Author

Paula Inés Buonfiglio

Consejo Nacional de Investigaciones Científicas y TécnicasORCID 0000-0003-2985-4790Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 1 Assay:DNA methylation· 1 Assay:electrophysiology· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Viviana DalamóniD· 2 shared Ana Belén ElgoyheniD· 1 shared Carmen Llames MassiniiD· 1 shared Carolina WedemeyeriD· 1 shared Catherine J.C. WeisziD· 1 shared Eleonora KatziD· 1 shared Florencia GilibertoiD· 1 shared Gabriel Capellino· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersPhysiology

Viviana DalamónORCID

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2 papers

Recent·Most cited

PhysiologyJournal of NeurosciencePeer-reviewedOct 2, 2025

Co-release of GABA and ACh from medial olivocochlear neurons fine tunes cochlear efferent inhibition

Tais Castagnola, Valeria C. Castagna, Lester Torres Cadenas…·Carolina Wedemeyer

The paper shows that GABA and ACh are co-released from MOC terminals, modulating cholinergic inhibition at IHC synapses during development.

3 citations

mouseelectrophysiology

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintOct 3, 2024

From Past to Present: Pompe Disease, Pseudodeficiency Alleles, and Diagnostic Challenges

Florencia Giliberto, Paula Inés Buonfiglio, Gabriel Capellino…·Micaela Carcione

The paper investigates a pseudodeficiency allele in Pompe disease, clarifies its benign classification, and highlights the importance of accurate variant interpretation in genetic diagnosis.

DOI 10.1101/2024.10.03.24314698

humanDNA methylation

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