Paul Avan

9PUBLICATIONS
93CO-AUTHORS
Phonetics and speech scienceSensory systemsInfant and child healthAutonomic nervous systemEpigenetics (incl. genome methylation and epigenomics)
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Publications (9)

|Apr 22, 2026
A cross-domain test battery for comprehensive hearing loss characterisation using functional, physiological, and vestibular measures.

|Feb 18, 2025
Deciphering Auditory Hyperexcitability in Otogl Mutant Mice Unravels an Auditory Neuropathy Mechanism.

Mathilde Gagliardini, Sabrina Mechaussier, Carolina Campos Pina

|Dec 06, 2023
Prevalence of hearing loss and health vulnerability in children aged 25 to 36 months: an analysis of spatial distribution.

Aline Aparecida Lopes, Amélia Augusta de Lima Friche, Stela Maris Aguiar Lemos

|Oct 05, 2022
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice.

Konstantina Chachlaki, Andrea Messina, Virginia Delli

|Nov 24, 2020
Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.

Sophie Boucher, Fabienne Wong Jun Tai, Sedigheh Delmaghani

|May 04, 2018
Noninvasive in-ear monitoring of intracranial pressure during microgravity in parabolic flights.

Paul Avan, Hervé Normand, Fabrice Giraudet

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Frequent Collaborators

3 joint publications

Fabrice Giraudet

2 joint publications

Christine Petit

2 joint publications

Sirley Alves da Silva Carvalho

2 joint publications

Nicolas Michalski