Published in Pediatrics on March 01, 2009
The conundrums of understanding genetic risks for autism spectrum disorders. Nat Neurosci (2011) 2.61
Maternal infection and immune involvement in autism. Trends Mol Med (2011) 1.78
Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability. Am J Psychiatry (2010) 1.58
Gastrointestinal dysfunction in autism: parental report, clinical evaluation, and associated factors. Autism Res (2012) 1.55
Short-chain fatty acid fermentation products of the gut microbiome: implications in autism spectrum disorders. Microb Ecol Health Dis (2012) 1.35
Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase. J Neurosci (2011) 1.22
The mind-body-microbial continuum. Dialogues Clin Neurosci (2011) 1.20
Genetics of autistic disorders: review and clinical implications. Eur Child Adolesc Psychiatry (2009) 1.19
Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments. Neuropsychopharmacology (2011) 1.15
Medical comorbidities in autism: challenges to diagnosis and treatment. Neurotherapeutics (2010) 1.13
Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met. Curr Opin Neurobiol (2011) 1.12
Prader-Willi syndrome and autism spectrum disorders: an evolving story. J Neurodev Disord (2011) 1.05
Association of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression. Transl Psychiatry (2011) 1.02
Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET. Toxicol Sci (2010) 1.00
Decreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal Disease. Biomark Insights (2009) 0.96
Rigid-compulsive behaviors are associated with mixed bowel symptoms in autism spectrum disorder. J Autism Dev Disord (2014) 0.91
Immune dysregulation in autism spectrum disorder. Eur J Pediatr (2013) 0.88
Association of maternal report of infant and toddler gastrointestinal symptoms with autism: evidence from a prospective birth cohort. JAMA Psychiatry (2015) 0.88
Prenatal expression of MET receptor tyrosine kinase in the fetal mouse dorsal raphe nuclei and the visceral motor/sensory brainstem. Dev Neurosci (2013) 0.87
The bacterial peptidoglycan-sensing molecule Pglyrp2 modulates brain development and behavior. Mol Psychiatry (2016) 0.87
The Impact of Neuroimmune Alterations in Autism Spectrum Disorder. Front Psychiatry (2015) 0.86
Myeloid dendritic cells frequencies are increased in children with autism spectrum disorder and associated with amygdala volume and repetitive behaviors. Brain Behav Immun (2012) 0.85
The clinical-basic interface in defining pathogenesis in disorders of neurodevelopmental origin. Neuron (2010) 0.85
Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome. Transl Psychiatry (2013) 0.85
MET receptor tyrosine kinase as an autism genetic risk factor. Int Rev Neurobiol (2013) 0.84
Parent-reported gastro-intestinal symptoms in children with autism spectrum disorders. J Autism Dev Disord (2013) 0.83
Patterns of Risk for Multiple Co-Occurring Medical Conditions Replicate Across Distinct Cohorts of Children with Autism Spectrum Disorder. Autism Res (2015) 0.83
Enrichment of elevated plasma F2t-isoprostane levels in individuals with autism who are stratified by presence of gastrointestinal dysfunction. PLoS One (2013) 0.82
Risperidone-related improvement of irritability in children with autism is not associated with changes in serum of epidermal growth factor and interleukin-13. J Child Adolesc Psychopharmacol (2011) 0.80
Modeling autism: a systems biology approach. J Clin Bioinforma (2012) 0.79
The Pleiotropic MET Receptor Network: Circuit Development and the Neural-Medical Interface of Autism. Biol Psychiatry (2016) 0.78
Effects of food on physical and sleep complaints in children with ADHD: a randomised controlled pilot study. Eur J Pediatr (2010) 0.78
Autism Linked to Increased Oncogene Mutations but Decreased Cancer Rate. PLoS One (2016) 0.77
Gastrointestinal tract abnormalities induced by prenatal valproic Acid exposure in rat offspring. Toxicol Res (2013) 0.77
Characterizing genes with distinct methylation patterns in the context of protein-protein interaction network: application to human brain tissues. PLoS One (2013) 0.76
A Putative Blood-Based Biomarker for Autism Spectrum Disorder-Associated Ileocolitis. Sci Rep (2016) 0.75
The Genetic Intersection of Neurodevelopmental Disorders and Shared Medical Comorbidities - Relations that Translate from Bench to Bedside. Front Psychiatry (2016) 0.75
Maladaptive Behavior and Gastrointestinal Disorders in Children with Autism Spectrum Disorder. Pediatr Gastroenterol Hepatol Nutr (2015) 0.75
Brief Report: Association Between Autism Spectrum Disorder, Gastrointestinal Problems and Perinatal Risk Factors Within Sibling Pairs. J Autism Dev Disord (2017) 0.75
Strong association of de novo copy number mutations with autism. Science (2007) 27.84
Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet (2007) 14.05
Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature (2012) 13.71
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. N Engl J Med (2008) 10.88
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron (2011) 10.61
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature (2009) 9.47
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature (2009) 7.39
Autism spectrum disorders: developmental disconnection syndromes. Curr Opin Neurobiol (2007) 6.96
Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet (2009) 6.13
Synaptic, transcriptional and chromatin genes disrupted in autism. Nature (2014) 5.30
Contribution of SHANK3 mutations to autism spectrum disorder. Am J Hum Genet (2007) 5.04
Schizophrenia as a disorder of neurodevelopment. Annu Rev Neurosci (2002) 4.36
Dynamics of obesity and chronic health conditions among children and youth. JAMA (2010) 4.22
A genetic variant that disrupts MET transcription is associated with autism. Proc Natl Acad Sci U S A (2006) 3.55
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet (2009) 3.42
Induction and maintenance infliximab therapy for the treatment of moderate-to-severe Crohn's disease in children. Gastroenterology (2006) 3.32
Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007. Pediatrics (2009) 3.24
A multisite study of the clinical diagnosis of different autism spectrum disorders. Arch Gen Psychiatry (2011) 2.99
Treatment of attention-deficit/hyperactivity disorder: overview of the evidence. Pediatrics (2005) 2.88
A transient placental source of serotonin for the fetal forebrain. Nature (2011) 2.71
Serotonin modulates the response of embryonic thalamocortical axons to netrin-1. Nat Neurosci (2007) 2.70
Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism (2012) 2.67
The conundrums of understanding genetic risks for autism spectrum disorders. Nat Neurosci (2011) 2.61
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron (2013) 2.45
Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report. Pediatrics (2010) 2.45
The Food and Drug Administration's deliberations on antidepressant use in pediatric patients. Pediatrics (2005) 2.37
A review of the evidence for the medical home for children with special health care needs. Pediatrics (2008) 2.36
Prenatal exposure to drugs: effects on brain development and implications for policy and education. Nat Rev Neurosci (2009) 2.33
A national profile of the health care experiences and family impact of autism spectrum disorder among children in the United States, 2005-2006. Pediatrics (2008) 2.21
Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction. J Neurosci (2003) 2.18
Molecular evidence for increased expression of genes related to immune and chaperone function in the prefrontal cortex in schizophrenia. Biol Psychiatry (2007) 2.12
A smoking cessation intervention for parents of children who are hospitalized for respiratory illness: the stop tobacco outreach program. Pediatrics (2003) 2.05
Disruption of cerebral cortex MET signaling in autism spectrum disorder. Ann Neurol (2007) 2.02
How the timing and quality of early experiences influence the development of brain architecture. Child Dev (2010) 1.87
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proc Natl Acad Sci U S A (2012) 1.85
Gene expression profiling reveals alterations of specific metabolic pathways in schizophrenia. J Neurosci (2002) 1.79
Systematic evidence review of newborn screening and treatment of severe combined immunodeficiency. Pediatrics (2010) 1.77
Early experience modifies the postnatal assembly of autonomic emotional motor circuits in rats. J Neurosci (2005) 1.76
The organization of the transcriptional network in specific neuronal classes. Mol Syst Biol (2009) 1.74
Cardiovascular monitoring and stimulant drugs for attention-deficit/hyperactivity disorder. Pediatrics (2008) 1.72
Association and linkage analyses of RGS4 polymorphisms in schizophrenia. Hum Mol Genet (2002) 1.68
Critical appraisal of DNA microarrays in psychiatric genomics. Biol Psychiatry (2006) 1.66
Cardiovascular risk of stimulant treatment in pediatric attention-deficit/hyperactivity disorder: update and clinical recommendations. J Am Acad Child Adolesc Psychiatry (2011) 1.66
Response to joint attention in toddlers at risk for autism spectrum disorder: a prospective study. J Autism Dev Disord (2007) 1.65
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. Autism Res (2008) 1.61
Integration of neuronal clones in the radial cortical columns by EphA and ephrin-A signalling. Nature (2009) 1.59
RGS4-dependent attenuation of M4 autoreceptor function in striatal cholinergic interneurons following dopamine depletion. Nat Neurosci (2006) 1.58
Gastrointestinal dysfunction in autism: parental report, clinical evaluation, and associated factors. Autism Res (2012) 1.55
Incomplete specialty referral among children in community health centers. J Pediatr (2011) 1.54
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. PLoS Genet (2013) 1.53
Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase. Proc Natl Acad Sci U S A (2005) 1.53
Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics (2013) 1.51
Financial burden for families of children with special health care needs. Matern Child Health J (2005) 1.51
Breastfeeding advice given to African American and white women by physicians and WIC counselors. Public Health Rep (2003) 1.50
Television viewing and initiation of smoking among youth. Pediatrics (2002) 1.50
Mental health conditions among school-aged children: geographic and sociodemographic patterns in prevalence and treatment. J Dev Behav Pediatr (2012) 1.48
Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior. Proc Natl Acad Sci U S A (2012) 1.48
Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. PLoS Genet (2013) 1.48
Strategies for addressing barriers to publishing pediatric quality improvement research. Pediatrics (2011) 1.47
Dissociation of corticothalamic and thalamocortical axon targeting by an EphA7-mediated mechanism. Neuron (2005) 1.44
Head lag in infants at risk for autism: a preliminary study. Am J Occup Ther (2012) 1.44
Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. BMC Med Genet (2005) 1.44
Transition of the patient with inflammatory bowel disease from pediatric to adult care: recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition. J Pediatr Gastroenterol Nutr (2002) 1.43
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet (2011) 1.43
Intervention with parental smokers in an outpatient pediatric clinic using counseling and nicotine replacement. Pediatrics (2003) 1.40
Amygdala gene expression correlates of social behavior in monkeys experiencing maternal separation. J Neurosci (2007) 1.35
Diagnostic practices for attention deficit hyperactivity disorder: a national survey of primary care physicians. Ambul Pediatr (2005) 1.35
Single-neuron RNA-Seq: technical feasibility and reproducibility. Front Genet (2012) 1.32
Autism-associated promoter variant in MET impacts functional and structural brain networks. Neuron (2012) 1.29
Built environment and weight disparities among children in high- and low-income towns. Acad Pediatr (2009) 1.28
Obesity and the built environment among Massachusetts children. Clin Pediatr (Phila) (2009) 1.27
Association and mutation analyses of 16p11.2 autism candidate genes. PLoS One (2009) 1.27
Enhanced activity of human serotonin transporter variants associated with autism. Philos Trans R Soc Lond B Biol Sci (2009) 1.25
RGS4 is a negative regulator of insulin release from pancreatic beta-cells in vitro and in vivo. Proc Natl Acad Sci U S A (2010) 1.25
Correlates of use of specialty care. Pediatrics (2004) 1.24
A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. Am J Med Genet B Neuropsychiatr Genet (2004) 1.23
Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase. J Neurosci (2011) 1.22
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Hum Mol Genet (2011) 1.22
Evidence for family-centered care for children with special health care needs: a systematic review. Acad Pediatr (2011) 1.22
Genetic analysis of biological pathway data through genomic randomization. Hum Genet (2011) 1.20
Fetal mechanisms in neurodevelopmental disorders. Pediatr Neurol (2008) 1.18
Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. J Neurodev Disord (2011) 1.17
Latent class analysis of early developmental trajectory in baby siblings of children with autism. J Child Psychol Psychiatry (2012) 1.16
Recommendations for evaluation and treatment of common gastrointestinal problems in children with ASDs. Pediatrics (2010) 1.16
Trends in attention deficit hyperactivity disorder ambulatory diagnosis and medical treatment in the United States, 2000-2010. Acad Pediatr (2012) 1.15
Association between parents' and children's use of oral health services. Pediatrics (2010) 1.14
Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain. J Comp Neurol (2009) 1.13
Weighing the evidence for newborn screening for early-infantile Krabbe disease. Genet Med (2010) 1.12
Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait. Biol Psychiatry (2013) 1.11
Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia. Biol Psychiatry (2007) 1.10
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Eur J Hum Genet (2006) 1.10
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes. BMC Med Genet (2004) 1.10