SCZ phenotype

Aliases: SCZ, Schizophrenia, schizophrenia

Evidence from: primary | all sources

Related entities (32)

Subject	Relation	Object	p-value	Evidence
22q11.2 deletion	risk_factor_for	SCZ	—	1
ASD	associated_with	SCZ	—	1
BiP	associated_with	SCZ	—	2
BiP	risk_factor_for	SCZ	—	1
CAD	risk_factor_for	SCZ	—	1
CAD	associated_with	SCZ	—	1
cannabis use	risk_factor_for	SCZ	—	1
CSMD1	risk_factor_for	SCZ	—	1
de novo variant	risk_factor_for	SCZ	—	2
de novo variant	associated_with	SCZ	—	2
FMR1	risk_factor_for	SCZ	—	1
inherited CNVs	risk_factor_for	SCZ	—	1
large rare CNVs	risk_factor_for	SCZ	—	1
MEF2C	risk_factor_for	SCZ	—	1
p-factor	associated_with	SCZ	—	1
PGC	associated_with	SCZ	—	1
polygenic risk score	associated_with	SCZ	—	1
Post-Traumatic Stress Disorder	associated_with	SCZ	—	1
rare CNV	associated_with	SCZ	—	1
rare CNVs	risk_factor_for	SCZ	—	1
risk allele	risk_factor_for	SCZ	—	1
rs2239547	associated_with	SCZ	6e-08	1
rs77378271	risk_factor_for	SCZ	2.13e-08	1
SCZ	associated_with	BiP	—	1
SCZ	associated_with	bipolar disorder	—	1
SCZ	associated_with	cognition	—	1
SCZ	associated_with	executive functioning	—	1
SCZ	associated_with	GABA	—	1
SCZ	associated_with	major depressive disorder	—	1
SCZ	associated_with	mood disorders	—	1
SCZ	associated_with	prefrontal cortex	—	1
SCZ	associated_with	TS	—	1

Mentioned in (25)

Papers in which this entity is mentioned.

Mapping the genetic landscape across 14 psychiatric disorders. (2026)
Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis. (2022)
Virtual Ontogeny of Cortical Growth Preceding Mental Illness. (2022)
Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data. (2022)
FXR1 regulation of parvalbumin interneurons in the prefrontal cortex is critical for schizophrenia-like behaviors. (2021)
Shared genetic architecture across psychiatric disorders. (2021)
The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences. (2021)
Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia. (2020)
ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (2020)
Increased power by harmonizing structural MRI site differences with the ComBat batch adjustment method in ENIGMA. (2020)
Impact of Proliferator-Activated Receptor γ Gene Polymorphisms on Risk of Schizophrenia: A Case-Control Study and Computational Analyses. (2020)
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders. (2019)
Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy children. (2015)
Genetics and genomics of psychiatric disease. (2015)
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
The psychiatric GWAS consortium: big science comes to psychiatry. (2010)

Merged raw entities (1)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.

Raw name	Type	Papers	Mentions
scz	phenotype	25	176