NIMH Data Archive - Data

Genomics

Neuroimaging

Phenotype¹

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Clinical Trial

¹ Numbers reported are subjects by age

New Project
Grant/Project Number

Format should be in the following format: Activity Code, Institute Abbreviation, and Serial Number. Grant Type, Support Year, and Suffix should be excluded. For example, grant 1R01MH123456-01A1 should be entered R01MH123456

Collection - Use Existing Experiment

To associate an experiment to the current collection, just select an axperiment from the table below then click the associate experiment button to persist your changes (saving the collection is not required). Note that once an experiment has been associated to two or more collections, the experiment will not longer be editable.

The table search feature is case insensitive and targets the experiment id, experiment name and experiment type columns. The experiment id is searched only when the search term entered is a number, and filtered using a startsWith comparison. When the search term is not numeric the experiment name is used to filter the results.

Select	Experiment Id	Experiment Name	Experiment Type	Created On

24	HI-NGS_R1	Omics	02/16/2011
475	MB1-10 (CHOP)	Omics	06/07/2016
490	Discovery and CRISPR validation of genetic factors associated with antipsychotic-induced weight gain and cardiometabolic risk	Omics	07/07/2016
501	PharmacoBOLD Resting State	fMRI	07/27/2016
506	PVPREF	Omics	08/05/2016
509	ABC-CT Resting v2	EEG	08/18/2016
13	Comparison of FI expression in Autistic and Neurotypical Homo Sapiens	Omics	12/28/2010
18	AGRE/Broad Affymetrix 5.0 Genotype Experiment	Omics	01/06/2011
22	Stitching PCR Sequencing	Omics	02/14/2011
26	ASD_Methylation	Omics	03/01/2011
29	Microarray family 03 (father, mother, sibling)	Omics	03/24/2011
37	Standard paired-end sequencing of BCRs	Omics	04/19/2011
38	Illumina Mate-Pair BCR sequencing	Omics	04/19/2011
39	Custom Jumping Libraries	Omics	04/19/2011
40	Custom CapBP	Omics	04/19/2011
41	Immunofluorescence	Omics	05/11/2011
43	Autism brain sample genotyping, Illumina	Omics	05/16/2011
47	ARRA Autism Sequencing Collaboration at Baylor. SOLiD 4 System	Omics	08/01/2011
53	AGRE Omni1-quad	Omics	10/11/2011
59	AGP genotyping	Omics	04/03/2012
60	Ultradeep 454 sequencing of synaptic genes from postmortem cerebella of individuals with ASD and neurotypical controls	Omics	06/23/2012
63	Microemulsion PCR and Targeted Resequencing for Variant Detection in ASD	Omics	07/20/2012
76	Whole Genome Sequencing in Autism Families	Omics	01/03/2013
519	Resting	fMRI	11/08/2016
90	Genotyped IAN Samples	Omics	07/09/2013
91	NJLAGS Axiom Genotyping Array	Omics	07/16/2013
93	AGP genotyping (CNV)	Omics	09/06/2013
106	Longitudinal Sleep Study. H20 200. Channel set 2	EEG	11/07/2013
107	Longitudinal Sleep Study. H20 200. Channel set 3	EEG	11/07/2013
108	Longitudinal Sleep Study. AURA 200	EEG	11/07/2013
105	Longitudinal Sleep Study. H20 200. Channel set 1	EEG	11/07/2013
109	Longitudinal Sleep Study. AURA 400	EEG	11/07/2013
116	Gene Expression Analysis WG-6	Omics	01/07/2014
131	Jeste Lab UCLA ACEii: Charlie Brown and Sesame Street - Project 1	Eye Tracking	02/27/2014
132	Jeste Lab UCLA ACEii: Animacy - Project 1	Eye Tracking	02/27/2014
133	Jeste Lab UCLA ACEii: Mom Stranger - Project 2	Eye Tracking	02/27/2014
134	Jeste Lab UCLA ACEii: Face Emotion - Project 3	Eye Tracking	02/27/2014
145	AGRE/FMR1_Illumina.JHU	Omics	04/14/2014
146	AGRE/MECP2_Sanger.JHU	Omics	04/14/2014
147	AGRE/MECP2_Junior.JHU	Omics	04/14/2014
151	Candidate Gene Identification in familial Autism	Omics	06/09/2014
152	NJLAGS Whole Genome Sequencing	Omics	07/01/2014
154	Math Autism Study - Vinod Menon	fMRI	07/15/2014
155	Resting	fMRI	07/25/2014
156	Speech	fMRI	07/25/2014
159	Emotion	fMRI	07/25/2014
160	syllable contrast	EEG	07/29/2014
167	School-age naturalistic stimuli	Eye Tracking	09/19/2014
44	AGRE/Broad Affymetrix 5.0 Genotype Experiment	Omics	06/27/2011
45	Exome Sequencing of 20 Sporadic Cases of Autism Spectrum Disorder	Omics	07/15/2011

Collection - Add Experiment

Add Supporting Documentation

Funding Source:
URL:

To add an existing Data Structure, enter its title in the search bar. If you need to request changes, select the indicator "No, it requires changes to meet research needs" after selecting the Structure, and upload the file with the request changes specific to the selected Data Structure. Your file should follow the Request Changes Procedure. If the Data Structure does not exist, select "Request New Data Structure" and upload the appropriate zip file.

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Trajectories of Aging in Psychotic Disorders Over 27 Years #2477

General
Experiments (4)
Shared Data
Publications (38)
Data Expected (24)
Associated Studies (3)

Collection Title	Collection Investigators	Collection Description
Collection Title:	Trajectories of Aging in Psychotic Disorders Over 27 Years
Collection Investigators:	Roman Kotov
Collection Description:	Life expectancy is approximately 20 years shorter in schizophrenia and 10 years shorter in mood disorder with psychosis than in the general population, which is almost entirely due to natural-cause mortality. One proposed explanation is that psychotic disorders are associated with accelerated aging. Substantial evidence indicates that this population experiences premature declines in three functional domains internal i.e., age-related medical disorders, cognitive, and physical. However, it is unknown whether these declines are explainable by exposure to risk factors highly elevated in psychotic disorders obesity, poverty, smoking, low physical activity, poor diet, inadequate medical care, etc or are also due to pathophysiology of psychosis itself. Indeed, biological processes associated with psychosis genetic, neural P3 and mismatch negativity, and allostatic load metabolic problems, increased inflammation, hypothalamic-pituitary-adrenal axis dysregulation, and hypertension were found to predict accelerated aging in the general population, but this has not been tested in psychotic disorders. Moreover, it remains uncertain when accelerated aging starts and how rapidly it progresses, as prior studies typically began with older patients. Prevention of premature aging in psychotic disorders would extend life and improve health of millions of people, but it is unclear how to target such efforts, because fundamental information is lacking on trajectories of aging and their determinants in psychosis. The Suffolk County Mental Health Project SCMHP MH094398 offers a unique opportunity to fill these crucial gaps. It is the only US epidemiologic study designed to examine health, cognition, and physical performance in psychotic disorders over 27 years following first admission from mean age 30 to 57. In addition, the study has gathered a wealth of information on premorbid risk factors. It also includes a geographically and demographically matched never-psychotic comparison group. Thorough assessments of cases were done 6 times during the first two decades. At Year 20 mean age 49, both case N385 and never-psychotic N261 groups completed a comprehensive psychiatric evaluation, medical history, physical performance tests, anthropometric exam, cognitive testing, event-related potentials battery, assays of blood samples, and genotyping. The present proposal is to reassess cases and never-psychotic participants at ages 54 and 57 to trace divergence of aging trajectories during a pivotal period age 49 to 57, when medical morbidity is expected to double and cognitive and physical functioning begin to decline and identify risk factors and biological vulnerabilities that help to determine what path aging takes. This innovative design will enable us to clarify when and why aging is accelerated in psychotic disorders, and where interventions can be applied most productively to extend life expectancy and health of this population.
Data Repository:	NIMH Data Archive
Permission Group:
Collection Creation Date:	09/19/2016
Collection Phase:	Funding Completed
Collection Sub-Phase:	Close Out
Blinded Clinical Trial:	No
Total Funded Amount:	$1,529,400.00
Subjects Shared:	628
Collection DOI:	10.15154/h2e4-8f41

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Funding Sources:

Funding Source Name	Funding Source URL
NIH - Extramural	None

Supporting Documentation:

Grant Information:

Project Number	Title	Start Date	Original End Date	End Date	Planned Enrollment	Actual Enrollment	Organization	Funds Obligated
R01MH110434-01	Trajectories of Aging in Psychotic Disorders Over 27 Years	08/19/2016	07/31/2021	07/31/2021	833	769	STATE UNIVERSITY NEW YORK STONY BROOK	$1,529,400.00

Clinical Trials:

helpcenter.collection.general-tab

Collection - General Tab

Fields available for edit on the top portion of the page include:

Collection Title
Investigators
Collection Description
Collection Phase
Funding Source
Clinical Trials

Collection Phase: The current status of a research project submitting data to an NDA Collection, based on the timing of the award and/or the data that have been submitted.

Pre-Enrollment: The default entry made when the NDA Collection is created.
Enrolling: Data have been submitted to the NDA Collection or the NDA Data Expected initial submission date has been reached for at least one data structure category in the NDA Collection.
Data Analysis: Subject level data collection for the research project is completed and has been submitted to the NDA Collection. The NDA Collection owner or the NDA Help Desk may set this phase when they’ve confirmed data submission is complete and submitted subject counts match at least 90% of the target enrollment numbers in the NDA Data Expected. Data submission reminders will be turned off for the NDA Collection.
Funding Completed: The NIH grant award (or awards) associated with the NDA Collection has reached its end date. NDA Collections in Funding Completed phase are assigned a subphase to indicate the status of data submission.
- The Data Expected Subphase indicates that NDA expects more data will be submitted
- The Closeout Subphase indicates the data submission is complete.
- The Sharing Not Met Subphase indicates that data submission was not completed as expected.

Blinded Clinical Trial Status:

This status is set by a Collection Owner and indicates the research project is a double blinded clinical trial. When selected, the public view of Data Expected will show the Data Expected items and the Submission Dates, but the targeted enrollment and subjects submitted counts will not be displayed.
Targeted enrollment and subjects submitted counts are visible only to NDA Administrators and to the NDA Collection or as the NDA Collection Owner.
When an NDA Collection that is flagged Blinded Clinical Trial reaches the maximum data sharing date for that Data Repository (see https://nda.nih.gov/nda/sharing-regimen.html), the embargo on Data Expected information is released.

Funding Source

The organization(s) responsible for providing the funding is listed here.

Supporting Documentation

Users with Submission privileges, as well as Collection Owners, Program Officers, and those with Administrator privileges, may upload and attach supporting documentation. By default, supporting documentation is shared to the general public, however, the option is also available to limit this information to qualified researchers only.

Grant Information

Identifiable details are displayed about the Project of which the Collection was derived from. You may click in the Project Number to view a full report of the Project captured by the NIH.

Clinical Trials

Any data that is collected to support or further the research of clinical studies will be available here. Collection Owners and those with Administrator privileges may add new clinical trials.

Frequently Asked Questions

How does the NIMH Data Archive (NDA) determine which Permission Group data are submitted into?

During Collection creation, NDA staff determine the appropriate Permission Group based on the type of data to be submitted, the type of access that will be available to data access users, and the information provided by the Program Officer during grant award.
How do I know when a NDA Collection has been created?

When a Collection is created by NDA staff, an email notification will automatically be sent to the PI(s) of the grant(s) associated with the Collection to notify them.
Is a single grant number ever associated with more than one Collection?

The NDA system does not allow for a single grant to be associated with more than one Collection; therefore, a single grant will not be listed in the Grant Information section of a Collection for more than one Collection.
Why is there sometimes more than one grant included in a Collection?

In general, each Collection is associated with only one grant; however, multiple grants may be associated if the grant has multiple competing segments for the same grant number or if multiple different grants are all working on the same project and it makes sense to hold the data in one Collection (e.g., Cooperative Agreements).

Glossary

Administrator Privilege

A privilege provided to a user associated with an NDA Collection or NDA Study whereby that user can perform a full range of actions including providing privileges to other users.
Collection Owner

Generally, the Collection Owner is the contact PI listed on a grant. Only one NDA user is listed as the Collection owner. Most automated emails are primarily sent to the Collection Owner.
Collection Phase
The Collection Phase provides information on data submission as opposed to grant/project completion so while the Collection phase and grant/project phase may be closely related they are often different. Collection users with Administrative Privileges are encouraged to edit the Collection Phase. The Program Officer as listed in eRA (for NIH funded grants) may also edit this field. Changes must be saved by clicking the Save button at the bottom of the page. This field is sortable alphabetically in ascending or descending order. Collection Phase options include:
- Pre-Enrollment: A grant/project has started, but has not yet enrolled subjects.
- Enrolling: A grant/project has begun enrolling subjects. Data submission is likely ongoing at this point.
- Data Analysis: A grant/project has completed enrolling subjects and has completed all data submissions.
- Funding Completed: A grant/project has reached the project end date.
Collection Title

An editable field with the title of the Collection, which is often the title of the grant associated with the Collection.
Grant

Provides the grant number(s) for the grant(s) associated with the Collection. The field is a hyperlink so clicking on the Grant number will direct the user to the grant information in the NIH Research Portfolio Online Reporting Tools (RePORT) page.
Supporting Documentation

Various documents and materials to enable efficient use of the data by investigators unfamiliar with the project and may include the research protocol, questionnaires, and study manuals.
NIH Research Initiative

NDA Collections may be organized by scientific similarity into NIH Research Initiatives, to facilitate query tool user experience. NIH Research Initiatives map to one or multiple Funding Opportunity Announcements.
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.
Planned Enrollment

Number of human subject participants to be enrolled in an NIH-funded clinical research study. The data is provided in competing applications and annual progress reports.
Actual Enrollment

Number of human subjects enrolled in an NIH-funded clinical research study. The data is provided in annual progress reports.
NDA Collection

A virtual container and organization structure for data and associated documentation from one grant or one large project/consortium. It contains tools for tracking data submission and allows investigators to define a wide array of other elements that provide context for the data, including all general information regarding the data and source project, experimental parameters used to collect any event-based data contained in the Collection, methods, and other supporting documentation. They also allow investigators to link underlying data to an NDA Study, defining populations and subpopulations specific to research aims.
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.
Total Subjects Shared

The total number of unique subjects for whom data have been shared and are available for users with permission to access data.

Contact NDA Help Desk

ID	Name	Created Date	Status	Type
755	Doors	07/26/2017	Approved	EEG
756	Flankers	07/27/2017	Approved	EEG
757	P300	07/27/2017	Approved	EEG
758	PWMMN	07/27/2017	Approved	EEG

helpcenter.collection.experiments-tab

Collection - Experiments

The number of Experiments included is displayed in parentheses next to the tab name. You may download all experiments associated with the Collection via the Download button. You may view individual experiments by clicking the Experiment Name and add them to the Filter Cart via the Add to Cart button.

Collection Owners, Program Officers, and users with Submission or Administrative Privileges for the Collection may create or edit an Experiment.

Please note: The creation of an NDA Experiment does not necessarily mean that data collected, according to the defined Experiment, has been submitted or shared.

Frequently Asked Questions

Can an Experiment be associated with more than one Collection?
Yes -see the “Copy” button in the bottom left when viewing an experiment. There are two actions that can be performed via this button:
1. Copy the experiment with intent for modifications.
2. Associate the experiment to the collection. No modifications can be made to the experiment.

Glossary

Experiment Status

An Experiment must be Approved before data using the associated Experiment_ID may be uploaded.
Experiment ID

The ID number automatically generated by NDA which must be included in the appropriate file when uploading data to link the Experiment Definition to the subject record.

Contact NDA Help Desk

Shared Data:

Title	Type	Number of Subjects
Big Five Inventory 44 Items	Clinical Assessments	569
Bradburn Scale of Psychological Well-Being	Clinical Assessments	569
Brief Assessment of Cognition	Clinical Assessments	569
Brief Psychiatric Rating Scale	Clinical Assessments	569
Clinical Global Impression (CGI)	Clinical Assessments	569
Color Reading Interference (Stroop)	Clinical Assessments	569
Controlled Oral Word Association Test	Clinical Assessments	569
DSM-IV Checklist (Early Steps; SOFAS)	Clinical Assessments	569
Digit Symbol Substitution Test	Clinical Assessments	569
EEG Subject Files	Imaging	419
Height and Weight	Clinical Assessments	569
PROMIS Support	Clinical Assessments	569
Physical Health Interview	Clinical Assessments	569
Predictors of Relapse and Rehospitalization	Clinical Assessments	569
Psychological Functioning Form	Clinical Assessments	569
Research Subject	Clinical Assessments	569
Scales for the Assessment of Positive/Negative Symptoms	Clinical Assessments	569
Schedule for Nonadaptive and Adaptive Personality	Clinical Assessments	569
Short Form Health Survey	Clinical Assessments	569
Short Physical Performance Battery	Clinical Assessments	569
Structured Clinical Interview for DSM-IV	Clinical Assessments	569
The Inventory of Depression and Anxiety Symptoms	Clinical Assessments	569
Trail Making Test, Child and Adult	Clinical Assessments	569
WHO Disability Assessment Schedule	Clinical Assessments	569

helpcenter.collection.shared-data-tab

Collection - Shared Data

This tab provides a quick overview of the Data Structure title, Data Type, and Number of Subjects that are currently Shared for the Collection. The information presented in this tab is automatically generated by NDA and cannot be edited. If no information is visible on this tab, this would indicate the Collection does not have shared data or the data is private.

The shared data is available to other researchers who have permission to access data in the Collection's designated Permission Group(s). Use the Download button to get all shared data from the Collection to the Filter Cart.

Frequently Asked Questions

How will I know if another researcher uses data that I shared through the NIMH Data Archive (NDA)?

To see what data your project have submitted are being used by a study, simply go the Associated Studies tab of your collection. Alternatively, you may review an NDA Study Attribution Report available on the General tab.
Can I get a supplement to share data from a completed research project?

Often it becomes more difficult to organize and format data electronically after the project has been completed and the information needed to create a GUID may not be available; however, you may still contact a program staff member at the appropriate funding institution for more information.
Can I get a supplement to share data from a research project that is still ongoing?

Unlike completed projects where researchers may not have the information needed to create a GUID and/or where the effort needed to organize and format data becomes prohibitive, ongoing projects have more of an opportunity to overcome these challenges. Please contact a program staff member at the appropriate funding institution for more information.

Glossary

Data Structure

A defined organization and group of Data Elements to represent an electronic definition of a measure, assessment, questionnaire, or collection of data points. Data structures that have been defined in the NDA Data Dictionary are available at https://nda.nih.gov/general-query.html?q=query=data-structure
Data Type

A grouping of data by similar characteristics such as Clinical Assessments, Omics, or Neurosignal data.
Shared

The term 'Shared' generally means available to others; however, there are some slightly different meanings based on what is Shared. A Shared NDA Study is viewable and searchable publicly regardless of the user's role or whether the user has an NDA account. A Shared NDA Study does not necessarily mean that data used in the NDA Study have been shared as this is independently determined. Data are shared according the schedule defined in a Collection's Data Expected Tab and/or in accordance with data sharing expectations in the NDA Data Sharing Terms and Conditions. Additionally, Supporting Documentation uploaded to a Collection may be shared independent of whether data are shared.

Contact NDA Help Desk

Collection Owners and those with Collection Administrator permission, may edit a collection. The following is currently available for Edit on this page:

Publications

Publications relevant to NDA data are listed below. Most displayed publications have been associated with the grant within Pubmed. Use the "+ New Publication" button to add new publications. Publications relevant/not relevant to data expected are categorized. Relevant publications are then linked to the underlying data by selecting the Create Study link. Study provides the ability to define cohorts, assign subjects, define outcome measures and lists the study type, data analysis and results. Analyzed data and results are expected in this way.

PubMed ID	Study	Title	Journal	Authors	Date	Status
41266786	Create Study	The impact of collider bias on genetic prediction in psychotic disorders.	Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology	Asim, Amna; Yang, Yuan; PsyCourse Study; Heilbronner, Urs; Schulze, Thomas; Lencz, Todd; Vassos, Evangelos; Clouston, Sean A P; Kotov, Roman; Jonas, Katherine	January 1, 2026	Not Determined
41220310	Create Study	Where is mania in the meta-structure of psychopathology?	Psychological medicine	Ruggero, Camilo J; Jonas, Katherine G; Busso, Cheyanne; Lian, Wenxuan; Docherty, Anna R; Shabalin, Andrey A; Carlson, Gabrielle A; Bromet, Evelyn J; Kotov, Roman	November 12, 2025	Not Determined
40383906	Create Study	Predictors and Outcomes Associated with 25-Year Cognitive Decline in Psychotic Disorders.	Schizophrenia bulletin	Yang, Yuan; Clouston, Sean A P; Reichenberg, Abraham; Callahan, Jennifer L; Ruggero, Camilo Javier; Carlson, Gabrielle A; Bromet, Evelyn J; Kotov, Roman; Jonas, Katherine	January 16, 2026	Not Determined
40080555	Create Study	Personality in psychosis decades after onset: Tests of models of the relations between psychopathology and personality.	Journal of psychopathology and clinical science	Martin, Elizabeth A; Blank, Jennifer M; Jonas, Katherine G; Lian, Wenxuan; Kotov, Roman	April 1, 2025	Not Determined
39957549	Create Study	Impact of ERP Reliability Cutoffs on Sample Characteristics and Effect Sizes: Performance-Monitoring ERPs in Psychosis and Healthy Controls.	Psychophysiology	Heindorf, Gavin; Holbrook, Amanda; Park, Bohyun; Light, Gregory A; Rast, Philippe; Foti, Dan; Kotov, Roman; Clayson, Peter E	February 1, 2025	Not Determined
39864302	Create Study	Emotional intelligence as a predictor of functional outcomes in psychotic disorders.	Schizophrenia research	Blank, Jennifer M; Kotov, Roman; Jonas, Katherine G; Lian, Wenxuan; Martin, Elizabeth A	February 1, 2025	Not Determined
38774642	Create Study	Inferring Trajectories of Psychotic Disorders Using Dynamic Causal Modeling.	Computational psychiatry (Cambridge, Mass.)	Jin, Jingwen; Zeidman, Peter; Friston, Karl J; Kotov, Roman	January 1, 2023	Not Determined
38745457	Create Study	Long-Term Course of Remission and Recovery in Psychotic Disorders.	The American journal of psychiatry	Tramazzo, Sara; Lian, Wenxuan; Ajnakina, Olesya; Carlson, Gabrielle; Bromet, Evelyn; Kotov, Roman; Jonas, Katherine	June 1, 2024	Not Determined
38530896	Create Study	Automating the analysis of facial emotion expression dynamics: A computational framework and application in psychotic disorders.	Proceedings of the National Academy of Sciences of the United States of America	Hall, Nathan T; Hallquist, Michael N; Martin, Elizabeth A; Lian, Wenxuan; Jonas, Katherine G; Kotov, Roman	April 2, 2024	Not Determined
38351173	Create Study	Psychosis superspectrum II: neurobiology, treatment, and implications.	Molecular psychiatry	Kotov, Roman; Carpenter, William T; Cicero, David C; Correll, Christoph U; Martin, Elizabeth A; Young, Jared W; Zald, David H; Jonas, Katherine G	May 1, 2024	Not Determined
36317338	Create Study	Distinguishing the Effects of Lead-Time Bias and Duration of Untreated Psychosis.	The American journal of psychiatry	Jonas, Katherine G; Fochtmann, Laura J; Perlman, Greg; Kane, John M; Bromet, Evelyn J; Kotov, Roman	November 1, 2022	Not Determined
36226640	Create Study	Mismatch negativity and clinical trajectories in psychotic disorders: Five-year stability and predictive utility.	Psychological medicine	Donaldson, Kayla R; Jonas, Katherine; Foti, Dan; Larsen, Emmett M; Mohanty, Aprajita; Kotov, Roman	September 1, 2023	Not Determined
36084492	Create Study	Pleasant and unpleasant odor identification ability is associated with distinct dimensions of negative symptoms transdiagnostically in psychotic disorders.	Schizophrenia research	Larsen, Emmett M; Donaldson, Kayla R; Jonas, Katherine G; Lian, Wenxuan; Bromet, Evelyn J; Kotov, Roman; Mohanty, Aprajita	October 1, 2022	Not Determined
35583896	Create Study	The Course of General Cognitive Ability in Individuals With Psychotic Disorders.	JAMA psychiatry	Jonas, Katherine; Lian, Wenxuan; Callahan, Jennifer; Ruggero, Camilo J; Clouston, Sean; Reichenberg, Avraham; Carlson, Gabrielle A; Bromet, Evelyn J; Kotov, Roman	July 1, 2022	Not Determined
35144862	Create Study	Reconceptualizing schizophrenia in the Hierarchical Taxonomy Of Psychopathology (HiTOP).	Schizophrenia research	Kotov, Roman; Jonas, Katherine G; Lian, Wenxuan; Docherty, Anna R; Carpenter, William T	April 1, 2022	Not Determined
34695710	Create Study	Mismatch negativity amplitude in first-degree relatives of individuals with psychotic disorders: Links with cognition and schizotypy.	Schizophrenia research	Donaldson, Kayla R; Larsen, Emmett M; Jonas, Katherine; Tramazzo, Sara; Perlman, Greg; Foti, Dan; Mohanty, Aprajita; Kotov, Roman	December 1, 2021	Not Determined
34524413	Create Study	Two Hypotheses on the High Incidence of Dementia in Psychotic Disorders.	JAMA psychiatry	Jonas, Katherine; Abi-Dargham, Anissa; Kotov, Roman	December 1, 2021	Not Determined
34425381	Create Study	Performance-based assessment of social skills in a large sample of participants with schizophrenia, bipolar disorder and healthy controls: Correlates of social competence and social appropriateness.	Schizophrenia research	Miller, Michelle L; Strassnig, Martin T; Bromet, Evelin; Depp, Colin A; Jonas, Katherine; Lin, Wenxuan; Moore, Raeanne C; Patterson, Thomas L; Penn, David L; Pinkham, Amy E; Kotov, Roman A; Harvey, Philip D	October 1, 2021	Not Determined
34031357	Create Study	PTSD is associated with accelerated transcriptional aging in World Trade Center responders.	Translational psychiatry	Kuan, Pei-Fen; Ren, Xu; Clouston, Sean; Yang, Xiaohua; Jonas, Katherine; Kotov, Roman; Bromet, Evelyn; Luft, Benjamin J	May 24, 2021	Not Determined
33890112	Create Study	Predicting Long-Term Outcomes in First-Admission Psychosis: Does the Hierarchical Taxonomy of Psychopathology Aid DSM in Prognostication?	Schizophrenia bulletin	Martin, Elizabeth A; Jonas, Katherine G; Lian, Wenxuan; Foti, Dan; Donaldson, Kayla R; Bromet, Evelyn J; Kotov, Roman	August 21, 2021	Not Determined
33143787	Create Study	Dynamic interplay between life events and course of psychotic disorders: 10-year longitudinal study following first admission.	Psychological medicine	Donaldson, Kayla R; Jonas, Katherine G; Tian, Yuan; Larsen, Emmett M; Klein, Daniel N; Mohanty, Aprajita; Bromet, Evelyn J; Kotov, Roman	August 1, 2022	Not Determined
32757601	Create Study	Associations of mismatch negativity with psychotic symptoms and functioning transdiagnostically across psychotic disorders.	Journal of abnormal psychology	Donaldson, Kayla R; Novak, Keisha D; Foti, Dan; Marder, Maya; Perlman, Greg; Kotov, Roman; Mohanty, Aprajita	August 1, 2020	Not Determined
32317045	Create Study	Pathways from performance monitoring to negative symptoms and functional outcomes in psychotic disorders.	Psychological medicine	Foti, Dan; Perlman, Greg; Bromet, Evelyn J; Harvey, Philip D; Hajcak, Greg; Mathalon, Daniel H; Kotov, Roman	September 2021	Not Determined
32046533	Create Study	Lead-Time Bias Confounds Association Between Duration of Untreated Psychosis and Illness Course in Schizophrenia.	The American journal of psychiatry	Jonas, Katherine G; Fochtmann, Laura J; Perlman, Greg; Tian, Yuan; Kane, John M; Bromet, Evelyn J; Kotov, Roman	April 2020	Not Determined
31825511	Create Study	Long-term Changes in Cognitive Functioning in Individuals With Psychotic Disorders: Findings From the Suffolk County Mental Health Project.	JAMA psychiatry	Fett, Anne-Kathrin J; Velthorst, Eva; Reichenberg, Abraham; Ruggero, Camilo J; Callahan, Jennifer L; Fochtmann, Laura J; Carlson, Gabrielle A; Perlman, Greg; Bromet, Evelyn J; Kotov, Roman	April 2020	Not Determined

helpcenter.collection.publications-tab

Collection - Publications

The number of Publications is displayed in parentheses next to the tab name. Clicking on any of the Publication Titles will open the Publication in a new internet browsing tab.

Collection Owners, Program Officers, and users with Submission or Administrative Privileges for the Collection may mark a publication as either Relevant or Not Relevant in the Status column.

Frequently Asked Questions

How can I determine if a publication is relevant?

Publications are considered relevant to a collection when the data shared is directly related to the project or collection.
Where does the NDA get the publications?

PubMed, an online library containing journals, articles, and medical research. Sponsored by NiH and National Library of Medicine (NLM).

Glossary

Create Study

A link to the Create an NDA Study page that can be clicked to start creating an NDA Study with information such as the title, journal and authors automatically populated.
Not Determined Publication

Indicates that the publication has not yet been reviewed and/or marked as Relevant or Not Relevant so it has not been determined whether an NDA Study is expected.
Not Relevant Publication

A publication that is not based on data related to the aims of the grant/project associated with the Collection or not based on any data such as a review article and, therefore, an NDA Study is not expected to be created.
PubMed

PubMed provides citation information for biomedical and life sciences publications and is managed by the U.S. National Institutes of Health's National Library of Medicine.
PubMed ID

The PUBMed ID is the unique ID number for the publication as recorded in the PubMed database.
Relevant Publication

A publication that is based on data related to the aims of the grant/project associated with the Collection and, therefore, an NDA Study is expected to be created.

Contact NDA Help Desk

Data Expected List: Mandatory Data Structures

These data structures are mandatory for your NDA Collection. Please update the Targeted Enrollment number to accurately represent the number of subjects you expect to submit for the entire study.

For NIMH HIV-related research that involves human research participants: Select the dictionary or dictionaries most appropriate for your research. If your research does not require all three data dictionaries, just ignore the ones you do not need. There is no need to delete extra data dictionaries from your NDA Collection. You can adjust the Targeted Enrollment column in the Data Expected tab to “0” for those unnecessary data dictionaries. At least one of the three data dictionaries must have a non-zero value.

Data Expected	Targeted Enrollment	Initial Submission	Subjects Submitted	Initial Share	Subjects Shared	Status
Research Subject and Pedigree	120	01/15/2018	569	05/15/2018	569	Approved

To create your project's Data Expected list, use the "+New Data Expected" to add or request existing structures and to request new Data Structures that are not in the NDA Data Dictionary.

If the Structure you need already exists, locate it and specify your dates and enrollment when adding it to your Data Expected list. If you require changes to the Structure you need, select the indicator stating "No, it requires changes to meet research needs," and upload a file containing your requested changes.

If the structure you need is not yet defined in the Data Dictionary, you can select "Upload Definition" and attach the necessary materials to request its creation.

When selecting the expected dates for your data, make sure to follow the standard Data Sharing Regimen and choose dates within the date ranges that correspond to your project start and end dates.

Please visit the Completing Your Data Expected Tutorial for more information.

Data Expected List: Data Structures per Research Aims

These data structures are specific to your research aims and should list all data structures in which data will be collected and submitted for this NDA Collection. Please update the Targeted Enrollment number to accurately represent the number of subjects you expect to submit for the entire study.

Data Expected	Targeted Enrollment	Initial Submission	Subjects Submitted	Initial Share	Subjects Shared	Status
Medical History	120	01/15/2018	569	05/15/2018	569	Approved
Clinical Global Impression (CGI)	120	01/15/2018	569	05/15/2018	569	Approved
Structured Clinical Interview for DSM (SCID)	120	01/15/2018	569	05/15/2018	569	Approved
Scales for the Assessment of Positive/Negative Symptoms	120	01/15/2018	569	05/15/2018	569	Approved
Big Five Inventory	120	01/15/2018	569	05/15/2018	569	Approved
DSM IV Criteria	120	01/15/2018	569	05/15/2018	569	Approved
Physical Exam	120	01/15/2018	569	05/15/2018	569	Approved
Brief Psychiatric Rating Scale	120	01/15/2018	569	05/15/2018	569	Approved
Brief Assessment of Cognition	120	01/15/2018	569	05/15/2018	569	Approved
Trail Making Test (Child and Adult)	120	01/15/2018	569	05/15/2018	569	Approved
WHO Disability Assessment Schedule	120	01/15/2018	569	05/15/2018	569	Approved
Color Reading Interference (Stroop)	120	01/15/2018	569	05/15/2018	569	Approved
Inventory of Depression and Anxiety Symptoms	120	01/15/2018	569	05/15/2018	569	Approved
Controlled Oral Word Association Test	120	01/15/2018	569	05/15/2018	569	Approved
Digit Symbol Substitution Test	120	01/15/2018	569	05/15/2018	569	Approved
Short Form Health Survey	120	01/15/2018	569	05/15/2018	569	Approved
EEG	120	01/15/2018	419	05/15/2018	419	Approved
Psychological Functioning	120	01/15/2018	569	05/15/2018	569	Approved
PROMIS Support	120	01/15/2018	569	05/15/2018	569	Approved
Schedule for Nonadaptive and Adaptive Personality	120	01/15/2018	569	05/15/2018	569	Approved
Affect Balance Scale	120	01/15/2018	569	05/15/2018	569	Approved
Short Physical Performance Battery	120	01/15/2018	569	05/15/2018	569	Approved
Predictors of Relapse and Rehospitalization	120	01/15/2018	569	05/15/2018	569	Approved

Structure not yet defined

No Status history for this Data Expected has been recorded yet

helpcenter.collection.data-expected-tab

Collection - Data Expected

The Data Expected tab displays the list of all data that NDA expects to receive in association with the Collection as defined by the contributing researcher, as well as the dates for the expected initial upload of the data, and when it is first expected to be shared, or with the research community. Above the primary table of Data Expected, any publications determined to be relevant to the data within the Collection are also displayed - members of the contributing research group can use these to define NDA Studies, connecting those papers to underlying data in NDA.

The tab is used both as a reference for those accessing shared data, providing information on what is expected and when it will be shared, and as the primary tracking mechanism for contributing projects. It is used by both contributing primary researchers, secondary researchers, and NIH Program and Grants Management staff.

Researchers who are starting their project need to update their Data Expected list to include all the Data Structures they are collecting under their grant and set their initial submission and sharing schedule according to the NDA Data Sharing Regimen.

To add existing Data Structures from the Data Dictionary, to request new Data Structure that are not in the Dictionary, or to request changes to existing Data Structures, click "+New Data Expected".

For step-by-step instructions on how to add existing Data Structures, request changes to an existing Structure, or request a new Data Structure, please visit the Completing Your Data Expected Tutorial.

If you are a contributing researcher creating this list for the first time, or making changes to the list as your project progress, please note the following:

Although items you add to the list and changes you make are displayed, they are not committed to the system until you Save the entire page using the "Save" button at the bottom of your screen. Please Save after every change to ensure none of your work is lost.
If you attempt to add a new structure, the title you provide must be unique - if another structure exists with the same name your change will fail.
Adding a new structure to this list is the only way to request the creation of a new Data Dictionary definition.

Frequently Asked Questions

What is an NDA Data Structure?

An NDA Data Structure is comprised of multiple Data Elements to make up an electronic definition of an assessment, measure, questionnaire, etc will have a corresponding Data Structure.
What is the NDA Data Dictionary?

The NDA Data Dictionary is comprised of electronic definitions known as Data Structures.

Glossary

Analyzed Data

Data specific to the primary aims of the research being conducted (e.g. outcome measures, other dependent variables, observations, laboratory results, analyzed images, volumetric data, etc.) including processed images.
Data Item

Items listed on the Data Expected list in the Collection which may be an individual and discrete Data Structure, Data Structure Category, or Data Structure Group.
Data Structure

A defined organization and group of Data Elements to represent an electronic definition of a measure, assessment, questionnaire, or collection of data points. Data structures that have been defined in the NDA Data Dictionary are available at https://nda.nih.gov/general-query.html?q=query=data-structure
Data Structure Category

An NDA term describing the affiliation of a Data Structure to a Category, which may be disease/disorder or diagnosis related (Depression, ADHD, Psychosis), specific to data type (MRI, eye tracking, omics), or type of data (physical exam, IQ).
Data Structure Group

A Data Item listed on the Data Expected tab of a Collection that indicates a group of Data Structures (e.g., ADOS or SCID) for which data may be submitted instead of a specific Data Structure identified by version, module, edition, etc. For example, the ADOS Data Structure Category includes every ADOS Data Structure such as ADOS Module 1, ADOS Module 2, ADOS Module 1 - 2nd Edition, etc. The SCID Data Structure Group includes every SCID Data Structure such as SCID Mania, SCID V Mania, SCID PTSD, SCID-V Diagnosis, and more.
Evaluated Data

A new Data Structure category, Evaluated Data is analyzed data resulting from the use of computational pipelines in the Cloud and can be uploaded directly back to a miNDAR database. Evaluated Data is expected to be listed as a Data Item in the Collection's Data Expected Tab.
Imaging Data

Imaging+ is an NDA term which encompasses all imaging related data including, but not limited to, images (DTI, MRI, PET, Structural, Spectroscopy, etc.) as well as neurosignal data (EEG, fMRI, MEG, EGG, eye tracking, etc.) and Evaluated Data.
Initial Share Date

Initial Submission and Initial Share dates should be populated according to the NDA Data Sharing Terms and Conditions. Any modifications to these will go through the approval processes outlined above. Data will be shared with authorized users upon publication (via an NDA Study) or 1-2 years after the grant end date specified on the first Notice of Award, as defined in the applicable Data Sharing Terms and Conditions.
Initial Submission Date

Initial Submission and Initial Share dates should be populated according to these NDA Data Sharing Terms and Conditions. Any modifications to these will go through the approval processes outlined above. Data for all subjects is not expected on the Initial Submission Date and modifications may be made as necessary based on the project's conduct.
Research Subject and Pedigree

An NDA created Data Structure used to convey basic information about the subject such as demographics, pedigree (links family GUIDs), diagnosis/phenotype, and sample location that are critical to allow for easier querying of shared data.
Submission Cycle

The NDA has two Submission Cycles per year - January 15 and July 15.
Submission Exemption

An interface to notify NDA that data may not be submitted during the upcoming/current submission cycle.

Contact NDA Help Desk

Collection Owners and those with Collection Administrator permission, may edit a collection. The following is currently available for Edit on this page:

Associated Studies

Studies that have been defined using data from a Collection are important criteria to determine the value of data shared. The number of subjects column displays the counts from this Collection that are included in a Study, out of the total number of subjects in that study. The Data Use column represents whether or not the study is a primary analysis of the data or a secondary analysis. State indicates whether the study is private or shared with the research community.

Study NameFilter by Study Name	DOIFilter by DOI	AbstractFilter by Abstract	Collection/Study SubjectsFilter by Collection/Study Subjects	Data UsageFilter by Data Usage	StateFilter by State
Intraindividual Variability of Event-Related Potentials in Psychosis: A Registered Report	10.15154/5vm9-f928	Background: Neurophysiological tools have yielded valuable insights into the pathophysiology and treatment of psychosis. However, studies using event-related potentials (ERPs) primarily focus on mean scores and neglect within-person variability of ERP scores. The neglect of within-person variability of ERPs in the search for biomarkers might result in missed crucial differences related to psychosis. This registered report aimed to determine whether distinct patterns of intraindividual variability in ERP biomarkers are observed in people with a lifetime psychosis diagnosis. Methods: Publicly available data posted to the NIMH Data Archive for 1R01MH110434-01 was obtained for 162 patients with a lifetime history of psychosis and 178 never-psychotic controls. Participants completed tasks that measured auditory mismatch negativity (MMN), P300, error-related negativity (ERN), and reward positivity (RewP). Multilevel location-scale models were used to determine whether patients show greater intraindividual variability of ERP scores than controls. Results: Contrary to predictions, groups did not differ in within-person variability of MMN-frequency, P3, or ERN; patients showed less variability in MMN-duration than controls. Exploratory analyses of a subset of patients with schizophrenia showed greater variability in this group than in controls for MMN. Greater severity of thought disorder and activation symptoms were associated with higher intraindividual MMN variability. Discussion: Distinct patterns of intraindividual variability in the measured ERPs were not observed for the broad group of people with lifetime psychotic disorders. Exploratory analyses suggest that intraindividual differences in ERPs are more relevant to schizophrenia and certain symptom dimensions than to psychotic disorders broadly, but research is needed to confirm these exploratory findings.	340/340	Secondary Analysis	Shared
The Impact of ERP Reliability Cutoffs on Sample Characteristics and Effect Sizes: Performance-Monitoring ERPs in Psychosis and Healthy Controls	10.15154/0pxp-hh95	In studies of event-related brain potentials (ERPs), it is common practice to exclude participants for having too few trials for analysis to ensure adequate score reliability (i.e., internal consistency). However, in research involving clinical samples, the impact of increasingly rigorous reliability standards on factors such as sample generalizability, patient vs. control effect sizes, and effect sizes for within-group correlations with external variables is unclear. This study systematically evaluated whether different ERP reliability cutoffs impacted these factors in psychosis. Error-related negativity (ERN) and error positivity (Pe) were assessed during a modified flanker task in 97 patients with psychosis and 104 healthy comparison participants, who also completed measures of cognition and psychiatric symptoms. ERP reliability cutoffs had notably different effects on the factors considered. A recommended reliability cutoff of .80 resulted in sample bias due to systematic exclusion of patients with relatively few task errors, lower reported psychiatric symptoms, and higher levels of cognitive functioning. ERP score reliability lower than .80 resulted in generally smaller between- and within-group effect sizes, likely misrepresenting effect sizes. Imposing rigorous ERP reliability standards in studies of psychotic disorders might exclude high-functioning patients, which raises important considerations for the generalizability of clinical ERP research.	201/201	Secondary Analysis	Shared
Trial-By-Trial ERP-Behavior Relationships in Psychosis: Between- and Within-Person Variability in Performance Monitoring Adjustments	10.15154/2pt7-8962	Cognitive impairment in schizophrenia, characterized by deficits in performance monitoring, predicts clinical and functional outcomes. The error-related negativity (ERN), a neurophysiological index of error detection, is reduced in psychosis, but it is unclear why this impaired error detection is not closely linked to post-error behavioral adjustments. A possibility is that research has overrelied on examining between-person relationships of average ERN and behavior, rather than focusing on within-person, trial-by-trial changes. This study aimed to determine whether neurophysiological indices of error detection (ERN, error positivity [Pe]) predict within-person post-error behavioral adjustments in psychotic disorders and whether these relationships are weaker in people with psychosis than in controls. ERN and Pe were assessed during a modified flanker task in 72 patients with psychosis and 82 healthy comparison participants. Multilevel location-scale models were used to examine trial-by-trial changes in the relationships between ERPs and behavior (response [RTs], accuracy). Results showed that ERP-RT relationships were similar across patients and controls. In both groups, greater within-person increases in ERN amplitude predicted longer and mor variable RTs following correct trials. Larger within-person increases in Pe predicted shorter and more variable RTs following correct trials, but less variable RTs following error trials. Exploratory analyses in a subset of patients with schizophrenia showed a similar pattern of effects as in the overall analyses. ERP-accuracy relationships were neither observed nor moderated by diagnostic groups. Within-person ERP-behavior relationships were preserved in psychosis, indicating intact performance monitoring at the individual level. This supports performance-monitoring as a transdiagnostic construct and underscores the importance of examining intraindividual variability to understand performance monitoring in psychotic disorders.	154/154	Secondary Analysis	Shared

* Data not on individual level

helpcenter.collection.associated-studies-tab

Collection - Associated Studies

Clicking on the Study Title will open the study details in a new internet browser tab. The Abstract is available for viewing, providing the background explanation of the study, as provided by the Collection Owner.

Primary v. Secondary Analysis: The Data Usage column will have one of these two choices. An associated study that is listed as being used for Primary Analysis indicates at least some and potentially all of the data used was originally collected by the creator of the NDA Study. Secondary Analysis indicates the Study owner was not involved in the collection of data, and may be used as supporting data.

Private v. Shared State: Studies that remain private indicate the associated study is only available to users who are able to access the collection. A shared study is accessible to the general public.

Frequently Asked Questions

How do I associate a study to my collection?

Studies are associated to the Collection automatically when the data is defined in the Study.

Glossary

Associated Studies Tab

A tab in a Collection that lists the NDA Studies that have been created using data from that Collection including both Primary and Secondary Analysis NDA Studies.

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