| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2009PNAS..10618638K |
| P356 | DOI | 10.1073/PNAS.0905497106 |
| P932 | PMC publication ID | 2767361 |
| P698 | PubMed publication ID | 19858497 |
| P5875 | ResearchGate publication ID | 38037819 |
| P50 | author | Joshua B. Plotkin | Q57242660 |
| P2093 | author name string | Sergey Kryazhimskiy | |
| Gasper Tkacik | |||
| P2860 | cites work | Genome evolution and adaptation in a long-term experiment with Escherichia coli | Q22122199 |
| The Distribution of Fitness Effects Among Beneficial Mutations | Q24543521 | ||
| Adaptive molecular evolution for 13,000 phage generations: a possible arms race | Q24545052 | ||
| The rate of adaptation in asexuals | Q24548116 | ||
| Frequency of fixation of adaptive mutations is higher in evolving diploid than haploid yeast populations | Q59092867 | ||
| Properties of adaptive walks on uncorrelated landscapes under strong selection and weak mutation. | Q64939522 | ||
| On evolution in a population with an infinite number of types | Q70739411 | ||
| A simple stochastic gene substitution model | Q71016135 | ||
| Continuity in evolution: on the nature of transitions | Q74594348 | ||
| The population genetics of adaptation: the adaptation of DNA sequences | Q74699508 | ||
| Evolution in a rugged fitness landscape | Q77863377 | ||
| The population genetics of adaptation on correlated fitness landscapes: the block model | Q80068725 | ||
| Adaptive evolution of asexual populations under Muller's ratchet | Q80514758 | ||
| The nk model and population genetics | Q81561603 | ||
| Neutral evolution of mutational robustness | Q24655790 | ||
| Beneficial mutation selection balance and the effect of linkage on positive selection | Q24685465 | ||
| Long-term experimental evolution in Escherichia coli. XI. Rejection of non-transitive interactions as cause of declining rate of adaptation | Q24794572 | ||
| Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations | Q28245607 | ||
| Effects of selective neutrality on the evolution of molecular species | Q28766080 | ||
| Experimental rugged fitness landscape in protein sequence space | Q33267358 | ||
| Extracting characteristic properties of fitness landscape from in vitro molecular evolution: a case study on infectivity of fd phage to E.coli | Q33275054 | ||
| Understanding the evolutionary fate of finite populations: the dynamics of mutational effects | Q33281050 | ||
| On the accessibility of adaptive phenotypes of a bacterial metabolic network | Q33495538 | ||
| Protein evolution on partially correlated landscapes | Q33860729 | ||
| The population genetics of ecological specialization in evolving Escherichia coli populations | Q33922714 | ||
| A study on a nearly neutral mutation model in finite populations | Q33957845 | ||
| Exceptional convergent evolution in a virus. | Q33971443 | ||
| The dynamical theory of coevolution: a derivation from stochastic ecological processes | Q34062882 | ||
| Protein evolution on rugged landscapes | Q34296709 | ||
| The solitary wave of asexual evolution | Q34470274 | ||
| Digital genetics: unravelling the genetic basis of evolution | Q34485612 | ||
| The speed of adaptation in large asexual populations | Q34645731 | ||
| Clonal interference in large populations | Q36156834 | ||
| Defining genetic interaction | Q36491179 | ||
| Epistasis between deleterious mutations and the evolution of recombination | Q36751300 | ||
| Evolutionary genetics: a piggyback ride to adaptation and diversity | Q36807008 | ||
| A general extreme value theory model for the adaptation of DNA sequences under strong selection and weak mutation | Q36969656 | ||
| The contribution of epistasis to the architecture of fitness in an RNA virus | Q37593251 | ||
| The effect of deleterious alleles on adaptation in asexual populations. | Q42534673 | ||
| The NK model of rugged fitness landscapes and its application to maturation of the immune response | Q42643980 | ||
| EVOLUTIONARY DYNAMICS OF FITNESS RECOVERY FROM THE DEBILITATING EFFECTS OF MULLER'S RATCHET. | Q46218646 | ||
| Towards a general theory of adaptive walks on rugged landscapes | Q47593883 | ||
| Protein Polymorphism as a Phase of Molecular Evolution | Q47760423 | ||
| An equivalence principle for the incorporation of favorable mutations in asexual populations. | Q50736355 | ||
| A minimum on the mean number of steps taken in adaptive walks. | Q52026868 | ||
| The fate of competing beneficial mutations in an asexual population. | Q54262235 | ||
| Fitness effects of fixed beneficial mutations in microbial populations. | Q54541810 | ||
| How Mutational Networks Shape Evolution: Lessons from RNA Models | Q57015492 | ||
| Evolutionary Dynamics of Fitness Recovery from the Debilitating Effects of Muller's Ratchet | Q57052392 | ||
| P433 | issue | 44 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 18638-18643 | |
| P577 | publication date | 2009-10-26 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | The dynamics of adaptation on correlated fitness landscapes | |
| P478 | volume | 106 |
| Q51826213 | A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social trait. |
| Q41986173 | Adaptation in tunably rugged fitness landscapes: the rough Mount Fuji model |
| Q35175854 | Adaptation of a cyanobacterium to a biochemically rich environment in experimental evolution as an initial step toward a chloroplast-like state |
| Q64933411 | Adaptive dynamics of unstable cancer populations: The canonical equation. |
| Q48248281 | Author’s response: Humans, fruit flies, and automatons. |
| Q35672470 | Backbones of evolutionary history test biodiversity theory for microbes |
| Q47106674 | Beneficial mutation-selection dynamics in finite asexual populations: a free boundary approach. |
| Q37173084 | Benefit of transferred mutations is better predicted by the fitness of recipients than by their ecological or genetic relatedness |
| Q34537612 | Changes in selective effects over time facilitate turnover of enhancer sequences |
| Q92126113 | Computational Complexity as an Ultimate Constraint on Evolution |
| Q42633184 | Detecting epistasis from an ensemble of adapting populations. |
| Q39954065 | Diminishing returns epistasis among beneficial mutations decelerates adaptation |
| Q54219938 | Diminishing-returns epistasis decreases adaptability along an evolutionary trajectory. |
| Q51332673 | Epistasis from functional dependence of fitness on underlying traits. |
| Q34760482 | Epistasis increases the rate of conditionally neutral substitution in an adapting population |
| Q41309636 | Evolution of new regulatory functions on biophysically realistic fitness landscapes. |
| Q90414037 | Evolving generalists in switching rugged landscapes |
| Q33523627 | Experimental evolution with E. coli in diverse resource environments. I. Fluctuating environments promote divergence of replicate populations |
| Q35962233 | Exploiting the Adaptation Dynamics to Predict the Distribution of Beneficial Fitness Effects |
| Q43184230 | Genetic background affects epistatic interactions between two beneficial mutations |
| Q37184676 | How Good Are Statistical Models at Approximating Complex Fitness Landscapes? |
| Q36368892 | Identification of the potentiating mutations and synergistic epistasis that enabled the evolution of inter-species cooperation |
| Q59867557 | Impact of epistasis and pleiotropy on evolutionary adaptation |
| Q33730568 | Inferring fitness landscapes by regression produces biased estimates of epistasis. |
| Q52735819 | Insertions and deletions trigger adaptive walks in Drosophila proteins. |
| Q42706151 | Introduction to focus issue: genetic interactions |
| Q45261637 | Long-term dynamics of adaptation in asexual populations |
| Q35105723 | Mapping the fitness landscape of gene expression uncovers the cause of antagonism and sign epistasis between adaptive mutations. |
| Q38053191 | Mechanisms and selection of evolvability: experimental evidence. |
| Q92141659 | Microbial Experimental Evolution - a proving ground for evolutionary theory and a tool for discovery |
| Q39169158 | Microbial evolution. Global epistasis makes adaptation predictable despite sequence-level stochasticity |
| Q47112377 | Molecular ensembles make evolution unpredictable. |
| Q44010374 | Negative epistasis between beneficial mutations in an evolving bacterial population |
| Q45362198 | On the findability of genotypes |
| Q45994253 | Parallel emergence of negative epistasis across experimental lineages. |
| Q92568694 | Patterns and Mechanisms of Diminishing Returns from Beneficial Mutations |
| Q21145317 | Predictability of evolutionary trajectories in fitness landscapes |
| Q28477179 | Prevalence of epistasis in the evolution of influenza A surface proteins |
| Q35077513 | Quantifying the similarity of monotonic trajectories in rough and smooth fitness landscapes |
| Q58570337 | Remote optimization of an ultracold atoms experiment by experts and citizen scientists |
| Q34504896 | Replaying the tape of life: quantification of the predictability of evolution |
| Q47378055 | Selecting among three basic fitness landscape models: Additive, multiplicative and stickbreaking |
| Q42324334 | Selection Limits to Adaptive Walks on Correlated Landscapes |
| Q35748281 | Stickbreaking: a novel fitness landscape model that harbors epistasis and is consistent with commonly observed patterns of adaptive evolution |
| Q92488321 | Stochastic tunneling across fitness valleys can give rise to a logarithmic long-term fitness trajectory |
| Q47136281 | The Nonstationary Dynamics of Fitness Distributions: Asexual Model with Epistasis and Standing Variation |
| Q26860873 | The causes of epistasis |
| Q58570246 | The causes of evolvability and their evolution |
| Q42145476 | The dynamics of adapting, unregulated populations and a modified fundamental theorem |
| Q46297608 | The dynamics of molecular evolution over 60,000 generations. |
| Q34671988 | The environment affects epistatic interactions to alter the topology of an empirical fitness landscape |
| Q35912265 | The genetic consequences of selection in natural populations. |
| Q34864177 | The impact of macroscopic epistasis on long-term evolutionary dynamics |
| Q42427784 | The peaks and geometry of fitness landscapes |
| Q40587253 | The strength of genetic interactions scales weakly with mutational effects |
| Q36153034 | Theory of prokaryotic genome evolution |
| Q34239196 | Young proteins experience more variable selection pressures than old proteins |
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