Author

Walid Abuhammour

Al Jalila FoundationORCID 0000-0001-5748-549XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-exome sequencing· 3 Research Focus:variant calling· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Ahmad N. Abou TayouniD· 3 shared Alawi A.A. Alsheikh-AliiD· 3 shared Lemis YavuziD· 3 shared Maha El Naofal· 3 shared Sathishkumar RamaswamyiD· 3 shared Abdulla Al Khayat· 2 shared Alan TayloriD· 2 shared Ali AlsarhaniD· 2 shared

Activity by Year

2022-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Ahmad N. Abou TayounORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 13, 2023

IFIH1 loss-of-function predisposes to inflammatory and SARS-CoV-2-related infectious diseases

Rania Najm, Lemis Yavuz, Ruchi Jain…·Richard K. Kandasamy

This study identifies IFIH1 loss-of-function variants in patients with inflammatory and SARS-CoV-2-related diseases, showing impaired immune responses and increased susceptibility.

DOI 10.1101/2023.10.13.23297034

humanwhole-exome sequencing

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Genetic & Genomic MedicineGenome MedicinePeer-reviewedJan 26, 2023

The Genomic Landscape of Rare Disorders in the Middle East

Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan…·Ahmad N. Abou Tayoun

This study evaluates genomic diagnostic yield and clinical impact in rare disease patients from the Middle East, finding higher yields with sequencing than microarrays and highlighting diagnostic delays due to limited access.

47 citationstop 1%

humanwhole-exome sequencing

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Genetic & Genomic MedicineJAMA Network OpenPeer-reviewedMay 31, 2022

Genomic and phenotypic characterization of Multisystem Inflammatory Syndrome in Children (MIS-C): a prospective multicenter study from the Middle East

Walid Abuhammour, Lemis Yavuz, Ruchi Jain…·Ahmad N. Abou Tayoun

This study identifies rare genetic variants in MIS-C patients from the Middle East, linking them to disease onset and treatment resistance.

29 citationstop 3%

humanwhole-exome sequencing

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