Crystel Bonnet

Institut Pasteur

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Articles (18)

Collaborators (4)

Christian Lorenzi

olivier sperandio

Université Paris-Saclay

Léo Varnet

Nicolas Michalski

Université Paris Cité

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Crystel Bonnet

Research Interests

Explore related searches

Contact this professor

Articles (18)

Collaborators (4)

Christian Lorenzi

olivier sperandio

Léo Varnet

Nicolas Michalski

Make your next move.

Crystel Bonnet

Research Interests

Explore related searches

Contact this professor

Articles (18)

Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment.

Biallelic variants in TMIE and PDE6B genes mimic Usher syndrome

Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control study.

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.

Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.

Deafness: from genetic architecture to gene therapy

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

Screening of BRCA1/2 variants in Mauritanian breast cancer patients

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco

Retinal Phenotype of Patients with <i>CLRN1</i>-Associated Usher 3A Syndrome in French Light4Deaf Cohort

Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference Analysis.

Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

Characteristics of Retinitis Pigmentosa Associated with ADGRV1 and Comparison with USH2A in Patients from a Multicentric Usher Syndrome Study Treatrush

Mutated CCDC51 Coding for a Mitochondrial Protein, MITOK Is a Candidate Gene Defect for Autosomal Recessive Rod-Cone Dystrophy

Phylogenetic analysis of Harmonin homology domains

Collaborators (4)

Christian Lorenzi

olivier sperandio

Léo Varnet

Nicolas Michalski

Make your next move.