Loss of Nicastrin from Oligodendrocytes Results in Hypomyelination and Schizophrenia with Compulsive Behavior

The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans

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Presenilins and  -Secretase: Structure, Function, and Role in Alzheimer Disease

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Treating the Developing Brain: Implications from Human Imaging and Mouse Genetics

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Paying more attention to attention: Towards more comprehensive cognitive translation using mouse models of Alzheimer's disease

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White Matter Predictors of Cognitive Functioning in Older Adults

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Behavioral alterations associated with targeted disruption of exons 2 and 3 of the Disc1 gene in the mouse

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Death receptor 6 negatively regulates oligodendrocyte survival, maturation and myelination

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Erroneous analyses of interactions in neuroscience: a problem of significance

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Biochemical and Functional Interaction of Disrupted-in-Schizophrenia 1 and Amyloid Precursor Protein Regulates Neuronal Migration during Mammalian Cortical Development

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Neuroligin-1 Deletion Results in Impaired Spatial Memory and Increased Repetitive Behavior

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Integrating common and rare genetic variation in diverse human populations

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Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive–like behaviors in mice

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Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia

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 -Secretase Gene Mutations in Familial Acne Inversa

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Glu-333 of Nicastrin Directly Participates in γ-Secretase Activity

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Conditional Forebrain Inactivation of Nicastrin Causes Progressive Memory Impairment and Age-Related Neurodegeneration

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The Dopamine Hypothesis of Schizophrenia: Version III--The Final Common Pathway

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Neurodevelopmental mechanisms of schizophrenia: understanding disturbed postnatal brain maturation through neuregulin-1–ErbB4 and DISC1

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Assembly, Maturation, and Trafficking of the γ-Secretase Complex in Alzheimers Disease

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The role of protease activity in ErbB biology

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Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

(2008) Frank Dudbridge   HUMAN HEREDITY

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

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Deficiency of Aph1B/C- -secretase disturbs Nrg1 cleavage and sensorimotor gating that can be reversed with antipsychotic treatment

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Alteration of BACE1-dependent NRG1/ErbB4 signaling and schizophrenia-like phenotypes in BACE1-null mice

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Psychiatric Comorbidities and Schizophrenia

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White matter in learning, cognition and psychiatric disorders

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