Author

Kamila Lee

Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel;ORCID 0009-0005-5049-7646Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:variant effect prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Rivka Birnbaum· 2 shared Tamar HareliD· 2 shared Ben Pode-Shakked· 1 shared Carol PerelmaniD· 1 shared Dan Raved· 1 shared Dov Popper· 1 shared Elias Elias Charua- Levy· 1 shared Hagar Mor· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Rivka Birnbaum

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 9, 2026

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

Rivka Birnbaum, Kamila Lee, Yaron Mazor…·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.

DOI 10.64898/2026.11.07.26367371

humanwhole-exome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintOct 23, 2026

Exome-based Preconception Carrier Screening for the Mexican Jewish Community; Yields and Implications

Rivka Birnbaum, Kamila Lee, Teresa Metta-Harari…·Hagar Mor‐Shaked

This study uses exome sequencing to identify genetic variants in the Mexican Jewish Community, finding higher rates of carrier status and novel alleles compared to standard panels.

DOI 10.64898/2026.10.21.26366106

humanwhole-exome sequencing

𝕏 PostBluesky