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Genomic analysis of local variation and recent evolution in Plasmodium vivax

https://doi.org/10.1038/ng.3599
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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/b978-0-12-397900-1.00001-3openalex-snapshot
The Global Public Health Significance of Plasmodium vivax
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Extensive microsatellite diversity in the human malaria parasite Plasmodium vivax
inferredcites →https://doi.org/10.1016/s1473-3099(14)70855-2openalex-snapshot
Global extent of chloroquine-resistant Plasmodium vivax: a systematic review and meta-analysis
inferredcites →https://doi.org/10.1021/acsinfecdis.5b00049openalex-snapshot
Next-Generation Sequencing of Plasmodium vivax Patient Samples Shows Evidence of Direct Evolution in Drug-Resistance Genes
inferredcites →https://doi.org/10.1038/nature06250openalex-snapshot
Genome-wide detection and characterization of positive selection in human populations
inferredcites →https://doi.org/10.1038/nature07327openalex-snapshot
Comparative genomics of the neglected human malaria parasite Plasmodium vivax
inferredcites →https://doi.org/10.1038/nature11174openalex-snapshot
Analysis of Plasmodium falciparum diversity in natural infections by deep sequencing
inferredcites →https://doi.org/10.1038/ncomms1265openalex-snapshot
The global distribution of the Duffy blood group
inferredcites →https://doi.org/10.1038/ng.2373openalex-snapshot
The malaria parasite Plasmodium vivax exhibits greater genetic diversity than Plasmodium falciparum
inferredcites →https://doi.org/10.1038/ng.2375openalex-snapshot
Plasmodium cynomolgi genome sequences provide insight into Plasmodium vivax and the monkey malaria clade
inferredcites →https://doi.org/10.1038/ng.3189openalex-snapshot
Genetic architecture of artemisinin-resistant Plasmodium falciparum
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/nrmicro1994openalex-snapshot
The porin and the permeating antibiotic: a selective diffusion barrier in Gram-negative bacteria
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03627.xopenalex-snapshot
Multiple transporters associated with malaria parasite responses to chloroquine and quinine
inferredcites →https://doi.org/10.1056/nejm197608052950602openalex-snapshot
The Resistance Factor toPlasmodium vivaxin Blacks
inferredcites →https://doi.org/10.1073/pnas.0807404105openalex-snapshot
The transcriptome of Plasmodium vivax reveals divergence and diversity of transcriptional regulation in malaria parasites
inferredcites →https://doi.org/10.1073/pnas.0912496107openalex-snapshot
Plasmodium vivax clinical malaria is commonly observed in Duffy-negative Malagasy people
inferredcites →https://doi.org/10.1073/pnas.1003776107openalex-snapshot
Whole-genome sequencing and microarray analysis of ex vivo Plasmodium vivax reveal selective pressure on putative drug resistance genes
inferredcites →https://doi.org/10.1074/jbc.m806944200openalex-snapshot
Disruption of a Plasmodium falciparum Multidrug Resistance-associated Protein (PfMRP) Alters Its Fitness and Transport of Antimalarial Drugs and Glutathione
inferredcites →https://doi.org/10.1086/501357openalex-snapshot
Mefloquine Is Highly Efficacious against Chloroquine-Resistant Plasmodium vivax Malaria and Plasmodium falciparum Malaria in Papua, Indonesia
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1086/592451openalex-snapshot
Amplification ofpvmdr1Associated with Multidrug‐ResistantPlasmodium vivax
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/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/cid/ciq249openalex-snapshot
Plasmodium vivax Recurrence Following Falciparum and Mixed Species Malaria: Risk Factors and Effect of Antimalarial Kinetics
inferredcites →https://doi.org/10.1093/infdis/jir806openalex-snapshot
The First Plasmodium vivax Relapses of Life Are Usually Genetically Homologous
inferredcites →https://doi.org/10.1093/infdis/jiv142openalex-snapshot
Using Amplicon Deep Sequencing to Detect Genetic Signatures of Plasmodium vivax Relapse
inferredcites →https://doi.org/10.1093/nar/gkr1032openalex-snapshot
GeneDB--an annotation database for pathogens
inferredcites →https://doi.org/10.1101/024182openalex-snapshot
Genome variation and meiotic recombination in Plasmodium falciparum : insights from deep sequencing of genetic crosses
inferredcites →https://doi.org/10.1101/gr.094052.109openalex-snapshot
Fast model-based estimation of ancestry in unrelated individuals
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1101/gr.168286.113openalex-snapshot
Single-cell genomics for dissection of complex malaria infections
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1128/aac.00691-10openalex-snapshot
Tracking Origins and Spread of Sulfadoxine-Resistant Plasmodium falciparum dhps Alleles in Thailand
inferredcites →https://doi.org/10.1128/aac.02207-15openalex-snapshot
Expression of Plasmodium vivax crt-o Is Related to Parasite Stage but Not Ex Vivo Chloroquine Susceptibility
inferredcites →https://doi.org/10.1128/aac.47.5.1514-1521.2003openalex-snapshot
Novel Point Mutations in the Dihydrofolate Reductase Gene of Plasmodium vivax : Evidence for Sequential Selection by Drug Pressure
inferredcites →https://doi.org/10.1128/aac.48.6.2214-2222.2004openalex-snapshot
Sulfadoxine Resistance in Plasmodium vivax Is Associated with a Specific Amino Acid in Dihydropteroate Synthase at the Putative Sulfadoxine-Binding Site
inferredcites →https://doi.org/10.1179/2047773215y.0000000012openalex-snapshot
Uncovering the transmission dynamics ofPlasmodium vivaxusing population genetics
inferredcites →https://doi.org/10.1186/1475-2875-10-251openalex-snapshot
Development and evaluation of a prototype non-woven fabric filter for purification of malaria-infected blood
inferredcites →https://doi.org/10.1186/1475-2875-10-297openalex-snapshot
Determinants of relapse periodicity in Plasmodium vivax malaria
inferredcites →https://doi.org/10.1371/journal.pbio.0040072openalex-snapshot
A Map of Recent Positive Selection in the Human Genome
inferredcites →https://doi.org/10.1371/journal.pntd.0000653openalex-snapshot
A Systems-Based Analysis of Plasmodium vivax Lifecycle Transcription from Human to Mosquito
inferredcites →https://doi.org/10.1371/journal.pntd.0001811openalex-snapshot
Whole Genome Sequencing of Field Isolates Provides Robust Characterization of Genetic Diversity in Plasmodium vivax
inferredcites →https://doi.org/10.1371/journal.pntd.0001814openalex-snapshot
A Long Neglected World Malaria Map: Plasmodium vivax Endemicity in 2010
inferredcites →https://doi.org/10.1371/journal.pntd.0002489openalex-snapshot
Whole Genome Sequencing of Field Isolates Reveals a Common Duplication of the Duffy Binding Protein Gene in Malagasy Plasmodium vivax Strains
inferredcites →https://doi.org/10.1371/journal.pntd.0002569openalex-snapshot
De Novo Assembly of a Field Isolate Genome Reveals Novel Plasmodium vivax Erythrocyte Invasion Genes
inferredcites →https://doi.org/10.1371/journal.pntd.0002882openalex-snapshot
A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
inferredcites →https://doi.org/10.1371/journal.pntd.0003539openalex-snapshot
Development of a Single Nucleotide Polymorphism Barcode to Genotype Plasmodium vivax Infections
inferredcites →https://doi.org/10.1371/journal.pntd.0003872openalex-snapshot
Plasmodium vivax Diversity and Population Structure across Four Continents
inferredcites →https://doi.org/10.1371/journal.pntd.0004252openalex-snapshot
Whole Genome Sequencing of Field Isolates Reveals Extensive Genetic Diversity in Plasmodium vivax from Colombia
inferredcites →https://doi.org/10.1371/journal.pone.0001089openalex-snapshot
Chloroquine Resistant Plasmodium vivax: In Vitro Characterisation and Association with Molecular Polymorphisms
inferredcites →https://doi.org/10.1371/journal.pone.0032891openalex-snapshot
Characterization of Within-Host Plasmodium falciparum Diversity Using Next-Generation Sequence Data
inferredcites →https://doi.org/10.1371/journal.pone.0053160openalex-snapshot
Effective Preparation of Plasmodium vivax Field Isolates for High-Throughput Whole Genome Sequencing
inferredcites →https://doi.org/10.4161/fly.19695openalex-snapshot
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
inferredcites →https://doi.org/10.4269/ajtmh.2007.77.79openalex-snapshot
Vivax Malaria: Neglected and Not Benign

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Population genomic evidence of structured and connected Plasmodium vivax populations under host selection in Latin America
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Malaria Situation in Latin America and the Caribbean: Residual and Resurgent Transmission and Challenges for Control and Elimination
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Plasmodium genomics: an approach for learning about and ending human malaria
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Antimalarial Drug Resistance and Implications for the WHO Global Technical Strategy
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In silico analysis of putative dormancy genes in Plasmodium vivax
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Co-transmission of Related Malaria Parasite Lineages Shapes Within-Host Parasite Diversity
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Single-genome sequencing reveals within-host evolution of human malaria parasites
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Dissecting malaria biology and epidemiology using population genetics and genomics
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Plasmodium vivax vaccine research – we’ve only just begun
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Geographical spread and structural basis of sulfadoxine-pyrimethamine drug-resistant malaria parasites
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The prevalence of molecular markers of drug resistance in Plasmodium vivax from the border regions of Thailand in 2008 and 2014
inferred← citeshttps://doi.org/10.1016/j.ijpddr.2021.04.002openalex-snapshot
The molecular basis of antimalarial drug resistance in Plasmodium vivax
inferred← citeshttps://doi.org/10.1016/j.ijpddr.2021.06.002openalex-snapshot
Longitudinal ex vivo and molecular trends of chloroquine and piperaquine activity against Plasmodium falciparum and P. vivax before and after introduction of artemisinin-based combination therapy in Papua, Indonesia
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Genetic diversity of Plasmodium vivax isolates from pregnant women in the Western Brazilian Amazon: a prospective cohort study
inferred← citeshttps://doi.org/10.1016/j.lana.2022.100420openalex-snapshot
Population-based genomic study of Plasmodium vivax malaria in seven Brazilian states and across South America
inferred← citeshttps://doi.org/10.1016/j.lanmic.2025.101335openalex-snapshot
Assessing the effect of parasite antigen genetic diversity on performance of Plasmodium vivax serological exposure markers for malaria: a multicentre observational diagnostic accuracy study
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Genetic diversity of the Plasmodium vivax multidrug resistance 1 gene in Thai parasite populations
inferred← citeshttps://doi.org/10.1016/j.meegid.2021.104908openalex-snapshot
Variation in selective constraints along the Plasmodium life cycle
inferred← citeshttps://doi.org/10.1016/j.meegid.2024.105605openalex-snapshot
Genetic Diversity and Natural Selection of Plasmodium vivax Merozoite Surface Protein 8 in Global Populations
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Malaria Epidemiology at the Clone Level
inferred← citeshttps://doi.org/10.1016/j.pt.2018.02.006openalex-snapshot
Plasmodium vivax Infections of Duffy-Negative Erythrocytes: Historically Undetected or a Recent Adaptation?
inferred← citeshttps://doi.org/10.1016/s1473-3099(16)30409-1openalex-snapshot
Genetic markers associated with dihydroartemisinin–piperaquine failure in Plasmodium falciparum malaria in Cambodia: a genotype–phenotype association study
inferred← citeshttps://doi.org/10.1038/ng.3630openalex-snapshot
An unsettling picture emerges from population genomic studies of Plasmodium vivax
inferred← citeshttps://doi.org/10.1038/s41467-018-04965-4openalex-snapshot
Genomic analysis of a pre-elimination Malaysian Plasmodium vivax population reveals selective pressures and changing transmission dynamics
inferred← citeshttps://doi.org/10.1038/s41467-019-12256-9openalex-snapshot
Plasmodium vivax chloroquine resistance links to pvcrt transcription in a genetic cross
inferred← citeshttps://doi.org/10.1038/s41467-019-13412-xopenalex-snapshot
Resolving the cause of recurrent Plasmodium vivax malaria probabilistically
inferred← citeshttps://doi.org/10.1038/s41467-020-14574-9openalex-snapshot
Amplification of Duffy binding protein-encoding gene allows Plasmodium vivax to evade host anti-DBP humoral immunity
inferred← citeshttps://doi.org/10.1038/s41467-021-21811-2openalex-snapshot
Naturally acquired blocking human monoclonal antibodies to Plasmodium vivax reticulocyte binding protein 2b
inferred← citeshttps://doi.org/10.1038/s41467-021-23422-3openalex-snapshot
Distinctive genetic structure and selection patterns in Plasmodium vivax from South Asia and East Africa
inferred← citeshttps://doi.org/10.1038/s41467-022-33804-wopenalex-snapshot
Genome-wide functional screening of drug-resistance genes in Plasmodium falciparum
inferred← citeshttps://doi.org/10.1038/s41467-024-51949-8openalex-snapshot
Single-cell analyses of polyclonal Plasmodium vivax infections and their consequences on parasite transmission
inferred← citeshttps://doi.org/10.1038/s41467-024-54731-yopenalex-snapshot
High-throughput genotyping of Plasmodium vivax in the Peruvian Amazon via molecular inversion probes
inferred← citeshttps://doi.org/10.1038/s41467-024-54964-xopenalex-snapshot
Genomic analysis of global Plasmodium vivax populations reveals insights into the evolution of drug resistance
inferred← citeshttps://doi.org/10.1038/s41467-025-62357-xopenalex-snapshot
Microhaplotype deep sequencing assays to capture Plasmodium vivax infection lineages
inferred← citeshttps://doi.org/10.1038/s41467-026-73664-2openalex-snapshot
The spatial proteome of the Plasmodium falciparum schizont illuminates the composition and evolutionary trajectories of its organelles
inferred← citeshttps://doi.org/10.1038/s41576-021-00349-5openalex-snapshot
Advances and opportunities in malaria population genomics
inferred← citeshttps://doi.org/10.1038/s41586-018-0249-1openalex-snapshot
Cryo-EM structure of an essential Plasmodium vivax invasion complex
inferred← citeshttps://doi.org/10.1038/s41598-019-46398-zopenalex-snapshot
Whole genome sequencing of amplified Plasmodium knowlesi DNA from unprocessed blood reveals genetic exchange events between Malaysian Peninsular and Borneo subpopulations
inferred← citeshttps://doi.org/10.1038/s41598-020-67568-4openalex-snapshot
Selective whole genome amplification of Plasmodium malariae DNA from clinical samples reveals insights into population structure
inferred← citeshttps://doi.org/10.1038/s41598-023-46076-1openalex-snapshot
Genomics of Plasmodium vivax in Colombia reveals evidence of local bottle-necking and inter-country connectivity in the Americas
inferred← citeshttps://doi.org/10.1038/s41598-023-47889-wopenalex-snapshot
Genomic analysis of Plasmodium vivax describes patterns of connectivity and putative drivers of adaptation in Ethiopia
inferred← citeshttps://doi.org/10.1038/s41598-026-48246-3openalex-snapshot
Parasite population dynamics shaped P. falciparum pfhrp2 and pfhrp3 deletion expansion in the Peruvian Amazon
inferred← citeshttps://doi.org/10.1038/s42003-022-04352-2openalex-snapshot
A molecular barcode and web-based data analysis tool to identify imported Plasmodium vivax malaria
inferred← citeshttps://doi.org/10.1038/s42003-025-08276-5openalex-snapshot
Genomic analysis of Plasmodium vivax field isolates circulating in sub-Saharan Africa
inferred← citeshttps://doi.org/10.1039/c8nr04917copenalex-snapshot
Accurate and sensitive single-cell-level detection of copy number variations by micro-channel multiple displacement amplification (μcMDA)
inferred← citeshttps://doi.org/10.1073/pnas.1606113113openalex-snapshot
Role of Plasmodium vivax Duffy-binding protein 1 in invasion of Duffy-null Africans
inferred← citeshttps://doi.org/10.1073/pnas.1611017113openalex-snapshot
Mitochondrial DNA from the eradicated European Plasmodium vivax and P. falciparum from 70-year-old slides from the Ebro Delta in Spain
inferred← citeshttps://doi.org/10.1073/pnas.1810053115openalex-snapshot
Evolutionary history of human Plasmodium vivax revealed by genome-wide analyses of related ape parasites
inferred← citeshttps://doi.org/10.1073/pnas.1818485116openalex-snapshot
Transcriptome profiling of Plasmodium vivax in Saimiri monkeys identifies potential ligands for invasion
inferred← citeshttps://doi.org/10.1080/14760584.2021.1880898openalex-snapshot
Progress towards the development of a P. vivax vaccine
inferred← citeshttps://doi.org/10.1093/bioinformatics/btx410openalex-snapshot
Panoptes: web-based exploration of large scale genome variation data
inferred← citeshttps://doi.org/10.1093/bioinformatics/btx530openalex-snapshot
Deconvolution of multiple infections in Plasmodium falciparum from high throughput sequencing data
inferred← citeshttps://doi.org/10.1093/database/baaa036openalex-snapshot
PvP01-DB: computational structural and functional characterization of soluble proteome of PvP01 strain of Plasmodium vivax
inferred← citeshttps://doi.org/10.1093/femsre/fuab047openalex-snapshot
A population genetic perspective on the origin, spread and adaptation of the human malaria agents Plasmodium falciparum and Plasmodium vivax
inferred← citeshttps://doi.org/10.1093/gbe/evx256openalex-snapshot
High-Resolution Single-Cell Sequencing of Malaria Parasites
inferred← citeshttps://doi.org/10.1093/infdis/jiab214openalex-snapshot
Plasmodium simium : Population Genomics Reveals the Origin of a Reverse Zoonosis
inferred← citeshttps://doi.org/10.1093/infdis/jiae111openalex-snapshot
Functional and Immunologic Mapping of Domains of the Reticulocyte-Binding Protein Plasmodium vivax PvRBP2a
inferred← citeshttps://doi.org/10.1093/infdis/jiae388openalex-snapshot
Copy Number Variations of Plasmodium vivax DBP1, EBP/DBP2, and RBP2b in Ethiopians Who Are Duffy Positive and Duffy Negative
inferred← citeshttps://doi.org/10.1093/infdis/jiaf322openalex-snapshot
Digital PCR Reveals High PvDBP 1 but not PvEBP/DBP 2 and PvRBP 2b Copy Number in Plasmodium vivax From Duffy-Negative Individuals in Central Africa
inferred← citeshttps://doi.org/10.1093/infdis/jiaf539openalex-snapshot
Extreme Genetic Diversity and Signatures of Balancing Selection in Plasmodium vivax Blood-Stage Antigens
inferred← citeshttps://doi.org/10.1093/infdis/jiw323openalex-snapshot
Genomic Analysis Reveals a Common Breakpoint in Amplifications of the Plasmodium vivax Multidrug Resistance 1 Locus in Thailand
inferred← citeshttps://doi.org/10.1093/infdis/jix106openalex-snapshot
Frequent Spread of Plasmodium vivax Malaria Maintains High Genetic Diversity at the Myanmar-China Border, Without Distance and Landscape Barriers
inferred← citeshttps://doi.org/10.1093/infdis/jiz016openalex-snapshot
Genomic Analysis of Plasmodium vivax in Southern Ethiopia Reveals Selective Pressures in Multiple Parasite Mechanisms
inferred← citeshttps://doi.org/10.1093/infdis/jiz019openalex-snapshot
A Solid Beginning to Understanding Plasmodium vivax in Africa
inferred← citeshttps://doi.org/10.1093/molbev/msz154openalex-snapshot
Ancient Hybridization and Adaptive Introgression of an Invadolysin Gene in Schistosome Parasites
inferred← citeshttps://doi.org/10.1093/molbev/msz264openalex-snapshot
Plasmodium vivax Malaria Viewed through the Lens of an Eradicated European Strain
inferred← citeshttps://doi.org/10.1093/nar/gkab1237openalex-snapshot
GIP: an open-source computational pipeline for mapping genomic instability from protists to cancer cells
inferred← citeshttps://doi.org/10.1098/rsbm.2025.0043openalex-snapshot
Dominic Kwiatkowski
inferred← citeshttps://doi.org/10.1099/mgen.0.001386openalex-snapshot
Detection of novel Plasmodium falciparum haplotypes under treatment pressure in paediatric severe malaria
inferred← citeshttps://doi.org/10.1101/2022.11.30.22282917openalex-snapshot
No association between the Plasmodium vivax crt-o MS334 or In9 pvcrt polymorphisms and chloroquine failure in a clinical cohort from Malaysia
inferred← citeshttps://doi.org/10.1101/2023.02.16.528793openalex-snapshot
Comparative transcriptomics reveal differential gene expression in Plasmodium vivax geographical isolates and implications on erythrocyte invasion mechanisms
inferred← citeshttps://doi.org/10.1101/2024.04.29.591731openalex-snapshot
Copy number variations of Plasmodium vivax DBP1 , EBP/DBP2 , and RBP2b in Duffy-positive and Duffy-negative Ethiopians
inferred← citeshttps://doi.org/10.1101/2024.08.20.24312296openalex-snapshot
Detection of novel Plasmodium falciparum haplotypes under treatment pressure in pediatric severe malaria
inferred← citeshttps://doi.org/10.1101/2024.10.14.24315131openalex-snapshot
Microhaplotype deep sequencing assays to capture Plasmodium vivax infection lineages
inferred← citeshttps://doi.org/10.1101/2025.03.09.25323469openalex-snapshot
Cambodian Plasmodium vivax parasites with reduced hemoglobin digestion display delayed clearance upon artesunate treatment
inferred← citeshttps://doi.org/10.1101/2025.05.26.25327775openalex-snapshot
Understanding Plasmodium vivax recurrent infections using an amplicon deep sequencing assay, PvAmpSeq, identity-by-descent and model-based classification
inferred← citeshttps://doi.org/10.1101/2025.07.07.663616openalex-snapshot
Navigating parasite antigen genetic diversity in the design of Plasmodium vivax serological exposure markers for malaria
inferred← citeshttps://doi.org/10.1101/2025.11.04.25339464openalex-snapshot
PvGTSeq and PvCRiSP: two amplicon-based targeted sequencing panels for Plasmodium vivax
inferred← citeshttps://doi.org/10.1101/2025.11.27.690946openalex-snapshot
The spatial proteome of the Plasmodium falciparum schizont illuminates the composition and evolutionary trajectories of its organelles
inferred← citeshttps://doi.org/10.1101/391268openalex-snapshot
Resolving within-host malaria parasite diversity using single-cell sequencing
inferred← citeshttps://doi.org/10.1101/505594openalex-snapshot
Estimating the probable cause of recurrence in Plasmodium vivax malaria: relapse, reinfection or recrudescence?
inferred← citeshttps://doi.org/10.1101/817320openalex-snapshot
Monitoring of Plasmodium falciparum and Plasmodium vivax using microsatellite markers indicates limited changes in population structure after substantial transmission decline in Papua New Guinea
inferred← citeshttps://doi.org/10.1101/cshperspect.a025585openalex-snapshot
The Biology of Plasmodium vivax
inferred← citeshttps://doi.org/10.1111/biom.13226openalex-snapshot
Relapse or reinfection: Classification of malaria infection using transition likelihoods
inferred← citeshttps://doi.org/10.1111/mec.15654openalex-snapshot
Monitoring Plasmodium falciparum and Plasmodium vivax using microsatellite markers indicates limited changes in population structure after substantial transmission decline in Papua New Guinea
inferred← citeshttps://doi.org/10.1126/sciadv.abc3713openalex-snapshot
Population genomic evidence of Plasmodium vivax Southeast Asian origin
inferred← citeshttps://doi.org/10.1126/science.aan1078openalex-snapshot
Transferrin receptor 1 is a reticulocyte-specific receptor for Plasmodium vivax
inferred← citeshttps://doi.org/10.1128/aac.00095-21openalex-snapshot
High Proportion of Genome-Wide Homology and Increased Pretreatment pvcrt Levels in Plasmodium vivax Late Recurrences: a Chloroquine Therapeutic Efficacy Study
inferred← citeshttps://doi.org/10.1128/aac.00355-17openalex-snapshot
Plasmodium falciparum and Plasmodium vivax Demonstrate Contrasting Chloroquine Resistance Reversal Phenotypes
inferred← citeshttps://doi.org/10.1128/aac.01610-22openalex-snapshot
No Association between the Plasmodium vivax crt-o MS334 or In9 pvcrt Polymorphisms and Chloroquine Failure in a Pre-Elimination Clinical Cohort from Malaysia with a Large Clonal Expansion
inferred← citeshttps://doi.org/10.1128/cmr.00019-19openalex-snapshot
Plasmodium Genomics and Genetics: New Insights into Malaria Pathogenesis, Drug Resistance, Epidemiology, and Evolution
inferred← citeshttps://doi.org/10.1128/mbio.02257-16openalex-snapshot
Selective Whole-Genome Amplification Is a Robust Method That Enables Scalable Whole-Genome Sequencing of Plasmodium vivax from Unprocessed Clinical Samples
inferred← citeshttps://doi.org/10.1128/spectrum.00726-22openalex-snapshot
Development and Optimization of a Selective Whole-Genome Amplification To Study Plasmodium ovale Spp.
inferred← citeshttps://doi.org/10.1146/annurev-micro-020518-115628openalex-snapshot
Ape Origins of Human Malaria
inferred← citeshttps://doi.org/10.11606/d.42.2017.tde-14032017-141656openalex-snapshot
Genômica populacional de Plasmodium vivax: níveis e mecanismos de diversidade genética na América.
inferred← citeshttps://doi.org/10.11606/t.42.2017.tde-19052017-130115openalex-snapshot
Perspectivas para eliminação da malária residual em área rural da Amazônia brasileira: estratégia de busca ativa reativa na identificação de reservatórios de Plasmodium vivax.
inferred← citeshttps://doi.org/10.11606/t.42.2018.tde-12032018-170059openalex-snapshot
Anticorpos contra a proteína de ligação em Duffy (PvDBP) e proteção contra a malária vivax na Amazônia rural brasileira.
inferred← citeshttps://doi.org/10.1172/jci.insight.152465openalex-snapshot
Controlled human malaria infection with a clone of Plasmodium vivax with high-quality genome assembly
inferred← citeshttps://doi.org/10.1186/s12711-018-0390-1openalex-snapshot
A survey of functional genomic variation in domesticated chickens
inferred← citeshttps://doi.org/10.1186/s12864-017-3523-yopenalex-snapshot
Whole-genome sequencing of a Plasmodium vivax clinical isolate exhibits geographical characteristics and high genetic variation in China-Myanmar border area
inferred← citeshttps://doi.org/10.1186/s12864-023-09707-5openalex-snapshot
A new Plasmodium vivax reference genome for South American isolates
inferred← citeshttps://doi.org/10.1186/s12936-016-1531-zopenalex-snapshot
Approaches to estimating inbreeding coefficients in clinical isolates of Plasmodium falciparum from genomic sequence data
inferred← citeshttps://doi.org/10.1186/s12936-016-1592-zopenalex-snapshot
Genetic diversity of the Pvk12 gene in Plasmodium vivax from the China-Myanmar border area
inferred← citeshttps://doi.org/10.1186/s12936-016-1595-9openalex-snapshot
Plasmodium vivax multidrug resistance-1 gene polymorphism in French Guiana
inferred← citeshttps://doi.org/10.1186/s12936-017-1762-7openalex-snapshot
A systematic review on malaria sero-epidemiology studies in the Brazilian Amazon: insights into immunological markers for exposure and protection
inferred← citeshttps://doi.org/10.1186/s12936-017-1882-0openalex-snapshot
Genome-wide scans for the identification of Plasmodium vivax genes under positive selection
inferred← citeshttps://doi.org/10.1186/s12936-017-1905-xopenalex-snapshot
Genetic diversity and natural selection of Plasmodium vivax multi-drug resistant gene (pvmdr1) in Mesoamerica
inferred← citeshttps://doi.org/10.1186/s12936-017-1912-yopenalex-snapshot
Chloroquine efficacy for Plasmodium vivax in Myanmar in populations with high genetic diversity and moderate parasite gene flow
inferred← citeshttps://doi.org/10.1186/s12936-017-2002-xopenalex-snapshot
Plasmodium vivax genetic diversity and heterozygosity in blood samples and resulting oocysts at the Thai–Myanmar border
inferred← citeshttps://doi.org/10.1186/s12936-020-03221-9openalex-snapshot
Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.1186/s12936-020-03330-5openalex-snapshot
Implementing parasite genotyping into national surveillance frameworks: feedback from control programmes and researchers in the Asia–Pacific region
inferred← citeshttps://doi.org/10.1186/s12936-020-03372-9openalex-snapshot
The biology of unconventional invasion of Duffy-negative reticulocytes by Plasmodium vivax and its implication in malaria epidemiology and public health
inferred← citeshttps://doi.org/10.1186/s12936-020-03386-3openalex-snapshot
Use of a Plasmodium vivax genetic barcode for genomic surveillance and parasite tracking in Sri Lanka
inferred← citeshttps://doi.org/10.1186/s12936-020-03440-0openalex-snapshot
SNP barcodes provide higher resolution than microsatellite markers to measure Plasmodium vivax population genetics
inferred← citeshttps://doi.org/10.1186/s12936-024-04852-yopenalex-snapshot
Genomic insights into Plasmodium vivax population structure and diversity in central Africa
inferred← citeshttps://doi.org/10.1186/s12936-024-04895-1openalex-snapshot
Epidemiology of Plasmodium vivax in Duffy negatives and Duffy positives from community and health centre collections in Ethiopia
inferred← citeshttps://doi.org/10.1186/s12936-025-05690-2openalex-snapshot
The pattern of gene amplification of members of the Plasmodium vivax erythrocyte binding-like proteins family across the Amazon rainforest
inferred← citeshttps://doi.org/10.1186/s13071-022-05296-6openalex-snapshot
Genetic diversity of Plasmodium vivax reticulocyte binding protein 2b in global parasite populations
inferred← citeshttps://doi.org/10.1186/s13071-022-05422-4openalex-snapshot
Genomic analysis of single nucleotide polymorphisms in malaria parasite drug targets
inferred← citeshttps://doi.org/10.1186/s13073-016-0343-7openalex-snapshot
Recent advances in malaria genomics and epigenomics
inferred← citeshttps://doi.org/10.1186/s13073-018-0563-0openalex-snapshot
Exploration of Plasmodium vivax transmission dynamics and recurrent infections in the Peruvian Amazon using whole genome sequencing
inferred← citeshttps://doi.org/10.1186/s40249-022-00964-2openalex-snapshot
Polymorphisms of potential drug resistant molecular markers in Plasmodium vivax from China–Myanmar border during 2008‒2017
inferred← citeshttps://doi.org/10.12688/f1000research.10255.1openalex-snapshot
Divergent pattern of genomic variation in Plasmodium falciparum and P. vivax
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.12741.1openalex-snapshot
Scale up of a Plasmodium falciparum elimination program and surveillance system in Kayin State, Myanmar
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.12741.2openalex-snapshot
Scale up of a Plasmodium falciparum elimination program and surveillance system in Kayin State, Myanmar
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.17795.1openalex-snapshot
An open dataset of Plasmodium vivax genome variation in 1,895 worldwide samples
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.9876.1openalex-snapshot
A new Plasmodium vivax reference sequence with improved assembly of the subtelomeres reveals an abundance of pir genes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008576openalex-snapshot
A molecular barcode to inform the geographical origin and transmission dynamics of Plasmodium vivax malaria
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009604openalex-snapshot
Population-level genome-wide STR discovery and validation for population structure and genetic diversity assessment of Plasmodium species
inferred← citeshttps://doi.org/10.1371/journal.pmed.1003560openalex-snapshot
The changing epidemiology of Plasmodium vivax: Insights from conventional and novel surveillance tools
inferred← citeshttps://doi.org/10.1371/journal.pntd.0005091openalex-snapshot
Independent Origin and Global Distribution of Distinct Plasmodium vivax Duffy Binding Protein Gene Duplications
inferred← citeshttps://doi.org/10.1371/journal.pntd.0005824openalex-snapshot
Genome-wide diversity and differentiation in New World populations of the human malaria parasite Plasmodium vivax
inferred← citeshttps://doi.org/10.1371/journal.pntd.0005930openalex-snapshot
Substantial population structure of Plasmodium vivax in Thailand facilitates identification of the sources of residual transmission
inferred← citeshttps://doi.org/10.1371/journal.pntd.0006146openalex-snapshot
Increasingly inbred and fragmented populations of Plasmodium vivax associated with the eastward decline in malaria transmission across the Southwest Pacific
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007222openalex-snapshot
Frequent expansion of Plasmodium vivax Duffy Binding Protein in Ethiopia and its epidemiological significance
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007470openalex-snapshot
Plasmodium knowlesi as a model system for characterising Plasmodium vivax drug resistance candidate genes
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007596openalex-snapshot
Antibodies to Plasmodium vivax reticulocyte binding protein 2b are associated with protection against P. vivax malaria in populations living in low malaria transmission regions of Brazil and Thailand
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008202openalex-snapshot
Genetic diversity and neutral selection in Plasmodium vivax erythrocyte binding protein correlates with patient antigenicity
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008234openalex-snapshot
Whole genome sequencing of Plasmodium vivax isolates reveals frequent sequence and structural polymorphisms in erythrocyte binding genes
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008506openalex-snapshot
Population genomics identifies a distinct Plasmodium vivax population on the China-Myanmar border of Southeast Asia
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008808openalex-snapshot
Population genomics reveals the expansion of highly inbred Plasmodium vivax lineages in the main malaria hotspot of Brazil
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008945openalex-snapshot
Multi-locus genotyping reveals established endemicity of a geographically distinct Plasmodium vivax population in Mauritania, West Africa
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010492openalex-snapshot
Geographical distribution and genetic diversity of Plasmodium vivax reticulocyte binding protein 1a correlates with patient antigenicity
inferred← citeshttps://doi.org/10.1371/journal.pntd.0010991openalex-snapshot
Long read single cell RNA sequencing reveals the isoform diversity of Plasmodium vivax transcripts
inferred← citeshttps://doi.org/10.1371/journal.pntd.0011598openalex-snapshot
Preliminary characterization of Plasmodium vivax sporozoite antigens as pre-erythrocytic vaccine candidates
inferred← citeshttps://doi.org/10.1371/journal.pntd.0011926openalex-snapshot
Comparative transcriptomics reveal differential gene expression among Plasmodium vivax geographical isolates and implications on erythrocyte invasion mechanisms
inferred← citeshttps://doi.org/10.1371/journal.pntd.0012299openalex-snapshot
Plasmodium vivax populations in the western Greater Mekong Subregion evaluated using a genetic barcode
inferred← citeshttps://doi.org/10.1371/journal.pntd.0013663openalex-snapshot
PvGTSeq and PvCRiSP: Two amplicon-based targeted sequencing panels for Plasmodium vivax
inferred← citeshttps://doi.org/10.1371/journal.pntd.0014053openalex-snapshot
Host kinase regulation of Plasmodium vivax dormant and replicating liver stages
inferred← citeshttps://doi.org/10.1371/journal.pntd.0014472openalex-snapshot
Spatiotemporal differentiation of Plasmodium vivax populations in the western Greater Mekong Subregion using a 22-SNP barcode
inferred← citeshttps://doi.org/10.1371/journal.pone.0177134openalex-snapshot
Genomic variation in Plasmodium vivax malaria reveals regions under selective pressure
inferred← citeshttps://doi.org/10.1371/journal.ppat.1008258openalex-snapshot
The enigmatic mechanisms by which Plasmodium vivax infects Duffy-negative individuals
inferred← citeshttps://doi.org/10.1371/journal.ppat.1012418openalex-snapshot
Turning the needle into the haystack: Culture-independent amplification of complex microbial genomes directly from their native environment
inferred← citeshttps://doi.org/10.15212/zoonoses-2021-0015openalex-snapshot
Zoonotic Transmission and Host Switches of Malaria Parasites
inferred← citeshttps://doi.org/10.17533/udea.hm.v15n2a03openalex-snapshot
Explorando los mecanismos de invasión celular de Plasmodium Vivax a través del sistema de grupo sanguíneo Duffy
inferred← citeshttps://doi.org/10.21203/rs.2.19786/v1openalex-snapshot
Evolution of Plasmodium vivax populations in border areas of the Greater Mekong Subregion during malaria elimination
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1023914/v1openalex-snapshot
Genetic Diversity of Plasmodium vivax Reticulocyte Binding Protein 2b in Global Parasite Populations
inferred← citeshttps://doi.org/10.22459/ta58.2024.06openalex-snapshot
Deep histories in New Guinea: Insights from genetics on human adaptation to malaria and diverse environments
inferred← citeshttps://doi.org/10.22541/au.159015516.68850426openalex-snapshot
Monitoring Plasmodium falciparum and Plasmodium vivax using microsatellite markers indicates limited changes in population structure after substantial transmission decline in Papua New Guinea
inferred← citeshttps://doi.org/10.3347/kjp.2017.55.5.473openalex-snapshot
Genetic Diversity and Natural Selection in 42 kDa Region of Plasmodium vivax Merozoite Surface Protein-1 from China-Myanmar Endemic Border
inferred← citeshttps://doi.org/10.3389/fcimb.2018.00034openalex-snapshot
Plasmodium vivax Biology: Insights Provided by Genomics, Transcriptomics and Proteomics
inferred← citeshttps://doi.org/10.3389/fcimb.2021.738075openalex-snapshot
Molecular Surveillance and Ex Vivo Drug Susceptibilities of Plasmodium vivax Isolates From the China–Myanmar Border
inferred← citeshttps://doi.org/10.3389/fcimb.2021.789417openalex-snapshot
Gene Polymorphisms Among Plasmodium vivax Geographical Isolates and the Potential as New Biomarkers for Gametocyte Detection
inferred← citeshttps://doi.org/10.3389/fcimb.2022.1011692openalex-snapshot
Band 3–mediated Plasmodium vivax invasion is associated with transcriptional variation in PvTRAg genes
inferred← citeshttps://doi.org/10.3389/fcimb.2022.953187openalex-snapshot
Novel highly-multiplexed AmpliSeq targeted assay for Plasmodium vivax genetic surveillance use cases at multiple geographical scales
inferred← citeshttps://doi.org/10.3389/fimmu.2022.862851openalex-snapshot
Multiple-Allele MHC Class II Epitope Engineering by a Molecular Dynamics-Based Evolution Protocol
inferred← citeshttps://doi.org/10.3389/fmicb.2020.01930openalex-snapshot
New Plasmodium vivax Genomes From the China-Myanmar Border
inferred← citeshttps://doi.org/10.3389/fmicb.2022.984394openalex-snapshot
Population genomics in neglected malaria parasites
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1071689openalex-snapshot
Retrospective analysis of Plasmodium vivax genomes from a pre-elimination China inland population in the 2010s
inferred← citeshttps://doi.org/10.3390/agriculture12060844openalex-snapshot
Positive Selection and Adaptive Introgression of Haplotypes from Bos indicus Improve the Modern Bos taurus Cattle
inferred← citeshttps://doi.org/10.3390/genes12060843openalex-snapshot
Malaria in the ‘Omics Era’
inferred← citeshttps://doi.org/10.3390/microorganisms10102021openalex-snapshot
Molecular Profiles of Multiple Antimalarial Drug Resistance Markers in Plasmodium falciparum and Plasmodium vivax in the Mandalay Region, Myanmar
inferred← citeshttps://doi.org/10.4269/ajtmh.16-0160openalex-snapshot
Implications of Plasmodium vivax Biology for Control, Elimination, and Research
inferred← citeshttps://doi.org/10.4269/ajtmh.16-0268openalex-snapshot
Epidemiology of Plasmodium vivax Malaria in Peru
inferred← citeshttps://doi.org/10.4269/ajtmh.17-0254openalex-snapshot
Plasmodium vivax Infections over 3 Years in Duffy Blood Group Negative Malians in Bandiagara, Mali
inferred← citeshttps://doi.org/10.4269/ajtmh.17-0869openalex-snapshot
Malaria Elimination: Time to Target All Species
inferred← citeshttps://doi.org/10.4269/ajtmh.18-0277openalex-snapshot
Plasmodium vivax Infections in Duffy-Negative Individuals in the Democratic Republic of the Congo
inferred← citeshttps://doi.org/10.47665/tb.37.4.911openalex-snapshot
Purification of Plasmodium and Babesia- infected erythrocytes using a non-woven fabric filter
inferred← citeshttps://doi.org/10.48550/arxiv.1612.06050openalex-snapshot
Long-term sustained malaria control leads to inbreeding and fragmentation of Plasmodium vivax populations
inferred← citeshttps://doi.org/10.5772/intechopen.96604openalex-snapshot
Elimination ofPlasmodium vivaxMalaria: Problems and Solutions
inferred← citeshttps://doi.org/10.5802/crbiol.95openalex-snapshot
Plasmodium vivax blood stage invasion pathways: Contribution of omics technologies in deciphering molecular and cellular mechanisms
inferred← citeshttps://doi.org/10.6084/m9.figshare.12101730openalex-snapshot
Additional file 1 of Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.6084/m9.figshare.12101742openalex-snapshot
Additional file 2 of Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.6084/m9.figshare.12101748openalex-snapshot
Additional file 3 of Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.6084/m9.figshare.12101754openalex-snapshot
Additional file 4 of Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.6084/m9.figshare.12101757openalex-snapshot
Additional file 5 of Dynamics of Plasmodium vivax populations in border areas of the Greater Mekong sub-region during malaria elimination
inferred← citeshttps://doi.org/10.6084/m9.figshare.12986817openalex-snapshot
Additional file 3 of Use of a Plasmodium vivax genetic barcode for genomic surveillance and parasite tracking in Sri Lanka
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120828openalex-snapshot
Additional file 1 of SNP barcodes provide higher resolution than microsatellite markers to measure Plasmodium vivax population genetics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120831openalex-snapshot
Additional file 2 of SNP barcodes provide higher resolution than microsatellite markers to measure Plasmodium vivax population genetics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120834openalex-snapshot
Additional file 3 of SNP barcodes provide higher resolution than microsatellite markers to measure Plasmodium vivax population genetics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120837openalex-snapshot
Additional file 4 of SNP barcodes provide higher resolution than microsatellite markers to measure Plasmodium vivax population genetics
inferred← citeshttps://doi.org/10.6084/m9.figshare.19646290openalex-snapshot
Additional file 1 of Polymorphisms of potential drug resistant molecular markers in Plasmodium vivax from China–Myanmar border during 2008‒2017
inferred← citeshttps://doi.org/10.6084/m9.figshare.20064221openalex-snapshot
Additional file 1 of Genetic diversity of Plasmodium vivax reticulocyte binding protein 2b in global parasite populations
inferred← citeshttps://doi.org/10.6084/m9.figshare.20745191openalex-snapshot
Additional file 1 of Genomic analysis of single nucleotide polymorphisms in malaria parasite drug targets
inferred← citeshttps://doi.org/10.6084/m9.figshare.20745194openalex-snapshot
Additional file 2 of Genomic analysis of single nucleotide polymorphisms in malaria parasite drug targets
inferred← citeshttps://doi.org/10.6084/m9.figshare.20745197openalex-snapshot
Additional file 3 of Genomic analysis of single nucleotide polymorphisms in malaria parasite drug targets
inferred← citeshttps://doi.org/10.6084/m9.figshare.25025891openalex-snapshot
Additional file 1 of Genomic insights into Plasmodium vivax population structure and diversity in central Africa
inferred← citeshttps://doi.org/10.6084/m9.figshare.25026033openalex-snapshot
Additional file 2 of Genomic insights into Plasmodium vivax population structure and diversity in central Africa
inferred← citeshttps://doi.org/10.64898/2026.04.28.26351930openalex-snapshot
Clinical malaria cases reflect the parasite population diversity of the asymptomatic reservoir in West Africa
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