Author

Y. Unger

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

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

B. Pode-Shakked· 1 shared D. Raved· 1 shared H. Shani· 1 shared Hagar Mor· 1 shared I. Grundwag· 1 shared K. Lee· 1 shared L. Greenbaum· 1 shared M. Chalk· 1 shared

Activity by Year

2026-2026 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

B. Pode-Shakked

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1 paper

Recent·Most cited

A Framework for Variant Filtering to Improve Diagnostic Outcomes in Genome Sequencing

R. Birnbaum, K. Lee, Y. Mazor, Y. Unger, S. Yanovsky-Dagan, I. Grundwag, M. Chalk, N. Shaul-Lotan, L. Greenbaum, O. Freireich, T. Klopstock, T. Dror, M. Sebbagh, R. Beeri, O. Murik, , Hagar Mor

This paper introduces a variant filtering framework called SMART filtering to improve diagnostic outcomes in genome sequencing by prioritizing non-coding and regulatory variants.

medRxiv · Nov 9, 2026 · PreprintGenetic & Genomic Medicine