Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion
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Title
Linking spatial gene expression patterns to sex-specific brain structural changes on a mouse model of 16p11.2 hemideletion
Authors
Keywords
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Journal
Translational Psychiatry
Volume 8, Issue 1, Pages -
Publisher
Springer Nature
Online
2018-05-29
DOI
10.1038/s41398-018-0157-z
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Note: Only part of the references are listed.- Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders
- (2017) N M Grissom et al. MOLECULAR PSYCHIATRY
- TAOK2 Kinase Mediates PSD95 Stability and Dendritic Spine Maturation through Septin7 Phosphorylation
- (2017) Smita Yadav et al. NEURON
- Association of White Matter Structure With Autism Spectrum Disorder and Attention-Deficit/Hyperactivity Disorder
- (2017) Yuta Aoki et al. JAMA Psychiatry
- Males are from Mars, and females are from Venus: sex-specific fetal brain gene expression signatures in a mouse model of maternal diet-induced obesity
- (2016) Andrea G. Edlow et al. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
- A Diffusion Tensor Imaging Study in Children With ADHD, Autism Spectrum Disorder, OCD, and Matched Controls: Distinct and Non-Distinct White Matter Disruption and Dimensional Brain-Behavior Relationships
- (2016) Stephanie H. Ameis et al. AMERICAN JOURNAL OF PSYCHIATRY
- Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism
- (2016) Christopher C. Angelakos et al. Autism Research
- Diffusion Tensor Imaging Provides Evidence of Possible Axonal Overconnectivity in Frontal Lobes in Autism Spectrum Disorder Toddlers
- (2016) Stephanie Solso et al. BIOLOGICAL PSYCHIATRY
- Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications
- (2016) Yi Shin Chang et al. HUMAN BRAIN MAPPING
- Attention deficit hyperactivity disorder
- (2016) Anita Thapar et al. LANCET
- Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes
- (2016) Thomas Arbogast et al. PLoS Genetics
- Decreased Left Caudate Volume Is Associated with Increased Severity of Autistic-Like Symptoms in a Cohort of ADHD Patients and Their Unaffected Siblings
- (2016) Laurence O’Dwyer et al. PLoS One
- The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population
- (2015) Ellen Hanson et al. BIOLOGICAL PSYCHIATRY
- Zn2+-dependent Activation of the Trk Signaling Pathway Induces Phosphorylation of the Brain-enriched Tyrosine Phosphatase STEP
- (2015) Ranjana Poddar et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Cathepsin D and its newly identified transport receptor SEZ6L2 can modulate neurite outgrowth
- (2015) Marielle Boonen et al. JOURNAL OF CELL SCIENCE
- Measuring the Neural Basis of Reward Anticipation and Reward Receipt in Attention-Deficit/Hyperactivity Disorder: The Importance of Task Design
- (2015) Michael M. Plichta et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- The molecular genetic architecture of attention deficit hyperactivity disorder
- (2015) Z Hawi et al. MOLECULAR PSYCHIATRY
- An assessment of sex bias in neurodevelopmental disorders
- (2015) Andrew Polyak et al. Genome Medicine
- The relative contribution of common and rare genetic variants to ADHD
- (2015) J Martin et al. Translational Psychiatry
- Abnormal auditory and language pathways in children with 16p11.2 deletion
- (2015) Jeffrey I. Berman et al. NeuroImage-Clinical
- A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders
- (2014) Sébastien Jacquemont et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Neural networks related to dysfunctional face processing in autism spectrum disorder
- (2014) Thomas Nickl-Jockschat et al. Brain Structure & Function
- Aberrant White Matter Microstructure in Children with 16p11.2 Deletions
- (2014) J. P. Owen et al. JOURNAL OF NEUROSCIENCE
- Opposing Brain Differences in 16p11.2 Deletion and Duplication Carriers
- (2014) A. Y. Qureshi et al. JOURNAL OF NEUROSCIENCE
- The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity
- (2014) A M Maillard et al. MOLECULAR PSYCHIATRY
- Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneity
- (2014) J Ellegood et al. MOLECULAR PSYCHIATRY
- Permutation inference for the general linear model
- (2014) Anderson M. Winkler et al. NEUROIMAGE
- Autism as a disorder of prediction
- (2014) Pawan Sinha et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: A systematic review of literature and meta-analysis
- (2014) Giovanni Giaroli et al. SCHIZOPHRENIA RESEARCH
- Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome
- (2014) Thomas Portmann et al. Cell Reports
- Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants
- (2013) Li Yang et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Social reward requires coordinated activity of nucleus accumbens oxytocin and serotonin
- (2013) Gül Dölen et al. NATURE
- Examining and interpreting the female protective effect against autistic behavior
- (2013) E. B. Robinson et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Neuroimaging Endophenotypes in Animal Models of Autism Spectrum Disorders: Lost or Found in Translation?
- (2013) Marija M. Petrinovic et al. PSYCHOPHARMACOLOGY
- The role of the striatum in social behavior
- (2013) Raymundo Báez-Mendoza et al. Frontiers in Neuroscience
- Differences in White Matter Fiber Tract Development Present From 6 to 24 Months in Infants With Autism
- (2012) Jason J. Wolff et al. AMERICAN JOURNAL OF PSYCHIATRY
- Changes in grey matter development in autism spectrum disorder
- (2012) Ellen Greimel et al. Brain Structure & Function
- CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics
- (2012) Dheeraj Malhotra et al. CELL
- Autism spectrum disorder susceptibility gene TAOK2 affects basal dendrite formation in the neocortex
- (2012) Froylan Calderon de Anda et al. NATURE NEUROSCIENCE
- Emergence of context-associated GluR1 and ERK phosphorylation in the nucleus accumbens core during withdrawal from cocaine self-administration
- (2011) Scott Edwards et al. ADDICTION BIOLOGY
- Brain structure anomalies in autism spectrum disorder-a meta-analysis of VBM studies using anatomic likelihood estimation
- (2011) Thomas Nickl-Jockschat et al. HUMAN BRAIN MAPPING
- Common alterations in sensitivity to type but not amount of reward in ADHD and autism spectrum disorders
- (2011) Ellen Demurie et al. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
- FSL
- (2011) Mark Jenkinson et al. NEUROIMAGE
- 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
- Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism
- (2011) G. Horev et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- MVP interacts with YPEL4 and inhibits YPEL4-mediated activities of the ERK signal pathway
- (2010) Pei Liang et al. Biochemistry and Cell Biology
- Abnormal white matter integrity in young children with autism
- (2010) Maya Weinstein et al. HUMAN BRAIN MAPPING
- Acquisition and Performance of Goal-Directed Instrumental Actions Depends on ERK Signaling in Distinct Regions of Dorsal Striatum in Rats
- (2010) M. W. Shiflett et al. JOURNAL OF NEUROSCIENCE
- Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
- (2010) Nigel M Williams et al. LANCET
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- Waxholm Space: An image-based reference for coordinating mouse brain research
- (2010) G. Allan Johnson et al. NEUROIMAGE
- An anatomic gene expression atlas of the adult mouse brain
- (2009) Lydia Ng et al. NATURE NEUROSCIENCE
- Magnetic resonance imaging and biological properties of pancreatic islets labeled with iron oxide nanoparticles
- (2009) Hoe Suk Kim et al. NMR IN BIOMEDICINE
- Review of Pathological Hallmarks of Schizophrenia: Comparison of Genetic Models With Patients and Nongenetic Models
- (2009) Hanna Jaaro-Peled et al. SCHIZOPHRENIA BULLETIN
- Structural Variation of Chromosomes in Autism Spectrum Disorder
- (2008) Christian R. Marshall et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The integrative function of the basal ganglia in instrumental conditioning
- (2008) Bernard W. Balleine et al. BEHAVIOURAL BRAIN RESEARCH
- Structural brain change in Attention Deficit Hyperactivity Disorder identified by meta-analysis
- (2008) Ian Ellison-Wright et al. BMC Psychiatry
- Major Vault Protein is Expressed along the Nucleus-Neurite Axis and Associates with mRNAs in Cortical Neurons
- (2008) C. D. Paspalas et al. CEREBRAL CORTEX
- Opposing Patterns of Signaling Activation in Dopamine D1 and D2 Receptor-Expressing Striatal Neurons in Response to Cocaine and Haloperidol
- (2008) J. Bertran-Gonzalez et al. JOURNAL OF NEUROSCIENCE
- Association between Microdeletion and Microduplication at 16p11.2 and Autism
- (2008) Lauren A. Weiss et al. NEW ENGLAND JOURNAL OF MEDICINE
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