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View Cohort
        helpcenter.ndastudy.view-cohort

        NDA Help Center

        NDA Study - View Cohort

        The View Cohort shows the Study cohort characteristics which will includes the name, type, sex and age in months range criteria. Note that age and sex restrict the data that can be added to the cohort. Medical criteria and phenotype are also included. Of particular importance on this page are any comments related to included subjects, which may be different than published results, often attributed to data sharing consent.

        Frequently Asked Questions

        • How do I know the characteristics of the cohort?
          The appropriate Medical Criteria, Phenotype, and Sub Type defined by the Study Owner are highlighted. The option trees are automatically expanded so the highlighted options are immediately viewable.

        Glossary

        • Age Range
          Age is expressed in months from 0 (birth) to 1200 (100 years old).
        • Medical Criteria
          NDA defines Medical Criteria as a diagnostically based determination of an individual's disease or condition.
        • Phenotype
          NDA defines Phenotype as any physical, morphologic, or biochemical characteristics that are observable in an individual.
        • Sub Types
          NDA defines Sub Type as a subordinate condition or disease that further characterizes an individual.
        • Cohort Name
          A user defined name for the cohort with a 200 character limit.
        • Cohort Type
          Cohort Type options include Baseline, Control, and Test.
        • Cohort Comments
          Comments further characterize the cohort beyond the options provided in the interface to define the cohort.
        • Cohort Subjects
          The Cohort Subjects provides the number of unique subjects for whom data have been associated with the cohort.
        • Cohort
          Summarizes the characteristics of a group of research subjects. The subject count is noted in parentheses.
        Add URL
        Add File
        Select File
        Study DOI
        Study DOI Status Info
        • DOI: 10.15154/khn8-jf08
        • DataCite Status: Findable
        • NDAR Status: Registered
        • DOI Registered with DataCite
        • Public URL Resolves at DOI
        Edit Subjects Dialog
        Select Subjects
        Selected
        No records found.
        Jeff Waugh jeff.waugh@utsouthwestern.edu Analysis Shared
        Click for more info Waugh, JL; Hassan AAO; Funk AT; Maldjian JA
        Background: Autism spectrum disorder (ASD) is the second-most common neurodevelopmental disorder in childhood. This complex developmental disorder that manifests with restricted interests, repetitive behaviors, and difficulties in communication and social awareness. The inherited and acquired causes of ASD impact many and diverse brain regions, challenging efforts to identify a shared neuroanatomical substrate for this range of symptoms. The striatum and its connections are among the most implicated sites of abnormal structure and/or function in ASD. Striatal projection neurons develop in segregated tissue compartments, the matrix and striosome, that are histochemically, pharmacologically, and functionally distinct. Immunohistochemical assessment of ASD and animal models of autism described abnormal matrix:striosome volume ratios, with an possible shift from striosome to matrix volume. Shifting the matrix:striosome ratio could result from expansion in matrix, reduction in striosome, spatial redistribution of the compartments, or a combination of these changes. Each type of ratio-shifting abnormality may predispose to ASD but yield different combinations of ASD features. Methods: We developed a cohort of 426 children and adults (213 matched ASD-control pairs) and performed connectivity-based parcellation (diffusion tractography) of the striatum. This identified voxels with matrix-like and striosome-like patterns of structural connectivity. Results: Matrix-like volume was increased in ASD, with no evident change in the volume or organization of the striosome-like compartment. The inter-compartment volume difference (matrix minus striosome) within each individual was 31% larger in ASD. Matrix-like volume was increased in both caudate and putamen, and in somatotopic zones throughout the rostral-caudal extent of the striatum. Subjects with moderate elevations in ADOS (Autism Diagnostic Observation Schedule) scores had increased matrix-like volume, but those with highly elevated ADOS scores had 3.7-fold larger increases in matrix-like volume. Conclusions: Matrix and striosome are embedded in distinct structural and functional networks, suggesting that compartment-selective injury or maldevelopment may mediate specific and distinct clinical features. Previously, assessing the striatal compartments in humans required post mortem tissue. Striatal parcellation provides a means to assess neuropsychiatric diseases for compartment-specific abnormalities in vivo. While this ASD cohort had increased matrix-like volume, other mechanisms that shift the matrix:striosome ratio may also increase the chance of developing the diverse social, sensory, and motor phenotypes of ASD.
        10.15154/khn8-jf08
        Click for more info Secondary Analysis
        Click for more info
        IDCollectionDOIPermission GroupSubjects
        2021 Multimodal Developmental Neurogenetics of Females with ASD 10.15154/4dat-5683NIMH Data Archive1,042
        2026 Biomarkers of Developmental Trajectories and Treatment in ASD 10.15154/39tn-yj66NIMH Data Archive628
        2358 Neural networks for attention to internal and external sensory cues in ASD 10.15154/pc6x-rp60NIMH Data Archive297
        1906 Atypical Late Neurodevelopment in Autism 10.15154/bx96-q537NIMH Data Archive174
        2804 Multimodal Developmental Neurogenetics of Females with ASD 10.15154/kr38-n898NIMH Data Archive135
        2075 Mapping Thalamocortical Networks Across Development in ASD 10.15154/49n6-qn82NIMH Data Archive100
        2129 Biological Determinants of Brain Variation in Autism 10.15154/vz1e-k126NIMH Data Archive79
        2400 Atypical Late Neurodevelopment in Autism: A Longitudinal Clinical Phenotype and Multimodal Brain Imaging Study 10.15154/44zw-jc80NIMH Data Archive77
        3005 Parsing ASD Heterogeneity: Neuroendophenotypes of Social Attention and Sensory Responsivity 10.15154/f5s5-t470NIMH Data Archive75
        2179 Neural markers of shared gaze during simulated social interactions in ASD \-Modal Automated Assessment of Behavior during Social Interactions in Children with ASD 10.15154/tabd-sm79NIMH Data Archive36
        2130 Recurrent de novo mutations implicate novel genes underlying simplex autism risk 10.15154/h0s3-bn42NIMH Data Archive22
        2042 SSC total recall project 10.15154/wtpt-qn32NIMH Data Archive20
        10 UCLA Sigman/Bookheimer ACE and ARRA 10.15154/mks4-e786NIMH Data Archive16
        1971 Rapid Phenotyping for Rare Variant Discovery in Autism 10.15154/z8cr-tx40NIMH Data Archive6
        1936 Deep sequencing of autism candidate genes in 2000 families from the Simons Simplex Collection (SSC) 10.15154/9sc9-de27NIMH Data Archive5
        2203 Change-sensitive Measurement of Emotion Dysregulation in ASD 10.15154/vxbc-wq93NIMH Data Archive5
        2030 Electrophysiological Response to Executive Control Training in Autism 10.15154/832m-tq21NIMH Data Archive5
        2101 Phenotypic Characterization of Gene Disrupting Mutations in ASD 10.15154/g2cd-kb44NIMH Data Archive5
        3906 The Influence of Social, Educational, and Work Experiences on Psychological Health for Transition-Aged Youth with Autism Spectrum Disorders 10.15154/36k2-cg92NIMH Data Archive4
        2312 Multimodel Assessment of Social Process Systems across Neurodevelopmental Disorders 10.15154/danj-a358NIMH Data Archive4
        2035 Autism Genetics, Phase II: Increasing Representation of Human Diversity 10.15154/c8p8-vx52NIMH Data Archive3
        2254 The neurobiological basis of heterogeneous social and motor deficits in ASD 10.15154/rw82-na31NIMH Data Archive3
        3957 Chromatin regulation during brain development and in ASD 10.15154/wh5x-yn58NIMH Data Archive3
        3670 The Autism Biomarkers Consortium for Clinical Trials 10.15154/kjye-gg81NIMH Data Archive3
        2683 Examining Stress and Arousal Across Pubertal Development in ASD 10.15154/th9d-5273NIMH Data Archive3
        2424 Neurobiology of Autism With Macrocephaly 10.15154/y2eh-hf59NIMH Data Archive3
        2288 The Autism Biomarkers Consortium for Clinical Trials 10.15154/3y3w-8z64NIMH Data Archive3
        1650 SFARI - DNA Methylation Analysis Cohort 10.15154/gkaw-vz58NIMH Data Archive3
        2004 1/3, 2/3, and 3/3: Sequencing Autism Spectrum Disorder Extended Pedigrees 10.15154/04r0-ka50NIMH Data Archive2
        2929 Social-communicative deficits in Autism Spectrum Disorder as measured by mGluR5 positron emission tomography 10.15154/skb0-3w31NIMH Data Archive2
        2292 Molecular Mechanisms of Atypical Habituation in Autism Spectrum Disorders 10.15154/vs5g-4k54NIMH Data Archive2
        3275 Testing a computational model of neural responses in autism 10.15154/qzkh-3v06NIMH Data Archive2
        2525 Neural Mechanisms for Social Interactions and Eye Contact in ASD 10.15154/82yh-9828NIMH Data Archive2
        1999 NIMH Genetics 10.15154/0hqy-6p91NIMH Data Archive2
        4218 A Longitudinal Study of Employment and Educational Instability for Young Adults with Autism Spectrum Disorder 10.15154/39nk-af12NIMH Data Archive1
        2650 Trajectories of Brain Maturation among Youth at Risk for Anxiety 10.15154/h879-qb33NIMH Data Archive1
        3850 Neural mechanisms of sensory reactivity and regulation in autism across development 10.15154/c3y6-5381NIMH Data Archive1
        2007 Treatment of Autism Symptoms in Children (TASC): Initial RCT with Active Control 10.15154/57s7-jz46NIMH Data Archive1
        2821 Cellular, molecular, and functional imaging approaches to understanding early neurodevelopment in autism 10.15154/77j6-7y28NIMH Data Archive1
        1854 Studies to Advance Autism Research and Treatment (STAART). 10.15154/m0m2-gq48NIMH Data Archive1
        2022 The Social Brain in Schizophrenia and Autism Spectrum Disorders 10.15154/g4mp-bq05NIMH Data Archive1
        1850 CBT for anxiety in adolescents with autism 10.15154/g338-jc55NIMH Data Archive1
        2076 1/3 to 3/3 Treatment of anxiety in autism spectrum disorder 10.15154/qfqr-6q70NIMH Data Archive1
        1654 UW ACE Extended Family Study 10.15154/yqmk-gc77NIMH Data Archive1
        2328 Simons Simplex Collection (SSC) Genome Studies 10.15154/6nft-5w58NIMH Data Archive1
        2009 Study of Oxytocin in Autism to Improve Reciprocal Social Behaviors (SOARS-B) 10.15154/gx26-h668NIMH Data Archive1
        3458 1/5, 2/5, 3/5, 4/5, 5/5 CAPR: Computerized assessment of psychosis risk 10.15154/gcth-2d46NIMH Data Archive1
        2266 Inhibitory dysfunction in autism 10.15154/xn3k-2181NIMH Data Archive1
        2070 Eyeblink conditioning in school-aged children with ASD 10.15154/pn22-x635NIMH Data Archive1
        2017 Wireless EEG System for Training Attention and Eye Movement in ASD 10.15154/wqc2-px14NIMH Data Archive1
        1880 Computer Adaptive Testing of Adaptive Behavior of Children and Youth with Autism 10.15154/20qm-mf27NIMH Data Archive1
        Analysis
        Age: 0 to 1,440 months
        Sex: Both
        helpcenter.ndastudy.summary-tab

        NDA Help Center

        NDA Study - Summary Tab

        An NDA Study describes an analysis, pipeline result, or curated data release - including the cohorts, measures, and methods - referencing the underlying source data in the NDA. Once the data is referenced and the study is shared, the underlying data will not change. It will be immutable allowing others to access those data without change into near perpetuity. Only the assessments (i.e. typically rows in a database) and outcome measures (i.e. columns in a database) included in the study are shared. By sharing data this way (e.g. specific outcome measures by subject/timepoint) an ongoing project's other unpublished data - typically other research aims - will remain embargoed according to a project's established data sharing schedule (see collection).

        When a study is created, a Digital Object Identifier (DOI) is reserved by the NDA, but will not be active. Once the study is shared, the DOI will then be issued and if associated with a publication, the NDA DOI will be linked to the publication's DOI.

        Frequently Asked Questions

        • How can I get access to an NDA Study if I am involved in creating/modifying the NDA Study?
          The individual listed as an Investigator on the General tab of the NDA Collection and any individuals defined as administrators can be provided this privilege. When the study is shared, all of those that have approved access to the data are given read-only access.

        Glossary

        • Abstract
          The Abstract of the publication or other public disclosure of analysis results. The publication abstract is automatically imported when creating a new NDA Study from a Create Study link associated with a Publication listed in a Collection. The field is editable.
        • Documents
          Provides links to additional documentation to help explain the NDA Study.
        • Cohort
          Summarizes the characteristics of a group of research subjects. The subject count is noted in parentheses.
        • Data Analysis
          Summarizes the Data Analysis methods used.
        • Data Usage
          Identifies the NDA Study as a Primary Analysis or Secondary Analysis.
        • Digital Object Identifier (DOI)
          A persistent and unique identifier that is issued for each NDA Study that may increase the visibility of a researcher's work. Authors are expected to reference the location of data in the publication using the DOI.
        • Download Button
          Adds all data from the current Collection or NDA Study to the Filter Cart.
        • Investigators
          The authors of the publication or other public disclosure of analysis results. The publication's authors are automatically imported when creating a new NDA Study from a Create Study link associated with a Publication listed in a Collection. The field is editable and uses a last name, first name format with multiple names separated by semicolons.
        • Primary Analysis
          Primary Analysis is one of the Data Use types NDA recognizes for NDA Studies. It indicates that the NDA Study's creator was involved in the collection of the data (in whole or in part) used in the NDA Study. In other words, at least some and potentially all of the data used was originally collected by the creator of the NDA Study. A Primary Analysis Study.
        • NDA Study Owner
          The NDA user, who does not necessarily have to be one of the Investigators listed in the NDA Study, primarily involved in creating the NDA Study who is serving as the point of contact. The NDA user who creates the NDA Study is automatically assigned as the Study Owner.
        • Private
          The term 'Private' generally means not available to others; however, there are some slightly different meanings based on what is Private. The default state for an NDA Collection, NDA Study, Supporting Documentation, and data is Private and, therefore, accessible only to those users with appropriate Privileges so it will not be viewable and searchable publicly. A Collection may be Shared while the data and Supporting Documentation remain Private.
        • Results
          Provides a link to the publication or other public disclosure of analysis results defined in the NDA Study.
        • Secondary Analysis
          Secondary Analysis is one of the Data Use types NDA recognizes for NDA Studies. It indicates that the NDA Study's creator was not involved in the collection of the data (in whole or in part) used in the NDA Study, but was involved in the analysis of those data. In other words, none of the data used was originally collected by the creator of the NDA Study. A Secondary Analysis Study will provide an Attribution Report listing the Collections and the researchers responsible for collecting and depositing the original data.
        • Study Type
          The NDA Study Type can be either Analysis (i.e. often associated with a computational pipeline), Clinical Trial, Finding (i.e. a result associated with a publication, or Release (i.e. a dataset release, often annually) to indicate the type of work defined in the NDA Study. Studies, once shared do not change.
        • Analysis Study Type
          The Analysis Study Type is primarily used to share a pipeline; however, it could be used to share a statistical analysis or method.
        • Release Study Type
          A static, curated data set.
        • Finding Study Type
          The Finding Study Type associates data to a publication or some type of result.
        • Clinical Trial Study Type
          A Clinical Trial Study is a finding specific to a clinical trial.
        • Study ID Number
          The Study ID number is a unique three digit number routinely expressed as S### that is assigned by the NDA.
        • Study State
          The Study State indicates whether the Study is viewable, searchable, and if the associated data can be accessed by users with appropriate data access Permissions. The default Study State is Private, which means that only the Collection Owner and users with Read Only Privileges. Only the Study Owner can Share the Study.
        • Study Title
          The Study Title is generally the title of the publication or other public disclosure of analysis results. The publication title is automatically imported when creating a new NDA Study from a Create Study link associated with a Publication listed in a Collection. The field is editable.
        • Edit Button
          The Edit Button allows a user to modify or add information once authenticated and if the user has appropriate permissions.
        • Return Button (Study)
          The Return Button brings the user back to the Data from Papers page.
        • Sex
          Sex is defined at birth and can only be Male or Female. In some places in the NDA, we incorrectly used the data_element name of Gender. Users are encouraged to review definitions and not make assumptions based upon a data element name.
        • Data Use Limitations
          Data Use Limitations (DULs) describe the appropriate secondary use of a dataset and are based on the original informed consent of a research participant. NDA only accepts consent-based data use limitations defined by the NIH Office of Science Policy.
        • Permission Group
          Access to shared record-level data in NDA is provisioned at the level of a Permission Group. NDA Permission Groups consist of one or multiple NDA Collections that contain data with the same subject consents.