| human | Q5 |
| P2038 | ResearchGate profile ID | Joseph_Piven |
| P735 | given name | Joseph | Q471788 |
| Joseph | Q471788 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q42029670 | A JOINT FRAMEWORK FOR 4D SEGMENTATION AND ESTIMATION OF SMOOTH TEMPORAL APPEARANCE CHANGES |
| Q58575698 | A Novel Framework for the Local Extraction of Extra-Axial Cerebrospinal Fluid from MR Brain Images |
| Q42114486 | A PRELIMINARY STUDY ON THE EFFECT OF MOTION CORRECTION ON HARDI RECONSTRUCTION. |
| Q50306241 | A case of autism and uniparental disomy of chromosome 1. |
| Q30726611 | A framework for longitudinal data analysis via shape regression |
| Q55272112 | A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees. |
| Q28943508 | A genome-wide scan for common alleles affecting risk for autism |
| Q57797728 | A longitudinal study of parent-reported sensory responsiveness in toddlers at-risk for autism |
| Q37364504 | A molecular genetic study of autism and related phenotypes in extended pedigrees |
| Q35828248 | A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder |
| Q34569558 | Abnormal use of facial information in high-functioning autism |
| Q30897515 | Accurate age classification of 6 and 12 month-old infants based on resting-state functional connectivity magnetic resonance imaging data |
| Q36443925 | Adaptive prior probability and spatial temporal intensity change estimation for segmentation of the one-year-old human brain |
| Q27303731 | Altered corpus callosum morphology associated with autism over the first 2 years of life |
| Q50303437 | Analysis of face gaze in autism using "Bubbles". |
| Q34707526 | Anorexia nervosa and autism spectrum disorders: guided investigation of social cognitive endophenotypes |
| Q36835082 | Autism and the broad autism phenotype: familial patterns and intergenerational transmission |
| Q24629598 | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes |
| Q44903204 | Autism spectrum disorder screening with the CBCL/1½-5: Findings for young children at high risk for autism spectrum disorder. |
| Q34233402 | Autism spectrum disorders in older adults: toward defining a research agenda |
| Q30658653 | Behavioral, cognitive, and adaptive development in infants with autism spectrum disorder in the first 2 years of life |
| Q49337205 | Brain and behavior development in autism from birth through infancy |
| Q55184259 | Brain structure in sagittal craniosynostosis. |
| Q37097365 | Brain volume findings in 6-month-old infants at high familial risk for autism |
| Q22241878 | Broader autism phenotype: evidence from a family history study of multiple-incidence autism families |
| Q48147016 | Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism |
| Q50763852 | Commentary from the DSM-5 Workgroup on Neurodevelopmental Disorders. |
| Q24603204 | Common genetic variants on 5p14.1 associate with autism spectrum disorders |
| Q50302014 | Communicative competence in parents of children with autism and parents of children with specific language impairment |
| Q53644961 | Compressive Sensing Based Q-Space Resampling for Handling Fast Bulk Motion in Hardi Acquisitions. |
| Q48789764 | Cortical gray and white brain tissue volume in adolescents and adults with autism |
| Q47157147 | Cover art description |
| Q54996743 | Cover art description. |
| Q24646514 | Current developments in the genetics of autism: from phenome to genome |
| Q37088013 | Defining genetically meaningful language and personality traits in relatives of individuals with fragile X syndrome and relatives of individuals with autism |
| Q42559323 | Defining key features of the broad autism phenotype: a comparison across parents of multiple- and single-incidence autism families |
| Q37026392 | Development of cortical shape in the human brain from 6 to 24months of age via a novel measure of shape complexity |
| Q36040731 | Differences in white matter fiber tract development present from 6 to 24 months in infants with autism |
| Q41879803 | Diffusion imaging quality control via entropy of principal direction distribution |
| Q31095444 | Diffusion tensor imaging: Application to the study of the developing brain |
| Q57511982 | Discrimination analysis using multi-object statistics of shape and pose |
| Q36825133 | Distinct face-processing strategies in parents of autistic children |
| Q38959207 | Early brain development in infants at high risk for autism spectrum disorder |
| Q35859835 | Early brain overgrowth in autism associated with an increase in cortical surface area before age 2 years |
| Q37274205 | Early white-matter abnormalities of the ventral frontostriatal pathway in fragile X syndrome |
| Q42433488 | Emerging Executive Functioning and Motor Development in Infants at High and Low Risk for Autism Spectrum Disorder |
| Q38272216 | Erratum to: Cover essay |
| Q33960148 | Evaluation of FOXP2 as an autism susceptibility gene |
| Q28250510 | Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene |
| Q37007579 | Evidence for three subtypes of repetitive behavior in autism that differ in familiality and association with other symptoms |
| Q36443043 | Evidence of a distinct behavioral phenotype in young boys with fragile X syndrome and autism |
| Q36637859 | Frontolimbic neural circuitry at 6 months predicts individual differences in joint attention at 9 months |
| Q24596191 | Functional impact of global rare copy number variation in autism spectrum disorders |
| Q28296286 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs |
| Q36006297 | High rates of parkinsonism in adults with autism |
| Q38732844 | Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism |
| Q28943296 | Individual common variants exert weak effects on the risk for autism spectrum disorders |
| Q34784066 | Introduction to the Special Section Contribution of the UNC Neurodevelopmental Disorders Research Center (NDRC). |
| Q33749714 | Joint Attention and Brain Functional Connectivity in Infants and Toddlers |
| Q57511236 | Joint Longitudinal Modeling of Brain Appearance in Multimodal MRI for the Characterization of Early Brain Developmental Processes |
| Q21198725 | Journal of Neurodevelopmental Disorders is now a fully open access journal |
| Q43134240 | Journal of Neurodevelopmental Disorders reviewer acknowledgement 2012. |
| Q41896137 | Journal of Neurodevelopmental Disorders reviewer acknowledgement 2013. |
| Q42079435 | Journal of Neurodevelopmental Disorders reviewer acknowledgement 2014. |
| Q38337230 | Journal of Neurodevelopmental Disorders reviewer acknowledgement 2015. |
| Q47964770 | Longitudinal identification of clinically distinct neurophenotypes in young children with fragile X syndrome |
| Q33935017 | Longitudinal patterns of repetitive behavior in toddlers with autism |
| Q34296019 | Longitudinal profiles of adaptive behavior in fragile X syndrome |
| Q35165580 | Longitudinal study of amygdala volume and joint attention in 2- to 4-year-old children with autism |
| Q36913121 | Looking you in the mouth: abnormal gaze in autism resulting from impaired top-down modulation of visual attention |
| Q41873445 | MODELING LONGITUDINAL MRI CHANGES IN POPULATIONS USING A LOCALIZED, INFORMATION-THEORETIC MEASURE OF CONTRAST. |
| Q47358712 | Magnetic resonance imaging and head circumference study of brain size in autism: birth through age 2 years |
| Q27315912 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements |
| Q57511475 | Mixed-Effects Shape Models for Estimating Longitudinal Changes in Anatomy |
| Q46497731 | Moderate sedation for MRI in young children with autism |
| Q33829145 | Morphometric spatial patterns differentiating boys with fragile X syndrome, typically developing boys, and developmentally delayed boys aged 1 to 3 years |
| Q35054523 | Multi-object analysis of volume, pose, and shape using statistical discrimination |
| Q57511866 | Multivariate nonlinear mixed model to analyze longitudinal image data: MRI study of early brain development |
| Q47955281 | Naturalistic Language Recordings Reveal "Hypervocal" Infants at High Familial Risk for Autism |
| Q42550743 | Neural bases for impaired social cognition in schizophrenia and autism spectrum disorders |
| Q37700970 | Neural circuitry at age 6 months associated with later repetitive behavior and sensory responsiveness in autism |
| Q35204726 | Neuroanatomical Differences in Toddler Boys With Fragile X Syndrome and Idiopathic Autism |
| Q37411441 | Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP). |
| Q50305841 | Neurodevelopmental disorders: Accelerating progress in autism through developmental research |
| Q37235434 | Neuropsychological profile of autism and the broad autism phenotype |
| Q28741116 | Offering to share: how to put heads together in autism neuroimaging |
| Q50342461 | On the misapplication of the broad autism phenotype questionnaire in a study of autism |
| Q36248060 | Orienting to social stimuli differentiates social cognitive impairment in autism and schizophrenia |
| Q39308598 | Parent Support of Preschool Peer Relationships in Younger Siblings of Children with Autism Spectrum Disorder |
| Q36854360 | Perception of affect in biological motion cues in anorexia nervosa |
| Q35640808 | Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16. |
| Q37742597 | Potential Risk Factors for the Development of Self-Injurious Behavior among Infants at Risk for Autism Spectrum Disorder |
| Q37360303 | Prevalence of selected clinical problems in older adults with autism and intellectual disability |
| Q24631049 | Rapid automatized naming as an index of genetic liability to autism |
| Q57167275 | Rapid face orienting in infants and school-age children with and without autism: Exploring measurement invariance in eye-tracking |
| Q48345690 | Reduced relationship to cortical white matter volume revealed by tractography-based segmentation of the corpus callosum in young children with developmental delay |
| Q33927318 | Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome |
| Q40630474 | Repetitive and self-injurious behaviors: associations with caudate volume in autism and fragile X syndrome |
| Q34625213 | Repetitive behavior in 12-month-olds later classified with autism spectrum disorder |
| Q44709442 | Resting-state fMRI in sleeping infants more closely resembles adult sleep than adult wakefulness |
| Q50301795 | Social-cognition and the broad autism phenotype: identifying genetically meaningful phenotypes |
| Q50342950 | Splenium development and early spoken language in human infants |
| Q30712946 | Structural and functional magnetic resonance imaging of autism |
| Q60651199 | Subcortical Brain and Behavior Phenotypes Differentiate Infants With Autism Versus Language Delay |
| Q35533617 | Subject-Motion Correction in HARDI Acquisitions: Choices and Consequences |
| Q50302751 | Systematic screening for subtelomeric anomalies in a clinical sample of autism |
| Q34052031 | Teasing apart the heterogeneity of autism: Same behavior, different brains in toddlers with fragile X syndrome and autism |
| Q37703321 | Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome |
| Q38810604 | The Emergence of Network Inefficiencies in Infants With Autism Spectrum Disorder |
| Q35177022 | The Social Orienting Continuum and Response Scale (SOC-RS): a dimensional measure for preschool-aged children |
| Q50302174 | The broad autism phenotype questionnaire |
| Q36867719 | The broad autism phenotype questionnaire: prevalence and diagnostic classification |
| Q30585077 | Topological methods reveal high and low functioning neuro-phenotypes within fragile X syndrome |
| Q36192790 | Trajectories of early brain volume development in fragile X syndrome and autism |
| Q49054557 | Translation of the Broad Autism Phenotype Questionnaire to an Indian language: A description of the process |
| Q41860688 | UNC-Utah NA-MIC framework for DTI fiber tract analysis |
| Q47969068 | Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes |
| Q50309416 | Visual scanning of faces in autism |
| Q47302530 | Walking, Gross Motor Development, and Brain Functional Connectivity in Infants and Toddlers |
| Q48477513 | When father doesn't know best: selective disagreement between self-report and informant report of the broad autism phenotype in parents of a child with autism |
| Q37392632 | White matter microstructure and atypical visual orienting in 7-month-olds at risk for autism |
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