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Author Details

Julie R Korenberg
University of Utah
1974
187
56
PMIDPaper TitleJournal TitlePublished Year
33564861Core transcriptional networks in Williams syndrome: IGF1-PI3K-AKT-mTOR, MAPK and actin signaling at the synapse echo autism.Hum Mol Genet2021
27834117Reward, salience, and attentional networks are activated by religious experience in devout Mormons.Soc Neurosci2018
26214361Structural integrity of the limbic-prefrontal connection: Neuropathological correlates of anxiety in Williams syndrome.Soc Neurosci2016
27509850A human neurodevelopmental model for Williams syndrome.Nature2016
26919477Assessment of the Characteristics of Orientation Distribution Functions in HARDI Using Morphological Metrics.PLoS One2016
26230578Morphological differences in the mirror neuron system in Williams syndrome.Soc Neurosci2016
26131023Violence: heightened brain attentional network response is selectively muted in Down syndrome.J Neurodev Disord2015
26464329Quantitative representation and description of intravoxel fiber complexity in HARDI.Phys Med Biol2015
24339224Dentate gyrus mediates cognitive function in the Ts65Dn/DnJ mouse model of Down syndrome.Hippocampus2014
24973601Morphometry of anatomical shape complexes with dense deformations and sparse parameters.Neuroimage2014
25105779Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome.PLoS One2014
23332975The social phenotype of Williams syndrome.Curr Opin Neurobiol2013
24219698Genetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing.Dev Neuropsychol2013
24179822Abnormal brain synchrony in Down Syndrome.Neuroimage Clin2013
22465678Serial section registration of axonal confocal microscopy datasets for long-range neural circuit reconstruction.J Neurosci Methods2012
23286134Topology preserving atlas construction from shape data without correspondence using sparse parameters.Med Image Comput Comput Assist Interv2012
22993292Patient-empowerment interactive technologies.Sci Transl Med2012
23049519Sensitivity of the autonomic nervous system to visual and auditory affect across social and non-social domains in williams syndrome.Front Psychol2012
22719898Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior.PLoS One2012
22072978Over-expression of DSCAM and COL6A2 cooperatively generates congenital heart defects.PLoS Genet2011
19822162Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome.Neuropsychologia2010
21304831A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome.J Neurodev Disord2010
20422020Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex.PLoS One2010
20385151Affiliative behavior in Williams syndrome: social perception and real-life social behavior.Neuropsychologia2010
20005238Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome.Neuropsychologia2010
19282872William's syndrome: gene expression is related to parental origin and regional coordinate control.J Hum Genet2009
19597142The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies.Proc Natl Acad Sci U S A2009
19690507Down syndrome: the crucible for treating genomic imbalance.Genet Med2009
19458618Down's syndrome suppression of tumour growth and the role of the calcineurin inhibitor DSCR1.Nature2009
19205026Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.Am J Med Genet A2009
19261893DSCAM deficiency causes loss of pre-inspiratory neuron synchroneity and perinatal death.J Neurosci2009
18211726Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.Dev Psychopathol2008
18924169Association between cerebral shape and social use of language in Williams syndrome.Am J Med Genet A2008
16996488Frontostriatal dysfunction during response inhibition in Williams syndrome.Biol Psychiatry2007
17978036More is not always better: increased fractional anisotropy of superior longitudinal fasciculus associated with poor visuospatial abilities in Williams syndrome.J Neurosci2007
17973792Nature and nurture: Williams syndrome across cultures.Dev Sci2007
17518929Reduced parietal and visual cortical activation during global processing in Williams syndrome.Dev Med Child Neurol2007
175127563D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.Neuroimage2007
16418593Deletion of chromosome 21 disturbs human brain morphogenesis.Genet Med2006
16707799Symmetry of cortical folding abnormalities in Williams syndrome revealed by surface-based analyses.J Neurosci2006
16810457The neurobiology of Williams syndrome: cascading influences of visual system impairment?Cell Mol Life Sci2006
16806978To modulate or not to modulate: differing results in uniquely shaped Williams syndrome brains.Neuroimage2006
16876437Anomalous sylvian fissure morphology in Williams syndrome.Neuroimage2006
16901723Increased local gyrification mapped in Williams syndrome.Neuroimage2006
15670775Molecular and cellular characterization of the Down syndrome critical region protein 2.Biochem Biophys Res Commun2005
15843618Abnormal cortical complexity and thickness profiles mapped in Williams syndrome.J Neurosci2005
15642924Evidence for superior parietal impairment in Williams syndrome.Neurology2005
15777750Relative sparing of primary auditory cortex in Williams Syndrome.Brain Res2005
15072519The relationship between age and IQ in adults with Williams syndrome.Am J Ment Retard2004
14708099"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.Am J Med Genet A2004
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Collaborators

Xiao-Ning Chen
College of Geographic and Environmental Science, Northwest Normal University
Co-authored papers 72
Melvin I Simon
Co-authored papers 7
Kazuhiro Yamakawa
RIKEN Center for Brain Science
Co-authored papers 7
Mark A Eckert
Medical University of South Carolina
Co-authored papers 7
Gary E Lyons
University of Wisconsin-Madison
Co-authored papers 5
Ren?? S Hubert
Amgen Inc.
Co-authored papers 5
Guido Gerig
New York University
Co-authored papers 4
Bruce W Birren
Broad Institute of MIT and Harvard
Co-authored papers 4
David R Cox
Rinat (Pfizer Inc.)
Co-authored papers 4
Paul M Thompson
University of Southern California
Co-authored papers 4
Timothy T Brown
University of California San Diego
Co-authored papers 3
Jerome I Rotter
Co-authored papers 3
Arthur W Toga
Keio University School of Medicine
Co-authored papers 3
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Knight Cancer Institute, Oregon Health and Science University
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University of Wisconsin Medical School, 1300 University Avenue
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Jennifer A Geaga
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Katheleen J Gardiner
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Kiralee M Hayashi
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Kazutoyo Osoegawa
Co-authored papers 2
David Haussler
Genomics Institute, University of California Santa Cruz
Co-authored papers 2
Matthew Erhart
University of California San Diego
Co-authored papers 2
Vernon R Sutton
Baylor College of Medicine
Co-authored papers 2
Pieter J de Jong
Center for Genetics, Children's Hospital Oakland Research Institute
Co-authored papers 2
Bruno Dallapiccola
Co-authored papers 2
Jean Weissenbach
Institut Francois Jacob, CNRS, Universite Paris-Saclay
Co-authored papers 2
John M Greally
Co-authored papers 2
Eric M Sobel
Co-authored papers 2
Maria Cristina Digilio
Co-authored papers 2
Release 1.2