| scholarly article | Q13442814 |
| P50 | author | Allan L. Reiss | Q52274856 |
| P2093 | author name string | Shelli Kesler | |
| Mark A Eckert | |||
| Hower Kwon | |||
| Asya Karchemskiy | |||
| Melody Chang | |||
| Fredric E Rose | |||
| Margaret F Reynolds | |||
| Al Galaburda | |||
| P2860 | cites work | Neural components of topographical representation | Q24600411 |
| Emotion circuits in the brain | Q27860733 | ||
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| A voxel-based morphometric study of ageing in 465 normal adult human brains | Q28214553 | ||
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| A cortical representation of the local visual environment | Q28268818 | ||
| Cognitive and emotional influences in anterior cingulate cortex | Q29547440 | ||
| The amygdala: vigilance and emotion | Q29615014 | ||
| Regional differences in synaptogenesis in human cerebral cortex | Q29616105 | ||
| Music skills and the expressive interpretation of music in children with Williams-Beuren syndrome: pitch, rhythm, melodic imagery, phrasing, and musical affect. | Q30329500 | ||
| Increased gyrification in Williams syndrome: evidence using 3D MRI methods. | Q30330376 | ||
| Visual and visuospatial development in young children with Williams syndrome. | Q52135088 | ||
| Anomalous brain activation during face and gaze processing in Williams syndrome. | Q53742102 | ||
| Explicit and implicit neural mechanisms for processing of social information from facial expressions: A functional magnetic resonance imaging study | Q57773817 | ||
| Vision: a window on consciousness | Q74092820 | ||
| Neural correlates of auditory perception in Williams syndrome: an fMRI study. | Q30332364 | ||
| Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome | Q30577163 | ||
| Maturation of white matter in the human brain: a review of magnetic resonance studies | Q30644997 | ||
| Effects of image orientation on the comparability of pediatric brain volumes using three-dimensional MR data | Q30651839 | ||
| Prefrontal cortical networks related to visceral function and mood | Q33692819 | ||
| Genetic influences on brain structure | Q33955853 | ||
| I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses | Q34011145 | ||
| Dissociable prefrontal brain systems for attention and emotion | Q34038744 | ||
| Multiple routes to memory: distinct medial temporal lobe processes build item and source memories | Q34176480 | ||
| Is the human amygdala specialized for processing social information? | Q34193930 | ||
| Anxiety, Fears, and Phobias in Persons With Williams Syndrome | Q34194633 | ||
| Localization and globalization in conscious vision | Q34205337 | ||
| Shared neural control of attentional shifts and eye movements | Q34405709 | ||
| Behavioral and emotional disturbance in individuals with Williams syndrome | Q34434106 | ||
| The functional anatomy of attention to visual motion. A functional MRI study | Q38839154 | ||
| Hemispheric and gender-related differences in the gross morphology of the anterior cingulate/paracingulate cortex in normal volunteers: an MRI morphometric study | Q40735098 | ||
| The effects of pretectal and superior collicular lesions on binocular vision | Q41474028 | ||
| IV. Neuroanatomy of Williams syndrome: a high-resolution MRI study | Q41757188 | ||
| Face and place processing in Williams syndrome: evidence for a dorsal-ventral dissociation | Q43889830 | ||
| Pathways for emotion: interactions of prefrontal and anterior temporal pathways in the amygdala of the rhesus monkey. | Q44230550 | ||
| Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans | Q44575175 | ||
| Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex | Q47177921 | ||
| "Frog, where are you?" Narratives in children with specific language impairment, early focal brain injury, and Williams syndrome | Q47203700 | ||
| Automated Talairach atlas-based parcellation and measurement of cerebral lobes in children | Q48106484 | ||
| Common and distinct neural responses during direct and incidental processing of multiple facial emotions. | Q48180387 | ||
| Attentional Characteristics of Infants and Toddlers With Williams Syndrome During Triadic Interactions | Q48318374 | ||
| Emotional valence modulates activity in the posterior fusiform gyrus and inferior medial prefrontal cortex in social perception | Q48349742 | ||
| Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservation. | Q48425546 | ||
| Reliability and validity of an algorithm for fuzzy tissue segmentation of MRI. | Q48459211 | ||
| Distributional assumptions in voxel-based morphometry. | Q48469787 | ||
| A neuromodulatory role for the human amygdala in processing emotional facial expressions. | Q48487002 | ||
| Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders | Q48498911 | ||
| Neural interaction of the amygdala with the prefrontal and temporal cortices in the processing of facial expressions as revealed by fMRI. | Q48652333 | ||
| Selective and divided attention during visual discriminations of shape, color, and speed: functional anatomy by positron emission tomography. | Q48680997 | ||
| A specific deficit of dorsal stream function in Williams' syndrome. | Q48704698 | ||
| Enlarged cerebellar vermis in Williams syndrome. | Q48771509 | ||
| Medial temporal lobe activity associated with active maintenance of novel information. | Q48785279 | ||
| Corpus callosum morphology of Williams syndrome: relation to genetics and behavior. | Q48943927 | ||
| Functional magnetic resonance imaging of human visual cortex during face matching: a comparison with positron emission tomography. | Q48944875 | ||
| Analysis of cerebral shape in Williams syndrome. | Q49029320 | ||
| II. Hypersociability in Williams Syndrome. | Q50312678 | ||
| Adults with Williams syndrome. Preliminary study of social, emotional and behavioural difficulties. | Q51097316 | ||
| Social-emotional and behavioral adjustment in children with Williams-Beuren syndrome. | Q51129644 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 5009-5015 | |
| P577 | publication date | 2004-05-01 | |
| P1433 | published in | Journal of Neuroscience | Q1709864 |
| P1476 | title | An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome | |
| P478 | volume | 24 |
| Q30353059 | (A)musicality in Williams syndrome: examining relationships among auditory perception, musical skill, and emotional responsiveness to music. |
| Q39257738 | 1H magnetic resonance spectroscopy evidence for occipital involvement in treatment-naive paediatric obsessive-compulsive disorder. |
| Q30542532 | 3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry |
| Q46558020 | A 1H magnetic resonance spectroscopy study in adults with obsessive compulsive disorder: relationship between metabolite concentrations and symptom severity |
| Q57110933 | A Different Brain: Anomalies of Functional and Structural Connections in Williams Syndrome |
| Q30483036 | A developmental neurobiological model of motivated behavior: anatomy, connectivity and ontogeny of the triadic nodes |
| Q28655504 | A dual comparative approach: integrating lines of evidence from human evolutionary neuroanatomy and neurodevelopmental disorders |
| Q37322461 | A genetic model for understanding higher order visual processing: functional interactions of the ventral visual stream in Williams syndrome |
| Q47177999 | A postmortem stereological study of the amygdala in Williams syndrome |
| Q34554168 | A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome |
| Q34464442 | A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome. |
| Q44912828 | Abnormal cortical complexity and thickness profiles mapped in Williams syndrome. |
| Q33720054 | Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders. |
| Q42362277 | Abnormalities in early visual processes are linked to hypersociability and atypical evaluation of facial trustworthiness: An ERP study with Williams syndrome |
| Q34454420 | Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content |
| Q56805722 | Affect, Social Behavior, and the Brain in Williams Syndrome |
| Q33897194 | Affiliative behavior in Williams syndrome: social perception and real-life social behavior |
| Q48624989 | Altered functional connectivity of the default mode network in Williams syndrome: a multimodal approach. |
| Q34396199 | Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome |
| Q36277157 | An event related potential study of ihibitory and attentional control in Williams syndrome adults |
| Q38286122 | Annual research review: Rare genotypes and childhood psychopathology--uncovering diverse developmental mechanisms of ADHD risk |
| Q40309602 | Applying tensor-based morphometry to parametric surfaces can improve MRI-based disease diagnosis |
| Q34482041 | Are genes destiny? Have adenine, cytosine, guanine and thymine replaced Lachesis, Clotho and Atropos as the weavers of our fate? |
| Q79615649 | Association between cerebral shape and social use of language in Williams syndrome |
| Q30476786 | Atypical hemispheric asymmetry in the perception of negative human vocalizations in individuals with Williams syndrome |
| Q51968569 | Atypical unfamiliar face processing in Williams syndrome: what can it tell us about typical familiarity effects? |
| Q36240284 | Autonomic response to approachability characteristics, approach behavior, and social functioning in Williams syndrome |
| Q37131277 | Autonomic responses to dynamic displays of facial expressions in adolescents and adults with Williams syndrome |
| Q49027562 | Biological motion processing as a hallmark of social cognition. |
| Q48416971 | Brain gray matter decrease in chronic pain is the consequence and not the cause of pain. |
| Q30472917 | Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes |
| Q35401581 | Callosal morphology in Williams syndrome: a new evaluation of shape and thickness |
| Q47829927 | Capacity to improve fine motor skills in Williams syndrome. |
| Q28279730 | Challenging the use of adult neuropsychological models for explaining neurodevelopmental disorders: developed versus developing brains |
| Q33625247 | Cingulate gyrus morphology in children and adolescents with fetal alcohol spectrum disorders |
| Q24613296 | Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome |
| Q30381566 | Cross-modal influences of affect across social and non-social domains in individuals with Williams syndrome. |
| Q60926670 | Decreased Neuron Density and Increased Glia Density in the Ventromedial Prefrontal Cortex (Brodmann Area 25) in Williams Syndrome |
| Q31143422 | Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior |
| Q41815519 | Developmental changes in mental rotation ability and visual perspective-taking in children and adults with Williams syndrome |
| Q34398230 | Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome |
| Q34080999 | Developmental profiles for multiple object tracking and spatial memory: typically developing preschoolers and people with Williams syndrome |
| Q35542205 | Effect of nonrigid registration algorithms on deformation-based morphometry: a comparative study with control and Williams syndrome subjects |
| Q35187194 | Electrophysiological study of local/global processing in Williams syndrome |
| Q31029871 | Exploiting human anatomical variability as a link between genome and cognome |
| Q91385580 | Extending the positive bias in Williams syndrome: The influence of biographical information on attention allocation |
| Q47834494 | Facial emotion recognition in Williams syndrome and Down syndrome: A matching and developmental study |
| Q33842946 | Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome |
| Q51926627 | Genetic contributions to human gyrification: sulcal morphometry in Williams syndrome. |
| Q36002649 | Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome |
| Q35960747 | Genomic sister-disorders of neurodevelopment: an evolutionary approach |
| Q36301072 | Gray matter abnormalities in social anxiety disorder: primary, replication, and specificity studies |
| Q39469297 | Handedness and corpus callosal morphology in Williams syndrome |
| Q48658363 | Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder. |
| Q49089991 | Hypersociability in Williams syndrome: a role for the amygdala? |
| Q46475542 | Increased glia density in the caudate nucleus in williams syndrome: Implications for frontostriatal dysfunction in autism |
| Q48449936 | Increased local gyrification mapped in Williams syndrome. |
| Q35213067 | Individual differences in social behavior predict amygdala response to fearful facial expressions in Williams syndrome |
| Q37450139 | Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome |
| Q30736046 | Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome |
| Q83320994 | Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays |
| Q35680708 | Language and sociability: insights from Williams syndrome |
| Q47245157 | Learning by observation and learning by doing in Down and Williams syndromes. |
| Q50778073 | Learning without representational change: development of numerical estimation in individuals with Williams syndrome. |
| Q21136169 | Leftward lateralization of auditory cortex underlies holistic sound perception in Williams syndrome |
| Q37404997 | MRI assessment of superior temporal gyrus in Williams syndrome |
| Q37308191 | Manual MRI parcellation of the frontal lobe |
| Q34020534 | Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome |
| Q36183641 | Mathematical skill in individuals with Williams syndrome: evidence from a standardized mathematics battery |
| Q46635683 | Mathematical skills in Williams syndrome: insight into the importance of underlying representations |
| Q51886517 | Mental rotation in Williams syndrome: an impaired ability. |
| Q42029377 | More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams-Beuren syndrome |
| Q33445868 | Morphing voxels: the hype around structural imaging of headache patients |
| Q48488192 | Morphometry of corpus callosum in Williams syndrome: shape as an index of neural development. |
| Q33618603 | Morphometry of human insular cortex and insular volume reduction in Williams syndrome |
| Q35663499 | NIRS-based hyperscanning reveals increased interpersonal coherence in superior frontal cortex during cooperation |
| Q48813102 | Neural correlates of genetically abnormal social cognition in Williams syndrome. |
| Q31043640 | Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour |
| Q36874111 | Neural phenotypes of common and rare genetic variants |
| Q37411441 | Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP). |
| Q57452982 | Neurodevelopmental Disorders Affecting Sociability: Recent Research Advances and Future Directions in Autism Spectrum Disorder and Williams Syndrome |
| Q31107088 | Neurodevelopmental and behavioral issues in Williams syndrome |
| Q46114621 | Neuron density is decreased in the prefrontal cortex in Williams syndrome |
| Q90215956 | Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug |
| Q37350700 | Normal susceptibility to visual illusions in abnormal development: evidence from Williams syndrome |
| Q35840644 | Out with the Old and in with the New--Is Backward Inhibition a Domain-Specific Process? |
| Q50190394 | Processing of stimulus content but not of emotional valence is altered in persons with Williams syndrome. |
| Q35834942 | Quantitative analysis of gray and white matter in Williams syndrome |
| Q36880990 | Reduced hippocampal volume and verbal memory performance associated with interleukin-6 and tumor necrosis factor-alpha levels in chemotherapy-treated breast cancer survivors |
| Q34166509 | Regional brain differences in cortical thickness, surface area and subcortical volume in individuals with Williams syndrome |
| Q37117117 | Regionally specific increased volume of the amygdala in Williams syndrome: evidence from surface-based modeling |
| Q35744171 | Relations between social-perceptual ability in multi- and unisensory contexts, autonomic reactivity, and social functioning in individuals with Williams syndrome |
| Q45813120 | Relationship between brain abnormalities and cognitive profile in Williams syndrome |
| Q30543830 | Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype. |
| Q27307963 | Resting-State Functional Connectivity in Individuals with Down Syndrome and Williams Syndrome Compared with Typically Developing Controls |
| Q34955409 | Retinotopically defined primary visual cortex in Williams syndrome |
| Q37672826 | Short Latency Gray Matter Changes in Voxel-Based Morphometry following High Frequent Visual Stimulation |
| Q37144616 | Social Cognition in Williams Syndrome: Face Tuning |
| Q38018931 | Social brain development in williams syndrome: the current status and directions for future research |
| Q48312360 | Structural imaging reveals anatomical alterations in inferotemporal cortex in congenital prosopagnosia |
| Q46072521 | Surface-based morphometry reveals distinct cortical thickness and surface area profiles in Williams syndrome |
| Q48535068 | Symmetry of cortical folding abnormalities in Williams syndrome revealed by surface-based analyses. |
| Q35887093 | The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function |
| Q36897261 | The fusiform face area is enlarged in Williams syndrome |
| Q44056677 | The interplay between executive control and motor functioning in Williams syndrome. |
| Q36630925 | The regulatory function of social referencing in preschoolers with Down syndrome or Williams syndrome |
| Q34323414 | The social phenotype of Williams syndrome |
| Q37360554 | Typical visual search performance and atypical gaze behaviors in response to faces in Williams syndrome |
| Q45063390 | Visually guided step descent in children with Williams syndrome |
| Q35661641 | White matter integrity deficits in prefrontal-amygdala pathways in Williams syndrome |
| Q36567458 | William's syndrome: gene expression is related to parental origin and regional coordinate control |
| Q64079906 | Williams Syndrome, Human Self-Domestication, and Language Evolution |
| Q38530082 | Williams syndrome and its cognitive profile: the importance of eye movements |
| Q45906112 | Williams syndrome and memory: a neuroanatomic and cognitive approach. |
| Q44800134 | Williams syndrome: a genetic deletion disorder presenting clues to the biology of sociability and clinical challenges of hypersociability |
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