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“Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autism.”, Sci Signal, vol. 11, no. 513, 2018.
, “Age-Related Effects and Sex Differences in Gray Matter Density, Volume, Mass, and Cortical Thickness from Childhood to Young Adulthood.”, J Neurosci, vol. 37, no. 20, pp. 5065-5073, 2017.
, “Common and Dissociable Mechanisms of Executive System Dysfunction Across Psychiatric Disorders in Youth.”, Am J Psychiatry, vol. 173, no. 5, pp. 517-26, 2016.
, “The impact of quality assurance assessment on diffusion tensor imaging outcomes in a large-scale population-based cohort.”, Neuroimage, vol. 125, pp. 903-919, 2016.
, “The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth.”, Neuroimage, vol. 124, no. Pt B, pp. 1115-1119, 2016.
, “The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder.”, Sci Rep, vol. 6, p. 19372, 2016.
, “Structural Brain Abnormalities in Youth With Psychosis Spectrum Symptoms.”, JAMA Psychiatry, vol. 73, no. 5, pp. 515-24, 2016.
, “Functional neuroimaging abnormalities in youth with psychosis spectrum symptoms.”, JAMA Psychiatry, vol. 72, no. 5, pp. 456-65, 2015.
, , “Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.”, Hum Genet, vol. 134, no. 6, pp. 539-51, 2015.
, “Imaging patterns of brain development and their relationship to cognition.”, Cereb Cortex, vol. 25, no. 6, pp. 1676-84, 2015.
, “Linked Sex Differences in Cognition and Functional Connectivity in Youth.”, Cereb Cortex, vol. 25, no. 9, pp. 2383-94, 2015.
, “The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative.”, J Child Psychol Psychiatry, vol. 56, no. 12, pp. 1356-1369, 2015.
, “Psychometric properties of the Penn Computerized Neurocognitive Battery.”, Neuropsychology, vol. 29, no. 2, pp. 235-46, 2015.
, “Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.”, Am J Hum Genet, vol. 94, no. 5, pp. 677-94, 2014.
, “Etiology of autism spectrum disorder: a genomics perspective.”, Curr Psychiatry Rep, vol. 16, no. 11, p. 501, 2014.
, “Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population.”, Mol Autism, vol. 5, no. 1, p. 5, 2014.
, “The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.”, Nat Commun, vol. 5, p. 4074, 2014.
, “Neuroimaging of the Philadelphia neurodevelopmental cohort.”, Neuroimage, vol. 86, pp. 544-53, 2014.
, “Sex differences in the structural connectome of the human brain.”, Proc Natl Acad Sci U S A, vol. 111, no. 2, pp. 823-8, 2014.
, “Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.”, Mol Autism, vol. 5, no. 1, p. 18, 2014.
, “Within-individual variability in neurocognitive performance: age- and sex-related differences in children and youths from ages 8 to 21.”, Neuropsychology, vol. 28, no. 4, pp. 506-18, 2014.
, “Common variation contributes to the genetic architecture of social communication traits.”, Mol Autism, vol. 4, no. 1, p. 34, 2013.
, “The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future.”, Genet Med, vol. 15, no. 10, pp. 761-71, 2013.
, “Functional maturation of the executive system during adolescence.”, J Neurosci, vol. 33, no. 41, pp. 16249-61, 2013.
, “Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.”, Nat Genet, vol. 45, no. 9, pp. 984-94, 2013.
, “Heterogeneous impact of motion on fundamental patterns of developmental changes in functional connectivity during youth.”, Neuroimage, vol. 83, pp. 45-57, 2013.
, “Practical challenges in integrating genomic data into the electronic health record.”, Genet Med, vol. 15, no. 10, pp. 772-8, 2013.
, “Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth.”, Neuroimage, vol. 60, no. 1, pp. 623-32, 2012.
, “Individual common variants exert weak effects on the risk for autism spectrum disorders.”, Hum Mol Genet, vol. 21, no. 21, pp. 4781-92, 2012.
, “A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.”, Hum Genet, vol. 131, no. 4, pp. 565-79, 2012.
, “Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.”, Biol Psychiatry, vol. 71, no. 5, pp. 392-402, 2012.
, “Rare genomic deletions and duplications and their role in neurodevelopmental disorders.”, Curr Top Behav Neurosci, vol. 12, pp. 345-60, 2012.
, “An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males.”, Mol Autism, vol. 2, no. 1, p. 18, 2011.
, “Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.”, Am J Psychiatry, vol. 167, no. 11, pp. 1364-72, 2010.
, “Functional impact of global rare copy number variation in autism spectrum disorders.”, Nature, vol. 466, no. 7304, pp. 368-72, 2010.
, “A genome-wide scan for common alleles affecting risk for autism.”, Hum Mol Genet, vol. 19, no. 20, pp. 4072-82, 2010.
, “A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.”, Mol Autism, vol. 1, no. 1, p. 5, 2010.
, “Population-based study of genetic variation in individuals with autism spectrum disorders from Croatia.”, BMC Med Genet, vol. 11, p. 134, 2010.
, “Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.”, Nature, vol. 459, no. 7246, pp. 569-73, 2009.
, “Common genetic variants on 5p14.1 associate with autism spectrum disorders.”, Nature, vol. 459, no. 7246, pp. 528-33, 2009.
, “Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.”, PLoS Genet, vol. 5, no. 6, p. e1000536, 2009.
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