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Purifying selection can reduce intraspecific mitochondrial gene variation to that of nuclear rRNA
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ece3.4937openalex-snapshot
Genetic structure, phylogeography, and demography of Anadara tuberculosa (Bivalvia) from East Pacific as revealed by mtDNA: Implications to conservation
inferredcites →https://doi.org/10.1006/mpev.1994.1013openalex-snapshot
Root Probabilities for Intraspecific Gene Trees under Neutral Coalescent Theory
inferredcites →https://doi.org/10.1007/bf02111234openalex-snapshot
Calibration of mitochondrial DNA evolution in geese
inferredcites →https://doi.org/10.1016/b978-1-4832-3211-9.50009-7openalex-snapshot
Evolution of Protein Molecules
inferredcites →https://doi.org/10.1016/j.ajhg.2009.05.001openalex-snapshot
Correcting for Purifying Selection: An Improved Human Mitochondrial Molecular Clock
inferredcites →https://doi.org/10.1016/j.jcz.2016.10.002openalex-snapshot
Pleistocene demographic expansion and high gene flow in the Globe Skimmer dragonfly Pantala flavescens Fabricius (Odonata: Libellulidae) in Peninsular Malaysia
inferredcites →https://doi.org/10.1016/j.tig.2007.03.008openalex-snapshot
Positive and negative selection on the mitochondrial genome
inferredcites →https://doi.org/10.1016/s0168-9525(01)02338-1openalex-snapshot
Natural selection and the evolution of mtDNA-encoded peptides: evidence for intergenomic co-adaptation
inferredcites →https://doi.org/10.1016/s0169-5347(00)89195-8openalex-snapshot
Is mitochondrial DNA a strictly neutral marker?
inferredcites →https://doi.org/10.1017/cbo9780511623486openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1038/30724openalex-snapshot
Rapid evolution to terrestrial life in Jamaican crabs
inferredcites →https://doi.org/10.1038/351652a0openalex-snapshot
Adaptive protein evolution at the Adh locus in Drosophila
inferredcites →https://doi.org/10.1038/nrg2396openalex-snapshot
Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease
inferredcites →https://doi.org/10.1038/s41598-018-25138-9openalex-snapshot
Mitochondrial DNA is unsuitable to test for isolation by distance
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1080/07474946.2011.563710openalex-snapshot
Off-Line Detection of Multiple Change Points by the Filtered Derivative withp-Value Method
inferredcites →https://doi.org/10.1080/24701394.2018.1467411openalex-snapshot
Levels and patterns of genetic variation in Japanese whiting ( Sillago japonica ) based on mitochondrial DNA control region
inferredcites →https://doi.org/10.1080/24701394.2019.1570173openalex-snapshot
Genetic homogeneity of the Pacific thread herring ( Opisthonema libertate ) (Günther, 1867) in the Eastern Pacific, inferred from mtDNA sequences
inferredcites →https://doi.org/10.1093/jhered/esv020openalex-snapshot
Problems and Cautions With Sequence Mismatch Analysis and Bayesian Skyline Plots to Infer Historical Demography
inferredcites →https://doi.org/10.1093/molbev/msi103openalex-snapshot
Bayesian Coalescent Inference of Past Population Dynamics from Molecular Sequences
inferredcites →https://doi.org/10.1093/nar/gkn337openalex-snapshot
Standard and generalized McDonald-Kreitman test: a website to detect selection by comparing different classes of DNA sites
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025554openalex-snapshot
Mitochondrial DNA phylogeny and the reconstruction of the population history of a species: the case of the European anchovy (Engraulis encrasicolus)
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026036openalex-snapshot
Median-joining networks for inferring intraspecific phylogenies
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040727openalex-snapshot
Population growth makes waves in the distribution of pairwise genetic differences.
inferredcites →https://doi.org/10.1098/rspb.1998.0568openalex-snapshot
New dates and new rates for divergence across the Isthmus of Panama
inferredcites →https://doi.org/10.1098/rspb.2014.0528openalex-snapshot
King penguin demography since the last glaciation inferred from genome-wide data
inferredcites →https://doi.org/10.1111/2041-210x.12410openalex-snapshot
popart : full‐feature software for haplotype network construction
inferredcites →https://doi.org/10.1111/imb.12501openalex-snapshot
Evolutionary divergence of mitochondrial genomes in two Tetranychus species distributed across different climates
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb00732.xopenalex-snapshot
IS THE POPULATION SIZE OF A SPECIES RELEVANT TO ITS EVOLUTION?
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01600.xopenalex-snapshot
SPECIATION AND DIVERSITY ON TROPICAL ROCKY SHORES: A GLOBAL PHYLOGENY OF SNAILS OF THE GENUS ECHINOLITTORINA
inferredcites →https://doi.org/10.1111/j.1096-3642.1979.tb01084.xopenalex-snapshot
On the taxonomy of Littorina africana (Mollusca: Gastropoda)
inferredcites →https://doi.org/10.1111/j.1365-2699.2009.02118.xopenalex-snapshot
Tethyan vicariance, relictualism and speciation: evidence from a global molecular phylogeny of the opisthobranch genus Bulla
inferredcites →https://doi.org/10.1111/j.1755-0998.2010.02847.xopenalex-snapshot
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows
inferredcites →https://doi.org/10.1111/mec.14488openalex-snapshot
Climate‐driven mitochondrial selection: A test in Australian songbirds
inferredcites →https://doi.org/10.1126/science.1122033openalex-snapshot
Population Size Does Not Influence Mitochondrial Genetic Diversity in Animals
inferredcites →https://doi.org/10.1146/annurev.ecolsys.36.091704.175513openalex-snapshot
The Population Biology of Mitochondrial DNA and Its Phylogenetic Implications
inferredcites →https://doi.org/10.1371/journal.pgen.1003527openalex-snapshot
Strong Purifying Selection at Synonymous Sites in D. melanogaster
inferredcites →https://doi.org/10.1371/journal.pone.0100755openalex-snapshot
DNA Barcoding Works in Practice but Not in (Neutral) Theory
inferredcites →https://doi.org/10.3853/j.0067-1975.56.2004.1393openalex-snapshot
The subfamily Littorininae (Gastropoda: Littorinidae) in the temperate Southern Hemisphere: the genera Nodilittorina, Austrolittorina and Afrolittorina
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