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Hybrid inferiority and genetic incompatibilities drive divergence of fungal pathogens infecting the same host
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471250953.bi1110s43openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.cub.2010.06.022openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.fgb.2009.12.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.fgb.2012.07.003openalex-snapshot
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QGene 4.0, an extensible Java QTL-analysis platform
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inferredcites →https://doi.org/10.1094/phyto.1999.89.2.176openalex-snapshot
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inferredcites →https://doi.org/10.1094/phyto.2002.92.3.314openalex-snapshot
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inferredcites →https://doi.org/10.1098/rspb.2002.1989openalex-snapshot
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Scaling accurate genetic variant discovery to tens of thousands of samples
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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
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Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00628.xopenalex-snapshot
THE EVOLUTION OF POSTZYGOTIC ISOLATION: ACCUMULATING DOBZHANSKY-MULLER INCOMPATIBILITIES
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb01515.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1364-3703.2010.00649.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1420-9101.2008.01511.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.1439-0434.1977.tb02858.xopenalex-snapshot
Inheritance of Genetic Factors for Symptoms and Pathogenicity in Hybrids of Pyrenophora teres and Pyrenophora graminea
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00863.xopenalex-snapshot
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inferredcites →https://doi.org/10.1111/j.2517-6161.1995.tb02031.xopenalex-snapshot
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Improved prediction of fungal effector proteins from secretomes with EffectorP 2.0
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Research advances in the Pyrenophora teres– barley interaction
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Evolution, selection and isolation: a genomic view of speciation in fungal plant pathogens
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A Test of the Snowball Theory for the Rate of Evolution of Hybrid Incompatibilities
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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.17.171995zenodo-depositor-declared
Interconnected worlds: a comprehensive review of fungal defenses, antimicrobial resistance, and their evolutionary dynamics
inferred← citeshttps://doi.org/10.1002/csc2.70088openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.micpath.2025.107278openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/evolut/qpaf175openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/g3journal/jkae259openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/gbe/evag172openalex-snapshot
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inferred← citeshttps://doi.org/10.1094/phyto-01-25-0002-ropenalex-snapshot
Pyrenophora teres f. maculata, Causal Agent of Spot Form Net Blotch of Barley, Is an Emerging Pathogen of Durum Wheat
inferred← citeshttps://doi.org/10.1094/phyto-11-23-0442-ropenalex-snapshot
Global Spread, Genetic Differentiation, and Selection of Barley Spot Form Net Blotch Isolates
inferred← citeshttps://doi.org/10.1099/mgen.0.001241openalex-snapshot
Deep population structure linked to host vernalization requirement in the barley net blotch fungal pathogen
inferred← citeshttps://doi.org/10.1101/2024.03.17.585425openalex-snapshot
High resolution mapping of novel non-transgressive hybrid susceptibility in barley exploited by P. teres f. maculata maps to a single pentatricopeptide repeat-containing protein
inferred← citeshttps://doi.org/10.1186/s12870-024-05303-1openalex-snapshot
High resolution mapping of a novel non-transgressive hybrid susceptibility locus in barley exploited by P. teres f. maculata
inferred← citeshttps://doi.org/10.3389/fagro.2024.1451281openalex-snapshot
Colocalization of genetic regions that confer resistance/susceptibility against Puccinia species and association with Pyrenophora teres loci within the barley genome
inferred← citeshttps://doi.org/10.6084/m9.figshare.26143743openalex-snapshot
Additional file 1 of High resolution mapping of a novel non-transgressive hybrid susceptibility locus in barley exploited by P. teres f. maculata
inferred← citeshttps://doi.org/10.6084/m9.figshare.26143853openalex-snapshot
Additional file 2 of High resolution mapping of a novel non-transgressive hybrid susceptibility locus in barley exploited by P. teres f. maculata
inferred← citeshttps://doi.org/10.6084/m9.figshare.26741174openalex-snapshot
Additional file 3 of High resolution mapping of a novel non-transgressive hybrid susceptibility locus in barley exploited by P. teres f. maculata
inferred← citeshttps://doi.org/10.6084/m9.figshare.26741177openalex-snapshot
Additional file 4 of High resolution mapping of a novel non-transgressive hybrid susceptibility locus in barley exploited by P. teres f. maculata
inferred← citeshttps://doi.org/10.70675/1e709feaz1914z44dbz844fz3bd311e92c25openalex-snapshot
Structure des populations, évaluation de la résistance de l'hôte et analyse génomique comparative du mycète responsable de l'helminthosporiose de l'orge Pyrenophora teres
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