Author

Ahror Belaid

Centre de Recherche sur l'Information Scientifique et TechniqueORCID 0000-0003-4610-8239Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Organism:human· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ahlam MihoubiiD· 1 shared Belaïd ImessaoudeneiD· 1 shared Djamal BelazzouguiiD· 1 shared Hassen MoutchachouiD· 1 shared Kouider BeladghamiD· 1 shared Mohamed El Amine BouabidiD· 1 shared Nadia GagiiD· 1 shared Saïd YahiaouiiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahlam MihoubiORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 25, 2026

Challenges and perspectives in implementing whole-exome sequencing in Algeria lessons from a fully autonomous in-country cohort

Tarik Ait Mouhoub, Kouider Beladgham, Sihem Brahimi…·Belaïd Imessaoudene

This study implements whole-exome sequencing in Algeria for neurodevelopmental disorders, achieving molecular diagnoses in 8/14 cases and highlighting challenges in variant interpretation and database underrepresentation.

DOI 10.64898/2026.03.23.26348909

humanwhole-exome sequencing

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