Author

Boris Rosin

Hebrew University of JerusalemORCID 0000-0001-7070-0879Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Organism:mouse· 1 Organism:rat· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

Eyal BaniniD· 2 shared Alaa AlTalbishiiD· 1 shared Alki C. LiasisiD· 1 shared Ana Berta SousaiD· 1 shared Andrew R. WebsteriD· 1 shared Anfisa AyaloniD· 1 shared Anna LarsoniD· 1 shared Anne B. FultoniD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersPhysiology

Eyal BaninORCID

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2 papers

Recent·Most cited

PhysiologybioRxivPreprintOct 2, 2026

Wavelet Transform improves time-frequency characterization of the Electroretinographic Oscillatory Potentials as compared to Short-Time Fourier Transform across experimental and clinical models

Patrick Reiman, Sean Ghiam, Avigail Beryozkin…·Boris Rosin

This study compares wavelet transform and short-time Fourier transform for analyzing electroretinographic oscillatory potentials, finding wavelet transform provides better time-frequency resolution and disease-specific insights.

DOI 10.64898/2026.09.26.754708

ratmouse

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Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedJun 29, 2021

Early onset non-syndromic retinal degeneration due to variants in INPP5E: phenotypic expansion of the ciliary gene previously associated with Joubert syndrome

Riccardo Sangermano, Iris Deitch, Virginie G. Peter…·Kinga M. Bujakowska

The paper identifies INPP5E variants in non-syndromic retinal degenerations, expanding the known phenotypic spectrum of this ciliary gene.

22 citations

humanstatistical model

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