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Molecular clocks: four decades of evolution
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf01659391openalex-snapshot
On the constancy of the evolutionary rate of cistrons
inferredcites →https://doi.org/10.1007/bf01659392openalex-snapshot
The structure of cytochromec and the rates of molecular evolution
inferredcites →https://doi.org/10.1007/bf01732067openalex-snapshot
Molecular evolution of mRNA: A method for estimating evolutionary rates of synonymous and amino acid substitutions from homologous nucleotide sequences and its application
inferredcites →https://doi.org/10.1007/bf01732751openalex-snapshot
Are evolutionary rates really variable?
inferredcites →https://doi.org/10.1007/bf01797451openalex-snapshot
An examination of the constancy of the rate of molecular evolution
inferredcites →https://doi.org/10.1007/bf02111287openalex-snapshot
Man's place in Hominoidea as inferred from molecular clocks of DNA
inferredcites →https://doi.org/10.1007/bf02202109openalex-snapshot
Determinants of rate variation in mammalian DNA sequence evolution
inferredcites →https://doi.org/10.1007/bf02603075openalex-snapshot
On the rate of DNA sequence evolution inDrosophila
inferredcites →https://doi.org/10.1007/pl00013150openalex-snapshot
Early Metazoan Divergence Was About 830 Million Years Ago
inferredcites →https://doi.org/10.1007/s002399910034openalex-snapshot
The Power of Relative Rates Tests Depends on the Data
inferredcites →https://doi.org/10.1016/0076-6879(90)83036-9openalex-snapshot
[34] Converting distance to time: Application to human evolution
inferredcites →https://doi.org/10.1016/0169-5347(94)90176-7openalex-snapshot
Thermal habit, metabolic rate and the evolution of mitochondrial DNA
inferredcites →https://doi.org/10.1016/0959-437x(93)90011-dopenalex-snapshot
So, what about the molecular clock hypothesis?
inferredcites →https://doi.org/10.1016/1055-7903(92)90017-bopenalex-snapshot
Higher rates of amino acid substitution in rodents than in humans
inferredcites →https://doi.org/10.1016/b978-1-4832-2734-4.50017-6openalex-snapshot
Evolutionary Divergence and Convergence in Proteins
inferredcites →https://doi.org/10.1016/b978-1-4832-2734-4.50023-1openalex-snapshot
Structural and Functional Aspects of Cytochrome c in Relation to Evolution
inferredcites →https://doi.org/10.1016/j.gde.2003.10.008openalex-snapshot
Mutation rate variation in the mammalian genome
inferredcites →https://doi.org/10.1016/j.tig.2004.03.004openalex-snapshot
Precision of molecular time estimates
inferredcites →https://doi.org/10.1016/j.tig.2004.12.006openalex-snapshot
Molecular dating: ape bones agree with chicken entrails
inferredcites →https://doi.org/10.1016/s0168-9525(03)00053-2openalex-snapshot
Genomic clocks and evolutionary timescales
inferredcites →https://doi.org/10.1016/s0168-9525(04)00072-1openalex-snapshot
Precision of molecular time estimates
inferredcites →https://doi.org/10.1016/s0169-5347(97)84100-6openalex-snapshot
The origin and evolution of birds
inferredcites →https://doi.org/10.1016/s0959-437x(96)80034-7openalex-snapshot
Neutral theory of molecular evolution
inferredcites →https://doi.org/10.1017/cbo9780511623486openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1017/s0033583500004765openalex-snapshot
Evolution of higher-organism DNA
inferredcites →https://doi.org/10.1023/a:1004394418084openalex-snapshot
Emile Zuckerkandl, Linus Pauling, and the Molecular Evolutionary Clock, 1959–1965
inferredcites →https://doi.org/10.1038/18872openalex-snapshot
Absolute measures of the completeness of the fossil record
inferredcites →https://doi.org/10.1038/202147a0openalex-snapshot
Amino-Acid Sequence Investigations of Fibrinopeptides from Various Mammals: Evolutionary Implications
inferredcites →https://doi.org/10.1038/217624a0openalex-snapshot
Evolutionary Rate at the Molecular Level
inferredcites →https://doi.org/10.1038/224149a0openalex-snapshot
Rate of Fixation of Nucleotide Substitutions in Evolution
inferredcites →https://doi.org/10.1038/253603a0openalex-snapshot
Darwinian evolution in the genealogy of haemoglobin
inferredcites →https://doi.org/10.1038/267275a0openalex-snapshot
Preponderance of synonymous changes as evidence for the neutral theory of molecular evolution
inferredcites →https://doi.org/10.1038/281230a0openalex-snapshot
A selectively driven molecular clock
inferredcites →https://doi.org/10.1038/303546a0openalex-snapshot
Evidence on human origins from haemoglobins of African apes
inferredcites →https://doi.org/10.1038/305017a0openalex-snapshot
Evolutionary biology: Taxonomy by nucleotides
inferredcites →https://doi.org/10.1038/31927openalex-snapshot
A molecular timescale for vertebrate evolution
inferredcites →https://doi.org/10.1038/326093a0openalex-snapshot
The molecular clock runs more slowly in man than in apes and monkeys
inferredcites →https://doi.org/10.1038/35102048openalex-snapshot
Late Cretaceous relatives of rabbits, rodents, and other extant eutherian mammals
inferredcites →https://doi.org/10.1038/357153a0openalex-snapshot
Rates of mitochondrial DNA evolution in sharks are slow compared with mammals
inferredcites →https://doi.org/10.1038/381226a0openalex-snapshot
Continental breakup and the ordinal diversification of birds and mammals
inferredcites →https://doi.org/10.1038/40386openalex-snapshot
Endemic African mammals shake the phylogenetic tree
inferredcites →https://doi.org/10.1038/416726aopenalex-snapshot
Using the fossil record to estimate the age of the last common ancestor of extant primates
inferredcites →https://doi.org/10.1038/nature01262openalex-snapshot
Initial sequencing and comparative analysis of the mouse genome
inferredcites →https://doi.org/10.1038/nature03150openalex-snapshot
Definitive fossil evidence for the extant avian radiation in the Cretaceous
inferredcites →https://doi.org/10.1038/nrg1044openalex-snapshot
Phylogeny estimation: traditional and Bayesian approaches
inferredcites →https://doi.org/10.1038/scientificamerican1179-98openalex-snapshot
The Neutral Theory of Molecular Evolution
inferredcites →https://doi.org/10.1042/bj1280971openalex-snapshot
The amino acid sequence of cytochrome c from Helix aspersa Müller (garden snail)
inferredcites →https://doi.org/10.1073/pnas.022629899openalex-snapshot
Mutation rates in mammalian genomes
inferredcites →https://doi.org/10.1073/pnas.0334222100openalex-snapshot
Placental mammal diversification and the Cretaceous–Tertiary boundary
inferredcites →https://doi.org/10.1073/pnas.0401670101openalex-snapshot
Estimating metazoan divergence times with a molecular clock
inferredcites →https://doi.org/10.1073/pnas.0404142101openalex-snapshot
Bayesian Markov chain Monte Carlo sequence analysis reveals varying neutral substitution patterns in mammalian evolution
inferredcites →https://doi.org/10.1073/pnas.051611498openalex-snapshot
Estimation of divergence times from multiprotein sequences for a few mammalian species and several distantly related organisms
inferredcites →https://doi.org/10.1073/pnas.50.4.672openalex-snapshot
PRIMARY STRUCTURE AND EVOLUTION OF CYTOCHROME C
inferredcites →https://doi.org/10.1073/pnas.58.1.142openalex-snapshot
Rates of albumin evolution in primates.
inferredcites →https://doi.org/10.1073/pnas.76.1.381openalex-snapshot
Evolutionary change in 5S RNA secondary structure and a phylogenic tree of 54 5S RNA species.
inferredcites →https://doi.org/10.1073/pnas.77.12.7328openalex-snapshot
Nucleotide sequence divergence and functional constraint in mRNA evolution.
inferredcites →https://doi.org/10.1073/pnas.81.24.8009openalex-snapshot
The molecular clock may be an episodic clock.
inferredcites →https://doi.org/10.1073/pnas.82.6.1741openalex-snapshot
Evidence for higher rates of nucleotide substitution in rodents than in man.
inferredcites →https://doi.org/10.1073/pnas.90.9.4087openalex-snapshot
Body size, metabolic rate, generation time, and the molecular clock.
inferredcites →https://doi.org/10.1073/pnas.94.15.7776openalex-snapshot
Vagaries of the molecular clock
inferredcites →https://doi.org/10.1073/pnas.94.24.13028openalex-snapshot
Determining divergence times with a protein clock: Update and reevaluation
inferredcites →https://doi.org/10.1073/pnas.95.2.606openalex-snapshot
Origin of the metazoan phyla: Molecular clocks confirm paleontological estimates
inferredcites →https://doi.org/10.1073/pnas.98.1.1openalex-snapshot
Afrotheria: Plate tectonics meets genomics
inferredcites →https://doi.org/10.1080/03919710210001714503openalex-snapshot
'Molecules and monkeys': George Gaylord Simpson and the challenge of molecular evolution
inferredcites →https://doi.org/10.1080/10635150290102456openalex-snapshot
Divergence Time and Evolutionary Rate Estimation with Multilocus Data
inferredcites →https://doi.org/10.1093/bioinformatics/19.2.301openalex-snapshot
r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock
inferredcites →https://doi.org/10.1093/genetics/116.1.169openalex-snapshot
On the Overdispersed Molecular Clock
inferredcites →https://doi.org/10.1093/genetics/132.1.269openalex-snapshot
Testing for equality of evolutionary rates.
inferredcites →https://doi.org/10.1093/genetics/135.2.599openalex-snapshot
Simple methods for testing the molecular evolutionary clock hypothesis.
inferredcites →https://doi.org/10.1093/genetics/139.2.975openalex-snapshot
A generalized least-squares estimate for the origin of sporophytic self-incompatibility.
inferredcites →https://doi.org/10.1093/genetics/158.3.1321openalex-snapshot
Disparity Index: A Simple Statistic to Measure and Test the Homogeneity of Substitution Patterns Between Molecular Sequences
inferredcites →https://doi.org/10.1093/molbev/msg226openalex-snapshot
Bayesian Models of Episodic Evolution Support a Late Precambrian Explosive Diversification of the Metazoa
inferredcites →https://doi.org/10.1093/molbev/msg236openalex-snapshot
Temporal Patterns of Fruit Fly (Drosophila) Evolution Revealed by Mutation Clocks
inferredcites →https://doi.org/10.1093/molbev/msh087openalex-snapshot
Similar Rates but Different Modes of Sequence Evolution in Introns and at Exonic Silent Sites in Rodents: Evidence for Selectively Driven Codon Usage
inferredcites →https://doi.org/10.1093/molbev/msi039openalex-snapshot
Molecular Clocks Do Not Support the Cambrian Explosion
inferredcites →https://doi.org/10.1093/oso/9780195068832.001.0001openalex-snapshot
The Causes of Molecular Evolution
inferredcites →https://doi.org/10.1093/oso/9780195135848.001.0001openalex-snapshot
Molecular Evolution and Phylogenetics
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004043openalex-snapshot
Slow Molecular Clocks in Old World Monkeys, Apes, and Humans
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004083openalex-snapshot
Molecular Clocks in Reptiles: Life History Influences Rate of Molecular Evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025656openalex-snapshot
Relative rates of nuclear DNA evolution in human and Old World monkey lineages
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025731openalex-snapshot
A Nonparametric Approach to Estimating Divergence Times in the Absence of Rate Constancy
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025892openalex-snapshot
Estimating the rate of evolution of the rate of molecular evolution
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026373openalex-snapshot
How Important Is DNA Replication for Mutagenesis?
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040259openalex-snapshot
Phylogenetic test of the molecular clock and linearized trees.
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040343openalex-snapshot
A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes.
inferredcites →https://doi.org/10.1098/rspb.1999.0617openalex-snapshot
Divergence time estimates for the early history of animal phyla and the origin of plants, animals and fungi
inferredcites →https://doi.org/10.1126/science.1107808openalex-snapshot
Stem Lagomorpha and the Antiquity of Glires
inferredcites →https://doi.org/10.1126/science.146.3651.1535openalex-snapshot
Organisms and Molecules in Evolution
inferredcites →https://doi.org/10.1126/science.147.3653.68openalex-snapshot
Evolving Genes and Proteins
inferredcites →https://doi.org/10.1126/science.158.3805.1200openalex-snapshot
Immunological Time Scale for Hominid Evolution
inferredcites →https://doi.org/10.1126/science.161.3841.529openalex-snapshot
Repeated Sequences in DNA
inferredcites →https://doi.org/10.1126/science.271.5248.470openalex-snapshot
Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock
inferredcites →https://doi.org/10.1126/science.272.5265.1150openalex-snapshot
Fossil Evidence for a Late Cretaceous Origin of “Hoofed” Mammals
inferredcites →https://doi.org/10.1126/science.274.5287.568openalex-snapshot
Molecular Evidence for Deep Precambrian Divergences Among Metazoan Phyla
inferredcites →https://doi.org/10.1126/science.275.5303.1109openalex-snapshot
Mass Survival of Birds Across the Cretaceous- Tertiary Boundary: Molecular Evidence
inferredcites →https://doi.org/10.1126/science.285.5436.2031aopenalex-snapshot
Divergence Times of Eutherian Mammals
inferredcites →https://doi.org/10.1126/science.3082006openalex-snapshot
Rates of DNA Sequence Evolution Differ Between Taxonomic Groups
inferredcites →https://doi.org/10.1146/annurev.bi.46.070177.003041openalex-snapshot
Biochemical Evolution
inferredcites →https://doi.org/10.1146/annurev.earth.30.091201.140057openalex-snapshot
Dating the Time of Origin of Major Clades: Molecular Clocks and the Fossil Record
inferredcites →https://doi.org/10.1186/1471-2105-6-53openalex-snapshot
Evolutionary sequence analysis of complete eukaryote genomes
inferredcites →https://doi.org/10.1186/1471-2148-1-4openalex-snapshot
A genomic timescale for the origin of eukaryotes
inferredcites →https://doi.org/10.1186/1471-2148-4-2openalex-snapshot
A molecular timescale of eukaryote evolution and the rise of complex multicellular life
inferredcites →https://doi.org/10.1266/ggs.78.267openalex-snapshot
Time scale of eutherian evolution estimated without assuming a constant rate of molecular evolution.
inferredcites →https://doi.org/10.1266/jjg.64.243openalex-snapshot
Heterogeneity of tempo and mode of mitochondrial DNA evolution among mammalian orders.
inferredcites →https://doi.org/10.4159/harvard.9780674865327openalex-snapshot
Animal Species and Evolution
inferredcites →https://doi.org/10.5860/choice.30-2064openalex-snapshot
The causes of molecular evolution
inferredcites →https://doi.org/10.5860/choice.34-3307openalex-snapshot
The origin and evolution of birds
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.meegid.2012.07.015openalex-snapshot
Insights into origins of Human T-cell Lymphotropic Virus Type 1 based on new strains from aboriginal people of Canada
inferred← citeshttps://doi.org/10.1016/j.palwor.2015.01.005openalex-snapshot
Molecular paleobiology — Progress and perspectives
inferred← citeshttps://doi.org/10.1016/j.pt.2013.03.011openalex-snapshot
How can we determine the molecular clock of malaria parasites?
inferred← citeshttps://doi.org/10.1016/j.quaint.2017.04.040openalex-snapshot
Genetic studies of the peopling of the Americas: What insights do diachronic mitochondrial genome datasets provide?
inferred← citeshttps://doi.org/10.1016/j.quascirev.2018.12.003openalex-snapshot
Evidence of Ice Age humans in eastern Beringia suggests early migration to North America
inferred← citeshttps://doi.org/10.1016/j.shpsa.2015.09.002openalex-snapshot
Histories of molecules: Reconciling the past
inferred← citeshttps://doi.org/10.1016/j.tig.2024.11.002openalex-snapshot
A more elaborate genetic clock for clonal species
inferred← citeshttps://doi.org/10.1016/j.tree.2007.05.005openalex-snapshot
Rocks and clocks: calibrating the Tree of Life using fossils and molecules
inferred← citeshttps://doi.org/10.1016/j.tree.2007.06.013openalex-snapshot
Estimating diversification rates from phylogenetic information
inferred← citeshttps://doi.org/10.1016/j.tree.2014.07.004openalex-snapshot
The changing face of the molecular evolutionary clock
inferred← citeshttps://doi.org/10.1016/j.tree.2021.11.005openalex-snapshot
The earliest history of eukaryotic life: uncovering an evolutionary story through the integration of biological and geological data
inferred← citeshttps://doi.org/10.1016/j.ttbdis.2018.09.010openalex-snapshot
Argasid and ixodid systematics: Implications for soft tick evolution and systematics, with a new argasid species list
inferred← citeshttps://doi.org/10.1016/j.tvjl.2009.04.013openalex-snapshot
Chronobiology and the horse: Recent revelations and future directions
inferred← citeshttps://doi.org/10.1016/j.ygeno.2016.03.002openalex-snapshot
The genetic equidistance phenomenon at the proteomic level
inferred← citeshttps://doi.org/10.1016/j.ympev.2012.05.004openalex-snapshot
Three genome-based phylogeny of Cupressaceae s.l.: Further evidence for the evolution of gymnosperms and Southern Hemisphere biogeography
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.08.004openalex-snapshot
Evolutionary analysis of Chironius snakes unveils cryptic diversity and provides clues to diversification in the Neotropics
inferred← citeshttps://doi.org/10.1017/s003118201500133xopenalex-snapshot
Genetic population structure ofGyrodactylus thymalli(Monogenea) in a large Norwegian river system
inferred← citeshttps://doi.org/10.1021/jacs.8b07612openalex-snapshot
Building Strain with Large Macrocycles and Using It To Tune the Thermal Half-Lives of Hydrazone Photochromes
inferred← citeshttps://doi.org/10.1038/ncomms3708openalex-snapshot
Baiji genomes reveal low genetic variability and new insights into secondary aquatic adaptations
inferred← citeshttps://doi.org/10.1038/ncomms4502openalex-snapshot
Ancient diversification of Hyposmocoma moths in Hawaii
inferred← citeshttps://doi.org/10.1038/npre.2008.1676.2openalex-snapshot
Ancient fossil specimens of extinct species are genetically more distant to an outgroup than extant sister species are
inferred← citeshttps://doi.org/10.1038/npre.2008.1751openalex-snapshot
Inverse relationship between genetic diversity and epigenetic complexity
inferred← citeshttps://doi.org/10.1038/nrg.2015.8openalex-snapshot
Bayesian molecular clock dating of species divergences in the genomics era
inferred← citeshttps://doi.org/10.1038/nrg1838openalex-snapshot
An integrated view of protein evolution
inferred← citeshttps://doi.org/10.1038/nrg3456openalex-snapshot
Functional and evolutionary implications of gene orthology
inferred← citeshttps://doi.org/10.1038/nrg3950openalex-snapshot
Determinants of the rate of protein sequence evolution
inferred← citeshttps://doi.org/10.1038/nri3299openalex-snapshot
Dietary influences on intestinal immunity
inferred← citeshttps://doi.org/10.1038/s41559-024-02418-4openalex-snapshot
A clock for clonal organisms
inferred← citeshttps://doi.org/10.1038/srep30851openalex-snapshot
Evolutionary dynamics of selfish DNA explains the abundance distribution of genomic subsequences
inferred← citeshttps://doi.org/10.1042/bst20180186openalex-snapshot
The molecular clock and evolutionary timescales
inferred← citeshttps://doi.org/10.1073/pnas.0509585102openalex-snapshot
Placing confidence limits on the molecular age of the human–chimpanzee divergence
inferred← citeshttps://doi.org/10.1073/pnas.0801924105openalex-snapshot
Three ambitious (and rather unorthodox) assignments for the field of biodiversity genetics
inferred← citeshttps://doi.org/10.1073/pnas.1201889109openalex-snapshot
Evolution of centralized nervous systems: Two schools of evolutionary thought
inferred← citeshttps://doi.org/10.1073/pnas.1600374113openalex-snapshot
Variation in the molecular clock of primates
inferred← citeshttps://doi.org/10.1073/pnas.1913071117openalex-snapshot
Epistatic contributions promote the unification of incompatible models of neutral molecular evolution
inferred← citeshttps://doi.org/10.1073/pnas.2220473120openalex-snapshot
Wilson and Sarich (1969): The birth of a molecular evolution research paradigm
inferred← citeshttps://doi.org/10.1073/pnas.2301674120openalex-snapshot
Classic QnAs with Rasmus Grønfeldt Winther and Eske Willerslev
inferred← citeshttps://doi.org/10.1073/pnas.2303578120openalex-snapshot
A variant-dependent molecular clock with anomalous diffusion models SARS-CoV-2 evolution in humans
inferred← citeshttps://doi.org/10.1080/00071668.2026.2630729openalex-snapshot
Mitogenomic characterisation of the Ispenc chicken: a genetically distinct Turkish miniature breed
inferred← citeshttps://doi.org/10.1080/00438243.2019.1683466openalex-snapshot
Archaeogenetics and human evolution: the ontogeny of a biological discipline
inferred← citeshttps://doi.org/10.1080/07391102.2012.687520openalex-snapshot
Structural phylogenomics uncovers the early and concurrent origins of cysteine biosynthesis and iron-sulfur proteins
inferred← citeshttps://doi.org/10.1080/09553002.2019.1606957openalex-snapshot
Study of mutation from DNA to biological evolution
inferred← citeshttps://doi.org/10.1080/14772000.2015.1135196openalex-snapshot
Areas of endemism: travelling through space and the unexplored dimension
inferred← citeshttps://doi.org/10.1080/15627020.2011.11407499openalex-snapshot
Exploring the Diversity and Molecular Evolution of Shrews (Family Soricidae) using mtDNA CytochromebData
inferred← citeshttps://doi.org/10.1080/24701394.2018.1462347openalex-snapshot
Evolutionary history of genus Macrobrachium inferred from mitochondrial markers: a molecular clock approach
inferred← citeshttps://doi.org/10.1086/679527openalex-snapshot
Mitochondrial Eve and the Affective Politics of Human Ancestry
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.001.0001openalex-snapshot
Computational Molecular Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.002.0004openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0001openalex-snapshot
Models of nucleotide substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0002openalex-snapshot
Models of amino acid and codon substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0003openalex-snapshot
Phylogeny reconstruction: overview
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0004openalex-snapshot
Maximum likelihood methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0005openalex-snapshot
Bayesian methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0006openalex-snapshot
Comparison of methods and tests on trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0007openalex-snapshot
Molecular clock and estimation of species divergence times
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0008openalex-snapshot
Neutral and adaptive protein evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0009openalex-snapshot
Simulating molecular evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780198567028.003.0010openalex-snapshot
Perspectives
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.001.0001openalex-snapshot
Molecular Evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.002.0003openalex-snapshot
Copyright Page
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0001openalex-snapshot
Models of nucleotide substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0002openalex-snapshot
Models of amino acid and codon substitution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0003openalex-snapshot
Phylogeny reconstruction: overview
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0004openalex-snapshot
Maximum likelihood methods
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0005openalex-snapshot
Comparison of phylogenetic methods and tests on trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0006openalex-snapshot
Bayesian theory
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0007openalex-snapshot
Bayesian computation (MCMC)
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0008openalex-snapshot
Bayesian phylogenetics
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0009openalex-snapshot
Coalescent theory and species trees
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0010openalex-snapshot
Molecular clock and estimation of species divergence times
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0011openalex-snapshot
Neutral and adaptive protein evolution
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199602605.003.0012openalex-snapshot
Simulating molecular evolution
inferred← citeshttps://doi.org/10.1093/bib/bbr045openalex-snapshot
Models, algorithms and programs for phylogeny reconciliation
inferred← citeshttps://doi.org/10.1093/bioinformatics/btad221openalex-snapshot
Phylogenomic branch length estimation using quartets
inferred← citeshttps://doi.org/10.1093/bioinformatics/btag085openalex-snapshot
PyEvoMotion: a Python tool for population-based time-course analysis of genome evolution
inferred← citeshttps://doi.org/10.1093/bioinformatics/btl505openalex-snapshot
TimeTree: a public knowledge-base of divergence times among organisms
inferred← citeshttps://doi.org/10.1093/bioinformatics/btm239openalex-snapshot
Bioinformatics software for biologists in the genomics era
inferred← citeshttps://doi.org/10.1093/bioinformatics/btr315openalex-snapshot
TimeTree2: species divergence times on the iPhone
inferred← citeshttps://doi.org/10.1093/cz/zow018openalex-snapshot
Phylogenetic framework for coevolutionary studies: a compass for exploring jungles of tangled trees
inferred← citeshttps://doi.org/10.1093/gbe/evaa248openalex-snapshot
Proteome-Scale Detection of Differential Conservation Patterns at Protein and Subprotein Levels with BLUR
inferred← citeshttps://doi.org/10.1093/gbe/evu223openalex-snapshot
The Influence of Selection for Protein Stability on dN/dS Estimations
inferred← citeshttps://doi.org/10.1093/gbe/evv146openalex-snapshot
The Evolution of Bony Vertebrate Enhancers at Odds with Their Coding Sequence Landscape
inferred← citeshttps://doi.org/10.1093/genetics/iyad036openalex-snapshot
Evolutionary genetics of the mitochondrial genome: insights from Drosophila
inferred← citeshttps://doi.org/10.1093/imaiai/iaad032openalex-snapshot
Spectral top-down recovery of latent tree models
inferred← citeshttps://doi.org/10.1093/jambio/lxag056openalex-snapshot
Tracing ancient life through the genomic record
inferred← citeshttps://doi.org/10.1093/jole/lzz009openalex-snapshot
Best practices in justifying calibrations for dating language families
inferred← citeshttps://doi.org/10.1093/molbev/msaa130openalex-snapshot
Gradients Do Grow on Trees: A Linear-Time O ( N )-Dimensional Gradient for Statistical Phylogenetics
inferred← citeshttps://doi.org/10.1093/molbev/msaa193openalex-snapshot
Additive Uncorrelated Relaxed Clock Models for the Dating of Genomic Epidemiology Phylogenies
inferred← citeshttps://doi.org/10.1093/molbev/msaa222openalex-snapshot
Log Transformation Improves Dating of Phylogenies
inferred← citeshttps://doi.org/10.1093/molbev/msag093openalex-snapshot
DiagnoDating: diagnostics for dated phylogenies in microbial population genetics
inferred← citeshttps://doi.org/10.1093/molbev/msn024openalex-snapshot
Divergence Times in Caenorhabditis and Drosophila Inferred from Direct Estimates of the Neutral Mutation Rate
inferred← citeshttps://doi.org/10.1093/molbev/msq014openalex-snapshot
Performance of Relaxed-Clock Methods in Estimating Evolutionary Divergence Times and Their Credibility Intervals
inferred← citeshttps://doi.org/10.1093/molbev/msq232openalex-snapshot
A Universal Molecular Clock of Protein Folds and Its Power in Tracing the Early History of Aerobic Metabolism and Planet Oxygenation
inferred← citeshttps://doi.org/10.1093/molbev/msr045openalex-snapshot
Approximate Likelihood Calculation on a Phylogeny for Bayesian Estimation of Divergence Times
inferred← citeshttps://doi.org/10.1093/molbev/msr266openalex-snapshot
Inconsistencies in Estimating the Age of HIV-1 Subtypes Due to Heterotachy
inferred← citeshttps://doi.org/10.1093/molbev/mss140openalex-snapshot
The Influence of Rate Heterogeneity among Sites on the Time Dependence of Molecular Rates
inferred← citeshttps://doi.org/10.1093/molbev/msu091openalex-snapshot
Covariance between Testes Size and Substitution Rates in Primates
inferred← citeshttps://doi.org/10.1093/molbev/msu200openalex-snapshot
Prospects for Building Large Timetrees Using Molecular Data with Incomplete Gene Coverage among Species
inferred← citeshttps://doi.org/10.1093/molbev/msv139openalex-snapshot
Mitogenomic Meta-Analysis Identifies Two Phases of Migration in the History of Eastern Eurasian Sheep
inferred← citeshttps://doi.org/10.1093/molbev/msv154openalex-snapshot
Evaluating the Adequacy of Molecular Clock Models Using Posterior Predictive Simulations
inferred← citeshttps://doi.org/10.1093/molbev/msw026openalex-snapshot
Advances in Time Estimation Methods for Molecular Data
inferred← citeshttps://doi.org/10.1093/molbev/msw194openalex-snapshot
Evolution of Protein Domain Repeats in Metazoa
inferred← citeshttps://doi.org/10.1093/molbev/msw234openalex-snapshot
Spontaneous Mutation Accumulation inDaphnia pulexin Selection-Free vs. Competitive Environments
inferred← citeshttps://doi.org/10.1093/molbev/msw247openalex-snapshot
Fast and Accurate Estimates of Divergence Times from Big Data
inferred← citeshttps://doi.org/10.1093/molbev/msx308openalex-snapshot
Unbiased Estimate of Synonymous and Nonsynonymous Substitution Rates with Nonstationary Base Composition
inferred← citeshttps://doi.org/10.1093/molbev/msy133openalex-snapshot
Estimating TimeTrees with MEGA and the TimeTree Resource
inferred← citeshttps://doi.org/10.1093/molbev/msz014openalex-snapshot
A Machine Learning Method for Detecting Autocorrelation of Evolutionary Rates in Large Phylogenies
inferred← citeshttps://doi.org/10.1093/molbev/msz283openalex-snapshot
Mutations Beget More Mutations—Rapid Evolution of Mutation Rate in Response to the Risk of Runaway Accumulation
inferred← citeshttps://doi.org/10.1093/mollus/eym014openalex-snapshot
Origin and diversification of the soldier meadow springsnails (Hydrobiidae: Pyrgulopsis), a species flock in the northwestern Great Basin, United States
inferred← citeshttps://doi.org/10.1093/mollus/eyu068openalex-snapshot
Phylogeography of Neptune whelk (Neptunea arthritica) suggests sex-biased impact of tributyltin pollution and overfishing around northern Japan
inferred← citeshttps://doi.org/10.1093/nc/niab013openalex-snapshot
Minimal physicalism as a scale-free substrate for cognition and consciousness
inferred← citeshttps://doi.org/10.1093/oso/9780198868125.002.0009openalex-snapshot
Preface and acknowledgements
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