Author

Deena Wafadari

Al Jalila Foundation

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2

Frequent Co-Authors

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

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Abdulla Al Khayat

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2 papers

Recent·Most cited

The Genomic Landscape of Rare Disorders in the Middle East

Maha El Naofal, Sathishkumar Ramaswamy, Ali Alsarhan, Ahmed Abd Alwahab Nugud, Fatima Sarfraz, Hiba Janbaz, Alan Taylor, Ruchi Jain, Nour Halabi, Sawsan Yaslam, Roudha Alfalasi, Shruti Shenbagam, Fatma Rabea, Martin M. Bitzan, Lemis Yavuz, , 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.

Genome Medicine · Jan 26, 2023Peer-reviewedGenetic & Genomic Medicine

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, Khawla Abu Hammour, Ghalia F. Al-Hammouri, Maha El Naofal, Nour Halabi, Sawsan Yaslam, Sathishkumar Ramaswamy, Alan Taylor, Deena Wafadari, Ali Alsarhan, Hamda Hassan Khansaheb, Zulfa Deesi, Rupa Murthy Varghese, , 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.

JAMA Network Open · May 31, 2022Peer-reviewedGenetic & Genomic Medicine