相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder
Ghayda M. Mirzaa et al.
GENETICS IN MEDICINE (2020)
Autism Spectrum Disorder as a Brain-Gut-Microbiome Axis Disorder
Virginia Saurman et al.
DIGESTIVE DISEASES AND SCIENCES (2020)
Epigenetic modification of the oxytocin receptor gene: implications for autism symptom severity and brain functional connectivity
Elissar Andari et al.
NEUROPSYCHOPHARMACOLOGY (2020)
Locus-specific DNA methylation of Mecp2 promoter leads to autism-like phenotypes in mice
Zongyang Lu et al.
CELL DEATH & DISEASE (2020)
Stem Cell-Derived Exosomes in Autism Spectrum Disorder
Nicola Alessio et al.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH (2020)
Differential effects of Foxp2 disruption in distinct motor circuits
Catherine A. French et al.
MOLECULAR PSYCHIATRY (2019)
Zinc and vitamin A deficiency in a cohort of children with autism spectrum disorder
Deirdre U. Sweetman et al.
CHILD CARE HEALTH AND DEVELOPMENT (2019)
Shank3 Transgenic and Prenatal Zinc-Deficient Autism Mouse Models Show Convergent and Individual Alterations of Brain Structures in MRI
Michael Schoen et al.
FRONTIERS IN NEURAL CIRCUITS (2019)
The influence of neuroinflammation in Autism Spectrum Disorder
Samantha M. Matta et al.
BRAIN BEHAVIOR AND IMMUNITY (2019)
Atypical behaviour and connectivity in SHANK3-mutant macaques
Yang Zhou et al.
NATURE (2019)
SETD5 Regulates Chromatin Methylation State and Preserves Global Transcriptional Fidelity during Brain Development and Neuronal Wiring
Alessandro Sessa et al.
NEURON (2019)
First behavioural assessment of a novel Immp2l knockdown mouse model with relevance for Gilles de la Tourette syndrome and Autism spectrum disorder
Fabian Kreilaus et al.
BEHAVIOURAL BRAIN RESEARCH (2019)
The use of iPSC technology for modeling Autism Spectrum Disorders
Fabiele Baldino Russo et al.
NEUROBIOLOGY OF DISEASE (2019)
A large data resource of genomic copy number variation across neurodevelopmental disorders
Mehdi Zarrei et al.
NPJ GENOMIC MEDICINE (2019)
Altered social behavior in mice carrying a cortical Foxp2 deletion
Vera P. Medvedeva et al.
HUMAN MOLECULAR GENETICS (2019)
Both rare and common genetic variants contribute to autism in the Faroe Islands
Claire S. Leblond et al.
NPJ GENOMIC MEDICINE (2019)
Neural Lineage Differentiation From Pluripotent Stem Cells to Mimic Human Brain Tissues
Yean Ju Hong et al.
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY (2019)
Curcumin-primed exosomes potently ameliorate cognitive function in AD mice by inhibiting hyperphosphorylation of the Tau protein through the AKT/GSK-3β pathway
Hao Wang et al.
NANOSCALE (2019)
Epigenetics at the crossroads between genes, environment and resilience in anxiety disorders
M. A. Schiele et al.
GENES BRAIN AND BEHAVIOR (2018)
Genetics and epigenetics of autism: A Review
Mary M. Y. Waye et al.
PSYCHIATRY AND CLINICAL NEUROSCIENCES (2018)
Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review
Lara J. Duffney et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2018)
Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice
Philipp Suetterlin et al.
CEREBRAL CORTEX (2018)
The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports
Aafke Engwerda et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2018)
Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition
Luye Qin et al.
NATURE NEUROSCIENCE (2018)
Sexually dimorphic behavior, neuronal activity, and gene expression in Chd8-mutant mice
Hwajin Jung et al.
NATURE NEUROSCIENCE (2018)
22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype
Laura Ponson et al.
TRANSLATIONAL PSYCHIATRY (2018)
Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition
Elena Deliu et al.
NATURE NEUROSCIENCE (2018)
Effect of age and autism spectrum disorder on oxytocin receptor density in the human basal forebrain and midbrain
Sara M. Freeman et al.
TRANSLATIONAL PSYCHIATRY (2018)
Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years - Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2014
Jon Baio et al.
MMWR SURVEILLANCE SUMMARIES (2018)
Association Testing of Vasopressin Receptor 1a Microsatellite Polymorphisms in Non-Clinical Autism Spectrum Phenotypes
Tanya L. Procyshyn et al.
AUTISM RESEARCH (2017)
A Single Dose, Randomized, Controlled Proof-Of-Mechanism Study of a Novel Vasopressin 1a Receptor Antagonist (RG7713) in High-Functioning Adults with Autism Spectrum Disorder
Daniel Umbricht et al.
NEUROPSYCHOPHARMACOLOGY (2017)
Foxp1 regulation of neonatal vocalizations via cortical development
Noriyoshi Usui et al.
GENES & DEVELOPMENT (2017)
Advanced paternal age and childhood cancer in offspring: A nationwide register-based cohort study
Stine Kjaer Urhoj et al.
INTERNATIONAL JOURNAL OF CANCER (2017)
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice
Mihiro Shibutani et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2017)
The de novo autism spectrum disorder RELN R2290C mutation reduces Reelin secretion and increases protein disulfide isomerase expression
Dawn B. Lammert et al.
JOURNAL OF NEUROCHEMISTRY (2017)
Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity
Daniel J. Araujo et al.
JOURNAL OF NEUROSCIENCE (2017)
Environmental factors influencing the risk of autism
Padideh Karimi et al.
JOURNAL OF RESEARCH IN MEDICAL SCIENCES (2017)
Kctd13 deletion reduces synaptic transmission via increased RhoA
Christine Ochoa Escamilla et al.
NATURE (2017)
Arid1b haploinsufficiency disrupts cortical interneuron development and mouse behavior
Eui-Man Jung et al.
NATURE NEUROSCIENCE (2017)
Oxytocin and vasopressin neural networks: Implications for social behavioral diversity and translational neuroscience
Zachary V. Johnson et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2017)
Fetal and postnatal metal dysregulation in autism
Manish Arora et al.
NATURE COMMUNICATIONS (2017)
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort
Hui Guo et al.
SCIENTIFIC REPORTS (2017)
Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment
Cemre Celen et al.
ELIFE (2017)
CpG and Non-CpG Methylation in Epigenetic Gene Regulation and Brain Function
Hyun Sik Jang et al.
GENES (2017)
Maternal Immunoreactivity to Herpes Simplex Virus 2 and Risk of Autism Spectrum Disorder in Male Offspring
Milada Mahic et al.
MSPHERE (2017)
The RELN Locus in Alzheimer's Disease
Davide Seripa et al.
JOURNAL OF ALZHEIMERS DISEASE (2017)
Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3
Stefanie Pfaender et al.
SCIENTIFIC REPORTS (2017)
Setd5 is essential for mammalian development and the co-transcriptional regulation of histone acetylation
Anna B. Osipovich et al.
DEVELOPMENT (2016)
Heavy metals (Pb, Cd, As and MeHg) as risk factors for cognitive dysfunction: A general review of metal mixture mechanism in brain
Venkatanaidu Karri et al.
ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY (2016)
Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects
Carla Lintas et al.
JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2016)
CHD8 haploinsufficiency results in autistic-like phenotypes in mice
Yuta Katayama et al.
NATURE (2016)
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
Yi-Chuan Chen et al.
NATURE NEUROSCIENCE (2016)
The landscape of DNA methylation amid a perfect storm of autism aetiologies
Annie Vogel Ciernia et al.
NATURE REVIEWS NEUROSCIENCE (2016)
The emerging roles of MicroRNAs in autism spectrum disorders
Julien Fregeac et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2016)
Metals and Neuronal Metal Binding Proteins Implicated in Alzheimer's Disease
Joana S. Cristovao et al.
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2016)
Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons
Fei Yi et al.
SCIENCE (2016)
RELN Mutations in Autism Spectrum Disorder
Dawn B. Lammert et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2016)
Reelin Exerts Structural, Biochemical and Transcriptional Regulation Over Presynaptic and Postsynaptic Elements in the Adult Hippocampus
Carles Bosch et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2016)
Epigenetic Effect of Environmental Factors on Autism Spectrum Disorders
Takeo Kubota et al.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH (2016)
A rare de novo interstitial duplication of 15q15.3q21.2 in a boy with severe short stature, hypogonadism, global developmental delay and intellectual disability
Haiming Yuan et al.
MOLECULAR CYTOGENETICS (2016)
FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders
Jessica Mariani et al.
CELL (2015)
FoxP1 orchestration of ASD-relevant signaling pathways in the striatum
Daniel J. Araujo et al.
GENES & DEVELOPMENT (2015)
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci
Stephan J. Sanders et al.
NEURON (2015)
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Justin Cotney et al.
NATURE COMMUNICATIONS (2015)
Hypomethylation of miR-142 promoter and upregulation of microRNAs that target the oxytocin receptor gene in the autism prefrontal cortex
Michal Mor et al.
MOLECULAR AUTISM (2015)
Kalirin-9 and Kalirin-12 Play Essential Roles in Dendritic Outgrowth and Branching
Yan Yan et al.
CEREBRAL CORTEX (2015)
Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour
C. Bacon et al.
MOLECULAR PSYCHIATRY (2015)
The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis
D. LoParo et al.
MOLECULAR PSYCHIATRY (2015)
Maternal Infection During Pregnancy and Autism Spectrum Disorders
Ousseny Zerbo et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2015)
Reelin Gene Variants and Risk of Autism Spectrum Disorders: An Integrated Meta-Analysis
Zhenling Wang et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2014)
Zinc deficiency dysregulates the synaptic ProSAP/Shank scaffold and might contribute to autism spectrum disorders
Stefanie Grabrucker et al.
BRAIN (2014)
A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains
Manuel Irimia et al.
CELL (2014)
Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
Raphael Bernier et al.
CELL (2014)
A Role for Synaptic Zinc in ProSAP/Shank PSD Scaffold Malformation in Autism Spectrum Disorders
Andreas M. Grabrucker
DEVELOPMENTAL NEUROBIOLOGY (2014)
KDM5C mutational screening among males with intellectual disability suggestive of X-Linked inheritance and review of the literature
Thaina Fernandez Goncalves et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2014)
Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders
Li Zhu et al.
HUMAN MOLECULAR GENETICS (2014)
Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population
Shuang Liang et al.
JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B (2014)
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits
C. C. Y. Wong et al.
MOLECULAR PSYCHIATRY (2014)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis et al.
NATURE (2014)
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov et al.
NATURE (2014)
Microfluidic organs-on-chips
Sangeeta N. Bhatia et al.
NATURE BIOTECHNOLOGY (2014)
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
Celine Helsmoortel et al.
NATURE GENETICS (2014)
De Novo Mutations in Moderate or Severe Intellectual Disability
Fadi F. Hamdan et al.
PLOS GENETICS (2014)
Increased binding of MeCP2 to the GAD1 and RELN promoters may be mediated by an enrichment of 5-hmC in autism spectrum disorder (ASD) cerebellum
A. Zhubi et al.
TRANSLATIONAL PSYCHIATRY (2014)
Epigenetic Control of the Genome-Lessons from Genomic Imprinting
Bjorn T. Adalsteinsson et al.
GENES (2014)
Brief Report: Functional MRI of a Patient with 7q11.23 Duplication Syndrome and Autism Spectrum Disorder
Paolo Prontera et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2014)
Prevalence of Parent-Reported ASD and ADHD in the UK: Findings from the Millennium Cohort Study
Ginny Russell et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2014)
The Behavioral Phenotype in MECP2 Duplication Syndrome: A Comparison With Idiopathic Autism
Sarika U. Peters et al.
AUTISM RESEARCH (2013)
SHANK3 as an autism spectrum disorder-associated gene
Shigeo Uchino et al.
BRAIN & DEVELOPMENT (2013)
cPLA2α knockout mice exhibit abnormalities in the architecture and synapses of cortical neurons
Bao-Xi Qu et al.
BRAIN RESEARCH (2013)
Progress in microRNA delivery
Yu Zhang et al.
JOURNAL OF CONTROLLED RELEASE (2013)
Epigenomic strategies at the interface of genetic and environmental risk factors for autism
Janine M. LaSalle
JOURNAL OF HUMAN GENETICS (2013)
RIM3γ and RIM4γ Are Key Regulators of Neuronal Arborization
Elena Alvarez-Baron et al.
JOURNAL OF NEUROSCIENCE (2013)
Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism
E. Ben-David et al.
MOLECULAR PSYCHIATRY (2013)
SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients
Aleksandr Shcheglovitov et al.
NATURE (2013)
From neural development to cognition: unexpected roles for chromatin
Jehnna L. Ronan et al.
NATURE REVIEWS GENETICS (2013)
Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2
Claudio Toma et al.
PSYCHIATRIC GENETICS (2013)
Prevalence of autism spectrum disorders in an Icelandic birth cohort
Evald Saemundsen et al.
BMJ OPEN (2013)
The Dynamics of Autism Spectrum Disorders: How Neurotoxic Compounds and Neurotransmitters Interact
Ilona Quaak et al.
INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH (2013)
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
Brett S. Abrahams et al.
MOLECULAR AUTISM (2013)
Paternal factors in spontaneous first trimester miscarriage
Riffat Jaleel et al.
PAKISTAN JOURNAL OF MEDICAL SCIENCES (2013)
Epigenetic Signatures of Autism Trimethylated H3K4 Landscapes in Prefrontal Neurons
Hennady P. Shulha et al.
ARCHIVES OF GENERAL PSYCHIATRY (2012)
Advancing Maternal Age Is Associated With Increasing Risk for Autism: A Review and Meta-Analysis
Sven Sandin et al.
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2012)
Phosphorylation of Distinct Sites in MeCP2 Modifies Cofactor Associations and the Dynamics of Transcriptional Regulation
Michael L. Gonzales et al.
MOLECULAR AND CELLULAR BIOLOGY (2012)
KCTD13 is a major driver of mirrored neuroanatomical phenotypes of the 16p11.2 copy number variant
Christelle Golzio et al.
NATURE (2012)
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Benjamin M. Neale et al.
NATURE (2012)
The interplay between the intestinal microbiota and the brain
Stephen M. Collins et al.
NATURE REVIEWS MICROBIOLOGY (2012)
De Novo Gene Disruptions in Children on the Autistic Spectrum
Ivan Iossifov et al.
NEURON (2012)
Prevalence of Autism Spectrum Disorders in a Total Population Sample
Young Shin Kim et al.
AMERICAN JOURNAL OF PSYCHIATRY (2011)
Gene and miRNA expression profiles in autism spectrum disorders
Mohammad M. Ghahramani Seno et al.
BRAIN RESEARCH (2011)
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
Jennifer C. Darnell et al.
CELL (2011)
Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study
Patricia L. Kramer et al.
NEUROBIOLOGY OF AGING (2011)
The Genetic Variation of RELN Expression in Schizophrenia and Bipolar Disorder
Galit Ovadia et al.
PLOS ONE (2011)
Autism-Associated Gene Expression in Peripheral Leucocytes Commonly Observed between Subjects with Autism and Healthy Women Having Autistic Children
Yuki Kuwano et al.
PLOS ONE (2011)
Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice
Stephen E. P. Smith et al.
SCIENCE TRANSLATIONAL MEDICINE (2011)
Infantile zinc deficiency: Association with autism spectrum disorders
Hiroshi Yasuda et al.
SCIENTIFIC REPORTS (2011)
ADVANCING PATERNAL AND MATERNAL AGE ARE BOTH IMPORTANT FOR AUTISM RISK
Abraham Reichenberg et al.
AMERICAN JOURNAL OF PUBLIC HEALTH (2010)
Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice
Monique C. M. Balemans et al.
BEHAVIOURAL BRAIN RESEARCH (2010)
Maternal Influenza Infection During Pregnancy Impacts Postnatal Brain Development in the Rhesus Monkey
Sarah J. Short et al.
BIOLOGICAL PSYCHIATRY (2010)
FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies
Amparo Tolosa et al.
BMC MEDICAL GENETICS (2010)
Correlation between EEG abnormalities and symptoms of autism spectrum disorder (ASD)
Akihiro Yasuhara
BRAIN & DEVELOPMENT (2010)
An extended Family with a Dominantly Inherited Speech Disorder
J. A. Hurst et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Parental Autoimmune Diseases Associated With Autism Spectrum Disorders in Offspring
Alexander Keil et al.
EPIDEMIOLOGY (2010)
Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome
Marjolein H. Willemsen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Histone Methylation Regulates Memory Formation
Swati Gupta et al.
JOURNAL OF NEUROSCIENCE (2010)
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility
E. Maestrini et al.
MOLECULAR PSYCHIATRY (2010)
Detection of cytomegalovirus in preserved umbilical cord from a boy with autistic disorder
Masao Kawatani et al.
PEDIATRICS INTERNATIONAL (2010)
Promoting social behavior with oxytocin in high-functioning autism spectrum disorders
Elissar Andari et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish women
Yaping Liu et al.
PSYCHIATRIC GENETICS (2010)
Maternal Infection Requiring Hospitalization During Pregnancy and Autism Spectrum Disorders
Hjordis O. Atladottir et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2010)
Novel De Novo SHANK3 Mutation in Autistic Patients
Julie Gauthier et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2009)
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Simon G. Gregory et al.
BMC MEDICINE (2009)
BSACI guidelines for the management of drug allergy
R. Mirakian et al.
CLINICAL AND EXPERIMENTAL ALLERGY (2009)
Different Timings of Dicer Deletion Affect Neurogenesis and Gliogenesis in the Developing Mouse Central Nervous System
Yoko Kawase-Koga et al.
DEVELOPMENTAL DYNAMICS (2009)
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang et al.
NATURE (2009)
Ube3a is required for experience-dependent maturation of the neocortex
Koji Yashiro et al.
NATURE NEUROSCIENCE (2009)
Zinc and copper modulate Alzheimer Aβ levels in human cerebrospinal fluid
Dorothea Strozyk et al.
NEUROBIOLOGY OF AGING (2009)
Control of Cognition and Adaptive Behavior by the GLP/G9a Epigenetic Suppressor Complex
Anne Schaefer et al.
NEURON (2009)
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
Mamta Tahiliani et al.
SCIENCE (2009)
Sleep problems in autism spectrum disorders: Prevalence, nature, & possible biopsychosocial aetiologies
Amanda L. Richdale et al.
SLEEP MEDICINE REVIEWS (2009)
Alzheimer's disease, metal ions and metal homeostatic therapy
Paolo Zatta et al.
TRENDS IN PHARMACOLOGICAL SCIENCES (2009)
Anxiety in children and adolescents with autism spectrum disorders
Susan W. White et al.
CLINICAL PSYCHOLOGY REVIEW (2009)
Advanced Parental Age and the Risk of Autism Spectrum Disorder
Maureen S. Durkin et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2008)
Structural variation of chromosomes in autism spectrum disorder
Christian R. Marshall et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
Dan E. Arking et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Disruption of neurexin 1 associated with autism spectrum disorder
Hyung-Goo Kim et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Molecular implementation and physiological roles for histone H3 lysine 4 (H3K4) methylation
Ali Shilatifard
CURRENT OPINION IN CELL BIOLOGY (2008)
Global DNA Hypomethylation Is Associated with High Serum-Persistent Organic Pollutants in Greenlandic Inuit
Jennifer A. Rusiecki et al.
ENVIRONMENTAL HEALTH PERSPECTIVES (2008)
Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus
Tigwa H. Davis et al.
JOURNAL OF NEUROSCIENCE (2008)
Increased GAD67 mRNA expression in cerebellar interneurons in autism:: Implications for Purkinje cell dysfunction
Jane Yip et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2008)
Heterogeneous dysregulation of microRNAs across the autism spectrum
Kawther Abu-Elneel et al.
NEUROGENETICS (2008)
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Gary J. Bassell et al.
NEURON (2008)
Identifying autism loci and genes by tracing recent shared ancestry
Eric M. Morrow et al.
SCIENCE (2008)
Oxytocin, Vasopressin, and the Neurogenetics of Sociality
Zoe R. Donaldson et al.
SCIENCE (2008)
Recurrent 16p11.2 microdeletions in autism
Ravinesh A. Kumar et al.
HUMAN MOLECULAR GENETICS (2008)
Contribution of SHANK3 mutations to autism spectrum disorder
Rainald Moessner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Maternal immune activation alters fetal brain development through interleukin-6
Stephen E. P. Smith et al.
JOURNAL OF NEUROSCIENCE (2007)
Autoimmune diseases in parents of children with infantile autism: a case-control study
Svend Erik Mouridsen et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2007)
Congenital cytomegalovirus infections
Gunillat Malm et al.
SEMINARS IN FETAL & NEONATAL MEDICINE (2007)
Decreased GAD67 mRNA levels in cerebellar purkinje cells in autism: pathophysiological implications
Jane Yip et al.
ACTA NEUROPATHOLOGICA (2007)
Strong association of de novo copy number mutations with autism
Jonathan Sebat et al.
SCIENCE (2007)
Maternal and paternal age and risk of autism spectrum disorders
Lisa A. Croen et al.
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE (2007)
Epilepsy in autism spectrum disorders
Roberto Canitano
EUROPEAN CHILD & ADOLESCENT PSYCHIATRY (2007)
The role of RELN in lissencephaly and neuropsychiatric disease
Bernard S. Chang et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2007)
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
Christelle M. Durand et al.
NATURE GENETICS (2007)
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome
Erwin Petek et al.
MOLECULAR GENETICS AND GENOMICS (2007)
Epigenetic gene regulation: Linking early developmental environment to adult disease
Dana C. Dolinoy et al.
REPRODUCTIVE TOXICOLOGY (2007)
Environmental epigenomics and disease susceptibility
Randy L. Jirtle et al.
NATURE REVIEWS GENETICS (2007)
Parental age and risk of childhood cancers: a population-based cohort study from Sweden
Benjamin H. Yip et al.
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY (2006)
Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation
Raman P. Nagarajan et al.
EPIGENETICS (2006)
Perinatal risk factors and infantile autism
R. D. Maimburg et al.
ACTA PSYCHIATRICA SCANDINAVICA (2006)
Advancing paternal age and autism
Abraham Reichenberg et al.
ARCHIVES OF GENERAL PSYCHIATRY (2006)
Paternal age and spontaneous abortion
K. Kleinhaus et al.
OBSTETRICS AND GYNECOLOGY (2006)
A role for zinc in postsynaptic density asSAMbly and plasticity?
Eckart D. Gundelfinger et al.
TRENDS IN BIOCHEMICAL SCIENCES (2006)
Association between the arginine vasopressin 1a receptor (AVPR1a) gene and autism in a family-based study:: mediation by socialization skills
N Yirmiya et al.
MOLECULAR PSYCHIATRY (2006)
Frequency of gastrointestinal symptoms in children with autistic spectrum disorders and association with family history of autoimmune disease
Maria Valicenti-McDermott et al.
JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS (2006)
The crucial role of metal ions in neurodegeneration: the basis for a promising therapeutic strategy
A Gaeta et al.
BRITISH JOURNAL OF PHARMACOLOGY (2005)
Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene
WG Shu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Analysis of the RELN gene as a genetic risk factor for autism
DA Skaar et al.
MOLECULAR PSYCHIATRY (2005)
Influence of paternal age on the risk of spontaneous abortion
R Slama et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2005)
Reelin signaling is impaired in autism
SH Fatemi et al.
BIOLOGICAL PSYCHIATRY (2005)
Epigenetic overlap in autism-spectrum neurodevelopmental disorders:: MECP2 deficiency causes reduced expression of UBE3A and GABRB3
RC Samaco et al.
HUMAN MOLECULAR GENETICS (2005)
Autistic disorder and viral infections
JE Libbey et al.
JOURNAL OF NEUROVIROLOGY (2005)
Advanced paternal age and risk of fetal death: A cohort study
AMN Andersen et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2004)
Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
SJ James et al.
AMERICAN JOURNAL OF CLINICAL NUTRITION (2004)
Paternal age and schizophrenia: a population based cohort study
A Sipos et al.
BMJ-BRITISH MEDICAL JOURNAL (2004)
Perinatal factors and the development of autism - A population study
EJ Glasson et al.
ARCHIVES OF GENERAL PSYCHIATRY (2004)
Brief report: Autistic disorder in three children with cytomegalovirus infection
TL Sweeten et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2004)
Micronutrient deficiencies and cognitive functioning
MM Black
JOURNAL OF NUTRITION (2003)
Dicer is essential for mouse development
E Bernstein et al.
NATURE GENETICS (2003)
Paternal age ≥40 years:: An important risk factor for infertility
E de La Rochebrochard et al.
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY (2003)
Possible association between congenital cytomegalovirus infection and autistic disorder
Y Yamashita et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2003)
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
S Jamain et al.
NATURE GENETICS (2003)
Defining the autism minimum candidate gene region on chromosome 7
HB Hutcheson et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2003)
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder
CSL Lai et al.
BRAIN (2003)
Paternal age and risk for schizophrenia
S Zammit et al.
BRITISH JOURNAL OF PSYCHIATRY (2003)
A population-based study of measles, mumps, and rubella vaccination and autism
KM Madsen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system
JB Vincent et al.
GENOMICS (2002)
Paternal age and risk of schizophrenia in adult offspring
AS Brown et al.
AMERICAN JOURNAL OF PSYCHIATRY (2002)
Perinatal risk factors for infantile autism
CM Hultman et al.
EPIDEMIOLOGY (2002)
Paternal age and maternal age are risk factors for miscarriage; results of a multicentre European study
E de La Rochebrochard et al.
HUMAN REPRODUCTION (2002)
FOXP2 is not a major susceptibility gene for autism or specific language impairment
DF Newbury et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder
SH Fatemi et al.
CELLULAR AND MOLECULAR NEUROBIOLOGY (2002)
Genomic screen and follow-up analysis for autistic disorder
YJ Shao et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2002)
Reelin gene alleles and susceptibility to autism spectrum disorders
H Zhang et al.
MOLECULAR PSYCHIATRY (2002)
A tumor necrosis factor α- and interleukin 6-inducible protein that interacts with the small subunit of DNA polymerase δ and proliferating cell nuclear antigen
H He et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
A forkhead-domain gene is mutated in a severe speech and language disorder
CSL Lai et al.
NATURE (2001)
Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors
WG Shu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Zinc and cognitive development
S Bhatnagar et al.
BRITISH JOURNAL OF NUTRITION (2001)
Advancing paternal age and the risk of schizophrenia
D Malaspina et al.
ARCHIVES OF GENERAL PSYCHIATRY (2001)
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
AM Persico et al.
MOLECULAR PSYCHIATRY (2001)
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual
JB Vincent et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Reelin controls position of autonomic neurons in the spinal cord
JW Yip et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Reelin binds α3β1 integrin and inhibits neuronal migration
L Dulabon et al.
NEURON (2000)
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations
SE Hong et al.
NATURE GENETICS (2000)