31 Aug 2026Open access
Mutational Landscape of Primary Hyperoxaluria in Morocco: Update and Implications for DiagnosisPublisher siteGenes, Kidney Stones and Urolithiasis Treatments
UniversitiesOurayna Batta
Active, last published 2026
In metabolism and genetic disorders
Ourayna
Batta
Scholar“Research focused on Metabolism and Genetic Disorders and adjacent fields.”
Mohammed V University
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01 · About the work
What I study
urayna Batta is a researcher working on Metabolism and Genetic Disorders. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Ourayna's work has been cited 0 times across 2 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Metabolism and Genetic Disorders×2Genetic and Kidney Cyst Diseases×2Kidney Stones and Urolithiasis Treatments×1
04 · Where I am
Affiliations
Affiliation on published researchMohammed V UniversityDrawn from the institution listed on this researcher’s published work.
05 · Selected work
Recent publications
3 works25 Feb 2026Open access
Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome SequencingPublisher siteMolecular Genetics & Genomic Medicine, Muscle Physiology and Disorders
4 Dec 2024
Genotype First Approach as a Diagnostic Strategy for Precision Medicine in Moroccan Families with NephronophthisisPublisher siteJournal of Pediatric Genetics, Genetic and Kidney Cyst Diseases
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