| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.TREE.2013.09.009 |
| P8608 | Fatcat ID | release_spnxphu6ffdozdyoyss7qktzsu |
| P698 | PubMed publication ID | 24148292 |
| P50 | author | Hanna Kokko | Q4354510 |
| Adam Eyre-Walker | Q30001938 | ||
| Robert Lanfear | Q30347654 | ||
| P2860 | cites work | Evidence that adaptation in Drosophila is not limited by mutation at single sites | Q21030632 |
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| IS THE POPULATION SIZE OF A SPECIES RELEVANT TO ITS EVOLUTION? | Q22065713 | ||
| The distribution of fitness effects of new mutations | Q22122013 | ||
| Sex releases the speed limit on evolution | Q22122522 | ||
| Weak selection and protein evolution | Q22305972 | ||
| Accelerated evolution and Muller's rachet in endosymbiotic bacteria | Q24568178 | ||
| Evolution of the mutation rate | Q24602069 | ||
| Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
| How does adaptation sweep through the genome? Insights from long-term selection experiments | Q26853716 | ||
| Reference-free population genomics from next-generation transcriptome data and the vertebrate-invertebrate gap | Q27323073 | ||
| Evolutionary dynamics on graphs | Q28303517 | ||
| Effective population size is positively correlated with levels of adaptive divergence among annual sunflowers | Q28740903 | ||
| The genome as a life-history character: why rate of molecular evolution varies between mammal species | Q28742524 | ||
| Fluctuating selection: the perpetual renewal of adaptation in variable environments | Q28748404 | ||
| The erratic mitochondrial clock: variations of mutation rate, not population size, affect mtDNA diversity across birds and mammals | Q28755001 | ||
| Evidence for variation in the effective population size of animal mitochondrial DNA | Q28755556 | ||
| Determination of mitochondrial genetic diversity in mammals | Q28755918 | ||
| Estimation of census and effective population sizes: the increasing usefulness of DNA-based approaches | Q58748176 | ||
| COMPENSATING FOR OUR LOAD OF MUTATIONS: FREEZING THE MELTDOWN OF SMALL POPULATIONS | Q63379853 | ||
| Compensatory nearly neutral mutations: selection without adaptation | Q71835485 | ||
| Molecular evolution of functional genes on the mammalian Y chromosome | Q74676538 | ||
| Population size and molecular evolution on islands | Q81278519 | ||
| Mutation and evolutionary rates in adélie penguins from the antarctic | Q28757071 | ||
| Accumulation of slightly deleterious mutations in mitochondrial protein-coding genes of large versus small mammals | Q28757218 | ||
| Evolutionary rescue: an emerging focus at the intersection between ecology and evolution. | Q30580050 | ||
| Accounting for missing data in the estimation of contemporary genetic effective population size (N(e) ). | Q30583854 | ||
| Population size and rate of evolution | Q30686217 | ||
| Estimating the distribution of selection coefficients from phylogenetic data with applications to mitochondrial and viral DNA. | Q30798810 | ||
| Population size does not influence mitochondrial genetic diversity in animals | Q33241444 | ||
| A general multivariate extension of Fisher's geometrical model and the distribution of mutation fitness effects across species | Q33342879 | ||
| Similar rates of protein adaptation in Drosophila miranda and D. melanogaster, two species with different current effective population sizes | Q33394067 | ||
| Genetic estimates of contemporary effective population size: what can they tell us about the importance of genetic stochasticity for wild population persistence? | Q33401810 | ||
| Slower tempo of microevolution in island birds: implications for conservation biology | Q33453868 | ||
| Effects of linkage on rates of molecular evolution | Q33644420 | ||
| Mutation rate is linked to diversification in birds | Q33741325 | ||
| Molecular hyperdiversity and evolution in very large populations | Q33784387 | ||
| The population genetics of beneficial mutations | Q33856621 | ||
| Recombination yet inefficient selection along the Drosophila melanogaster subgroup's fourth chromosome | Q33881169 | ||
| Patterns of DNA sequence polymorphism along chromosome 1 of maize (Zea mays ssp. mays L.). | Q33930146 | ||
| Estimating the distribution of selection coefficients from phylogenetic data using sitewise mutation-selection models | Q34115062 | ||
| Linkage limits the power of natural selection in Drosophila | Q34160190 | ||
| Anchored hybrid enrichment for massively high-throughput phylogenomics | Q34273260 | ||
| Experimental evolution | Q34289524 | ||
| How does the 50/500 rule apply to MVPs? | Q34367864 | ||
| Recombination enhances protein adaptation in Drosophila melanogaster | Q34451827 | ||
| Mutational effects and population dynamics during viral adaptation challenge current models | Q34477455 | ||
| Molecular hyperdiversity defines populations of the nematode Caenorhabditis brenneri | Q34775455 | ||
| From fitness landscapes to seascapes: non-equilibrium dynamics of selection and adaptation. | Q34949551 | ||
| Genetic variation and the fate of beneficial mutations in asexual populations | Q35222738 | ||
| The lower bound to the evolution of mutation rates | Q35362334 | ||
| Quantifying the variation in the effective population size within a genome. | Q35620472 | ||
| Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution | Q35748281 | ||
| Distribution of fixed beneficial mutations and the rate of adaptation in asexual populations | Q35882382 | ||
| The effect of variation in the effective population size on the rate of adaptive molecular evolution in eukaryotes. | Q36054035 | ||
| The other side of the nearly neutral theory, evidence of slightly advantageous back-mutations | Q36089115 | ||
| Clonal interference in the evolution of influenza | Q36268135 | ||
| Adaptive evolution and effective population size in wild house mice | Q36278205 | ||
| Life-history traits drive the evolutionary rates of mammalian coding and noncoding genomic elements | Q36300009 | ||
| No effect of recombination on the efficacy of natural selection in primates | Q36517937 | ||
| Effective population size and the rate and pattern of nucleotide substitutions | Q37443408 | ||
| Genetic recombination and molecular evolution | Q37592858 | ||
| Watching the clock: studying variation in rates of molecular evolution between species | Q37775232 | ||
| The population genomics of plant adaptation. | Q37778860 | ||
| Variation in the mutation rate across mammalian genomes | Q37942062 | ||
| Non-random mutation: the evolution of targeted hypermutation and hypomutation | Q38071050 | ||
| A unified treatment of the probability of fixation when population size and the strength of selection change over time | Q38517913 | ||
| A comparison of models to infer the distribution of fitness effects of new mutations | Q39218552 | ||
| The role of population size in molecular evolution | Q41665292 | ||
| The nearly neutral and selection theories of molecular evolution under the fisher geometrical framework: substitution rate, population size, and complexity. | Q42123470 | ||
| Genetic linkage and natural selection | Q42430166 | ||
| The relationship of nucleotide polymorphism, recombination rate and selection in wild tomato species. | Q42705463 | ||
| A Neutral Explanation for the Correlation of Diversity with Recombination Rates in Humans | Q42927602 | ||
| Increased rates of sequence evolution in endosymbiotic bacteria and fungi with small effective population sizes | Q44169518 | ||
| Genomic evidence for large, long-lived ancestors to placental mammals | Q44542979 | ||
| Substitution rates at neutral genes depend on population size under fluctuating demography and overlapping generations | Q44568331 | ||
| Ultraconserved elements anchor thousands of genetic markers spanning multiple evolutionary timescales | Q46198301 | ||
| 50/500 rule and minimum viable populations: response to Jamieson and Allendorf | Q46271487 | ||
| Effective population size | Q47175639 | ||
| Selection efficiency and effective population size in Drosophila species | Q47198433 | ||
| Joint reconstruction of divergence times and life-history evolution in placental mammals using a phylogenetic covariance model | Q47198891 | ||
| Strong variations of mitochondrial mutation rate across mammals--the longevity hypothesis | Q47285264 | ||
| The effect of population structure on the rate of evolution. | Q51530388 | ||
| A Phylogenetic Model for Investigating Correlated Evolution of Substitution Rates and Continuous Phenotypic Characters | Q51650584 | ||
| Characteristics, causes and evolutionary consequences of male-biased mutation. | Q51775095 | ||
| Fast accumulation of nonsynonymous mutations on the female-specific W chromosome in birds. | Q51830204 | ||
| Divergence and polymorphism under the nearly neutral theory of molecular evolution. | Q51868323 | ||
| Transitions to asexuality result in excess amino acid substitutions. | Q51950373 | ||
| Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster | Q52443577 | ||
| Evolution of protein-coding genes in Drosophila. | Q52688311 | ||
| The rate of molecular adaptation in a changing environment. | Q52751267 | ||
| The Nearly Neutral Theory of Molecular Evolution | Q55968685 | ||
| Effective population size/adult population size ratios in wildlife: a review | Q56029135 | ||
| A Mathematical Theory of Natural and Artificial Selection, Part V: Selection and Mutation | Q56169900 | ||
| Diminishing Returns from Mutation Supply Rate in Asexual Populations | Q56920120 | ||
| P433 | issue | 1 | |
| P1104 | number of pages | 9 | |
| P304 | page(s) | 33-41 | |
| P577 | publication date | 2013-10-20 | |
| P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
| P1476 | title | Population size and the rate of evolution | |
| P478 | volume | 29 |
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