Author

Roudha Alfalasi

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 Maha El Naofal· 2 shared Nour Halabi· 2 shared Ruchi JainiD· 2 shared Sathishkumar RamaswamyiD· 2 shared

Activity by Year

2023-2023 · peak 2/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

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 MedicinemedRxivPreprintJan 11, 2023

Genetic determinants of severe COVID-19 in young Asian and Middle Eastern patients

Beshr Abdulaziz Badla, Mohamed Samer Hanifa, Ruchi Jain…·Ahmad N. Abou Tayoun

This study identifies rare genetic variants associated with severe COVID-19 in young Asian and Middle Eastern patients using whole exome sequencing.

3 citations

humanwhole-exome sequencing

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