| scholarly article | Q13442814 |
| P50 | author | Andrius J Dagilis | Q88414121 |
| Daniel I. Bolnick | Q45679730 | ||
| P2093 | author name string | Mark Kirkpatrick | |
| P2860 | cites work | The genetics of speciation: Insights from Fisher's geometric model. | Q50892004 |
| A Test of the Snowball Theory for the Rate of Evolution of Hybrid Incompatibilities | Q51619902 | ||
| Systematic analysis of complex genetic interactions. | Q52315036 | ||
| "PATTERNS OF SPECIATION IN DROSOPHILA" REVISITED. | Q54626249 | ||
| Incompatibility of nuclear and mitochondrial genomes causes hybrid sterility between two yeast species. | Q54781969 | ||
| Coadapted genomes and selection on hybrids: Fisher's geometric model explains a variety of empirical patterns | Q57133869 | ||
| Hybridization is a recurrent evolutionary stimulus in wild yeast speciation | Q64106183 | ||
| The evolution of postzygotic isolation: accumulating Dobzhansky-Muller incompatibilities | Q74273365 | ||
| Contributions of heterosis and epistasis to hybrid fitness | Q81350792 | ||
| Speciation genetics: search for the missing snowball | Q82965512 | ||
| Hybrid Incompatibility “Snowballs” Between Solanum Species | Q85041068 | ||
| Evolution in the light of fitness landscape theory | Q90743445 | ||
| Dominance, overdominance and epistasis condition the heterosis in two heterotic rice hybrids | Q36969692 | ||
| The pattern and distribution of deleterious mutations in maize | Q37460697 | ||
| The polymorphic prelude to Bateson-Dobzhansky-Muller incompatibilities | Q37966407 | ||
| PATTERNS OF SPECIATION IN DROSOPHILA. | Q38751832 | ||
| Heterosis and Outbreeding Depression in Interpopulation Crosses Spanning a Wide Range of Divergence | Q38753144 | ||
| Species-wide survey reveals the various flavors of intraspecific reproductive isolation in yeast. | Q38861954 | ||
| Spiraling Complexity: A Test of the Snowball Effect in a Computational Model of RNA Folding | Q39070449 | ||
| A global genetic interaction network maps a wiring diagram of cellular function | Q39318959 | ||
| Epistasis together with partial dominance, over-dominance and QTL by environment interactions contribute to yield heterosis in upland cotton | Q39451300 | ||
| Epistasis and the Structure of Fitness Landscapes: Are Experimental Fitness Landscapes Compatible with Fisher's Geometric Model? | Q40725548 | ||
| The fitness effect of mutations across environments: Fisher's geometrical model with multiple optima | Q41020117 | ||
| Determinants of divergent adaptation and Dobzhansky-Muller interaction in experimental yeast populations | Q42147858 | ||
| The limits to parapatric speciation: Dobzhansky-Muller incompatibilities in a continent-island model | Q42225942 | ||
| Incomplete dominance of deleterious alleles contributes substantially to trait variation and heterosis in maize. | Q42708328 | ||
| Heterosis | Q45327381 | ||
| Heterosis in hybrids within and between yeast species | Q46448570 | ||
| The genetic architecture of hybrid incompatibilities and their effect on barriers to introgression in secondary contact | Q46700797 | ||
| Tempo of hybrid inviability in centrarchid fishes (Teleostei: Centrarchidae). | Q46836574 | ||
| Effective population size and the faster-X effect: an extended model | Q47182566 | ||
| The probability of speciation on an interaction network with unequal substitution rates | Q49209238 | ||
| A stochastic model for the development of Bateson-Dobzhansky-Muller incompatibilities that incorporates protein interaction networks | Q49258345 | ||
| PERSPECTIVE: MODELS OF SPECIATION: WHAT HAVE WE LEARNED IN 40 YEARS? | Q22065124 | ||
| On the probability of fixation of mutant genes in a population | Q24533316 | ||
| Haldane's Rule: Genetic Bases and Their Empirical Support | Q26745539 | ||
| Progress toward understanding heterosis in crop plants | Q26809978 | ||
| The role of hybridization in evolution | Q26810047 | ||
| Evidence for archaic adaptive introgression in humans | Q26830001 | ||
| The genetic landscape of a cell | Q28131628 | ||
| The barrier to genetic exchange between hybridising populations | Q28304986 | ||
| Asymmetric postmating isolation: Darwin's corollary to Haldane's rule | Q28757542 | ||
| Widespread Genetic Incompatibilities between First-Step Mutations during Parallel Adaptation of Saccharomyces cerevisiae to a Common Environment | Q28818537 | ||
| The genetic architecture necessary for transgressive segregation is common in both natural and domesticated populations | Q30445209 | ||
| Transgressive Hybrids as Hopeful Monsters | Q30628476 | ||
| The faster-X effect: integrating theory and data | Q30650832 | ||
| Accumulating Dobzhansky-Muller incompatibilities: reconciling theory and data | Q30946080 | ||
| Adaptive introgression between Anopheles sibling species eliminates a major genomic island but not reproductive isolation | Q31075931 | ||
| A screen for recessive speciation genes expressed in the gametes of F1 hybrid yeast | Q33274201 | ||
| Are species real? The shape of the species boundary with exponential failure, reinforcement, and the "missing snowball". | Q33506735 | ||
| Explaining Darwin's corollary to Haldane's rule: the role of mitonuclear interactions in asymmetric postzygotic isolation among toads | Q33779642 | ||
| Transgressive segregation, adaptation and speciation. | Q33785749 | ||
| Haldane's rule in the 21st century | Q33790794 | ||
| Pervasive antagonistic interactions among hybrid incompatibility loci | Q33834859 | ||
| The population genetics of speciation: the evolution of hybrid incompatibilities | Q33964957 | ||
| The weaker sex is heterogametic: 75 years of Haldane's rule. | Q33971314 | ||
| Functional coadaptation between cytochrome c and cytochrome c oxidase within allopatric populations of a marine copepod | Q34190799 | ||
| Adaptive introgression across species boundaries in Heliconius butterflies. | Q34318245 | ||
| Multiple rounds of speciation associated with reciprocal gene loss in polyploid yeasts | Q34502616 | ||
| Dominance, epistasis and the genetics of postzygotic isolation | Q34609169 | ||
| A fine-scale genetic analysis of hybrid incompatibilities in Drosophila. | Q34617291 | ||
| Incipient speciation by divergent adaptation and antagonistic epistasis in yeast | Q34632967 | ||
| A rapidly evolving MYB-related protein causes species isolation in Drosophila | Q34982785 | ||
| Partial Dominance, Overdominance and Epistasis as the Genetic Basis of Heterosis in Upland Cotton (Gossypium hirsutum L.). | Q35855584 | ||
| Speciation driven by hybridization and chromosomal plasticity in a wild yeast | Q36116121 | ||
| Accelerated mitochondrial evolution and "Darwin's corollary": asymmetric viability of reciprocal F1 hybrids in Centrarchid fishes | Q36470614 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ggplot2 | Q326489 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | speciation | Q39350 |
| P304 | page(s) | e1008125 | |
| P577 | publication date | 2019-05-06 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | The evolution of hybrid fitness during speciation | |
| P478 | volume | 15 |
| Q94585502 | Genomic evidence for a hybrid origin of the yeast opportunistic pathogen Candida albicans | cites work | P2860 |
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