Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements

The impact of genetics on future drug discovery in schizophrenia

(2017) Mitsuyuki Matsumoto et al.   Expert Opinion on Drug Discovery

Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studies

(2017) X Xiao et al.   MOLECULAR PSYCHIATRY

Altered fucosyltransferase expression in the superior temporal gyrus of elderly patients with schizophrenia

(2017) Toni M. Mueller et al.   SCHIZOPHRENIA RESEARCH

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics

(2017) Ina Giegling et al.   WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY

Chromosome conformation elucidates regulatory relationships in developing human brain

(2016) Hyejung Won et al.   NATURE

Mental disorders of known aetiology and precision medicine in psychiatry: a promising but neglected alliance

(2016) D. Fraguas et al.   PSYCHOLOGICAL MEDICINE

Molecular Risk Factors for Schizophrenia

(2016) Shira Modai et al.   TRENDS IN MOLECULAR MEDICINE

Sensory Processing Dysfunction in the Personal Experience and Neuronal Machinery of Schizophrenia

(2015) Daniel C. Javitt et al.   AMERICAN JOURNAL OF PSYCHIATRY

The Brief Negative Symptom Scale (BNSS): Independent validation in a large sample of Italian patients with schizophrenia

(2015) A. Mucci et al.   EUROPEAN PSYCHIATRY

De novo mutations from sporadic schizophrenia cases highlight important signaling genes in an independent sample

(2015) Thorsten M. Kranz et al.   SCHIZOPHRENIA RESEARCH

Genetic studies of schizophrenia: an update

(2015) Jingchun Chen et al.   Neuroscience Bulletin

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia

(2015) E Rees et al.   Translational Psychiatry

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

(2014) S E McCarthy et al.   MOLECULAR PSYCHIATRY

De novo mutations in schizophrenia implicate synaptic networks

(2014) Menachem Fromer et al.   NATURE

An atlas of active enhancers across human cell types and tissues

(2014) Robin Andersson et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

(2014) Ivan Iossifov et al.   NATURE

Biological insights from 108 schizophrenia-associated genetic loci

(2014)   NATURE

The influence of illness-related variables, personal resources and context-related factors on real-life functioning of people with schizophrenia

(2014) Silvana Galderisi et al.   World Psychiatry

A Role for Noncoding Variation in Schizophrenia

(2014) Panos Roussos et al.   Cell Reports

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

(2013) Jennifer Gladys Mulle et al.   BIOLOGICAL PSYCHIATRY

Analysis of copy number variations at 15 schizophrenia-associated loci

(2013) Elliott Rees et al.   BRITISH JOURNAL OF PSYCHIATRY

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

(2013) Stephan Ripke et al.   NATURE GENETICS

Wnt1-regulated genetic networks in midbrain dopaminergic neuron development

(2013) W. Wurst et al.   Journal of Molecular Cell Biology

The Enhancer Landscape during Early Neocortical Development Reveals Patterns of Dense Regulation and Co-option

(2013) Aaron M. Wenger et al.   PLoS Genetics

MAGI1 Copy Number Variation in Bipolar Affective Disorder and Schizophrenia

(2012) Robert Karlsson et al.   BIOLOGICAL PSYCHIATRY

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia

(2012) Bin Xu et al.   NATURE GENETICS

The X-Linked Intellectual Disability Protein TSPAN7 Regulates Excitatory Synapse Development and AMPAR Trafficking

(2012) Silvia Bassani et al.   NEURON

Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients

(2012) Takayoshi Koide et al.   PLoS One

Enhancer Chip: Detecting Human Copy Number Variations in Regulatory Elements

(2012) Marco Savarese et al.   PLoS One

Systematic Localization of Common Disease-Associated Variation in Regulatory DNA

(2012) M. T. Maurano et al.   SCIENCE

Motor Chip: A Comparative Genomic Hybridization Microarray for Copy-Number Mutations in 245 Neuromuscular Disorders

(2011) G. Piluso et al.   CLINICAL CHEMISTRY

α1,6-Fucosyltransferase-deficient Mice Exhibit Multiple Behavioral Abnormalities Associated with a Schizophrenia-like Phenotype

(2011) Tomohiko Fukuda et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

(2011) G Kirov et al.   MOLECULAR PSYCHIATRY

Exome sequencing supports a de novo mutational paradigm for schizophrenia

(2011) Bin Xu et al.   NATURE GENETICS

Increased exonic de novo mutation rate in individuals with schizophrenia

(2011) Simon L Girard et al.   NATURE GENETICS

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

(2011) Dheeraj Malhotra et al.   NEURON

MAGUKs, Synaptic Development, and Synaptic Plasticity

(2011) Chan-Ying Zheng et al.   NEUROSCIENTIST

Accuracy of CNV Detection from GWAS Data

(2011) Dandan Zhang et al.   PLoS One

Schizophrenia risk gene CAV1 is both pro-psychotic and required for atypical antipsychotic drug actions in vivo

(2011) J A Allen et al.   Translational Psychiatry

Microdeletions of 3q29 Confer High Risk for Schizophrenia

(2010) Jennifer Gladys Mulle et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Association of Genetic Variation in theMETProto-Oncogene With Schizophrenia and General Cognitive Ability

(2010) Katherine E. Burdick et al.   AMERICAN JOURNAL OF PSYCHIATRY

Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

(2010) A Piton et al.   MOLECULAR PSYCHIATRY

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function

(2010) David Warde-Farley et al.   NUCLEIC ACIDS RESEARCH

Loss of Caveolin-1 Accelerates Neurodegeneration and Aging

(2010) Brian P. Head et al.   PLoS One

CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila

(2009) Christiane Zweier et al.   AMERICAN JOURNAL OF HUMAN GENETICS

MAGI-1 Modulates AMPA Receptor Synaptic Localization and Behavioral Plasticity in Response to Prior Experience

(2009) Lesley Emtage et al.   PLoS One

Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder

(2009) Abdul Noor et al.   PSYCHIATRIC GENETICS

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

(2008) Maricela Alarcón et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The MATRICS Consensus Cognitive Battery, Part 2: Co-Norming and Standardization

(2008) Robert S. Kern et al.   AMERICAN JOURNAL OF PSYCHIATRY

The MATRICS Consensus Cognitive Battery, Part 1: Test Selection, Reliability, and Validity

(2008) Keith H. Nuechterlein et al.   AMERICAN JOURNAL OF PSYCHIATRY

Multiple Molecular Interactions Determine the Clustering of Caspr2 and Kv1 Channels in Myelinated Axons

(2008) I. Horresh et al.   JOURNAL OF NEUROSCIENCE

Evidence for disruption of sphingolipid metabolism in schizophrenia

(2008) Sujatha Narayan et al.   JOURNAL OF NEUROSCIENCE RESEARCH

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE

GeneMANIA: a real-time multiple association network integration algorithm for predicting gene function

(2008) Sara Mostafavi et al.   GENOME BIOLOGY