A case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population | Behavioral and Brain Functions | Full Text
Information about each variant of interest in NRXN1. a Diagram of... | Download Scientific Diagram
JPM | Free Full-Text | Is NRXN1 Gene Expression an Important Marker of Treatment of Depressive Disorders? A Pilot Study
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression | Genetics in Medicine
Neuronal impact of patient-specific aberrant NRXN1α splicing | Nature Genetics
Allelic contribution of Nrxn1α to autism-relevant behavioral phenotypes in mice | PLOS Genetics
NRXN1 | Science Over a Cuppa
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1 - ScienceDirect
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Identification of Nrxn1γ protein as a Nrxn1 gene-derived CA10 receptor.... | Download Scientific Diagram
Cross-Platform Validation of Neurotransmitter Release Impairments in Schizophrenia Patient-Derived NRXN1-Mutant Neurons | bioRxiv
Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders - Ching - 2010 - American Journal of Medical Genetics Part B: Neuropsychiatric Genetics - Wiley Online Library
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases - Alfieri - 2020 - Genes, Brain and Behavior - Wiley Online Library
Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous
Disruption of Neurexin 1 Associated with Autism Spectrum Disorder - ScienceDirect
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila - ScienceDirect
A deletion of approximately 70 kb encompassing two exons (3,4) from the... | Download Scientific Diagram
Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders | Molecular Psychiatry
Frontiers | NRXN1 Deletion and Exposure to Methylmercury Increase Astrocyte Differentiation by Different Notch-Dependent Transcriptional Mechanisms
Table 1 from Resequencing and follow-up of neurexin 1 (NRXN1) in schizophrenia patients | Semantic Scholar
NRXN1 deletions and the double hit hypothesis of idiopathic epilepsy | Beyond the Ion Channel
2p16.3 (NRXN1) deletions
NRXN1 Gene - GeneCards | NRX1B Protein | NRX1B Antibody
Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived NRXN1-mutant neurons
Neurexin 1 variants as risk factors for suicide death | Molecular Psychiatry
Neurexin 1 (NRXN1) Deletions in Schizophrenia
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila - ScienceDirect
