Author

Lemis Yavuz

Al Jalila FoundationORCID 0000-0002-1970-6930Unclaimed 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 Maha El Naofal· 3 shared Sathishkumar RamaswamyiD· 3 shared Walid AbuhammouriD· 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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Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenetic & Genomic Medicine

Ahmad N. Abou TayounORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

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

Rania Najm, Lemis Yavuz, Ruchi Jain, Maha El Naofal, Sathishkumar Ramaswamy, Walid Abuhammour, Tom Loney, Norbert R. Nowotny, Alawi A.A. Alsheikh-Ali, Ahmad N. Abou Tayoun, 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.

medRxiv · Oct 13, 2023 · PreprintGenetic & Genomic Medicine

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