Author

Tony Yammine

Lyon 1 UniversitéORCID 0000-0002-1545-6794Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Boris KereniD· 2 shared Caroline Schluth‐BolardiD· 2 shared Damien SanlavilleiD· 2 shared Laurence Olivier FaivreiD· 2 shared Achille Lolascon· 1 shared Alexander HoischeniD· 1 shared Alexander P.A. StegmanniD· 1 shared Alexandra AfenjariD· 1 shared

Activity by Year

2020-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 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

Boris KerenORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintAug 5, 2025

Genotype-Phenotype Correlation in RBM10-Associated Syndromes. How Variant Function Shapes a Broad Phenotypic Landscape

Jeanne Mari V. Bang, Christina Ringmann Fagerberg, Thomas Koed Doktor…·Brage Storstein Andresen

The paper reports 37 new cases of RBM10 variants, identifies two phenotypic groups, and establishes a genotype-phenotype correlation based on functional studies.

DOI 10.1101/2025.08.05.25330579

humanstatistical model

𝕏 PostBluesky

GenomicsbioRxivPreprintJul 17, 2020

The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms

Nicolas Chatron, Giuliana Giannuzzi, Pierre‐Antoine Rollat‐Farnier…·Caroline Schluth‐Bolard

The paper analyzes chromoanagenesis breakpoints in constitutional and cancer cases, finding enrichment in late-replicating chromatin and suggesting similar mechanisms for both.

14 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 15, 2020

Next generation cytogenetics: genome-imaging enables comprehensive structural variant detection for 100 constitutional chromosomal aberrations in 85 samples

Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard…·Laïla El Khattabi

This study evaluates high-resolution optical mapping for detecting chromosomal aberrations in 85 samples, achieving 100% concordance with standard tests for non-centromeric breakpoints.

24 citations

humanwhole-genome sequencing

𝕏 PostBluesky