Author

Evyatar Mor

Ben-Gurion University of the Negev

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· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Hagar Mor-ShakediD· 2 shared Christopher T. GordoniD· 1 shared Divya PachatiD· 1 shared Eden EngaliD· 1 shared Eldar Dedic· 1 shared Giovanni ZifarelliiD· 1 shared Hane LeeiD· 1 shared Henry HouldeniD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetics

Hagar Mor-ShakedORCID

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2 papers

Recent·Most cited

SeverYX: An ensemble framework for robust variant severity classification

Evyatar Mor, Eldar Dedic, Yaron Mazor, Suzanne Drury, Hagar Mor-Shaked, Lina Zelinger

SeverYX is an ensemble framework that classifies genetic variants into severity tiers, achieving high concordance with ClinVar and improving predictive accuracy through threshold optimization and additional predictors.

bioRxiv · Nov 4, 2026 · PreprintGenetics

Biallelic loss of function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome

Eden Engal, Kaisa Teele Oja, Reza Maroofian, Ophir Geminder, Thuy-Linh Le, Evyatar Mor, Naama Tzvi, Naama Elefant, Maha Saad Zaki, Joseph G. Gleeson, Kai Muru, Sander Pajusalu, Monica Hsiung Wojcik, Divya Pachat, Marwa Saeed Abd Elmaksoud, , Hagar Mor‐Shaked

This study identifies biallelic loss-of-function variants in WBP4 as a cause of a neurodevelopmental syndrome with variable manifestations.

medRxiv · Jun 19, 2023 · PreprintGenetic & Genomic Medicine