(Q52884385)

English

Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports.

scientific article published on 16 February 2016

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Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports. (English)

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Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

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Catherine A. Brownstein

1

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

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Europe PubMed Central

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Robin J Kleiman

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Robin J Kleiman

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9 May 2018

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Kaya Bilguvar

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9 May 2018

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Elizabeth C Engle

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Meghan C Towne

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http://europepmc.org/abstract/PMC/4833544

Eugene J D'Angelo

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Jonathan Picker

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http://europepmc.org/abstract/PMC/4833544

Jason M Fogler

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Devon Carroll

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http://europepmc.org/abstract/PMC/4833544

Rachel C O Schmitt

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Robert R Wolff

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Yiping Shen

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Va Lip

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http://europepmc.org/abstract/PMC/4833544

April Kim

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http://europepmc.org/abstract/PMC/4833544

Sahil Tembulkar

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Kyle O'Donnell

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

Joseph Gonzalez-Heydrich

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

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16 February 2016

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http://europepmc.org/abstract/PMC/4833544

American Journal of Medical Genetics

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

170A

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9 May 2018

http://europepmc.org/abstract/PMC/4833544

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http://europepmc.org/abstract/PMC/4833544

1165-1173

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Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

1 reference

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Ubiquitin-proteasome dependent degradation of GABAAα1 in autism spectrum disorder

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Sequencing and expression analyses of the synaptic lipid raft adapter gene PAG1 in schizophrenia

1 reference

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Transcriptional targets of the schizophrenia risk gene MIR137.

1 reference

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Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.

1 reference

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22 May 2018

Genetic association between the dopamine D1-receptor gene and paranoid schizophrenia in a northern Han Chinese population

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22 May 2018

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

1 reference

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22 May 2018

Copy number variation in schizophrenia in Sweden

1 reference

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22 May 2018

Relationship between genetic polymorphisms in the DRD5 gene and paranoid schizophrenia in northern Han Chinese

1 reference

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22 May 2018

Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci

1 reference

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22 May 2018

Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex

1 reference

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22 May 2018

Analysis of copy number variations at 15 schizophrenia-associated loci.

1 reference

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22 May 2018

New findings in the genetics of schizophrenia

1 reference

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22 May 2018

Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus

1 reference

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22 May 2018

Chronic exposure of mutant DISC1 mice to lead produces sex-dependent abnormalities consistent with schizophrenia and related mental disorders: a gene-environment interaction study

1 reference

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22 May 2018

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

1 reference

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22 May 2018

The ubiquitin-proteasome system as a critical regulator of synaptic plasticity and long-term memory formation

1 reference

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22 May 2018

Dysfunction of the ubiquitin proteasome and ubiquitin-like systems in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4833544

22 May 2018

Copy number variations in neurodevelopmental disorders

1 reference

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Activity-dependent growth of new dendritic spines is regulated by the proteasome

1 reference

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Expression and biochemical characterization of the human enzyme N-terminal asparagine amidohydrolase

1 reference

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Phenotypic manifestations of copy number variation in chromosome 16p13.11.

1 reference

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Behavioural phenotyping assays for mouse models of autism

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LIS1 and NudE induce a persistent dynein force-producing state

1 reference

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

1 reference

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22 May 2018

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

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22 May 2018

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

1 reference

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22 May 2018

DISC1, PDE4B, and NDE1 at the centrosome and synapse

1 reference

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22 May 2018

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

1 reference

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22 May 2018

22q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features keywords

1 reference

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22 May 2018

Mitotic spindle regulation by Nde1 controls cerebral cortical size

1 reference

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

1 reference

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1 reference

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1 reference

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22 May 2018

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1 reference

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

1 reference

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22 May 2018

ANK3 gene expression in bipolar disorder and schizophrenia.

1 reference

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13 August 2018

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1 reference

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13 August 2018

DNA hypermethylation of serotonin transporter gene promoter in drug naïve patients with schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4833544

13 August 2018

Efficient strategy for detecting gene × gene joint action and its application in schizophrenia

1 reference

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13 August 2018

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4833544

13 August 2018

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4833544

13 August 2018

Standardizing ADOS scores for a measure of severity in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.37595

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1 reference

https://pubmed.ncbi.nlm.nih.gov/26887912

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1 reference

https://pubmed.ncbi.nlm.nih.gov/26887912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TPH2 gene polymorphisms in the regulatory region are associated with paranoid schizophrenia in Northern Han Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/26887912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distal Xq28 microdeletions: clarification of the spectrum of contiguous gene deletions involving ABCD1, BCAP31, and SLC6A8 with a new case and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/26887912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.37595

1 reference

Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 May 2018

http://europepmc.org/abstract/PMC/4833544

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