Reference health
The association of Boeremia lilacis with necrotic lesions on shoots and leaf petioles and its pathogenicity towards Fraxinus excelsior
39/39 checkable references clean · checked 2026-07-22
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
11 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 39 checked references that resolve
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Genetic differentiation of Phoma exigua varieties by means of AFLP fingerprints
resolves10.1111/j.1364-3703.2009.00540.x
Development of taxon‐specific sequence characterized amplified region (SCAR) markers based on actin sequences and DNA amplification fingerprinting (DAF): a case study in the
<i>Phoma exigua</i>
species complex
resolves10.3114/sim.2010.65.01
Highlights of the Didymellaceae: A polyphasic approach to characterise Phoma and related pleosporalean genera
resolves10.1111/j.1365-3059.2008.01977.x
Investigations concerning the role of
<i>Chalara fraxinea</i>
in declining
<i>Fraxinus excelsior</i>
resolves10.1080/21501203.2014.963720
<i>Hymenoscyphus fraxineus</i>
vs.
<i>Hymenoscyphus albidus</i>
– A comparative light microscopic study on the causal agent of European ash dieback and related foliicolous, stroma-forming species
resolves10.5598/imafungus.2014.05.01.09
Hymenoscyphus fraxineus, the correct scientific name for the fungus causing ash dieback in Europe
resolves10.1016/j.biocontrol.2014.11.009
Assessment of Boeremia exigua var. rhapontica, as a biological control agent of Russian knapweed (Rhaponticum repens)
resolves10.1094/PDIS.1999.83.2.200C
First Report of <i>Phoma herbarum</i> and <i>Phoma exigua</i> as Pathogens of Dandelion in Southern Ontario
resolves10.1080/00275514.1999.12061051
A method for designing primer sets for speciation studies in filamentous ascomycetes
resolves10.1111/ppa.12048
Light and scanning electron microscopy studies of the early infection stages of
<i>
<scp>H</scp>
ymenoscyphus pseudoalbidus
</i>
on
<i>
<scp>F</scp>
raxinus excelsior
</i>
resolves10.1111/j.1439-0434.1998.tb04773.x
Taxonomy and Pathogenicity of <i>Phoma exigua</i> var. <i>populi</i> var. nov. Causing Necrotic Bark Lesions on Poplars
resolves10.1111/ppa.12588
<i>Hymenoscyphus fraxineus</i>
is a leaf pathogen of local
<i>Fraxinus</i>
species in the Russian Far East
resolves10.1128/AEM.61.4.1323-1330.1995
Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes
resolves10.1111/ppa.12450
Virulence of
<i>Hymenoscyphus albidus</i>
and native and introduced
<i>Hymenoscyphus fraxineus</i>
on
<i>Fraxinus excelsior</i>
and
<i>Fraxinus pennsylvanica</i>
resolves10.1111/mpp.12073
<i>
<scp>H</scp>
ymenoscyphus pseudoalbidus
</i>
, the causal agent of
<scp>E</scp>
uropean ash dieback
resolves10.1007/BF02101694
Dating of the human-ape splitting by a molecular clock of mitochondrial DNA
resolves10.1111/j.1365-3059.2011.02578.x
Occurrence of
<i>Hymenoscyphus pseudoalbidus</i>
on infected ash logs
resolves10.1016/j.funeco.2017.05.001
Communities of fungal endophytes in leaves of Fraxinus ornus are highly diverse
resolves10.1093/molbev/mst010
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
resolves10.1093/bioinformatics/bts199
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
resolves10.1023/A:1007528101452
Rapid Isolation of DNA from Dry and Fresh Samples of Plants Producing Large Amounts of Secondary Metabolites and Essential Oils
resolves10.1016/j.funbio.2017.11.002
Fungal communities associated with species of Fraxinus tolerant to ash dieback, and their potential for biological control
resolves10.1111/j.1439-0329.2006.00453.x
<i>Chalara fraxinea</i> sp. nov. associated with dieback of ash (<i>Fraxinus excelsior</i>) in Poland
resolves10.1371/journal.pone.0141592
Virulence of Hymenoscyphus albidus and H. fraxineus on Fraxinus excelsior and F. pennsylvanica
resolves10.1007/s10342-016-0955-x
Fungi on stems and twigs in initial and advanced stages of dieback of European ash (Fraxinus excelsior) in Poland
resolves10.1111/ppa.12667
Pathogenicity of fungi associated with ash dieback towards
<i>Fraxinus excelsior</i>
resolves10.1093/molbev/msw054
MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets
resolves10.1111/ppa.12196
The ash dieback crisis: genetic variation in resistance can prove a long‐term solution
resolves10.1080/10408410902975992
<i>Phoma Saccardo</i>
: Distribution, secondary metabolite production and biotechnological applications
resolves10.1111/j.1439-0329.2009.00599.x
Associations among symptoms of dieback in even‐aged stands of ash (<i>Fraxinus excelsior</i>L.)
resolves10.1073/pnas.0404206101
Prospects for inferring very large phylogenies by using the neighbor-joining method
resolves10.1111/j.1365-2338.2010.02429.x
Ash dieback: pathogen spread and diurnal patterns of ascospore dispersal, with special emphasis on Norway*
The 11 references without a DOI — listed, not checked
no DOI — not checkedAa, H. A., van der Boerema, G. H., & de Gruyter, J. (2000). Contributions towards a monograph of Phoma (Coelomycetes) VI — 1. Section Phyllostictoides: Characteristics and nomenclature of its type species Phoma exigua. Persoonia, 17, 435–456.
no DOI — not checkedBoerema, G. H., & Höweler, L. H. (1967). Phoma exigua Desm. and its varieties. Persoonia, 5, 15–28.
no DOI — not checkedBoerema, G. H., de Gruyter, J., Noordeloos, M. E. & Hamers, M. E. C. (2004). Phoma Identification Manual. Differentiation of Specific and Infra-specific Taxa in Culture. (Wallingford, Oxfordshire, UK, CAB International: CABI Publishing).
no DOI — not checkedBoudier, B. (1994). Le chancre des jeunes plants de frênes, une maladie grave certaines années mais des perspectives de lutte. Phytoma, 461, 35–36.
no DOI — not checkedChen, J. (2012). Fungal community survey of Fraxinus excelsior in New Zealand. Dissertation, University of Agricultural Sciences, Uppsala, Swedish.
no DOI — not checkedFarr, D. F., Bills, G. F., Chamuris, G. P., & Rossman, A. Y. (1989). Fungi on plants and plant products in the United States. St Paul: APS Press.
no DOI — not checkedKowalski, T., & Kehr, R. (2016). Stand des Eschentriebsterbens und zunehmende Schäden an Buche und Berg-Ahorn. In D. Dujesiefken (Ed.), Jahrbuch der Baumpflege (pp. 63–83). Braunschweig: Haymarket Media.
no DOI — not checkedPower, M. W. P., Hopkins, A. J. M., Chen, J., Bengtsson, S. B. K., Vasaitis, R., & Cleary, M. R. (2017). European Fraxinus species introduced into New Zealand retain many of their native endophytic fungi. Baltic Forestry, 23, 74–81.
no DOI — not checkedSchmitz, S., Zini, J., Etienne, M., Moreau, J.-M., Chandelier, A., & Cavelier, M. (2006). Effectiveness of thiophanatemethyl, trifloxystrobin and vinclozolin on canker caused by Phoma exigua Desm. On ash tree seedlings. Biotechnologie Agronomie Societe et Environement, 10, 25–31.
no DOI — not checkedTrapiello, E., Schoebel, C. N., & Rigling, D. (2017). Fungal community in symptomatic ash leaves in Spain. Baltic Forestry, 23, 68–73.
no DOI — not checkedWhite, T. J., Bruns, T. D., Lee, S., & Taylor, J. (1990). Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In M. A. Innis, D. H. Gelfand, J. J. Sninsky, & T. J. White (Eds.), PCR Protocols: A Guide to Methods and Applications (pp. 315–322). New York: Academic Press.
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