Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia
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Title
Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia
Authors
Keywords
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Journal
SCHIZOPHRENIA BULLETIN
Volume -, Issue -, Pages -
Publisher
Oxford University Press (OUP)
Online
2021-01-14
DOI
10.1093/schbul/sbab007
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Note: Only part of the references are listed.- c.753A>G genome editing of a Cdh23 allele delays age-related hearing loss and degeneration of cochlear hair cells in C57BL/6J mice
- (2020) Shumpei P. Yasuda et al. HEARING RESEARCH
- The mutational constraint spectrum quantified from variation in 141,456 humans
- (2020) Konrad J. Karczewski et al. NATURE
- Emerging phenotyping strategies will advance our understanding of psychiatric genetics
- (2020) Sandra Sanchez-Roige et al. NATURE NEUROSCIENCE
- Evidence for Altered Metabolism of Sphingosine-1-Phosphate in the Corpus Callosum of Patients with Schizophrenia
- (2020) Kayoko Esaki et al. SCHIZOPHRENIA BULLETIN
- Prefecture-level population structure of the Japanese based on SNP genotypes of 11,069 individuals
- (2020) Yusuke Watanabe et al. JOURNAL OF HUMAN GENETICS
- Evaluation of the role of fatty acid-binding protein 7 in controlling schizophrenia-relevant phenotypes using newly established knockout mice
- (2019) Chie Shimamoto-Mitsuyama et al. SCHIZOPHRENIA RESEARCH
- Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis
- (2019) Stephan C. Collins et al. Nature Communications
- Investigation of betaine as a novel psychotherapeutic for schizophrenia
- (2019) Tetsuo Ohnishi et al. EBioMedicine
- Excess hydrogen sulfide and polysulfides production underlies a schizophrenia pathophysiology
- (2019) Masayuki Ide et al. EMBO Molecular Medicine
- Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study
- (2019) Tiffany A. Greenwood et al. JAMA Psychiatry
- Psychiatric genetics and the structure of psychopathology
- (2018) Jordan W. Smoller et al. MOLECULAR PSYCHIATRY
- Digital gene atlas of neonate common marmoset brain
- (2018) Tomomi Shimogori et al. NEUROSCIENCE RESEARCH
- Sensorimotor gating deficits in schizophrenia: Advancing our understanding of the phenotype, its neural circuitry and genetic substrates
- (2018) Neal R. Swerdlow et al. SCHIZOPHRENIA RESEARCH
- Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction
- (2017) Baptiste Libé-Philippot et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Deficient prepulse inhibition in schizophrenia in a multi-site cohort: Internal replication and extension
- (2017) Neal R. Swerdlow et al. SCHIZOPHRENIA RESEARCH
- Beyond Cell–Cell Adhesion: Sensational Cadherins for Hearing and Balance
- (2017) Avinash Jaiganesh et al. Cold Spring Harbor Perspectives in Biology
- Genetic tests in major psychiatric disorders—integrating molecular medicine with clinical psychiatry—why is it so difficult?
- (2017) U Demkow et al. Translational Psychiatry
- Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains
- (2017) Kenneth R. Johnson et al. Scientific Reports
- The Relationship of Common Risk Variants and Polygenic Risk for Schizophrenia to Sensorimotor Gating
- (2016) Panos Roussos et al. BIOLOGICAL PSYCHIATRY
- Heterozygous mutation ofUsh1g/Sansin mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation inCdh23
- (2016) Yuki Miyasaka et al. HUMAN MOLECULAR GENETICS
- Sensorimotor gating of the startle reflex: what we said 25 years ago, what has happened since then, and what comes next
- (2016) Neal R Swerdlow et al. JOURNAL OF PSYCHOPHARMACOLOGY
- Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair
- (2016) Joffrey Mianné et al. Genome Medicine
- Diversification of behavior and postsynaptic properties by netrin-G presynaptic adhesion family proteins
- (2016) Qi Zhang et al. Molecular Brain
- Analysis of induced pluripotent stem cells carrying 22q11.2 deletion
- (2016) M Toyoshima et al. Translational Psychiatry
- Genomic resources for wild populations of the house mouse, Mus musculus and its close relative Mus spretus
- (2016) Bettina Harr et al. Scientific Data
- Factor structure and heritability of endophenotypes in schizophrenia: Findings from the Consortium on the Genetics of Schizophrenia (COGS-1)
- (2015) Larry J. Seidman et al. SCHIZOPHRENIA RESEARCH
- MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencing
- (2014) Evan A. Boyle et al. BIOINFORMATICS
- Functional characterization of FABP3, 5 and 7 gene variants identified in schizophrenia and autism spectrum disorder and mouse behavioral studies
- (2014) Chie Shimamoto et al. HUMAN MOLECULAR GENETICS
- Rat subthalamic nucleus and zona incerta share extensively overlapped representations of cortical functional territories
- (2014) Takako Kita et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Deficient prepulse inhibition in schizophrenia detected by the multi-site COGS
- (2014) Neal R. Swerdlow et al. SCHIZOPHRENIA RESEARCH
- Sorting out a promiscuous superfamily: towards cadherin connectomics
- (2014) Marcos Sotomayor et al. TRENDS IN CELL BIOLOGY
- One-Step Generation of Mice Carrying Mutations in Multiple Genes by CRISPR/Cas-Mediated Genome Engineering
- (2013) Haoyi Wang et al. CELL
- Compound Heterozygosity of the Functionally Null Cdh23v-ngt and Hypomorphic Cdh23ahl Alleles Leads to Early-onset Progressive Hearing Loss in Mice
- (2013) Yuki Miyasaka et al. EXPERIMENTAL ANIMALS
- The anatomy of the caudal zona incerta in rodents and primates
- (2013) Charles Watson et al. JOURNAL OF ANATOMY
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- Deep brain stimulation of the subthalamic nucleus in the 6-hydroxydopamine rat model of Parkinson's disease: Effects on sensorimotor gating
- (2012) Christoph Lindemann et al. BEHAVIOURAL BRAIN RESEARCH
- Comparative Anatomy of Marmoset and Mouse Cortex from Genomic Expression
- (2012) H. Mashiko et al. JOURNAL OF NEUROSCIENCE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- Cadherins in Brain Morphogenesis and Wiring
- (2012) Shinji Hirano et al. PHYSIOLOGICAL REVIEWS
- Subthalamic nucleus stimulation for Parkinson disease with severe medication-induced hallucinations or delusions
- (2011) Atsushi Umemura et al. JOURNAL OF NEUROSURGERY
- Research Domain Criteria (RDoC): Toward a New Classification Framework for Research on Mental Disorders
- (2010) Thomas Insel et al. AMERICAN JOURNAL OF PSYCHIATRY
- Japanese Population Structure, Based on SNP Genotypes from 7003 Individuals Compared to Other Ethnic Groups: Effects on Population-Based Association Studies
- (2008) Yumi Yamaguchi-Kabata et al. AMERICAN JOURNAL OF HUMAN GENETICS
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