| scholarly article | Q13442814 |
| P50 | author | Matthew W Hahn | Q64856494 |
| P2860 | cites work | Non-Darwinian Evolution | Q7048737 |
| Population history and natural selection shape patterns of genetic variation in 132 genes | Q21146407 | ||
| Population genomics: whole-genome analysis of polymorphism and divergence in Drosophila simulans | Q21563561 | ||
| The distribution of fitness effects of new deleterious amino acid mutations in humans | Q22065135 | ||
| IS THE POPULATION SIZE OF A SPECIES RELEVANT TO ITS EVOLUTION? | Q22065713 | ||
| Evolutionary Rate at the Molecular Level | Q22122432 | ||
| The spandrels of San Marco and the Panglossian paradigm: a critique of the adaptationist programme | Q28237797 | ||
| The status of the neutral theory: the neutral theory of molecular evolution | Q28244805 | ||
| Adaptive protein evolution at the Adh locus in Drosophila | Q28302478 | ||
| Natural selection on protein-coding genes in the human genome | Q29615352 | ||
| Testing the neutral theory of molecular evolution with genomic data from Drosophila. | Q30677368 | ||
| Genomic scans for selective sweeps using SNP data | Q31013520 | ||
| SelSim: a program to simulate population genetic data with natural selection and recombination | Q33205144 | ||
| The scale of mutational variation in the murid genome | Q33219707 | ||
| Population size does not influence mitochondrial genetic diversity in animals | Q33241444 | ||
| Widespread positive selection in synonymous sites of mammalian genes | Q33285587 | ||
| Multilocus patterns of nucleotide variability and the demographic and selection history of Drosophila melanogaster populations | Q33841555 | ||
| Fitting background-selection predictions to levels of nucleotide variation and divergence along the human autosomes | Q33942576 | ||
| Adjusting the focus on human variation | Q33945651 | ||
| Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens" and "Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans". | Q33997612 | ||
| Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels | Q34020571 | ||
| Methods to detect selection in populations with applications to the human | Q34101053 | ||
| Adaptive protein evolution in Drosophila | Q34116884 | ||
| Abundant raw material for cis-regulatory evolution in humans | Q34157325 | ||
| Bayesian analysis suggests that most amino acid replacements in Drosophila are driven by positive selection | Q34303973 | ||
| Disentangling the effects of demography and selection in human history | Q34346838 | ||
| The neutral theory is dead. Long live the neutral theory | Q34392820 | ||
| Statistical tests of selective neutrality in the age of genomics | Q34397732 | ||
| The neutral theory in the genomic era. | Q34420764 | ||
| Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens. | Q34449464 | ||
| Recombination and linkage disequilibrium in Arabidopsis thaliana. | Q34659467 | ||
| Human SNP variability and mutation rate are higher in regions of high recombination | Q34750287 | ||
| Natural selection at linked sites in humans | Q35017925 | ||
| Reduced recombination rate and genetic differentiation between the M and S forms of Anopheles gambiae s.s. | Q35221538 | ||
| Detecting natural selection on cis-regulatory DNA. | Q36586560 | ||
| Progress and prospects in mapping recent selection in the genome. | Q36808696 | ||
| Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens". | Q41918632 | ||
| 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 | ||
| Why do human diversity levels vary at a megabase scale? | Q42953750 | ||
| Proceedings of the SMBE Tri-National Young Investigators' Workshop 2005. Accurate inference and estimation in population genomics | Q46374136 | ||
| Adaptive evolution of non-coding DNA in Drosophila | Q46601551 | ||
| Inference of positive and negative selection on the 5' regulatory regions of Drosophila genes | Q47336207 | ||
| Genetic variation versus recombination rate in a structured population of mice | Q47336237 | ||
| Protein Polymorphism as a Phase of Molecular Evolution | Q47760423 | ||
| Selection at linked sites in the partial selfer Caenorhabditis elegans | Q47990114 | ||
| The rate of adaptive evolution in enteric bacteria | Q50081882 | ||
| Levels of naturally occurring DNA polymorphism correlate with recombination rates in D. melanogaster | Q52443577 | ||
| The cost of inbreeding in Arabidopsis. | Q52595244 | ||
| The genomic rate of adaptive amino acid substitution in Drosophila. | Q52646887 | ||
| Gene expression, synteny, and local similarity in human noncoding mutation rates. | Q52841911 | ||
| Local similarity in evolutionary rates extends over whole chromosomes in human-rodent and mouse-rat comparisons: implications for understanding the mechanistic basis of the male mutation bias. | Q52935162 | ||
| Evolutionary Divergence and Convergence in Proteins | Q56689213 | ||
| Regional similarities in polymorphism in the human genome extend over many megabases | Q57251631 | ||
| Positive Selection on a Human-Specific Transcription Factor Binding Site Regulating IL4 Expression | Q57309676 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 255-65 | |
| P577 | publication date | 2008-02-01 | |
| P1433 | published in | Evolution | Q4038411 |
| P1476 | title | Toward a selection theory of molecular evolution | |
| P478 | volume | 62 |
| Q34815429 | "Reverse ecology" and the power of population genomics |
| Q35953671 | A Continuous Correlated Beta Process Model for Genetic Ancestry in Admixed Populations |
| Q51436032 | A conceptual framework for organismal biology: linking theories, models, and data. |
| Q36936736 | A fundamental relationship between genotype frequencies and fitnesses |
| Q37216758 | A population genomic approach to map recent positive selection in model species |
| Q30396862 | Aquaporins in the wild: natural genetic diversity and selective pressure in the PIP gene family in five Neotropical tree species |
| Q37534066 | Assessing the spatial dependence of adaptive loci in 43 European and Western Asian goat breeds using AFLP markers |
| Q33811797 | Background selection as baseline for nucleotide variation across the Drosophila genome |
| Q30981029 | Bayesian inference of selection in a heterogeneous environment from genetic time-series data |
| Q30831579 | Climatic adaptation and ecological divergence between two closely related pine species in Southeast China |
| Q33998296 | Comparative genomics based on massive parallel transcriptome sequencing reveals patterns of substitution and selection across 10 bird species |
| Q42177825 | Contrasting patterns of nucleotide polymorphism suggest different selective regimes within different parts of the PgiC1 gene in Festuca ovina L. |
| Q39173779 | Cross-species outlier detection reveals different evolutionary pressures between sister species |
| Q30701255 | Detecting natural selection in genomic data |
| Q46638613 | Detecting spatial genetic signatures of local adaptation in heterogeneous landscapes |
| Q35118137 | Distinguishing the effects of selection from demographic history in the genetic variation of two sister passerines based on mitochondrial-nuclear comparison |
| Q93106464 | Divergent selection and genetic structure of Sideritis scardica populations from southern Balkan Peninsula as revealed by AFLP fingerprinting |
| Q34994057 | Ecologically and evolutionarily important SNPs identified in natural populations |
| Q39412676 | Effects of Linked Selective Sweeps on Demographic Inference and Model Selection |
| Q92111567 | Effects of life history and ecology on virus evolutionary potential |
| Q34760482 | Epistasis increases the rate of conditionally neutral substitution in an adapting population |
| Q57583265 | Evolving social influence in large populations |
| Q41760677 | Extreme Mitogenomic Variation in Natural Populations of Chaetognaths. |
| Q28654599 | Extremely low nucleotide polymorphism in Pinus krempfii Lecomte, a unique flat needle pine endemic to Vietnam |
| Q22122004 | Fitness and its role in evolutionary genetics |
| Q33352330 | Fully Bayesian tests of neutrality using genealogical summary statistics |
| Q38874683 | Gene conversion and linkage: effects on genome evolution and speciation. |
| Q33688892 | Gene genealogies strongly distorted by weakly interfering mutations in constant environments. |
| Q51858880 | Genome-wide comparison of nucleotide-binding site-leucine-rich repeat-encoding genes in Arabidopsis. |
| Q44761567 | Genome-wide evidence for efficient positive and purifying selection in Capsella grandiflora, a plant species with a large effective population size |
| Q33368642 | Genomic analysis of differentiation between soil types reveals candidate genes for local adaptation in Arabidopsis lyrata |
| Q34768275 | Genomic basis of ecological niche divergence among cryptic sister species of non-biting midges |
| Q27028044 | Genomic signatures of selection at linked sites: unifying the disparity among species |
| Q36268123 | Genomic variation in natural populations of Drosophila melanogaster |
| Q30764360 | High evolutionary potential of marine zooplankton |
| Q34382818 | High level of structural polymorphism driven by mobile elements in the Hox genomic region of the Chaetognath Spadella cephaloptera |
| Q36079788 | High-throughput SNP genotyping of historical and modern samples of five bird species via sequence capture of ultraconserved elements |
| Q35765322 | How closely does genetic diversity in finite populations conform to predictions of neutral theory? Large deficits in regions of low recombination |
| Q34783993 | Integrating phylogenetics, phylogeography and population genetics through genomes and evolutionary theory |
| Q37945702 | Joint analysis of demography and selection in population genetics: where do we stand and where could we go? |
| Q61642423 | Lipidome Evolution in Mammalian Tissues |
| Q34414598 | Longevity and plasticity of CFTR provide an argument for noncanonical SNP organization in hominid DNA |
| Q28084988 | Mitonuclear Ecology |
| Q37142674 | Models of frequency-dependent selection with mutation from parental alleles |
| Q92872735 | Molecular Evolution of the Glutathione S-Transferase Family in the Bemisia tabaci Species Complex |
| Q52864185 | Molecular Population Genetics. |
| Q37243134 | Molecular evolution and population genetics of two Drosophila mettleri cytochrome P450 genes involved in host plant utilization |
| Q41966519 | More accurate phylogenies inferred from low-recombination regions in the presence of incomplete lineage sorting |
| Q42623839 | Multilocus analyses reveal little evidence for lineage-wide adaptive evolution within major clades of soft pines (Pinus subgenus Strobus). |
| Q36151738 | Multilocus approaches for the measurement of selection on correlated genetic loci. |
| Q28757155 | Multilocus patterns of nucleotide polymorphism and the demographic history of Populus tremula |
| Q22065772 | Natural selection shapes nucleotide polymorphism across the genome of the nematode Caenorhabditis briggsae |
| Q46669644 | Neutralism and selectionism: a network-based reconciliation |
| Q27301368 | Non-Selective Evolution of Growing Populations |
| Q37810545 | Nonadaptive processes in primate and human evolution |
| Q34131510 | Patterns and processes of genome-wide divergence between North American and African Drosophila melanogaster. |
| Q33463271 | Pervasive natural selection in the Drosophila genome? |
| Q37247032 | Pervasive, genome-wide positive selection leading to functional divergence in the bacterial genus Campylobacter. |
| Q42638351 | Population genetic evidence for complex evolutionary histories of four high altitude juniper species in the Qinghai-Tibetan Plateau. |
| Q45761685 | Positive relationships between genetic diversity and abundance in fishes |
| Q30940992 | Problems and Cautions With Sequence Mismatch Analysis and Bayesian Skyline Plots to Infer Historical Demography |
| Q57583263 | Quality versus mere popularity: a conceptual map for understanding human behavior |
| Q58759625 | Random Genetic Drift and Selective Pressures Shaping the Blattabacterium Genome |
| Q34420759 | Reanalysis suggests that genomic islands of speciation are due to reduced diversity, not reduced gene flow |
| Q21563525 | Recombination modulates how selection affects linked sites in Drosophila |
| Q35465413 | Reconstructing the demographic history of orang-utans using Approximate Bayesian Computation. |
| Q57093794 | Repeated Selection of Alternatively Adapted Haplotypes Creates Sweeping Genomic Remodeling in Stickleback |
| Q34274126 | Rethinking Hardy-Weinberg and genetic drift in undergraduate biology |
| Q28749184 | Scaling expectations for the time to establishment of complex adaptations |
| Q33688912 | Signatures of recent directional selection under different models of population expansion during colonization of new selective environments |
| Q36119961 | Similar Efficacies of Selection Shape Mitochondrial and Nuclear Genes in Both Drosophila melanogaster and Homo sapiens |
| Q37089714 | Simulation of DNA sequence evolution under models of recent directional selection |
| Q35579812 | Soft shoulders ahead: spurious signatures of soft and partial selective sweeps result from linked hard sweeps |
| Q36295354 | Synonymous Genetic Variation in Natural Isolates of Escherichia coli Does Not Predict Where Synonymous Substitutions Occur in a Long-Term Experiment |
| Q36771745 | Targeted capture in evolutionary and ecological genomics. |
| Q30485345 | Testing comparative phylogeographic models of marine vicariance and dispersal using a hierarchical Bayesian approach |
| Q88555310 | The Neutral Theory in Light of Natural Selection |
| Q42156118 | The Selective Maintenance of Allelic Variation Under Generalized Dominance |
| Q90380825 | The evolution of metabolism: How to test evolutionary hypotheses at the genomic level |
| Q28661554 | The evolutionary genetics of the genes underlying phenotypic associations for loblolly pine (Pinus taeda, Pinaceae) |
| Q36969627 | The generation and maintenance of genetic variation by frequency-dependent selection: constructing polymorphisms under the pairwise interaction model |
| Q46700797 | The genetic architecture of hybrid incompatibilities and their effect on barriers to introgression in secondary contact |
| Q38206695 | The impact of linked selection on plant genomic variation |
| Q93263268 | The importance of the Neutral Theory in 1968 and 50 years on: A response to Kern and Hahn 2018 |
| Q40503221 | The maintenance of single-locus polymorphism by maternal selection |
| Q34116848 | The standard of neutrality: still flapping in the breeze? |
| Q36901012 | The structure of allelic diversity in the presence of purifying selection |
| Q35748213 | The structure of genealogies in the presence of purifying selection: a fitness-class coalescent |
| Q35257048 | Weighing the evidence for adaptation at the molecular level |
| Q50186021 | What do we mean when we talk about hybrid speciation? |
| Q37238238 | Whole-genome sequencing of two North American Drosophila melanogaster populations reveals genetic differentiation and positive selection |
| Q92146681 | Widespread selection and gene flow shape the genomic landscape during a radiation of monkeyflowers |
| Q36744941 | ZRT1 Harbors an Excess of Nonsynonymous Polymorphism and Shows Evidence of Balancing Selection in Saccharomyces cerevisiae |
Search more.