| scholarly article | Q13442814 |
| P2093 | author name string | Barton NH | |
| P2860 | cites work | Non-Darwinian Evolution | Q7048737 |
| Sexual reproduction as an adaptation to resist parasites (a review) | Q22066201 | ||
| Evolutionary Rate at the Molecular Level | Q22122432 | ||
| The effect of deleterious mutations on neutral molecular variation | Q24532876 | ||
| A molecular approach to the study of genic heterozygosity in natural populations. II. Amount of variation and degree of heterozygosity in natural populations of Drosophila pseudoobscura | Q24533326 | ||
| The evolutionary advantage of recombination | Q24533419 | ||
| The hitch-hiking effect of a favourable gene | Q28241578 | ||
| Possibility of extensive neutral evolution under stabilizing selection with special reference to nonrandom usage of synonymous codons | Q28776243 | ||
| Effects of linkage on rates of molecular evolution | Q33644420 | ||
| Organization and evolution of the mammalian genome: I. Polymorphism of H-2 linked loci. | Q33948928 | ||
| Limits of adaptation: the evolution of selective neutrality | Q33951427 | ||
| Allelic genealogy under overdominant and frequency-dependent selection and polymorphism of major histocompatibility complex loci | Q33956460 | ||
| The selection-mutation-drift theory of synonymous codon usage | Q33958751 | ||
| Comparing evolvability and variability of quantitative traits | Q33958894 | ||
| A ruby in the rubbish: beneficial mutations, deleterious mutations and the evolution of sex | Q33963090 | ||
| Effective size of populations under selection. | Q33964375 | ||
| "Silent" sites in Drosophila genes are not neutral: evidence of selection among synonymous codons | Q34049120 | ||
| Deleterious mutations and the evolution of sexual reproduction | Q34164458 | ||
| The molecular basis of dominance. | Q34283978 | ||
| Confidence interval for the number of selectively neutral amino acid polymorphisms | Q34343443 | ||
| Population structure of the human pseudoautosomal boundary | Q42636302 | ||
| Does natural selection increase or decrease variability at linked Loci | Q42958315 | ||
| Does associative overdominance account for the extensive polymorphism of h-2-linked Loci | Q42958317 | ||
| Models of host-parasite interaction and MHC polymorphism | Q42963490 | ||
| The number of balanced polymorphisms that can be maintained in a natural population | Q42971739 | ||
| Heterosis as a major cause of heterozygosity in nature. | Q42971743 | ||
| Coevolution of codon usage and transfer RNA abundance | Q43851327 | ||
| "Haldane's dilemma" and the rate of evolution. | Q51338527 | ||
| Redundancies, development and the flow of information | Q52231934 | ||
| The genomic mutation rate for fitness in Drosophila | Q52443296 | ||
| Genetic recombination. Patterns in the genome. | Q52541664 | ||
| The fixation of chromosomal rearrangements in a subdivided population with local extinction and colonization. | Q52668581 | ||
| Fitness effects of amino acid replacements in the beta-galactosidase of Escherichia coli. | Q54742523 | ||
| An estimate of heterosis inDrosophila melanogaster | Q67250408 | ||
| The effect of selected linked locus on heterozygosity of neutral alleles (the hitch-hiking effect) | Q67324548 | ||
| Fixation probability in spatially changing environments | Q67875793 | ||
| The probability of establishment of an advantageous mutant in a subdivided population | Q69398164 | ||
| Associative overdominance caused by linked detrimental mutations | Q70710194 | ||
| On the fixation probability of mutant genes in a subdivided population | Q71595745 | ||
| The effect of linkage on limits to artificial selection | Q72951099 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 821-841 | |
| P577 | publication date | 1995-06-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Linkage and the limits to natural selection | |
| P478 | volume | 140 |
| Q30862512 | A genome-wide scan for selection signatures in Yorkshire and Landrace pigs based on sequencing data |
| Q32064787 | A test of the background selection hypothesis based on nucleotide data from Drosophila ananassae. |
| Q34589967 | Adaptation in sexuals vs. asexuals: clonal interference and the Fisher-Muller model |
| Q33277177 | Adaptation of HIV-1 depends on the host-cell environment |
| Q35589220 | Adaptive gene introgression after secondary contact |
| Q34587933 | Allele frequency distribution under recurrent selective sweeps |
| Q34605822 | An adaptive hypothesis for the evolution of the Y chromosome |
| Q90095299 | An approximate full-likelihood method for inferring selection and allele frequency trajectories from DNA sequence data |
| Q83232098 | An integrative genomic analysis of the Longshanks selection experiment for longer limbs in mice |
| Q24685465 | Beneficial mutation selection balance and the effect of linkage on positive selection |
| Q33856627 | Beneficial mutations and the dynamics of adaptation in asexual populations. |
| Q34606746 | Beneficial mutations, hitchhiking and the evolution of mutation rates in sexual populations |
| Q52880031 | Between migration load and evolutionary rescue: dispersal, adaptation and the response of spatially structured populations to environmental change. |
| Q54251489 | Clonal interference can cause wavelet-like oscillations of multilocus linkage disequilibrium. |
| Q37203984 | Coalescence and genetic diversity in sexual populations under selection |
| Q28763574 | Comparative sequence analyses reveal rapid and divergent evolutionary changes of the WFDC locus in the primate lineage |
| Q33839433 | Correlated evolution of nearby residues in Drosophilid proteins |
| Q36837117 | Cut thy neighbor: cyclic birth and death of recombination hotspots via genetic conflict |
| Q29011147 | Deleterious Passengers in Adapting Populations |
| Q29543946 | Differential Strengths of Positive Selection Revealed by Hitchhiking Effects at Small Physical Scales in Drosophila melanogaster |
| Q35542057 | Distinguishing driver and passenger mutations in an evolutionary history categorized by interference |
| Q28474346 | Does mutational robustness inhibit extinction by lethal mutagenesis in viral populations? |
| Q53566921 | Dynamics and Fate of Beneficial Mutations Under Lineage Contamination by Linked Deleterious Mutations. |
| Q42571310 | Effective size and polymorphism of linked neutral loci in populations under directional selection. |
| Q37126633 | Effects of the population pedigree on genetic signatures of historical demographic events |
| Q35620493 | Emergent neutrality in adaptive asexual evolution |
| Q64233145 | Environmental fitness heterogeneity in the Moran process |
| Q92440432 | Epistasis detectably alters correlations between genomic sites in a narrow parameter window |
| Q36076919 | Establishment of new mutations in changing environments |
| Q34013656 | Evidence for hitchhiking of deleterious mutations within the human genome |
| Q40100301 | Evolution of Caenorhabditis elegans host defense under selection by the bacterial parasite Serratia marcescens |
| Q42128822 | Evolution of recombination due to random drift |
| Q30794348 | Evolutionary genomics of Borrelia burgdorferi sensu lato: findings, hypotheses, and the rise of hybrids |
| Q33325656 | Experimental evolution and genome sequencing reveal variation in levels of clonal interference in large populations of bacteriophage phiX174. |
| Q35854631 | Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits |
| Q91805925 | Exploiting selection at linked sites to infer the rate and strength of adaptation |
| Q40995314 | Fixation probability in a two-locus model by the ancestral recombination-selection graph |
| Q55382193 | Fixation probability of a beneficial mutation conferring decreased generation time in changing environments. |
| Q36883976 | Frequent adaptation and the McDonald-Kreitman test. |
| Q89517152 | From Drift to Draft: How Much Do Beneficial Mutations Actually Contribute to Predictions of Ohta's Slightly Deleterious Model of Molecular Evolution? |
| Q22065128 | Genetic draft and quasi-neutrality in large facultatively sexual populations |
| Q42430166 | Genetic linkage and natural selection |
| Q34625893 | Genetic load in sexual and asexual diploids: segregation, dominance and genetic drift. |
| Q35213699 | Genome-wide scan of gastrointestinal nematode resistance in closed Angus population selected for minimized influence of MHC |
| Q27028044 | Genomic signatures of selection at linked sites: unifying the disparity among species |
| Q63916629 | High-Resolution Evolutionary Analysis of Within-Host Hepatitis C Virus Infection |
| Q36873700 | Hitchhiking both ways: effect of two interfering selective sweeps on linked neutral variation |
| Q89027271 | In silico approaches to discover the functional impact of non-synonymous single nucleotide polymorphisms in selective sweep regions of the Landrace genome |
| Q52368963 | Inferring Fitness Effects from Time-Resolved Sequence Data with a Delay-Deterministic Model. |
| Q30501790 | Interplay of recombination and selection in the genomes of Chlamydia trachomatis |
| Q34609915 | Joint effects of genetic hitchhiking and background selection on neutral variation |
| Q90475013 | Landscape limits gene flow and drives population structure in Agassiz's desert tortoise (Gopherus agassizii) |
| Q36976920 | Limits to Adaptation in Partially Selfing Species |
| Q21144916 | Limits to the rate of adaptive substitution in sexual populations |
| Q34160190 | Linkage limits the power of natural selection in Drosophila |
| Q34608082 | Local recombination and mutation effects on molecular evolution in Drosophila |
| Q36756563 | Lytic phages obscure the cost of antibiotic resistance in Escherichia coli |
| Q37390406 | Male fitness increases when females are eliminated from gene pool: implications for the Y chromosome |
| Q45087918 | Molecular basis of the size polymorphism of the first intron of the Adh-1 gene of the mediterranean fruit fly, Ceratitis capitata. |
| Q33968789 | Molecular evolution between Drosophila melanogaster and D. simulans: reduced codon bias, faster rates of amino acid substitution, and larger proteins in D. melanogaster |
| Q33856660 | Mutation and the evolution of recombination |
| Q34279988 | Mutation load and rapid adaptation favour outcrossing over self-fertilization. |
| Q38517810 | On the fixation process of a beneficial mutation in a variable environment |
| Q33811376 | Outcrossing and the maintenance of males within C. elegans populations |
| Q41548380 | Phase III of Wright's shifting balance process and the variance among demes in migration rate |
| Q36094044 | Population genetic processes affecting the mode of selective sweeps and effective population size in influenza virus H3N2. |
| Q34612936 | Positive and negative selection on the human genome |
| Q42908236 | Predictions of patterns of response to artificial selection in lines derived from natural populations |
| Q34617001 | Probability of fixation of an advantageous mutant in a viral quasispecies. |
| Q33789108 | Purging deleterious mutations under self fertilization: paradoxical recovery in fitness with increasing mutation rate in Caenorhabditis elegans |
| Q21283965 | Quasispecies theory in the context of population genetics |
| Q33688865 | Rate of adaptation in large sexual populations |
| Q41911214 | Rates of fitness decline and rebound suggest pervasive epistasis |
| Q48521753 | Recombination Alters the Dynamics of Adaptation on Standing Variation in Laboratory Yeast Populations. |
| Q28540044 | Recombination accelerates adaptation on a large-scale empirical fitness landscape in HIV-1 |
| Q33525265 | Recombination and its impact on the genome of the haplodiploid parasitoid wasp Nasonia |
| Q30838915 | Recombination rate and protein evolution in yeast |
| Q37324343 | Relative effects of segregation and recombination on the evolution of sex in finite diploid populations |
| Q57055367 | Replicability of Introgression Under Linked, Polygenic Selection |
| Q34587456 | Selection for recombination in structured populations |
| Q47158568 | Selection on non-antigenic gene segments of seasonal influenza A virus and its impact on adaptive evolution |
| Q34617552 | Selective Sweeps in the Presence of Interference Among Partially Linked Loci |
| Q36969662 | Selective sweep at a quantitative trait locus in the presence of background genetic variation |
| Q34604996 | Selfish genes, pleiotropy and the origin of recombination |
| Q38952339 | Sex in a test tube: testing the benefits of in vitro recombination |
| Q35221557 | Sex-specific incompatibility generates locus-specific rates of introgression between species |
| Q58084796 | Slower environmental change hinders adaptation from standing genetic variation |
| Q33266807 | Soft sweeps III: the signature of positive selection from recurrent mutation |
| Q24544984 | Soft sweeps: molecular population genetics of adaptation from standing genetic variation |
| Q34936638 | The Effect of Interference on the CD8(+) T Cell Escape Rates in HIV. |
| Q92687083 | The Effects on Neutral Variability of Recurrent Selective Sweeps and Background Selection |
| Q42421139 | The Hill-Robertson effect and the evolution of recombination |
| Q73373285 | The approach to mutation-selection balance in an infinite asexual population, and the evolution of mutation rates |
| Q33924285 | The correlation between intron length and recombination in drosophila. Dynamic equilibrium between mutational and selective forces. |
| Q33929033 | The degeneration of Y chromosomes |
| Q33897315 | The dynamics of mutations associated with anti-malarial drug resistance in Plasmodium falciparum |
| Q33831372 | The ecology of sexual reproduction |
| Q42534673 | The effect of deleterious alleles on adaptation in asexual populations. |
| Q33575819 | The effect of linkage on establishment and survival of locally beneficial mutations |
| Q33903943 | The effects of Hill-Robertson interference between weakly selected mutations on patterns of molecular evolution and variation |
| Q36177833 | The effects of a deleterious mutation load on patterns of influenza A/H3N2's antigenic evolution in humans |
| Q35644757 | The effects of deleterious mutations on evolution at linked sites |
| Q41845604 | The effects of deleterious mutations on linked, neutral variation in small populations |
| Q34610474 | The evolution of recombination in a heterogeneous environment. |
| Q33971025 | The evolution of recombination: removing the limits to natural selection. |
| Q31061059 | The evolution of sex is favoured during adaptation to new environments |
| Q37229521 | The fixation probability of beneficial mutations |
| 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 |
| Q38206695 | The impact of linked selection on plant genomic variation |
| Q34081814 | The influence of deleterious mutations on adaptation in asexual populations |
| Q24533194 | The pattern of neutral molecular variation under the background selection model |
| Q35224710 | The population genetics of evolutionary rescue |
| Q24533249 | The probability of fixation in populations of changing size. |
| Q24548116 | The rate of adaptation in asexuals |
| Q34141931 | The rate of fitness-valley crossing in sexual populations. |
| Q35917364 | The role of background selection in shaping patterns of molecular evolution and variation: evidence from variability on the Drosophila X chromosome |
| Q34645731 | The speed of adaptation in large asexual populations |
| Q34330675 | The speed of evolution and maintenance of variation in asexual populations |
| Q36665927 | The stochastic edge in adaptive evolution |
| Q35247990 | The time scale of evolutionary innovation |
| Q41853709 | The traveling-wave approach to asexual evolution: Muller's ratchet and speed of adaptation |
| Q55038485 | Two steps forward, one step back: the pleiotropic effects of favoured alleles. |
| Q90399281 | Variability in fitness effects can preclude selection of the fittest |
| Q89934202 | Weak Correlation between Nucleotide Variation and Recombination Rate across the House Mouse Genome |
| Q50058827 | Weak Epistasis May Drive Adaptation in Recombining Bacteria |
| Q22305972 | Weak selection and protein evolution |
Search more.