| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Guillaume Martin | Q56754583 |
| Thomas Lenormand | Q30518257 | ||
| P2860 | cites work | The fate of competing beneficial mutations in an asexual population. | Q54262235 |
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| Perspective: Spontaneous Deleterious Mutation | Q57933462 | ||
| The genome sequence of Caenorhabditis briggsae: a platform for comparative genomics | Q21092840 | ||
| Fitness effects of advantageous mutations in evolving Escherichia coli populations | Q22066182 | ||
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| The genetic theory of adaptation: a brief history | Q22122021 | ||
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| Contribution of individual random mutations to genotype-by-environment interactions in Escherichia coli | Q33944549 | ||
| Limits to natural selection | Q34085649 | ||
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| Theories of adaptation: what they do and don't say. | Q36120420 | ||
| Genotype-environment interactions of spontaneous mutations for vegetative fitness in the human pathogenic fungus Cryptococcus neoformans | Q42910035 | ||
| Estimate of the genomic mutation rate deleterious to overall fitness in E. coli. | Q51030744 | ||
| THE EVOLUTION OF CANALIZATION AND THE BREAKING OF VON BAER'S LAWS: MODELING THE EVOLUTION OF DEVELOPMENT WITH EPISTASIS. | Q52187296 | ||
| Some evolutionary consequences of deleterious mutations. | Q52237149 | ||
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| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | multivariate statistics | Q1952580 |
| species distribution model | Q122175981 | ||
| P1104 | number of pages | 15 | |
| P304 | page(s) | 893-907 | |
| P577 | publication date | 2006-05-01 | |
| P1433 | published in | Evolution | Q4038411 |
| P1476 | title | A general multivariate extension of Fisher's geometrical model and the distribution of mutation fitness effects across species | |
| P478 | volume | 60 |
| Q37628802 | A bayesian MCMC approach to assess the complete distribution of fitness effects of new mutations: uncovering the potential for adaptive walks in challenging environments |
| Q37514471 | A comparative view of the evolution of grasses under domestication |
| Q28754894 | A framework for evolutionary systems biology |
| Q111629295 | A note on gene pleiotropy estimation from phylogenetic analysis of protein sequences |
| Q51147065 | A population genetic interpretation of GWAS findings for human quantitative traits. |
| Q41021919 | A statistical guide to the design of deep mutational scanning experiments |
| Q42371063 | Accumulation of Deleterious Mutations During Bacterial Range Expansions |
| Q35960742 | Adaptation, extinction and global change |
| Q46274966 | Adaptive Evolution under Extreme Genetic Drift in Oxidatively Stressed Caenorhabditis elegans |
| Q27309280 | Adaptive Protein Evolution in Animals and the Effective Population Size Hypothesis |
| Q51544118 | Antibiotic resistance and stress in the light of Fisher's model. |
| Q33339383 | Assessing the evolutionary impact of amino acid mutations in the human genome |
| Q33895095 | Balancing selection in species with separate sexes: insights from Fisher's geometric model |
| Q28082810 | Can the experimental evolution programme help us elucidate the genetic basis of adaptation in nature? |
| Q36071255 | Catch Me if You Can: Adaptation from Standing Genetic Variation to a Moving Phenotypic Optimum |
| Q34537612 | Changes in selective effects over time facilitate turnover of enhancer sequences |
| Q49866098 | Chaos and the (un)predictability of evolution in a changing environment |
| Q51122897 | Chaos and unpredictability in evolution. |
| Q57133869 | Coadapted genomes and selection on hybrids: Fisher's geometric model explains a variety of empirical patterns |
| Q42379133 | Competition and fixation of cohorts of adaptive mutations under Fisher geometrical model |
| Q90029099 | Comprehensive fitness maps of Hsp90 show widespread environmental dependence |
| Q34003200 | Cost of adaptation and fitness effects of beneficial mutations in Pseudomonas fluorescens. |
| Q64926740 | Cross-sex genetic correlations for fitness and fitness components: Connecting theoretical predictions to empirical patterns. |
| Q46281390 | Determinants of the Efficacy of Natural Selection on Coding and Noncoding Variability in Two Passerine Species |
| Q33620151 | Determining the factors driving selective effects of new nonsynonymous mutations |
| Q54444950 | Distributions of epistasis in microbes fit predictions from a fitness landscape model. |
| Q51868323 | Divergence and polymorphism under the nearly neutral theory of molecular evolution. |
| Q50424274 | Effects of mutation and selection on plasticity of a promoter activity in Saccharomyces cerevisiae |
| Q30828514 | Effects of new mutations on fitness: insights from models and data |
| Q35620493 | Emergent neutrality in adaptive asexual evolution |
| Q37764210 | Environmental duress and epistasis: how does stress affect the strength of selection on new mutations? |
| Q40771994 | Epigenetic mutations can both help and hinder adaptive evolution. |
| Q53156835 | Epistatic interactions between ancestral genotype and beneficial mutations shape evolvability in Pseudomonas aeruginosa. |
| Q53702273 | Evolutionary Rescue over a Fitness Landscape. |
| Q51670388 | Evolutionary epidemiology and the dynamics of adaptation. |
| Q42059556 | Evolutionary framework for protein sequence evolution and gene pleiotropy |
| Q54443680 | Evolutionary inevitability of sexual antagonism. |
| Q30671403 | Fisher's geometric model of adaptation meets the functional synthesis: data on pairwise epistasis for fitness yields insights into the shape and size of phenotype space |
| Q51313054 | Fisher's geometric model predicts the effects of random mutations when tested in the wild. |
| Q34851593 | Fisher's geometric model with a moving optimum |
| Q39224677 | Fisher's geometrical model and the mutational patterns of antibiotic resistance across dose gradients |
| Q33575800 | Fisher's geometrical model emerges as a property of complex integrated phenotypic networks |
| Q38599116 | Fitness effects of derived deleterious mutations in four closely related wild tomato species with spatial structure. |
| Q35541962 | Fitness landscapes: an alternative theory for the dominance of mutation |
| Q34203627 | Fitness recovery and compensatory evolution in natural mutant lines of C. elegans |
| Q30248269 | Forecasting Epidemiological and Evolutionary Dynamics of Infectious Diseases |
| Q42565608 | From adaptation to molecular evolution |
| Q43111621 | Genepleio software for effective estimation of gene pleiotropy from protein sequences. |
| Q38883864 | Genetic Diversity and the Efficacy of Purifying Selection across Plant and Animal Species |
| Q44458030 | Genetic constraints on adaptation to a changing environment. |
| Q34140433 | Genomic patterns of pleiotropy and the evolution of complexity |
| Q28728043 | Horizontal gene transfer dynamics and distribution of fitness effects during microbial in silico evolution |
| Q39024444 | How does epistasis influence the response to selection? |
| Q36315799 | Inbreeding depression maintained by recessive lethal mutations interacting with stabilizing selection on quantitative characters in a partially self-fertilizing population |
| Q33642802 | Inference of the Distribution of Selection Coefficients for New Nonsynonymous Mutations Using Large Samples |
| Q28540172 | Influenza virus drug resistance: a time-sampled population genetics perspective |
| Q58764752 | Information Theory, Developmental Psychology, and the Baldwin Effect |
| Q40863246 | Lethal mutagenesis and evolutionary epidemiology |
| Q42031438 | Molecular evolution, mutation size and gene pleiotropy: a geometric reexamination. |
| Q36779247 | Multidimensional adaptive evolution of a feed-forward network and the illusion of compensation |
| Q37011403 | Multivariate QST-FST comparisons: a neutrality test for the evolution of the g matrix in structured populations |
| Q41920654 | Multivariate genetic analysis of plant responses to water deficit and high temperature revealed contrasting adaptive strategies |
| Q34491304 | Multivariate phenotypic divergence due to the fixation of beneficial mutations in experimentally evolved lineages of a filamentous fungus |
| Q42219041 | Next generation genetics |
| Q46948022 | Niche dimensionality and the genetics of ecological speciation. |
| Q42076622 | On measuring selection in experimental evolution. |
| Q51026723 | On the effect of phenotypic dimensionality on adaptation and optimality. |
| Q60691926 | Phenotypic lag and population extinction in the moving-optimum model: insights from a small-jumps limit |
| Q36512966 | Phenotypic plasticity in evolutionary rescue experiments |
| Q33389164 | Pleiotropic scaling and QTL data |
| Q51691507 | Pleiotropic scaling of gene effects and the 'cost of complexity'. |
| Q42544122 | Pleiotropy can be effectively estimated without counting phenotypes through the rank of a genotype-phenotype map. |
| Q38154687 | Population size and the rate of evolution. |
| Q35079781 | Properties of selected mutations and genotypic landscapes under Fisher's geometric model. |
| Q55208702 | Quantifying natural seasonal variation in mutation parameters with mutation accumulation lines. |
| Q30829788 | Quantifying organismal complexity using a population genetic approach |
| Q30740418 | Rapid evolution of quantitative traits: theoretical perspectives |
| Q90244482 | Recent insights into the genotype-phenotype relationship from massively parallel genetic assays |
| Q27323073 | Reference-free population genomics from next-generation transcriptome data and the vertebrate-invertebrate gap |
| Q54708052 | Restricted pleiotropy facilitates mutational erosion of major life-history traits. |
| Q88932496 | Robustness and evolvability of heterogeneous cell populations |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q37215211 | Selection for chaperone-like mediated genetic robustness at low mutation rate: impact of drift, epistasis and complexity |
| Q90131153 | Selective Sweep at a QTL in a Randomly Fluctuating Environment |
| Q36969662 | Selective sweep at a quantitative trait locus in the presence of background genetic variation |
| Q44019766 | Sensitivity of the distribution of mutational fitness effects to environment, genetic background, and adaptedness: a case study with Drosophila |
| Q39282789 | Sex-specific selection under environmental stress in seed beetles |
| Q37373507 | Shifting fitness landscapes in response to altered environments. |
| Q49803782 | Stochastic Evolutionary Demography under a Fluctuating Optimum Phenotype |
| Q37380183 | Stochasticity in evolution. |
| Q43092006 | Synergistic fitness interactions and a high frequency of beneficial changes among mutations accumulated under relaxed selection in Saccharomyces cerevisiae |
| Q47136281 | The Nonstationary Dynamics of Fitness Distributions: Asexual Model with Epistasis and Standing Variation |
| Q38689208 | The Utility of Fisher's Geometric Model in Evolutionary Genetics |
| Q36724374 | The distribution of beneficial and fixed mutation fitness effects close to an optimum |
| Q90243144 | The distribution of epistasis on simple fitness landscapes |
| Q41914227 | The distribution of fitness effects in an uncertain world |
| Q50021304 | The distribution of mutational fitness effects of phage φX174 on different hosts |
| Q31040305 | The emergence of complexity and restricted pleiotropy in adapting networks |
| Q43138629 | The evolution of epistasis and its links with genetic robustness, complexity and drift in a phenotypic model of adaptation |
| Q41020117 | The fitness effect of mutations across environments: Fisher's geometrical model with multiple optima |
| Q42030850 | The genetic basis of phenotypic adaptation I: fixation of beneficial mutations in the moving optimum model |
| Q42693809 | The genetic basis of phenotypic adaptation II: the distribution of adaptive substitutions in the moving optimum model |
| Q35912265 | The genetic consequences of selection in natural populations. |
| Q50892004 | The genetics of speciation: Insights from Fisher's geometric model. |
| Q41227395 | The inclusive fitness controversy: finding a way forward. |
| Q34310887 | The many faces of pleiotropy |
| Q42123470 | The nearly neutral and selection theories of molecular evolution under the fisher geometrical framework: substitution rate, population size, and complexity. |
| Q37844408 | The pleiotropic structure of the genotype-phenotype map: the evolvability of complex organisms. |
| Q37755968 | The population genetics of antibiotic resistance: integrating molecular mechanisms and treatment contexts. |
| Q30947119 | The properties of adaptive walks in evolving populations of fungus |
| Q50476213 | The role of pleiotropy and linkage in genes affecting a sexual ornament and bone allocation in the chicken. |
| Q39024576 | The rule of declining adaptability in microbial evolution experiments. |
| Q55424984 | Two sides of the same coin: A population genetics perspective on lethal mutagenesis and mutational meltdown. |
| Q60620239 | Uneven Distribution of Mutational Variance Across the Transcriptome of Revealed by High-Dimensional Analysis of Gene Expression |
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