Pcdh15 | List of Frontiers open access articles

Original Research

Published on 22 May 2025

Outcomes of cochlear implants in patients with PCDH15 mutations: a clinical study

in Genetics of Common and Rare Diseases

Qingling Bi
Zhongyan Chen
Baoling Kang
Yong Lv
Yongyi Yuan
Yang Liu
Jianfeng Liu
Yuan Li

Frontiers in Genetics

doi 10.3389/fgene.2025.1541333

2,266 views
1 citation

Case Report

Published on 02 Jul 2020

A 4.6 Mb Inversion Leading to PCDH15-LINC00844 and BICC1-PCDH15 Fusion Transcripts as a New Pathogenic Mechanism Implicated in Usher Syndrome Type 1

in Genetics of Common and Rare Diseases

Christel Vaché
Jacques Puechberty
Valérie Faugère
Floriane Darmaisin
Alessandro Liquori
David Baux
Catherine Blanchet
Gema Garcia-Garcia
Isabelle Meunier
Franck Pellestor

Frontiers in Genetics

doi 10.3389/fgene.2020.00623

4,739 views
11 citations

Original Research

Published on 20 Feb 2018

TRPV6, TRPM6 and TRPM7 Do Not Contribute to Hair-Cell Mechanotransduction

in Cellular Neurophysiology

Clive P. Morgan
Hongyu Zhao
Meredith LeMasurier
Wei Xiong
Bifeng Pan
Piotr Kazmierczak
Matthew R. Avenarius
Michael Bateschell
Ruby Larisch
Anthony J. Ricci

Frontiers in Cellular Neuroscience

doi 10.3389/fncel.2018.00041

7,127 views
8 citations

Original Research

Published on 15 Jan 2020

The lhfpl5 Ohnologs lhfpl5a and lhfpl5b Are Required for Mechanotransduction in Distinct Populations of Sensory Hair Cells in Zebrafish

in Methods and Model Organisms

Timothy Erickson
Itallia V. Pacentine
Alexandra Venuto
Rachel Clemens
Teresa Nicolson

Frontiers in Molecular Neuroscience

doi 10.3389/fnmol.2019.00320

7,362 views
36 citations

Original Research

Published on 27 Mar 2020

Genome-Wide Association Study Identifies Genomic Loci Associated With Neurotransmitter Concentration in Cattle

in Livestock Genomics

Qiuming Chen
Kaixing Qu
Zhijie Ma
Jingxi Zhan
Fengwei Zhang
Jiafei Shen
Qingqing Ning
Peng Jia
Jicai Zhang
Ningbo Chen

Frontiers in Genetics

doi 10.3389/fgene.2020.00139

6,603 views
20 citations

Original Research

Published on 22 May 2019

Genetic Screening of the Usher Syndrome in Cuba

in Genetics of Common and Rare Diseases

Elayne E. Santana
Carla Fuster-García
Elena Aller
Teresa Jaijo
Belén García-Bohórquez
Gema García-García
José M. Millán
Araceli Lantigua

Frontiers in Genetics

doi 10.3389/fgene.2019.00501

6,778 views
11 citations

Articles

Outcomes of cochlear implants in patients with PCDH15 mutations: a clinical study

A 4.6 Mb Inversion Leading to PCDH15-LINC00844 and BICC1-PCDH15 Fusion Transcripts as a New Pathogenic Mechanism Implicated in Usher Syndrome Type 1

TRPV6, TRPM6 and TRPM7 Do Not Contribute to Hair-Cell Mechanotransduction

The lhfpl5 Ohnologs lhfpl5a and lhfpl5b Are Required for Mechanotransduction in Distinct Populations of Sensory Hair Cells in Zebrafish

Genome-Wide Association Study Identifies Genomic Loci Associated With Neurotransmitter Concentration in Cattle

Genetic Screening of the Usher Syndrome in Cuba