On the public citation graph
The Genomics of Selfing in Maize ( Zea mays ssp. mays ): Catching Purging in the Act
0 signed · 91 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471250953.bi1112s47openalex-snapshot
BEDTools: The Swiss‐Army Tool for Genome Feature Analysis
inferredcites →https://doi.org/10.1007/bf02860861openalex-snapshot
Evolution of DNA content in higher plants
inferredcites →https://doi.org/10.1016/j.tplants.2010.05.003openalex-snapshot
A triptych of the evolution of plant transposable elements
inferredcites →https://doi.org/10.1016/j.tree.2016.09.005openalex-snapshot
Understanding Inbreeding Depression, Purging, and Genetic Rescue
inferredcites →https://doi.org/10.1016/s0959-437x(00)00254-9openalex-snapshot
Breeding systems and genome evolution
inferredcites →https://doi.org/10.1017/s0016672300010156openalex-snapshot
The effect of linkage on limits to artificial selection
inferredcites →https://doi.org/10.1017/s0016672300012684openalex-snapshot
Associative overdominance caused by linked detrimental mutations
inferredcites →https://doi.org/10.1038/347380a0openalex-snapshot
Genetic loads and estimates of mutation rates in highly inbred plant populations
inferredcites →https://doi.org/10.1038/hdy.1994.183openalex-snapshot
Purging inbreeding depression and the probability of extinction: full-sib mating
inferredcites →https://doi.org/10.1038/nature08496openalex-snapshot
Mutation load and rapid adaptation favour outcrossing over self-fertilization
inferredcites →https://doi.org/10.1038/nature22971openalex-snapshot
Improved maize reference genome with single-molecule technologies
inferredcites →https://doi.org/10.1038/ng.2313openalex-snapshot
Maize HapMap2 identifies extant variation from a genome in flux
inferredcites →https://doi.org/10.1038/ng.2678openalex-snapshot
Massive genomic variation and strong selection in Arabidopsis thaliana lines from Sweden
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/ng.807openalex-snapshot
The Arabidopsis lyrata genome sequence and the basis of rapid genome size change
inferredcites →https://doi.org/10.1038/nprot.2009.86openalex-snapshot
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
inferredcites →https://doi.org/10.1038/nprot.2015.123openalex-snapshot
SIFT missense predictions for genomes
inferredcites →https://doi.org/10.1038/nrg2664openalex-snapshot
The genetics of inbreeding depression
inferredcites →https://doi.org/10.1038/s41588-018-0158-0openalex-snapshot
The maize W22 genome provides a foundation for functional genomics and transposon biology
inferredcites →https://doi.org/10.1038/s41588-018-0182-0openalex-snapshot
Extensive intraspecific gene order and gene structural variations between Mo17 and other maize genomes
inferredcites →https://doi.org/10.1038/s41598-017-06153-8openalex-snapshot
Maize (Zea mays L.) genome size indicated by 180-bp knob abundance is associated with flowering time
inferredcites →https://doi.org/10.1073/pnas.0509810102openalex-snapshot
Recombination, rearrangement, reshuffling, and divergence in a centromeric region of rice
inferredcites →https://doi.org/10.1073/pnas.0605618103openalex-snapshot
Analysis of retrotransposon structural diversity uncovers properties and propensities in angiosperm genome evolution
inferredcites →https://doi.org/10.1073/pnas.1018222108openalex-snapshot
Transposable elements and small RNAs contribute to gene expression divergence between Arabidopsis thaliana and Arabidopsis lyrata
inferredcites →https://doi.org/10.1073/pnas.110587497openalex-snapshot
Genome evolution of wild barley ( Hordeum spontaneum ) by BARE -1 retrotransposon dynamics in response to sharp microclimatic divergence
inferredcites →https://doi.org/10.1073/pnas.1413864112openalex-snapshot
Recombination in diverse maize is stable, predictable, and associated with genetic load
inferredcites →https://doi.org/10.1086/523366openalex-snapshot
Genomic Consequences of Outcrossing and Selfing in Plants
inferredcites →https://doi.org/10.1093/aob/mci011openalex-snapshot
The Large Genome Constraint Hypothesis: Evolution, Ecology and Phenotype
inferredcites →https://doi.org/10.1093/aob/mci013openalex-snapshot
Mechanisms and Control of Rapid Genomic Changes in Flax
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btq454openalex-snapshot
MASiVE: Mapping and Analysis of SireVirus Elements in plant genome sequences
inferredcites →https://doi.org/10.1093/bioinformatics/btt730openalex-snapshot
CrossMap: a versatile tool for coordinate conversion between genome assemblies
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/btu356openalex-snapshot
Toward better understanding of artifacts in variant calling from high-coverage samples
inferredcites →https://doi.org/10.1093/bioinformatics/btv351openalex-snapshot
BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs
inferredcites →https://doi.org/10.1093/gbe/evr008openalex-snapshot
Genome Size and Transposable Element Content as Determined by High-Throughput Sequencing in Maize and Zea luxurians
inferredcites →https://doi.org/10.1093/genetics/134.4.1289openalex-snapshot
The effect of deleterious mutations on neutral molecular variation.
inferredcites →https://doi.org/10.1093/genetics/141.3.1209openalex-snapshot
Individual variation in inbreeding depression: the roles of inbreeding history and mutation.
inferredcites →https://doi.org/10.1093/genetics/26.6.608openalex-snapshot
GENETIC CHARACTERISTICS OF THE B CHROMOSOMES IN MAIZE
inferredcites →https://doi.org/10.1093/genetics/93.1.237openalex-snapshot
SELECTION FOR RECOMBINATION IN PARTIALLY SELF-FERTILIZING POPULATIONS
inferredcites →https://doi.org/10.1093/molbev/msw296openalex-snapshot
Deleterious variants in Asian rice and the potential cost of domestication
inferredcites →https://doi.org/10.1093/nar/gkg509openalex-snapshot
SIFT: predicting amino acid changes that affect protein function
inferredcites →https://doi.org/10.1098/rspb.1979.0082openalex-snapshot
The evolutionary genetics of sexual systems in flowering plants
inferredcites →https://doi.org/10.1098/rspb.2013.0133openalex-snapshot
Evolutionary consequences of self-fertilization in plants
inferredcites →https://doi.org/10.1101/gr.081851.108openalex-snapshot
Detecting heterozygosity in shotgun genome assemblies: Lessons from obligately outcrossing nematodes
inferredcites →https://doi.org/10.1101/gr.091678.109openalex-snapshot
Epigenetic silencing of transposable elements: A trade-off between reduced transposition and deleterious effects on neighboring gene expression
inferredcites →https://doi.org/10.1101/gr.132102openalex-snapshot
Genome Size Reduction through Illegitimate Recombination Counteracts Genome Expansion in Arabidopsis
inferredcites →https://doi.org/10.1101/gr.5347007openalex-snapshot
Allelic variation and heterosis in maize: How do two halves make more than a whole?
inferredcites →https://doi.org/10.1111/eva.12414openalex-snapshot
Genomics advances the study of inbreeding depression in the wild
inferredcites →https://doi.org/10.1111/j.0014-3820.2002.tb00160.xopenalex-snapshot
PERSPECTIVE: PURGING THE GENETIC LOAD: A REVIEW OF THE EXPERIMENTAL EVIDENCE
inferredcites →https://doi.org/10.1111/j.1365-313x.2011.04806.xopenalex-snapshot
The turbulent life of Sirevirus retrotransposons and the evolution of the maize genome: more than ten thousand elements tell the story
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00965.xopenalex-snapshot
Inbreeding depression and heterosis in populations of Schiedea viscosa, a highly selfing species
inferredcites →https://doi.org/10.1111/j.1439-0523.1994.tb00690.xopenalex-snapshot
Selection for Early Flowering Results in Simultaneous Selection for Reduced Nuclear DNA Content in Maize
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.1469-8137.2008.02528.xopenalex-snapshot
Genome size is a strong predictor of cell size and stomatal density in angiosperms
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03335.xopenalex-snapshot
Stabilizing selection on genome size in a population of Festuca pallens under conditions of intensive intraspecific competition
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/nph.12247openalex-snapshot
Genome size variation in wild and cultivated maize along altitudinal gradients
inferredcites →https://doi.org/10.1111/nph.13639openalex-snapshot
Examining the cause of high inbreeding depression: analysis of whole‐genome sequence data in 28 selfed progeny of Eucalyptus grandis
inferredcites →https://doi.org/10.1111/nph.14784openalex-snapshot
Convergent adaptive evolution in marginal environments: unloading transposable elements as a common strategy among mangrove genomes
inferredcites →https://doi.org/10.1126/science.1174320openalex-snapshot
Genetic Properties of the Maize Nested Association Mapping Population
inferredcites →https://doi.org/10.1126/science.1177837openalex-snapshot
A First-Generation Haplotype Map of Maize
inferredcites →https://doi.org/10.1126/science.1178534openalex-snapshot
The B73 Maize Genome: Complexity, Diversity, and Dynamics
inferredcites →https://doi.org/10.1126/science.aao0827openalex-snapshot
Rapid genome shrinkage in a self-fertile nematode reveals sperm competition proteins
inferredcites →https://doi.org/10.1126/science.aar3684openalex-snapshot
Natural selection interacts with recombination to shape the evolution of hybrid genomes
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103827openalex-snapshot
Progress Toward Understanding Heterosis in Crop Plants
inferredcites →https://doi.org/10.1146/annurev.ecolsys.30.1.479openalex-snapshot
Do Plant Populations Purge Their Genetic Load? Effects of Population Size and Mating History on Inbreeding Depression
inferredcites →https://doi.org/10.1146/annurev.genet.42.110807.091612openalex-snapshot
Mid-Century Controversies in Population Genetics
inferredcites →https://doi.org/10.1371/journal.pgen.1003258openalex-snapshot
Properties and Modeling of GWAS when Complex Disease Risk Is Due to Non-Complementing, Deleterious Mutations in Genes of Large Effect
inferredcites →https://doi.org/10.1371/journal.pgen.1003604openalex-snapshot
From Many, One: Genetic Control of Prolificacy during Maize Domestication
inferredcites →https://doi.org/10.1371/journal.pgen.1004298openalex-snapshot
Three Groups of Transposable Elements with Contrasting Copy Number Dynamics and Host Responses in the Maize (Zea mays ssp. mays) Genome
inferredcites →https://doi.org/10.1371/journal.pgen.1005323openalex-snapshot
Reproductive Mode and the Evolution of Genome Size and Structure in Caenorhabditis Nematodes
inferredcites →https://doi.org/10.1371/journal.pgen.1006666openalex-snapshot
Independent introductions and admixtures have contributed to adaptation of European maize and its American counterparts
inferredcites →https://doi.org/10.1371/journal.pgen.1007162openalex-snapshot
Parallel altitudinal clines reveal trends in adaptive evolution of genome size in Zea mays
inferredcites →https://doi.org/10.1371/journal.pone.0014473openalex-snapshot
Purging Deleterious Mutations under Self Fertilization: Paradoxical Recovery in Fitness with Increasing Mutation Rate in Caenorhabditis elegans
inferredcites →https://doi.org/10.1534/g3.113.008870openalex-snapshot
The Pattern and Distribution of Deleterious Mutations in Maize
inferredcites →https://doi.org/10.1534/g3.115.023184openalex-snapshot
On the Consequences of Purging and Linkage on Fitness and Genetic Diversity
inferredcites →https://doi.org/10.1534/genetics.104.036384openalex-snapshot
Self-Fertilization and the Evolution of Recombination
inferredcites →https://doi.org/10.1534/genetics.105.048322openalex-snapshot
The Maize Ab10 Meiotic Drive System Maps to Supernumerary Sequences in a Large Complex Haplotype
inferredcites →https://doi.org/10.1534/genetics.108.097238openalex-snapshot
Historical Divergence and Gene Flow in the Genus Zea
inferredcites →https://doi.org/10.1534/genetics.114.172809openalex-snapshot
The Evolution of Selfing Is Accompanied by Reduced Efficacy of Selection and Purging of Deleterious Mutations
inferredcites →https://doi.org/10.2307/3558325openalex-snapshot
Is self‐fertilization an evolutionary dead end? Revisiting an old hypothesis with genetic theories and a macroevolutionary approach
inferredcites →https://doi.org/10.32614/rj-2016-021openalex-snapshot
mclust 5: Clustering, Classification and Density Estimation Using Gaussian Finite Mixture Models
inferredcites →https://doi.org/10.5962/bhl.title.110800openalex-snapshot
The effects of cross and self fertilisation in the vegetable kingdom /
inferredcites →https://doi.org/10.7554/elife.15716openalex-snapshot
The Arabidopsis thaliana mobilome and its impact at the species level
inferredcites →https://doi.org/10.7554/elife.25762openalex-snapshot
Pervasive epigenetic effects of Drosophila euchromatic transposable elements impact their evolution
inferredcites →https://doi.org/10.7717/peerj.2408openalex-snapshot
Testing the link between genome size and growth rate in maize
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.04.012openalex-snapshot
Lactuca dregeana DC. (Asteraceae: Chicorieae) – A South African crop relative under threat from hybridization and climate change
inferred← citeshttps://doi.org/10.1038/s41477-019-0507-8openalex-snapshot
The population genetics of structural variants in grapevine domestication
inferred← citeshttps://doi.org/10.3390/plants8090354openalex-snapshot
Population Genomic Approaches for Weed Science
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.