| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | H. Allen Orr | Q5628056 |
| P2860 | cites work | EVOLUTION IN MENDELIAN POPULATIONS | Q5418627 |
| Population genomics: whole-genome analysis of polymorphism and divergence in Drosophila simulans | Q21563561 | ||
| Molecular Evolution Over the Mutational Landscape | Q22064602 | ||
| The Propensity Interpretation of Fitness | Q22066138 | ||
| The genetic theory of adaptation: a brief history | Q22122021 | ||
| Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation | Q22122024 | ||
| An empirical test of the mutational landscape model of adaptation using a single-stranded DNA virus | Q22122043 | ||
| The genomic rate of adaptive evolution | Q22162494 | ||
| The Distribution of Fitness Effects Among Beneficial Mutations | Q24543521 | ||
| Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations | Q28245607 | ||
| Toward a selection theory of molecular evolution | Q28270306 | ||
| Adaptive protein evolution at the Adh locus in Drosophila | Q28302478 | ||
| Genomewide patterns of substitution in adaptively evolving populations of the RNA bacteriophage MS2 | Q28754815 | ||
| The locus of evolution: evo devo and the genetics of adaptation | Q29615067 | ||
| Detecting the form of selection from DNA sequence data. | Q31833185 | ||
| Daniel Bernoulli (1738): evolution and economics under risk | Q33181208 | ||
| Understanding the evolutionary fate of finite populations: the dynamics of mutational effects | Q33281050 | ||
| Protein evolution on partially correlated landscapes | Q33860729 | ||
| Long-term experimental evolution in Escherichia coli. IV. Targets of selection and the specificity of adaptation | Q33967274 | ||
| Exceptional convergent evolution in a virus. | Q33971443 | ||
| The estimation of fitnesses from population data | Q34015373 | ||
| Adaptive protein evolution in Drosophila | Q34116884 | ||
| Perspective: Here's to Fisher, additive genetic variance, and the fundamental theorem of natural selection | Q34147025 | ||
| Extension of covariance selection mathematics | Q34227739 | ||
| Natural Selection and the Concept of a Protein Space | Q34233063 | ||
| Selection and Covariance | Q34233418 | ||
| Maintenance of genetic heterogeneity | Q34241342 | ||
| Protein evolution on rugged landscapes | Q34296709 | ||
| The neutral theory is dead. Long live the neutral theory | Q34392820 | ||
| Evolution of high mutation rates in experimental populations of E. coli | Q34429727 | ||
| Different trajectories of parallel evolution during viral adaptation | Q34504264 | ||
| Profiles of adaptation in two similar viruses | Q34613893 | ||
| A review of some fundamental concepts and problems of population genetics | Q35245265 | ||
| Theories of adaptation: what they do and don't say. | Q36120420 | ||
| A general extreme value theory model for the adaptation of DNA sequences under strong selection and weak mutation | Q36969656 | ||
| The loci of evolution: how predictable is genetic evolution? | Q37035424 | ||
| CHARACTER CHANGE, SPECIATION, AND THE HIGHER TAXA. | Q38752015 | ||
| PERSPECTIVE: A CRITIQUE OF SEWALL WRIGHT'S SHIFTING BALANCE THEORY OF EVOLUTION. | Q39343164 | ||
| The fundamental theorem of natural selection | Q40654752 | ||
| Detecting a local signature of genetic hitchhiking along a recombining chromosome. | Q41778534 | ||
| Alternative fitness models with the same allele frequency dynamics. | Q42125092 | ||
| An optimizing principle of natural selection in evolutionary population genetics | Q43794620 | ||
| EVOLUTIONARY DYNAMICS OF FITNESS RECOVERY FROM THE DEBILITATING EFFECTS OF MULLER'S RATCHET. | Q46218646 | ||
| The effects of artificial selection on the maize genome | Q46515058 | ||
| Adaptive evolution of non-coding DNA in Drosophila | Q46601551 | ||
| Towards a general theory of adaptive walks on rugged landscapes | Q47593883 | ||
| Absolute fitness, relative fitness, and utility. | Q51902038 | ||
| Fisher's fundamental theorem of natural selection revisited. | Q52254001 | ||
| An interpretation and proof of the Fundamental Theorem of Natural Selection. | Q52518395 | ||
| A mathematical model of the culling process in dairy cattle | Q56341509 | ||
| Big-benefit mutations in a bacteriophage inhibited with heat | Q56901737 | ||
| Dynamics of polymorphisms. I. Selection components in an experimental population of Drosophila melanogaster | Q69374635 | ||
| Selection component analysis of natural polymorphisms using population samples including mother-offspring combinations | Q69658168 | ||
| A simple stochastic gene substitution model | Q71016135 | ||
| Selection in animals: synthesis | Q74511196 | ||
| The population genetics of adaptation: the adaptation of DNA sequences | Q74699508 | ||
| The probability of parallel evolution | Q81578520 | ||
| The Rate of Change of a Character Correlated with Fitness | Q87989049 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 531-9 | |
| P577 | publication date | 2009-08-01 | |
| P1433 | published in | Nature Reviews Genetics | Q1071824 |
| P1476 | title | Fitness and its role in evolutionary genetics | |
| P478 | volume | 10 |
| Q40379657 | A framework for how environment contributes to cancer risk. |
| Q34411888 | A gene family derived from transposable elements during early angiosperm evolution has reproductive fitness benefits in Arabidopsis thaliana |
| Q28817124 | A genetically distinct hybrid zone occurs for two globally invasive mosquito fish species with striking phenotypic resemblance |
| Q24606375 | A high level of mutation tolerance in the multifunctional sequence encoding the RNA encapsidation signal of an avian hepatitis B virus and slow evolution rate revealed by in vivo infection |
| Q37556879 | A mechanistic explanation linking adaptive mutation, niche change, and fitness advantage for the wrinkly spreader |
| Q42779145 | A reinforcement learning mechanism responsible for the valuation of free choice |
| Q41021919 | A statistical guide to the design of deep mutational scanning experiments |
| Q35678619 | Accurate Alternative Measurements for Female Lifetime Reproductive Success in Drosophila melanogaster |
| Q50532537 | Adaptation of Drosophila melanogaster to increased NaCl concentration due to dominant beneficial mutations. |
| Q51823286 | Altruism can evolve when relatedness is low: evidence from bacteria committing suicide upon phage infection. |
| Q38594823 | Antagonistic within-host interactions between plant viruses: molecular basis and impact on viral and host fitness. |
| Q28709173 | As it happens: current directions in experimental evolution |
| Q58565233 | Asexual reproduction and growth rate: independent and plastic life history traits in Neurospora crassa |
| Q36558529 | Assessing the cost-benefit effect of a Plasmodium falciparum drug resistance mutation on parasite growth in vitro |
| Q34985567 | Bacterial growth laws reflect the evolutionary importance of energy efficiency |
| Q27319462 | Bet hedging in yeast by heterogeneous, age-correlated expression of a stress protectant |
| Q42140623 | BioJazz: in silico evolution of cellular networks with unbounded complexity using rule-based modeling |
| Q34086939 | Biogeography of species richness gradients: linking adaptive traits, demography and diversification |
| Q35204371 | Biophysical fitness landscapes for transcription factor binding sites |
| Q38997863 | Bridging the physical scales in evolutionary biology: from protein sequence space to fitness of organisms and populations |
| Q41522217 | Can They Make It on Their Own? Hosts, Microbes, and the Holobiont Niche. |
| Q50499548 | Can a Network Approach Resolve How Adaptive vs Nonadaptive Plasticity Impacts Evolutionary Trajectories? |
| Q45902054 | Cancer and intercellular cooperation. |
| Q28602368 | Causes and consequences of intra-specific variation in vertebral number |
| Q28550306 | Comparative Fitness of a Parent Leishmania donovani Clinical Isolate and Its Experimentally Derived Paromomycin-Resistant Strain |
| Q39676882 | Competitive and cooperative metabolic interactions in bacterial communities. |
| Q39834738 | Computational optimization and biological evolution |
| Q38752296 | Constraints, Trade-offs and the Currency of Fitness |
| Q28650546 | Contextual modulation of social and endocrine correlates of fitness: insights from the life history of a sex changing fish |
| Q34807160 | Contrasted Fitness Costs of Docking and Antibacterial Constructs in the EE and EVida3 Strains Validates Two-Phase Anopheles gambiae Genetic Transformation System |
| Q37428442 | Contribution of selection for protein folding stability in shaping the patterns of polymorphisms in coding regions |
| Q26825267 | Culture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transition |
| Q58837963 | Dental Reduction and the Transition to Agriculture in Europe |
| Q29543946 | Differential Strengths of Positive Selection Revealed by Hitchhiking Effects at Small Physical Scales in Drosophila melanogaster |
| Q51163955 | Dispersal and selection mediate hybridization between a native and invasive species. |
| Q35772715 | Diversity Waves in Collapse-Driven Population Dynamics |
| Q42594318 | Drug resistance in cancer: molecular evolution and compensatory proliferation |
| Q38040818 | Drug-resistant microorganisms with a higher fitness--can medicines boost pathogens? |
| Q59299964 | Eco-evolutionary dynamics in plants: interactive processes at overlapping time-scales and their implications |
| Q90524173 | Effects of demographic stochasticity and life-history strategies on times and probabilities to fixation |
| Q30828514 | Effects of new mutations on fitness: insights from models and data |
| Q64243784 | Elucidating fitness components of the invasive dermestid beetle Trogoderma granarium combining deterministic and stochastic demography |
| Q47830315 | Ensemble variant interpretation methods to predict enzyme activity and assign pathogenicity in the CAGI4 NAGLU (Human N-acetyl-glucosaminidase) and UBE2I (Human SUMO-ligase) challenges. |
| Q39014583 | Evaluating drug resistance in visceral leishmaniasis: the challenges |
| Q38780287 | Evidence for microbial local adaptation in nature |
| Q53120855 | Evidence of a drug-specific impact of experimentally selected paromomycin and miltefosine resistance on parasite fitness in Leishmania infantum. |
| Q31145383 | Evolution in fluctuating environments: decomposing selection into additive components of the Robertson-Price equation |
| Q51526488 | Evolution of a plastic quantitative trait in an age-structured population in a fluctuating environment. |
| Q42365796 | Evolutionary algorithms and synthetic biology for directed evolution: commentary on "on the mapping of genotype to phenotype in evolutionary algorithms" by Peter A. Whigham, Grant Dick, and James Maclaurin |
| Q34731158 | Evolutionary and neuropsychological perspectives on addictive behaviors and addictive substances: relevance to the "food addiction" construct |
| Q40396005 | Evolutionary interplay between structure, energy and epistasis in the coat protein of the ϕX174 phage family |
| Q35560450 | Evolutionary molecular medicine |
| Q39030938 | Evolutionary scalpels for dissecting tumor ecosystems |
| Q91940726 | Evolutionary stasis of a heritable morphological trait in a wild fish population despite apparent directional selection |
| Q58650569 | Evolvability and Speed of Evolutionary Algorithms in Light of Recent Developments in Biology |
| Q57174769 | Experimental Design, Population Dynamics, and Diversity in Microbial Experimental Evolution |
| Q87933762 | Experimental determination of invasive fitness in Caenorhabditis elegans |
| Q34383507 | Explaining human recreational use of 'pesticides': The neurotoxin regulation model of substance use vs. the hijack model and implications for age and sex differences in drug consumption. |
| Q88334043 | Feedback between environment and traits under selection in a seasonal environment: consequences for experimental evolution |
| Q58601263 | Fitness costs associated with multiple resistance to dicamba and atrazine in Chenopodium album |
| Q37976151 | Fitness effects of mutations in bacteria. |
| Q46346757 | Fitness of drug resistant Mycobacterium tuberculosis and the impact on the transmission among household contacts |
| Q57467597 | Free-energy minimization in joint agent-environment systems: A niche construction perspective |
| Q34244125 | Functional organization and its implication in evolution of the human protein-protein interaction network |
| Q38703264 | Genetic load makes cancer cells more sensitive to common drugs: evidence from Cancer Cell Line Encyclopedia |
| Q28651650 | Genome dynamics during experimental evolution |
| Q90049157 | Genome-wide analysis reveals molecular convergence underlying domestication in 7 bird and mammals |
| Q44855793 | Genomic studies of disease-outcome in host--pathogen dynamics |
| Q33356734 | Hamiltonian inclusive fitness: a fitter fitness concept |
| Q30881998 | How eco-evolutionary principles can guide tree breeding and tree biotechnology for enhanced productivity |
| Q42480395 | Humanized Foxp2 specifically affects cortico-basal ganglia circuits |
| Q37799532 | Identifying genetic markers of adaptation for surveillance of viral host jumps |
| Q92573678 | Individuals' expected genetic contributions to future generations, reproductive value, and short-term metrics of fitness in free-living song sparrows (Melospiza melodia) |
| Q47102776 | Inferring genetic interactions from comparative fitness data. |
| Q30921954 | Inferring positive selection in humans from genomic data |
| Q30574878 | Insecticide resistance and malaria vector control: the importance of fitness cost mechanisms in determining economically optimal control trajectories. |
| Q52735819 | Insertions and deletions trigger adaptive walks in Drosophila proteins. |
| Q89055694 | Insight into the evolution of nidovirus endoribonuclease based on the finding that nsp15 from porcine Deltacoronavirus functions as a dimer |
| Q47602609 | Interaction rates, vital rates, background fitness and replicator dynamics: how to embed evolutionary game structure into realistic population dynamics |
| Q41886122 | Interpretations arising from Wrightian and Malthusian fitness under strong frequency dependent selection. |
| Q43718616 | Interspecific competition alters nonlinear selection on offspring size in the field. |
| Q37945702 | Joint analysis of demography and selection in population genetics: where do we stand and where could we go? |
| Q92668480 | Large-effect flowering time mutations reveal conditionally adaptive paths through fitness landscapes in Arabidopsis thaliana |
| Q91473489 | Learning dynamical information from static protein and sequencing data |
| Q42929210 | Limits of neutral drift: lessons from the in vitro evolution of two ribozymes. |
| Q57133292 | Lineages evolved under stronger sexual selection show superior ability to invade conspecific competitor populations |
| Q61642423 | Lipidome Evolution in Mammalian Tissues |
| Q38100662 | Mammary stroma in development and carcinogenesis |
| Q27331437 | Mapping the environmental fitness landscape of a synthetic gene circuit |
| Q37640957 | Mathematical model of adult stem cell regeneration with cross-talk between genetic and epigenetic regulation |
| Q92955773 | Measuring intolerance to mutation in human genetics |
| Q40384168 | Measuring microbial fitness in a field reciprocal transplant experiment |
| Q28659333 | Measuring natural selection on genotypes and phenotypes in the wild |
| Q33501885 | Measuring the sensitivity of single-locus "neutrality tests" using a direct perturbation approach |
| Q58606303 | Metanetwork Transmission Model for Predicting a Malaria-Control Strategy |
| Q33590430 | Modeling Tumor Clonal Evolution for Drug Combinations Design |
| Q90617354 | Modeling cell population dynamics |
| Q28742971 | Molecular evolution of rbcL in three gymnosperm families: identifying adaptive and coevolutionary patterns |
| Q41445226 | Monotonicity of fitness landscapes and mutation rate control. |
| Q51098001 | Multiplex growth rate phenotyping of synthetic mutants in selection to engineer glucose and xylose co-utilization in Escherichia coli. |
| Q39145276 | Mutation rate plasticity in rifampicin resistance depends on Escherichia coli cell-cell interactions. |
| Q42130432 | Network of epistatic interactions within a yeast snoRNA. |
| Q47607244 | On the origin of obesity: identifying the biological, environmental and cultural drivers of genetic risk among human populations |
| Q47343783 | On the stochastic evolution of finite populations |
| Q49483771 | Onychomycosis and Chronic Fungal Disease: Exploiting a Commensal Disguise to Stage a Covert Invasion |
| Q92456740 | Optimal foraging and the information theory of gambling |
| Q54150482 | Optimization of lag phase shapes the evolution of a bacterial enzyme. |
| Q63641385 | Optimizing Genomic Selection for a Sorghum Breeding Program in Haiti: A Simulation Study |
| Q46308637 | Perspectives on non-target site mechanisms of herbicide resistance in weedy plant species using evolutionary physiology. |
| Q40898690 | Phenotypic and genotypic convergences are influenced by historical contingency and environment in yeast |
| Q33787403 | Phenotypic plasticity can facilitate adaptive evolution in gene regulatory circuits |
| Q46281751 | Predicted global warming scenarios impact on the mother plant to alter seed dormancy and germination behaviour in Arabidopsis |
| Q84324563 | Probing the basis for genotype-phenotype relationships |
| Q38787151 | Quantifying and understanding the fitness effects of protein mutations: Laboratory versus nature |
| Q33641547 | Quasispecies theory and the behavior of RNA viruses |
| Q38254854 | Recent advances in the evolutionary engineering of industrial biocatalysts |
| Q47609415 | Red ochre and shells: clues to human evolution |
| Q64280270 | Release from natural enemies mitigates inbreeding depression in native and invasive populations |
| Q58105771 | Reply to 'Currently available bulk sequencing data do not necessarily support a model of neutral tumor evolution' |
| Q36727650 | Role of Multicellular Aggregates in Biofilm Formation |
| Q33928337 | Selection on crop-derived traits and QTL in sunflower (Helianthus annuus) crop-wild hybrids under water stress |
| Q27333840 | Self-organized centripetal movement of corneal epithelium in the absence of external cues. |
| Q92279436 | Shifting Paradigms for Studying Parasitism in Hybridising Hosts: Response to Theodosopoulos, Hund, and Taylor |
| Q37433924 | Signatures of natural selection on genetic variants affecting complex human traits |
| Q36018297 | Slow-growing cells within isogenic populations have increased RNA polymerase error rates and DNA damage |
| Q47844600 | Soft selective sweeps in fungicide resistance evolution: recurrent mutations without fitness costs in grapevine downy mildew. |
| Q90029019 | Soil compaction and the architectural plasticity of root systems |
| Q38610766 | Stochastic Cell Fate and Longevity of Offspring |
| Q38335985 | Studying the evolutionary ecology of cognition in the wild: a review of practical and conceptual challenges. |
| Q38287400 | Synthetic biology for the directed evolution of protein biocatalysts: navigating sequence space intelligently |
| Q22065137 | The Awesome Power of Yeast Evolutionary Genetics: New Genome Sequences and Strain Resources for the Saccharomyces sensu stricto Genus |
| Q49835177 | The Genetic/Non-genetic Duality of Drug 'Resistance' in Cancer |
| Q55002438 | The Influence of Higher-Order Epistasis on Biological Fitness Landscape Topography. |
| Q36116006 | The Mutational Robustness of Influenza A Virus |
| Q37410740 | The Reproductive Ecology of Industrial Societies, Part I : Why Measuring Fertility Matters. |
| Q36490860 | The basis of antagonistic pleiotropy in hfq mutations that have opposite effects on fitness at slow and fast growth rates |
| Q26744394 | The benefits of expanding studies of trait exaggeration to hemimetabolous insects and beyond morphology |
| Q36365457 | The ecology of cooperative breeding behaviour. |
| Q45998210 | The effect of leg-to-body ratio on male attractiveness depends on the ecological validity of the figures. |
| Q38525366 | The effects of hyalurodinase upon tumor formation in BALB/c mice painted with 7,12-dimethylbenz-(a)anthracene |
| Q50265047 | The quick and the dead: microbial demography at the yeast thermal limit |
| Q48094290 | The relevance of the philosophical 'mind-body problem' for the status of psychosomatic medicine: a conceptual analysis of the biopsychosocial model |
| Q47336035 | The roles of cell size and cell number in determining ovariole number in Drosophila |
| Q41439409 | Theory of fads: traveling-wave solution of evolutionary dynamics in a one-dimensional trait space. |
| Q28384546 | Toward an evolutionary model of cancer: Considering the mechanisms that govern the fate of somatic mutations |
| Q87790201 | Trade-offs between microbial growth phases lead to frequency-dependent and non-transitive selection |
| Q28484459 | Treatment of visceral leishmaniasis: model-based analyses on the spread of antimony-resistant L. donovani in Bihar, India |
| Q90571692 | Understanding the evolution of interspecies interactions in microbial communities |
| Q36255485 | Upon Accounting for the Impact of Isoenzyme Loss, Gene Deletion Costs Anticorrelate with Their Evolutionary Rates. |
| Q58548124 | Using accelerometers to develop time-energy budgets of wild fur seals from captive surrogates |
| Q35080225 | Utility rate equations of group population dynamics in biological and social systems |
| Q90399281 | Variability in fitness effects can preclude selection of the fittest |
| Q37105626 | Variation in parent-offspring kinship in socially monogamous systems with extra-pair reproduction and inbreeding. |
| Q52347585 | Viral fitness correlates with the magnitude and direction of the perturbation induced in the host's transcriptome: the tobacco etch potyvirus - tobacco case study. |
| Q36449318 | What keeps cells in tissues behaving normally in the face of myriad mutations? |
| Q38539322 | When is dispersal for dispersal? Unifying marine and terrestrial perspectives |
| Q36179896 | r- and K-selection in fluctuating populations is determined by the evolutionary trade-off between two fitness measures: Growth rate and lifetime reproductive success |
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