Association testing of copy number variants in schizophrenia and autism spectrum disorders
Published 2012 View Full Article
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Title
Association testing of copy number variants in schizophrenia and autism spectrum disorders
Authors
Keywords
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Journal
Journal of Neurodevelopmental Disorders
Volume 4, Issue 1, Pages -
Publisher
Springer Nature
Online
2012-08-21
DOI
10.1186/1866-1955-4-15
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Note: Only part of the references are listed.- CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
- (2012) Dheeraj Malhotra et al. CELL
- Evidence for involvement of GNB1L in autism
- (2011) Ying-Zhang Chen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness
- (2011) Andrés Ingason et al. AMERICAN JOURNAL OF PSYCHIATRY
- Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications
- (2011) Douglas F. Levinson et al. AMERICAN JOURNAL OF PSYCHIATRY
- Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems
- (2011) Trilochan Sahoo et al. GENETICS IN MEDICINE
- An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
- (2011) Erin B. Kaminsky et al. GENETICS IN MEDICINE
- Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
- (2011) Julie Gauthier et al. HUMAN GENETICS
- Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
- (2011) Rachel D. Burnside et al. HUMAN GENETICS
- 16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders
- (2011) Arivudainambi Ramalingam et al. JOURNAL OF HUMAN GENETICS
- Criteria, Categories, and Continua: Autism and Related Disorders in DSM-5
- (2011) Francesca Happé JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
- (2011) Sébastien Jacquemont et al. NATURE
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
- (2011) Stephan J. Sanders et al. NEURON
- From lumping to splitting and back again: Atypical social and language development in individuals with clinical-high-risk for psychosis, first episode schizophrenia, and autism spectrum disorders
- (2011) Marjorie Solomon et al. SCHIZOPHRENIA RESEARCH
- Why Are Autism Spectrum Conditions More Prevalent in Males?
- (2011) Simon Baron-Cohen et al. PLOS BIOLOGY
- Microdeletions of 3q29 Confer High Risk for Schizophrenia
- (2010) Jennifer Gladys Mulle et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia
- (2010) Daniel Moreno-De-Luca et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Sibling Recurrence and the Genetic Epidemiology of Autism
- (2010) John N. Constantino et al. AMERICAN JOURNAL OF PSYCHIATRY
- 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
- Is schizophrenia on the autism spectrum?
- (2010) Bryan H. King et al. BRAIN RESEARCH
- Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder
- (2010) Jill Clayton-Smith et al. CLINICAL DYSMORPHOLOGY
- 15q11.2 microdeletion – Seven new patients with delayed development and/or behavioural problems
- (2010) C. von der Lippe et al. European Journal of Medical Genetics
- Penetrance for copy number variants associated with schizophrenia
- (2010) E. Vassos et al. HUMAN MOLECULAR GENETICS
- Cognitive and Behavioral Characterization of 16p11.2 Deletion Syndrome
- (2010) Ellen Hanson et al. JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS
- The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment
- (2010) Noah J. Sasson et al. Journal of Neurodevelopmental Disorders
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion
- (2010) Chantal Loirat et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- New Copy Number Variations in Schizophrenia
- (2010) Chiara Magri et al. PLoS One
- Strong synaptic transmission impact by copy number variations in schizophrenia
- (2010) J. T. Glessner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Social skill and social cognition in adolescents at genetic risk for psychosis
- (2010) Clare M. Gibson et al. SCHIZOPHRENIA RESEARCH
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic Disease
- (2009) Andy Itsara et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation
- (2009) Audrey Guilmatre et al. ARCHIVES OF GENERAL PSYCHIATRY
- Copy number and sequence variants implicateAPBA2as an autism candidate gene
- (2009) Timothy D. Babatz et al. Autism Research
- Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study
- (2009) Gian Paolo Ramelli et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12
- (2009) Sandesh Chakravarthy Sreenath Nagamani et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances
- (2009) Marianne Doornbos et al. European Journal of Medical Genetics
- Microduplication 22q11.2: A new chromosomal syndrome
- (2009) Marie-France Portnoï European Journal of Medical Genetics
- Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
- (2009) E.K. Bijlsma et al. European Journal of Medical Genetics
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders
- (2009) S Ben-Shachar et al. JOURNAL OF MEDICAL GENETICS
- Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder
- (2009) B. A. Fernandez et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size
- (2009) M. Shinawi et al. JOURNAL OF MEDICAL GENETICS
- Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome
- (2009) B W M van Bon et al. JOURNAL OF MEDICAL GENETICS
- Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications
- (2009) Jill A. Rosenfeld et al. Journal of Neurodevelopmental Disorders
- Copy number variations of chromosome 16p13.1 region associated with schizophrenia
- (2009) A Ingason et al. MOLECULAR PSYCHIATRY
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
- (2009) Joseph T. Glessner et al. NATURE
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Association of Syndromic Mental Retardation and Autism with 22q11.2 Duplication
- (2009) A. Lo-Castro et al. NEUROPEDIATRICS
- Comparative genomics of autism and schizophrenia
- (2009) B. Crespi et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Premorbid adjustment in schizophrenia and schizoaffective disorder
- (2009) Ricardo Saracco-Alvarez et al. PSYCHIATRY RESEARCH
- What Is the Role of Theories in the Study of Schizophrenia?
- (2009) T. D. Cannon SCHIZOPHRENIA BULLETIN
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Schizophrenia, “just the facts” 4. Clinical features and conceptualization
- (2009) Rajiv Tandon et al. SCHIZOPHRENIA RESEARCH
- The genetics of childhood-onset schizophrenia: When madness strikes the prepubescent
- (2009) Anjené M. Addington et al. Current Psychiatry Reports
- Pervasive developmental disorders and psychosis
- (2009) Jean Starling et al. Current Psychiatry Reports
- Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes
- (2009) Maja Bucan et al. PLoS Genetics
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Microduplication 22q11.2: A benign polymorphism or a syndrome with a very large clinical variability and reduced penetrance?—Report of two families
- (2008) Winnie Courtens et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
- (2008) Anna Brunet et al. Behavioral and Brain Functions
- Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
- (2008) Susan L. Christian et al. BIOLOGICAL PSYCHIATRY
- Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome
- (2008) Doron Gothelf et al. Developmental Disabilities Research Reviews
- Velo-cardio-facial syndrome: 30 Years of study
- (2008) Robert J. Shprintzen Developmental Disabilities Research Reviews
- Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome
- (2008) Sarah E. Prasad et al. Developmental Disabilities Research Reviews
- Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
- (2008) Zhishuo Ou et al. GENETICS IN MEDICINE
- Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
- (2008) D T Miller et al. JOURNAL OF MEDICAL GENETICS
- Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
- (2008) F D Hannes et al. JOURNAL OF MEDICAL GENETICS
- Autism Spectrum Disorders and Childhood-Onset Schizophrenia: Clinical and Biological Contributions to a Relation Revisited
- (2008) Judith Rapoport et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Rare chromosomal deletions and duplications increase risk of schizophrenia
- (2008) Jennifer L. Stone et al. NATURE
- Large recurrent microdeletions associated with schizophrenia
- (2008) Hreinn Stefansson et al. NATURE
- Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
- (2008) Nicola Brunetti-Pierri et al. NATURE GENETICS
- The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13
- (2008) Amber Hogart et al. NEUROBIOLOGY OF DISEASE
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
- Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
- (2008) Heather C. Mefford et al. NEW ENGLAND JOURNAL OF MEDICINE
- Parental Psychiatric Disorders Associated With Autism Spectrum Disorders in the Offspring
- (2008) J. L. Daniels et al. PEDIATRICS
- The Antecedents of Schizophrenia: A Review of Birth Cohort Studies
- (2008) J. Welham et al. SCHIZOPHRENIA BULLETIN
- Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication
- (2008) Blake C Ballif et al. Molecular Cytogenetics
- Pathways to psychosis: A comparison of the pervasive developmental disorder subtype Multiple Complex Developmental Disorder and the “At Risk Mental State”
- (2007) M. Sprong et al. SCHIZOPHRENIA RESEARCH
- Social functioning in individuals at clinical high risk for psychosis
- (2007) Jean Addington et al. SCHIZOPHRENIA RESEARCH
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