Rebecca Crudale Source Confirmed

Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.

Researcher

John Brown University

faculty

5 h-index 36 pubs 88 cited

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Biography and Research Information

OverviewAI-generated summary

Rebecca Crudale is a faculty member at John Brown University whose research focuses on combating infectious diseases, particularly malaria and HIV/AIDS. Her work encompasses both computational drug discovery and the study of genetic variations that impact disease transmission and treatment efficacy. Crudale's recent research has investigated antimalarial drug resistance in diverse populations and geographic regions. This includes studies identifying artemisinin partial resistance mutations in the Great Lakes region and examining the prevalence of antimalarial drug resistance markers in Ugandan refugees. She also employs high-throughput genotyping methods to study Plasmodium vivax in South America. Her research extends to genotype-phenotype association studies of Plasmodium falciparum in Africa, evaluating ex vivo susceptibility to antimalarial drugs. Crudale's broader research interests include mosquito-borne diseases and their control.

Metrics

  • h-index: 5
  • Publications: 36
  • Citations: 88

Selected Publications

  • COATswga: A Coverage Optimizing and Accurate Toolkit for fast primer design in selective whole genome amplification (2025) DOI
  • Genome-wide SNP genotyping of <i>Plasmodium falciparum</i> isolates across Mali reveals major impacts of <i>Pfsa1</i> and PfCRT K76T selections on parasite populations (2025) DOI
  • Highly multiplex molecular inversion probe panel in Plasmodium falciparum targeting common SNPs approximates whole genome sequencing assessments for selection and relatedness (2025) DOI
  • Author response: Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI
  • Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI
  • Author response: Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI
  • Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI
  • <i>Ex vivo</i> susceptibility to antimalarial drugs and polymorphisms in drug resistance genes of African <i>Plasmodium falciparum</i> , 2016-2023: a genotype-phenotype association study (2024) DOI
  • High frequency of artemisinin partial resistance mutations in the great lake region revealed through rapid pooled deep sequencing (2024) DOI
  • Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI
  • Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3 (2024) DOI

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