Abstract is: Sarah Perin "Sally" Otto FRSC (born October 23, 1967) is a theoretical biologist, Canada Research Chair in Theoretical and Experimental Evolution, and is currently a Killam Professor at the University of British Columbia. From 2008-2016, she was the director of the Biodiversity Research Centre at the University of British Columbia. Otto was named a 2011 MacArthur Fellow. In 2015 the American Society of Naturalists gave her the Sewall Wright Award for fundamental contributions to the unification of biology. In 2021, she was awarded the Darwin-Wallace Medal for contributing major advances to the mathematical theory of evolution.
human | Q5 |
P268 | Bibliothèque nationale de France ID | 16027417x |
P5361 | BNB person ID | OttoSarahP1967- |
P8179 | Canadiana Name Authority ID | ncf12120008 |
P2456 | DBLP author ID | 142/1762 |
P6178 | Dimensions author ID | 0603061110.46 |
P646 | Freebase ID | /m/0h64hn_ |
P227 | GND ID | 132966867 |
P1960 | Google Scholar author ID | -bIc5H0AAAAJ |
P6594 | Guggenheim fellows ID | sarah-perin-otto |
P269 | IdRef ID | 117723533 |
P213 | ISNI | 0000000114925707 |
P244 | Library of Congress authority ID | n2006019538 |
P3388 | LittleSis people ID | 106450 |
P9541 | MacArthur Fellows Program ID | 12 |
class-of-2011/sarah-otto | ||
P549 | Mathematics Genealogy Project ID | 44595 |
P4955 | MR Author ID | 264710 |
P5380 | National Academy of Sciences member ID | 20029948 |
P8189 | National Library of Israel J9U ID | 987007604320305171 |
P1006 | Nationale Thesaurus voor Auteursnamen ID | 310601894 |
P691 | NL CR AUT ID | jcu2012739185 |
P1015 | NORAF ID | 7025119 |
P1375 | NSK ID | 000587046 |
P1207 | NUKAT ID | n2008131611 |
P856 | official website | http://www.zoology.ubc.ca/~otto |
P496 | ORCID iD | 0000-0003-3042-0818 |
P3065 | RERO ID (obsolete) | 02-A014177012 |
P3987 | SHARE Catalogue author ID | 311064 |
P3430 | SNAC ARK ID | w60m4pcr |
P214 | VIAF ID | 62723727 |
P10832 | WorldCat Entities ID | E39PBJkhFrRhk8tW7Ffr667GpP |
P2002 | X username | sarperotto |
P1556 | zbMATH author ID | otto.sarah-perin |
P512 | academic degree | Doctor of Philosophy | Q752297 |
P166 | award received | Guggenheim Fellowship | Q1316544 |
MacArthur Fellows Program | Q1543268 | ||
Fellow of the Royal Society of Canada | Q3305342 | ||
ASN Award for Distinguished Achievement in the Conceptual Unification of the Biological Sciences | Q7458154 | ||
Weldon Memorial Prize | Q11804209 | ||
Fellow of the Royal Society | Q15631401 | ||
P27 | country of citizenship | Canada | Q16 |
United States of America | Q30 | ||
P184 | doctoral advisor | Marcus W. Feldman | Q15989759 |
P69 | educated at | Stanford University | Q41506 |
Washington International School | Q7971982 | ||
P108 | employer | University of British Columbia | Q391028 |
P734 | family name | Otto | Q2791874 |
Otto | Q2791874 | ||
Otto | Q2791874 | ||
P735 | given name | Sarah | Q18201513 |
Sarah | Q18201513 | ||
P1412 | languages spoken, written or signed | English | Q1860 |
P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
WikiProject Invasion Biology | Q56241615 | ||
P463 | member of | National Academy of Sciences | Q270794 |
American Academy of Arts and Sciences | Q463303 | ||
P106 | occupation | evolutionary biologist | Q16063497 |
P21 | sex or gender | female | Q6581072 |
P8687 | social media followers | 9742 |
Q90488796 | "Any news?" Special issue in honor of Marcus Feldman's 75th birthday |
Q63379862 | A Comparative Approach to the Population-Genetics Theory of Segregation Distortion |
Q63379840 | A MODEL OF THE EVOLUTION OF DICHOGAMY INCORPORATING SEX-RATIO SELECTION, ANTHER-STIGMA INTERFERENCE, AND INBREEDING DEPRESSION |
Q63379842 | A MODEL OF THE EVOLUTION OF DICHOGAMY INCORPORATING SEX-RATIO SELECTION, ANTHER-STIGMA INTERFERENCE, AND INBREEDING DEPRESSION |
Q43029588 | A likelihood method for detecting trait-dependent shifts in the rate of molecular evolution |
Q93095810 | A sheep in wolf's clothing: levels of deceit and detection in the evolution of cue-mimicry |
Q51713425 | A short history of recombination in yeast. |
Q37941231 | About PAR: the distinct evolutionary dynamics of the pseudoautosomal region |
Q28597774 | Adaptation to elevated CO2 in different biodiversity contexts |
Q59807739 | Adaptation, speciation and extinction in the Anthropocene |
Q60305188 | Adaptive epigenetic memory of ancestral temperature regime in Arabidopsis thalianaThis paper is one of a selection of papers published in a Special Issue from the National Research Council of Canada – Plant Biotechnology Institute |
Q33680997 | Aging in a long-lived clonal tree |
Q37227170 | Antibiotic overuse: the influence of social norms |
Q51198166 | Asymmetric competition impacts evolutionary rescue in a changing environment. |
Q52880022 | Balanced Polymorphisms and the Evolution of Dominance. |
Q63379853 | COMPENSATING FOR OUR LOAD OF MUTATIONS: FREEZING THE MELTDOWN OF SMALL POPULATIONS |
Q47200088 | Can clone size serve as a proxy for clone age? An exploration using microsatellite divergence in Populus tremuloides |
Q33997612 | Comment on "Ongoing adaptive evolution of ASPM, a brain size determinant in Homo sapiens" and "Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans". |
Q46947042 | Comparative analysis reveals that polyploidy does not decelerate diversification in fish. |
Q125461780 | Conceptual and empirical bridges between micro- and macroevolution |
Q63379834 | Condition‐Dependent Sex and the Rate of Adaptation |
Q36665918 | Contrasting patterns of transposable-element insertion polymorphism and nucleotide diversity in autotetraploid and allotetraploid Arabidopsis species |
Q36008800 | Costs of reproduction can explain the correlated evolution of semelparity and egg size: theory and a test with salmon |
Q92726157 | Crossover Interference: Shedding Light on the Evolution of Recombination |
Q28741669 | Cryptic fitness advantage: diploids invade haploid populations despite lacking any apparent advantage as measured by standard fitness assays |
Q41486670 | Deleterious mutations, variable epistatic interactions, and the evolution of recombination. |
Q31833185 | Detecting the form of selection from DNA sequence data. |
Q51365377 | Differential selection between the sexes and selection for sex. |
Q34497994 | Dioecy does not consistently accelerate or slow lineage diversification across multiple genera of angiosperms |
Q43929626 | Driven apart: the evolution of ploidy differences between the sexes under antagonistic selection |
Q63379830 | ESTABLISHMENT AND MAINTENANCE OF ADAPTIVE GENETIC DIVERGENCE UNDER MIGRATION, SELECTION, AND DRIFT |
Q22121995 | EVOLUTION OF SEXRESOLVING THE PARADOX OF SEX AND RECOMBINATION |
Q63379854 | Ecology and the Evolution of Biphasic Life Cycles |
Q51204801 | Ecology and the Evolution of Biphasic Life Cycles. |
Q34895148 | Effect of varying epistasis on the evolution of recombination |
Q63379849 | Eliminating the cost of sex with sexual selection |
Q63379825 | Erratum |
Q29618906 | Estimating a binary character's effect on speciation and extinction |
Q51692157 | Estimating trait-dependent speciation and extinction rates from incompletely resolved phylogenies. |
Q24671542 | Evidence that plant-like genes in Chlamydia species reflect an ancestral relationship between Chlamydiaceae, cyanobacteria, and the chloroplast |
Q51851033 | Evolution by fisherian sexual selection in diploids. |
Q63379861 | Evolution of Sex Determination in the Conchostracan Shrimp Eulimnadia texana |
Q36435329 | Evolution of haploid selection in predominantly diploid organisms |
Q33668331 | Evolution of movement rate increases the effectiveness of marine reserves for the conservation of pelagic fishes |
Q42128822 | Evolution of recombination due to random drift |
Q39675173 | Evolution of sex: Using experimental genomics to select among competing theories |
Q52610038 | Evolution: Zeroing In on the Rate of Genome Doubling. |
Q44909318 | Evolutionarily stable sex ratios and mutation load |
Q60586695 | Evolutionary dynamics of a quantitative trait in a finite asexual population |
Q35895628 | Evolutionary dynamics of a quantitative trait in a finite asexual population |
Q92287316 | Evolutionary potential for genomic islands of sexual divergence on recombining sex chromosomes |
Q44933702 | Evolutionary rescue in structured populations |
Q63379847 | Evolving beyond point mutations |
Q47383300 | Fitness-valley crossing with generalized parent-offspring transmission |
Q58034961 | Fixation Probabilities and Times |
Q58034967 | Fixation Probabilities and Times |
Q39171424 | Fixation Probability in a Haploid-Diploid Population |
Q29463194 | Frequency-dependent selection and the evolution of assortative mating |
Q48702042 | Functional pleiotropy and mating system evolution in plants: frequency-independent mating |
Q36439810 | Gene functional trade-offs and the evolution of pleiotropy. |
Q63379826 | Gene-culture co-evolution: teaching, learning, and correlations between relatives |
Q30580618 | Genes and other samples of DNA sequence data for phylogenetic inference |
Q91852635 | Genetic Paths to Evolutionary Rescue and the Distribution of Fitness Effects Along Them |
Q35960906 | Genetic control of invasive plants species using selfish genetic elements |
Q52600983 | Genomes and evolution Population genetics and molecular evolution of whole genomes. |
Q33258468 | Genomic convergence toward diploidy in Saccharomyces cerevisiae |
Q47604405 | Haploid Selection Favors Suppressed Recombination Between Sex Chromosomes Despite Causing Biased Sex Ratios |
Q63379821 | Haploid selection, sex ratio bias, and transitions between sex-determining systems |
Q63379822 | Haploid selection, sex ratio bias, and transitions between sex-determining systems |
Q33772117 | Haploids adapt faster than diploids across a range of environments |
Q50716196 | Host-parasite coevolution and selection on sex through the effects of segregation. |
Q24794881 | Host-parasite interactions and the evolution of gene expression. |
Q22066379 | Host-parasite interactions and the evolution of ploidy |
Q63379844 | In polyploids, one plus one does not equal two |
Q96433681 | Insights from Fisher's geometric model on the likelihood of speciation under different histories of environmental change |
Q22122238 | Interference among deleterious mutations favours sex and recombination in finite populations |
Q47570016 | Joint coevolutionary-epidemiological models dampen Red Queen cycles and alter conditions for epidemics |
Q47336884 | Keeping Pace with the Red Queen: Identifying the Genetic Basis of Susceptibility to Infectious Disease. |
Q34199925 | Liberating genetic variance through sex. |
Q35696836 | Liking the good guys: amplifying local adaptation via the evolution of condition-dependent mate choice. |
Q34327654 | Linking the investigations of character evolution and species diversification |
Q90249989 | Little Evidence of Antagonistic Selection in the Evolutionary Strata of Fungal Mating-Type Chromosomes (Microbotryum lychnidis-dioicae) |
Q35457373 | Loss of sexual recombination and segregation is associated with increased diversification in evening primroses |
Q35164402 | Loss-of-heterozygosity facilitates passage through Haldane's sieve for Saccharomyces cerevisiae undergoing adaptation |
Q51150731 | Macroevolutionary Patterns of Flowering Plant Speciation and Extinction. |
Q38770777 | Macroevolutionary synthesis of flowering plant sexual systems |
Q63379850 | Masking and purging mutations following EMS treatment in haploid, diploid and tetraploid yeast (Saccharomyces cerevisiae) |
Q63379858 | Mating systems and the evolutionary transition between haploidy and diploidy |
Q51387507 | Methods for studying polyploid diversification and the dead end hypothesis: a reply to Soltis et al. (2014). |
Q53566124 | Mitotic recombination counteracts the benefits of genetic segregation. |
Q42990076 | More on recombination and selection in the modifier theory of sex-ratio distortion |
Q39538117 | Multiple reproductive barriers separate recently diverged sunflower ecotypes |
Q63379835 | Mutating away from your enemies: The evolution of mutation rate in a host–parasite system |
Q91174284 | National contributions to global ecosystem values |
Q88207495 | ON GENETIC SEGREGATION AND THE EVOLUTION OF SEX |
Q63379859 | On the evolution of recombination in haploids and diploids: I. Deterministic models |
Q63379860 | On the evolution of recombination in haploids and diploids: II. Stochastic models |
Q98200163 | On the evolutionary epidemiology of SARS-CoV-2 |
Q117215734 | On the fast track: hybrids adapt more rapidly than parental populations in a novel environment |
Q36198245 | Parallel genetic changes and nonparallel gene-environment interactions characterize the evolution of drug resistance in yeast |
Q31118000 | Phylogenetic evidence for cladogenetic polyploidization in land plants |
Q51370089 | Ploidally antagonistic selection maintains stable genetic polymorphism. |
Q37558967 | Ploidy and the causes of genomic evolution |
Q63379829 | Ploidy and the evolution of parasitism |
Q36699581 | Ploidy reduction in Saccharomyces cerevisiae |
Q22065392 | Polyploid Incidence and Evolution |
Q41291263 | Population genetic perspectives on the evolution of recombination. |
Q51629165 | Probabilistic models of chromosome number evolution and the inference of polyploidy. |
Q41642365 | Probing the Depths of Biological Diversity During the Second Century of GENETICS. |
Q33996502 | Recently formed polyploid plants diversify at lower rates |
Q43989379 | Recombination and hitchhiking of deleterious alleles |
Q97592970 | Relative genomic impacts of translocation history, hatchery practices, and farm selection in Pacific oyster Crassostrea gigas throughout the Northern Hemisphere |
Q37509533 | Relaxed selection in the wild |
Q63379851 | SELECTION FOR RECOMBINATION IN SMALL POPULATIONS |
Q96428556 | Samarium doped titanium dioxide nanoparticles as theranostic agents in radiation therapy |
Q42184891 | Segregation and the evolution of sex under overdominant selection. |
Q77401068 | Selection for recombination in small populations |
Q34587456 | Selection for recombination in structured populations |
Q100526704 | Selective Interference and the Evolution of Sex |
Q35094686 | Selective maintenance of recombination between the sex chromosomes |
Q21092698 | Sex determination: why so many ways of doing it? |
Q51838045 | Sexual selection can resolve sex-linked sexual antagonism. |
Q34216097 | Sexual selection enables long-term coexistence despite ecological equivalence |
Q92463012 | Somatic mutations substantially increase the per-generation mutation rate in the conifer Picea sitchensis |
Q90798929 | Some topics in theoretical population genetics: Editorial commentaries on a selection of Marc Feldman's TPB papers |
Q28653264 | Specialization and generalization in the diversification of phytophagous insects: tests of the musical chairs and oscillation hypotheses |
Q34320816 | Species interactions and the evolution of sex. |
Q57835595 | Stimulating a Canadian narrative for climate |
Q63379852 | THE CONSEQUENCES OF DIOECY FOR SEED DISPERSAL: MODELING THE SEED-SHADOW HANDICAP |
Q63379828 | THE MAINTENANCE OF OBLIGATE SEX IN FINITE, STRUCTURED POPULATIONS SUBJECT TO RECURRENT BENEFICIAL AND DELETERIOUS MUTATION |
Q92348862 | TRY plant trait database - enhanced coverage and open access |
Q90387928 | Testing the socioeconomic and environmental determinants of better child-health outcomes in Africa: a cross-sectional study among nations |
Q63379838 | The Dynamic Nature of Apomixis in the Angiosperms |
Q63379832 | The Evolution of Sex Ratio Adjustment in the Presence of Sexually Antagonistic Selection |
Q56889202 | The Evolutionary Consequences of Selection at the Haploid Gametic Stage |
Q22066104 | The Evolutionary Enigma of Sex |
Q63379841 | The Role of Local Species Abundance in the Evolution of Pollinator Attraction in Flowering Plants |
Q34215620 | The advantages of segregation and the evolution of sex. |
Q41081632 | The distribution of beneficial mutant effects under strong selection. |
Q35910948 | The evolution of condition-dependent sex in the face of high costs |
Q34586458 | The evolution of gene duplicates |
Q44592265 | The evolution of genomic base composition in bacteria |
Q63379836 | The evolution of haploidy and diploidy |
Q56874668 | The evolution of life cycles with haploid and diploid phases |
Q39111447 | The evolution of offspring size across life-history stages |
Q34589752 | The evolution of plastic recombination |
Q63379855 | The evolution of recombination in changing environments |
Q35757735 | The evolution of sex and recombination in response to abiotic or coevolutionary fluctuations in epistasis |
Q46787473 | The evolution of sex chromosomes in organisms with separate haploid sexes |
Q34709080 | The evolutionary consequences of polyploidy |
Q63379843 | The first steps in adaptive evolution |
Q63379824 | The genome-wide rate and spectrum of spontaneous mutations differ between haploid and diploid yeast |
Q33520068 | The impact of epistatic selection on the genomic traces of selection |
Q37402961 | The magnitude of local adaptation under genotype-dependent dispersal |
Q126309823 | The phoenix hypothesis of speciation |
Q34154985 | The red queen coupled with directional selection favours the evolution of sex. |
Q40413453 | The role of advantageous mutations in enhancing the evolution of a recombination modifier |
Q50630572 | The role of epistasis on the evolution of recombination in host-parasite coevolution. |
Q82538694 | The role of local species abundance in the evolution of pollinator attraction in flowering plants |
Q42874950 | The role of pleiotropy in the maintenance of sex in yeast |
Q89526607 | Theory in Service of Narratives in Evolution and Ecology |
Q35050923 | Too much of a good thing: the unique and repeated paths toward copper adaptation |
Q41775956 | Toothpaste allergy diagnosis and management |
Q55038485 | Two steps forward, one step back: the pleiotropic effects of favoured alleles. |
Q37715308 | Two-locus autosomal sex determination: on the evolutionary genetic stability of the even sex ratio. |
Q126309836 | Unbalanced selection: the challenge of maintaining a social polymorphism when a supergene is selfish |
Q50920609 | Unravelling gene interactions. |
Q63379839 | Unravelling the evolutionary advantage of sex: a commentary on ‘Mutation–selection balance and the evolutionary advantage of sex and recombination’ by Brian Charlesworth |
Q34515406 | Use of Ecotilling as an efficient SNP discovery tool to survey genetic variation in wild populations of Populus trichocarpa |
Q44920334 | Variation in the strength of male mate choice allows long-term coexistence of sperm-dependent asexuals and their sexual hosts |
Q63379857 | Waiting with and without Recombination: The Time to Production of a Double Mutant |
Q46349684 | When Predators Help Prey Adapt and Persist in a Changing Environment |
Q63379837 | When do host-parasite interactions drive the evolution of non-random mating? |
Q63379845 | When looks can kill: the evolution of sexually dimorphic floral display and the extinction of dioecious plants |
Q22121967 | Why have sex? The population genetics of sex and recombination |
Q46620070 | Why wait? Three mechanisms selecting for environment-dependent developmental delays. |
Q28818537 | Widespread Genetic Incompatibilities between First-Step Mutations during Parallel Adaptation of Saccharomyces cerevisiae to a Common Environment |
Q51799692 | Women editors: we need more female scientists. |
Q28603215 | Women in evolution - highlighting the changing face of evolutionary biology |
Q35628971 | Y fuse? Sex chromosome fusions in fishes and reptiles |
Q15989759 | Marcus W. Feldman | doctoral student | P185 |