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The evolutionary dynamics of Oropouche Virus (OROV) in South America
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.epidem.2012.09.002openalex-snapshot
Evolutionary and molecular analysis of the emergent severe fever with thrombocytopenia syndrome virus
inferredcites →https://doi.org/10.1016/j.ijid.2017.07.016openalex-snapshot
Silent emergence of Mayaro and Oropouche viruses in humans in Central Brazil
inferredcites →https://doi.org/10.1016/j.jcv.2008.11.006openalex-snapshot
Oropouche fever epidemic in Northern Brazil: Epidemiology and molecular characterization of isolates
inferredcites →https://doi.org/10.1016/j.jmb.2019.04.016openalex-snapshot
Protein and Glycan Mimicry in HIV Vaccine Design
inferredcites →https://doi.org/10.1016/j.meegid.2018.11.020openalex-snapshot
Oropouche orthobunyavirus: Genetic characterization of full-length genomes and development of molecular methods to discriminate natural reassortments
inferredcites →https://doi.org/10.1016/j.micinf.2017.11.013openalex-snapshot
Oropouche fever, an emergent disease from the Americas
inferredcites →https://doi.org/10.1016/j.tmaid.2016.11.001openalex-snapshot
Mayaro, Oropouche and Venezuelan Equine Encephalitis viruses: Following in the footsteps of Zika?
inferredcites →https://doi.org/10.1016/j.virol.2005.12.026openalex-snapshot
Characterization of Maguari orthobunyavirus mutants suggests the nonstructural protein NSm is not essential for growth in tissue culture
inferredcites →https://doi.org/10.1016/j.virol.2006.09.035openalex-snapshot
The NSm proteins of Rift Valley fever virus are dispensable for maturation, replication and infection
inferredcites →https://doi.org/10.1016/j.virol.2013.07.030openalex-snapshot
Viruses of the family Bunyaviridae: Are all available isolates reassortants?
inferredcites →https://doi.org/10.1016/s0168-1702(01)00262-3openalex-snapshot
Jatobal virus is a reassortant containing the small RNA of Oropouche virus
inferredcites →https://doi.org/10.1016/s0169-5347(03)00216-7openalex-snapshot
Measurably evolving populations
inferredcites →https://doi.org/10.1038/nrmicro3332openalex-snapshot
Orthobunyaviruses: recent genetic and structural insights
inferredcites →https://doi.org/10.1038/s41467-017-02789-2openalex-snapshot
Shielding and activation of a viral membrane fusion protein
inferredcites →https://doi.org/10.1038/s41467-019-08832-8openalex-snapshot
Orthobunyavirus spike architecture and recognition by neutralizing antibodies
inferredcites →https://doi.org/10.1038/srep11353openalex-snapshot
Reassortment and distinct evolutionary dynamics of Rift Valley Fever virus genomic segments
inferredcites →https://doi.org/10.1038/srep42500openalex-snapshot
The N-terminal domain of Schmallenberg virus envelope protein Gc is highly immunogenic and can provide protection from infection
inferredcites →https://doi.org/10.1073/pnas.1603364113openalex-snapshot
Bunyamwera orthobunyavirus glycoprotein precursor is processed by cellular signal peptidase and signal peptide peptidase
inferredcites →https://doi.org/10.1073/pnas.1803990115openalex-snapshot
Structure of the Lassa virus glycan shield provides a model for immunological resistance
inferredcites →https://doi.org/10.1093/bioinformatics/bti079openalex-snapshot
HyPhy: hypothesis testing using phylogenies
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp698openalex-snapshot
Fast and accurate long-read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/bts580openalex-snapshot
A counting renaissance: combining stochastic mapping and empirical Bayes to quickly detect amino acid sites under positive selection
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/molbev/msi103openalex-snapshot
Bayesian Coalescent Inference of Past Population Dynamics from Molecular Sequences
inferredcites →https://doi.org/10.1093/molbev/msi105openalex-snapshot
Not So Different After All: A Comparison of Methods for Detecting Amino Acid Sites Under Selection
inferredcites →https://doi.org/10.1093/molbev/msv022openalex-snapshot
Less Is More: An Adaptive Branch-Site Random Effects Model for Efficient Detection of Episodic Diversifying Selection
inferredcites →https://doi.org/10.1093/molbev/msv035openalex-snapshot
Gene-Wide Identification of Episodic Selection
inferredcites →https://doi.org/10.1093/molbev/msx335openalex-snapshot
Datamonkey 2.0: A Modern Web Application for Characterizing Selective and Other Evolutionary Processes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004152openalex-snapshot
Accuracy and Power of Bayes Prediction of Amino Acid Sites Under Positive Selection
inferredcites →https://doi.org/10.1093/ve/vev003openalex-snapshot
RDP4: Detection and analysis of recombination patterns in virus genomes
inferredcites →https://doi.org/10.1093/ve/vew007openalex-snapshot
Exploring the temporal structure of heterochronous sequences using TempEst (formerly Path-O-Gen)
inferredcites →https://doi.org/10.1093/ve/vey016openalex-snapshot
Bayesian phylogenetic and phylodynamic data integration using BEAST 1.10
inferredcites →https://doi.org/10.1099/0022-1317-73-9-2255openalex-snapshot
Non-random reassortment between the tripartite RNA genomes of La Crosse and snowshoe hare viruses
inferredcites →https://doi.org/10.1099/vir.0.000108openalex-snapshot
Genetic analysis of members of the species Oropouche virus and identification of a novel M segment sequence
inferredcites →https://doi.org/10.1111/j.1863-2378.2008.01166.xopenalex-snapshot
Role of the NSs Protein in the Zoonotic Capacity of Orthobunyaviruses
inferredcites →https://doi.org/10.1128/jvi.00476-06openalex-snapshot
NSm and 78-Kilodalton Proteins of Rift Valley Fever Virus Are Nonessential for Viral Replication in Cell Culture
inferredcites →https://doi.org/10.1128/jvi.00579-06openalex-snapshot
Requirement of the N-Terminal Region of Orthobunyavirus Nonstructural Protein NSm for Virus Assembly and Morphogenesis
inferredcites →https://doi.org/10.1128/jvi.01238-07openalex-snapshot
NSm Protein of Rift Valley Fever Virus Suppresses Virus-Induced Apoptosis
inferredcites →https://doi.org/10.1128/jvi.02192-12openalex-snapshot
The C-Terminal Region of Rift Valley Fever Virus NSm Protein Targets the Protein to the Mitochondrial Outer Membrane and Exerts Antiapoptotic Function
inferredcites →https://doi.org/10.1128/jvi.02448-05openalex-snapshot
Batai and Ngari Viruses: M Segment Reassortment and Association with Severe Febrile Disease Outbreaks in East Africa
inferredcites →https://doi.org/10.1128/jvi.37.1.383-394.1981openalex-snapshot
Genetic interactions among viruses of the Bunyamwera complex
inferredcites →https://doi.org/10.1128/jvi.79.21.13725-13734.2005openalex-snapshot
Role of N-Linked Glycans on Bunyamwera Virus Glycoproteins in Intracellular Trafficking, Protein Folding, and Virus Infectivity
inferredcites →https://doi.org/10.1146/annurev-virology-110615-035747openalex-snapshot
Genomic Analysis of Viral Outbreaks
inferredcites →https://doi.org/10.1186/s13073-015-0220-9openalex-snapshot
Rapid metagenomic identification of viral pathogens in clinical samples by real-time nanopore sequencing analysis
inferredcites →https://doi.org/10.1371/journal.pbio.0040088openalex-snapshot
Relaxed Phylogenetics and Dating with Confidence
inferredcites →https://doi.org/10.1371/journal.pgen.1002764openalex-snapshot
Detecting Individual Sites Subject to Episodic Diversifying Selection
inferredcites →https://doi.org/10.1371/journal.pntd.0000787openalex-snapshot
Arboviral Etiologies of Acute Febrile Illnesses in Western South America, 2000–2007
inferredcites →https://doi.org/10.1371/journal.pntd.0001315openalex-snapshot
Iquitos Virus: A Novel Reassortant Orthobunyavirus Associated with Human Illness in Peru
inferredcites →https://doi.org/10.1371/journal.pntd.0001639openalex-snapshot
Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection
inferredcites →https://doi.org/10.1371/journal.pone.0143081openalex-snapshot
Assessment of the Utility of Whole Genome Sequencing of Measles Virus in the Characterisation of Outbreaks
inferredcites →https://doi.org/10.1371/journal.ppat.1003374openalex-snapshot
Orthobunyavirus Ultrastructure and the Curious Tripodal Glycoprotein Spike
inferredcites →https://doi.org/10.1590/0074-02760150123openalex-snapshot
Detection of Oropouche virus segment S in patients and inCulex quinquefasciatus in the state of Mato Grosso, Brazil
inferredcites →https://doi.org/10.1590/0074-02760160415openalex-snapshot
Vegetation loss and the 2016 Oropouche fever outbreak in Peru
inferredcites →https://doi.org/10.3201/eid1110.050464openalex-snapshot
Oropouche Virus Isolation, Southeast Brazil
inferredcites →https://doi.org/10.3201/eid1306.061114openalex-snapshot
Reemergence of Oropouche Fever, Northern Brazil
inferredcites →https://doi.org/10.3201/eid1502.080401openalex-snapshot
Sporadic Oropouche Infection, Acre, Brazil
inferredcites →https://doi.org/10.3201/eid1705.101333openalex-snapshot
Molecular Epidemiology of Oropouche Virus, Brazil
inferredcites →https://doi.org/10.3201/eid2405.171569openalex-snapshot
Isolation of Oropouche Virus from Febrile Patient, Ecuador
inferredcites →https://doi.org/10.3390/v5102447openalex-snapshot
Non-Structural Proteins of Arthropod-Borne Bunyaviruses: Roles and Functions
inferredcites →https://doi.org/10.3390/v8050149openalex-snapshot
N-Glycans on the Rift Valley Fever Virus Envelope Glycoproteins Gn and Gc Redundantly Support Viral Infection via DC-SIGN
inferredcites →https://doi.org/10.4269/ajtmh.15-0679openalex-snapshot
Isolation of Madre de Dios Virus (Orthobunyavirus; Bunyaviridae), an Oropouche Virus Species Reassortant, from a Monkey in Venezuela
inferredcites →https://doi.org/10.4269/ajtmh.16-0672openalex-snapshot
Oropouche Virus: Clinical, Epidemiological, and Molecular Aspects of a Neglected Orthobunyavirus
inferredcites →https://doi.org/10.4269/ajtmh.1961.10.574openalex-snapshot
Oropouche Virus: a New Human Disease Agent from Trinidad, West Indies
inferredcites →https://doi.org/10.4269/ajtmh.1997.56.148openalex-snapshot
Oropouche Virus Transmission in the Amazon River Basin of Peru
inferredcites →https://doi.org/10.4269/ajtmh.2009.81.146openalex-snapshot
Etiology of Acute Undifferentiated Febrile Illness in the Amazon Basin of Ecuador
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1099/jgv.0.002027openalex-snapshot
Oropouche Virus: An Emerging Orthobunyavirus
inferred← citeshttps://doi.org/10.1099/jgv.0.002076openalex-snapshot
Characterisation of the virome of Culicoides brevitarsis Kieffer (Diptera: Ceratopogonidae), a vector of bluetongue virus in Australia
inferred← citeshttps://doi.org/10.1101/2025.02.28.25323068openalex-snapshot
Spatiotemporal disease suitability prediction for Oropouche virus and the role of vectors across the Americas
inferred← citeshttps://doi.org/10.1128/jvi.01127-19openalex-snapshot
Evolutionary Dynamics of Oropouche Virus in South America
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