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Selfing, adaptation and background selection in finite populations

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What this work says

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

inferredcites →https://doi.org/10.1006/tpbi.1995.1025openalex-snapshot

Statistical Properties of Segregating Sites

inferredcites →https://doi.org/10.1006/tpbi.1997.1301openalex-snapshot

Deleterious Mutations, Variable Epistatic Interactions, and the Evolution of Recombination

inferredcites →https://doi.org/10.1007/978-94-011-5210-5_22openalex-snapshot

Evolution of intermediate selfing rates in plants: pollination ecology versus deleterious mutations

inferredcites →https://doi.org/10.1016/0022-5193(76)90138-7openalex-snapshot

A model for the evolution of self-fertilization and vegetative reproduction

inferredcites →https://doi.org/10.1016/0040-5809(86)90035-3openalex-snapshot

The interdependence of mating structure and inbreeding depression

inferredcites →https://doi.org/10.1016/0040-5809(91)90045-hopenalex-snapshot

Coevolution of self-fertilization and inbreeding depression I. Mutation-selection balance at one and two loci

inferredcites →https://doi.org/10.1016/0040-5809(91)90052-hopenalex-snapshot

Coevolution of self-fertilization and inbreeding depression. III. Homozygous lethal mutations at multiple loci

inferredcites →https://doi.org/10.1016/j.cub.2005.06.022openalex-snapshot

High Local Genetic Diversity and Low Outcrossing Rate in Caenorhabditis elegans Natural Populations

inferredcites →https://doi.org/10.1016/j.tree.2010.05.003openalex-snapshot

Environmental duress and epistasis: how does stress affect the strength of selection on new mutations?

inferredcites →https://doi.org/10.1016/s0022-5193(80)80026-9openalex-snapshot

The cost of sex in relation to mating system

inferredcites →https://doi.org/10.1017/s0016672300010156openalex-snapshot

The effect of linkage on limits to artificial selection

inferredcites →https://doi.org/10.1017/s0016672300029256openalex-snapshot

Multilocus models of inbreeding depression with synergistic selection and partial self-fertilization

inferredcites →https://doi.org/10.1017/s0016672300030160openalex-snapshot

The effect of linkage and population size on inbreeding depression due to mutational load

inferredcites →https://doi.org/10.1017/s0016672300033619openalex-snapshot

The effect of recombination on background selection

inferredcites →https://doi.org/10.1017/s001667230800949xopenalex-snapshot

The effect of linkage on limits to artificial selection

inferredcites →https://doi.org/10.1017/s0016672399004048openalex-snapshot

Inbreeding depression due to mildly deleterious mutations in finite populations: size does matter

inferredcites →https://doi.org/10.1017/s0016672399004152openalex-snapshot

The genetic basis of inbreeding depression

inferredcites →https://doi.org/10.1023/a:1017039010191openalex-snapshot

Evolution of intermediate selfing rates in plants: pollination ecology versus deleterious mutations

inferredcites →https://doi.org/10.1038/hdy.1989.56openalex-snapshot

Population genetic structure and outcrossing rate of Arabidopsis thaliana (L.) Heynh.

inferredcites →https://doi.org/10.1038/hdy.1993.189openalex-snapshot

Outcrossing and selfing evolution in populations under directional selection

inferredcites →https://doi.org/10.1038/nature05049openalex-snapshot

Interference among deleterious mutations favours sex and recombination in finite populations

inferredcites →https://doi.org/10.1038/nrg1985openalex-snapshot

The evolution of sex: empirical insights into the roles of epistasis and drift

inferredcites →https://doi.org/10.1086/281999openalex-snapshot

Self Fertilization and Population Variability in the Higher Plants

inferredcites →https://doi.org/10.1086/283365openalex-snapshot

Some Reproductive Factors Affecting the Selection of Self-Fertilization in Plants

inferredcites →https://doi.org/10.1086/284287openalex-snapshot

The Evolution of Self-Fertilization in Plants: A Population Genetic Model

inferredcites →https://doi.org/10.1086/285237openalex-snapshot

Mass-Action Models of Plant Mating Systems: The Evolutionary Stability of Mixed Mating Systems

inferredcites →https://doi.org/10.1086/297041openalex-snapshot

Self- and Cross-Fertilization in Plants. II. The Selection of Self- Fertilization

inferredcites →https://doi.org/10.1086/599083openalex-snapshot

Diploidy, Population Structure, and the Evolution of Recombination

inferredcites →https://doi.org/10.1086/669675openalex-snapshot

The Effects of Selective History and Environmental Heterogeneity on Inbreeding Depression in Experimental Populations ofDrosophila melanogaster

inferredcites →https://doi.org/10.1093/genetics/111.3.635openalex-snapshot

DELETERIOUS MUTATIONS AS AN EVOLUTIONARY FACTOR. II. FACULTATIVE APOMIXIS AND SELFING

inferredcites →https://doi.org/10.1093/genetics/131.2.493openalex-snapshot

Effects of partial inbreeding on fixation rates and variation of mutant genes.

inferredcites →https://doi.org/10.1093/genetics/140.2.821openalex-snapshot

Linkage and the limits to natural selection.

inferredcites →https://doi.org/10.1093/genetics/141.4.1605openalex-snapshot

Deleterious background selection with recombination.

inferredcites →https://doi.org/10.1093/genetics/146.4.1501openalex-snapshot

Structured Coalescent Processes on Different Time Scales

inferredcites →https://doi.org/10.1093/genetics/165.4.2249openalex-snapshot

Recombination Can Evolve in Large Finite Populations Given Selection on Sufficient Loci

inferredcites →https://doi.org/10.1093/genetics/78.2.737openalex-snapshot

THE EVOLUTIONARY ADVANTAGE OF RECOMBINATION

inferredcites →https://doi.org/10.1093/molbev/msq062openalex-snapshot

Genome-Wide Evidence for Efficient Positive and Purifying Selection in Capsella grandiflora, a Plant Species with a Large Effective Population Size

inferredcites →https://doi.org/10.1098/rspb.2013.0133openalex-snapshot

Evolutionary consequences of self-fertilization in plants

inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00604.xopenalex-snapshot

PARASITES AND THE EVOLUTION OF SELF-FERTILIZATION

inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00525.xopenalex-snapshot

ANIMALS MIX IT UP TOO: THE DISTRIBUTION OF SELF-FERTILIZATION AMONG HERMAPHRODITIC ANIMALS

inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00905.xopenalex-snapshot

The evolution of self‐fertilization and inbreeding depression under pollen discounting and pollen limitation

inferredcites →https://doi.org/10.1111/j.1469-1809.1941.tb02272.xopenalex-snapshot

AVERAGE EXCESS AND AVERAGE EFFECT OF A GENE SUBSTITUTION

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb04077.xopenalex-snapshot

THE EVOLUTION OF SELF‐FERTILIZATION AND INBREEDING DEPRESSION IN PLANTS. I. GENETIC MODELS

inferredcites →https://doi.org/10.1111/j.1558-5646.1988.tb04183.xopenalex-snapshot

INBREEDING DEPRESSION DOESN'T MATTER: THE GENETIC BASIS OF MATING-SYSTEM EVOLUTION

inferredcites →https://doi.org/10.1111/j.1558-5646.1990.tb03839.xopenalex-snapshot

INBREEDING DEPRESSION, GENETIC LOAD, AND THE EVOLUTION OF OUTCROSSING RATES IN A MULTILOCUS SYSTEM WITH NO LINKAGE

inferredcites →https://doi.org/10.1111/j.1558-5646.2012.01778.xopenalex-snapshot

ADAPTATION AND MALADAPTATION IN SELFING AND OUTCROSSING SPECIES: NEW MUTATIONS VERSUS STANDING VARIATION

inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.091704.175539openalex-snapshot

The Evolutionary Enigma of Mixed Mating Systems in Plants: Occurrence, Theoretical Explanations, and Empirical Evidence

inferredcites →https://doi.org/10.1146/annurev.es.18.110187.001321openalex-snapshot

INBREEDING DEPRESSION AND ITS EVOLUTIONARY CONSEQUENCES

inferredcites →https://doi.org/10.1201/9780429246593openalex-snapshot

An Introduction to the Bootstrap

inferredcites →https://doi.org/10.1371/journal.pgen.1000890openalex-snapshot

Local-Scale Patterns of Genetic Variability, Outcrossing, and Spatial Structure in Natural Stands of Arabidopsis thaliana

inferredcites →https://doi.org/10.1534/genetics.104.032821openalex-snapshot

Evolution of Recombination Due to Random Drift

inferredcites →https://doi.org/10.1534/genetics.104.036384openalex-snapshot

Self-Fertilization and the Evolution of Recombination

inferredcites →https://doi.org/10.1534/genetics.105.048207openalex-snapshot

Nucleotide Polymorphism and Linkage Disequilibrium in Wild Populations of the Partial Selfer Caenorhabditis elegans

inferredcites →https://doi.org/10.1534/genetics.108.086637openalex-snapshot

Sex and Deleterious Mutations

inferredcites →https://doi.org/10.1534/genetics.109.112920openalex-snapshot

The Role of Advantageous Mutations in Enhancing the Evolution of a Recombination Modifier

inferredcites →https://doi.org/10.1534/genetics.111.134288openalex-snapshot

The Effects of Deleterious Mutations on Evolution at Linked Sites

inferredcites →https://doi.org/10.1554/0014-3820(2001)055[0869:pateos]2.0.co;2openalex-snapshot

PARASITES AND THE EVOLUTION OF SELF-FERTILIZATION

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.518.4.5zenodo-depositor-declared

Molecular studies of Iranian populations support the morphology-based taxonomic separation of Medicago rigidula and M. rigiduloides

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inferred← citeshttps://doi.org/10.1002/ece3.8555openalex-snapshot

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inferred← citeshttps://doi.org/10.1007/978-1-0716-0199-0_11openalex-snapshot

Population Genomics of Transitions to Selfing in Brassicaceae Model Systems

inferred← citeshttps://doi.org/10.1007/978-1-4939-9074-0_11openalex-snapshot

Genome Evolution in Outcrossing vs. Selfing vs. Asexual Species

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Comparative analysis of molecular and morphological diversity in two diploid Paspalum species (Poaceae) with contrasting mating systems

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Genomic studies of adaptive evolution in outcrossing Arabidopsis species

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Maintenance of andromonoecy in an autogamous species: Superior male function in male flowers of the endangered Sagittaria guayanensis

inferred← citeshttps://doi.org/10.1016/j.tig.2017.04.002openalex-snapshot

The Evolutionary Interplay between Adaptation and Self-Fertilization

inferred← citeshttps://doi.org/10.1016/j.tpb.2025.05.003openalex-snapshot

Conditional gene genealogies given the population pedigree for a diploid Moran model with selfing

inferred← citeshttps://doi.org/10.1038/s41437-019-0182-6openalex-snapshot

Structure of multilocus genetic diversity in predominantly selfing populations

inferred← citeshttps://doi.org/10.1073/pnas.1501820112openalex-snapshot

Evolutionary perspectives on clonal reproduction in vertebrate animals

inferred← citeshttps://doi.org/10.1073/pnas.1707492115openalex-snapshot

Demography and mating system shape the genome-wide impact of purifying selection in Arabis alpina

inferred← citeshttps://doi.org/10.1080/17550874.2019.1610914openalex-snapshot

Diverse yet endangered: pollen dispersal and mating system reveal inbreeding in a narrow endemic plant

inferred← citeshttps://doi.org/10.1086/690009openalex-snapshot

Selfing, Local Mate Competition, and Reinforcement

inferred← citeshttps://doi.org/10.1086/700875openalex-snapshot

Anther Rubbing, a New Mechanism That Actively Promotes Selfing in Plants

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When Synchrony Makes the Best of Both Worlds Even Better: How Well Do We Really Understand Facultative Sex?

inferred← citeshttps://doi.org/10.1086/743597openalex-snapshot

Coexistence of sexual and asexual reproduction in facultatively parthenogenetic populations under sexual conflict: an agent-based simulation

inferred← citeshttps://doi.org/10.1093/aob/mcv025openalex-snapshot

Pollen dispersal and breeding structure in a hawkmoth-pollinated Pampa grasslands speciesPetunia axillaris(Solanaceae)

inferred← citeshttps://doi.org/10.1093/botlinnean/boag039openalex-snapshot

Reproductive flexibility and plant–pollinator coupling in a carnivorous plant from campos rupestres Utricularia damazioi Beauverd (Lentibulariaceae)

inferred← citeshttps://doi.org/10.1093/evolut/qpac013openalex-snapshot

The efficacy of selection may increase or decrease with selfing depending upon the recombination environment

inferred← citeshttps://doi.org/10.1093/evolut/qpac029openalex-snapshot

The effects of selfing on multi-step adaptation

inferred← citeshttps://doi.org/10.1093/evolut/qpae168openalex-snapshot

Hill-Robertson interference may bias the inference of fitness effects of new mutations in highly selfing species

inferred← citeshttps://doi.org/10.1093/gbe/evae261openalex-snapshot

Selfing Shapes Fixation of a Mutant Allele Under Flux Equilibrium

inferred← citeshttps://doi.org/10.1093/gbe/evag224openalex-snapshot

High levels of mitotic gene conversion are needed to effectively purge deleterious mutations in asexual organisms

inferred← citeshttps://doi.org/10.1093/gbe/evx098openalex-snapshot

Selfing in Haploid Plants and Efficacy of Selection: Codon Usage Bias in the Model Moss Physcomitrella patens

inferred← citeshttps://doi.org/10.1093/genetics/iyab123openalex-snapshot

Interplay between extreme drift and selection intensities favors the fixation of beneficial mutations in selfing maize populations

inferred← citeshttps://doi.org/10.1093/genetics/iyac114openalex-snapshot

The evolution of recombination in self-fertilizing organisms

inferred← citeshttps://doi.org/10.1093/genetics/iyaf169openalex-snapshot

A gene-based model of fitness and its implications for genetic variation: genetic and inbreeding loads

inferred← citeshttps://doi.org/10.1093/jeb/voaf009openalex-snapshot

Perspectives on mating–system evolution: comparing concepts in plants and animals

inferred← citeshttps://doi.org/10.1093/molbev/msaa199openalex-snapshot

The Genomic Selfing Syndrome Accompanies the Evolutionary Breakdown of Heterostyly

inferred← citeshttps://doi.org/10.1093/molbev/msae273openalex-snapshot

Selection Can Favor a Recombination Landscape That Limits Polygenic Adaptation

inferred← citeshttps://doi.org/10.1093/molbev/msag004openalex-snapshot

Estimating the Reduction in Genetic Diversity from Background Selection under Non-equilibrium Demography and Partial Selfing

inferred← citeshttps://doi.org/10.1093/molbev/msv121openalex-snapshot

Molecular Evolution of Freshwater Snails with Contrasting Mating Systems

inferred← citeshttps://doi.org/10.1098/rspb.2017.1652openalex-snapshot

Give one species the task to come up with a theory that spans them all: what good can come out of that?

inferred← citeshttps://doi.org/10.1101/2020.12.22.423930openalex-snapshot

Interplay between extreme drift and selection intensities favors the fixation of beneficial mutations in selfing maize populations

inferred← citeshttps://doi.org/10.1101/2021.05.20.445016openalex-snapshot

Genetic load may increase or decrease with selfing depending upon the recombination environment

inferred← citeshttps://doi.org/10.1101/210005openalex-snapshot

Partial selfing eliminates inbreeding depression while maintaining genetic diversity

inferred← citeshttps://doi.org/10.1101/809814openalex-snapshot

Epistasis, inbreeding depression and the evolution of self-fertilization

inferred← citeshttps://doi.org/10.1101/810515openalex-snapshot

Hidden genetic variance contributes to increase the short-term adaptive potential of selfing populations

inferred← citeshttps://doi.org/10.1111/1365-2745.12377openalex-snapshot

High‐elevation range limit of an annual herb is neither caused nor reinforced by declining pollinator service

inferred← citeshttps://doi.org/10.1111/ele.12703openalex-snapshot

Shifts in outcrossing rates and changes to floral traits are associated with the evolution of herbicide resistance in the common morning glory

inferred← citeshttps://doi.org/10.1111/eva.12398openalex-snapshot

Spatial pattern of invasion and the evolutionary responses of native plant species

inferred← citeshttps://doi.org/10.1111/evo.13222openalex-snapshot

The double edged sword: The demographic consequences of the evolution of self-fertilization

inferred← citeshttps://doi.org/10.1111/evo.13363openalex-snapshot

Feed-backs among inbreeding, inbreeding depression in sperm traits, and sperm competition can drive evolution of costly polyandry

inferred← citeshttps://doi.org/10.1111/evo.13449openalex-snapshot

Effects of partial selfing on the equilibrium genetic variance, mutation load, and inbreeding depression under stabilizing selection

inferred← citeshttps://doi.org/10.1111/evo.13553openalex-snapshot

Mutation accumulation in selfing populations under fluctuating selection

inferred← citeshttps://doi.org/10.1111/evo.13812openalex-snapshot

Effect of partial selfing and polygenic selection on establishment in a new habitat

inferred← citeshttps://doi.org/10.1111/evo.13961openalex-snapshot

Epistasis, inbreeding depression, and the evolution of self‐fertilization

inferred← citeshttps://doi.org/10.1111/evo.14189openalex-snapshot

Addressing Darwin's dilemma: Can pseudo‐overdominance explain persistent inbreeding depression and load?

inferred← citeshttps://doi.org/10.1111/evo.14194openalex-snapshot

Balancing selection in self‐fertilizing populations

inferred← citeshttps://doi.org/10.1111/jeb.12424openalex-snapshot

Sex uncovered: the evolutionary biology of reproductive systems

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Evolutionary genetic consequences of facultative sex and outcrossing

inferred← citeshttps://doi.org/10.1111/jeb.13660openalex-snapshot

Hidden genetic variance contributes to increase the short‐term adaptive potential of selfing populations

inferred← citeshttps://doi.org/10.1111/jeb.13968openalex-snapshot

Mutation accumulation in inbreeding populations under evolution of the selfing rate

inferred← citeshttps://doi.org/10.1111/mec.14933openalex-snapshot

Mutational load, inbreeding depression and heterosis in subdivided populations

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Genomic insights into inter‐ and intraspecific mating system shifts in Primulina

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Population genomics of the facultatively asexual duckweed Spirodela polyrhiza

inferred← citeshttps://doi.org/10.1111/nph.16186openalex-snapshot

Mating system impacts the genetic architecture of adaptation to heterogeneous environments

inferred← citeshttps://doi.org/10.1111/nph.19522openalex-snapshot

Parallel evolution of morphological and genomic selfing syndromes accompany the breakdown of heterostyly

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The Ecology of Mating and Its Evolutionary Consequences in Seed Plants

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On the Trail of Linked Selection

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Slower environmental change hinders adaptation from standing genetic variation

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Polygenic selection to a changing optimum under self–fertilisation

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Effects of Interference Between Selected Loci on the Mutation Load, Inbreeding Depression, and Heterosis

inferred← citeshttps://doi.org/10.1534/genetics.115.181024openalex-snapshot

Coalescence with Background and Balancing Selection in Systems with Bi- and Uniparental Reproduction: Contrasting Partial Asexuality and Selfing

inferred← citeshttps://doi.org/10.1534/genetics.116.187955openalex-snapshot

Background Selection in Partially Selfing Populations

inferred← citeshttps://doi.org/10.1534/genetics.116.188821openalex-snapshot

Limits to Adaptation in Partially Selfing Species

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Polygenicity and Epistasis Underlie Fitness-Proximal Traits in the Caenorhabditis elegans Multiparental Experimental Evolution (CeMEE) Panel

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Species boundary and extensive hybridization and introgression in Petunia

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Why do Inbreeding Depression and Load Resist Both Purging and Fixation?

inferred← citeshttps://doi.org/10.3389/fpls.2021.619154openalex-snapshot

How and When Does Outcrossing Occur in the Predominantly Selfing Species Medicago truncatula?

inferred← citeshttps://doi.org/10.3389/fpls.2024.1379730openalex-snapshot

How should we measure population-level inbreeding depression? Impacts of standing genetic associations between selfing rate and deleterious mutations

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Why Self-fertilizing Plants Still Exist in Wild Populations: Diversity Assurance through Stress-Induced Male Sterility May Promote Selective Outcrossing and Recombination

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Fisher vs. the Worms: Extraordinary Sex Ratios in Nematodes and the Mechanisms that Produce Them

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The Joint Evolution of Herbivory Defense and Mating System in Plants: A Simulation Approach

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Postpollination discrimination between self and outcross pollen covaries with the mating system of a self‐compatible flowering plant

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Analyse temporelle de la diversité en régime autogame ˸ approches théorique et empirique

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The evolution of recombination in self-fertilising species : theoretical approach and genomic study of linkage disequilibrium between deleterious mutations in several Angiosperm species

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Conséquences de l'autogamie sur le potentiel évolutif des populations ˸ approches empirique, expérimentale et théorique

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The dynamics of the response to selection under high drift-high selection : insights from Saclay’s divergent selection experiments for flowering time in maize

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Selfing is the safest sex for Caenorhabditis tropicalis

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The Drivers of Invasive Species Establishment and Impact on Ecological and Evolutionary Aspects of Resident Plant Communities

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