(Q38260604)

1 September 2017

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title

Whole genome/exome sequencing in mood and psychotic disorders (English)

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1 September 2017

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whole genome sequencing

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1

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1 September 2017

language of work or name

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9 November 2014

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Psychiatry and Clinical Neurosciences

1 September 2017

published in

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1 September 2017

volume

69

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1 September 2017

issue

2

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1 September 2017

page(s)

65-76

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Guideline for treatment of bipolar disorder by the Japanese Society of Mood Disorders, 2012

1 September 2017

cites work

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“Meta-guidelines” for the management of patients with schizophrenia

21 January 2018

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Lost in translation: confusion about depression and antidepressant therapy in Japan

21 January 2018

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Review of mental-health-related stigma in Japan

21 January 2018

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Analysis of genetic inheritance in a family quartet by whole-genome sequencing

21 January 2018

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A de novo convergence of autism genetics and molecular neuroscience

21 January 2018

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A hybrid likelihood model for sequence-based disease association studies

21 January 2018

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Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder

21 January 2018

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Rare Genomic Variants Link Bipolar Disorder with Anxiety Disorders to CREB-Regulated Intracellular Signaling Pathways

21 January 2018

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Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate

21 January 2018

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A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder

21 January 2018

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Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data.

21 January 2018

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Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study.

21 January 2018

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Preliminary genome-wide association study of bipolar disorder in the Japanese population.

21 January 2018

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Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder

21 January 2018

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Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

21 January 2018

1 reference

The genetics of major depression

21 January 2018

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One gene, many neuropsychiatric disorders: lessons from Mendelian diseases.

21 January 2018

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A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk

21 January 2018

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Exome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegia

21 January 2018

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A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions

21 January 2018

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Mitochondrial dysfunction as the molecular basis of bipolar disorder: therapeutic implications.

21 January 2018

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MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions

21 January 2018

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Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic Variability

21 January 2018

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

21 January 2018

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Whole-exome sequencing identifies a polymorphism in the BMP5 gene associated with SSRI treatment response in major depression.

21 January 2018

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Molecular neurobiology of bipolar disorder: a disease of 'mood-stabilizing neurons'?

21 January 2018

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Exome sequencing supports a de novo mutational paradigm for schizophrenia.

21 January 2018

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

21 January 2018

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Loss-of-function variants in schizophrenia risk and SETD1A as a candidate susceptibility gene

21 January 2018

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Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism

21 January 2018

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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

21 January 2018

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Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

21 January 2018

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De novo mutations in schizophrenia implicate synaptic networks

21 January 2018

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Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

21 January 2018

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A polygenic burden of rare disruptive mutations in schizophrenia

21 January 2018

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Patterns of variation influencing antipsychotic treatment outcomes in South African first-episode schizophrenia patients

21 January 2018

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Increased l1 retrotransposition in the neuronal genome in schizophrenia

21 January 2018

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A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing.

21 January 2018

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Genic intolerance to functional variation and the interpretation of personal genomes

21 January 2018

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Rate of de novo mutations and the importance of father's age to disease risk

21 January 2018

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Role of immunological factors in the pathophysiology and diagnosis of bipolar disorder: comparison with schizophrenia

21 January 2018

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Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders

21 January 2018

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Somatic activation of AKT3 causes hemispheric developmental brain malformations

21 January 2018

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De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

21 January 2018

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Copy-number variation in the pathogenesis of autism spectrum disorder

21 January 2018

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The role of DNA copy number variation in schizophrenia.

21 January 2018

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De novo CNVs in bipolar affective disorder and schizophrenia

21 January 2018

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Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

21 January 2018

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

21 January 2018

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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

21 January 2018

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A population-specific uncommon variant in GRIN3A associated with schizophrenia.

21 January 2018

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Deep resequencing and association analysis of schizophrenia candidate genes.

21 January 2018

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A genotype-first approach to defining the subtypes of a complex disease

21 January 2018

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Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping

21 January 2018

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Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities

21 January 2018

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SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties

21 January 2018

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Disruptive CHD8 mutations define a subtype of autism early in development

21 January 2018

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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

21 January 2018

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Rare-variant association analysis: study designs and statistical tests

21 January 2018

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Rare-variant association testing for sequencing data with the sequence kernel association test

21 January 2018

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Testing for an unusual distribution of rare variants

21 January 2018

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A framework for the interpretation of de novo mutation in human disease

21 January 2018

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Performance comparison of four exome capture systems for deep sequencing

21 January 2018

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Performance comparison of whole-genome sequencing platforms

21 January 2018

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Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/PCN.12247

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release_f35o5eq2avaozau7ljpiwja6cm

1 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/f35o5eq2avaozau7ljpiwja6cm

mapped directly with Wikidata item

24 November 2022

based on heuristic

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