Pablo Naranjo-Roman
Granada, AN 18071, Spain
Last Updated: 09/26/2026
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Found 11 publications
Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction.
Journal: Genes
Published: March 08, 2023
A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases.
Journal: Journal of biomedical informatics
Published: January 28, 2023
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus.
Journal: NPJ genomic medicine
Published: May 25, 2022
A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss.
Journal: European journal of human genetics : EJHG
Published: May 14, 2022
Defective α-tectorin may involve tectorial membrane in familial Meniere disease.
Journal: Clinical and translational medicine
Published: March 01, 2022
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.
Journal: Ear and hearing
Published: November 02, 2020
Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease.
Journal: Genes
Published: October 01, 2020
Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease.
Journal: Journal of medical genetics
Published: March 18, 2019
Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease.
Journal: Frontiers in genetics
Published: September 06, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026