On the public citation graph
On the rate of molecular evolution
0 signed · 233 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known work and none has been retracted — and get a dated CiteStamped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/food.19710150234openalex-snapshot
Margaret O. Dayhoff: Atlas of Protein Sequence and Structure 1969 (Volume 4) XXIV u. 361 S., 21 Ausklapptafeln, 68 Abb. und zahlreiche Tabellen. National Biomedical Research Foundation, Silver Spring/Maryland 1969. Preis $ 12,50
inferredcites →https://doi.org/10.1007/978-3-642-46244-3_5openalex-snapshot
Genetic Loads and the Cost of Natural Selection
inferredcites →https://doi.org/10.1007/bf00486096openalex-snapshot
An improved method for determining codon variability in a gene and its application to the rate of fixation of mutations in evolution
inferredcites →https://doi.org/10.1007/bf02985336openalex-snapshot
Optimum mutation rate and degree of dominance as determined by the principle of minimum genetic load
inferredcites →https://doi.org/10.1007/bf02987241openalex-snapshot
More precise expressions for the cost of natural selection
inferredcites →https://doi.org/10.1016/0009-2541(72)90017-4openalex-snapshot
Biochemical evolution and the origin of life
inferredcites →https://doi.org/10.1016/b978-1-4832-2734-4.50017-6openalex-snapshot
Evolutionary Divergence and Convergence in Proteins
inferredcites →https://doi.org/10.1017/s0016672300002846openalex-snapshot
Natural selection and gene substitution
inferredcites →https://doi.org/10.1017/s0016672300011459openalex-snapshot
Genetic variability maintained in a finite population due to mutational production of neutral and nearly neutral isoalleles
inferredcites →https://doi.org/10.1017/s0021900200108368openalex-snapshot
Diffusion models in population genetics
inferredcites →https://doi.org/10.1017/s0031819100038146openalex-snapshot
Reason and Existenz,. By Karl Jaspers. Translated, with an introduction, by William Earle. (London: Routledge and Kegan Paul. Pp. 157. Price 14s.)
inferredcites →https://doi.org/10.1017/s0305004100015644openalex-snapshot
A Mathematical Theory of Natural and Artificial Selection, Part V: Selection and Mutation
inferredcites →https://doi.org/10.1038/201847a0openalex-snapshot
A Preliminary Estimate of the Number of Human Genes
inferredcites →https://doi.org/10.1038/217624a0openalex-snapshot
Evolutionary Rate at the Molecular Level
inferredcites →https://doi.org/10.1038/2251025a0openalex-snapshot
Non-Darwinian Evolution: A Critique
inferredcites →https://doi.org/10.1038/hdy.1969.10openalex-snapshot
The substitutional load in a finite population
inferredcites →https://doi.org/10.1073/pnas.58.1.142openalex-snapshot
Rates of albumin evolution in primates.
inferredcites →https://doi.org/10.1073/pnas.58.5.1895openalex-snapshot
Altered base ratios in the DNA of an Escherichia coli mutator strain.
inferredcites →https://doi.org/10.1073/pnas.63.4.1181openalex-snapshot
THE RATE OF MOLECULAR EVOLUTION CONSIDERED FROM THE STANDPOINT OF POPULATION GENETICS
inferredcites →https://doi.org/10.1086/282389openalex-snapshot
Evolution in Sexual and Asexual Populations
inferredcites →https://doi.org/10.1086/282698openalex-snapshot
On the Biological Significance of the Cost of Gene Substitution
inferredcites →https://doi.org/10.1090/s0002-9904-1958-10191-3openalex-snapshot
Evolution by mutation
inferredcites →https://doi.org/10.1093/genetics/47.6.713openalex-snapshot
ON THE PROBABILITY OF FIXATION OF MUTANT GENES IN A POPULATION
inferredcites →https://doi.org/10.1093/genetics/61.3.763openalex-snapshot
THE AVERAGE NUMBER OF GENERATIONS UNTIL FIXATION OF A MUTANT GENE IN A FINITE POPULATION
inferredcites →https://doi.org/10.1093/genetics/61.4.893openalex-snapshot
THE NUMBER OF HETEROZYGOUS NUCLEOTIDE SITES MAINTAINED IN A FINITE POPULATION DUE TO STEADY FLUX OF MUTATIONS
inferredcites →https://doi.org/10.1093/genetics/63.3.701openalex-snapshot
THE AVERAGE NUMBER OF GENERATIONS UNTIL EXTINCTION OF AN INDIVIDUAL MUTANT GENE IN A FINITE POPULATION
inferredcites →https://doi.org/10.1093/genetics/64.3-4.387openalex-snapshot
STATISTICAL ANALYSIS OF THE BASE COMPOSITION OF GENES USING DATA ON THE AMINO ACID COMPOSITION OF PROTEINS
inferredcites →https://doi.org/10.1111/j.1558-5646.1949.tb00004.xopenalex-snapshot
SUGGESTIONS AS TO QUANTITATIVE MEASUREMENT OF RATES OF EVOLUTION
inferredcites →https://doi.org/10.1111/j.1558-5646.1963.tb03281.xopenalex-snapshot
THE MEASUREMENT OF EFFECTIVE POPULATION NUMBER
inferredcites →https://doi.org/10.1126/science.147.3653.68openalex-snapshot
Evolving Genes and Proteins
inferredcites →https://doi.org/10.1126/science.168.3938.1469openalex-snapshot
Eukaryotes versus Prokaryotes: An Estimate of Evolutionary Distance
inferredcites →https://doi.org/10.1126/science.169.3946.686openalex-snapshot
Fitness of an Escherichia coli Mutator Gene
inferredcites →https://doi.org/10.1214/aoms/1177706791openalex-snapshot
Some Problems of Stochastic Processes in Genetics
inferredcites →https://doi.org/10.2307/1529706openalex-snapshot
An Introduction to Population Genetics Theory
inferredcites →https://doi.org/10.2307/2412074openalex-snapshot
Atlas of Protein Sequence and Structure, 1966.
inferredcites →https://doi.org/10.4159/harvard.9780674865327openalex-snapshot
Animal Species and Evolution
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/zookeys.1256.153772zenodo-depositor-declared
Genome sequencing provides novel insights into diadromous migration adaptations in the roughskin sculpin, Trachidermus fasciatus (Scorpaeniformes, Cottidae)
inferred← citeshttps://doi.org/10.1002/9780470122839.ch4openalex-snapshot
A Theory on the Origin of Life
inferred← citeshttps://doi.org/10.1002/9780470143810.ch11openalex-snapshot
The Molecular Variations of Cytochrome c as a Function of the Evolution of Species
inferred← citeshttps://doi.org/10.1002/ange.19720841802openalex-snapshot
Selbstorganisation molekularer Systeme und die Evolution des genetischen Apparats
inferred← citeshttps://doi.org/10.1002/anie.197207981openalex-snapshot
Self‐Organization of Molecular Systems and Evolution of the Genetic Apparatus
inferred← citeshttps://doi.org/10.1002/ece3.8562openalex-snapshot
Does effective population size affect rates of molecular evolution: Mitochondrial data for host/parasite species pairs in bees suggests not
inferred← citeshttps://doi.org/10.1002/prot.25702openalex-snapshot
Effect of site‐directed point mutations on protein misfolding: A simulation study
inferred← citeshttps://doi.org/10.1007/0-387-26887-1_10openalex-snapshot
Origin and Evolution of DNA and DNA Replication Machineries
inferred← citeshttps://doi.org/10.1007/13836_2018_58openalex-snapshot
Population Genomics and Biogeography of the Northern Acorn Barnacle (Semibalanus balanoides) Using Pooled Sequencing Approaches
inferred← citeshttps://doi.org/10.1007/978-0-387-45083-4_2openalex-snapshot
Dating Methods and Corresponding Chronometers in Astrobiology
inferred← citeshttps://doi.org/10.1007/978-1-4615-6781-3_9openalex-snapshot
Phylogeny and Classification of Birds Based on the Data of DNA-DNA Hybridization
inferred← citeshttps://doi.org/10.1007/978-1-4615-6968-8_2openalex-snapshot
Evolution on a Petri Dish
inferred← citeshttps://doi.org/10.1007/978-1-4615-8267-0_2openalex-snapshot
Population Genetics Theory in Relation to the Neutralist-Selectionist Controversy
inferred← citeshttps://doi.org/10.1007/978-3-030-60181-2_2openalex-snapshot
Molecular Evolution: A Brief Introduction
inferred← citeshttps://doi.org/10.1007/978-3-642-50124-1_11openalex-snapshot
The Changing Role of Population Genetics Theory
inferred← citeshttps://doi.org/10.1007/978-3-642-66894-4_6openalex-snapshot
Mechanisms Controlling the Oxygen Affinity of Bird and Reptile Blood: A Comparison Between the Funtional Properties of Chicken and Crocodile Hemoglobin
inferred← citeshttps://doi.org/10.1007/978-3-642-93360-8_16openalex-snapshot
Population Genetical Mechanism of Molecular Evolution
inferred← citeshttps://doi.org/10.1007/978-94-011-5210-5_30openalex-snapshot
The molecular clock revisited: the rate of synonymous vs. replacement change in Drosophila
inferred← citeshttps://doi.org/10.1007/bf01323098openalex-snapshot
Theoretical considerations on probabilities of biopolymers and life's origin
inferred← citeshttps://doi.org/10.1007/bf01653962openalex-snapshot
Non-randomness of base replacement in point mutation
inferred← citeshttps://doi.org/10.1007/bf01659159openalex-snapshot
Theoretical foundations for a quantitative approach to paleogenetics
inferred← citeshttps://doi.org/10.1007/bf01659160openalex-snapshot
Theoretical foundations for a quantitative approach to paleogenetics
inferred← citeshttps://doi.org/10.1007/bf01659161openalex-snapshot
Evolutionary rate of cistrons and DNA divergence
inferred← citeshttps://doi.org/10.1007/bf01730998openalex-snapshot
Evolution of DNA structure: Direction, mechanism, rate
inferred← citeshttps://doi.org/10.1007/bf01732948openalex-snapshot
Evolution of the amino acid substitution in the mammalian myoglobin gene
inferred← citeshttps://doi.org/10.1007/bf01739097openalex-snapshot
Criteria for optimising phylogenetic trees and the problem of determining the root of a tree
inferred← citeshttps://doi.org/10.1007/bf01743626openalex-snapshot
Evolutionary processes and evolutionary noise at the molecular level
inferred← citeshttps://doi.org/10.1007/bf01797452openalex-snapshot
Evolutionary clock: The rate of evolution of rattlesnake cytochromec
inferred← citeshttps://doi.org/10.1007/bf02100622openalex-snapshot
Molecular evolution inDrosophila and the higher diptera
inferred← citeshttps://doi.org/10.1007/bf02111279openalex-snapshot
Molecular evolutionary clock and the neutral theory
inferred← citeshttps://doi.org/10.1007/s00239-003-2543-1openalex-snapshot
Model-Based Inference of Recombination Hotspots in a Highly, Variable Oncogene
inferred← citeshttps://doi.org/10.1007/s00239-004-9921-1openalex-snapshot
Model-Based Inference of Recombination Hotspots in a Highly Variable Oncogene
inferred← citeshttps://doi.org/10.1007/s00239-010-9407-2openalex-snapshot
The Last Universal Common Ancestor (LUCA) and the Ancestors of Archaea and Bacteria were Progenotes
inferred← citeshttps://doi.org/10.1007/s00239-020-09932-6openalex-snapshot
Emerging Frontiers in the Study of Molecular Evolution
inferred← citeshttps://doi.org/10.1007/s00239-025-10270-8openalex-snapshot
Fascination with RNA Editing: In the Lights of Evolution and Biology
inferred← citeshttps://doi.org/10.1007/s00239-026-10318-3openalex-snapshot
Functionality versus Adaptation: Insights from Transcriptional Adaptation
inferred← citeshttps://doi.org/10.1007/s00438-009-0509-8openalex-snapshot
Molecular characterization of the Sasanda LTR copia retrotransposon family uncovers their recent amplification in Triticum aestivum (L.) genome
inferred← citeshttps://doi.org/10.1007/s10905-017-9603-7openalex-snapshot
Sex Ratios in a Socially Parasitic Bee and Implications for Host-Parasite Interactions
inferred← citeshttps://doi.org/10.1007/s11033-007-9057-7openalex-snapshot
RAPD typing of Aspergillus chevalieri, Aspergillus nidulans, Aspergillus tetrazonus (quadrilineatus) and their teleomorphs using 5′-d[AACGCGCAAC]-3′ and 5′-d[CCCGTCAGCA]-3′ primers
inferred← citeshttps://doi.org/10.1007/s11038-006-9086-6openalex-snapshot
2. Dating Methods and Corresponding Chronometers in Astrobiology
inferred← citeshttps://doi.org/10.1007/s11427-013-4452-xopenalex-snapshot
The genetic equidistance result: misreading by the molecular clock and neutral theory and reinterpretation nearly half of a century later
inferred← citeshttps://doi.org/10.1016/0005-2787(73)90095-6openalex-snapshot
The relationship between mismatched base pairs and the thermal stability of DNA duplexes
inferred← citeshttps://doi.org/10.1016/0005-2787(73)90096-8openalex-snapshot
The relationship between mismatched base pairs and the thermal stability of DNA duplexes
inferred← citeshttps://doi.org/10.1016/0005-2787(75)90106-9openalex-snapshot
Sequence homology of nuclear and mitochondrial DNAs of different yeasts
inferred← citeshttps://doi.org/10.1016/0022-5193(83)90346-6openalex-snapshot
Some theoretical aspects of protein coevolution in the ecosystem “phage-bacteria” I. The problem
inferred← citeshttps://doi.org/10.1016/0040-5809(71)90014-1openalex-snapshot
Theoretical foundation of population genetics at the molecular level
inferred← citeshttps://doi.org/10.1016/0047-2484(72)90003-6openalex-snapshot
Differential rates of evolution in the carbonic anhydrase isozymes of catarrhine primates
inferred← citeshttps://doi.org/10.1016/0047-2484(72)90007-3openalex-snapshot
Molecular evolution of human immunoglobulins
inferred← citeshttps://doi.org/10.1016/b978-0-08-021378-1.50034-8openalex-snapshot
PHOSPHOGLUCOISOMERASE ALLELE FREQUENCY DATA IN Mytilus edulis (L) FROM IRISH COASTAL SITES: ITS ECOLOGICAL SIGNIFICANCE
inferred← citeshttps://doi.org/10.1016/b978-0-12-005215-8.50010-3openalex-snapshot
Time in Organic Evolution
inferred← citeshttps://doi.org/10.1016/b978-0-12-635501-7.50011-3openalex-snapshot
The Evolution of Proteins
inferred← citeshttps://doi.org/10.1016/b978-0-12-643150-6.50024-5openalex-snapshot
Evolutionary Adaptation of Mitochondrial Cytochrome c to Its Functional Milieu
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.02.203openalex-snapshot
The human pandemic coronaviruses on the show: The spike glycoprotein as the main actor in the coronaviruses play
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.07.017openalex-snapshot
Biological evidence against the panspermia theory
inferred← citeshttps://doi.org/10.1016/j.shpsc.2008.12.006openalex-snapshot
Molecular evolution: concepts and the origin of disciplines
inferred← citeshttps://doi.org/10.1016/j.tig.2013.05.009openalex-snapshot
The faster-X effect: integrating theory and data
inferred← citeshttps://doi.org/10.1016/j.ygeno.2016.01.008openalex-snapshot
New thoughts on an old riddle: What determines genetic diversity within and between species?
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.ygeno.2017.03.002openalex-snapshot
Genetic equidistance at nucleotide level
inferred← citeshttps://doi.org/10.1016/s1369-8486(00)00026-1openalex-snapshot
Satellite-DNA: A case-study for the evolution of experimental techniques
inferred← citeshttps://doi.org/10.1017/s0001867800038568openalex-snapshot
Evolution processes with continuity of types
inferred← citeshttps://doi.org/10.1017/s0016672300018930openalex-snapshot
The rate of mutant substitution in populations with overlapping generations
inferred← citeshttps://doi.org/10.1017/s0016672300020036openalex-snapshot
Genetic variation in varying environments
inferred← citeshttps://doi.org/10.1023/a:1017035109224openalex-snapshot
The molecular clock revisited: the rate of synonymous vs. replacement change in Drosophila
inferred← citeshttps://doi.org/10.1023/a:1024707801415openalex-snapshot
Rates of Molecular Evolution of Primates
inferred← citeshttps://doi.org/10.1034/j.1399-0004.2002.610401.xopenalex-snapshot
Genetics of population isolates
inferred← citeshttps://doi.org/10.1038/280599a0openalex-snapshot
Use of Panamanian sea urchins to test the molecular clock
inferred← citeshttps://doi.org/10.1038/302495a0openalex-snapshot
Frequency of fixation of adaptive mutations is higher in evolving diploid than haploid yeast populations
inferred← citeshttps://doi.org/10.1038/ng.2656openalex-snapshot
Mycobacterium tuberculosis mutation rate estimates from different lineages predict substantial differences in the emergence of drug-resistant tuberculosis
inferred← citeshttps://doi.org/10.1038/npre.2008.1733.1openalex-snapshot
The genetic equidistance result of molecular evolution is independent of mutation rates
inferred← citeshttps://doi.org/10.1038/npre.2008.1733.2openalex-snapshot
The genetic equidistance result of molecular evolution is independent of mutation rates
inferred← citeshttps://doi.org/10.1038/s41437-021-00446-5openalex-snapshot
Pedigree-based and phylogenetic methods support surprising patterns of mutation rate and spectrum in the gray mouse lemur
inferred← citeshttps://doi.org/10.1038/s41467-020-19818-2openalex-snapshot
No evidence for increased transmissibility from recurrent mutations in SARS-CoV-2
inferred← citeshttps://doi.org/10.1038/s41559-024-02439-zopenalex-snapshot
A somatic genetic clock for clonal species
inferred← citeshttps://doi.org/10.1038/s41588-021-00836-9openalex-snapshot
Large-scale sequencing of flatfish genomes provides insights into the polyphyletic origin of their specialized body plan
inferred← citeshttps://doi.org/10.1038/s41598-026-64001-0openalex-snapshot
Gene function predicts divergence across molecular levels
inferred← citeshttps://doi.org/10.1042/bcj20200915openalex-snapshot
Tick–human interactions: from allergic klendusity to the α-Gal syndrome
inferred← citeshttps://doi.org/10.1073/pnas.71.10.3863openalex-snapshot
Solutions to the Cost-of-Selection Dilemma
inferred← citeshttps://doi.org/10.1073/pnas.74.6.2514openalex-snapshot
Spontaneous mutation rates at enzyme loci in Drosophila melanogaster.
inferred← citeshttps://doi.org/10.1080/00219266.1975.9654039openalex-snapshot
Investigating the causes of changes in allele frequency during evolution
inferred← citeshttps://doi.org/10.1080/10635150490522278openalex-snapshot
Explosive Radiations and the Reliability of Molecular Clocks: Island Endemic Radiations as a Test Case
inferred← citeshttps://doi.org/10.1080/11250008609355508openalex-snapshot
Place et rôle de l'adaptation dans l'évolution des organismes
inferred← citeshttps://doi.org/10.1086/282856openalex-snapshot
Estimation of Number of Amino Acid Substitutions when Back Mutations Can Occur
inferred← citeshttps://doi.org/10.1086/677571openalex-snapshot
Modeling Evolution Using the Probability of Fixation: History and Implications
inferred← citeshttps://doi.org/10.1093/biosci/biad021openalex-snapshot
So overt it's covert: Wildlife coloration in the city
inferred← citeshttps://doi.org/10.1093/evlett/qrac004openalex-snapshot
Slower-X: reduced efficiency of selection in the early stages of X chromosome evolution
inferred← citeshttps://doi.org/10.1093/gbe/evs133openalex-snapshot
Patterns of Evolutionary Conservation of Microsatellites (SSRs) Suggest a Faster Rate of Genome Evolution in Hymenoptera Than in Diptera
inferred← citeshttps://doi.org/10.1093/genetics/152.1.269openalex-snapshot
Synonymous Rates at the RpII215 Gene of Drosophila: Variation Among Species and Across the Coding Region
inferred← citeshttps://doi.org/10.1093/genetics/iyae043openalex-snapshot
Fixation times of de novo and standing beneficial variants in subdivided populations
inferred← citeshttps://doi.org/10.1093/genetics/iyaf011openalex-snapshot
Substitution load revisited: a high proportion of deaths can be selective
inferred← citeshttps://doi.org/10.1093/genetics/iyag081openalex-snapshot
A model for background selection in nonequilibrium populations
inferred← citeshttps://doi.org/10.1093/hmg/ddi408openalex-snapshot
Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer
inferred← citeshttps://doi.org/10.1093/jeb/voae157openalex-snapshot
Skewed X chromosome inactivation as a response to sexually antagonistic selection
inferred← citeshttps://doi.org/10.1093/jhered/esae040openalex-snapshot
Quantitative trait loci concentrate in specific regions of the Mexican cavefish genome and reveal key candidate genes for cave-associated evolution
inferred← citeshttps://doi.org/10.1093/molbev/msg167openalex-snapshot
Increased Rates of Sequence Evolution in Endosymbiotic Bacteria and Fungi with Small Effective Population Sizes
inferred← citeshttps://doi.org/10.1093/molbev/msq009openalex-snapshot
A Generation Time Effect on the Rate of Molecular Evolution in Invertebrates
inferred← citeshttps://doi.org/10.1093/molbev/msr227openalex-snapshot
Expansion Dating: Calibrating Molecular Clocks in Marine Species from Expansions onto the Sunda Shelf Following the Last Glacial Maximum
inferred← citeshttps://doi.org/10.1093/molbev/mss057openalex-snapshot
Impact of Genetic Architecture on the Relative Rates of X versus Autosomal Adaptive Substitution
inferred← citeshttps://doi.org/10.1093/nar/11.3.901openalex-snapshot
cDNa cloning and nucleotide sequence comparison of Chinese hamster metallothionein I and II mRNAs
inferred← citeshttps://doi.org/10.1093/sysbio/24.2.209openalex-snapshot
Primate Phylogeny, Neutral Mutations, and "Molecular Clocks"
inferred← citeshttps://doi.org/10.1093/sysbio/syz022openalex-snapshot
The Molecular Clock in the Evolution of Protein Structures
inferred← citeshttps://doi.org/10.1098/rsif.2014.1010openalex-snapshot
Evolution on neutral networks accelerates the ticking rate of the molecular clock
inferred← citeshttps://doi.org/10.1098/rspb.2026.1143openalex-snapshot
Ornaments evolve faster than weapons
inferred← citeshttps://doi.org/10.1098/rsta.2020.0422openalex-snapshot
The simple emergence of complex molecular function
inferred← citeshttps://doi.org/10.1101/2021.06.27.450095openalex-snapshot
Evolution and favored change: a principle of least selection
inferred← citeshttps://doi.org/10.1101/2022.10.25.513737openalex-snapshot
Time in allopatry does not predict the outcome of secondary contact in lowland Panamanian birds
inferred← citeshttps://doi.org/10.1101/2023.07.07.548167openalex-snapshot
Fixation times of de novo and standing beneficial variants in subdivided populations
inferred← citeshttps://doi.org/10.1101/2023.07.19.549703openalex-snapshot
Patterns of diversity under loose genetic draft
inferred← citeshttps://doi.org/10.1101/2023.11.07.566010openalex-snapshot
Precise age estimation in clonal species using a somatic genetic clock
inferred← citeshttps://doi.org/10.1101/2024.03.29.587360openalex-snapshot
Loci associated with cave-derived traits concentrate in specific regions of the Mexican cavefish genome
inferred← citeshttps://doi.org/10.1101/2024.10.23.619029openalex-snapshot
Paternal genome elimination, monogenic reproduction, and the evolutionary genetics of atypical sex chromosome systems
inferred← citeshttps://doi.org/10.1101/2025.01.14.633008openalex-snapshot
Integrated model of the protein molecular clock across mammalian species
inferred← citeshttps://doi.org/10.1101/259507openalex-snapshot
The Rate of Molecular Evolution When Mutation May Not Be Weak
inferred← citeshttps://doi.org/10.1101/724880openalex-snapshot
Pedigree-based measurement of the de novo mutation rate in the gray mouse lemur reveals a high mutation rate, few mutations in CpG sites, and a weak sex bias
inferred← citeshttps://doi.org/10.1101/821736openalex-snapshot
Testing the basic tenet of the molecular clock and neutral theory by using ancient proteomes
inferred← citeshttps://doi.org/10.1101/cshperspect.a041453openalex-snapshot
Combining Molecular, Macroevolutionary, and Macroecological Perspectives on the Generation of Diversity
inferred← citeshttps://doi.org/10.1109/e-science.2009.17openalex-snapshot
Phylogenetic Predictions on Grids
inferred← citeshttps://doi.org/10.1111/1755-0998.13841openalex-snapshot
Validation of machine learning approach for direct mutation rate estimation
inferred← citeshttps://doi.org/10.1111/brv.13010openalex-snapshot
Moderating the neutralist–selectionist debate: exactly which propositions are we debating, and which arguments are valid?
inferred← citeshttps://doi.org/10.1111/eva.13649openalex-snapshot
Rare, long‐distance dispersal underpins genetic connectivity in the pink sea fan, Eunicella verrucosa
inferred← citeshttps://doi.org/10.1111/evo.13360openalex-snapshot
Fitness change in relation to mutation number in spontaneous mutation accumulation lines ofChlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1111/j.1469-185x.1975.tb00989.xopenalex-snapshot
THE MOLECULAR EVOLUTION OF PITUITARY HORMONES
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1981.tb04950.xopenalex-snapshot
GENETIC VARIABILITY OF THE FACE FLY,MUSCA AUTUMNALISDE GEER, IN RELATION TO A POPULATION BOTTLENECK
inferred← citeshttps://doi.org/10.1111/j.1558-5646.1999.tb05361.xopenalex-snapshot
PERSPECTIVE: SPONTANEOUS DELETERIOUS MUTATION
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2011.01458.xopenalex-snapshot
SUBSTITUTION RATES AT NEUTRAL GENES DEPEND ON POPULATION SIZE UNDER FLUCTUATING DEMOGRAPHY AND OVERLAPPING GENERATIONS
inferred← citeshttps://doi.org/10.1111/j.1601-5223.1973.tb01092.xopenalex-snapshot
Genetics of Zoarces populations
inferred← citeshttps://doi.org/10.1111/j.1601-5223.1981.tb01420.xopenalex-snapshot
Genetics of Zoarces populations
inferred← citeshttps://doi.org/10.1111/jeb.12031openalex-snapshot
The determinants of the molecular substitution process in turtles
inferred← citeshttps://doi.org/10.1111/jzo.12325openalex-snapshot
Small effective population sizes of bee social parasites compared to their hosts raise important questions for evolutionary arms race
inferred← citeshttps://doi.org/10.1111/mec.13113openalex-snapshot
Variation in promiscuity and sexual selection drives avian rate of Faster‐Z evolution
inferred← citeshttps://doi.org/10.1126/science.174.4005.150openalex-snapshot
Amino Acid Composition of Proteins as a Product of Molecular Evolution
inferred← citeshttps://doi.org/10.1126/science.179.4078.1144openalex-snapshot
Generation Time and Genomic Evolution in Primates
inferred← citeshttps://doi.org/10.1126/science.182.4116.1024openalex-snapshot
Electrophoretic Variation in Escherichia coli from Natural Sources
inferred← citeshttps://doi.org/10.1126/science.183.4123.446openalex-snapshot
Analysis of Neutrality in Protein Polymorphism
inferred← citeshttps://doi.org/10.1126/science.183.4123.446-bopenalex-snapshot
Analysis of Neutrality in Protein Polymorphism
inferred← citeshttps://doi.org/10.1126/science.183.4123.446.bopenalex-snapshot
Analysis of Neutrality in Protein Polymorphism
inferred← citeshttps://doi.org/10.1126/science.271.5248.470openalex-snapshot
Determining Divergence Times of the Major Kingdoms of Living Organisms with a Protein Clock
inferred← citeshttps://doi.org/10.1128/jb.110.3.793-802.1972openalex-snapshot
Enzyme Evolution in the Enterobacteriaceae
inferred← citeshttps://doi.org/10.1134/s0016702906130015openalex-snapshot
Phenomenon of life: Between equilibrium and non-linearity. Origin and principles of evolution
inferred← citeshttps://doi.org/10.1134/s2079086422050024openalex-snapshot
The Concept of the Modern Molecular Clock and Experience in Estimating Divergence Times of Eulipotyphla and Rodentia
inferred← citeshttps://doi.org/10.1139/g77-024openalex-snapshot
ESTIMATION OF TIME OF DIVERGENCE FROM PHYLOGENETIC STUDIES
inferred← citeshttps://doi.org/10.1146/annurev-arplant-070522-062509openalex-snapshot
The Evolution and Evolvability of Photosystem II
inferred← citeshttps://doi.org/10.1146/annurev.es.14.110183.000453openalex-snapshot
The Molecular Basis of Adaptation: A Critical Review of Relevant Ideas and Observations
inferred← citeshttps://doi.org/10.1159/000394568openalex-snapshot
The Molecular Variations of Cytochrome c as a Function of the Evolution of Species1
inferred← citeshttps://doi.org/10.11606/t.44.2018.tde-26042018-095244openalex-snapshot
Análises estatísticas de Cloudina spp. no sul da faixa Paraguai e Namíbia. E suas implicações filogenéticas e evolutivas.
inferred← citeshttps://doi.org/10.1161/01.hyp.25.3.320openalex-snapshot
Association of the α-Adducin Locus With Essential Hypertension
inferred← citeshttps://doi.org/10.1162/biot_a_00021openalex-snapshot
The Overlap Feature of the Genetic Equidistance Result—A Fundamental Biological Phenomenon Overlooked for Nearly Half of a Century
inferred← citeshttps://doi.org/10.1186/1471-2148-6-7openalex-snapshot
Genome-wide acceleration of protein evolution in flies (Diptera)
inferred← citeshttps://doi.org/10.1201/b17795-3openalex-snapshot
Identifying Evolution Signatures in Molecules
inferred← citeshttps://doi.org/10.1201/b17795-5openalex-snapshot
Identifying Natural Selection with Molecular Data
inferred← citeshttps://doi.org/10.1266/ggs.76.159openalex-snapshot
Comparison of DNA and protein polymorphisms between humans and chimpanzees.
inferred← citeshttps://doi.org/10.1266/jjg.46.393openalex-snapshot
GENETIC LOAD DUE TO MUTATIONS WITH VERY SMALL EFFECTS
inferred← citeshttps://doi.org/10.1360/zc2013-43-4-275openalex-snapshot
遗传等距离现象: 分子钟和中性理论的误读及其近半世纪后的重新解谜
inferred← citeshttps://doi.org/10.1525/9780520313897-001openalex-snapshot
DARWINIAN AND NON-DARWINIAN EVOLUTION
inferred← citeshttps://doi.org/10.1525/9780520313897-016openalex-snapshot
THEORETICAL FOUNDATIONS OF PALEOGENETICS
inferred← citeshttps://doi.org/10.1534/genetics.104.75135openalex-snapshot
Molecular Clock: An Anti-neo-Darwinian Legacy
inferred← citeshttps://doi.org/10.1534/genetics.110.125997openalex-snapshot
Epistasis Increases the Rate of Conditionally Neutral Substitution in an Adapting Population
inferred← citeshttps://doi.org/10.1534/genetics.112.140178openalex-snapshot
Weak Selection and Protein Evolution
inferred← citeshttps://doi.org/10.2307/2640707openalex-snapshot
Perspective: Spontaneous Deleterious Mutation
inferred← citeshttps://doi.org/10.2478/biocosmos-2025-0009openalex-snapshot
The Maximum Genetic Diversity Theory: A Comprehensive Framework for Understanding Evolutionary Processes
inferred← citeshttps://doi.org/10.2984/67.4.7openalex-snapshot
Diversity and Origins of Fijian Leaf-Cutter Bees (Megachilidae)
inferred← citeshttps://doi.org/10.31274/rtd-180813-8590openalex-snapshot
Some effects of subdivision of finite populations on genetic diversity measures
inferred← citeshttps://doi.org/10.3161/150811009x465668openalex-snapshot
A Relaxed Molecular Clock Places an Evolutionary Timescale on the Origins of North American Big-Eared Bats (Vespertilionidae:Corynorhinus)
inferred← citeshttps://doi.org/10.3389/fpls.2022.888049openalex-snapshot
Does IR-loss promote plastome structural variation and sequence evolution?
inferred← citeshttps://doi.org/10.3390/ijms241612892openalex-snapshot
Genome Sequencing Provides Novel Insights into Mudflat Burrowing Adaptations in Eel Goby Taenioides sp. (Teleost: Amblyopinae)
inferred← citeshttps://doi.org/10.3390/life13081751openalex-snapshot
Speciation on the Roof of the World: Parallel Fast Evolution of Cryptic Mole Vole Species in the Pamir-Alay—Tien Shan Region
inferred← citeshttps://doi.org/10.3390/v14061225openalex-snapshot
Characterization of the Cross-Species Transmission Potential for Porcine Deltacoronaviruses Expressing Sparrow Coronavirus Spike Protein in Commercial Poultry
inferred← citeshttps://doi.org/10.3390/v3040379openalex-snapshot
An Ecological and Conservation Perspective on Advances in the Applied Virology of Zoonoses
inferred← citeshttps://doi.org/10.4172/jcsb.1000009openalex-snapshot
The Genetic Equidistance Result of Molecular Evolution is Independent of Mutation Rates
inferred← citeshttps://doi.org/10.4310/cis.2023.v23.n4.a1openalex-snapshot
The maximum genetic diversity theory of molecular evolution
inferred← citeshttps://doi.org/10.59717/j.tiis.2026.100009openalex-snapshot
Comparative RNA editomics prioritizes candidate adaptive RNA editing sites
inferred← citeshttps://doi.org/10.64898/2026.02.08.704128openalex-snapshot
Rapid termite diversification is associated with increased transposable element activity
inferred← citeshttps://doi.org/10.64898/2026.02.19.706750openalex-snapshot
Rapid speciation in small populations challenges the dominance of ecological speciation
inferred← citeshttps://doi.org/10.70675/28835658ze3c8z4a59z94bcz6db7a7e22084openalex-snapshot
Les causes des variations du taux d’évolution moléculaire entre lignées
inferred← citeshttps://doi.org/10.70675/428a7961z0409z47adzaabbz52baacd50dc3openalex-snapshot
Origine des variations de taux d’évolution moléculaire inter-spécifiques : apport d’un modèle génomique en milieu souterrain
inferred← citeshttps://doi.org/10.70675/dde8eaf9zf176z4523z9998z19703368ae00openalex-snapshot
Intégrer des approches expérimentales et d’évolution moléculaire en génomique de la spéciation afin d’identifier les mécanismes impliqués dans la divergence entre bar atlantique et loup méditerranéen
inferred← citeshttps://doi.org/10.7554/elife.88456openalex-snapshot
Somatic mutation rates scale with time not growth rate in long-lived tropical trees
inferred← citeshttps://doi.org/10.7554/elife.88456.1openalex-snapshot
The molecular clock in long-lived tropical trees is independent of growth rate
inferred← citeshttps://doi.org/10.7554/elife.88456.1.sa0openalex-snapshot
Reviewer #3 (Public Review): The molecular clock in long-lived tropical trees is independent of growth rate
inferred← citeshttps://doi.org/10.7554/elife.88456.1.sa2openalex-snapshot
Reviewer #1 (Public Review): The molecular clock in long-lived tropical trees is independent of growth rate
inferred← citeshttps://doi.org/10.7554/elife.88456.1.sa3openalex-snapshot
eLife Assessment: The molecular clock in long-lived tropical trees is independent of growth rate
inferred← citeshttps://doi.org/10.7554/elife.88456.2openalex-snapshot
Somatic mutation rates scale with time not growth rate in long-lived tropical trees
inferred← citeshttps://doi.org/10.7554/elife.88456.3openalex-snapshot
Somatic mutation rates scale with time not growth rate in long-lived tropical trees
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.