human | Q5 |
P227 | GND ID | 1165691914 |
P269 | IdRef ID | 111889715 |
P8189 | National Library of Israel J9U ID | 987007366802205171 |
P496 | ORCID iD | 0000-0002-5731-8808 |
P4012 | Semantic Scholar author ID | 2935634 |
P214 | VIAF ID | 275148874394249621085 |
P166 | award received | Fellow of the American Association for the Advancement of Science | Q5442484 |
P108 | employer | Indiana University Bloomington | Q1079140 |
P734 | family name | Hahn | Q1362661 |
Hahn | Q1362661 | ||
Hahn | Q1362661 | ||
P735 | given name | Matthew | Q4927231 |
Matthew | Q4927231 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q34815429 | "Reverse ecology" and the power of population genomics |
Q92364906 | A Three-Sample Test for Introgression |
Q33633516 | A complex suite of forces drives gene traffic from Drosophila X chromosomes. |
Q56529735 | A multispecies coalescent model for quantitative traits |
Q114690139 | A new class of metrics for learning on real-valued and structured data |
Q31115851 | AGOUTI: improving genome assembly and annotation using transcriptome data |
Q35563213 | Abundant genetic variation in transcript level during early Drosophila development |
Q36287723 | Accelerated rate of gene gain and loss in primates |
Q37176321 | Adaptive evolution of young gene duplicates in mammals. |
Q33503331 | All human-specific gene losses are present in the genome as pseudogenes |
Q21146079 | Ancient and recent positive selection transformed opioid cis-regulation in humans |
Q91720507 | Association mapping desiccation resistance within chromosomal inversions in the African malaria vector Anopheles gambiae |
Q114109250 | Author Correction: Comparative and demographic analysis of orang-utan genomes |
Q36570626 | Bias in phylogenetic tree reconciliation methods: implications for vertebrate genome evolution |
Q104482508 | CAFE 5 models variation in evolutionary rates among gene families |
Q53657643 | COMPUTATIONAL APPROACHES TO UNDERSTANDING THE EVOLUTION OF MOLECULAR FUNCTION. |
Q60488154 | Clonal polymorphism and high heterozygosity in the celibate genome of the Amazon molly |
Q31061806 | Coding sequence divergence between two closely related plant species: Arabidopsis thaliana and Brassica rapa ssp. pekinensis |
Q34447196 | Comparative analysis of the domestic cat genome reveals genetic signatures underlying feline biology and domestication |
Q22122185 | Comparative and demographic analysis of orang-utan genomes |
Q81191524 | Comparative genomics of centrality and essentiality in three eukaryotic protein-interaction networks |
Q35549129 | Convergent evolution of the genomes of marine mammals |
Q41628098 | Detecting highly differentiated copy-number variants from pooled population sequencing. |
Q36586560 | Detecting natural selection on cis-regulatory DNA. |
Q41049748 | Detection and Polarization of Introgression in a Five-Taxon Phylogeny |
Q28648492 | Determining the Null Model for Detecting Adaptive Convergence from Genomic Data: A Case Study using Echolocating Mammals |
Q104511215 | Determining the probability of hemiplasy in the presence of incomplete lineage sorting and introgression |
Q36897193 | Differential gene expression in incipient species of Anopheles gambiae |
Q34712340 | Discovery of functional elements in 12 Drosophila genomes using evolutionary signatures |
Q34346838 | Disentangling the effects of demography and selection in human history |
Q89313364 | Dissecting the basis of novel trait evolution in a radiation with widespread phylogenetic discordance |
Q34992045 | Distinguishing among evolutionary models for the maintenance of gene duplicates |
Q34615149 | Distinguishing between selection and population expansion in an experimental lineage of bacteriophage T7. |
Q36938896 | Divergent transcriptional response to thermal stress by Anopheles gambiae larvae carrying alternative arrangements of inversion 2La |
Q111321579 | Does a complex life cycle affect adaptation to environmental change? Genome-informed insights for characterizing selection across complex life cycle |
Q55036811 | Drift as a mechanism for cultural change: an example from baby names. |
Q35863100 | Ecological genomics of Anopheles gambiae along a latitudinal cline: a population-resequencing approach |
Q113034035 | Erratum to: Genus-wide characterization of bumblebee genomes provides insights into their evolution and variation in ecological and behavioral traits |
Q44820810 | Estimating gene gain and loss rates in the presence of error in genome assembly and annotation using CAFE 3. |
Q30997971 | Estimating the tempo and mode of gene family evolution from comparative genomic data |
Q47240532 | Evaluating methods to visualize patterns of genetic differentiation on a landscape. |
Q22122220 | Evolution of genes and genomes on the Drosophila phylogeny |
Q22065872 | Evolutionary and Biomedical Insights from the Rhesus Macaque Genome |
Q46034913 | Evolutionary genomics: codon bias and selection on single genomes. |
Q92392784 | Evolutionary superscaffolding and chromosome anchoring to improve Anopheles genome assemblies |
Q35488229 | Extensive error in the number of genes inferred from draft genome assemblies |
Q44164287 | Female-biased gene expression in the malaria mosquito Anopheles gambiae |
Q43063740 | Gain and loss of phosphorylation sites in human cancer |
Q46488833 | Gene Tree Discordance Can Generate Patterns of Diminishing Convergence over Time |
Q39958900 | Gene Tree Discordance Causes Apparent Substitution Rate Variation |
Q92857694 | Gene content evolution in the arthropods |
Q51827237 | Gene conversion among paralogs results in moderate false detection of positive selection using likelihood methods. |
Q21144898 | Gene copy-number polymorphism caused by retrotransposition in humans |
Q55498998 | Gene copy-number polymorphism in nature. |
Q33668536 | Gene expression divergence between malaria vector sibling species Anopheles gambiae and An. coluzzii from rural and urban Yaoundé Cameroon. |
Q21145221 | Gene family evolution across 12 Drosophila genomes |
Q38832262 | Gene-tree reconciliation with MUL-trees to resolve polyploidy events |
Q33735743 | Genome-Wide Estimates of Transposable Element Insertion and Deletion Rates in Drosophila Melanogaster |
Q35581559 | Genome-wide analysis of retrogene polymorphisms in Drosophila melanogaster |
Q40026368 | Genome-wide patterns of regulatory divergence revealed by introgression lines |
Q46425281 | Genomic evidence of gene flow during reinforcement in Texas Phlox. |
Q24816847 | Genomic islands of speciation in Anopheles gambiae |
Q44151749 | Genomic islands of speciation or genomic islands and speciation? |
Q36268123 | Genomic variation in natural populations of Drosophila melanogaster |
Q99568928 | Genus-wide characterization of bumblebee genomes provides insights into their evolution and variation in ecological and behavioral traits |
Q34437895 | Gibbon genome and the fast karyotype evolution of small apes |
Q36744616 | How reticulated are species? |
Q83336634 | Identifying parent-daughter relationships among duplicated genes |
Q112756317 | Inferring the Genetic Basis of Sex Determination from the Genome of a Dioecious Nightshade |
Q35748310 | Inferring the history of interchromosomal gene transposition in Drosophila using n-dimensional parsimony |
Q35791522 | Interlocus gene conversion events introduce deleterious mutations into at least 1% of human genes associated with inherited disease |
Q46627864 | Irrational exuberance for resolved species trees |
Q57017848 | Leveraging evolutionary relationships to improve Anopheles genome assemblies |
Q33309462 | Localization of candidate regions maintaining a common polymorphic inversion (2La) in Anopheles gambiae |
Q44172979 | Locus- and population-specific selection and differentiation between incipient species of Anopheles gambiae |
Q33881264 | Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications |
Q37215228 | Minimal effect of ectopic gene conversion among recent duplicates in four mammalian genomes. |
Q43791663 | Molecular evolution in large genetic networks: does connectivity equal constraint? |
Q38872866 | Molecular mechanisms of postmating prezygotic reproductive isolation uncovered by transcriptome analysis |
Q41966519 | More accurate phylogenies inferred from low-recombination regions in the presence of incomplete lineage sorting |
Q28650801 | Mosquito genomics. Extensive introgression in a malaria vector species complex revealed by phylogenomics |
Q34456356 | Mosquito genomics. Highly evolvable malaria vectors: the genomes of 16 Anopheles mosquitoes |
Q64907663 | Multinucleotide mutations cause false inferences of lineage-specific positive selection. |
Q57812147 | Natural diversity of the malaria vector Anopheles gambiae |
Q99402388 | New Approaches for Inferring Phylogenies in the Presence of Paralogs |
Q62564168 | New methods to calculate concordance factors for phylogenomic datasets |
Q94512540 | New methods to calculate concordance factors for phylogenomic datasets |
Q35601067 | No evidence for biased co-transmission of speciation islands in Anopheles gambiae. |
Q35622998 | No excess gene movement is detected off the avian or lepidopteran Z chromosome |
Q33853245 | Nonallelic gene conversion in the genus Drosophila |
Q34140299 | Noncoding sequences near duplicated genes evolve rapidly |
Q102329221 | Origins and long-term patterns of copy-number variation in rhesus macaques |
Q37007882 | Parallel Evolution of Copy-Number Variation across Continents in Drosophila melanogaster |
Q95930784 | Paternal age in rhesus macaques is positively associated with germline mutation accumulation but not with measures of offspring sociability |
Q93366119 | Patterns of transposable element variation and clinality in Drosophila |
Q36553453 | Pervasive multinucleotide mutational events in eukaryotes |
Q28600841 | Phylogenomics Reveals Three Sources of Adaptive Variation during a Rapid Radiation |
Q34645182 | Population genetic and phylogenetic evidence for positive selection on regulatory mutations at the factor VII locus in humans |
Q21563561 | Population genomics: whole-genome analysis of polymorphism and divergence in Drosophila simulans |
Q57309676 | Positive Selection on a Human-Specific Transcription Factor Binding Site Regulating IL4 Expression |
Q38337161 | Positive selection on MMP3 regulation has shaped heart disease risk |
Q35946609 | Powerful methods for detecting introgressed regions from population genomic data |
Q104059243 | Primate phylogenomics uncovers multiple rapid radiations and ancient interspecific introgression |
Q46374136 | Proceedings of the SMBE Tri-National Young Investigators' Workshop 2005. Accurate inference and estimation in population genomics |
Q40514157 | Proteomic evidence for in-frame and out-of-frame alternatively spliced isoforms in human and mouse |
Q60311370 | Quantifying the risk of hemiplasy in phylogenetic inference |
Q103825890 | Radiation with reticulation marks the origin of a major malaria vector |
Q36821371 | Radical remodeling of the Y chromosome in a recent radiation of malaria mosquitoes |
Q57583313 | Random drift and culture change |
Q57583315 | Random drift and large shifts in popularity of dog breeds |
Q37063145 | Rates and genomic consequences of spontaneous mutational events in Drosophila melanogaster |
Q34420759 | Reanalysis suggests that genomic islands of speciation are due to reduced diversity, not reduced gene flow |
Q64285726 | Referee: Reference Assembly Quality Scores |
Q56502978 | Regular rates of popular culture change reflect random copying |
Q57074331 | Reproductive Longevity Predicts Mutation Rates in Primates |
Q40064499 | Reticulate evolutionary history and extensive introgression in mosquito species revealed by phylogenetic network analysis |
Q34196373 | Retrogenes reveal the direction of sex-chromosome evolution in mosquitoes |
Q35921011 | Revisiting classic clines in Drosophila melanogaster in the age of genomics |
Q33761700 | Sequencing, assembling, and correcting draft genomes using recombinant populations |
Q42014235 | Sex chromosomes evolved from independent ancestral linkage groups in winged insects |
Q21092698 | Sex determination: why so many ways of doing it? |
Q36119961 | Similar Efficacies of Selection Shape Mitochondrial and Nuclear Genes in Both Drosophila melanogaster and Homo sapiens |
Q35579812 | Soft shoulders ahead: spurious signatures of soft and partial selective sweeps result from linked hard sweeps |
Q47211008 | Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host |
Q46323522 | Speciation as a sieve for ancestral polymorphism. |
Q57134585 | Speciation genes are more likely to have discordant gene trees |
Q56358012 | Systems genetic analysis of inversion polymorphisms in the malaria mosquito |
Q21145323 | Testing the ortholog conjecture with comparative functional genomic data from mammals |
Q37738644 | The Effects of Increasing the Number of Taxa on Inferences of Molecular Convergence |
Q60312624 | The Genomic Basis of Arthropod Diversity |
Q88555310 | The Neutral Theory in Light of Natural Selection |
Q112710902 | The Potential for a Released Autosomal X-Shredder Becoming a Driving-Y Chromosome and Invasively Suppressing Wild Populations of Malaria Mosquitoes |
Q91167590 | The Timing and Direction of Introgression Under the Multispecies Network Coalescent |
Q64004670 | The comparative genomics and complex population history of baboons |
Q39890656 | The contribution of gene movement to the "two rules of speciation". |
Q115020606 | The effects of introgression across thousands of quantitative traits revealed by gene expression in wild tomatoes |
Q52950810 | The effects of selection against spurious transcription factor binding sites. |
Q21092262 | The evolution of mammalian gene families |
Q36991910 | The evolution of the Anopheles 16 genomes project |
Q29618447 | The evolution of transcriptional regulation in eukaryotes |
Q44160035 | The fixation of malaria refractoriness in mosquitoes |
Q74070251 | The g-value paradox |
Q35777965 | The genome of the vervet (Chlorocebus aethiops sabaeus) |
Q44173808 | The human mutation rate is increasing, even as it slows |
Q34925251 | The life and death of gene families |
Q30882819 | The limited contribution of reciprocal gene loss to increased speciation rates following whole-genome duplication. |
Q97542285 | The ortholog conjecture revisited: the value of orthologs and paralogs in function prediction |
Q92469401 | The perils of intralocus recombination for inferences of molecular convergence |
Q60300916 | The sequencing and interpretation of the genome obtained from a Serbian individual |
Q30493305 | The strength of transcription-factor binding modulates co-variation in transcriptional networks |
Q57468607 | Three new genome assemblies support a rapid radiation in Musa acuminata (wild banana) |
Q28270306 | Toward a selection theory of molecular evolution |
Q33595653 | Transcriptomic analysis links gene expression to unilateral pollen-pistil reproductive barriers |
Q21135000 | Very few RNA and DNA sequence differences in the human transcriptome |
Q39577960 | Very low rate of gene conversion in the yeast genome |
Q46295966 | Why Concatenation Fails Near the Anomaly Zone |
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