Author

Virginie G. Peter

University Hospital of BernORCID 0000-0001-8157-9568Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Carlo RivoltaiD· 2 shared Dror SharoniD· 2 shared Mathieu QuinodoziD· 2 shared Alaa AlTalbishiiD· 1 shared Ana Berta SousaiD· 1 shared Andrew R. WebsteriD· 1 shared Anna LarsoniD· 1 shared Anne B. FultoniD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersGenetics

Carlo RivoltaORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJun 8, 2025

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

Mathieu Quinodoz, Elifnaz Çelik, Dhryata Kamdar…·Carlo Rivolta

RetiGene provides a curated gene atlas for inherited retinal diseases, integrating variant data and RNA sequencing to support gene prioritization and therapeutic development.

3 citations

humanbulk RNA-seq

𝕏 PostBluesky

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

𝕏 PostBluesky