population structure of H ymenoscyphus fraxineus surveyed by an enlarged set of microsatellite markers
inferred← citeshttps://doi.org/10.1111/efp.12236openalex-snapshot
Analyses of the ash dieback pathogen, H ymenoscyphus fraxineus, suggest role of tree species diversity on colonization and population structure differentiation
inferred← citeshttps://doi.org/10.1111/efp.12481openalex-snapshot
Hymenoscyphus pusillus , a new species on leaves of Fraxinus pennsylvanica in Poland
inferred← citeshttps://doi.org/10.1111/efp.12520openalex-snapshot
Fungal colonization patterns in necrotic rootstocks and stem bases of dieback‐affected Fraxinus excelsior L.
inferred← citeshttps://doi.org/10.1111/efp.12657openalex-snapshot
Aqueous leaf extract of Ligustrum vulgare inhibits ascospore germination and mycelial growth of Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.1111/ele.70394openalex-snapshot
Native‐Alien Dichotomy in Pathogen Genomics: Host Specialization Versus Environmental Decoupling
inferred← citeshttps://doi.org/10.1111/eva.12562openalex-snapshot
Planting exotic relatives has increased the threat posed by Dothistroma septosporum to the Caledonian pine populations of Scotland
inferred← citeshttps://doi.org/10.1111/eva.12853openalex-snapshot
Genomic biosurveillance of forest invasive alien enemies: A story written in code
inferred← citeshttps://doi.org/10.1111/mec.14048openalex-snapshot
Population genetic analysis of a parasitic mycovirus to infer the invasion history of its fungal host
inferred← citeshttps://doi.org/10.1111/nph.14204openalex-snapshot
Fungal diversity and seasonal succession in ash leaves infected by the invasive ascomycete Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.1111/ppa.12450openalex-snapshot
Virulence of Hymenoscyphus albidus and native and introduced Hymenoscyphus fraxineus on Fraxinus excelsior and Fraxinus pennsylvanica
inferred← citeshttps://doi.org/10.1111/ppa.12499openalex-snapshot
Pathogenicity of Hymenoscyphus fraxineus towards leaves of three European ash species: Fraxinus excelsior , F. angustifolia and F. ornus
inferred← citeshttps://doi.org/10.1111/ppa.12539openalex-snapshot
Ash dieback due to Hymenoscyphus fraxineus : what can be learnt from evolutionary ecology?
inferred← citeshttps://doi.org/10.1111/ppa.12588openalex-snapshot
Hymenoscyphus fraxineus is a leaf pathogen of local Fraxinus species in the Russian Far East
inferred← citeshttps://doi.org/10.1111/ppa.12635openalex-snapshot
Virulence of the invasive ash pathogen Hymenoscyphus fraxineus in old and recently established populations
inferred← citeshttps://doi.org/10.1111/ppa.12762openalex-snapshot
Population structure of the ash dieback pathogen, Hymenoscyphus fraxineus , in relation to its mode of arrival in the UK
inferred← citeshttps://doi.org/10.1111/ppa.13003openalex-snapshot
Limited genetic diversity across pathogen populations responsible for the global emergence of boxwood blight identified using SSR s
inferred← citeshttps://doi.org/10.1111/ppa.13876openalex-snapshot
Cryptic sexual reproduction in an emerging Eucalyptus shoot and foliar pathogen
inferred← citeshttps://doi.org/10.1111/ppa.14099openalex-snapshot
High Host Density Promotes Ash Dieback
inferred← citeshttps://doi.org/10.1126/article.1424677openalex-snapshot
Forest health in a changing world
inferred← citeshttps://doi.org/10.1128/9781555819583.ch17openalex-snapshot
Ecology of Fungal Plant Pathogens
inferred← citeshttps://doi.org/10.1128/9781555819583.ch38openalex-snapshot
Emerging Fungal Threats to Plants and Animals Challenge Agriculture and Ecosystem Resilience
inferred← citeshttps://doi.org/10.1128/microbiolspec.funk-0013-2016openalex-snapshot
Ecology of Fungal Plant Pathogens
inferred← citeshttps://doi.org/10.1128/microbiolspec.funk-0027-2016openalex-snapshot
Emerging Fungal Threats to Plants and Animals Challenge Agriculture and Ecosystem Resilience
inferred← citeshttps://doi.org/10.1139/cjfr-2015-0430openalex-snapshot
Genetic variation between and within two populations of Rhabdocline pseudotsugae in Germany
inferred← citeshttps://doi.org/10.1186/s12864-022-08363-5openalex-snapshot
Global invasion history of the emerging plant pathogen Phytophthora multivora
inferred← citeshttps://doi.org/10.1186/s12915-017-0376-4openalex-snapshot
NOXious gases and the unpredictability of emerging plant pathogens under climate change
inferred← citeshttps://doi.org/10.1186/s43008-023-00115-8openalex-snapshot
Endophytic fungi related to the ash dieback causal agent encode signatures of pathogenicity on European ash
inferred← citeshttps://doi.org/10.1371/journal.pone.0141592openalex-snapshot
Virulence of Hymenoscyphus albidus and H. fraxineus on Fraxinus excelsior and F. pennsylvanica
inferred← citeshttps://doi.org/10.1371/journal.pone.0141792openalex-snapshot
Genetic Differentiation and Spatial Structure of Phellinus noxius, the Causal Agent of Brown Root Rot of Woody Plants in Japan
inferred← citeshttps://doi.org/10.1371/journal.pone.0167104openalex-snapshot
Genetic Structure in the Northern Range Margins of Common Ash, Fraxinus excelsior L.
inferred← citeshttps://doi.org/10.1371/journal.ppat.1006381openalex-snapshot
Ash dieback epidemic in Europe: How can molecular technologies help?
inferred← citeshttps://doi.org/10.15177/seefor.22-03openalex-snapshot
Drivers of Forest Pathogen Invasions
inferred← citeshttps://doi.org/10.3389/ffgc.2023.1048971openalex-snapshot
Potential alternative tree species to Fraxinus excelsior in European forests
inferred← citeshttps://doi.org/10.3389/ffgc.2025.1588428openalex-snapshot
Point-of-care diagnostics and resistance phenotyping to combat ash dieback
inferred← citeshttps://doi.org/10.3389/fgene.2015.00208openalex-snapshot
Novel R tools for analysis of genome-wide population genetic data with emphasis on clonality
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02345openalex-snapshot
The Endophytic Mycobiome of European Ash and Sycamore Maple Leaves – Geographic Patterns, Host Specificity and Influence of Ash Dieback
inferred← citeshttps://doi.org/10.3390/d14080645openalex-snapshot
Three New Species of Dicephalospora (Helotiaceae, Helotiales) from Thailand
inferred← citeshttps://doi.org/10.3390/f16030506openalex-snapshot
Assessing Ash (Fraxinus excelsior L.) Dieback Dynamics in the Białowieża Forest, Poland, Using Bi-Temporal High-Resolution Remote Sensing Data
inferred← citeshttps://doi.org/10.3390/microorganisms14020395openalex-snapshot
Early-Stage Growth Restriction of Hymenoscyphus fraxineus on Tolerant Fraxinus excelsior Is Associated with Constitutive Chemical Defenses
inferred← citeshttps://doi.org/10.3390/v10110628openalex-snapshot
Detection of a Conspecific Mycovirus in Two Closely Related Native and Introduced Fungal Hosts and Evidence for Interspecific Virus Transmission
inferred← citeshttps://doi.org/10.3897/neobiota.62.52991openalex-snapshot
Harmonising the fields of invasion science and forest pathology
inferred← citeshttps://doi.org/10.4172/2168-9776.1000123openalex-snapshot
How do Size and Resource Availability Control Aboveground Biomass Allocation of Tree Seedlings?
inferred← citeshttps://doi.org/10.4172/2168-9776.1000131openalex-snapshot
Risk of Natural Spread of Hymenoscyphus fraxineus with Environmental Niche Modelling and Ensemble Forecasting Technique
inferred← citeshttps://doi.org/10.47371/mycosci.2020.05.002openalex-snapshot
Systematics, ecology, and application of Helotiales: Recent progress and future perspectives for research with special emphasis on activities within Japan
inferred← citeshttps://doi.org/10.5598/imafungus.2014.05.01.09openalex-snapshot
Hymenoscyphus fraxineus, the correct scientific name for the fungus causing ash dieback in Europe
inferred← citeshttps://doi.org/10.64898/2025.12.22.695959openalex-snapshot
Thermal plasticity of virulence differs between two latitudinally distant populations of the ash dieback pathogen
inferred← citeshttps://doi.org/10.70675/757a6433z8898z4332zbab4z8ccac2d8ecdfopenalex-snapshot
Épidémiologie de la chalarose du frêne, une maladie causée par l’agent pathogène Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.70675/f29cd56dz32c1z43a6z8cbbz031044d07ef9openalex-snapshot
Genetic architecture of the interactions between English oak (Quercus robur L.) and the microbial community of its phyllosphere
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