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Effect of DISC1 on the P300 Waveform in Psychosis

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DISC1 (disrupted-in-schizophrenia 1) is associated with cortical grey matter volumes in the human brain: a voxel-based morphometry (VBM) study.

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DBZ (DISC1-binding zinc finger protein)-deficient mice display abnormalities in basket cells in the somatosensory cortices.

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The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

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Gender-specific association of TSNAX/DISC1 locus for schizophrenia and bipolar affective disorder in South Indian population

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Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

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A Disrupted-in-Schizophrenia 1 Gene Variant is Associated with Clinical Symptomatology in Patients with First-Episode Psychosis

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A Tail of Two Signals: The C Terminus of the A2A-Adenosine Receptor Recruits Alternative Signaling Pathways

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Translating advances in the molecular basis of schizophrenia into novel cognitive treatment strategies

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Alterations in dendrite and spine morphology of cortical pyramidal neurons in DISC1-binding zinc finger protein (DBZ) knockout mice

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Pathophysiology of Schizophrenia

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Animal Models of Schizophrenia

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The cortical thickness phenotype of individuals with DISC1 translocation resembles schizophrenia

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Chasing genes for mood disorders and schizophrenia in genetically isolated populations

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DISC1 and Striatal Volume: A Potential Risk Phenotype For mental Illness

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The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484

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The Cognitive Genetics of Neuropsychiatric Disorders

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The Genetics of Schizophrenia Converge Upon the NMDA Glutamate Receptor

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Translin-Associated Factor X Gene (TSNAX) may be Associated with Female major Depressive Disorder in the Japanese Population

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Effects of a mis‐sense DISC1 variant on brain activation in two cohorts at high risk of bipolar disorder or schizophrenia

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Disease and genetic contributions toward local tissue volume disturbances in schizophrenia: A tensor‐based morphometry study

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Increased inhibition and enhancement of memory retrieval are associated with reduced hippocampal volume

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Microdissection‐based high‐resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes

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Clinical impact of recently detected susceptibility genes for schizophrenia

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Effect of DISC1 SNPs on brain structure in healthy controls and patients with a history of psychosis

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Molecular Genetic Models Related to Schizophrenia and Psychotic Illness: Heuristics and Challenges

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Effects of background mutations and single nucleotide polymorphisms (SNPs) on the Disc1 L100P behavioral phenotype associated with schizophrenia in mice

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Schizophrenia in the genetic era: a review from development history, clinical features and genomic research approaches to insights of susceptibility genes

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Interaction between DISC1 and CHL1 in regulation of neurite outgrowth

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Kognitive Störungen bei schizophrenen Patienten

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Primate-Accelerated Evolutionary Genes: Novel Routes to Drug Discovery in Psychiatric Disorders

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Unlocking the molecular mechanisms of antipsychotics – a new frontier for discovery

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Neurobiologicalendophenotypes of psychosis and schizophrenia

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Chromosomal abnormalities and psychosis

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The Neurodevelopmental Model of Schizophrenia: Updated

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Disrupted-in-Schizophrenia-1 SNPs and Susceptibility to Schizophrenia: Evidence from Malaysia

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Variants in regulatory elements of PDE4D associate with major mental illness in the Finnish population

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Gene expression changes related to immune processes associate with cognitive endophenotypes of schizophrenia

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In Silico Whole Genome Association Scan for Murine Prepulse Inhibition

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Mutations in DISC1 alter IP3R and voltage-gated Ca2+ channel functioning, implications for major mental illness

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Additive sex-specific influence of common non-synonymous DISC1 variants on amygdala, basal ganglia, and white cortical surface area in healthy young adults

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A prenatal interruption of DISC1 function in the brain exhibits a lasting impact on adult behaviors, brain metabolism, and interneuron development

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Markers of vulnerability in schizophrenia.

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Differential Contributions of Lateral Prefrontal Cortex Regions to Visual Memory Processes

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DISC1 mRNA expression is not influenced by common Cis‐acting regulatory polymorphisms or imprinting

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Association Study Between the Pericentrin (PCNT) Gene and Schizophrenia

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Deconstructing Schizophrenia: An Overview of the Use of Endophenotypes in Order to Understand a Complex Disorder

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Schizophrenia: Modeling a complex psychiatric disorder

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Association Study of Three Microsatellite Polymorphisms Located in Introns 1, 8, and 9 of DISC1 with Schizophrenia in the Chinese Han Population

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Effects of the Adverse Life Events and Disrupted in Schizophrenia-1 ( DISC1 ) Gene Polymorphisms on Acute Symptoms of Schizophrenia

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DISC1 gene polymorphisms and the risk of schizophrenia in an Iranian population: A preliminary study

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Intermediate Phenotypes in Genetic Studies of Schizophrenia

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The Center for Computational Biology: resources, achievements, and challenges

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Genetic Effects of DISC1 and G72 (DAOA) on Visual Learning of Patients with Schizophrenia

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Human Brain Volume: What’s in the Genes#

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Phospholipids and Insulin Resistance in Psychosis: A Lipidomics Study of Twin Pairs Discordant for Schizophrenia

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Association of DISC1, BDNF, and COMT polymorphisms with exploratory eye movement of schizophrenia in a Chinese Han population

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The Cognitive Neuroscience of Thought Disorder in Schizophrenia

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Effect of DISC1 Polymorphisms on the Long-term Course of Neurocognitive Deficits in Non-affective Psychosis

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Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia

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Preclinical neuroimaging of gene–environment interactions in psychiatric disease

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Classical Genetic Studies of Schizophrenia

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Forward and reverse genomic screens enhance the understanding of phenotypic variation in a large Chinese rhesus macaque cohort

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The associations between cognitive functions and TSNAX genetic variations in patients with schizophrenia

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The genetics of latent inhibition: studies of inbred and mutant mice

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Association of schizophrenia with the rs821633 polymorphism in the DISC1 gene among Han Chinese.

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Malformation of the Posterior Cerebellar Vermis Is a Common Neuroanatomical Phenotype of Genetically Engineered Mice on the C57BL/6 Background

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Chromosomal region 1q24.1 is associated with increased risk of schizophrenia in Pakistani population

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Neuropsychological Endophenotypes in Schizophrenia and Bipolar I Disorder: Yields from the Finnish Family and Twin Studies

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The Genetics of Schizophrenia

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Molecular Genetics of Schizophrenia: Focus on Symptom Dimensions

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Combining fMRI and DISC1 gene haplotypes to understand working memory-related brain activity in schizophrenia

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Impaired Neurogenesis as a Risk Factor for Schizophrenia and Related Mental Diseases

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Lack of association between translin-associated factor X gene (TSNAX) and methamphetamine dependence in the Japanese population

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Association study between schizophrenia and the DISC1 gene polymorphism.

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Prediction of Psychosis Through the Prodromal Syndrome

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Molecular Genetics of Schizophrenia and Related Intermediate Phenotypes in a Founder Population

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Genes, hypoxia and schizophrenia

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Dissecting the Molecular Causes of Schizophrenia

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