Author

Bassel W Abou-Khalil

Vanderbilt University Medical CenterORCID 0000-0002-6559-1329Unclaimed ORCID profile · follow to get notified of new preprints

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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

Ahmad A. BeydouniD· 1 shared 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 Beata Fonferko‐ShadrachiD· 1 shared

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2024-2024 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmad A. BeydounORCID

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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

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