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Dive into the research topics where Deanna J. Greene is active.

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Featured researches published by Deanna J. Greene.


The Journal of Neuroscience | 2014

Developmental changes in the organization of functional connections between the basal ganglia and cerebral cortex

Deanna J. Greene; Timothy O. Laumann; Joseph W. Dubis; S. Katie Ihnen; Maital Neta; Jonathan D. Power; John R. Pruett; Kevin J. Black; Bradley L. Schlaggar

The basal ganglia (BG) comprise a set of subcortical nuclei with sensorimotor, cognitive, and limbic subdivisions, indicative of functional organization. BG dysfunction in several developmental disorders suggests the importance of the healthy maturation of these structures. However, few studies have investigated the development of BG functional organization. Using resting-state functional connectivity MRI (rs-fcMRI), we compared human child and adult functional connectivity of the BG with rs-fcMRI-defined cortical systems. Because children move more than adults, customized preprocessing, including volume censoring, was used to minimize motion-induced rs-fcMRI artifact. Our results demonstrated functional organization in the adult BG consistent with subdivisions previously identified in anatomical tracing studies. Group comparisons revealed a developmental shift in bilateral posterior putamen/pallidum clusters from preferential connectivity with the somatomotor “face” system in childhood to preferential connectivity with control/attention systems (frontoparietal, ventral attention) in adulthood. This shift was due to a decline in the functional connectivity of these clusters with the somatomotor face system over development, and no change with control/attention systems. Applying multivariate pattern analysis, we were able to reliably classify individuals as children or adults based on BG–cortical system functional connectivity. Interrogation of the features driving this classification revealed, in addition to the somatomotor face system, contributions by the orbitofrontal, auditory, and somatomotor hand systems. These results demonstrate that BG–cortical functional connectivity evolves over development, and may lend insight into developmental disorders that involve BG dysfunction, particularly those involving motor systems (e.g., Tourette syndrome).


Developmental Cognitive Neuroscience | 2016

Considerations for MRI study design and implementation in pediatric and clinical populations.

Deanna J. Greene; Kevin J. Black; Bradley L. Schlaggar

Human neuroimaging, specifically magnetic resonance imaging (MRI), is being used with increasing popularity to study brain structure and function in development and disease. When applying these methods to developmental and clinical populations, careful consideration must be taken with regard to study design and implementation. In this article, we discuss two major considerations particularly pertinent to brain research in special populations. First, we discuss considerations for subject selection and characterization, including issues related to comorbid conditions, medication status, and clinical assessment. Second, we discuss methods and considerations for acquisition of adequate, useable MRI data. Given that children and patients may experience anxiety with the scanner environment, preventing participation, and that they have a higher risk of motion artifact, resulting in data loss, successful subject compliance and data acquisition are not trivial tasks. We conclude that, as researchers, we must consider a number of issues when using neuroimaging tools to study children and patients, and we should thoughtfully justify our choices of methods and study design.


Developmental Cognitive Neuroscience | 2015

REWARD ENHANCES TIC SUPPRESSION IN CHILDREN WITHIN MONTHS OF TIC DISORDER ONSET

Deanna J. Greene; Jonathan M. Koller; Amy Robichaux-Viehoever; Emily C. Bihun; Bradley L. Schlaggar; Kevin J. Black

Highlights • We examine a common, yet rarely studied, population: children with recent-onset tics.• The ability to suppress tics is present within months of tic onset.• Immediate, contingent reward enhances these childrens ability to suppress tics.


Developmental Science | 2016

Multivariate pattern classification of pediatric Tourette syndrome using functional connectivity MRI

Deanna J. Greene; Jessica A. Church; Nico U.F. Dosenbach; Ashley N. Nielsen; Babatunde Adeyemo; Binyam Nardos; Steven E. Petersen; Kevin J. Black; Bradley L. Schlaggar

Abstract Tourette syndrome (TS) is a developmental neuropsychiatric disorder characterized by motor and vocal tics. Individuals with TS would benefit greatly from advances in prediction of symptom timecourse and treatment effectiveness. As a first step, we applied a multivariate method – support vector machine (SVM) classification – to test whether patterns in brain network activity, measured with resting state functional connectivity (RSFC) MRI, could predict diagnostic group membership for individuals. RSFC data from 42 children with TS (8–15 yrs) and 42 unaffected controls (age, IQ, in‐scanner movement matched) were included. While univariate tests identified no significant group differences, SVM classified group membership with ~70% accuracy (p < .001). We also report a novel adaptation of SVM binary classification that, in addition to an overall accuracy rate for the SVM, provides a confidence measure for the accurate classification of each individual. Our results support the contention that multivariate methods can better capture the complexity of some brain disorders, and hold promise for predicting prognosis and treatment outcome for individuals with TS.


NeuroImage | 2017

Real-time motion analytics during brain MRI improve data quality and reduce costs

Nico U.F. Dosenbach; Jonathan M. Koller; Eric Earl; Oscar Miranda-Dominguez; Rachel L. Klein; Andrew N. Van; Abraham Z. Snyder; Bonnie J. Nagel; Joel T. Nigg; Annie L. Nguyen; Victoria Wesevich; Deanna J. Greene; Damien A. Fair

Abstract Head motion systematically distorts clinical and research MRI data. Motion artifacts have biased findings from many structural and functional brain MRI studies. An effective way to remove motion artifacts is to exclude MRI data frames affected by head motion. However, such post‐hoc frame censoring can lead to data loss rates of 50% or more in our pediatric patient cohorts. Hence, many scanner operators collect additional ‘buffer data’, an expensive practice that, by itself, does not guarantee sufficient high‐quality MRI data for a given participant. Therefore, we developed an easy‐to‐setup, easy‐to‐use Framewise Integrated Real‐time MRI Monitoring (FIRMM) software suite that provides scanner operators with head motion analytics in real‐time, allowing them to scan each subject until the desired amount of low‐movement data has been collected. Our analyses show that using FIRMM to identify the ideal scan time for each person can reduce total brain MRI scan times and associated costs by 50% or more. Graphical abstract Figure. No Caption available.


Molecular Psychiatry | 2017

Brain structure in pediatric Tourette syndrome

Deanna J. Greene; A C Williams; Jonathan M. Koller; Bradley L. Schlaggar; Kevin J. Black

Previous studies of brain structure in Tourette syndrome (TS) have produced mixed results, and most had modest sample sizes. In the present multicenter study, we used structural magnetic resonance imaging (MRI) to compare 103 children and adolescents with TS to a well-matched group of 103 children without tics. We applied voxel-based morphometry methods to test gray matter (GM) and white matter (WM) volume differences between diagnostic groups, accounting for MRI scanner and sequence, age, sex and total GM+WM volume. The TS group demonstrated lower WM volume bilaterally in orbital and medial prefrontal cortex, and greater GM volume in posterior thalamus, hypothalamus and midbrain. These results demonstrate evidence for abnormal brain structure in children and youth with TS, consistent with and extending previous findings, and they point to new target regions and avenues of study in TS. For example, as orbital cortex is reciprocally connected with hypothalamus, structural abnormalities in these regions may relate to abnormal decision making, reinforcement learning or somatic processing in TS.


The Journal of Pediatrics | 2015

Clinical Correlates of Parenting Stress in Children with Tourette Syndrome and in Typically Developing Children

Stephanie B. Stewart; Deanna J. Greene; Christina N. Lessov-Schlaggar; Jessica A. Church; Bradley L. Schlaggar

OBJECTIVE To determine the impact of tic severity in children with Tourette syndrome on parenting stress and the impact of comorbid attention-deficit hyperactivity disorder (ADHD) and obsessive-compulsive disorder (OCD) symptomatology on parenting stress in both children with Tourette syndrome and typically developing children. STUDY DESIGN Children with diagnosed Tourette syndrome (n=74) and tic-free typically developing control subjects (n=48) were enrolled in a cross-sectional study. RESULTS Parenting stress was greater in the group with Tourette syndrome than the typically developing group. Increased levels of parenting stress were related to increased ADHD symptomatology in both children with Tourette syndrome and typically developing children. Symptomatology of OCD was correlated with parenting stress in Tourette syndrome. Parenting stress was independent of tic severity in patients with Tourette syndrome. CONCLUSIONS For parents of children with Tourette syndrome, parenting stress appears to be related to the childs ADHD and OCD comorbidity and not to the severity of the childs tic. Subthreshold ADHD symptomatology also appears to be related to parenting stress in parents of typically developing children. These findings demonstrate that ADHD symptomatology impacts parental stress both in children with and without a chronic tic disorder.


Neuron | 2018

Functional Brain Networks Are Dominated by Stable Group and Individual Factors, Not Cognitive or Daily Variation

Caterina Gratton; Timothy O. Laumann; Ashley N. Nielsen; Deanna J. Greene; Evan M. Gordon; Adrian W. Gilmore; Steven M. Nelson; Rebecca S. Coalson; Abraham Z. Snyder; Bradley L. Schlaggar; Nico U.F. Dosenbach; Steven E. Petersen

The organization of human brain networks can be measured by capturing correlated brain activity with fMRI. There is considerable interest in understanding how brain networks vary across individuals or neuropsychiatric populations or are altered during the performance of specific behaviors. However, the plausibility and validity of such measurements is dependent on the extent to which functional networks are stable over time or are state dependent. We analyzed data from nine high-quality, highly sampled individuals to parse the magnitude and anatomical distribution of network variability across subjects, sessions, and tasks. Critically, we find that functional networks are dominated by common organizational principles and stable individual features, with substantially more modest contributions from task-state and day-to-day variability. Sources of variation were differentially distributed across the brain and differentially linked to intrinsic and task-evoked sources. We conclude that functional networks are suited to measuring stable individual characteristics, suggesting utility in personalized medicine.


F1000Research | 2016

Provisional tic disorder: What to tell parents when their child first starts ticcing

Kevin J. Black; Elizabeth Rose Black; Deanna J. Greene; Bradley L. Schlaggar

The child with recent onset of tics is a common patient in a pediatrics or child neurology practice. If the child’s first tic was less than a year in the past, the diagnosis is usually Provisional Tic Disorder (PTD). Published reviews by experts reveal substantial consensus on prognosis in this situation: the tics will almost always disappear in a few months, having remained mild while they lasted. Surprisingly, however, the sparse existing data may not support these opinions. PTD may have just as much importance for science as for clinical care. It provides an opportunity to prospectively observe the spontaneous remission of tics. Such prospective studies may aid identification of genes or biomarkers specifically associated with remission rather than onset of tics. A better understanding of tic remission may also suggest novel treatment strategies for Tourette syndrome, or may lead to secondary prevention of tic disorders. This review summarizes the limited existing data on the epidemiology, phenomenology, and outcome of PTD, highlights areas in which prospective study is sorely needed, and proposes that tic disorders may completely remit much less often than is generally believed.


NeuroImage | 2018

Behavioral interventions for reducing head motion during MRI scans in children

Deanna J. Greene; Jonathan M. Koller; Jacqueline M. Hampton; Victoria Wesevich; Andrew N. Van; Annie L. Nguyen; Catherine R. Hoyt; Lindsey McIntyre; Eric Earl; Rachel L. Klein; Joshua S. Shimony; Steven E. Petersen; Bradley L. Schlaggar; Damien A. Fair; Nico U.F. Dosenbach

&NA; A major limitation to structural and functional MRI (fMRI) scans is their susceptibility to head motion artifacts. Even submillimeter movements can systematically distort functional connectivity, morphometric, and diffusion imaging results. In patient care, sedation is often used to minimize head motion, but it incurs increased costs and risks. In research settings, sedation is typically not an ethical option. Therefore, safe methods that reduce head motion are critical for improving MRI quality, especially in high movement individuals such as children and neuropsychiatric patients. We investigated the effects of (1) viewing movies and (2) receiving real‐time visual feedback about head movement in 24 children (5–15 years old). Children completed fMRI scans during which they viewed a fixation cross (i.e., rest) or a cartoon movie clip, and during some of the scans they also received real‐time visual feedback about head motion. Head motion was significantly reduced during movie watching compared to rest and when receiving feedback compared to receiving no feedback. However, these results depended on age, such that the effects were largely driven by the younger children. Children older than 10 years showed no significant benefit. We also found that viewing movies significantly altered the functional connectivity of fMRI data, suggesting that fMRI scans during movies cannot be equated to standard resting‐state fMRI scans. The implications of these results are twofold: (1) given the reduction in head motion with behavioral interventions, these methods should be tried first for all clinical and structural MRIs in lieu of sedation; and (2) for fMRI research scans, these methods can reduce head motion in certain groups, but investigators must keep in mind the effects on functional MRI data. HighlightsIn young children, movie watching during MRI scans reduces head motion.Real‐time head motion feedback also reduces motion during MRI scans in young children.Motion effects were specific to younger (5‐10 years) not older children (11‐15 years).Movies, but not feedback, significantly alter functional connectivity MRI data.

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Bradley L. Schlaggar

Washington University in St. Louis

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Kevin J. Black

Washington University in St. Louis

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Nico U.F. Dosenbach

Washington University in St. Louis

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Steven E. Petersen

Washington University in St. Louis

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Caterina Gratton

Washington University in St. Louis

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Jonathan M. Koller

Washington University in St. Louis

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Abraham Z. Snyder

Washington University in St. Louis

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Timothy O. Laumann

Washington University in St. Louis

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Annie L. Nguyen

Washington University in St. Louis

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Evan M. Gordon

University of Texas at Dallas

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