Related references
Note: Only part of the references are listed.Psychiatric genetics and the structure of psychopathology
Jordan W. Smoller et al.
MOLECULAR PSYCHIATRY (2019)
Genetics of attention deficit hyperactivity disorder
Stephen V. Faraone et al.
MOLECULAR PSYCHIATRY (2019)
Psychiatric disorders in children with 16p11.2 deletion and duplication
Maria Niarchou et al.
TRANSLATIONAL PSYCHIATRY (2019)
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
Mehdi Zarrei et al.
GENETICS IN MEDICINE (2018)
A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data
Brett Trost et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing
Gregory Costain et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2018)
The nature of social cognitive deficits in children and adults with Klinefelter syndrome (47,XXY)
S. van Rijn et al.
GENES BRAIN AND BEHAVIOR (2018)
Executive Functions in Children and Adolescents with Turner Syndrome: A Systematic Review and Meta-Analysis
Claire Mauger et al.
NEUROPSYCHOLOGY REVIEW (2018)
The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders
Ambra Rizzo et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2018)
Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights
Itaru Kushima et al.
CELL REPORTS (2018)
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
Chelsea Lowther et al.
GENETICS IN MEDICINE (2017)
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
O. Mercati et al.
MOLECULAR PSYCHIATRY (2017)
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Christian R. Marshall et al.
NATURE GENETICS (2017)
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
Ryan K. C. Yuen et al.
NATURE NEUROSCIENCE (2017)
Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
Chelsea Lowther et al.
CURRENT PSYCHIATRY REPORTS (2017)
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
Chelsea Lowther et al.
GENOME MEDICINE (2017)
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
Kimberley M. Kendall et al.
BIOLOGICAL PSYCHIATRY (2017)
Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
Leticia Diaz-Beltran et al.
BMC GENOMICS (2017)
Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells
Pei-Chi Wei et al.
CELL (2016)
Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation
Matthew J. Gazzellone et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2016)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek et al.
NATURE (2016)
A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders
Andrea J. Gonzalez-Mantilla et al.
JAMA PSYCHIATRY (2016)
Genome-wide characteristics of de novo mutations in autism
Ryan K. C. Yuen et al.
NPJ GENOMIC MEDICINE (2016)
Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family
Linh T. T. Duong et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2015)
Integrative analysis of 111 reference human epigenomes
Anshul Kundaje et al.
NATURE (2015)
Whole-genome sequencing of quartet families with autism spectrum disorder
Ryan K. C. Yuen et al.
NATURE MEDICINE (2015)
A copy number variation map of the human genome
Mehdi Zarrei et al.
NATURE REVIEWS GENETICS (2015)
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui et al.
NATURE COMMUNICATIONS (2015)
A high-resolution copy-number variation resource for clinical and population genetics
Mohammed Uddin et al.
GENETICS IN MEDICINE (2015)
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
Anath C. Lionel et al.
HUMAN MOLECULAR GENETICS (2014)
Copy Number Variation in Obsessive-Compulsive Disorder and Tourette Syndrome: A Cross-Disorder Study
Lauren M. McGrath et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2014)
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing
Yong-hui Jiang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays
Gregory Costain et al.
HUMAN MOLECULAR GENETICS (2013)
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Jordan W. Smoller et al.
LANCET (2013)
Heterozygous mutations in PALB2 cause DNA replication and damage response defects
Jenni Nikkila et al.
NATURE COMMUNICATIONS (2013)
A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder
Aparna Prasad et al.
G3-GENES GENOMES GENETICS (2012)
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants
Hutton M. Kearney et al.
GENETICS IN MEDICINE (2011)
Risk factors for autism: translating genomic discoveries into diagnostics
Stephen W. Scherer et al.
HUMAN GENETICS (2011)
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
Anath C. Lionel et al.
SCIENCE TRANSLATIONAL MEDICINE (2011)
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
David T. Miller et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
The clinical context of copy number variation in the human genome
Charles Lee et al.
EXPERT REVIEWS IN MOLECULAR MEDICINE (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
A global map of human gene expression
Margus Lukk et al.
NATURE BIOTECHNOLOGY (2010)
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
Abdul Noor et al.
SCIENCE TRANSLATIONAL MEDICINE (2010)
AmiGO: online access to ontology and annotation data
Seth Carbon et al.
BIOINFORMATICS (2009)
Differences in the clinical presentation of Trisomy 21 with and without autism
C. A. Molloy et al.
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH (2009)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
NFAT signaling in neural development and axon growth
Tuan Nguyen et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2008)
Copy-number variations associated with neuropsychiatric conditions
Edwin H. Cook et al.
NATURE (2008)