Exome sequencing supports a de novo mutational paradigm for schizophrenia. (Q30405748)

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9 February 2020

title

Exome sequencing supports a de novo mutational paradigm for schizophrenia (English)

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9 February 2020

0 references

2

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9 February 2020

Phillip Dexheimer

3

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9 February 2020

Shawn Levy

6

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9 February 2020

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Joseph A Gogos

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9 February 2020

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Maria Karayiorgou

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9 February 2020

author name string

Bin Xu

1

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9 February 2020

Braden Boone

4

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9 February 2020

Brooks Plummer

5

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9 February 2020

publication date

7 August 2011

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9 February 2020

language of work or name

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9 February 2020

volume

43

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9 February 2020

issue

9

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9 February 2020

page(s)

864-868

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

9 February 2020

cites work

1 reference

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Deficiency of Dgcr8 , a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex

20 June 2018

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Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

20 June 2018

1 reference

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Type 7 Adenylyl Cyclase is Involved in the Ethanol and CRF Sensitivity of GABAergic Synapses in Mouse Central Amygdala

20 June 2018

1 reference

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A map of human genome variation from population-scale sequencing

20 June 2018

1 reference

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Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

20 June 2018

1 reference

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22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

20 June 2018

1 reference

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Uncovering the roles of rare variants in common disease through whole-genome sequencing

20 June 2018

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Impaired hippocampal–prefrontal synchrony in a genetic mouse model of schizophrenia

20 June 2018

1 reference

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Rate, molecular spectrum, and consequences of human mutation

20 June 2018

1 reference

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Cognition in mouse models of schizophrenia susceptibility genes

20 June 2018

1 reference

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Detection of nonneutral substitution rates on mammalian phylogenies

20 June 2018

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Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans

20 June 2018

1 reference

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Fast and accurate short read alignment with Burrows-Wheeler transform

20 June 2018

1 reference

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Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

20 June 2018

1 reference

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

20 June 2018

1 reference

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Accurate whole human genome sequencing using reversible terminator chemistry

20 June 2018

1 reference

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Large recurrent microdeletions associated with schizophrenia

20 June 2018

1 reference

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Rare chromosomal deletions and duplications increase risk of schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3196550

Strong association of de novo copy number mutations with sporadic schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3196550

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

20 June 2018

1 reference

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Genomic rearrangements and sporadic disease

20 June 2018

1 reference

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Modeling madness in mice: one piece at a time

20 June 2018

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Nine new human Rhodopsin family G-protein coupled receptors: identification, sequence characterisation and evolutionary relationship

20 June 2018

1 reference

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The human and mouse repertoire of the adhesion family of G-protein-coupled receptors

20 June 2018

1 reference

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Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1

20 June 2018

1 reference

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

20 June 2018

1 reference

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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

20 June 2018

1 reference

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Cloning of SEZ-12 encoding seizure-related and membrane-bound adhesion protein

20 June 2018

1 reference

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

20 June 2018

1 reference

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A polygenic theory of schizophrenia

20 June 2018

1 reference

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Amino acid difference formula to help explain protein evolution

20 June 2018

1 reference

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A de novo paradigm for mental retardation

20 June 2018

1 reference

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Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

26 November 2018

1 reference

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Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database

26 November 2018

1 reference

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26 November 2018

Identifiers

DOI

10.1038/NG.902

1 reference

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9 February 2020

1 reference

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9 February 2020

PubMed publication ID

21822266

1 reference