Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q34381708)
Watch
English
The genomics of schizophrenia: update and implications.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
title
The genomics of schizophrenia: update and implications
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
main subject
schizophrenia
0 references
genomics
0 references
author
Paola Giusti-Rodríguez
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
Patrick F. Sullivan
series ordinal
2
object named as
Patrick F Sullivan
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
language of work or name
English
0 references
publication date
1 November 2013
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
number of pages
7
1 reference
based on heuristic
inferred from page(s)
published in
Journal of Clinical Investigation
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
volume
123
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
page(s)
4557-4563
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
issue
11
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
cites work
Questions about DISC1 as a genetic risk factor for schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Major channels involved in neuropsychiatric disorders and therapeutic perspectives
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genetics of cardiac electrical disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
An integrated encyclopedia of DNA elements in the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Using summary data from the danish national registers to estimate heritabilities for schizophrenia, bipolar disorder, and major depressive disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genetic architectures of psychiatric disorders: the emerging picture and its implications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Patterns and rates of exonic de novo mutations in autism spectrum disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
CNVs: harbingers of a rare variant revolution in psychiatric genetics
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Five years of GWAS discovery
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
High frequencies of de novo CNVs in bipolar disorder and schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Chromosome 1p21.3 microdeletions comprising DPYD and MIR137 are associated with intellectual disability
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide association study identifies five new schizophrenia loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Signaling complexes of voltage-gated calcium channels
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Exome sequencing supports a de novo mutational paradigm for schizophrenia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Initial impact of the sequencing of the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
A map of human genome variation from population-scale sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genomic analysis of mental illness: a changing landscape
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Cross talk between microRNA and epigenetic regulation in adult neurogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Narrowing the boundaries of the genetic architecture of schizophrenia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Microduplications of 16p11.2 are associated with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common variants on chromosome 6p22.1 are associated with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common variants conferring risk of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common genetic variation and human traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Population analysis of large copy number variants and hotspots of human genetic disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
A framework for interpreting genome-wide association studies of psychiatric disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Disruption of the neurexin 1 gene is associated with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Schizophrenia and sudden cardiac death: a review
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Large recurrent microdeletions associated with schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Rare chromosomal deletions and duplications increase risk of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Structural neuroimaging in psychosis: a systematic review and economic evaluation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Structural variation of chromosomes in autism spectrum disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Association between microdeletion and microduplication at 16p11.2 and autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Recurrent 16p11.2 microdeletions in autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Strong association of de novo copy number mutations with autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Voltage-gated calcium channels in genetic diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Schizophrenia and increased risks of cardiovascular disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Role of hippocampal Cav1.2 Ca2+ channels in NMDA receptor-independent synaptic plasticity and spatial memory
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
The Economic Burden of Schizophrenia in the United States in 2002
2 references
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24177465
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Antipsychotic drugs and QT prolongation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Voltage-dependent calcium channels and cardiac pacemaker activity: from ionic currents to genes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
A systematic review of the prevalence of schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
The global burden of typhoid fever
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
The International HapMap Project
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
The molecular genetics of schizophrenia: new findings promise new insights
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Replication validity of genetic association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Initial sequencing and analysis of the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Epidemiology of schizophrenia: the global burden of disease and disability
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Medical comorbidity in schizophrenia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
The future of genetic studies of complex human diseases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Comorbidity of mental disorders with alcohol and other drug abuse. Results from the Epidemiologic Catchment Area (ECA) Study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
6 July 2018
Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
A system-level transcriptomic analysis of schizophrenia using postmortem brain tissue samples.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
Epigenetics as a unifying principle in the aetiology of complex traits and diseases.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
Conditional forebrain deletion of the L-type calcium channel Ca V 1.2 disrupts remote spatial memories in mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3809776
retrieved
27 October 2018
Depression in chronic schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24177465
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increased exonic de novo mutation rate in individuals with schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24177465
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Excess mortality of mental disorder
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24177465
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Schizophrenia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24177465
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI66031
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
PMCID
3809776
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
PubMed ID
24177465
1 reference
stated in
Europe PubMed Central
PMCID
3809776
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24177465%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 February 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit