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Assortment of flowering time and immunity alleles in natural Arabidopsis thaliana populations suggests immunity and vegetative lifespan strategies coevolve
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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/ece3.1270openalex-snapshot
Direct and indirect selection on flowering time, water‐use efficiency ( WUE , δ13C), and WUE plasticity to drought in Arabidopsis thaliana
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Optimal defense theory explains deviations from latitudinal herbivory defense hypothesis
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The floral transition is not the developmental switch that confers competence for the Arabidopsis age-related resistance response to Pseudomonas syringae pv. tomato
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Ecological immunology: costly parasite defences and trade-offs in evolutionary ecology
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The Genetics Underlying Natural Variation in the Biotic Interactions of Arabidopsis thaliana
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Host-Microbe Interactions: Shaping the Evolution of the Plant Immune Response
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Why did the acquired immune system of vertebrates evolve?
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The Red Queen's long race: human adaptation to pathogen pressure
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Genetic and evolutionary perspectives on the interplay between plant immunity and development
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Age-related resistance to Pseudomonas syringae pv. tomato is associated with the transition to flowering in Arabidopsis and is effective against Peronospora parasitica
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Regulation of the Arabidopsis defense transcriptome
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Trade-off between growth and immunity: role of brassinosteroids
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Red Queen: from populations to taxa and communities
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Life history lability underlies rapid climate niche evolution in the angiosperm clade Montiaceae
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Resampling-based false discovery rate controlling multiple test procedures for correlated test statistics
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The Toll receptor family and microbial recognition
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Trade‐offs in evolutionary immunology: just what is the cost of immunity?
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Dr. Pangloss restrained by the Red Queen – steps towards a unified defence theory
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Release of invasive plants from fungal and viral pathogens
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Fitness costs of R-gene-mediated resistance in Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/nature04878openalex-snapshot
Genetic mechanisms and evolutionary significance of natural variation in Arabidopsis
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Patterns of population epigenomic diversity
inferredcites →https://doi.org/10.1038/nature13439openalex-snapshot
The long-term maintenance of a resistance polymorphism through diffuse interactions
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Phylogenetic structure and host abundance drive disease pressure in communities
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Single base–resolution methylome of the silkworm reveals a sparse epigenomic map
inferredcites →https://doi.org/10.1038/ng1702openalex-snapshot
A unified mixed-model method for association mapping that accounts for multiple levels of relatedness
inferredcites →https://doi.org/10.1038/ng1818openalex-snapshot
The PHYTOCHROME C photoreceptor gene mediates natural variation in flowering and growth responses of Arabidopsis thaliana
inferredcites →https://doi.org/10.1038/ni.2083openalex-snapshot
NLR functions in plant and animal immune systems: so far and yet so close
inferredcites →https://doi.org/10.1038/nplants.2016.110openalex-snapshot
Genetic architecture and pleiotropy shape costs of Rps2-mediated resistance in Arabidopsis thaliana
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Count-based differential expression analysis of RNA sequencing data using R and Bioconductor
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Towards identifying genes underlying ecologically relevant traits in Arabidopsis thaliana
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The genetic basis of flowering responses to seasonal cues
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Evolution of plant resistance at the molecular level: ecological context of species interactions
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Salicylic acid regulates flowering time and links defence responses and reproductive development
inferredcites →https://doi.org/10.1073/pnas.0608379104openalex-snapshot
Rapid evolution of flowering time by an annual plant in response to a climate fluctuation
inferredcites →https://doi.org/10.1073/pnas.1517456113openalex-snapshot
Predicting the evolutionary dynamics of seasonal adaptation to novel climates in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1531467100openalex-snapshot
Attenuation of FLOWERING LOCUS C activity as a mechanism for the evolution of summer-annual flowering behavior in Arabidopsis
inferredcites →https://doi.org/10.1086/381407openalex-snapshot
The Evolutionary Economics of Immunity
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The Dilemma of Plants: To Grow or Defend
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Fitness Effects Associated with the Major Flowering Time GeneFRIGIDAinArabidopsis thalianain the Field
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Identifying the Molecular Basis of Host-Parasite Coevolution: Merging Models and Mechanisms
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Modeling the Influence of Genetic and Environmental Variation on the Expression of Plant Life Cycles across Landscapes
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The time of day effects of warm temperature on flowering time involve PIF4 and PIF5
inferredcites →https://doi.org/10.1093/molbev/msi247openalex-snapshot
Genetic Diversity and the Evolutionary History of Plant Immunity Genes in Two Species of Zea
inferredcites →https://doi.org/10.1093/molbev/mss011openalex-snapshot
Flagellin Perception Varies Quantitatively in Arabidopsis thaliana and Its Relatives
inferredcites →https://doi.org/10.1093/nar/30.1.207openalex-snapshot
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
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Reactive oxygen species as universal constraints in life-history evolution
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On sexual dimorphism in immune function
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Introduction. Ecological immunology
inferredcites →https://doi.org/10.1101/gad.245993.114openalex-snapshot
Multiple FLC haplotypes defined by independent cis-regulatory variation underpin life history diversity in Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.103.027094openalex-snapshot
A Developmental Response to Pathogen Infection in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.103.036749openalex-snapshot
The Transcriptional Innate Immune Response to flg22. Interplay and Overlap with Avr Gene-Dependent Defense Responses and Bacterial Pathogenesis
inferredcites →https://doi.org/10.1104/pp.111.183426openalex-snapshot
Altitudinal and Climatic Adaptation Is Mediated by Flowering Traits andFRI,FLC, andPHYCGenes in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.113.121111openalex-snapshot
The bHLH Transcription Factor HBI1 Mediates the Trade-Off between Growth and Pathogen-Associated Molecular Pattern–Triggered Immunity in Arabidopsis
inferredcites →https://doi.org/10.1111/ele.12744openalex-snapshot
Future directions in the ontogeny of plant defence: understanding the evolutionary causes and consequences
inferredcites →https://doi.org/10.1111/eva.12350openalex-snapshot
Directional selection for flowering time leads to adaptive evolution in Raphanus raphanistrum (Wild radish)
inferredcites →https://doi.org/10.1111/evo.12854openalex-snapshot
The Red Queen lives: Epistasis between linked resistance loci
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EVOLUTIONARY GENETICS OF RESISTANCE AND TOLERANCE TO NATURAL HERBIVORY IN ARABIDOPSIS THALIANA
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Host defence in a developmental context
inferredcites →https://doi.org/10.1111/j.1364-3703.2010.00657.xopenalex-snapshot
Co‐evolutionary interactions between host resistance and pathogen effector genes in flax rust disease
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01794.xopenalex-snapshot
Plant traits that predict resistance to herbivores
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01800.xopenalex-snapshot
Trade‐off between growth and immune function: a meta‐analysis of selection experiments
inferredcites →https://doi.org/10.1111/j.1365-2435.2010.01803.xopenalex-snapshot
The resource availability hypothesis revisited: a meta‐analysis
inferredcites →https://doi.org/10.1111/j.1365-2745.2010.01738.xopenalex-snapshot
Spatial variation in disease resistance: from molecules to metapopulations
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02722.xopenalex-snapshot
Variation at two flowering time genes within and among populations of Arabidopsis thaliana : comparison with markers and traits
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05709.xopenalex-snapshot
Characterizing genomic variation of Arabidopsis thaliana : the roles of geography and climate
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Life history in a model system: opening the black box with Arabidopsis thaliana
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Controls on pathogen species richness in plants’ introduced and native ranges: roles of residence time, range size and host traits
inferredcites →https://doi.org/10.1111/j.1461-0248.2011.01601.xopenalex-snapshot
Meta-analysis of phenotypic selection on flowering phenology suggests that early flowering plants are favoured
inferredcites →https://doi.org/10.1111/j.1461-0248.2011.01730.xopenalex-snapshot
Living fast and dying of infection: host life history drives interspecific variation in infection and disease risk
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02130.xopenalex-snapshot
Resistance to pathogens and host developmental stage: a multifaceted relationship within the plant kingdom
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03479.xopenalex-snapshot
Arabidopsis thaliana populations show clinal variation in a climatic gradient associated with altitude
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PLEIOTROPY CAUSES LONG‐TERM GENETIC CONSTRAINTS ON LIFE‐HISTORY EVOLUTION INBRASSICA RAPA
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HOST LIFE SPAN AND THE EVOLUTION OF RESISTANCE CHARACTERISTICS
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PLEIOTROPY IN THE WILD: THE DORMANCY GENEDOG1EXERTS CASCADING CONTROL ON LIFE CYCLES
inferredcites →https://doi.org/10.1111/jeb.12528openalex-snapshot
Natural selection on quantitative immune defence traits: a comparison between theory and data
inferredcites →https://doi.org/10.1111/mec.12285openalex-snapshot
Paths to selection on life history loci in different natural environments across the native range of A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/mec.12396openalex-snapshot
Investigation of the geographical scale of adaptive phenological variation and its underlying genetics in A rabidopsis thaliana
inferredcites →https://doi.org/10.1111/mec.14084openalex-snapshot
Divergence of annual and perennial species in the Brassicaceae and the contribution of cis‐acting variation at FLC orthologues
inferredcites →https://doi.org/10.1111/mec.14100openalex-snapshot
Natural variation in life history strategy ofArabidopsis thalianadetermines stress responses to drought and insects of different feeding guilds
inferredcites →https://doi.org/10.1111/pce.12734openalex-snapshot
Altitudinal and climatic associations of seed dormancy and flowering traits evidence adaptation of annual life cycle timing in Arabidopsis thaliana
inferredcites →https://doi.org/10.1126/science.1165826openalex-snapshot
Effects of Genetic Perturbation on Seasonal Life History Plasticity
inferredcites →https://doi.org/10.1126/science.1195568openalex-snapshot
Has the Microbiota Played a Critical Role in the Evolution of the Adaptive Immune System?
inferredcites →https://doi.org/10.1126/science.1209244openalex-snapshot
Adaptation to Climate Across the Arabidopsis thaliana Genome
inferredcites →https://doi.org/10.1126/science.1209271openalex-snapshot
A Map of Local Adaptation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154055openalex-snapshot
Hormonal Modulation of Plant Immunity
inferredcites →https://doi.org/10.1146/annurev.ecolsys.34.011802.132339openalex-snapshot
The Evolutionary Ecology of Novel Plant-Pathogen Interactions
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1186/s13059-017-1378-9openalex-snapshot
Adaptation of Arabidopsis thaliana to the Yangtze River basin
inferredcites →https://doi.org/10.1371/journal.pbio.0040137openalex-snapshot
A Nonparametric Test Reveals Selection for Rapid Flowering in the Arabidopsis Genome
inferredcites →https://doi.org/10.1371/journal.pgen.0010006openalex-snapshot
Diversity of Flowering Responses in Wild Arabidopsis thaliana Strains
inferredcites →https://doi.org/10.1371/journal.pgen.1005597openalex-snapshot
"Missing" G x E Variation Controls Flowering Time in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0061075openalex-snapshot
Co-Variation between Seed Dormancy, Growth Rate and Flowering Time Changes with Latitude in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0127699openalex-snapshot
Investigating the Association between Flowering Time and Defense in the Arabidopsis thaliana-Fusarium oxysporum Interaction
inferredcites →https://doi.org/10.1371/journal.pone.0178990openalex-snapshot
Temporal fitness fluctuations in experimental Arabidopsis thaliana populations
inferredcites →https://doi.org/10.1371/journal.ppat.1000124openalex-snapshot
Host Responses in Life-History Traits and Tolerance to Virus Infection in Arabidopsis thaliana
inferredcites →https://doi.org/10.1534/genetics.107.074393openalex-snapshot
Polymorphism in Multilocus Host–Parasite Coevolutionary Interactions
inferredcites →https://doi.org/10.1534/genetics.107.079707openalex-snapshot
Comparison of Mixed-Model Approaches for Association Mapping
inferredcites →https://doi.org/10.1534/genetics.107.083899openalex-snapshot
Quantitative Trait Loci Mapping in Five New Large Recombinant Inbred Line Populations of Arabidopsis thaliana Genotyped With Consensus Single-Nucleotide Polymorphism Markers
inferredcites →https://doi.org/10.1534/genetics.108.094268openalex-snapshot
Single Nucleotide Polymorphisms in the Allene Oxide Synthase 2 Gene Are Associated With Field Resistance to Late Blight in Populations of Tetraploid Potato Cultivars
inferredcites →https://doi.org/10.2307/2260858openalex-snapshot
Growth Analysis of Congeneric Annual and Perennial Grass Species
inferredcites →https://doi.org/10.3389/fpls.2015.00981openalex-snapshot
Flg22-Triggered Immunity Negatively Regulates Key BR Biosynthetic Genes
inferredcites →https://doi.org/10.3732/ajb.2007346openalex-snapshot
From annuals to perennials: phylogeny of subtribe Castillejinae (Orobanchaceae)
inferredcites →https://doi.org/10.7554/elife.05255openalex-snapshot
DNA methylation in Arabidopsis has a genetic basis and shows evidence of local adaptation
inferredcites →https://doi.org/10.7554/elife.05604openalex-snapshot
Natural genetic variation in Arabidopsis thaliana defense metabolism genes modulates field fitness
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/tpg2.20121openalex-snapshot
A near‐complete genome sequence of mungbean ( Vigna radiata L.) provides key insights into the modern breeding program
inferred← citeshttps://doi.org/10.24072/pci.evolbiol.100026openalex-snapshot
Towards an integrated scenario to understand evolutionary patterns in A. thaliana
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