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“Genome-wide population diversity in Hymenoscyphus fraxineus points to an eastern Russian origin of European Ash dieback”
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ece3.258openalex-snapshot
Complex genetic patterns in closely related colonizing invasive species
inferredcites →https://doi.org/10.1007/s10342-014-0811-9openalex-snapshot
Introduction of Mandshurian ash (Fraxinus mandshurica Rupr.) to Estonia: Is it related to the current epidemic on European ash (F. excelsior L.)?
inferredcites →https://doi.org/10.1007/s10530-015-0911-6openalex-snapshot
Genetic population structure of the invasive ash dieback pathogen Hymenoscyphus fraxineus in its expanding range
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/s11557-013-0945-zopenalex-snapshot
Hymenoscyphus albidoides sp. nov. and H. pseudoalbidus from China
inferredcites →https://doi.org/10.1007/s11557-016-1209-5openalex-snapshot
The earliest samples of Hymenoscyphus albidus vs. H. fraxineus in Estonian mycological herbaria
inferredcites →https://doi.org/10.1007/s12686-011-9548-7openalex-snapshot
STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method
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.fgb.2015.12.013openalex-snapshot
MAT – gene structure and mating behavior of Hymenoscyphus fraxineus and Hymenoscyphus albidus
inferredcites →https://doi.org/10.1016/j.funeco.2011.10.004openalex-snapshot
Population structure of Hymenoscyphus pseudoalbidus and its genetic relationship to Hymenoscyphus albidus
inferredcites →https://doi.org/10.1016/j.funeco.2012.05.004openalex-snapshot
Rapid invasion by an aggressive pathogenic fungus (Hymenoscyphus pseudoalbidus) replaces a native decomposer (Hymenoscyphus albidus): a case of local cryptic extinction?
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.2005.02.004openalex-snapshot
The role of propagule pressure in explaining species invasions
inferredcites →https://doi.org/10.1016/j.tree.2011.03.023openalex-snapshot
A proposed unified framework for biological invasions
inferredcites →https://doi.org/10.1038/s41559-017-0186openalex-snapshot
Global hotspots and correlates of alien species richness across taxonomic groups
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/10.1046/j.1439-0329.2002.00301.xopenalex-snapshot
Fungi associated with necrotic apical parts of Fraxinus excelsior shoots
inferredcites →https://doi.org/10.1073/pnas.1003577107openalex-snapshot
Dispersal of fungal spores on a cooperatively generated wind
inferredcites →https://doi.org/10.1073/pnas.1201403109openalex-snapshot
Fusion of two divergent fungal individuals led to the recent emergence of a unique widespread pathogen species
inferredcites →https://doi.org/10.1073/pnas.1602205113openalex-snapshot
Global threat to agriculture from invasive species
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/10.1086/521987openalex-snapshot
Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering
inferredcites →https://doi.org/10.1093/bioinformatics/btm233openalex-snapshot
CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure
inferredcites →https://doi.org/10.1093/bioinformatics/btr330openalex-snapshot
The variant call format and VCFtools
inferredcites →https://doi.org/10.1093/bioinformatics/btr642openalex-snapshot
PGDSpider: an automated data conversion tool for connecting population genetics and genomics programs
inferredcites →https://doi.org/10.1093/bioinformatics/bts606openalex-snapshot
A high-performance computing toolset for relatedness and principal component analysis of SNP data
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/genetics/164.4.1567openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies
inferredcites →https://doi.org/10.1093/molbev/msj030openalex-snapshot
Application of Phylogenetic Networks in Evolutionary Studies
inferredcites →https://doi.org/10.1093/molbev/msu136openalex-snapshot
PopGenome: An Efficient Swiss Army Knife for Population Genomic Analyses in R
inferredcites →https://doi.org/10.1101/004564openalex-snapshot
Crowdsourced analysis of ash and ash dieback through the Open Ash Dieback project: A year 1 report on datasets and analyses contributed by a self-organising community
inferredcites →https://doi.org/10.1101/gr.118851.110openalex-snapshot
The making of a new pathogen: Insights from comparative population genomics of the domesticated wheat pathogen Mycosphaerella graminicola and its wild sister species
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/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.1365-294x.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.2011.05121.xopenalex-snapshot
Amplified fragment length polymorphism and sequence analyses reveal massive gene introgression from the European fungal pathogen Heterobasidion annosum into its introduced congener H. irregulare
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.1439-0329.2008.00565.xopenalex-snapshot
Pathogenicity of Chalara fraxinea
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.1439-0329.2010.00647.xopenalex-snapshot
First record of Chalara fraxinea in Finland and genetic variation among isolates sampled from Åland, mainland Finland, Estonia and Latvia
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.1461-0248.2005.00792.xopenalex-snapshot
Predicting species distribution: offering more than simple habitat models
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.1752-4571.2012.00272.xopenalex-snapshot
The biology of small, introduced populations, with special reference to biological control
inferredcites →https://doi.org/10.1111/j.1755-0998.2011.02987.xopenalex-snapshot
Comparison of FST outlier tests for SNP loci under selection
inferredcites →https://doi.org/10.1111/mec.12792openalex-snapshot
Population structure of the invasive forest pathogen H ymenoscyphus pseudoalbidus
inferredcites →https://doi.org/10.1111/mec.14039openalex-snapshot
What was old is new again: thermal adaptation within clonal lineages during range expansion in a fungal pathogen
inferredcites →https://doi.org/10.1111/mec.14048openalex-snapshot
Population genetic analysis of a parasitic mycovirus to infer the invasion history of its fungal host
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.12384openalex-snapshot
A gapless genome sequence of the fungus Botrytis cinerea
inferredcites →https://doi.org/10.1111/nph.14204openalex-snapshot
Fungal diversity and seasonal succession in ash leaves infected by the invasive ascomycete Hymenoscyphus fraxineus
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.12588openalex-snapshot
Hymenoscyphus fraxineus is a leaf pathogen of local Fraxinus species in the Russian Far East
inferredcites →https://doi.org/10.1146/annurev-phyto-080614-115913openalex-snapshot
Population Genomics of Fungal and Oomycete Pathogens
inferredcites →https://doi.org/10.1353/hub.2012.a493568openalex-snapshot
PCAdmix: Principal Components-Based Assignment of Ancestry Along Each Chromosome in Individuals with Admixed Ancestry from Two or More Populations
inferredcites →https://doi.org/10.1371/journal.pgen.1002230openalex-snapshot
Genomic Analysis of the Necrotrophic Fungal Pathogens Sclerotinia sclerotiorum and Botrytis cinerea
inferredcites →https://doi.org/10.1371/journal.pone.0064479openalex-snapshot
Combining a Climatic Niche Model of an Invasive Fungus with Its Host Species Distributions to Identify Risks to Natural Assets: Puccinia psidii Sensu Lato in Australia
inferredcites →https://doi.org/10.1371/journal.pone.0167104openalex-snapshot
Genetic Structure in the Northern Range Margins of Common Ash, Fraxinus excelsior L.
inferredcites →https://doi.org/10.1534/genetics.108.092221openalex-snapshot
A Genome-Scan Method to Identify Selected Loci Appropriate for Both Dominant and Codominant Markers: A Bayesian Perspective
inferredcites →https://doi.org/10.3389/fgene.2013.00288openalex-snapshot
Sequencing quality assessment tools to enable data-driven informatics for high throughput genomics
inferredcites →https://doi.org/10.48550/arxiv.1207.3907openalex-snapshot
Haplotype-based variant detection from short-read sequencing
inferredcites →https://doi.org/10.5248/122.25openalex-snapshot
Hymenoscyphus pseudoalbidus, the correct name for Lambertella albida reported from Japan
inferredcites →https://doi.org/10.5598/imafungus.2014.05.01.09openalex-snapshot
Hymenoscyphus fraxineus, the correct scientific name for the fungus causing ash dieback in Europe
inferredcites →https://doi.org/10.5941/myco.2014.42.4.391openalex-snapshot
First Report of the Ash Dieback Pathogen Hymenoscyphus fraxineus in Korea
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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/10.1007/978-3-319-89833-9_11openalex-snapshot
Dieback of European Ash: What Can We Learn from the Microbial Community and Species-Specific Traits of Endophytic Fungi Associated with Ash?
inferred← citeshttps://doi.org/10.1007/s13595-019-0799-xopenalex-snapshot
Negative correlation between ash dieback susceptibility and reproductive success: good news for European ash forests
inferred← citeshttps://doi.org/10.1007/s42161-022-01108-zopenalex-snapshot
Infection potential of Botryodiplodia hypodermia, the causal agent of elm canker
inferred← citeshttps://doi.org/10.1079/pavsnnr201914025openalex-snapshot
An overview of ash ( Fraxinus spp.) and the ash dieback disease in Europe.
inferred← citeshttps://doi.org/10.1111/1365-2664.13255openalex-snapshot
Maintaining ecosystem properties after loss of ash in Great Britain
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/ppa.13948openalex-snapshot
Hymenoscyphus fraxineus persistence in the ash litter
inferred← citeshttps://doi.org/10.1515/fsmu-2017-0012openalex-snapshot
New problems in dendropathology – new and invasive pathogens
inferred← citeshttps://doi.org/10.3389/fpls.2018.01087openalex-snapshot
Propagule Pressure Build-Up by the Invasive Hymenoscyphus fraxineus Following Its Introduction to an Ash Forest Inhabited by the Native Hymenoscyphus albidus
inferred← citeshttps://doi.org/10.3390/jof6030150openalex-snapshot
The Relationship between Fungal Diversity and Invasibility of a Foliar Niche—The Case of Ash Dieback
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/10.3832/ifor2897-012openalex-snapshot
Lenticel infection in Fraxinus excelsior shoots in the context of ash dieback
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