A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity
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Title
A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity
Authors
Keywords
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Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Volume 171, Issue 2, Pages 290-299
Publisher
Wiley
Online
2015-12-01
DOI
10.1002/ajmg.b.32406
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Note: Only part of the references are listed.- A de novo proximal 3q29 chromosome microduplication in a patient with oculo auriculo vertebral spectrum
- (2015) Valentina Guida et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Developmental trajectories in 22q11.2 deletion syndrome
- (2015) Ann Swillen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS
- A clinical case report and literature review of the 3q29 microdeletion syndrome
- (2015) Devin M. Cox et al. CLINICAL DYSMORPHOLOGY
- Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
- (2015) Robert A. Kozol et al. HUMAN MOLECULAR GENETICS
- A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)
- (2015) Elisa Giorgio et al. HUMAN MOLECULAR GENETICS
- The 3q29 deletion confers >40-fold increase in risk for schizophrenia
- (2015) J G Mulle MOLECULAR PSYCHIATRY
- Copy number variation in bipolar disorder
- (2015) E K Green et al. MOLECULAR PSYCHIATRY
- A copy number variation map of the human genome
- (2015) Mehdi Zarrei et al. NATURE REVIEWS GENETICS
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
- (2014) Dalila Pinto et al. AMERICAN JOURNAL OF HUMAN GENETICS
- ‘Neonatal’ Nav1.2 reduces neuronal excitability and affects seizure susceptibility and behaviour
- (2014) Elena V. Gazina et al. HUMAN MOLECULAR GENETICS
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- De novo mutations in schizophrenia implicate synaptic networks
- (2014) Menachem Fromer et al. NATURE
- A polygenic burden of rare disruptive mutations in schizophrenia
- (2014) Shaun M. Purcell et al. NATURE
- Inhibition of Notch signaling promotes browning of white adipose tissue and ameliorates obesity
- (2014) Pengpeng Bi et al. NATURE MEDICINE
- Does employment alter the course and outcome of schizophrenia and other severe mental illnesses? A systematic review of longitudinal research
- (2014) Alison Luciano et al. SCHIZOPHRENIA RESEARCH
- Revisiting the Relationship Between Autism and Schizophrenia: Toward an Integrated Neurobiology
- (2013) Nina de Lacy et al. Annual Review of Clinical Psychology
- Notch/Rbpj signaling regulates progenitor maintenance and differentiation of hypothalamic arcuate neurons
- (2013) P. K. Aujla et al. DEVELOPMENT
- Concordance of white matter and gray matter abnormalities in autism spectrum disorders: A voxel-based meta-analysis study
- (2013) Franco Cauda et al. HUMAN BRAIN MAPPING
- Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
- (2013) S Hong Lee et al. NATURE GENETICS
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia
- (2013) Stephan Ripke et al. NATURE GENETICS
- Phenotypic impact of genomic structural variation: insights from and for human disease
- (2013) Joachim Weischenfeldt et al. NATURE REVIEWS GENETICS
- A Comparison of Neuroimaging Findings in Childhood Onset Schizophrenia and Autism Spectrum Disorder: A Review of the Literature
- (2013) Danielle A. Baribeau et al. Frontiers in Psychiatry
- Genetic architectures of psychiatric disorders: the emerging picture and its implications
- (2012) Patrick F. Sullivan et al. NATURE REVIEWS GENETICS
- Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) in adult psychiatry. A 20-year register study
- (2012) Lena Nylander et al. NORDIC JOURNAL OF PSYCHIATRY
- Whole brain resting state functional connectivity abnormalities in schizophrenia
- (2012) Archana Venkataraman et al. SCHIZOPHRENIA RESEARCH
- Functional and Structural MR Imaging in Neuropsychiatric Disorders, Part 2: Application in Schizophrenia and Autism
- (2011) S. Mueller et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- 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
- The Notch effector gene Hes1 regulates migration of hypothalamic neurons, neuropeptide content and axon targeting to the pituitary
- (2011) Paven K. Aujla et al. DEVELOPMENTAL BIOLOGY
- Cooperative functions of Hes/Hey genes in auditory hair cell and supporting cell development
- (2011) Tomoko Tateya et al. DEVELOPMENTAL BIOLOGY
- Grey matter abnormality in autism spectrum disorder: an activation likelihood estimation meta-analysis study
- (2011) F. Cauda et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
- (2011) G Kirov et al. MOLECULAR PSYCHIATRY
- Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
- (2011) Sébastien Jacquemont et al. NATURE
- High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia
- (2011) Dheeraj Malhotra et al. NEURON
- Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders
- (2011) Dan Levy et al. NEURON
- 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
- Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication
- (2011) Ozlem Bozdagi et al. Molecular Autism
- 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
- Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review
- (2010) Fabiola Quintero-Rivera et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Abnormal cell patterning at the cortical gray–white matter boundary in autism spectrum disorders
- (2010) Thomas A. Avino et al. BRAIN RESEARCH
- Neurological soft signs in juvenile patients with Asperger syndrome, early-onset psychosis, and healthy controls
- (2010) María Mayoral et al. Early Intervention in Psychiatry
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
- (2010) Sabine Endele et al. NATURE GENETICS
- Hes1 functions downstream of growth factors to maintain oligodendrocyte lineage cells in the early progenitor stage
- (2010) T. Ogata et al. NEUROSCIENCE
- Autistic Disorders and Schizophrenia: Related or Remote? An Anatomical Likelihood Estimation
- (2010) Charlton Cheung et al. PLoS One
- Metacognition in schizophrenia: Correlates and stability of deficits in theory of mind and self-reflectivity
- (2010) Paul H. Lysaker et al. PSYCHIATRY RESEARCH
- Overlap of autistic and schizotypal traits in adolescents with Autism Spectrum Disorders
- (2010) Petra S. Barneveld et al. SCHIZOPHRENIA RESEARCH
- 3q29 microdeletion: A mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs
- (2009) Maria Cristina Digilio et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The E646D-ATP13A4 Mutation Associated with Autism Reveals a Defect in Calcium Regulation
- (2009) Janaki Vallipuram et al. CELLULAR AND MOLECULAR NEUROBIOLOGY
- Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
- (2009) George Kirov et al. HUMAN MOLECULAR GENETICS
- Microduplications of 16p11.2 are associated with schizophrenia
- (2009) Shane E McCarthy et al. NATURE GENETICS
- Distinct contributions of Nav1.6 and Nav1.2 in action potential initiation and backpropagation
- (2009) Wenqin Hu et al. NATURE NEUROSCIENCE
- Neurexin 1 (NRXN1) Deletions in Schizophrenia
- (2009) G. Kirov et al. SCHIZOPHRENIA BULLETIN
- Mirror neurons: from discovery to autism
- (2009) Giacomo Rizzolatti et al. EXPERIMENTAL BRAIN RESEARCH
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations
- (2008) Jessica Lasky-Su et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Overrepresentation of mood and anxiety disorders in adults with autism and their first-degree relatives: what does it mean?
- (2008) Carla A. Mazefsky et al. Autism Research
- A Common Variant in DRD3 Receptor Is Associated with Autism Spectrum Disorder
- (2008) Mariken de Krom et al. BIOLOGICAL PSYCHIATRY
- The Glucocorticoid Receptor Controls Hepatic Dyslipidemia through Hes1
- (2008) Ulrike Lemke et al. Cell Metabolism
- 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
- Neuroligins and neurexins link synaptic function to cognitive disease
- (2008) Thomas C. Südhof NATURE
- 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
- Strong association of de novo copy number mutations with sporadic schizophrenia
- (2008) Bin Xu et al. NATURE GENETICS
- Corpus callosum shape alterations in individuals prior to the onset of psychosis
- (2008) Mark Walterfang et al. SCHIZOPHRENIA RESEARCH
- Reduced motor facilitation during action observation in schizophrenia: A mirror neuron deficit?
- (2008) P ENTICOTT et al. SCHIZOPHRENIA RESEARCH
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