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Ash dieback: From Asia to Europe

https://doi.org/10.1111/ppa.13859
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ndr2.12054openalex-snapshot
First report of Hymenoscyphus fraxineus causing ash dieback in Spain
inferredcites →https://doi.org/10.1002/ppp3.10060openalex-snapshot
The viability of a breeding programme for ash in the British Isles in the face of ash dieback
inferredcites →https://doi.org/10.1002/ppp3.11openalex-snapshot
Estimating mortality rates of European ash (Fraxinus excelsior) under the ash dieback (Hymenoscyphus fraxineus) epidemic
inferredcites →https://doi.org/10.1007/s00484-021-02211-zopenalex-snapshot
Meteorological factors associated with the timing and abundance of Hymenoscyphus fraxineus spore release
inferredcites →https://doi.org/10.1007/s00606-008-0005-3openalex-snapshot
Systematics of Fraxinus (Oleaceae) and evolution of dioecy
inferredcites →https://doi.org/10.1007/s10342-013-0717-yopenalex-snapshot
Temporal development of ash dieback symptoms and spatial distribution of collar rots in a provenance trial of Fraxinus excelsior
inferredcites →https://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
inferredcites →https://doi.org/10.1007/s10658-017-1179-8openalex-snapshot
Evaluation and validation of a loop-mediated isothermal amplification test kit for detection of Hymenoscyphus fraxineus
inferredcites →https://doi.org/10.1007/s10658-019-01814-yopenalex-snapshot
Endophytes vs tree pathogens and pests: can they be used as biological control agents to improve tree health?
inferredcites →https://doi.org/10.1007/s11557-010-0724-zopenalex-snapshot
Genetic variability of Chalara fraxinea, dieback cause of European ash (Fraxinus excelsior L.)
inferredcites →https://doi.org/10.1007/s13595-019-0799-xopenalex-snapshot
Negative correlation between ash dieback susceptibility and reproductive success: good news for European ash forests
inferredcites →https://doi.org/10.1007/s41348-023-00804-xopenalex-snapshot
Evaluation and identification of viruses for biocontrol of the ash dieback disease
inferredcites →https://doi.org/10.1016/j.agrformet.2011.06.019openalex-snapshot
Drought-sensitivity ranking of deciduous tree species based on thermal imaging of forest canopies
inferredcites →https://doi.org/10.1016/j.biocon.2012.08.026openalex-snapshot
European ash (Fraxinus excelsior) dieback – A conservation biology challenge
inferredcites →https://doi.org/10.1016/j.biocon.2014.04.019openalex-snapshot
Ash dieback in the UK: A review of the ecological and conservation implications and potential management options
inferredcites →https://doi.org/10.1016/j.biocon.2020.108516openalex-snapshot
Ash dieback risks an extinction cascade
inferredcites →https://doi.org/10.1016/j.cub.2019.03.033openalex-snapshot
The £15 billion cost of ash dieback in Britain
inferredcites →https://doi.org/10.1016/j.ecolecon.2009.09.004openalex-snapshot
Cost of potential emerald ash borer damage in U.S. communities, 2009–2019
inferredcites →https://doi.org/10.1016/j.fgb.2012.08.008openalex-snapshot
Reproductive mode and life cycle of the ash dieback pathogen Hymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1016/j.foreco.2016.09.032openalex-snapshot
Drivers of emerging fungal diseases of forest trees
inferredcites →https://doi.org/10.1016/j.foreco.2021.119177openalex-snapshot
Combined progress in symptoms caused by Hymenoscyphus fraxineus and Armillaria species, and corresponding mortality in young and old ash trees
inferredcites →https://doi.org/10.1016/j.funbio.2017.11.002openalex-snapshot
Fungal communities associated with species of Fraxinus tolerant to ash dieback, and their potential for biological control
inferredcites →https://doi.org/10.1016/j.funeco.2013.03.008openalex-snapshot
The invasive ash dieback pathogen Hymenoscyphus pseudoalbidus exerts maximal infection pressure prior to the onset of host leaf senescence
inferredcites →https://doi.org/10.1016/j.tree.2004.07.021openalex-snapshot
Emerging infectious diseases of plants: pathogen pollution, climate change and agrotechnology drivers
inferredcites →https://doi.org/10.1016/j.ufug.2006.03.002openalex-snapshot
An assessment of the drought tolerance of Fraxinus genotypes for urban landscape plantings
inferredcites →https://doi.org/10.1016/j.ufug.2017.06.017openalex-snapshot
Can pruning help maintain vitality of ash trees affected by ash dieback in urban landscapes?
inferredcites →https://doi.org/10.1017/s037689290000357xopenalex-snapshot
Dutch Elm Disease: A Review of the History, Environmental Implications, Control, and Research Needs
inferredcites →https://doi.org/10.1038/hdy.2010.119openalex-snapshot
Presence of natural genetic resistance in Fraxinus excelsior (Oleraceae) to Chalara fraxinea (Ascomycota): an emerging infectious disease
inferredcites →https://doi.org/10.1038/nature20786openalex-snapshot
Genome sequence and genetic diversity of European ash trees
inferredcites →https://doi.org/10.1038/s41558-021-01104-8openalex-snapshot
Plant pathogen infection risk tracks global crop yields under climate change
inferredcites →https://doi.org/10.1038/s41559-018-0548-9openalex-snapshot
The ash dieback invasion of Europe was founded by two genetically divergent individuals
inferredcites →https://doi.org/10.1038/s41559-019-1036-6openalex-snapshot
Genomic basis of European ash tree resistance to ash dieback fungus
inferredcites →https://doi.org/10.1038/s41598-017-16706-6openalex-snapshot
A first assessment of Fraxinus excelsior (common ash) susceptibility to Hymenoscyphus fraxineus (ash dieback) throughout the British Isles
inferredcites →https://doi.org/10.1038/s41598-020-61990-4openalex-snapshot
The invasive forest pathogen Hymenoscyphus fraxineus boosts mortality and triggers niche replacement of European ash (Fraxinus excelsior)
inferredcites →https://doi.org/10.1038/s43016-020-0075-0openalex-snapshot
Threats to global food security from emerging fungal and oomycete crop pathogens
inferredcites →https://doi.org/10.1038/srep19335openalex-snapshot
Molecular markers for tolerance of European ash (Fraxinus excelsior) to dieback disease identified using Associative Transcriptomics
inferredcites →https://doi.org/10.1038/srep21895openalex-snapshot
Friend or foe? Biological and ecological traits of the European ash dieback pathogen Hymenoscyphus fraxineus in its native environment
inferredcites →https://doi.org/10.1038/srep34638openalex-snapshot
A role for the asexual spores in infection of Fraxinus excelsior by the ash-dieback fungus Hymenoscyphus fraxineus
inferredcites →https://doi.org/10.1046/j.1439-0329.2002.00301.xopenalex-snapshot
Fungi associated with necrotic apical parts of Fraxinus excelsior shoots
inferredcites →https://doi.org/10.1073/pnas.2022239118openalex-snapshot
The persistent threat of emerging plant disease pandemics to global food security
inferredcites →https://doi.org/10.1079/cabicompendium.108083openalex-snapshot
Hymenoscyphus fraxineus (ash dieback)
inferredcites →https://doi.org/10.1080/00275514.2017.1418578openalex-snapshot
The use of fungal entomopathogens as endophytes in biological control: a review
inferredcites →https://doi.org/10.1080/09644016.2015.1118790openalex-snapshot
The discovery of ash dieback in the UK: the making of a focusing event
inferredcites →https://doi.org/10.1080/13669877.2017.1281339openalex-snapshot
The social amplification of risk on Twitter: the case of ash dieback disease in the United Kingdom
inferredcites →https://doi.org/10.1080/13669877.2018.1485170openalex-snapshot
Ash dieback and other tree pests and pathogens: dispersed risk events and the Social Amplification of Risk Framework
inferredcites →https://doi.org/10.1080/21501203.2014.963720openalex-snapshot
Hymenoscyphus fraxineus vs. Hymenoscyphus albidus – A comparative light microscopic study on the causal agent of European ash dieback and related foliicolous, stroma-forming species
inferredcites →https://doi.org/10.1093/femsec/fiy049openalex-snapshot
Tracking the invasion: dispersal of Hymenoscyphus fraxineus airborne inoculum at different scales
inferredcites →https://doi.org/10.1093/forestry/cpx012openalex-snapshot
Silvicultural strategies for Fraxinus excelsior in response to dieback caused by Hymenoscyphus fraxineus
inferredcites →https://doi.org/10.1093/forestry/cpx059openalex-snapshot
Evidence from mortality dating of Fraxinus excelsior indicates ash dieback (Hymenoscyphus fraxineus) was active in England in 2004–2005
inferredcites →https://doi.org/10.1093/forestry/cpy040openalex-snapshot
Responding to ash dieback (Hymenoscyphus fraxineus) in the UK: woodland composition and replacement tree species
inferredcites →https://doi.org/10.1093/jipm/pmx029openalex-snapshot
Under Siege: Ash Management in the Wake of the Emerald Ash Borer
inferredcites →https://doi.org/10.1098/rstb.2010.0395openalex-snapshot
Learning from history, predicting the future: the UK Dutch elm disease outbreak in relation to contemporary tree disease threats
inferredcites →https://doi.org/10.1099/00207713-49-4-1605openalex-snapshot
The phytoplasma associated with ash yellows and lilac witches'-broom: ‘Candidatus Phytoplasma fraxini’
inferredcites →https://doi.org/10.1101/154492openalex-snapshot
“Genome-wide population diversity in Hymenoscyphus fraxineus points to an eastern Russian origin of European Ash dieback”
inferredcites →https://doi.org/10.1111/1365-2664.13255openalex-snapshot
Maintaining ecosystem properties after loss of ash in Great Britain
inferredcites →https://doi.org/10.1111/1365-2745.12566openalex-snapshot
Biological Flora of the British Isles:Fraxinus excelsior
inferredcites →https://doi.org/10.1111/1365-2745.13383openalex-snapshot
Landscape epidemiology of ash dieback
inferredcites →https://doi.org/10.1111/1365-2745.14191openalex-snapshot
Neighbours matter and the weak succumb: Ash dieback infection is more severe in ash trees with fewer conspecific neighbours and lower prior growth rate
inferredcites →https://doi.org/10.1111/efp.12012openalex-snapshot
Natural infection of F raxinus excelsior seeds by C halara fraxinea
inferredcites →https://doi.org/10.1111/efp.12022openalex-snapshot
On the longevity of H ymenoscyphus pseudoalbidus in petioles of F raxinus excelsior
inferredcites →https://doi.org/10.1111/efp.12038openalex-snapshot
Temperature effect on C halara fraxinea: heat treatment of saplings as a possible disease control method
inferredcites →https://doi.org/10.1111/efp.12183openalex-snapshot
Ascocarp formation of Hymenoscyphus fraxineus on several‐year‐old pseudosclerotial leaf rachises of Fraxinus excelsior
inferredcites →https://doi.org/10.1111/efp.12258openalex-snapshot
Temporal evolution of collar lesions associated with ash dieback and the occurrence of Armillaria in Belgian forests
inferredcites →https://doi.org/10.1111/efp.12311openalex-snapshot
Efficacy of fungicides on Hymenoscyphus fraxineus and their potential for control of ash dieback in forest nurseries
inferredcites →https://doi.org/10.1111/efp.12370openalex-snapshot
Direct evidence of Hymenoscyphus fraxineus infection pathway through the petiole‐shoot junction
inferredcites →https://doi.org/10.1111/efp.12426openalex-snapshot
Do higher summer temperatures restrict the dissemination of Hymenoscyphus fraxineus in France?
inferredcites →https://doi.org/10.1111/epp.12130openalex-snapshot
The UK Plant Health Risk Register: a tool for prioritizing actions
inferredcites →https://doi.org/10.1111/geb.12599openalex-snapshot
Global trade networks determine the distribution of invasive non‐native species
inferredcites →https://doi.org/10.1111/j.1365-2338.2008.01210.xopenalex-snapshot
Occurrence of the emerald ash borer,Agrilus planipennisin Russia and its potential impact on European forestry
inferredcites →https://doi.org/10.1111/j.1365-2338.2010.02429.xopenalex-snapshot
Ash dieback: pathogen spread and diurnal patterns of ascospore dispersal, with special emphasis on Norway*
inferredcites →https://doi.org/10.1111/j.1365-3059.2008.01977.xopenalex-snapshot
Investigations concerning the role of Chalara fraxinea in declining Fraxinus excelsior
inferredcites →https://doi.org/10.1111/j.1365-3059.2009.02162.xopenalex-snapshot
Chalara fraxinea associated with dieback of narrow‐leafed ash ( Fraxinus angustifolia )
inferredcites →https://doi.org/10.1111/j.1365-3059.2011.02578.xopenalex-snapshot
Occurrence of Hymenoscyphus pseudoalbidus on infected ash logs
inferredcites →https://doi.org/10.1111/j.1439-0329.2006.00453.xopenalex-snapshot
Chalara fraxinea sp. nov. associated with dieback of ash (Fraxinus excelsior) in Poland
inferredcites →https://doi.org/10.1111/j.1439-0329.2008.00565.xopenalex-snapshot
Pathogenicity of Chalara fraxinea
inferredcites →https://doi.org/10.1111/j.1439-0329.2008.00589.xopenalex-snapshot
The teleomorph of Chalara fraxinea, the causal agent of ash dieback
inferredcites →https://doi.org/10.1111/j.1439-0329.2009.00599.xopenalex-snapshot
Associations among symptoms of dieback in even‐aged stands of ash (Fraxinus excelsiorL.)
inferredcites →https://doi.org/10.1111/j.1439-0329.2009.00610.xopenalex-snapshot
Detection of Chalara fraxinea in common ash (Fraxinus excelsior) using real time PCR
inferredcites →https://doi.org/10.1111/j.1439-0329.2009.00615.xopenalex-snapshot
Mycological and histological investigations of Fraxinus excelsior nursery saplings naturally infected by Chalara fraxinea
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.1752-4571.2011.00222.xopenalex-snapshot
Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogenHymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1111/jen.12369openalex-snapshot
A new forest pest in Europe: a review of Emerald ash borer (Agrilus planipennis) invasion
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/mpp.12542openalex-snapshot
Cryphonectria parasitica , the causal agent of chestnut blight: invasion history, population biology and disease control
inferredcites →https://doi.org/10.1111/ppa.12048openalex-snapshot
Light and scanning electron microscopy studies of the early infection stages of H ymenoscyphus pseudoalbidus on F raxinus excelsior
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/10.1111/ppa.12218openalex-snapshot
Detection and quantification of airborne inoculum of H ymenoscyphus pseudoalbidus using real‐time PCR assays
inferredcites →https://doi.org/10.1111/ppa.12450openalex-snapshot
Virulence of Hymenoscyphus albidus and native and introduced Hymenoscyphus fraxineus on Fraxinus excelsior and Fraxinus pennsylvanica
inferredcites →https://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
inferredcites →https://doi.org/10.1111/ppa.12542openalex-snapshot
Influence of site and stand factors on Hymenoscyphus fraxineus ‐induced basal lesions
inferredcites →https://doi.org/10.1111/ppa.12591openalex-snapshot
Detection of plant pathogens using real‐time PCR : how reliable are late C t values?
inferredcites →https://doi.org/10.1111/ppa.12667openalex-snapshot
Pathogenicity of fungi associated with ash dieback towards Fraxinus excelsior
inferredcites →https://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
inferredcites →https://doi.org/10.1111/ppa.13014openalex-snapshot
Life at the edge – the cytology and physiology of the biotroph to necrotroph transition in Hymenoscyphus fraxineus during lesion formation in ash
inferredcites →https://doi.org/10.1111/tran.12259openalex-snapshot
The post‐politics of plant biosecurity: The British Government's response to ash dieback in 2012
inferredcites →https://doi.org/10.1126/science.1235773openalex-snapshot
The Consequence of Tree Pests and Diseases for Ecosystem Services
inferredcites →https://doi.org/10.1126/science.adp2990openalex-snapshot
Rapid polygenic adaptation in a wild population of ash trees under a novel fungal epidemic
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114623openalex-snapshot
Fungal Effectors and Plant Susceptibility
inferredcites →https://doi.org/10.1146/annurev-ento-011613-162051openalex-snapshot
Emerald Ash Borer Invasion of North America: History, Biology, Ecology, Impacts, and Management
inferredcites →https://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
inferredcites →https://doi.org/10.1186/s43170-021-00034-xopenalex-snapshot
The eradication of Asian longhorned beetle at Paddock Wood, UK
inferredcites →https://doi.org/10.1371/journal.pone.0080431openalex-snapshot
The Phylogeny and Biogeographic History of Ashes (Fraxinus, Oleaceae) Highlight the Roles of Migration and Vicariance in the Diversification of Temperate Trees
inferredcites →https://doi.org/10.1371/journal.pone.0141592openalex-snapshot
Virulence of Hymenoscyphus albidus and H. fraxineus on Fraxinus excelsior and F. pennsylvanica
inferredcites →https://doi.org/10.1534/genetics.115.180968openalex-snapshot
The Impact of Recombination Hotspots on Genome Evolution of a Fungal Plant Pathogen
inferredcites →https://doi.org/10.1890/110145openalex-snapshot
Global change, global trade, and the next wave of plant invasions
inferredcites →https://doi.org/10.3389/fmicb.2020.590944openalex-snapshot
Analyzing Ash Leaf-Colonizing Fungal Communities for Their Biological Control of Hymenoscyphus fraxineus
inferredcites →https://doi.org/10.3390/f7010001openalex-snapshot
Detection of Airborne Inoculum of Hymenoscyphus fraxineus and H. albidus during Seasonal Fluctuations Associated with Absence of Apothecia
inferredcites →https://doi.org/10.3832/ifor2897-012openalex-snapshot
Lenticel infection in Fraxinus excelsior shoots in the context of ash dieback
inferredcites →https://doi.org/10.5248/122.25openalex-snapshot
Hymenoscyphus pseudoalbidus, the correct name for Lambertella albida reported from Japan
inferredcites →https://doi.org/10.5248/130.1017openalex-snapshot
Five new species of Hymenoscyphus (Helotiaceae, Ascomycota) with notes on the phylogeny of the genus
inferredcites →https://doi.org/10.5586/aa.2010.012openalex-snapshot
Morphologial variation in colonies of Chalara fraxinea isolated from ash (Fraxinus excelsior L.) stems with symptoms of dieback and effects of temperature on colony growth and structure
inferredcites →https://doi.org/10.5598/imafungus.2014.05.01.09openalex-snapshot
Hymenoscyphus fraxineus, the correct scientific name for the fungus causing ash dieback in Europe

What points at this work

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

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Drivers of Natural Colonisation and Regeneration within Planted Woodlands: Towards an Integrated Approach to Increase Resilience
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The extension of the taxon cycle model to island plants: insights from the Canarian vascular flora
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European Ash ( Fraxinus excelsior ) as a Functional Keystone Species Shaping Woodland Flora in the UK
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Rapid detection of Hymenoscyphus fraxineus using genome‐specific primers based on loop‐mediated isothermal amplification assay
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/s13280-026-02467-yopenalex-snapshot
“Rädda Asken”: A scientific perspective on Sweden’s efforts to conserve Ash Fraxinus excelsior since 2013
inferred← citeshttps://doi.org/10.1007/s41348-024-00989-9openalex-snapshot
Exploring the interaction between aminobutyric acid and epigenetics in modulating ash dieback response in european ash (Fraxinus excelsior)
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Plant pathology and diseases from a novel bibliometric method
inferred← citeshttps://doi.org/10.1016/j.foreco.2024.122476openalex-snapshot
Synergistic negative effects of ash dieback and Armillaria root rot on health and stability of mature ash trees
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Drivers of natural colonisation and regeneration within planted woodlands in England: towards an integrated approach to increase resilience
inferred← citeshttps://doi.org/10.1016/j.foreco.2025.122593openalex-snapshot
A new hope: Condition of young stands suggests natural recovery of European ash in Northern Europe
inferred← citeshttps://doi.org/10.1016/j.foreco.2025.122702openalex-snapshot
The impact of environmental variables on ash dieback mediated tree mortality and defoliation
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101646openalex-snapshot
Fungal endophytes with anti-fungal metabolites reduce symptoms of ash dieback in Fraxinus excelsior in a greenhouse experiment
inferred← citeshttps://doi.org/10.1016/j.funeco.2026.101522openalex-snapshot
Why sycamore and beech fall short: assessing the compensatory potential of alternative hosts for ash-associated saproxylic fungi
inferred← citeshttps://doi.org/10.1016/j.tfp.2024.100559openalex-snapshot
Modelling the potential range of Agrilus planipennis in Europe according to current and future climate conditions
inferred← citeshttps://doi.org/10.1016/j.tfp.2026.101383openalex-snapshot
Forestry stakeholders' perspectives on the prospects for restoring European ash in Sweden
inferred← citeshttps://doi.org/10.1016/j.ufug.2025.128674openalex-snapshot
Collaborative approaches to urban tree biosecurity: Stakeholder’s perceptions, actions and social networks
inferred← citeshttps://doi.org/10.1080/07388551.2024.2430478openalex-snapshot
RNAi-biofungicides: a quantum leap for tree fungal pathogen management
inferred← citeshttps://doi.org/10.1088/1748-9326/adf12eopenalex-snapshot
Asymmetric diurnal warming worsens forest pest hazards in China: evidence from a long-term dataset
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/10.1111/efp.70029openalex-snapshot
Evaluation of Methods for Resistance Testing of Fraxinus excelsior Genotypes Against Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.1111/gcb.70430openalex-snapshot
Forest Topsoil Organic Carbon Declines Under Ash Dieback
inferred← citeshttps://doi.org/10.1111/plb.13754openalex-snapshot
Linking sap flow and tree water deficit in an unmanaged, mixed beech forest during the summer drought 2022
inferred← citeshttps://doi.org/10.3390/f15050829openalex-snapshot
Use of Phosphite Preparations to Protect Ash Seedlings Fraxinus excelsior L. against Phytophthora spp. and Hymenoscyphus fraxineus Pathogens
inferred← citeshttps://doi.org/10.3390/f16010109openalex-snapshot
The Potential of European Beech (Fagus sylvatica L.) in the Hemiboreal Baltic Region: A Review
inferred← citeshttps://doi.org/10.3390/f16010141openalex-snapshot
Spring’s Signal: Can Bud Burst Timing Enhance Resistance to Ash Dieback in Europe?
inferred← citeshttps://doi.org/10.3390/f16010149openalex-snapshot
Detection of Hymenoscyphus fraxineus in Leaf Rachises from European Ash (Fraxinus excelsior) in Germany
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/f16071033openalex-snapshot
Determining Management Strategies to Control Ash Dieback Disease Through the Study of Molecular and Environmental Interactions
inferred← citeshttps://doi.org/10.3390/f17030389openalex-snapshot
Associations Between the Leaf Microbiome and the Health of Irish Ash Trees Affected by Hymenoscyphus fraxineus
inferred← citeshttps://doi.org/10.3390/microorganisms13061238openalex-snapshot
Diplodia fraxini: The Main Pathogen Involved in the Ash Dieback of Fraxinus angustifolia in Croatia
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/10.64898/2026.04.21.719819openalex-snapshot
Environment-aware genomic prediction enhances the transferability of polygenic resistance to ash dieback in Fraxinus excelsior
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