Author

Mathieu Cérino

InsermORCID 0000-0002-4992-5157Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Bioinformatics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:software / tool· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Marc BartoliiD· 3 shared Svetlana GorokhovaiD· 3 shared Martin KrahniD· 2 shared Nicolas LévyiD· 2 shared Anaı̈s BaudotiD· 1 shared Annamaria Molon· 1 shared Aurélien PerriniD· 1 shared Cécile AcquavivaiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 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

3 shared papersBioinformatics

Marc BartoliORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

BioinformaticsScientific ReportsPeer-reviewedMay 16, 2024

System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution

Ozan Özışık, Svetlana Gorokhova, Mathieu Cérino…·Anaı̈s Baudot

The paper analyzes genes mutated in muscular dystrophies to identify functional patterns linked to distal or proximal muscle weakness distribution.

3 citations

humanstatistical model

𝕏 PostBluesky

Genetic & Genomic MedicineInternational Journal of Molecular SciencesPeer-reviewedJul 31, 2022

Objective evaluation of clinical actionability for genes involved in myopathies: 63 genes with a medical value for patient care

Maude Vecten, Emmanuelle Pion, Marc Bartoli…·Mireille Cossée

The paper evaluates the clinical actionability of 63 myopathy-related genes using ClinGen criteria, finding that only 8 of the top 36 genes had prior ClinGen scores.

3 citations

humanstatistical model

𝕏 PostBluesky

BioinformaticsScientific ReportsPeer-reviewedApr 10, 2020

A new tool CovReport generates easy-to-understand sequencing coverage summary for diagnostic reports.

Mark Gorokhov, Mathieu Cérino, Jérémie Mortreux…·Svetlana Gorokhova

CovReport provides a user-friendly tool for generating sequencing coverage summaries to aid in diagnostic reporting and interpretation.

2 citations

whole-genome sequencingexperimental assay

𝕏 PostBluesky