A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

The Effectiveness and Safety of Antipsychotic and Antidepressant Medications in Individuals with 22q11.2 Deletion Syndrome

(2017) Netta Dori et al.   JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY

Altered Cortical Ensembles in Mouse Models of Schizophrenia

(2017) Jordan P. Hamm et al.   NEURON

A review of molecular genetic studies of neurocognitive deficits in schizophrenia

(2017) Gwyneth Zai et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

PEMapper and PECaller provide a simplified approach to whole-genome sequencing

(2017) H. Richard Johnston et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Integrated Post-GWAS Analysis Sheds New Light on the Disease Mechanisms of Schizophrenia

(2016) Jhih-Rong Lin et al.   GENETICS

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

(2016) Elisabeth E. Mlynarski et al.   HUMAN GENETICS

Clinical sequencing: is WGS the better WES?

(2016) Janine Meienberg et al.   HUMAN GENETICS

Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis

(2016) Xingyi Guo et al.   HUMAN MOLECULAR GENETICS

Developmental Inhibition of Gsk3 Rescues Behavioral and Neurophysiological Deficits in a Mouse Model of Schizophrenia Predisposition

(2016) Makoto Tamura et al.   NEURON

The ExAC browser: displaying reference data information from over 60 000 exomes

(2016) Konrad J. Karczewski et al.   NUCLEIC ACIDS RESEARCH

Integrated Post-GWAS Analysis Sheds New Light on the Disease Mechanisms of Schizophrenia

(2016) Jhih-Rong Lin et al.   GENETICS

Deconstructing Pretest Risk Enrichment to Optimize Prediction of Psychosis in Individuals at Clinical High Risk

(2016) Paolo Fusar-Poli et al.   JAMA Psychiatry

Association of Neurocognition With Transition to Psychosis

(2016) Larry J. Seidman et al.   JAMA Psychiatry

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

(2015) Elisabeth E. Mlynarski et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome

(2015) Maria Niarchou et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Response to clozapine in a clinically identifiable subtype of schizophrenia

(2015) Nancy J. Butcher et al.   BRITISH JOURNAL OF PSYCHIATRY

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms

(2015) Alina Guna et al.   Journal of Neurodevelopmental Disorders

Connectome-wide network analysis of youth with Psychosis-Spectrum symptoms

(2015) T D Satterthwaite et al.   MOLECULAR PSYCHIATRY

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

Whole-genome sequencing of quartet families with autism spectrum disorder

(2015) Ryan K C Yuen et al.   NATURE MEDICINE

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

(2015) Daniel W. Meechan et al.   PROGRESS IN NEUROBIOLOGY

The impact of psychosis on the course of cognition: a prospective, nested case-control study in individuals at clinical high-risk for psychosis

(2015) R. E. Carrión et al.   PSYCHOLOGICAL MEDICINE

Neurocognitive performance in family-based and case-control studies of schizophrenia

(2015) Ruben C. Gur et al.   SCHIZOPHRENIA RESEARCH

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome

(2015) Daniele Merico et al.   G3-Genes Genomes Genetics

Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

(2015) Jacob A. S. Vorstman et al.   JAMA Psychiatry

22q11.2 deletion syndrome

(2015) Donna M. McDonald-McGinn et al.   Nature Reviews Disease Primers

Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

(2014) Maude Schneider et al.   AMERICAN JOURNAL OF PSYCHIATRY

Subthreshold Psychotic Symptoms in 22q11.2 Deletion Syndrome

(2014) Sunny X. Tang et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities

(2014) R E Gur et al.   MOLECULAR PSYCHIATRY

Biological insights from 108 schizophrenia-associated genetic loci

(2014)   NATURE

A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

The psychosis spectrum in a young U.S. community sample: findings from the Philadelphia Neurodevelopmental Cohort

(2014) Monica E. Calkins et al.   World Psychiatry

Neurocognitive Growth Charting in Psychosis Spectrum Youths

(2014) Ruben C. Gur et al.   JAMA Psychiatry

Neuropsychological Decline in Schizophrenia From the Premorbid to the Postonset Period: Evidence From a Population-Representative Longitudinal Study

(2013) Madeline H. Meier et al.   AMERICAN JOURNAL OF PSYCHIATRY

The 22q11.2 Deletion Syndrome as a Window into Complex Neuropsychiatric Disorders Over the Lifespan

(2013) Rachel K. Jonas et al.   BIOLOGICAL PSYCHIATRY

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

(2013) G. Costain et al.   HUMAN MOLECULAR GENETICS

Risk Factors and the Evolution of Psychosis in 22q11.2 Deletion Syndrome: A Longitudinal 2-Site Study

(2013) Doron Gothelf et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

(2013) N Hiroi et al.   MOLECULAR PSYCHIATRY

Schizophrenia Is a Cognitive Illness

(2013) René S. Kahn et al.   JAMA Psychiatry

Using ERDS to Infer Copy-Number Variants in High-Coverage Genomes

(2012) Mingfu Zhu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

(2012) Seunggeun Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Cognitive development in children with 22q11.2 deletion syndrome

(2012) Sasja N. Duijff et al.   BRITISH JOURNAL OF PSYCHIATRY

Gene Ontology Annotations and Resources

(2012)   NUCLEIC ACIDS RESEARCH

Prevalence of psychotic symptoms in childhood and adolescence: a systematic review and meta-analysis of population-based studies

(2012) I. Kelleher et al.   PSYCHOLOGICAL MEDICINE

Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: A comparison of prodromal psychotic symptoms and general functioning

(2012) Marco Armando et al.   SCHIZOPHRENIA RESEARCH

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

(2012) J. A. Tennessen et al.   SCIENCE

Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways

(2012) Candice K. Silversides et al.   PLoS Genetics

CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

(2011) A. Abyzov et al.   GENOME RESEARCH

CREST maps somatic structural variation in cancer genomes with base-pair resolution

(2011) Jianmin Wang et al.   NATURE METHODS

Meta-analyses of cognitive and motor function in youth aged 16 years and younger who subsequently develop schizophrenia

(2011) H. Dickson et al.   PSYCHOLOGICAL MEDICINE

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

(2011) A. C. Lionel et al.   Science Translational Medicine

Copy Number Variations in Schizophrenia: Critical Review and New Perspectives on Concepts of Genetics and Disease

(2010) Anne S. Bassett et al.   AMERICAN JOURNAL OF PSYCHIATRY

Rethinking schizophrenia

(2010) Thomas R. Insel   NATURE

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

(2010) Maria Karayiorgou et al.   NATURE REVIEWS NEUROSCIENCE

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

(2009) K. Ye et al.   BIOINFORMATICS

Detection of nonneutral substitution rates on mammalian phylogenies

(2009) K. S. Pollard et al.   GENOME RESEARCH

Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome

(2009) Tamar Green et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Prediction of Psychosis in Youth at High Clinical Risk

(2008) Tyrone D. Cannon et al.   ARCHIVES OF GENERAL PSYCHIATRY

Intellectual disability co-occurring with schizophrenia and other psychiatric illness: population-based study

(2008) Vera A. Morgan et al.   BRITISH JOURNAL OF PSYCHIATRY

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

(2008) Anne S. Bassett et al.   HUMAN MOLECULAR GENETICS

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

(2008) T. Walsh et al.   SCIENCE