Laurence Jonard - Publications

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

Journal: Clinical genetics

Published: May 20, 2026

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

Journal: Genes

Published: April 25, 2026

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.

Journal: European journal of medical genetics

Published: December 03, 2025

Vestibular Deficit in Patients with Waardenburg Syndrome.

Journal: Biomedicines

Published: June 13, 2025

Bilateral Enlarged Vestibular Aqueduct: Auditory, Genetic and Radiological Characterization, and Benefits of Cochlear Implants.

Journal: Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery

Published: March 24, 2025

Unilateral, bilateral symmetric or asymmetric isolated hearing loss in patients with heterozygous KITLG variants.

Journal: Human genetics

Published: December 01, 2024

HDR syndrome: Large cohort and systematic review.

Journal: Clinical genetics

Published: March 21, 2024

RIPOR2: A new gene of non-syndromic cochleovestibular dysfunction, discrepancy between human pathology and animal models.

Journal: Clinical genetics

Published: July 26, 2023

Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions.

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: February 10, 2023

Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.

Journal: Audiology research

Published: January 18, 2023

Audiological phenotyping evaluation in KBG syndrome: Description of a multicenter review.

Journal: International journal of pediatric otorhinolaryngology

Published: December 02, 2022