Whole‐Exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal‐Recessive Nonsyndromic Hearing Loss DFNB99

No abstract is available for this paper.

• Publication year

  2015

• Venue

  Human Mutation

• Publication date

  2015-01-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/humu.22712PMID 25331638
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Are TMEM genes potential candidate genes for panic disorder?

  2014cited by this paper
• Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.

  2012cited by this paper
• Rare variants in TMEM132D in a case–control sample for panic disorder

  2012cited by this paper
• TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies

  2011cited by this paper
• Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28.

  2011cited by this paper
• A method and server for predicting damaging missense mutations

  2010cited by this paper
• Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

  2010cited by this paper
• Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.

  2010cited by this paper
• Knockdown of transmembrane protein 132A by RNA interference facilitates serum starvation-induced cell death in Neuro2a cells

  2010cited by this paper
• Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

  2010cited by this paper
• Function and expression pattern of nonsyndromic deafness genes.

  2009cited by this paper
• The transmembrane inner ear (Tmie) protein is essential for normal hearing and balance in the zebrafish

  2009cited by this paper
• Hearing loss: mechanisms revealed by genetics and cell biology.

  2009cited by this paper
• Clustal W and Clustal X version 2.0

  2007cited by this paper
• Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

  2006cited by this paper
• Mutation of the zebrafish choroideremia gene encoding Rab escort protein 1 devastates hair cells.

  2004cited by this paper
• [Gene mapping of a nonsyndromic hearing impairmint family].

  2003influential reference
• FM1-43 Dye Behaves as a Permeant Blocker of the Hair-Cell Mechanotransducer Channel

  2001cited by this paper
• Predicting deleterious amino acid substitutions.

  2001cited by this paper
• Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants.

  1998cited by this paper
• Selective labeling of sensory hair cells and neurons in auditory, vestibular, and lateral line systems by a monoclonal antibody

  1990cited by this paper
• The lateral-line and inner-ear afferents in larval and adult urodeles.

  1988cited by this paper
• Sensory neuron growth cones comigrate with posterior lateral line primordial cells in zebrafish

  1985cited by this paper

• Dissecting the genome in Ménière disease: a review

  2025cites this paper
• Genetic analysis of a Kaijiang duck conservation population through genome-wide scan

  2024cites this paper
• Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes

  2023cites this paper
• TMEM132A ensures mouse caudal neural tube closure and regulates integrin-based mesodermal migration.

  2022cites this paper
• ARNSHL gene identification: past, present and future

  2022cites this paper
• Differential expression of the Tmem132 family genes in the developing mouse nervous system.

  2022cites this paper
• An update on autosomal recessive hearing loss and loci involved in it

  2022cites this paper
• Efficient multiplexed genome engineering with a polycistronic tRNA and CRISPR guide-RNA reveals an important role of detonator in reproduction of Drosophila melanogaster

  2021cites this paper
• How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us

  2021cites this paper
• Genome-wide analysis of cell-Free DNA methylation profiling with MeDIP-seq identified potential biomarkers for colorectal cancer

  2021cites this paper
• Positive selection of skeleton-related genes during duck domestication revealed by whole genome sequencing

  2021cites this paper
• Genomic prediction of growth in a commercially, recreationally, and culturally important marine resource, the Australian snapper (Chrysophrys auratus)

  2021cites this paper
• Nicotinic acetylcholine receptor redux: Discovery of accessories opens therapeutic vistas

  2021cites this paper
• Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future

  2021cites this paper
• Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process

  2021cites this paper
• Systematic Review of Sequencing Studies and Gene Expression Profiling in Familial Meniere Disease

  2020cites this paper
• Small fish, big prospects: using zebrafish to unravel the mechanisms of hereditary hearing loss.

  2020cites this paper
• Practical aspects of inner ear gene delivery for research and clinical applications.

  2020cites this paper
• Development and Deafness

  2020cites this paper
• NCOA3 identified as a new candidate to explain autosomal dominant progressive hearing loss

  2020cites this paper
• Gene therapy development in hearing research in China

  2020cites this paper
• Hair cell α9α10 nicotinic acetylcholine receptor functional expression regulated by ligand binding and deafness gene products

  2020influential citation
• Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment

  2019influential citation
• Water Waves to Sound Waves: Using Zebrafish to Explore Hair Cell Biology

  2019cites this paper
• A Combined Multi-Cohort Approach Reveals Novel and Known Genome-Wide Selection Signatures for Wool Traits in Merino and Merino-Derived Sheep Breeds

  2019cites this paper
• Whole‐exome sequencing suggests multiallelic inheritance for childhood‐onset Ménière's disease

  2019cites this paper
• Genetic Hearing Loss and Gene Therapy

  2018cites this paper
• ANIMAL “ Genomics of Speciation in Humpback Dolphins ( Genus Sousa )

  2018cites this paper
• Zebrafish models of human eye and inner ear diseases.

  2017cites this paper
• TMEM132: an ancient architecture of cohesin and immunoglobulin domains define a new family of neural adhesion molecules

  2017cites this paper
• Genotype–Phenotype Relationship in Inherited Disorders of Hearing Impairment

  2017cites this paper
• Explorer TMEM 132 : an ancient architecture of cohesin and immunoglobulin domains define a new family of neural adhesion molecules

  2017cites this paper
• Genetics Of Human Hereditary Hearing Impairment.

  2017cites this paper
• Genetic Elucidation of Nonsyndromic Hearing Loss in the High-Throughput Sequencing Era

  2016cites this paper
• Genetics of Nonsyndromic Congenital Hearing Loss

  2016cites this paper
• Navigating genetic diagnostics in patients with hearing loss

  2016cites this paper
• Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea

  2016cites this paper
• Whole-exome sequencing and its impact in hereditary hearing loss.

  2015cites this paper
• NOVEL TRENDS IN THE MOLECULAR GENETICS OF HEARING LOSS

  2015cites this paper
• Pediatric otolaryngology, molecular diagnosis of hereditary hearing loss: next-generation sequencing approach

  2015cites this paper
• Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.

  2015cites this paper