High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy (Q34084054)

30 July 2017

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy (English)

1 reference

30 July 2017

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4

Chad A Shaw

1 reference

30 July 2017

Larissa R Stewart

1

1 reference

30 July 2017

April L Hall

series ordinal

2

1 reference

30 July 2017

Sung-Hae L Kang

series ordinal

3

1 reference

30 July 2017

Arthur L Beaudet

series ordinal

5

1 reference

30 July 2017

25 November 2011

1 reference

30 July 2017

1 reference

30 July 2017

12

1 reference

30 July 2017

154

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-12-154

30 July 2017

0 references

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Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism.

28 July 2018

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Detection of clinically relevant exonic copy-number changes by array CGH.

28 July 2018

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Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

28 July 2018

1 reference

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

28 July 2018

1 reference

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

28 July 2018

1 reference

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Genetics of early-onset obsessive-compulsive disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

28 July 2018

1 reference

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Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Nucleotide variation in central nervous system genes among male suicide attempters

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

15q13.3 microdeletions increase risk of idiopathic generalized epilepsy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Large recurrent microdeletions associated with schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

28 July 2018

1 reference

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Recurrent 16p11.2 microdeletions in autism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Global variation in copy number in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT

28 July 2018

1 reference

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Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Clinical features of 78 adults with 22q11 Deletion Syndrome.

28 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Penetrance for copy number variants associated with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Microdeletions of 3q29 confer high risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

The Internet-based MGS2 control sample: self report of mental illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Novel linkage to chromosome 20p using latent classes of psychotic illness in 270 Irish high-density families

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Changes in NMDA receptor subunits and interacting PSD proteins in dorsolateral prefrontal and anterior cingulate cortex indicate abnormal regional expression in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Upregulated expression of postsynaptic density-93 and N-methyl-D-aspartate receptors subunits 2B mRNA in temporal lobe tissue of epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Evidence for abnormal forward trafficking of AMPA receptors in frontal cortex of elderly patients with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Correlation of transcriptome profile with electrical activity in temporal lobe epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Structures and molecular mechanisms for common 15q13.3 microduplications involving CHRNA7: benign or pathological?

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Evidence of association of serotonin transporter gene polymorphisms with schizophrenia in a South Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Association of syndromic mental retardation and autism with 22q11.2 duplication.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Comorbidity of hospital-treated psychiatric and physical disorders with special reference to schizophrenia: a 28 year follow-up of the 1966 northern Finland general population birth cohort.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3239290

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

28 October 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-154

Pharmaco-genetically guided treatment of recurrent rage outbursts in an adult male with 15q13.3 deletion syndrome

21 January 2018

1 reference

12 December 2020

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

12 December 2020

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13

1 reference

12 December 2020

Gene expression of PSD95 in prefrontal cortex and hippocampus in schizophrenia

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-12-154

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference

30 July 2017

1 reference