(Q46504843)

22 December 2017

title

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder (English)

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22 December 2017

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Manuel Mattheisen

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Maria Grigoroiu-Serbanescu

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Markus M Nöthen

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Sven Cichon

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S Cichon

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Mark Lathrop

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object named as

M Lathrop

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M Leboyer

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M Rietschel

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W Maier

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2

F A Degenhardt

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author name string

L Priebe

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B Haenisch

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V Nieratschker

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M Weingarten

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S Witt

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R Breuer

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T Paul

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M Alblas

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S Moebus

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S Schreiber

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P Propping

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T W Mühleisen

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language of work or name

English

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publication date

1 March 2011

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22 December 2017

published in

Molecular Psychiatry

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volume

17

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issue

4

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page(s)

421-432

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https://scigraph.springernature.com/pub.10.1038/mp.2011.8

exact match

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cites work

Progress and pitfalls: bipolar molecular linkage studies

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A pilot Swedish twin study of affective illness, including hospital- and population-ascertained subsamples

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Psychiatric genetics: progress amid controversy

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Major changes in our DNA lead to major changes in our thinking

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

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Large recurrent microdeletions associated with schizophrenia

21 January 2018

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Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

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Singleton deletions throughout the genome increase risk of bipolar disorder

21 January 2018

1 reference

Genomic landscape of a three-generation pedigree segregating affective disorder

21 January 2018

1 reference

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

21 January 2018

1 reference

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

1 reference

Psychiatric disorders in the relatives of probands with affective disorders. The Yale University--National Institute of Mental Health Collaborative Study.

21 January 2018

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A family study of bipolar I disorder in adolescence. Early onset of symptoms linked to increased familial loading and lithium resistance

21 January 2018

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The genetics of pediatric-onset bipolar disorder

21 January 2018

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Different familial transmission patterns in bipolar I disorder with onset before and after age 25.

21 January 2018

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Age at onset and gender resemblance in bipolar siblings.

21 January 2018

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The Structured Clinical Interview for DSM-III-R (SCID). I: History, rationale, and description

21 January 2018

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Computer-assisted phenotype characterization for genetic research in psychiatry

21 January 2018

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Age at onset in bipolar I affective disorder: further evidence for three subgroups

21 January 2018

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Incidence and distribution of first-episode mania by age: results from a 35-year study.

21 January 2018

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Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups

21 January 2018

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PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships

21 January 2018

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Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Facto

21 January 2018

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A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

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QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

21 January 2018

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NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

21 January 2018

1 reference

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 January 2018

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PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

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A dynamic gradient of Wnt signaling controls initiation of neurogenesis in the mammalian cortex and cellular specification in the hippocampus.

21 January 2018

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Wnt signaling in neuroprotection and stem cell differentiation

21 January 2018

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Whole-genome association study of bipolar disorder

21 January 2018

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

21 January 2018

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The thioredoxin-related redox-regulating protein nucleoredoxin inhibits Wnt-beta-catenin signalling through dishevelled

21 January 2018

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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

21 January 2018

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Disruption of neurexin 1 associated with autism spectrum disorder

21 January 2018

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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

21 January 2018

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Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures

21 January 2018

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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

21 January 2018

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Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

21 January 2018

1 reference

The breakpoint cluster region gene on chromosome 22q11 is associated with bipolar disorder.

21 January 2018

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Early and late onset bipolar disorders: two different forms of manic-depressive illness?

21 January 2018

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Genetics of bipolar disorder.

21 January 2018

1 reference

7 January 2021

Increase inGSK3β gene copy number variation in bipolar disorder

1 reference

7 January 2021

Age at onset in bipolar-related major affective illness: clinical and genetic implications

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7 January 2021

Heterozygous deletion of mitotic arrest-deficient protein 1 (MAD1) increases the incidence of tumors in mice

1 reference

7 January 2021

Disruption of the neurexin 1 gene is associated with schizophrenia

1 reference

7 January 2021

Identifiers

DOI

10.1038/MP.2011.8

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22 December 2017

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22 December 2017