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Raphael Bernier et al.
GENETICS IN MEDICINE (2016)
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Dimitri J. Stavropoulos et al.
NPJ GENOMIC MEDICINE (2016)
Performance of case-control rare copy number variation annotation in classification of autism
Worrawat Engchuan et al.
BMC MEDICAL GENOMICS (2015)
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Kristiina Tammimies et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2015)
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Ryan K. C. Yuen et al.
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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.
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Mohammed Uddin et al.
GENETICS IN MEDICINE (2015)
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS
M. Mattheisen et al.
MOLECULAR PSYCHIATRY (2015)
Anxiety disorders and GABA neurotransmission: a disturbance of modulation
Philippe Nuss
NEUROPSYCHIATRIC DISEASE AND TREATMENT (2015)
Diagnostic validity of comorbid bipolar disorder and obsessive-compulsive disorder: a systematic review
A. Amerio et al.
ACTA PSYCHIATRICA SCANDINAVICA (2014)
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Dalila Pinto et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Analysis of copy number variations at 15 schizophrenia-associated loci
Elliott Rees et al.
BRITISH JOURNAL OF PSYCHIATRY (2014)
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)
Copy number variation in schizophrenia in Sweden
J. P. Szatkiewicz et al.
MOLECULAR PSYCHIATRY (2014)
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder
Mohammed Uddin et al.
NATURE GENETICS (2014)
Obsessive-compulsive disorder: an integrative genetic and neurobiological perspective
David L. Pauls et al.
NATURE REVIEWS NEUROSCIENCE (2014)
Copy number variation in Han Chinese individuals with autism spectrum disorder
Matthew J. Gazzellone et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2014)
Age of onset in obsessive-compulsive disorder: admixture analysis with a large sample
G. E. Anholt et al.
PSYCHOLOGICAL MEDICINE (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)
1q21.1 Microduplication expression in adults
Alessia Dolcetti et al.
GENETICS IN MEDICINE (2013)
The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cells
Lingling Shi et al.
HUMAN MOLECULAR GENETICS (2013)
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures
Anath C. Lionel et al.
HUMAN MOLECULAR GENETICS (2013)
Neuroligin1 Drives Synaptic and Behavioral Maturation through Intracellular Interactions
Jennifer L. Hoy et al.
JOURNAL OF NEUROSCIENCE (2013)
Genome-wide association study of obsessive-compulsive disorder
S. E. Stewart et al.
MOLECULAR PSYCHIATRY (2013)
Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts
D. Moreno-De-Luca et al.
MOLECULAR PSYCHIATRY (2013)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J. M. Verhoeven et al.
NATURE GENETICS (2013)
Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: A preliminary study
Ke Wu et al.
PSYCHIATRY RESEARCH-NEUROIMAGING (2013)
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
Slave Petrovski et al.
PLOS GENETICS (2013)
Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings
Robert A. Power et al.
JAMA PSYCHIATRY (2013)
Genetic architecture in autism spectrum disorder
Bernie Devlin et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2012)
Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways
Candice K. Silversides et al.
PLOS GENETICS (2012)
Replication and meta-analysis of TMEM132D gene variants in panic disorder
A. Erhardt et al.
TRANSLATIONAL PSYCHIATRY (2012)
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
Jennifer C. Darnell et al.
CELL (2011)
Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants
Dalila Pinto et al.
NATURE BIOTECHNOLOGY (2011)
High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
Dheeraj Malhotra et al.
NEURON (2011)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J. Sanders et al.
NEURON (2011)
How Prevalent Are Anxiety Disorders in Schizophrenia? A Meta-Analysis and Critical Review on a Significant Association
Amelie M. Achim et al.
SCHIZOPHRENIA BULLETIN (2011)
Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD
Anath C. Lionel et al.
SCIENCE TRANSLATIONAL MEDICINE (2011)
Long-term outcomes of obsessive-compulsive disorder: follow-up of 142 children and adolescents
N. Micali et al.
BRITISH JOURNAL OF PSYCHIATRY (2010)
OBSESSIVE-COMPULSIVE DISORDER: A REVIEW OF THE DIAGNOSTIC CRITERIA AND POSSIBLE SUBTYPES AND DIMENSIONAL SPECIFIERS FOR DSM-V
James E. Leckman et al.
DEPRESSION AND ANXIETY (2010)
The epidemiology of obsessive-compulsive disorder in the National Comorbidity Survey Replication
A. M. Ruscio et al.
MOLECULAR PSYCHIATRY (2010)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto et al.
NATURE (2010)
DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
Helen V. Firth et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Predictors of Early Adult Outcomes in Pediatric-Onset Obsessive-Compulsive Disorder
Michael H. Bloch et al.
PEDIATRICS (2009)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Familial deletion within NLGN4 associated with autism and Tourette syndrome
Amy Lawson-Yuen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2008)
Copy-number variations associated with neuropsychiatric conditions
Edwin H. Cook et al.
NATURE (2008)
PLINK: A tool set for whole-genome association and population-based linkage analyses
Shaun Purcell et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Strong association of de novo copy number mutations with autism
Jonathan Sebat et al.
SCIENCE (2007)
Novel genes identified in a high-density genome wide association study for nicotine dependence
Laura Jean Bierut et al.
HUMAN MOLECULAR GENETICS (2007)
Comorbid psychiatric disorders in children with autism: Interview development and rates of disorders
Ovsanna T. Leyfer et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2006)
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder
VL Willour et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Long-term outcome of pediatric obsessive-compulsive disorder: a meta-analysis and qualitative review of the literature
SE Stewart et al.
ACTA PSYCHIATRICA SCANDINAVICA (2004)
Association between the dopamine receptor D4 (DRD4) gene and obsessive-compulsive disorder
B Millet et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2003)
Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands
GL Hanna et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Adults with early-onset obsessive-compulsive disorder
MC do Rosario-Campos et al.
AMERICAN JOURNAL OF PSYCHIATRY (2001)