Christine Petit

Centre National de la Recherche Scientifique — France

Neuroscience · Life Sciences

99h-index32.1kcitations496works1.42yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Hearing, Cochlea, Tinnitus, Genetics(227), Connexins and lens biology(69), Vestibular and auditory disorders(57), Hearing Loss and Rehabilitation(38), RNA and protein synthesis mechanisms(31)

Publications495 total

Single-cell spatially resolved transcriptomic characterization of the developing mouse cochlea
2026
Genetic diversity of Usher syndrome in Moroccan patients
Human Genetics·2026
Hearing Impairment
Elsevier eBooks·2025
Deciphering Auditory Hyperexcitability in <i>Otogl</i> Mutant Mice Unravels an Auditory Neuropathy Mechanism (Adv. Sci. 19/2025)
Advanced Science·2025Open Access
Deciphering Auditory Hyperexcitability in <i>Otogl</i> Mutant Mice Unravels an Auditory Neuropathy Mechanism
Advanced Science·2025· 3 citedOpen Access
Whole exome sequencing identifies ABHD14A and MRNIP as novel candidate genes for developmental language disorder
Scientific Reports·2025· 2 citedOpen Access
Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment
Journal of Applied Genetics·2024· 1 citedOpen Access
A free intravesicular C-terminal of otoferlin is essential for synaptic vesicle docking and fusion at auditory inner hair cell ribbon synapses
Progress in Neurobiology·2024· 2 citedOpen Access
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families
Molecular Biology Reports·2024
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Frontiers in Genetics·2024· 1 citedOpen Access
Biallelic variants in TMIE and PDE6B genes mimic Usher syndrome
Gene Reports·2024Open Access
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Frontiers in Genetics·2024· 1 citedOpen Access
François Gros (1925–2022)
Comptes Rendus Biologies·2024Open Access
Extended time frame for restoring inner ear function through gene therapy in Usher1G preclinical model
JCI Insight·2024· 11 citedOpen Access
Novel pathogenic WHRN variant causing hearing loss in a moroccan family
Molecular Biology Reports·2023· 2 cited
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families
Biochemical Genetics·2023· 1 cited
Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies
Proceedings of the National Academy of Sciences·2023· 81 citedOpen Access
Deafness: from genetic architecture to gene therapy
Nature Reviews Genetics·2023· 130 citedOpen Access
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness
European Archives of Oto-Rhino-Laryngology·2023· 2 citedOpen Access
Groupes à médiation « danse » en pédopsychiatrie* - « La pensée naît aussi du mouvement. »
L information psychiatrique·2023
page 1 of 25Next →

Frequent Co-authors

Dominique Weil(17), A. Amraoui(12), Vincent Michel(10), Stéphane Blanchard(8), Jacqueline Levilliers(8), Jean‐Pierre Hardelin(8), Isabelle Perfettini(8), Michel Leibovici(7), Sandrine Marlin(6), Saaïd Safieddine(5), Paul Avan(5), Fabienne Lévi-Acobas(4), M’hamed Grati(4), Françoise Denoyelle(4), Mirna Mustapha(4), Jean-Pierre Hardelin(4), Richard J. Smith(4), Uwe Wolfrum(4), Guy P. Richardson(4), Catherine Dodé(3)