Exome sequencing supports a de novo mutational paradigm for schizophrenia. - Wikidata - wikimedia - TriplyDB

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

http://www.wikidata.org/entity/Q30405748

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Clinical application of exome sequencing in undiagnosed genetic conditions In search of low-frequency and rare variants affecting complex traits The dysconnection hypothesis (2016)Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology Toward a Deeper Understanding of the Genetics of Bipolar Disorder Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.Following the genes: a framework for animal modeling of psychiatric disorders Disease gene identification strategies for exome sequencing A review of post-GWAS prioritization approaches CNVs: harbingers of a rare variant revolution in psychiatric genetics The Use of Induced Pluripotent Stem Cell Technology to Advance Autism Research and Treatment Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss The contribution of de novo coding mutations to autism spectrum disorder Paternal age effect mutations and selfish spermatogonial selection: causes and consequences for human disease De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome Deleterious GRM1 mutations in schizophrenia Impairment of translation in neurons as a putative causative factor for autism Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects Properties and rates of germline mutations in humans Whole-genome sequencing in an autism multiplex family 'Sifting the significance from the data' - the impact of high-throughput genomic technologies on human genetics and health care Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations De Novo Gene Disruptions in Children on the Autistic Spectrum Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci De novo mutations revealed by whole-exome sequencing are strongly associated with autism Investigation of SHANK3 in schizophrenia.De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.Impact of the next-generation sequencing data depth on various biological result inferences.The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors.Integrating multiple genomic data to predict disease-causing nonsynonymous single nucleotide variants in exome sequencing studies.VariantDB: a flexible annotation and filtering portal for next generation sequencing data.Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.Neuroinflammation - using big data to inform clinical practice.Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence.Paternal age and psychiatric disorders: A review.Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathies

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

http://www.wikidata.org/entity/Q30405748

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2011 nî lūn-bûn

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2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի օգոստոսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

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Nature Genetics

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Exome sequencing supports a de novo mutational paradigm for schizophrenia

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P2093

Bin Xu

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Braden Boone

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Brooks Plummer

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Joseph A Gogos

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Maria Karayiorgou

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P2860

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

Rare chromosomal deletions and duplications increase risk of schizophrenia

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

A map of human genome variation from population-scale sequencing

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

Accurate whole human genome sequencing using reversible terminator chemistry

Fast and accurate short read alignment with Burrows-Wheeler transform

Large recurrent microdeletions associated with schizophrenia

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

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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9

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Phillip Dexheimer

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