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Journal of Neurodevelopmental Disorders is now a fully open access journalFunctional impact of global rare copy number variation in autism spectrum disordersCommon genetic variants on 5p14.1 associate with autism spectrum disordersAutism genome-wide copy number variation reveals ubiquitin and neuronal genesRapid automatized naming as an index of genetic liability to autismCurrent developments in the genetics of autism: from phenome to genomeAltered corpus callosum morphology associated with autism over the first 2 years of life.Mapping autism risk loci using genetic linkage and chromosomal rearrangements.Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility geneGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsOffering to share: how to put heads together in autism neuroimagingIndividual common variants exert weak effects on the risk for autism spectrum disordersA genome-wide scan for common alleles affecting risk for autismTopological methods reveal high and low functioning neuro-phenotypes within fragile X syndrome.Behavioral, cognitive, and adaptive development in infants with autism spectrum disorder in the first 2 years of life.Structural and functional magnetic resonance imaging of autism.A framework for longitudinal data analysis via shape regressionAccurate age classification of 6 and 12 month-old infants based on resting-state functional connectivity magnetic resonance imaging data.Diffusion tensor imaging: Application to the study of the developing brain.Joint Attention and Brain Functional Connectivity in Infants and ToddlersMorphometric spatial patterns differentiating boys with fragile X syndrome, typically developing boys, and developmentally delayed boys aged 1 to 3 yearsRegion-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome.Longitudinal patterns of repetitive behavior in toddlers with autism.Evaluation of FOXP2 as an autism susceptibility gene.Teasing apart the heterogeneity of autism: Same behavior, different brains in toddlers with fragile X syndrome and autism.Autism spectrum disorders in older adults: toward defining a research agenda.Longitudinal profiles of adaptive behavior in fragile X syndrome.Abnormal use of facial information in high-functioning autism.Repetitive behavior in 12-month-olds later classified with autism spectrum disorderAnorexia nervosa and autism spectrum disorders: guided investigation of social cognitive endophenotypes.Introduction to the Special Section Contribution of the UNC Neurodevelopmental Disorders Research Center (NDRC).Multi-object analysis of volume, pose, and shape using statistical discrimination.Longitudinal study of amygdala volume and joint attention in 2- to 4-year-old children with autism.The Social Orienting Continuum and Response Scale (SOC-RS): a dimensional measure for preschool-aged children.Neuroanatomical differences in toddler boys with fragile x syndrome and idiopathic autismSubject-Motion Correction in HARDI Acquisitions: Choices and ConsequencesPosterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Early brain overgrowth in autism associated with an increase in cortical surface area before age 2 yearsHigh rates of parkinsonism in adults with autism.
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P50
name
Joseph Piven
@ast
Joseph Piven
@en
Joseph Piven
@es
Joseph Piven
@nl
type
label
Joseph Piven
@ast
Joseph Piven
@en
Joseph Piven
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Joseph Piven
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prefLabel
Joseph Piven
@ast
Joseph Piven
@en
Joseph Piven
@es
Joseph Piven
@nl