The DOI matches its Crossref record; 63 of the 63 references it cites were found in a registry or an index.
Detecting Individual Sites Subject to Episodic Diversifying Selection
Open accessAbstract
The imprint of natural selection on protein coding genes is often difficult to identify because selection is frequently transient or episodic, i.e. it affects only a subset of lineages. Existing computational techniques, which are designed to identify sites subject to pervasive selection, may fail to recognize sites where selection is episodic: a large proportion of positively selected sites. We present a mixed effects model of evolution (MEME) that is capable of identifying instances of both episodic and pervasive positive selection at the level of an individual site. Using empirical and simulated data, we demonstrate the superior performance of MEME over older models under a broad range of scenarios. We find that episodic selection is widespread and conclude that the number of sites experiencing positive selection may have been vastly underestimated.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Positively selected sites were identified using two different methods: the Bayes Empirical Bayes (BEB) analysis from MA (with a cutoff of 0.90) and the Mixed Effects Model of Evolution (MEME) (with the default cutoff of 0.1)34.”
From Distinct selective forces and Neanderthal introgression shaped genetic diversity at genes involved in neurodevelopmental disorders (2017) · cites this paper as [34]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, this test can be misleading because estimates of ! can be increased by processes such as intensification of positive selection when selective pressures vary both along branches and sites (Murrell et al. 2012).”
From RELAX: Detecting Relaxed Selection in a Phylogenetic Framework (2015) · cites this paper as Murrell et al. 2012
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Standard methods for estimating the strength and extent of purifying or positive selection from molecular sequence data are not suitable for detecting relaxed selection, because they lack power and can mistake an increase in the intensity of positive selection for relaxation of both purifying and positive selection.”
From RELAX: Detecting Relaxed Selection in a Phylogenetic Framework (2015) · cites this paper as Murrell et al. 2012
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“To be conservative, we considered as positively selected only sites also detected by the Mixed Effects Model of Evolution (MEME) method34.”
From Distinct selective forces and Neanderthal introgression shaped genetic diversity at genes involved in neurodevelopmental disorders (2017) · cites this paper as [34]
The cited source says what the claim attributes to it.
In the citing paper
“This development vastly increased the detectable instances of positive selection (Murrell et al. 2012).”
From RELAX: Detecting Relaxed Selection in a Phylogenetic Framework (2015) · cites this paper as Murrell et al. 2012
The cited source says what the claim attributes to it.
In the citing paper
“Our random effects (Kosakovsky Pond et al. 2011) and mixed effects (Murrell et al. 2012) branch-site models allow detection of individual branches on which only a subset of sites are under positive selection or, conversely, individual sites which are under positive selection on only a subset of branches.”
From RELAX: Detecting Relaxed Selection in a Phylogenetic Framework (2015) · cites this paper as Murrell et al. 2012
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482
Evolutionary trees from DNA sequences: A maximum likelihood approach.
Felsenstein, J. (1981) · Journal of Molecular Evolution · doi:10.1007/bf01734359 · Cited by 14,571
Evolutionary Rate at the Molecular Level
KIMURA, M. (1968) · Nature · doi:10.1038/217624a0 · Cited by 3,747
Adaptive protein evolution at the Adh locus in Drosophila
McDonald, J. H., & Kreitman, M. (1991) · Nature · doi:10.1038/351652a0 · Cited by 3,313
Self, S., & Liang, K.-Y. (1987) · Journal of the American Statistical Association · doi:10.1080/01621459.1987.10478472 · Cited by 2,861
Not So Different After All: A Comparison of Methods for Detecting Amino Acid Sites Under Selection
Pond, S. L. K., & Frost, S. D. W. (2005) · Molecular Biology and Evolution · doi:10.1093/molbev/msi105 · Cited by 2,320
Codon-substitution models for heterogeneous selection pressure at amino acid sites
Yang, Z., Nielsen, R., Goldman, N., & Pedersen, A.-M. K. (2000) · Genetics · doi:10.1093/genetics/155.1.431 · Cited by 2,286
Hughes, A. L., & Nei, M. (1988) · Nature · doi:10.1038/335167a0 · Cited by 1,976
A codon-based model of nucleotide substitution for protein-coding DNA sequences.
(1994) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040153 · Cited by 1,960
Nielsen, R., & Yang, Z. (1998) · Genetics · doi:10.1093/genetics/148.3.929 · Cited by 1,622
Flagged first, then by citations
Cited by
Sorted by citations
Items 201–300 of 1,003
Ohshima, K., Matsumoto, K., Yasaka, R., Nishiyama, M., Soejima, K., Korkmaz, S., Ho, S. Y. W., Gibbs, A. J., & Takeshita, M. (2015) · Virology · doi:10.1016/j.virol.2015.09.024 · Cited by 49
Molecular Characterization and Evolutionary Analyses of Carnivore Protoparvovirus 1 NS1 Gene
Mira, F., Canuti, M., Purpari, G., Cannella, V., Bella, S. D., Occhiogrosso, L., Schirò, G., Chiaramonte, G., Barreca, S., Pisano, P., et al. (2019) · Viruses · doi:10.3390/v11040308 · Cited by 49
Martin, D. P., Weaver, S., Tegally, H., San, E. J., Shank, S. D., Wilkinson, E., Lucaci, A. G., Giandhari, J., Naidoo, S., Pillay, Y., et al. (2021) · PubMed · doi:10.34944/dspace/7022 · Cited by 49
Self-citationWeak selection on synonymous codons substantially inflates dN/dS estimates in bacteria
Rahman, S., Pond, S. L. K., Webb, A. E., & Hey, J. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2023575118 · Cited by 53
RNA Populations in Immunocompromised Patients as Reservoirs for Novel Norovirus Variants
Vega, E. M., Donaldson, E., Huynh, J., Barclay, L., Lopman, B. A., Baric, R. S., Chen, L. F., & Vinjé, J. (2014) · Journal of Virology · doi:10.1128/jvi.02494-14 · Cited by 48
The molecular evolutionary dynamics of oxidative phosphorylation (OXPHOS) genes in Hymenoptera
Li, Y., Zhang, R., Liu, S., Donath, A., Peters, R. S., Ware, J. L., Misof, B. Y., Niehuis, O., Pfrender, M. E., & Zhou, X. Y. (2017) · BMC Evolutionary Biology · doi:10.1186/s12862-017-1111-z · Cited by 46
Structural characterization and evolutionary analysis of fish-specific TLR27
Wang, J., Zhang, Z., Liu, J., Li, F., Chang, F., Fu, H., Zhao, J., & Yin, D. (2015) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2015.06.017 · Cited by 48
Yang, Z., Li, X., Yang, L. M., Peng, S., Song, W., Lin, Y., Xiang, G., Li, Y., Ye, S., Ma, C., et al. (2023) · Plant Communications · doi:10.1016/j.xplc.2023.100591 · Cited by 50
The emergence, impact, and evolution of human metapneumovirus variants from 2014 to 2021 in Spain
Piñana, M., Gónzalez‐Sánchez, A., Andrés, C., Abanto, M., Vila, J., Esperalba, J., Moral, N., Espartosa, E., Saubi, N., Creus‐Costa, A., et al. (2023) · Journal of Infection · doi:10.1016/j.jinf.2023.05.004 · Cited by 47
Understanding the evolution of immune genes in jawed vertebrates
Vinkler, M., Fiddaman, S. R., Těšický, M., O'Connor, E. A., Savage, A. E., Lenz, T. L., Smith, A. L., Kaufman, J., Bolnick, D. I., Davies, C. S., et al. (2023) · Journal of Evolutionary Biology · doi:10.1111/jeb.14181 · Cited by 55
The Phylogeography and Spatiotemporal Spread of South-Central Skunk Rabies Virus
Kuzmina, N. A., Lemey, P., Kuzmin, I. V., Mayes, B. C., Ellison, J. A., Orciari, L. A., Hightower, D., Taylor, S. T., & Rupprecht, C. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082348 · Cited by 47
Mitogenomics of recombinant mitochondrial genomes of Baltic Sea Mytilus mussels
Zbawicka, M., Wenne, R., & Burzyński, A. (2014) · Molecular Genetics and Genomics · doi:10.1007/s00438-014-0888-3 · Cited by 47
OASes and STING: Adaptive Evolution in Concert
Mozzi, A., Pontremoli, C., Forni, D., Clerici, M., Pozzoli, U., Bresolin, N., Cagliani, R., & Sironi, M. (2015) · Genome Biology and Evolution · doi:10.1093/gbe/evv046 · Cited by 46
Extremophile deep-sea viral communities from hydrothermal vents: Structural and functional analysis
Castelán-Sánchez, H. G., López‐Rosas, I., García-Suástegui, W. A., Peralta, R., Dobson, A. D. W., Batista‐García, R. A., & Dávila‐Ramos, S. (2019) · Marine Genomics · doi:10.1016/j.margen.2019.03.001 · Cited by 43
Moore, A. J., de Vos, J. M., Hancock, L. P., Goolsby, E. W., & Edwards, E. J. (2017) · Systematic Biology · doi:10.1093/sysbio/syx078 · Cited by 48
Wei, R., Xie, J., Theuns, S., & Nauwynck, H. (2019) · Virus Evolution · doi:10.1093/ve/vez026 · Cited by 47
Chaintoutis, S. C., Papa, A., Pervanidou, D., & Dovas, C. Ι. (2019) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2019.106617 · Cited by 47
Scobeyeva, V. A., Artyushin, I. V., Krinitsina, A. A., Nikitin, P., Antipin, M. I., Kuptsov, S., Belenikin, M. S., Omelchenko, D. O., Logacheva, M. D., Konorov, E. A., et al. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.674783 · Cited by 46
Signatures of mitonuclear coevolution in a warbler species complex
Wang, S., Ore, M. J., Mikkelsen, E. K., Lee‐Yaw, J. A., Toews, D. P. L., Rohwer, S. A., & Irwin, D. E. (2021) · Nature Communications · doi:10.1038/s41467-021-24586-8 · Cited by 46
Jacquet, S., Garros, C., Lombaert, É., Walton, C., Restrepo, J., Allène, X., Baldet, T., Cêtre-Sossah, C. B., Chaskopoulou, A., Delécolle, J., et al. (2015) · Molecular Ecology · doi:10.1111/mec.13422 · Cited by 46
González‐Romero, R., Eirin-Lopez, J. M., & Ausió, J. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu280 · Cited by 46
Bello, M. A., Cubas, P., Álvarez, I., Sanjuanbenito, G., & Aguilar, J. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00589 · Cited by 46
Evolutionary evidence for multi-host transmission of cetacean morbillivirus
Jo, W. K., Kruppa, J., Habierski, A., van de Bildt, M. W. G., Mazzariol, S., Guardo, G. D., Siebert, U., Kuiken, T., Jung, K., Osterhaus, A. D. M. E., et al. (2018) · Emerging Microbes & Infections · doi:10.1038/s41426-018-0207-x · Cited by 46
Reciprocal translocation of small numbers of inbred individuals rescues immunogenetic diversity
Grueber, C. E., Sutton, J. T., Heber, S., Briskie, J. V., Jamieson, I. G., & Robertson, B. C. (2017) · Molecular Ecology · doi:10.1111/mec.14063 · Cited by 47
Zhao, J., Dellicour, S., Yan, Z., Veit, M., Gill, M. S., He, W., Zhai, X., Ji, X., Suchard, M. A., Lemey, P., et al. (2022) · Journal of Virology · doi:10.1128/jvi.01091-22 · Cited by 46
Intrasubtype Reassortments Cause Adaptive Amino Acid Replacements in H3N2 Influenza Genes
Neverov, A. D., Lezhnina, K. V., Kondrashov, A. S., & Bazykin, G. A. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004037 · Cited by 49
Zhu, Z., Wang, R., Ren, L., & Xu, T. (2013) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2013.06.015 · Cited by 45
Genomic Analysis of the Emergence, Evolution, and Spread of Human Respiratory RNA Viruses
Lam, T. T., Zhu, H., Guan, Y., & Holmes, E. C. (2016) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083115-022628 · Cited by 46
Genetic analysis and evolutionary changes of Porcine circovirus 2
He, W., Zhao, J., Xing, G., Li, G., Wang, R., Wang, Z., Zhang, C., Franzo, G., Su, S., & Zhou, J. (2019) · Molecular Phylogenetics and Evolution · doi:10.1016/j.ympev.2019.106520 · Cited by 45
Filleton, F., Filleton, F., Gérossier, L., Paturel, A., Hall, J. A., Strubin, M., & Etienne, L. (2018) · Journal of Virology · doi:10.1128/jvi.00769-18 · Cited by 48
Franzo, G., He, W., Correa‐Fiz, F., Li, G., Legnardi, M., Su, S., & Segalés, J. (2019) · Advanced Science · doi:10.1002/advs.201901004 · Cited by 45
Genomic epidemiology of coxsackievirus A16 in mainland of China, 2000–18
Han, Z., Song, Y., Xiao, J., Jiang, L., Huang, W. E., Wei, H., Li, J., Zeng, H., Yu, Q., Li, J., et al. (2020) · Virus Evolution · doi:10.1093/ve/veaa084 · Cited by 45
Tian, R., Geng, Y., Yang, Y., Seim, I., & Yang, G. (2021) · Integrative Zoology · doi:10.1111/1749-4877.12521 · Cited by 46
Global Evolutionary History and Dynamics of Dengue Viruses Inferred from Whole Genome Sequences
Stica, C. J., Barrero, R. A., Murray, R. Z., Devine, G. J., Phillips, M. J., & Frentiu, F. D. (2022) · Viruses · doi:10.3390/v14040703 · Cited by 44
Xu, T., Zhu, Z., Sun, Y., Ren, L., & Wang, R. (2013) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2013.12.006 · Cited by 44
Global Diversity within and between Human Herpesvirus 1 and 2 Glycoproteins
Lamers, S. L., Newman, R. M., Laeyendecker, O. B., Tobian, A. A. R., Colgrove, R. C., Ray, S. C., Koelle, D. M., Cohen, J. I., Knipe, D. M., & Quinn, T. C. (2015) · Journal of Virology · doi:10.1128/jvi.01302-15 · Cited by 44
Genome-Wide Analysis of Human Metapneumovirus Evolution
Kim, J. I., Park, S., Lee, I., Park, K. S., Kwak, E. J., Moon, K. M., Lee, C. K., Bae, J., Park, M., & Song, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152962 · Cited by 45
Poczai, P., & Hyvönen, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187199 · Cited by 45
Genetic architecture and sex-specific selection govern modular, male-biased evolution of doublesex
Baral, S., Arumugam, G., Deshmukh, R., & Kunte, K. K. (2019) · Science Advances · doi:10.1126/sciadv.aau3753 · Cited by 42
Morin, P. A., Foote, A. D., Baker, C. S., Hancock‐Hanser, B. L., Kaschner, K., Mate, B. R., Mesnick, S. L., Pease, V. L., Rosel, P. E., & Alexander, A. M. (2018) · Molecular Ecology · doi:10.1111/mec.14698 · Cited by 47
Zhang, L., Sun, K., Csorba, G., Hughes, A. C., Jin, L., Xiao, Y., & Feng, J. (2021) · BMC Ecology and Evolution · doi:10.1186/s12862-021-01926-2 · Cited by 43
Origin, genetic diversity, adaptive evolution and transmission dynamics of Getah virus
Shi, N., Zhu, X., Qiu, X., Cao, X., Jiang, Z., Lu, H., & Jin, N. (2021) · Transboundary and Emerging Diseases · doi:10.1111/tbed.14395 · Cited by 43
Molecular epidemiology of R abbit H aemorrhagic D isease V irus in A ustralia: when one became many
Kovaliski, J., Sinclair, R. G., MUTZE, G. J., Peacock, D. E., Strive, T., Abrantes, J., Esteves, P. J., & Holmes, E. C. (2013) · Molecular Ecology · doi:10.1111/mec.12596 · Cited by 43
Undheim, E. A. B., Sunagar, K., Hamilton, B. R., Jones, A., Venter, D. J., Fry, B. G., & King, G. F. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.02.024 · Cited by 43
Population Structure and Evolution of Rhinoviruses
Waman, V., Kolekar, P. S., Kale, M. M., & Kulkarni‐Kale, U. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088981 · Cited by 43
Machnicka, M. A., Kaminska, K. H., Dunin-Horkawicz, S., & Bujnicki, J. M. (2015) · BMC Bioinformatics · doi:10.1186/s12859-015-0773-z · Cited by 43
Sun, J., Jin, P., Hoffmann, A. A., Duan, X., Dai, J., Hu, G., Xue, X., & Hong, X. (2018) · Insect Molecular Biology · doi:10.1111/imb.12501 · Cited by 43
Nardo, A. D., Luca Ferretti, A., Wadsworth, J., Mioulet, V., Gelman, B., Karniely, S., Scherbakov, A. V., Ziay, G. M., Özyörük, F., Parlak, Ü., et al. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab172 · Cited by 47
Ramírez-Medina, E., Vuono, E. A., Pruitt, S., Rai, A., Espinoza, N., Valladares, A., Silva, E. B., Velázquez-Salinas, L., Borca, M. V., & Gladue, D. P. (2022) · Viruses · doi:10.3390/v14051112 · Cited by 42
Emergence, phylogeography, and adaptive evolution of mpox virus
Guan, H., Gul, I., Xiao, C., Ma, S., Liang, Y., Yu, D., Liu, Y., Liu, H., Zhang, C. Y., Li, J., et al. (2023) · New Microbes and New Infections · doi:10.1016/j.nmni.2023.101102 · Cited by 43
Genotype-Specific Evolution of Hepatitis E Virus
Brayne, A. B., Dearlove, B. L., Lester, J. S., Pond, S. L. K., & Frost, S. D. W. (2017) · Journal of Virology · doi:10.1128/jvi.02241-16 · Cited by 42
As Blind as a Bat? Opsin Phylogenetics Illuminates the Evolution of Color Vision in Bats
Simões, B. F., Foley, N. M., Hughes, G. M., Zhao, H., Zhang, S., Rossiter, S. J., & Teeling, E. C. (2018) · Molecular Biology and Evolution · doi:10.1093/molbev/msy192 · Cited by 43
Saxenhofer, M., Schmidt, S., Ulrich, R. G., & Heckel, G. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000142 · Cited by 42
Han, Z., Zhang, Y., Huang, K., Wang, J., Tian, H., Song, Y., Yang, Q., Yan, D., Zhu, S., Yao, M., et al. (2019) · BMC Infectious Diseases · doi:10.1186/s12879-019-4107-z · Cited by 42
Potter, J. H. T., Davies, K. T. J., Yohe, L. R., Sánchez, M. K. R., Rengifo, E. M., Struebig, M., Warren, K., Tsagkogeorga, G., Lim, B. K., dos Reis, M., et al. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab028 · Cited by 45
Lucaci, A. G., Zehr, J. D., Enard, D., Thornton, J. W., & Pond, S. L. K. (2023) · Molecular Biology and Evolution · doi:10.1093/molbev/msad150 · Cited by 39
Minias, P., Bateson, Z. W., Whittingham, L. A., Johnson, J. A., Oyler‐McCance, S. J., & Dunn, P. O. (2016) · Heredity · doi:10.1038/hdy.2016.6 · Cited by 41
Lau, S. K. P., Wong, A. C. P., Lau, T. C., & Woo, P. C. Y. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102138 · Cited by 41
Maize chlorotic mottle virus exhibits low divergence between differentiated regional sub-populations
Braidwood, L., quito-avila, D. F., Cabanas, D., Bressan, A., Wangai, W., & Baulcombe, D. C. (2018) · Scientific Reports · doi:10.1038/s41598-018-19607-4 · Cited by 41
Li, Y., Metcalf, B. J., Chochua, S., Li, Z., Walker, H., Tran, T. N., Hawkins, P. A., Gierke, R., Pilishvili, T., McGee, L., et al. (2019) · Nature Communications · doi:10.1038/s41467-018-07997-y · Cited by 41
Palmer, S. N., Chappidi, S., Pinkham, C., & Hancks, D. C. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab256 · Cited by 43
Xie, B., Dashevsky, D., Rokyta, D. R., Ghezellou, P., Fathinia, B., Shi, Q., Richardson, M. K., & Fry, B. G. (2022) · BMC Biology · doi:10.1186/s12915-021-01208-9 · Cited by 45
Sikazwe, C. T., Neave, M. J., Michie, A., Mileto, P., Wang, J., Cooper, N., Levy, A., Imrie, A. A., Baird, R., Currie, B. J., et al. (2022) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0010754 · Cited by 41
Subfamily-Specific Specialization of RGH1/MLA Immune Receptors in Wild Barley
Maekawa, T., Kracher, B., Saur, I. M. L., Maekawa‐Yoshikawa, M., Kellner, R., Pankin, A., von Korff, M., & Schulze‐Lefert, P. (2018) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-07-18-0186-fi · Cited by 40
Gerdol, M., Greco, S., & Pallavicini, A. (2019) · Marine Drugs · doi:10.3390/md17100583 · Cited by 39
Martin, D. P., Lytras, S., Lucaci, A. G., Maier, W., Grüning, B. A., Shank, S. D., Weaver, S., MacLean, O. A., Orton, R. J., Lemey, P., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.14.476382 · Cited by 40
Self-citationPhadungsombat, J., Imad, H. A., Rahman, M., Nakayama, E. E., Kludkleeb, S., Ponam, T., Rahim, R., Hasan, A., Poltep, K., Yamanaka, A., et al. (2020) · Viruses · doi:10.3390/v12111319 · Cited by 39
Águeda-Pinto, A., Alves, L. Q., Neves, F., McFadden, G., Jacobs, B. L., Castro, L. F. C., Rahman, M. M., & Esteves, P. J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.747737 · Cited by 40
Adaptations to a cold climate promoted social evolution in Asian colobine primates
Qi, X., Wu, J., Zhao, L., Wang, L., Guang, X., Garber, P. A., Opie, C., Yuan, Y., Diao, R., Li, G., et al. (2023) · Science · doi:10.1126/science.abl8621 · Cited by 42
INCIPIENT SPECIATION OF SEA STAR POPULATIONS BY ADAPTIVE GAMETE RECOGNITION COEVOLUTION
Hart, M. W., Sunday, J. M., Popovic, I., Learning, K. J., & Konrad, C. M. (2014) · Evolution · doi:10.1111/evo.12352 · Cited by 39
Iraola, G., Pérez, R., Naya, H., Paolicchi, F. A., Pastor, E., Valenzuela, S., Calleros, L., Velilla, A. V., Hernández, M. A., & Morsella, C. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu195 · Cited by 39
Ancient Diversification of Three-Finger Toxins in Micrurus Coral Snakes
Dashevsky, D., & Fry, B. G. (2018) · Journal of Molecular Evolution · doi:10.1007/s00239-017-9825-5 · Cited by 39
Correa‐Fiz, F., Franzo, G., Llorens, A., Segalés, J., & Kekarainen, T. (2018) · Scientific Reports · doi:10.1038/s41598-018-33849-2 · Cited by 39
Song, Y., Zhang, Y., Han, Z., Xu, W. H., Xiao, J., Wang, X., Wang, J., Yang, J., Yu, Q., Yu, D., et al. (2020) · Virus Evolution · doi:10.1093/ve/veaa048 · Cited by 39
Origin and Spread of the Dengue Virus Type 1, Genotype V in Senegal, 2015–2019
Dieng, I., Cunha, M. D. P., Diagne, M. M., Sembène, P. M., Zanotto, P. M. D. A., Faye, O., Faye, O., & Sall, A. A. (2021) · Viruses · doi:10.3390/v13010057 · Cited by 39
Evolution of the interferon response: lessons from ISGs of diverse mammals
McDougal, M. B., Boys, I. N., Cruz-Rivera, P. C. D. L., & Schoggins, J. W. (2022) · Current Opinion in Virology · doi:10.1016/j.coviro.2022.101202 · Cited by 40
Fast fish face fewer mitochondrial mutations: Patterns of dN/dS across fish mitogenomes
Strohm, J. H. T., Gwiazdowski, R., & Hanner, R. (2015) · Gene · doi:10.1016/j.gene.2015.06.074 · Cited by 39
Hraber, P., Korber, B., Wagh, K., Giorgi, E. E., Tanmoy Bhattacharya, A., Gnanakaran, S., Lapedes, A. S., Learn, G. H., Kreider, E. F., Li, Y., et al. (2015) · Viruses · doi:10.3390/v7102881 · Cited by 36
Forni, D., Cagliani, R., Tresoldi, C., Pozzoli, U., GIOIA, L. D., Filippi, G., Riva, S., Menozzi, G., Colleoni, M., Biasin, M., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004189 · Cited by 37
Phylogeny and population dynamics of respiratory syncytial virus (Rsv) A and B
Martinelli, M., Frati, E. R., Zappá, A., Ebranati, E., Bianchi, S., Pariani, E., Amendola, A., Zehender, G., & Tanzi, E. (2014) · Virus Research · doi:10.1016/j.virusres.2014.06.006 · Cited by 38
Dipp-Álvarez, M., & Cruz‐Ramírez, A. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00017 · Cited by 38
Vizueta, J., Macías‐Hernández, N., Arnedo, M. A., Rozas, J., & Sánchez‐Gracia, A. (2019) · Molecular Ecology · doi:10.1111/mec.15199 · Cited by 38
Parallel evolution in the emergence of highly pathogenic avian influenza A viruses
Escalera‐Zamudio, M., Golden, M., Gutiérrez, B., Thézé, J., Keown, J. R., Carrique, L., Bowden, T. A., & Pybus, O. G. (2020) · Nature Communications · doi:10.1038/s41467-020-19364-x · Cited by 38
Franzo, G., Drigo, M., Legnardi, M., Grassi, L., Pasotto, D., Menandro, M. L., Cecchinato, M., & Tucciarone, C. M. (2020) · Viruses · doi:10.3390/v12111285 · Cited by 38
Kasparian, N. A., Bränström, R., Chang, Y., Affleck, P., Aspinwall, L. G., Tibben, A., Azizi, E., Baron‐Epel, O., Battistuzzi, L., Bruno, W., et al. (2012) · Archives of Dermatology · doi:10.1001/archdermatol.2012.1817 · Cited by 39
Gruber, D. F., Gaffney, J. P., Mehr, S., DeSalle, R., Sparks, J. S., Platiša, J., & Pieribone, V. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140972 · Cited by 38
Genome-Wide Comparative Analysis of Chemosensory Gene Families in Five Tsetse Fly Species
Macharia, R. W., Mireji, P. O., Murungi, E. K., Murilla, G. A., Christoffels, A. G., Aksoy, S., & Masiga, D. K. (2016) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0004421 · Cited by 37
Co-option of the same ancestral gene family gave rise to mammalian and reptilian toxins
Barua, A., Koludarov, I., & Mikheyev, A. S. (2021) · BMC Biology · doi:10.1186/s12915-021-01191-1 · Cited by 38
QTL Mapping of Sex Determination Loci Supports an Ancient Pathway in Ants and Honey Bees
Miyakawa, M. O., & Mikheyev, A. S. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005656 · Cited by 32
Filloux, D., Murrell, S., Koohapitagtam, M., Golden, M., Julian, C., Galzi, S., Uzest, M., Rodier-Goud, M., D’Hont, A., Vernerey, M.-S., et al. (2015) · Virus Evolution · doi:10.1093/ve/vev002 · Cited by 37
Self-citationAnalysis of Evolutionary Processes of Species Jump in Waterfowl Parvovirus
Fan, W., Sun, Z., Shen, T., Xu, D., Huang, K., Zhou, J., Song, S., & Yan, L. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00421 · Cited by 37
Zdenek, C. N., den Brouw, B. O., Dashevsky, D., Gloria, A., Youngman, N. J., Watson, E. R., Green, P. A., Hay, C., Dunstan, N. L., Allen, L., et al. (2019) · Toxicology Letters · doi:10.1016/j.toxlet.2019.08.014 · Cited by 37
Bazykin, G. A. (2015) · Biology Letters · doi:10.1098/rsbl.2015.0315 · Cited by 35
Genetic diversity and evolution of dengue virus serotype 3: A comparative genomics study
Waman, V., Kale, M. M., & Kulkarni‐Kale, U. (2017) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2017.01.022 · Cited by 36
Genetic Evolution and Molecular Selection of the HE Gene of Influenza C Virus
Zhang, W., Zhang, L., He, W., Zhang, X., Wen, B., Wang, C., Xu, Q., Li, G., Zhou, J., Veit, M., et al. (2019) · Viruses · doi:10.3390/v11020167 · Cited by 36
Zhai, X., Zhao, W. T., Li, K., Zhang, C., Wang, C., Su, S., Zhou, J., Lei, J., Xing, G., Sun, H., et al. (2019) · Virologica Sinica · doi:10.1007/s12250-019-00140-1 · Cited by 36
Symbiosis, Selection, and Novelty: Freshwater Adaptation in the Unique Sponges of Lake Baikal
Kenny, N. J., Pleše, B., Riesgo, A., & Itskovich, V. B. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz151 · Cited by 37
Benfield, C. T. O., Hill, S. C., Shatar, M., Shiilegdamba, E., Damdinjav, B., Fine, A. E., Willett, B. J., Kock, R. A., & Bataille, A. (2021) · Virus Evolution · doi:10.1093/ve/veab062 · Cited by 36
Suppressors of RNAi from plant viruses are subject to episodic positive selection
Murray, G. G. R., Pond, S. L. K., & Obbard, D. J. (2013) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2013.0965 · Cited by 36
Hashiguchi, Y., Lee, J. M., Shiraishi, M., Komatsu, S., Miki, S., Shimasaki, Y., Mochioka, N., Kusakabe, T., & Oshima, Y. (2015) · Journal of Evolutionary Biology · doi:10.1111/jeb.12634 · Cited by 35
Metadata
- Authors
- Murrell, B., Wertheim, J. O., Moola, S., Weighill, T., Scheffler, K., & Kosakovsky Pond, S. L.
- Affiliations
- Stellenbosch University (ZA)
- University of California San Diego (US)
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2012-07-12
- Volume
- 8
- Issue
- 7
- Pages
- e1002764
- ISSN
- 1553-7390 (ISSN-L)
- 1553-7404
- PMC
- PMC3395634
- OpenAlex
- W2118982822
- Cited by
- 1,811
- References
- 63
- Citations by year
- 2026: 147 · 2025: 135 · 2024: 169 · 2023: 162 · 2022: 161 · 2021: 183 · 2020: 172 · 2019: 123 · 2018: 115 · 2017: 99 · 2016: 87 · 2015: 100 · 2014: 83 · 2013: 66 · 2012: 9
- FWCI
- 49.72
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS Genetics (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- TUScholarShare (Temple University) (submittedVersion, cc-by)
- SUNScholar (Stellenbosch University) (submittedVersion)
- Funders
- National Science Foundation (0714991)
- European Commission
- National Research Foundation
- National Institutes of Health (AI47745, AI74621, AI-36214, AI57167, GM093939)
- Center for AIDS Research, University of Washington
- University of California, San Diego
- National Institute of General Medical Sciences (GM093939, R01GM093939)
- National Institute of Allergy and Infectious Diseases (R01AI057167, AI-74621, AI-47745, AI57167, R21AI047745, AI 43638, R24AI106039, R56AI047745, AI-36214, R01AI047745, U01AI043638, P01AI074621, P30AI036214, T32AI007384)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
- Keywords
- episodic selection, positive selection, memes, protein-coding genes, natural selection
- MeSH terms
- Amino Acids, Animals, Computer Simulation, Models, Theoretical, Phylogeny, Rhodopsin, Selection, Genetic, Vertebrates, Open Reading Frames, Evolution, Molecular, Computational Biology
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review