(Q36247979)

13 August 2017

0 references

A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband (English)

1 reference

13 August 2017

1 reference

7

Judith L Rapoport

1 reference

13 August 2017

Nicole K A Wilson

1

1 reference

13 August 2017

Yohan Lee

2

1 reference

13 August 2017

Robert Long

3

1 reference

13 August 2017

Karen Hermetz

4

1 reference

13 August 2017

M Katharine Rudd

5

1 reference

13 August 2017

Rachel Miller

6

1 reference

13 August 2017

Anjené M Addington

8

1 reference

13 August 2017

language of work or name

1 reference

12 September 2011

1 reference

13 August 2017

Case reports in genetics

1 reference

13 August 2017

2011

1 reference

13 August 2017

585893

1 reference

Creative Commons Attribution 3.0 Unported

13 August 2017

start time

1 January 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

WRP/srGAP3 facilitates the initiation of spine development by an inverse F-BAR domain, and its loss impairs long-term memory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Disrupted-in-Schizophrenia 1 (DISC1) regulates spines of the glutamate synapse via Rac1

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

A genome-wide investigation of SNPs and CNVs in schizophrenia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Molecular genetics of schizophrenia

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

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

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3447216

Penetrance for copy number variants associated with schizophrenia.

1 October 2017

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2011%2F585893

The neurodevelopmental model of schizophrenia: what can very early onset cases tell us?

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2011%2F585893

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1155%2F2011%2F585893

Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3-p26.1.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23074677

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1155/2011/585893

1 reference

13 August 2017

1 reference

13 August 2017

PubMed publication ID

23074677

1 reference