Sandrine Marlin

Paris, France

Last Updated: 09/26/2026

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Found 98 publications

Pediatric Cochlear Implant Outcomes in Auditory Neuropathy, Cochlear Nerve Deficiency, and Sensorineural Hearing Loss: An 8-Year Longitudinal Study.

Pediatric Cochlear Implant Outcomes in Auditory Neuropathy, Cochlear Nerve Deficiency, and Sensorineural Hearing Loss: An 8-Year Longitudinal Study.

Journal: Ear and hearing
Published: June 09, 2026

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Establishing a Prognosis When Identifying Pathogenic Variants in Usher Syndrome/DFNB-Related Genes: An Impossible Challenge?

Journal: Clinical genetics
Published: May 20, 2026

Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy.

Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy.

Journal: International journal of audiology
Published: April 27, 2026

Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy.

Transient disappearance of otoacoustic emissions after conventional hearing aid use in OTOF-related auditory neuropathy.

Journal: International journal of audiology
Published: April 27, 2026

COCH-Related Hearing Loss in a French Cohort: Novel Variants and Genotype-Phenotype Correlations.

COCH-Related Hearing Loss in a French Cohort: Novel Variants and Genotype-Phenotype Correlations.

Journal: Genes
Published: April 25, 2026

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Journal: European journal of human genetics : EJHG
Published: April 02, 2026

Genetic contributions to familial Ménière's disease: a systematic review.

Genetic contributions to familial Ménière's disease: a systematic review.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
Published: January 12, 2026

Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophy.

Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophy.

Journal: European journal of medical genetics
Published: December 03, 2025

The RNA-binding protein TRIM71 is essential for hearing in humans and mice and times auditory sensory organ development.

The RNA-binding protein TRIM71 is essential for hearing in humans and mice and times auditory sensory organ development.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: September 02, 2025

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function.

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function.

Journal: eLife
Published: August 27, 2025

Vestibular Deficit in Patients with Waardenburg Syndrome.

Vestibular Deficit in Patients with Waardenburg Syndrome.

Journal: Biomedicines
Published: June 13, 2025

The RNA-binding protein TRIM71 is essential for hearing in humans and mice and regulates the timing of auditory sensory organ development.

The RNA-binding protein TRIM71 is essential for hearing in humans and mice and regulates the timing of auditory sensory organ development.

Journal: bioRxiv : the preprint server for biology
Published: June 12, 2025
Showing 1-12 of 98

Last Updated: 09/26/2026