Exome Sequencing Identifies as a Novel Candidate Gene for Schizophrenia in the SCZD2 Locus at 11q14-21 (Q61807958)

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Jun Zhu

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Yu Wu

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Xi-Hang Zhuang

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Qu-Liang Chen

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Cai-Ru Wu

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Jin-Tao Hu

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Hou-Shi Zhou

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Wei-Hang Xie

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Xin Yi

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Shan-Shan Yu

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Zhi-Yu Peng

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Huan-Ming Yang

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Xiao-Hong Hong

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Jian-Huan Chen

Creative Commons Attribution 4.0 International

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language of work or name

English

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publication date

2018

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published in

Frontiers in Genetics

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volume

9

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page(s)

725

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copyright license

start time

28 January 2019

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Tena, a Drosophila gene related to tenascin, shows selective transcript localization.

1 reference

12 December 2020

Tenm, a Drosophila gene related to tenascin, is a new pair-rule gene

1 reference

12 December 2020

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1

1 reference

12 December 2020

Teneurin-1, a vertebrate homologue of the Drosophila pair-rule gene ten-m, is a neuronal protein with a novel type of heparin-binding domain

1 reference

12 December 2020

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

12 December 2020

Phylogenetic analysis of teneurin genes and comparison to the rearrangement hot spot elements of E. coli

1 reference

12 December 2020

Neuregulin 1 and susceptibility to schizophrenia

1 reference

12 December 2020

PRODH mutations and hyperprolinemia in a subset of schizophrenic patients

1 reference

12 December 2020

The murine Ten-m/Odz genes show distinct but overlapping expression patterns during development and in adult brain

1 reference

12 December 2020

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

1 reference

12 December 2020

Family-based association study of schizophrenia with 444 markers and analysis of a new susceptibility locus mapped to 11q13.3.

1 reference

12 December 2020

Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation

1 reference

12 December 2020

Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2).

1 reference

12 December 2020

A review of the evidence from family, twin and adoption studies for a genetic contribution to adult psychiatric disorders

1 reference

12 December 2020

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

12 December 2020

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

1 reference

12 December 2020

11-year follow-up of mortality in patients with schizophrenia: a population-based cohort study (FIN11 study).

1 reference

12 December 2020

GABRB2 in schizophrenia and bipolar disorder: disease association, gene expression and clinical correlations

1 reference

12 December 2020

Genetic structure of the Han Chinese population revealed by genome-wide SNP variation

1 reference

12 December 2020

Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy

1 reference

12 December 2020

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

1 reference

12 December 2020

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

1 reference

12 December 2020

A whole-genome analysis of premature termination codons

1 reference

12 December 2020

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

1 reference

12 December 2020

Mouse genomic variation and its effect on phenotypes and gene regulation

1 reference

12 December 2020

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

1 reference

12 December 2020

Genome-wide association studies of schizophrenia: does bigger lead to better results?

1 reference

12 December 2020

Genetic overlap of schizophrenia and bipolar disorder in a high-density linkage survey in the Portuguese Island population

1 reference

12 December 2020

Analysis of the DISC1 translocation partner (11q14.3) in genetic risk of schizophrenia

1 reference

12 December 2020

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

1 reference

12 December 2020

A mutation in NPAS3 segregates with mental illness in a small family

1 reference

12 December 2020

Deletion at the SLC1A1 glutamate transporter gene co-segregates with schizophrenia and bipolar schizoaffective disorder in a 5-generation family

1 reference

12 December 2020

An LRRTM4-HSPG complex mediates excitatory synapse development on dentate gyrus granule cells

1 reference

12 December 2020

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations

1 reference

12 December 2020

Autozygome sequencing expands the horizon of human knockout research and provides novel insights into human phenotypic variation.

1 reference

12 December 2020

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

1 reference

12 December 2020

A polygenic burden of rare disruptive mutations in schizophrenia

1 reference

12 December 2020

Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.

1 reference

12 December 2020

Biological insights from 108 schizophrenia-associated genetic loci

1 reference

12 December 2020

Rare variants in neuronal excitability genes influence risk for bipolar disorder

1 reference

12 December 2020

Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor

1 reference

12 December 2020

Comparative analysis of MBD-seq and MeDIP-seq and estimation of gene expression changes in a rodent model of schizophrenia

1 reference

12 December 2020

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

1 reference

12 December 2020

Shifting the focus toward rare variants in schizophrenia to close the gap from genotype to phenotype.

1 reference

12 December 2020

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.

1 reference

12 December 2020