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Invasive Everywhere? Phylogeographic Analysis of the Globally Distributed Tree Pathogen Lasiodiplodia theobromae

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Outgoing claims: the papers this work cites, builds on, or argues with.

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What points at this work

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

inferred← citeshttps://doi.org/10.3897/imafungus.16.147543zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1007/978-3-031-81770-0_19openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-87035-4_17openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-031-87035-4_22openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10327-018-0814-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10327-023-01118-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10327-024-01187-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10658-022-02587-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12600-024-01123-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s13225-024-00542-xopenalex-snapshot
One stop shop V: taxonomic update with molecular phylogeny for important phytopathogenic genera: 101–125 (2024)
inferred← citeshttps://doi.org/10.1007/s13313-017-0516-xopenalex-snapshot
Diversity of tree-infecting Botryosphaeriales on native and non-native trees in South Africa and Namibia
inferred← citeshttps://doi.org/10.1007/s13313-018-0577-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s41348-024-00933-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-85042-1.00040-9openalex-snapshot
Ecological, evolutionary, and societal impacts of invasions by emergent forest pathogens
inferred← citeshttps://doi.org/10.1016/j.crmicr.2023.100201openalex-snapshot
MALDI mass spectrometry-based identification of antifungal molecules from endophytic Bacillus strains with biocontrol potential of Lasiodiplodia theobromae, a grapevine trunk pathogen in Peru
inferred← citeshttps://doi.org/10.1016/j.fbr.2023.100352openalex-snapshot
From host to host: The taxonomic and geographic expansion of Botryosphaeriaceae
inferred← citeshttps://doi.org/10.1016/j.funbio.2018.05.005openalex-snapshot
Ophiostoma quercus: An unusually diverse and globally widespread tree-infecting fungus
inferred← citeshttps://doi.org/10.1016/j.funeco.2022.101179openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41598-022-13057-9openalex-snapshot
Lasiodiplodia theobromae as a causal pathogen of leaf blight, stem canker, and pod rot of Theobroma cacao in Malaysia
inferred← citeshttps://doi.org/10.1038/s41598-025-22739-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1080/03235408.2022.2116689openalex-snapshot
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inferred← citeshttps://doi.org/10.1080/07060661.2026.2673749openalex-snapshot
Canadian Plant Disease Survey 2026 Volume 106
inferred← citeshttps://doi.org/10.1094/mpmi-07-26-0067-irwopenalex-snapshot
Lasiodiplodia theobromae as a Model Latent Pathogen: Molecular Mechanisms, Global Impact, and Sustainable Management
inferred← citeshttps://doi.org/10.1094/pdis-03-22-0638-pdnopenalex-snapshot
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inferred← citeshttps://doi.org/10.1094/pdis-07-18-1131-reopenalex-snapshot
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inferred← citeshttps://doi.org/10.1094/pdis-07-23-1260-sropenalex-snapshot
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inferred← citeshttps://doi.org/10.1094/pdis-09-23-1939-sropenalex-snapshot
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inferred← citeshttps://doi.org/10.1094/pdis-11-21-2421-scopenalex-snapshot
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inferred← citeshttps://doi.org/10.1098/rsbl.2020.0820openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/efp.12491openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/efp.12504openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/efp.12737openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/efp.70077openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/nph.70209openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/ppa.12997openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/msphere.00034-26openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s43008-020-00043-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.14692/jfi.17.4.159-168openalex-snapshot
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inferred← citeshttps://doi.org/10.17159/sajs.2020/8038openalex-snapshot
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inferred← citeshttps://doi.org/10.17268/sci.agropecu.2021.068openalex-snapshot
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inferred← citeshttps://doi.org/10.18779/cyt.v15i2.583openalex-snapshot
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inferred← citeshttps://doi.org/10.18781/r.mex.fit.2301-1openalex-snapshot
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inferred← citeshttps://doi.org/10.20546/ijcmas.2022.1102.028openalex-snapshot
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inferred← citeshttps://doi.org/10.25268/bimc.invemar.2023.52.2.1231openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agriculture10100488openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/agronomy14112487openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/f12030313openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/f12121658openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/f13020341openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/f8110441openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/jof12040270openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/toxins12070457openalex-snapshot
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inferred← citeshttps://doi.org/10.36253/phyto-12576openalex-snapshot
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inferred← citeshttps://doi.org/10.36253/phyto-14198openalex-snapshot
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inferred← citeshttps://doi.org/10.36253/phyto-14711openalex-snapshot
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inferred← citeshttps://doi.org/10.36253/phyto-15292openalex-snapshot
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inferred← citeshttps://doi.org/10.55779/nsb14411284openalex-snapshot
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inferred← citeshttps://doi.org/10.5943/mycosphere/14/1/14openalex-snapshot
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