Published in Dialogues Clin Neurosci on September 01, 2012
A New Methodology of Viewing Extra-Axial Fluid and Cortical Abnormalities in Children with Autism via Transcranial Ultrasonography. Front Hum Neurosci (2014) 1.09
Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders. Biol Psychiatry (2014) 0.97
Autism spectrum disorder and low vitamin D at birth: a sibling control study. Mol Autism (2015) 0.94
Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders. Brain Res (2014) 0.93
Neurobiology of autism gene products: towards pathogenesis and drug targets. Psychopharmacology (Berl) (2014) 0.86
MTHFR Gene C677T Polymorphism in Autism Spectrum Disorders. Genet Res Int (2014) 0.81
Redox Regulation and the Autistic Spectrum: Role of Tryptophan Catabolites, Immuno-inflammation, Autoimmunity and the Amygdala. Curr Neuropharmacol (2014) 0.81
Neurofeedback training produces normalization in behavioural and electrophysiological measures of high-functioning autism. Philos Trans R Soc Lond B Biol Sci (2014) 0.80
Pre-clinical models of neurodevelopmental disorders: focus on the cerebellum. Rev Neurosci (2014) 0.79
An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options. Neurosci Bull (2017) 0.78
Modulation of the genome and epigenome of individuals susceptible to autism by environmental risk factors. Int J Mol Sci (2015) 0.78
Risk factors for autism spectrum disorder in the Thai population. Eur J Pediatr (2015) 0.77
Environmental risk factors for autism spectrum disorders. Nervenarzt (2016) 0.76
Uncovering the etiology of autism spectrum disorders: genomics, bioinformatics, environment, data collection and exploration, and future possibilities. Pac Symp Biocomput (2014) 0.76
An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview-Revised data. J Biomed Inform (2015) 0.75
Neuropsychological Development in Patients with Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase (LCHAD) Deficiency. JIMD Rep (2015) 0.75
Maternal C-Reactive Protein Concentration in Early Pregnancy and Child Autistic Traits in the General Population. Paediatr Perinat Epidemiol (2015) 0.75
A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3. Eur J Hum Genet (2016) 0.75
Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors. J Pediatr Genet (2016) 0.75
Meconium exposure and autism risk. J Perinatol (2016) 0.75
Metabolic Dysfunction Underlying Autism Spectrum Disorder and Potential Treatment Approaches. Front Mol Neurosci (2017) 0.75
Measurement of Serum Superoxide Dismutase and Its Relevance to Disease Intensity Autistic Children. Maedica (Buchar) (2015) 0.75
Exploring Health Situation of Indian Children with Autism Spectrum Disorder Using Autism Treatment Evaluation Checklist (ATEC) in an Urban Area of Odisha: A Case Study. J Clin Diagn Res (2015) 0.75
Interactive Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder. J Autism Dev Disord (2017) 0.75
Adult zebrafish in CNS disease modeling: a tank that's half-full, not half-empty, and still filling. Lab Anim (NY) (2017) 0.75
Supplementation of omega 3 fatty acids may improve hyperactivity, lethargy, and stereotypy in children with autism spectrum disorders: a meta-analysis of randomized controlled trials. Neuropsychiatr Dis Treat (2017) 0.75
A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report. Clin Case Rep (2017) 0.75
Retracted Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children. Lancet (1998) 36.93
Strong association of de novo copy number mutations with autism. Science (2007) 27.84
Association between microdeletion and microduplication at 16p11.2 and autism. N Engl J Med (2008) 19.71
Structural variation of chromosomes in autism spectrum disorder. Am J Hum Genet (2008) 15.51
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet (2003) 15.31
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
De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature (2012) 13.61
Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med (1995) 12.70
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat Genet (2011) 11.94
Prevalence of autism spectrum disorders--Autism and Developmental Disabilities Monitoring Network, 14 sites, United States, 2008. MMWR Surveill Summ (2012) 11.55
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet (2006) 11.14
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron (2011) 10.61
Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature (2011) 10.16
MeCP2, a key contributor to neurological disease, activates and represses transcription. Science (2008) 10.11
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature (2009) 9.47
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP). Lancet (2006) 8.00
Identifying autism loci and genes by tracing recent shared ancestry. Science (2008) 7.72
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature (2009) 7.39
Genetic heritability and shared environmental factors among twin pairs with autism. Arch Gen Psychiatry (2011) 6.98
Recurrent 16p11.2 microdeletions in autism. Hum Mol Genet (2007) 6.75
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat Genet (2010) 6.62
Microduplications of 16p11.2 are associated with schizophrenia. Nat Genet (2009) 6.13
Neuroglial activation and neuroinflammation in the brain of patients with autism. Ann Neurol (2005) 5.95
Prevalence of autism spectrum disorders in a total population sample. Am J Psychiatry (2011) 5.85
Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron (2011) 5.78
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol Psychiatry (2006) 5.63
Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry (1977) 5.55
Epidemiology of pervasive developmental disorders. Pediatr Res (2009) 5.52
Pervasive developmental disorders in preschool children: confirmation of high prevalence. Am J Psychiatry (2005) 5.52
Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. Brain Res (2010) 5.50
Autistic traits in the general population: a twin study. Arch Gen Psychiatry (2003) 5.40
Epidemiology of autistic disorder and other pervasive developmental disorders. J Clin Psychiatry (2005) 5.30
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Am J Hum Genet (2004) 5.15
A critical review of the first 10 years of candidate gene-by-environment interaction research in psychiatry. Am J Psychiatry (2011) 5.15
Contribution of SHANK3 mutations to autism spectrum disorder. Am J Hum Genet (2007) 5.04
A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet (2009) 5.01
A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet (1999) 4.96
The genetics of autism. Pediatrics (2004) 4.93
The genetics of autism spectrum disorders and related neuropsychiatric disorders in childhood. Am J Psychiatry (2010) 4.92
Diagnostic change and the increased prevalence of autism. Int J Epidemiol (2009) 4.81
A genome-wide linkage and association scan reveals novel loci for autism. Nature (2009) 4.76
A case-control family history study of autism. J Child Psychol Psychiatry (1994) 4.66
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron (2011) 4.66
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. J Med Genet (2006) 4.64
Maternal immune activation alters fetal brain development through interleukin-6. J Neurosci (2007) 4.06
Time to give up on a single explanation for autism. Nat Neurosci (2006) 3.87
Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation. Nat Genet (2010) 3.73
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes. Mol Psychiatry (2009) 3.56
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
Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status. Am J Epidemiol (2005) 3.36
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature (1997) 3.27
Epidemiology of autism spectrum disorders in adults in the community in England. Arch Gen Psychiatry (2011) 3.19
The National Children's Study: a 21-year prospective study of 100,000 American children. Pediatrics (2006) 3.16
Prenatal risk factors for autism: comprehensive meta-analysis. Br J Psychiatry (2009) 3.16
De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proc Natl Acad Sci U S A (2010) 3.13
Sibling recurrence and the genetic epidemiology of autism. Am J Psychiatry (2010) 3.07
Familial aggregation of quantitative autistic traits in multiplex versus simplex autism. Am J Med Genet B Neuropsychiatr Genet (2009) 2.98
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet (1995) 2.94
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. PLoS Genet (2012) 2.65
Use of antidepressant medications during pregnancy: a multisite study. Am J Obstet Gynecol (2007) 2.61
Recurrent CNVs disrupt three candidate genes in schizophrenia patients. Am J Hum Genet (2008) 2.61
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol Psychiatry (2008) 2.60
Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. J Autism Dev Disord (2010) 2.59
Autistic social impairment in the siblings of children with pervasive developmental disorders. Am J Psychiatry (2006) 2.57
Perinatal factors and the development of autism: a population study. Arch Gen Psychiatry (2004) 2.54
Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLoS Genet (2011) 2.46
Novel de novo SHANK3 mutation in autistic patients. Am J Med Genet B Neuropsychiatr Genet (2009) 2.43
Why are autism spectrum conditions more prevalent in males? PLoS Biol (2011) 2.35
Microglial activation and increased microglial density observed in the dorsolateral prefrontal cortex in autism. Biol Psychiatry (2010) 2.30
Perinatal and neonatal risk factors for autism: a comprehensive meta-analysis. Pediatrics (2011) 2.13
Prenatal interaction of mutant DISC1 and immune activation produces adult psychopathology. Biol Psychiatry (2010) 2.11
Antidepressant use during pregnancy and childhood autism spectrum disorders. Arch Gen Psychiatry (2011) 2.09
Migration and autism spectrum disorder: population-based study. Br J Psychiatry (2012) 2.07
Rethinking the nature of genetic vulnerability to autistic spectrum disorders. Trends Genet (2007) 2.04
Complex segregation analysis of autism. Am J Hum Genet (1991) 1.89
Thimerosal-containing vaccines and autistic spectrum disorder: a critical review of published original data. Pediatrics (2004) 1.88
Characteristics of fetal anticonvulsant syndrome associated autistic disorder. Dev Med Child Neurol (2005) 1.88
Abnormal melatonin synthesis in autism spectrum disorders. Mol Psychiatry (2007) 1.79
Long-term effect of in vitro culture of mouse embryos with serum on mRNA expression of imprinting genes, development, and behavior. Proc Natl Acad Sci U S A (2004) 1.74
The prevalence puzzle: Autism counts. Nature (2011) 1.72
Autism spectrum disorders and autistic like traits: similar etiology in the extreme end and the normal variation. Arch Gen Psychiatry (2012) 1.66
Penetrance for copy number variants associated with schizophrenia. Hum Mol Genet (2010) 1.64
The quantitative nature of autistic social impairment. Pediatr Res (2011) 1.60
Generation of the melatonin endocrine message in mammals: a review of the complex regulation of melatonin synthesis by norepinephrine, peptides, and other pineal transmitters. Pharmacol Rev (2003) 1.60
What causes autism? Exploring the environmental contribution. Curr Opin Pediatr (2010) 1.55
Phenotypic and genetic overlap between autistic traits at the extremes of the general population. J Am Acad Child Adolesc Psychiatry (2006) 1.54
The Autism Birth Cohort: a paradigm for gene-environment-timing research. Mol Psychiatry (2010) 1.51
Do common variants play a role in risk for autism? Evidence and theoretical musings. Brain Res (2010) 1.44
Melatonin receptors, heterodimerization, signal transduction and binding sites: what's new? Br J Pharmacol (2008) 1.42
Circulating autoantibodies to neuronal and glial filament proteins in autism. Pediatr Neurol (1997) 1.40
Neuroligin-deficient mutants of C. elegans have sensory processing deficits and are hypersensitive to oxidative stress and mercury toxicity. Dis Model Mech (2010) 1.33
Nocturnal excretion of 6-sulphatoxymelatonin in children and adolescents with autistic disorder. Biol Psychiatry (2005) 1.28
Prevalence of autism spectrum disorder in adolescents born weighing <2000 grams. Pediatrics (2011) 1.28
Networks of neuronal genes affected by common and rare variants in autism spectrum disorders. PLoS Genet (2012) 1.25
Th1- and Th2-like cytokines in CD4+ and CD8+ T cells in autism. J Neuroimmunol (1998) 1.25
A twin study of autism symptoms in Sweden. Mol Psychiatry (2010) 1.22
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet (2003) 15.31
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
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders. Nat Genet (2006) 11.14
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02
Promoting social behavior with oxytocin in high-functioning autism spectrum disorders. Proc Natl Acad Sci U S A (2010) 4.02
A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet (2011) 2.71
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. PLoS Genet (2012) 2.65
Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Hum Mol Genet (2012) 2.46
Ketamine administration in depressive disorders: a systematic review and meta-analysis. Psychopharmacology (Berl) (2014) 2.37
Impaired decision making in suicide attempters. Am J Psychiatry (2005) 2.37
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders. Trends Genet (2010) 2.14
Abnormal cortical voice processing in autism. Nat Neurosci (2004) 2.11
Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders. BMC Psychiatry (2009) 2.03
Longitudinal studies of cognition in schizophrenia: meta-analysis. Br J Psychiatry (2008) 1.89
Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet (2013) 1.68
ROAMER: roadmap for mental health research in Europe. Int J Methods Psychiatr Res (2014) 1.67
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly. Am J Med Genet B Neuropsychiatr Genet (2007) 1.65
SHANK1 Deletions in Males with Autism Spectrum Disorder. Am J Hum Genet (2012) 1.59
Fronto-striatal overactivation in euthymic bipolar patients during an emotional go/nogo task. Am J Psychiatry (2007) 1.45
Clinical staging in psychiatry: a cross-cutting model of diagnosis with heuristic and practical value. Br J Psychiatry (2013) 1.43
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet (2011) 1.43
Conscious and subliminal conflicts in normal subjects and patients with schizophrenia: the role of the anterior cingulate. Proc Natl Acad Sci U S A (2003) 1.36
Anxiety and depression comorbidities in irritable bowel syndrome (IBS): a systematic review and meta-analysis. Eur Arch Psychiatry Clin Neurosci (2014) 1.34
Age at onset in bipolar I affective disorder: further evidence for three subgroups. Am J Psychiatry (2003) 1.33
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders. Biol Psychiatry (2009) 1.32
Four-factor structure of obsessive-compulsive disorder symptoms in children, adolescents, and adults. J Am Acad Child Adolesc Psychiatry (2008) 1.28
Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet (2007) 1.27
Executive dysfunctions as potential markers of familial vulnerability to bipolar disorder and schizophrenia. Psychiatry Res (2004) 1.27
Neuroimaging-based markers of bipolar disorder: evidence from two meta-analyses. J Affect Disord (2011) 1.25
Progress toward treatments for synaptic defects in autism. Nat Med (2013) 1.24
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders. Am J Med Genet B Neuropsychiatr Genet (2006) 1.24
Admixture analysis of age at first suicide attempt. J Psychiatr Res (2009) 1.20
Immunological and autoimmune considerations of Autism Spectrum Disorders. J Autoimmun (2013) 1.17
Biomarkers in bipolar disorder: a positional paper from the International Society for Bipolar Disorders Biomarkers Task Force. Aust N Z J Psychiatry (2013) 1.12
Anxiety disorders in 318 bipolar patients: prevalence and impact on illness severity and response to mood stabilizer. J Clin Psychiatry (2003) 1.11
Tests of executive functions in first-degree relatives of schizophrenic patients: a meta-analysis. Psychol Med (2005) 1.11
Beyond genetics: childhood affective trauma in bipolar disorder. Bipolar Disord (2008) 1.11
Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations. Schizophr Bull (2014) 1.10
Affective lability and affect intensity as core dimensions of bipolar disorders during euthymic period. Psychiatry Res (2008) 1.10
A meta-analysis of whole-brain diffusion tensor imaging studies in bipolar disorder. Prog Neuropsychopharmacol Biol Psychiatry (2011) 1.09
A mechanistic basis for amplification differences between samples and between genome regions. BMC Genomics (2012) 1.06
Faux pas detection and intentional action in Asperger Syndrome. A replication on a French sample. J Autism Dev Disord (2008) 1.06
Treatment nonadherence and neurocognitive impairment in bipolar disorder. J Clin Psychiatry (2009) 1.05
Population-based and family-based association study of 5'UTR polymorphism of the reelin gene and schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2005) 1.05
Early-onset obsessive-compulsive disorder: a subgroup with a specific clinical and familial pattern? J Child Psychol Psychiatry (2005) 1.04
Association between the COMT locus and obsessive-compulsive disorder in females but not males. Am J Med Genet (2002) 1.04
Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder. Eur Psychiatry (2006) 1.04
The promise of biological markers for treatment response in first-episode psychosis: a systematic review. Schizophr Bull (2015) 1.03
Prefrontal cortex dysfunction in patients with suicidal behavior. Psychol Med (2006) 1.03
Influence of prefrontal target region on the efficacy of repetitive transcranial magnetic stimulation in patients with medication-resistant depression: a [(18)F]-fluorodeoxyglucose PET and MRI study. Int J Neuropsychopharmacol (2009) 1.02
Immuno- inflammatory markers of bipolar disorder: a review of evidence. Front Biosci (Elite Ed) (2012) 1.02
A genetic family-based association study of OLIG2 in obsessive-compulsive disorder. Arch Gen Psychiatry (2007) 1.02
A first national survey of knowledge, attitudes and behaviours towards schizophrenia, bipolar disorders and autism in France. BMC Psychiatry (2012) 1.02
The influence of four serotonin-related genes on decision-making in suicide attempters. Am J Med Genet B Neuropsychiatr Genet (2007) 0.99
Admixture analysis of age at onset in obsessive-compulsive disorder. Psychol Med (2005) 0.98
Preserved subliminal processing and impaired conscious access in schizophrenia. Arch Gen Psychiatry (2006) 0.98
Analysis of X chromosome inactivation in autism spectrum disorders. Am J Med Genet B Neuropsychiatr Genet (2008) 0.98
Preferential association between childhood emotional abuse and bipolar disorder. J Trauma Stress (2010) 0.95
Evidence for two types of bipolar depression using a dimensional approach. Psychother Psychosom (2007) 0.95
Executive deficits in psychotic and bipolar disorders - implications for our understanding of schizoaffective disorder. Eur Psychiatry (2007) 0.95
Possible association between the androgen receptor gene and autism spectrum disorder. Psychoneuroendocrinology (2009) 0.95
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother. Eur J Hum Genet (2012) 0.94
Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder. Neuroreport (2004) 0.94
Bipolar patients with suicidal behavior: toward the identification of a clinical subgroup. J Clin Psychiatry (2004) 0.94
Cortical folding difference between patients with early-onset and patients with intermediate-onset bipolar disorder. Bipolar Disord (2009) 0.93
Moral judgment in adults with autism spectrum disorders. Cognition (2011) 0.93
Comparative analysis of anti-toxoplasmic activity of antipsychotic drugs and valproate. Eur Arch Psychiatry Clin Neurosci (2013) 0.93
The role of causal and intentional judgments in moral reasoning in individuals with high functioning autism. J Autism Dev Disord (2013) 0.93
Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder. Hum Mol Genet (2012) 0.93
Factor analyses of the Suicidal Intent Scale (SIS) and the Risk-Rescue Rating Scale (RRRS): toward the identification of homogeneous subgroups of suicidal behaviors. J Affect Disord (2009) 0.92
Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a prospective follow-up study. BMC Psychiatry (2006) 0.92
Endogenous retrovirus type W GAG and envelope protein antigenemia in serum of schizophrenic patients. Biol Psychiatry (2008) 0.92
Familial aggregation of delusional proneness in schizophrenia and bipolar pedigrees. Am J Psychiatry (2003) 0.92
Clinical expression of bipolar disorder type I as a function of age and polarity at onset: convergent findings in samples from France and the United States. J Clin Psychiatry (2012) 0.92
Increased rate of twins among affected sibling pairs with autism. Am J Hum Genet (2002) 0.92
Familial resemblance for executive functions in families of schizophrenic and bipolar patients. Psychiatry Res (2006) 0.91
Schizotypal dimensions: an intermediate phenotype associated with the COMT high activity allele. Am J Med Genet B Neuropsychiatr Genet (2007) 0.91
Microstructural white matter changes in euthymic bipolar patients: a whole-brain diffusion tensor imaging study. Bipolar Disord (2009) 0.91
Correlations between objective and subjective sleep and circadian markers in remitted patients with bipolar disorder. Chronobiol Int (2014) 0.91
Reconsideration of bipolar disorder as a developmental disorder: importance of the time of onset. J Physiol Paris (2013) 0.90
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. J Pineal Res (2011) 0.90
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry (2014) 0.90
Immunity, inflammation, and bipolar disorder: diagnostic and therapeutic implications. Curr Psychiatry Rep (2013) 0.90
Childhood trauma is associated with severe clinical characteristics of bipolar disorders. J Clin Psychiatry (2013) 0.90
Anhedonia in schizophrenia: a distinct familial subtype? Schizophr Res (2003) 0.90
Autoantibodies to neurotransmitter receptors and ion channels: from neuromuscular to neuropsychiatric disorders. Front Genet (2013) 0.90
Schizotypal dimensions: continuity between schizophrenia and bipolar disorders. Schizophr Res (2005) 0.89
Cortical folding in patients with bipolar disorder or unipolar depression. J Psychiatry Neurosci (2009) 0.89
Fasting in mood disorders: neurobiology and effectiveness. A review of the literature. Psychiatry Res (2013) 0.88
Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report. PLoS One (2013) 0.88
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population. PLoS One (2010) 0.88
Emotional hyper-reactivity in normothymic bipolar patients. Bipolar Disord (2009) 0.88
[Genetics of autism: from genome scans to candidate genes]. Med Sci (Paris) (2003) 0.87
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects. Biol Psychiatry (2006) 0.87
Relationship between Toxoplasma gondii infection and bipolar disorder in a French sample. J Affect Disord (2012) 0.87
Biomarkers of bipolar disorder: specific or shared with schizophrenia? Front Biosci (Elite Ed) (2013) 0.86
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations. PLoS One (2011) 0.86
Advances in bipolar disorder: selected sessions from the 2011 International Conference on Bipolar Disorder. Ann N Y Acad Sci (2011) 0.86