NRXN1 gene
Evidence from:
primary |
all sources
Related entities (13)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| NRXN1 | risk_factor_for | addiction | — | 1 |
| NRXN1 | associated_with | alcohol abuse | — | 1 |
| NRXN1 | risk_factor_for | autism | — | 1 |
| NRXN1 | associated_with | autism | — | 1 |
| NRXN1 | risk_factor_for | autism spectrum disorder | — | 1 |
| NRXN1 | associated_with | autism spectrum disorder | — | 1 |
| NRXN1 | associated_with | cocaine | — | 1 |
| NRXN1 | risk_factor_for | cocaine | — | 1 |
| NRXN1 | associated_with | nicotine | 0.0001 | 2 |
| NRXN1 | risk_factor_for | opioid dependence | — | 1 |
| NRXN1 | associated_with | schizophrenia | — | 1 |
| NRXN1 | associated_with | tobacco dependence | — | 1 |
| NRXN1 | risk_factor_for | TS | — | 1 |
Mentioned in (23)
Papers in which this entity is mentioned.
- Connectome-seq: High-throughput Mapping of Neuronal Connectivity at Single-Synapse Resolution via Barcode Sequencing. (2025)
- Impact of alcohol exposure on neural development and network formation in human cortical organoids. (2023)
- TGF-β/Smad3 Signalling Modulates GABA Neurotransmission: Implications in Parkinson's Disease. (2020)
- Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
- Cannabis Teratology Explains Current Patterns of Coloradan Congenital Defects: The Contribution of Increased Cannabinoid Exposure to Rising Teratological Trends. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- Identification of novel candidate disease genes from de novo exonic copy number variants. (2017)
- The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
- Effect of Neuroinflammation on Synaptic Organization and Function in the Developing Brain: Implications for Neurodevelopmental and Neurodegenerative Disorders. (2017)
- DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
- Recent genetic findings in schizophrenia and their therapeutic relevance. (2015)
- Methylomic trajectories across human fetal brain development. (2015)
- The impact of environmental factors in severe psychiatric disorders. (2014)
- Distribution of disease-associated copy number variants across distinct disorders of cognitive development. (2013)
- Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. (2012)
- Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Divergent roles of ALS-linked proteins FUS/TLS and TDP-43 intersect in processing long pre-mRNAs. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- DISC1 at 10: connecting psychiatric genetics and neuroscience. (2011)
- Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. (2011)
- New insights into the genetics of addiction. (2009)
- Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking. (2008)
Merged raw entities (3)
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 |
|---|---|---|---|
| nrxn1 | gene | 23 | 35 |
| neurexin 1 | gene | 1 | 1 |
| neurexin-1α | gene | — | — |