Author

Carlos A. H. Fernandes

Centre National de la Recherche ScientifiqueORCID 0000-0001-6515-6872Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Biophysics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Assay:electrophysiology· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:structural biology· 1 Organism:Xenopus· 1

Frequent Co-Authors

Catherine Vénien‐BryaniD· 2 shared Alexandre PozzaiD· 1 shared Ana‐Andreea ArteniiD· 1 shared Andreas ZoumpoulakisiD· 1 shared Bruno CollinetiD· 1 shared Charles CirioiD· 1 shared Christelle ArrondeliD· 1 shared Corinne AntignaciD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersBiochemistry

Catherine Vénien‐BryanORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

BiochemistrybioRxivPreprintMar 3, 2026

Structure of the human KEOPS/tRNA complex and characterization of pathogenic variants responsible for the Galloway Mowat syndrome.

Charles Cirio, Sylvie Auxilien, Dominique Liger…·Bruno Collinet

The paper determines the structure of the human KEOPS/tRNA complex and characterizes pathogenic variants in the t6A pathway linked to Galloway-Mowat syndrome.

DOI 10.64898/2026.03.03.709218

humanstructural biology

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BiophysicsThe FASEB JournalPeer-reviewedNov 9, 2024

Biochemical, biophysical, and structural investigations of two mutants (C154Y and R312H) of the human Kir2.1 channel involved in the Andersen-Tawil syndrome.

Dania Zuniga, Andreas Zoumpoulakis, Rafael F. Veloso…·Catherine Vénien‐Bryan

This study investigates two Kir2.1 mutants linked to Andersen-Tawil syndrome, showing they impair channel function through distinct mechanisms, with C154Y causing dominant-negative effects.

9 citations

Xenopuselectrophysiology

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