Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities
Published 2017 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities
Authors
Keywords
Association study, ADI-R phenotypes, Genetic architecture, IQ
Journal
JOURNAL OF NEURAL TRANSMISSION
Volume 125, Issue 2, Pages 259-271
Publisher
Springer Nature
Online
2017-11-16
DOI
10.1007/s00702-017-1813-9
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Gray matter abnormalities in pediatric autism spectrum disorder: a meta-analysis with signed differential mapping
- (2017) Jieke Liu et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- Safety and Efficacy of Memantine in Children with Autism: Randomized, Placebo-Controlled Study and Open-Label Extension
- (2017) Michael G. Aman et al. JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY
- Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder
- (2016) Thorsten M. Kranz et al. Autism Research
- A Prospective Open-Label Trial of Memantine Hydrochloride for the Treatment of Social Deficits in Intellectually Capable Adults With Autism Spectrum Disorder
- (2016) Gagan Joshi et al. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY
- Reduced Glutamate Release in Adult BTBR Mouse Model of Autism Spectrum Disorder
- (2016) Hongen Wei et al. NEUROCHEMICAL RESEARCH
- NMDA receptor subunit mutations in neurodevelopmental disorders
- (2015) Nail Burnashev et al. CURRENT OPINION IN PHARMACOLOGY
- Heritability of autism spectrum disorders: a meta-analysis of twin studies
- (2015) Beata Tick et al. JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY
- Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
- (2015) Anthony J. Griswold et al. Molecular Autism
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
- (2014) Dalila Pinto et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
- (2014) Regina Waltes et al. HUMAN GENETICS
- Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range
- (2014) Regina Waltes et al. JOURNAL OF NEURAL TRANSMISSION
- Glutamatergic candidate genes in autism spectrum disorder: an overview
- (2014) Andreas G. Chiocchetti et al. JOURNAL OF NEURAL TRANSMISSION
- GABAergic/glutamatergic imbalance relative to excessive neuroinflammation in autism spectrum disorders
- (2014) Afaf El-Ansary et al. Journal of Neuroinflammation
- The Schizophrenia Susceptibility GeneDysbindinRegulates Dendritic Spine Dynamics
- (2014) Jie-Min Jia et al. JOURNAL OF NEUROSCIENCE
- Disturbed cingulate glutamate metabolism in adults with high-functioning autism spectrum disorder: evidence in support of the excitatory/inhibitory imbalance hypothesis
- (2014) L Tebartz van Elst et al. MOLECULAR PSYCHIATRY
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- The contribution of de novo coding mutations to autism spectrum disorder
- (2014) Ivan Iossifov et al. NATURE
- Most genetic risk for autism resides with common variation
- (2014) Trent Gaugler et al. NATURE GENETICS
- Reciprocal signaling between translational control pathways and synaptic proteins in autism spectrum disorders
- (2014) E. Santini et al. Science Signaling
- A-Kinase Anchoring Protein Lbc Coordinates a p38 Activating Signaling Complex Controlling Compensatory Cardiac Hypertrophy
- (2013) I. Perez Lopez et al. MOLECULAR AND CELLULAR BIOLOGY
- Recurrence of Autism Spectrum Disorders in Full- and Half-Siblings and Trends Over Time
- (2013) Therese K. Grønborg et al. JAMA Pediatrics
- Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
- (2013) Latha Soorya et al. Molecular Autism
- AKAPs integrate genetic findings for autism spectrum disorders
- (2013) G Poelmans et al. Translational Psychiatry
- Regulation of intracellular membrane trafficking and cell dynamics by syntaxin-6
- (2012) Jae‑Joon Jung et al. BIOSCIENCE REPORTS
- Animal model of autism induced by prenatal exposure to valproate: Altered glutamate metabolism in the hippocampus
- (2012) Roberta Bristot Silvestrin et al. BRAIN RESEARCH
- Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders
- (2012) Luigi Boccuto et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- AKAP13, CACNA1, GRIK4 and GRIA1 genetic variations may be associated with haloperidol efficacy during acute treatment
- (2012) Antonio Drago et al. EUROPEAN NEUROPSYCHOPHARMACOLOGY
- CAMK2A polymorphisms predict working memory performance in humans
- (2012) A C Easton et al. MOLECULAR PSYCHIATRY
- Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function
- (2012) Hyejung Won et al. NATURE
- Rare and common variants: twenty arguments
- (2012) Greg Gibson NATURE REVIEWS GENETICS
- High-Throughput Sequencing of mGluR Signaling Pathway Genes Reveals Enrichment of Rare Variants in Autism
- (2012) Raymond J. Kelleher III et al. PLoS One
- Elevated Glutamatergic Compounds in Pregenual Anterior Cingulate in Pediatric Autism Spectrum Disorder Demonstrated by 1H MRS and 1H MRSI
- (2012) Anthony Bejjani et al. PLoS One
- Common genetic variants, acting additively, are a major source of risk for autism
- (2012) Lambertus Klei et al. Molecular Autism
- Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability
- (2011) Fadi F. Hamdan et al. AMERICAN JOURNAL OF HUMAN GENETICS
- 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
- A-Kinase Anchoring Protein (AKAP)-Lbc Anchors a PKN-based Signaling Complex Involved in α1-Adrenergic Receptor-induced p38 Activation
- (2011) Luca Cariolato et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
- (2011) Veronica J. Vieland et al. Journal of Neurodevelopmental Disorders
- Genome-Wide Association Study of the Child Behavior Checklist Dysregulation Profile
- (2011) Eric Mick et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- mGluR5-Antagonist Mediated Reversal of Elevated Stereotyped, Repetitive Behaviors in the VPA Model of Autism
- (2011) Mili V. Mehta et al. PLoS One
- Gain-of-function glutamate receptor interacting protein 1 variants alter GluA2 recycling and surface distribution in patients with autism
- (2011) R. Mejias et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The ongoing dissection of the genetic architecture of autistic spectrum disorder
- (2011) Rob F Gillis et al. Molecular Autism
- Gene and miRNA expression profiles in autism spectrum disorders
- (2010) Mohammad M. Ghahramani Seno et al. BRAIN RESEARCH
- A genome-wide scan for common alleles affecting risk for autism
- (2010) R. Anney et al. HUMAN MOLECULAR GENETICS
- The Rho Guanine Nucleotide Exchange Factor AKAP13 (BRX) Is Essential for Cardiac Development in Mice
- (2010) Chantal M. Mayers et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Functional impact of global rare copy number variation in autism spectrum disorders
- (2010) Dalila Pinto et al. NATURE
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- Genetics of autistic disorders: review and clinical implications
- (2009) Christine M. Freitag et al. EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
- SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies
- (2009) Zongli Xu et al. NUCLEIC ACIDS RESEARCH
- Contact in the genetics of autism and schizophrenia
- (2009) J. Peter H. Burbach et al. TRENDS IN NEUROSCIENCES
- The Autistic Neuron: Troubled Translation?
- (2008) Raymond J. Kelleher et al. CELL
- The Splicing Factor SF2/ASF Regulates Translation Initiation by Enhancing Phosphorylation of 4E-BP1
- (2008) Gracjan Michlewski et al. MOLECULAR CELL
- Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disorders
- (2008) Nobuyuki Yamasaki et al. Molecular Brain
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started