(Q37953976)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Annual research review: impact of advances in genetics in understanding developmental psychopathology (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

2

Judith L Rapoport

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

8 November 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Child Psychology and Psychiatry

16 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

53

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

510-518

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22067053%20AND%20SRC:MED&resulttype=core&format=json

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

16 January 2020

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Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease

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Therapeutic implications of the mGluR theory of fragile X mental retardation

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Array-based DNA diagnostics: let the revolution begin

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A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.

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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

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Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

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Increased alpha-defensins as a blood marker for schizophrenia susceptibility

21 January 2018

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Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls

21 January 2018

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Mechanism-based approaches to treating fragile X

21 January 2018

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

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No evidence that rare coding variants in ZNF804A confer risk of schizophrenia.

21 January 2018

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Genomic medicine--an updated primer

21 January 2018

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Nature of the molecular defect in phenylketonuria and hyperphenylalaninaemia

21 January 2018

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De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

21 January 2018

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Novel de novo SHANK3 mutation in autistic patients

21 January 2018

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Neurodevelopmental disorders: hope for a new beginning.

21 January 2018

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The genetics of obsessive-compulsive disorder and Tourette syndrome: an epidemiological and pathway-based approach for gene discovery

21 January 2018

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Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome

21 January 2018

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

21 January 2018

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Recent advances in the genetics of autism

21 January 2018

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Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

21 January 2018

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Child and adolescent psychiatric genetics

21 January 2018

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Detection of large-scale variation in the human genome

21 January 2018

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Neurodevelopmental mechanisms of schizophrenia: understanding disturbed postnatal brain maturation through neuregulin-1-ErbB4 and DISC1.

21 January 2018

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

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The pursuit of genome-wide association studies: where are we now?

21 January 2018

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

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Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

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Schizophrenia as a disorder of neurodevelopment

21 January 2018

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Genetic mechanisms in childhood psychiatric disorders

21 January 2018

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Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

21 January 2018

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Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases.

21 January 2018

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Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

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Duplication hotspots, rare genomic disorders, and common disease

21 January 2018

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Disruption of two novel genes by a translocation co-segregating with schizophrenia

21 January 2018

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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

21 January 2018

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Predictive and diagnostic genetic testing in psychiatry

21 January 2018

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Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

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Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

21 January 2018

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The next exclusion debate: assessing technology, ethics, and intellectual disability after the Human Genome Project

21 January 2018

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Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

21 January 2018

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Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

21 January 2018

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Identification of loci associated with schizophrenia by genome-wide association and follow-up

21 January 2018

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Striatal and white matter predictors of estimated diagnosis for Huntington disease

21 January 2018

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The current status of urban-rural differences in psychiatric disorders

21 January 2018

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Imaging-genetics applications in child psychiatry

21 January 2018

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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.

21 January 2018

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The future of genetics in psychology and psychiatry: microarrays, genome-wide association, and non-coding RNA

21 January 2018

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Attention-deficit/hyperactivity disorder: advancing on pharmacogenomics

21 January 2018

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The neurodevelopmental model of schizophrenia: update 2005.

21 January 2018

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Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited

21 January 2018

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Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents

21 January 2018

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The future of genetic studies of complex human diseases

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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Childhood schizophrenia reconsidered

21 January 2018

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Relationships between child and adult psychiatric disorders. Some research considerations

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02478.X

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02478.X

Attention-deficit/hyperactivity disorder is characterized by a delay in cortical maturation

21 January 2018

1 reference

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Clinical genetic testing for patients with autism spectrum disorders

21 January 2018

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Interstitial deletion of (17)(p11.2p11.2) in nine patients

21 January 2018

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The Genetics of Child Psychiatric Disorders: Focus on Autism and Tourette Syndrome

21 January 2018

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Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

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Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

21 January 2018

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De novo truncating mutation in Kinesin 17 associated with schizophrenia

21 January 2018

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The genetics of attention deficit hyperactivity disorder

21 January 2018

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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

21 January 2018

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Transcriptomic analysis of autistic brain reveals convergent molecular pathology

21 January 2018

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A bivariate twin study of regional brain volumes and verbal and nonverbal intellectual skills during childhood and adolescence

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

21 January 2018

1 reference

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Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

21 January 2018

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Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

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21 January 2018

1 reference

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

21 January 2018

1 reference

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Phenotypic variations on the theme of CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-7610.2011.02478.X

21 January 2018

1 reference

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