Author

Ahmad A. Beydoun

American University of Beirut Medical CenterORCID 0000-0002-9047-1185Unclaimed 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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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alica M. GoldmaniD· 1 shared Alison AndersoniD· 1 shared Andrew J. ColeiD· 1 shared Annika B. FauconiD· 1 shared Antonio GambardellaiD· 1 shared Barbara CastellottiiD· 1 shared Bassel W Abou-KhaliliD· 1 shared Beata Fonferko‐ShadrachiD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alica M. GoldmanORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineNature NeurosciencePeer-reviewedOct 1, 2024

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Epi25 Collaborative, Siwei Chen, Bassel W Abou-Khalil…·Alica M. Goldman

This study identifies shared and distinct ultra-rare genetic risk factors for epilepsy subtypes using whole-exome sequencing of 20,979 patients and 33,444 controls.

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humanwhole-exome sequencing