Author

Blaise Didry‐Barca

InsermORCID 0009-0003-3261-7670Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:differential expression· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

Alice LepelleyiD· 2 shared Yanick Joseph CrowiD· 2 shared Adham SafieddineiD· 1 shared Adolfo SaiardiiD· 1 shared Alexandre Pierga· 1 shared Antria SavvidouiD· 1 shared Arnold MünnichiD· 1 shared Carina C. de Oliveira ManniD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersCell Biology

Alice LepelleyORCID

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3 papers

Recent·Most cited

Cell BiologybioRxivPreprintMay 7, 2026

Loss of MTPAP disrupts mitochondrial RNA processing causing upregulation of type I interferon signalling

Alexandre Pierga, Yan de Souza Angelo, Adham Safieddine…·Alice Lepelley

This study shows that MTPAP loss causes mitochondrial RNA processing defects, leading to type I interferon signaling upregulation through mt-dsRNA accumulation.

DOI 10.64898/2026.05.04.722669

humanmetagenomics

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Genetic & Genomic MedicinemedRxivPreprintApr 28, 2023

ARF1 prevents aberrant type I IFN induction by regulating STING activation and recycling

Maximilian Hirschenberger, Alice Lepelley, Ulrich Rupp…·Konstantin M. J. Sparrer

This study identifies ARF1 as a negative regulator of cGAS-STING signaling, showing it prevents type I IFN induction by regulating STING activation and recycling.

DOI 10.1101/2023.04.28.23289152

humanproteomics

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GeneticsNature CommunicationsPeer-reviewedNov 30, 2020

MINPP1 prevents intracellular accumulation of the cation chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia

Ekin Ucuncu, Karthyayani Rajamani, Miranda Wilson…·Vincent Cantagrel

This study identifies MINPP1 mutations as a cause of Pontocerebellar Hypoplasia, showing that MINPP1 deficiency leads to IP6 accumulation and cation chelation, disrupting brain development.

62 citationstop 2%

humanbulk RNA-seq

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