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    Query Data
    Data from Labs
    Data from Papers
    Query Instructions

    Use "Select Data" below to query the data available in NDAR. Then, select download to create a package and download your results. Use the Data tab above to search in other ways. For more information on search see our Methods.

    Data Distribution by Gender1

    Phenotypic Data Distribution1,2

    Neuroimaging Data Distribution2,3

    Genomic Data Distribution2
    1 Numbers reported are subjects by age 2 ~4,000 subjects have no phenotypic, neuroimaging, or genomic data 3 Currently, the vast majority of imaging data is control data from the PediatricMRI project
    Select Data:
    All
    Basic
    Phenotype
    Neuroimaging
    omicSEARCH:
    Experiment
    Results
    All None Clear
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    SUBJECT ID INTERVIEW AGE GENDER
    1  424  FEMALE 
    2  426  FEMALE 
    3  30  MALE 
    4  104  MALE 
    5  117  MALE 
    6  168  MALE 
    7  170  MALE 
    8  6  FEMALE 
    9  207  MALE 
    10  95  MALE 
    11  96  MALE 
    12  275  MALE 
    13  574  MALE 
    14  12  FEMALE 
    15  432  FEMALE 
    16  135  FEMALE 
    17  132  MALE 
    18  196  MALE 
    19  48  MALE 
    20  50  MALE 
    21  26  MALE 
    22  27  MALE 
    23  485  MALE 
    24  8  MALE 
    25  20  FEMALE 
    26  19  MALE 
    27  36  FEMALE 
    28  184  MALE 
    29  6  FEMALE 
    30  7  FEMALE 
    31  12  FEMALE 
    32  13  FEMALE 
    33  18  FEMALE 
    34  22  FEMALE 
    35  25  FEMALE 
    36  362  FEMALE 
    37  518  MALE 
    38  70  MALE 
    39  26  MALE 
    40  27  MALE 
    41  443  FEMALE 
    42  288   
    43  664  FEMALE 
    44  41  MALE 
    45  45  MALE 
    46  18  MALE 
    47  19  MALE 
    48  36  MALE 
    49  106  MALE 
    50  108  MALE 
    SUBJECT ID INTERVIEW AGE GENDER

    No Alterations for Selected Options

    For projects that share genomic or proteomic results, published and provided alterations are available for query using NDAR's omicSEARCH. To use this feature, search by alteration type (e.g. SNP, CNV, SNV), affected region, chromosome, cytoband, etc., returning specific alterations. Selected alterations can then be applied -- via Show Results -- against participant data, including phenotypic categories and imaging results in NDAR. Authenticated users will be able to search by significance values and download participant data.

    How to use this dialog
    • Enter your search criteria in the input fields. Most fields will take a comma-separated list of values. The system will suggest values as you type. To see all available values before typing, press the up or down arrow key. You may navigate through the suggestion list with the mouse or keyboard.
    • Once you have entered all values you wish to search by, click the "Show Results" button on the bottom of the dialog. This will populate the table with all alterations that match your criteria. You can use the table navigation controls to select how many alterations to see at a time and to navigate forward, back, or to a specific page of alterations.
    • Check the "Select" box next to all alterations you would like to see subjects for, then click the "Apply" button at the bottom of the dialog. The dialog will close and the main page will display the subjects that match your selected alterations, including selection criteria for phenotype, imaging, and basic demographics.