Author

Mohamed El Amine Bouabid

Centre de Recherche sur l'Information Scientifique et TechniqueORCID 0009-0008-4635-9867Unclaimed 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 Ahror BelaidiD· 1 shared Belaïd ImessaoudeneiD· 1 shared Djamal BelazzouguiiD· 1 shared Hassen MoutchachouiD· 1 shared Kouider BeladghamiD· 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

Mutual co-authors in cluster

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1 paper

Recent·Most cited

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, Nadia Gagi, Ahlam Mihoubi, Hassen Moutchachou, Mohamed El Amine Bouabid, Ahror Belaid, Saïd Yahiaoui, Djamal Belazzougui, 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.

medRxiv · Mar 25, 2026 · PreprintGenetic & Genomic Medicine