Developmental psychopathology: the role of structural variation in the genome (Q38051773)

27 August 2017

Developmental psychopathology: the role of structural variation in the genome (English)

1 reference

27 August 2017

1

1 reference

27 August 2017

1 November 2012

1 reference

Development and Psychopathology

27 August 2017

1 reference

27 August 2017

24

1 reference

27 August 2017

4

1 reference

27 August 2017

1319-1334

1 reference

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications

27 August 2017

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

De novo rates and selection of large copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Penetrance for copy number variants associated with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Phenotypic variability and genetic susceptibility to genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Young males have a higher risk of developing schizophrenia: a Danish register study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Chromosomal disorders and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Schizophrenia and velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Should children with ADHD and normal intelligence be routinely screened for underlying cytogenetic abnormalities?

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Association within a family of a balanced autosomal translocation with major mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

The array CGH and its clinical applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Genomic structural variation in psychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Copy number variation in human health, disease, and evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Genetics of early onset cognitive impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Functional impact of global rare copy number variation in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Mental disorders in first-degree relatives of schizophrenics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Clinically detectable copy number variations in a Canadian catchment population of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Tourette syndrome is associated with recurrent exonic copy number variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

A unified genetic theory for sporadic and inherited autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Epilepsy and the new cytogenetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Microdeletions of 3q29 confer high risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Psychiatric family history and schizophrenia risk in Denmark: which mental disorders are relevant?

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Chromosomal abnormalities and mental illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Clan genomics and the complex architecture of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Cryptic telomere imbalance: a 15-year update

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

A forkhead-domain gene is mutated in a severe speech and language disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Cytogenetic Abnormalities in Attention-Deficit/Hyperactivity Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Accurate distinction of pathogenic from benign CNVs in mental retardation

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Cytogenetic findings in 250 schizophrenics: evidence confirming an excess of the X chromosome aneuploidies and pericentric inversion of chromosome 9

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

An extended family with a dominantly inherited speech disorder

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Mechanisms for human genomic rearrangements

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Search for linkage to schizophrenia on the X and Y chromosomes

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1.

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Late paraphrenia and its bearing on the aetiology of schizophrenia

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Developmental psychopathology: concepts and challenges

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Chromosomal abnormalities and schizophrenia

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

The expression of schizophrenia, affective disorder and vulnerability to tardive dyskinesia in an extensive pedigree

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Genetically complex epilepsies, copy number variants and syndrome constellations

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

Computational neuroanatomy of speech production.

1 reference

https://api.crossref.org/works/10.1017%2FS0954579412000739

7 January 2021

10.1017/S0954579412000739

Identifiers

DOI

1 reference

27 August 2017

1 reference

PubMed ID

23062300