NIMH Data Archive - Data

Genomics

Neuroimaging

Phenotype¹

New Trial
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	Illumina Infinium PsychArray BeadChip Assay	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.

Use/Modify Existing Data Structure

Request New Data Structure

Targeted Enrollment:

Initial Submission Date:

Initial Share Date:

Data Structure Search:

Data Structures:

Submit

Request Submission Exemption

Not Eligible

The Data Expected list for this Collection shows some raw data as missing. Contact the NDA Help Desk with any questions.

Please confirm that you will not be enrolling any more subjects and that all raw data has been collected and submitted.

Collection Updated

Your Collection is now in Data Analysis phase and exempt from biannual submissions. Analyzed data is still expected prior to publication or no later than the project end date.

[CMS] Error

[CMS]

Unable to change collection phase where targeted enrollment is less than 90%

You have requested to move the sharing dates for the following assessments:

Data Expected Item	Original Sharing Date	New Sharing Date

Please provide a reason for this change, which will be sent to the Program Officers listed within this collection:

Explanation must be between 20 and 200 characters in length.

Please press Save or Cancel

Rett syndrome, MECP2 Duplications, and Rett-related Disorders Natural History #2388

General
Experiments (0)
Shared Data
Publications (104)
Data Expected (8)
Associated Studies (0)

Collection Title	Collection Investigators	Collection Description
Collection Title:	Rett syndrome, MECP2 Duplications, and Rett-related Disorders Natural History
Collection Investigators:	Alan Percy
Collection Description:	This Collection is from a multi-institutional group of investigators with longstanding interest in Rett syndrome (RTT) and RTT-related disorders continues a Rare Disease Clinical Research Center (RDCRC) within the Rare Diseases Clinical Research Network. This RDCRC will focus on three distinct disorders: RTT, MECP2 duplication disorder, and the RTT-related disorders including CDKL5, FOXG1, and individuals with MECP2 mutations but lacking clinical criteria for RTT. The near-term potential for meaningful therapies is tangible for RTT; the treatment potential for the other disorders is promising. Three overarching specific aims are proposed. 1) Perform longitudinal and neurobehavioral assessments on the core clinical features of each disorder: The on-going RTT NHS has provided critical data for organizing and advancing longitudinal studies. Substantial questions remain for RTT in terms of clinical variability not explainable solely by the specific mutations. Acquisition of similar data for the other disorders is equally important. 2) Perform robust biomarker and clinical outcome measures to identify biological factors that contribute to disease severity in each disorder: Providing critical guidance to effective and discriminant outcome measures is a crucial feature of any clinical trial and requires special consideration for these disorders. 3) Identify and characterize neurophysiological and neuroimaging correlates of disease severity in RTT and RTT-related disorders: Understanding alterations in specific volumetric measures, chemical composition, and neurophysiological measures such as EEG and Evoked Potentials are critical to advancing clinical knowledge. The RDCRC will maintain extensive training and pilot project programs cooperating directly with the respective CTSAs. The RDCRC will work with the Patient Advocacy Groups to ensure a full partnership and will rely principally on the Data Management and Coordinating Center for protocol management, data storage, a website portal, and biostatistical support. The UAB CCTS (CTSA) will fully cooperate with the RDCRC with pilot project development and additional biostatistical support. Website interfaces will be linked with the RDCRC, the DMCC, and the Patients Advocacy groups to ensure the widest reach of relevant information.
Data Repository:	NIMH Data Archive
Permission Group:
Collection Creation Date:	06/21/2016
Collection Phase:	Funding Completed
Collection Sub-Phase:	Close Out
Blinded Clinical Trial:	No
Total Funded Amount:	$5,096,669.00
Subjects Shared:	958

{"values":[]}

Loading Chart...

Funding Sources:

Funding Source Name	Funding Source URL
NIH - Extramural	None

Supporting Documentation:

Grant Information:

Project Number	Project Title	Start Date	End Date	Planned Enrollment	Actual Enrollment	Organization	Funds Obligated
U54HD061222-11	Rett syndrome, MECP2 Duplications, and Rett-related Disorders Natural History	09/17/2014	07/31/2020	1796	111	UNIVERSITY OF ALABAMA AT BIRMINGHAM	$5,096,669.00

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
No records found.

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
Clinical Assessment Form	Clinical Assessments	955
Demographics and Birth History	Clinical Assessments	958
Interval History Form	Clinical Assessments	942
Physician Initial History Form	Clinical Assessments	958
SF-36 Health Survey	Clinical Assessments	847

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
38496825	Create Study	Distribution of hand function by age in individuals with Rett syndrome.	Annals of the Child Neurology Society	Neul, Jeffrey L; Benke, Tim A; Marsh, Eric D; Lane, Jane B; Lieberman, David N; Skinner, Steven A; Glaze, Daniel G; Suter, Bernhard; Heydemann, Peter T; Beisang, Arthur A; Standridge, Shannon M; Ryther, Robin C C; Haas, Richard H; Edwards, Lloyd J; Ananth, Amitha; Percy, Alan K	September 1, 2023	Not Determined
38474085	Create Study	Mowat-Wilson Syndrome: Case Report and Review of ZEB2 Gene Variant Types, Protein Defects and Molecular Interactions.	International journal of molecular sciences	St Peter, Caroline; Hossain, Waheeda A; Lovell, Scott; Rafi, Syed K; Butler, Merlin G	February 29, 2024	Not Determined
37833681	Create Study	Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study.	Journal of neurodevelopmental disorders	Neul, Jeffrey L; Benke, Timothy A; Marsh, Eric D; Suter, Bernhard; Silveira, Lori; Fu, Cary; Peters, Sarika U; Percy, Alan K; Rett syndrome Natural History Study Group	October 13, 2023	Not Determined
37581718	Create Study	Adaptive Skills of Individuals with Angelman Syndrome Assessed Using the Vineland Adaptive Behavior Scales, 2nd Edition.	Journal of autism and developmental disorders	Gwaltney, Angela; Potter, Sarah Nelson; Peters, Sarika U; Barbieri-Welge, Rene L; Horowitz, Lucia T; Noll, Lisa M; Hundley, Rachel J; Bird, Lynne M; Tan, Wen-Hann; Sadhwani, Anjali; Wheeler, Anne	August 15, 2023	Not Determined
36993737	Create Study	Top Caregiver Concerns in Rett syndrome and related disorders: data from the US Natural History Study.	Research square	Neul, Jeffrey Lorenz; Benke, Timothy A; Marsh, Eric D; Suter, Bernhard; Silveira, Lori; Fu, Cary; Peters, Sarika U; Percy, Alan K; Rett syndrome Natural History Study Group	March 20, 2023	Not Determined
36870948	Create Study	Comparison of evoked potentials across four related developmental encephalopathies.	Journal of neurodevelopmental disorders	Saby, Joni N; Peters, Sarika U; Benke, Timothy A; Standridge, Shannon M; Swanson, Lindsay C; Lieberman, David N; Olson, Heather E; Key, Alexandra P; Percy, Alan K; Neul, Jeffrey L; Nelson, Charles A; Roberts, Timothy P L; Marsh, Eric D	March 4, 2023	Not Determined
36522453	Create Study	Neural complexity is a common denominator of human consciousness across diverse regimes of cortical dynamics.	Communications biology	Frohlich, Joel; Chiang, Jeffrey N; Mediano, Pedro A M; Nespeca, Mark; Saravanapandian, Vidya; Toker, Daniel; Dell'Italia, John; Hipp, Joerg F; Jeste, Shafali S; Chu, Catherine J; Bird, Lynne M; Monti, Martin M	December 15, 2022	Not Determined
36372969	Create Study	Analysis of electrocardiograms in individuals with CDKL5 deficiency disorder.	American journal of medical genetics. Part A	Stansauk, Jessica; Fidell, Andrea; Benke, Tim; Schaffer, Michael; Demarest, Scott T	January 1, 2023	Not Determined
35566699	Create Study	Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome.	Journal of clinical medicine	Mahmoud, Ranim; Swanson, Heidi D; Butler, Merlin G; Flodman, Pamela; Gold, June-Anne; Miller, Jennifer L; Roof, Elizabeth; Osann, Kathryn; Dykens, Elisabeth; Driscoll, Daniel J; Kimonis, Virginia	May 4, 2022	Not Determined
35483386	Create Study	CDKL5 deficiency disorder: clinical features, diagnosis, and management.	The Lancet. Neurology	Leonard, Helen; Downs, Jenny; Benke, Tim A; Swanson, Lindsay; Olson, Heather; Demarest, Scott	June 1, 2022	Not Determined
35063470	Create Study	Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome.	The Journal of pediatrics	Motil, Kathleen J; Geerts, Suzanne; Annese, Fran; Neul, Jeffrey L; Benke, Tim; Marsh, Eric; Lieberman, David; Skinner, Steven A; Glaze, Daniel G; Heydemann, Peter; Beisang, Arthur; Standridge, Shannon; Ryther, Robin; Lane, Jane B; Edwards, Lloyd; Percy, Alan K	May 1, 2022	Not Determined
34979033	Create Study	Anxiety in Angelman Syndrome.	American journal on intellectual and developmental disabilities	Grebe, Stacey C; Limon, Danica L; McNeel, Morgan M; Guzick, Andrew; Peters, Sarika U; Tan, Wen-Hann; Sadhwani, Anjali; Bacino, Carlos A; Bird, Lynne M; Samaco, Rodney C; Berry, Leandra N; Goodman, Wayne K; Schneider, Sophie C; Storch, Eric A	January 1, 2022	Not Determined
34841387	Create Study	Electrophysiological Abnormalities in Angelman Syndrome Correlate With Symptom Severity.	Biological psychiatry global open science	Hipp, Joerg F; Frohlich, Joel; Keute, Marius; Tan, Wen-Hann; Bird, Lynne M	September 1, 2021	Not Determined
34642905	Create Study	Electrophysiological Biomarkers in Genetic Epilepsies.	Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics	Armstrong, Caren; Marsh, Eric D	July 1, 2021	Not Determined
34595733	Create Study	Clinical Trial Design for Disease-Modifying Therapies for Genetic Epilepsies.	Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics	Brock, Dylan C; Demarest, Scott; Benke, Tim A	July 1, 2021	Not Determined
34547934	Create Study	Cerebral Visual Impairment in CDKL5 Deficiency Disorder Correlates With Developmental Achievement.	Journal of child neurology	Brock, Dylan; Fidell, Andrea; Thomas, Jacob; Juarez-Colunga, Elizabeth; Benke, Tim A; Demarest, Scott	October 1, 2021	Not Determined
34536900	Create Study	Clinical Characterization of Epilepsy in Children With Angelman Syndrome.	Pediatric neurology	Cassater, Daiana; Bustamante, Mariana; Sach-Peltason, Lisa; Rotenberg, Alexander; Nespeca, Mark; Tan, Wen-Hann; Bird, Lynne M; Hipp, Joerg F	November 1, 2021	Not Determined
34530725	Create Study	Current neurologic treatment and emerging therapies in CDKL5 deficiency disorder.	Journal of neurodevelopmental disorders	Olson, Heather E; Daniels, Carolyn I; Haviland, Isabel; Swanson, Lindsay C; Greene, Caitlin A; Denny, Anne Marie M; Demarest, Scott T; Pestana-Knight, Elia; Zhang, Xiaoming; Moosa, Ahsan N; Fidell, Andrea; Weisenberg, Judith L; Suter, Bernhard; Fu, Cary; Neul, Jeffrey L; Percy, Alan K; Marsh, Eric D; Benke, Timothy A; Poduri, Annapurna	September 16, 2021	Not Determined
34388423	Create Study	Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.	Pediatric neurology	Veatch, Olivia J; Malow, Beth A; Lee, Hye-Seung; Knight, Aryn; Barrish, Judy O; Neul, Jeffrey L; Lane, Jane B; Skinner, Steven A; Kaufmann, Walter E; Miller, Jennifer L; Driscoll, Daniel J; Bird, Lynne M; Butler, Merlin G; Dykens, Elisabeth M; Gold, June-Anne; Kimonis, Virginia; Bacino, Carlos A; Tan, Wen-Hann; Kothare, Sanjeev V; Peters, Sarika U; Percy, Alan K; Glaze, Daniel G	October 1, 2021	Not Determined
34028805	Create Study	Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure.	Developmental medicine and child neurology	Olson, Heather E; Costantini, Julia G; Swanson, Lindsay C; Kaufmann, Walter E; Benke, Timothy A; Fulton, Anne B; Hansen, Ronald; Poduri, Annapurna; Heidary, Gena	November 1, 2021	Not Determined
33517526	Create Study	Developmental Skills of Individuals with Angelman Syndrome Assessed Using the Bayley-III.	Journal of autism and developmental disorders	Sadhwani, Anjali; Wheeler, Anne; Gwaltney, Angela; Peters, Sarika U; Barbieri-Welge, Rene L; Horowitz, Lucia T; Noll, Lisa M; Hundley, Rachel J; Bird, Lynne M; Tan, Wen-Hann	January 30, 2021	Not Determined
33480039	Create Study	Multisite Study of Evoked Potentials in Rett Syndrome.	Annals of neurology	Saby, Joni N; Benke, Timothy A; Peters, Sarika U; Standridge, Shannon M; Matsuzaki, Junko; Cutri-French, Clare; Swanson, Lindsay C; Lieberman, David N; Key, Alexandra P; Percy, Alan K; Neul, Jeffrey L; Nelson, Charles A; Roberts, Timothy P L; Marsh, Eric D	April 1, 2021	Not Determined
33211820	Create Study	A Psychometric Evaluation of the Motor-Behavioral Assessment Scale for Use as an Outcome Measure in Rett Syndrome Clinical Trials.	American journal on intellectual and developmental disabilities	Raspa, Melissa; Bann, Carla M; Gwaltney, Angela; Benke, Timothy A; Fu, Cary; Glaze, Daniel G; Haas, Richard; Heydemann, Peter; Jones, Mary; Kaufmann, Walter E; Lieberman, David; Marsh, Eric; Peters, Sarika; Ryther, Robin; Standridge, Shannon; Skinner, Steven A; Percy, Alan K; Neul, Jeffrey L	November 1, 2020	Not Determined
33170557	Create Study	Phenotypic features in MECP2 duplication syndrome: Effects of age.	American journal of medical genetics. Part A	Peters, Sarika U; Fu, Cary; Marsh, Eric D; Benke, Tim A; Suter, Bernard; Skinner, Steve A; Lieberman, David N; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Glaze, Daniel G; Percy, Alan K; Neul, Jeffrey L	February 1, 2021	Not Determined
33024833	Create Study	Multisystem comorbidities in classic Rett syndrome: a scoping review.	BMJ paediatrics open	Fu, Cary; Armstrong, Dallas; Marsh, Eric; Lieberman, David; Motil, Kathleen; Witt, Rochelle; Standridge, Shannon; Lane, Jane; Dinkel, Tristen; Jones, Mary; Hale, Katie; Suter, Bernhard; Glaze, Daniel; Neul, Jeffrey; Percy, Alan; Benke, Timothy	January 1, 2020	Not Determined
32984552	Create Study	Consensus guidelines on managing Rett syndrome across the lifespan.	BMJ paediatrics open	Fu, Cary; Armstrong, Dallas; Marsh, Eric; Lieberman, David; Motil, Kathleen; Witt, Rochelle; Standridge, Shannon; Nues, Paige; Lane, Jane; Dinkel, Tristen; Coenraads, Monica; von Hehn, Jana; Jones, Mary; Hale, Katie; Suter, Bernhard; Glaze, Daniel; Neul, Jeffrey; Percy, Alan; Benke, Timothy	January 1, 2020	Not Determined
32792659	Create Study	Angelman syndrome genotypes manifest varying degrees of clinical severity and developmental impairment.	Molecular psychiatry	Keute, Marius; Miller, Meghan T; Krishnan, Michelle L; Sadhwani, Anjali; Chamberlain, Stormy; Thibert, Ronald L; Tan, Wen-Hann; Bird, Lynne M; Hipp, Joerg F	July 1, 2021	Not Determined
32698758	Create Study	Cortisol profiles and clinical severity in MECP2 duplication syndrome.	Journal of neurodevelopmental disorders	Peters, Sarika U; Fu, Cary; Neul, Jeffrey L; Granger, Douglas A	July 2020	Not Determined
32669918	Create Study	MeCP2 in the regulation of neural activity: Rett syndrome pathophysiological perspectives.	Degenerative neurological and neuromuscular disease	Cuddapah, Vishnu Anand; Sinifunanya, Elvee Nwaobi; Percy, Alan K; Olsen, Michelle Lynne	January 1, 2015	Not Determined
32551137	Create Study	High-voltage, diffuse delta rhythms coincide with wakeful consciousness and complexity in Angelman syndrome.	Neuroscience of consciousness	Frohlich, Joel; Bird, Lynne M; Dell'Italia, John; Johnson, Micah A; Hipp, Joerg F; Monti, Martin M	January 2020	Not Determined
32524756	Create Study	Differentiating molecular etiologies of Angelman syndrome through facial phenotyping using deep learning.	American journal of medical genetics. Part A	Gomez, Diego A; Bird, Lynne M; Fleischer, Nicole; Abdul-Rahman, Omar A	September 1, 2020	Not Determined
32472944	Create Study	Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study.	Annals of neurology	Cutri-French, Clare; Armstrong, Dallas; Saby, Joni; Gorman, Casey; Lane, Jane; Fu, Cary; Peters, Sarika U; Percy, Alan; Neul, Jeffrey L; Marsh, Eric D	August 2020	Not Determined
32203572	Create Study	Proof-of-concept for a gene replacement approach to CDKL5 deficiency disorder.	Brain : a journal of neurology	Benke, Tim A; Kind, Peter C	March 1, 2020	Not Determined
32161522	Create Study	Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings.	Frontiers in integrative neuroscience	Neul, Jeffrey L; Skinner, Steven A; Annese, Fran; Lane, Jane; Heydemann, Peter; Jones, Mary; Kaufmann, Walter E; Glaze, Daniel G; Percy, Alan K	January 1, 2020	Not Determined
31854050	Create Study	Neurodevelopmental profile of siblings with Angelman syndrome due to pathogenic UBE3A variants.	Journal of intellectual disability research : JIDR	Sadhwani, A; Willen, J M; Miller, H; Barbieri-Welge, R; Horowitz, L T; Noll, L M; Peters, S; Hundley, R; Bird, L M; Tan, W H	March 1, 2020	Not Determined
31684986	Create Study	An observational study of pediatric healthcare burden in Angelman syndrome: results from a real-world study.	Orphanet journal of rare diseases	Khan N, Cabo R, Tan WH, Tayag R, Bird LM	November 2019	Not Determined
31313283	Create Study	CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development.	Epilepsia	Demarest, Scott T; Olson, Heather E; Moss, Angela; Pestana-Knight, Elia; Zhang, Xiaoming; Parikh, Sumit; Swanson, Lindsay C; Riley, Katherine D; Bazin, Grace A; Angione, Katie; Niestroj, Lisa-Marie; Lal, Dennis; Juarez-Colunga, Elizabeth; Benke, Tim A	August 2019	Not Determined
31147226	Create Study	Severity Assessment in CDKL5 Deficiency Disorder.	Pediatric neurology	Demarest, Scott; Pestana-Knight, Elia M; Olson, Heather E; Downs, Jenny; Marsh, Eric D; Kaufmann, Walter E; Partridge, Carol-Anne; Leonard, Helen; Gwadry-Sridhar, Femida; Frame, Katheryn Elibri; Cross, J Helen; Chin, Richard F M; Parikh, Sumit; Panzer, Axel; Weisenberg, Judith; Utley, Karen; Jaksha, Amanda; Amin, Sam; Khwaja, Omar; Devinsky, Orrin; Neul, Jeffery L; Percy, Alan K; Benke, Tim A	August 2019	Not Determined
31090212	Create Study	Healthcare burden among individuals with Angelman syndrome: Findings from the Angelman Syndrome Natural History Study.	Molecular genetics & genomic medicine	Khan, Nasreen; Cabo, Raquel; Tan, Wen-Hann; Tayag, Regina; Bird, Lynne M	July 2019	Not Determined
31053667	Create Study	Hand stereotypies: Lessons from the Rett Syndrome Natural History Study.	Neurology	Stallworth, Jennifer L; Dy, Marisela E; Buchanan, Caroline B; Chen, Chin-Fu; Scott, Alexandra E; Glaze, Daniel G; Lane, Jane B; Lieberman, David N; Oberman, Lindsay M; Skinner, Steven A; Tierney, Aubin E; Cutter, Gary R; Percy, Alan K; Neul, Jeffrey L; Kaufmann, Walter E	May 28, 2019	Not Determined
30942555	Create Study	Maladaptive behaviors in individuals with Angelman syndrome.	American journal of medical genetics. Part A	Sadhwani, Anjali; Willen, Jennifer M; LaVallee, Nicole; Stepanians, Miganush; Miller, Hillary; Peters, Sarika U; Barbieri-Welge, Rene L; Horowitz, Lucia T; Noll, Lisa M; Hundley, Rachel J; Bird, Lynne M; Tan, Wen-Hann	June 2019	Not Determined
30928302	Create Study	Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review.	Pediatric neurology	Olson, Heather E; Demarest, Scott T; Pestana-Knight, Elia M; Swanson, Lindsay C; Iqbal, Sumaiya; Lal, Dennis; Leonard, Helen; Cross, J Helen; Devinsky, Orrin; Benke, Tim A	August 2019	Not Determined
30826071	Create Study	Electrophysiological Phenotype in Angelman Syndrome Differs Between Genotypes.	Biological psychiatry	Frohlich J, Miller MT, Bird LM, Garces P, Purtell H, Hoener MC, Philpot BD, Sidorov MS, Tan WH, Hernandez MC, Rotenberg A, Jeste SS, Krishnan M, Khwaja O, Hipp JF	May 2019	Not Determined
30788845	Create Study	Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome.	Clinical genetics	Peters SU, Fu C, Suter B, Marsh E, Benke TA, Skinner SA, Lieberman DN, Standridge S, Jones M, Beisang A, Feyma T, Heydeman P, Ryther R, Kaufmann WE, Glaze DG, Neul JL, Percy AK	May 2019	Not Determined
30664568	Create Study	Biliary Tract Disease in Girls and Young Women With Rett Syndrome.	Journal of pediatric gastroenterology and nutrition	Motil, Kathleen J; Lane, Jane B; Barrish, Judy O; Annese, Fran; Geerts, Suzanne; McNair, Lauren; Skinner, Steven A; Neul, Jeffrey L; Glaze, Daniel G; Percy, Alan K	June 2019	Not Determined
30649225	Create Study	Towards a better diagnosis and treatment of Rett syndrome: a model synaptic disorder.	Brain : a journal of neurology	Banerjee A, Miller MT, Li K, Sur M, Kaufmann WE	February 2019	Not Determined
30556641	Create Study	Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomes.	American journal of medical genetics. Part A	Mahmoud, Ranim; Singh, Preeti; Weiss, Lan; Lakatos, Anita; Oakes, Melanie; Hossain, Waheeda; Butler, Merlin G; Kimonis, Virginia	January 2019	Not Determined
30536762	Create Study	The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Neul, Jeffrey L; Benke, Timothy A; Marsh, Eric D; Skinner, Steven A; Merritt, Jonathan; Lieberman, David N; Standridge, Shannon; Feyma, Timothy; Heydemann, Peter; Peters, Sarika; Ryther, Robin; Jones, Mary; Suter, Bernhard; Kaufmann, Walter E; Glaze, Daniel G; Percy, Alan K	January 2019	Not Determined
30217666	Create Study	Behavioral profiles in Rett syndrome: Data from the natural history study.	Brain & development	Buchanan CB, Stallworth JL, Scott AE, Glaze DG, Lane JB, Skinner SA, Tierney AE, Percy AK, Neul JL, Kaufmann WE	February 2019	Not Determined
29737008	Create Study	Two Angelman families with unusually advanced neurodevelopment carry a start codon variant in the most highly expressed UBE3A isoform.	American journal of medical genetics. Part A	Sadhwani, Anjali; Sanjana, Neville E; Willen, Jennifer M; Calculator, Stephen N; Black, Emily D; Bean, Lora J H; Li, Hong; Tan, Wen-Hann	July 2018	Not Determined
29730598	Create Study	Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.	Journal of medical genetics	Butler MG, Hartin SN, Hossain WA, Manzardo AM, Kimonis V, Dykens E, Gold JA, Kim SJ, Weisensel N, Tamura R, Miller JL, Driscoll DJ	March 2019	Not Determined
29681103	Create Study	Comparison of perinatal factors in deletion versus uniparental disomy in Prader-Willi syndrome.	American journal of medical genetics. Part A	Gold, June-Anne; Mahmoud, Ranim; Cassidy, Suzanne B; Kimonis, Virginia	May 2018	Not Determined
29657083	Create Study	The course of awake breathing disturbances across the lifespan in Rett syndrome.	Brain & development	Tarquinio DC, Hou W, Neul JL, Berkmen GK, Drummond J, Aronoff E, Harris J, Lane JB, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Percy AK	April 2018	Not Determined
29264392	Create Study	CDKL5 variants: Improving our understanding of a rare neurologic disorder.	Neurology. Genetics	Hector, Ralph D; Kalscheuer, Vera M; Hennig, Friederike; Leonard, Helen; Downs, Jenny; Clarke, Angus; Benke, Tim A; Armstrong, Judith; Pineda, Mercedes; Bailey, Mark E S; Cobb, Stuart R	December 1, 2017	Not Determined
28944563	Create Study	A randomized controlled trial of levodopa in patients with Angelman syndrome.	American journal of medical genetics. Part A	Tan, Wen-Hann; Bird, Lynne M; Sadhwani, Anjali; Barbieri-Welge, Rene L; Skinner, Steven A; Horowitz, Lucia T; Bacino, Carlos A; Noll, Lisa M; Fu, Cary; Hundley, Rachel J; Wink, Logan K; Erickson, Craig A; Barnes, Gregory N; Slavotinek, Anne; Jeremy, Rita; Rotenberg, Alexander; Kothare, Sanjeev V; Olson, Heather E; Poduri, Annapurna; Nespeca, Mark P; Chu, Hillary C; Willen, Jennifer M; Haas, Kevin F; Weeber, Edwin J; Rufo, Paul A	May 2018	Not Determined
28838622	Create Study	Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective.	Pediatric neurology	Dy ME, Waugh JL, Sharma N, O'Leary H, Kapur K, D'Gama AM, Sahin M, Urion DK, Kaufmann WE	October 2017	Relevant
28347601	Create Study	Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.	Pediatric neurology	Killian, John T; Lane, Jane B; Lee, Hye-Seung; Skinner, Steve A; Kaufmann, Walter E; Glaze, Daniel G; Neul, Jeffrey L; Percy, Alan K	May 2017	Not Relevant
28163986	Create Study	Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.	Expert opinion on orphan drugs	Kaufmann, Walter E; Stallworth, Jennifer L; Everman, David B; Skinner, Steven A	October 2016	Not Determined
28132121	Create Study	Assessment of Caregiver Inventory for Rett Syndrome.	Journal of autism and developmental disorders	Lane JB, Salter AR, Jones NE, Cutter G, Horrigan J, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK	January 2017	Relevant
28007990	Create Study	Longitudinal course of epilepsy in Rett syndrome and related disorders.	Brain : a journal of neurology	Tarquinio DC, Hou W, Berg A, Kaufmann WE, Lane JB, Skinner SA, Motil KJ, Neul JL, Percy AK, Glaze DG	February 2017	Relevant
27929079	Create Study	From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.	Scientific reports	Sheikh TI, Ausió J, Faghfoury H, Silver J, Lane JB, Eubanks JH, Macleod P, Percy AK, Vincent JB	December 2016	Not Determined
27828991	Create Study	Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome.	PloS one	Ward CS, Huang TW, Herrera JA, Samaco RC, Pitcher MR, Herron A, Skinner SA, Kaufmann WE, Glaze DG, Percy AK, Neul JL	January 2016	Not Relevant
27815692	Create Study	Neurogenetics in Child Neurology: Redefining a Discipline in the Twenty-first Century.	Current neurology and neuroscience reports	Kaufmann WE	December 2016	Not Determined
27570781	Create Study	EVALUATION OF PLASMA SUBSTANCE P AND BETA-ENDORPHIN LEVELS IN CHILDREN WITH PRADER-WILLI SYNDROME.	The Journal of rare disorders	Butler, M G; Nelson, T A; Driscoll, D J; Manzardo, A M	September 2015	Not Relevant
27491553	Create Study	Progress in Rett Syndrome: from discovery to clinical trials.	Wiener medizinische Wochenschrift (1946)	Percy AK	September 2016	Not Relevant
27194034	Create Study	The partnership of patient advocacy groups and clinical investigators in the rare diseases clinical research network.	Orphanet journal of rare diseases	Merkel PA, Manion M, Gopal-Srivastava R, Groft S, Jinnah HA, Robertson D, Krischer JP,	May 2016	Not Relevant
27171548	Create Study	Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.	Genetics in medicine : official journal of the American College of Medical Genetics	Sajan, Samin A; Jhangiani, Shalini N; Muzny, Donna M; Gibbs, Richard A; Lupski, James R; Glaze, Daniel G; Kaufmann, Walter E; Skinner, Steven A; Annese, Fran; Friez, Michael J; Lane, Jane; Percy, Alan K; Neul, Jeffrey L	January 1, 2017	Not Relevant
26995066	Create Study	Caretaker Quality of Life in Rett Syndrome: Disorder Features and Psychological Predictors.	Pediatric neurology	Killian JT, Lane JB, Lee HS, Pelham JH, Skinner SA, Kaufmann WE, Glaze DG, Neul JL, Percy AK	May 2016	Relevant
26883647	Create Study	Life Satisfaction Among Mothers of Individuals with Prader-Willi Syndrome.	Journal of autism and developmental disorders	Shivers CM, Leonczyk CL, Dykens EM	June 2016	Not Determined
26615966	Create Study	Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblings.	American journal of medical genetics. Part A	Johnson, Lisa; Manzardo, Ann M; Miller, Jennifer L; Driscoll, Daniel J; Butler, Merlin G	March 2016	Not Determined
26332183	Create Study	Visual evoked potentials detect cortical processing deficits in Rett syndrome.	Annals of neurology	Leblanc JJ, Degregorio G, Centofante E, Vogel-Farley VK, Barnes K, Kaufmann WE, Fagiolini M, Nelson CA	November 2015	Relevant
26278631	Create Study	The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.	Pediatric neurology	Tarquinio DC, Hou W, Neul JL, Kaufmann WE, Glaze DG, Motil KJ, Skinner SA, Lee HS, Percy AK	November 2015	Relevant
26076992	Create Study	Therapeutic Advances in Autism and Other Neurodevelopmental Disorders.	Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics	Neul, Jeffrey L; Sahin, Mustafa	July 2015	Not Relevant
25914188	Create Study	Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.	American journal of medical genetics. Part A	Olson, Heather E; Tambunan, Dimira; LaCoursiere, Christopher; Goldenberg, Marti; Pinsky, Rebecca; Martin, Emilie; Ho, Eugenia; Khwaja, Omar; Kaufmann, Walter E; Poduri, Annapurna	September 2015	Not Relevant
25895911	Create Study	Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale.	Journal of child neurology	Neul JL, Glaze DG, Percy AK, Feyma T, Beisang A, Dinh T, Suter B, Anagnostou E, Snape M, Horrigan J, Jones NE	November 2015	Relevant
25861995	Create Study	Rett Syndrome: Reaching for Clinical Trials.	Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics	Pozzo-Miller, Lucas; Pati, Sandipan; Percy, Alan K	July 2015	Not Relevant
25801175	Create Study	Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis.	Pediatric neurology	Tarquinio DC, Hou W, Neul JL, Lane JB, Barnes KV, O'Leary HM, Bruck NM, Kaufmann WE, Motil KJ, Glaze DG, Skinner SA, Annese F, Baggett L, Barrish JO, Geerts SP, Percy AK	June 2015	Relevant
25713300	Create Study	Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.	Disease models & mechanisms	Herrera JA, Ward CS, Pitcher MR, Percy AK, Skinner S, Kaufmann WE, Glaze DG, Wehrens XH, Neul JL	April 2015	Not Relevant
25705109	Create Study	Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes.	Advances in genomics and genetics	Butler, Merlin G; Wang, Kun; Marshall, Jan D; Naggert, Jürgen K; Rethmeyer, Jasmine A; Gunewardena, Sumedha S; Manzardo, Ann M	2015	Not Relevant
25355237	Create Study	Hyperghrelinemia in Prader-Willi syndrome begins in early infancy long before the onset of hyperphagia.	American journal of medical genetics. Part A	Kweh, Frederick A; Miller, Jennifer L; Sulsona, Carlos R; Wasserfall, Clive; Atkinson, Mark; Shuster, Jonathan J; Goldstone, Anthony P; Driscoll, Daniel J	January 2015	Relevant
25283752	Create Study	Pubertal development in Rett syndrome deviates from typical females.	Pediatric neurology	Killian JT, Lane JB, Cutter GR, Skinner SA, Kaufmann WE, Tarquinio DC, Glaze DG, Motil KJ, Neul JL, Percy AK	December 2014	Relevant
25083850	Create Study	Localization of sleep spindles, k-complexes, and vertex waves with subdural electrodes in children.	Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society	Pinto AL, Fernández IS, Peters JM, Manganaro S, Singer JM, Vendrame M, Prabhu SP, Loddenkemper T, Kothare SV	August 2014	Relevant
25071871	Create Study	Developmental delay in Rett syndrome: data from the natural history study.	Journal of neurodevelopmental disorders	Neul JL, Lane JB, Lee HS, Geerts S, Barrish JO, Annese F, Baggett LM, Barnes K, Skinner SA, Motil KJ, Glaze DG, Kaufmann WE, Percy AK	2014	Relevant
24776956	Create Study	Induced gamma oscillations differentiate familiar and novel voices in children with MECP2 duplication and Rett syndromes.	Journal of child neurology	Peters SU, Gordon RL, Key AP	February 2015	Relevant
24515997	Create Study	Effect of genetic subtypes and growth hormone treatment on bone mineral density in Prader-Willi syndrome.	Journal of pediatric endocrinology & metabolism : JPEM	Khare M, Gold JA, Wencel M, Billimek J, Surampalli A, Duarte B, Pontello A, Galassetti P, Cassidy S, Kimonis VE	May 2014	Relevant
23953953	Create Study	Long-term response to high-dose diazepam treatment in continuous spikes and waves during sleep.	Pediatric neurology	Sánchez Fernández I, Peters JM, An S, Bergin AM, Takeoka M, Rotenberg A, Kothare SV, Riviello JJ, Loddenkemper T	September 2013	Relevant
23928912	Create Study	Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.	Genetics in medicine : official journal of the American College of Medical Genetics	Gold JA, Ruth C, Osann K, Flodman P, Mcmanus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE	February 2014	Relevant
23433655	Create Study	Effects of growth hormone treatment in adults with Prader-Willi syndrome.	Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society	Butler, M G; Smith, B K; Lee, J; Gibson, C; Schmoll, C; Moore, W V; Donnelly, J E	June 2013	Relevant
22484792	Create Study	Leisure activities in Prader-Wili syndrome: implications for health, cognition and adaptive functioning.	Journal of autism and developmental disorders	Dykens EM	February 2014	Relevant
22341959	Create Study	Analysis of EEG patterns and genotypes in patients with Angelman syndrome.	Epilepsy & behavior : E&B	Vendrame M, Loddenkemper T, Zarowski M, Gregas M, Shuhaiber H, Sarco DP, Morales A, Nespeca M, Sharpe C, Haas K, Barnes G, Glaze D, Kothare SV	March 2012	Relevant
22331013	Create Study	Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome.	Journal of pediatric gastroenterology and nutrition	Motil KJ, Caeg E, Barrish JO, Geerts S, Lane JB, Percy AK, Annese F, Mcnair L, Skinner SA, Lee HS, Neul JL, Glaze DG	September 2012	Relevant
22013176	Create Study	Clinical severity and quality of life in children and adolescents with Rett syndrome.	Neurology	Lane JB, Lee HS, Smith LW, Cheng P, Percy AK, Glaze DG, Neul JL, Motil KJ, Barrish JO, Skinner SA, Annese F, Mcnair L, Graham J, Khwaja O, Barnes K, Krischer JP	November 15, 2011	Relevant
22002941	Create Study	A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome.	American journal of medical genetics. Part A	Bird, Lynne M; Tan, Wen-Hann; Bacino, Carlos A; Peters, Sarika U; Skinner, Steven A; Anselm, Irina; Barbieri-Welge, Rene; Bauer-Carlin, Astrid; Gentile, Jennifer K; Glaze, Daniel G; Horowitz, Lucia T; Mohan, K Naga; Nespeca, Mark P; Sahoo, Trilochan; Sarco, Dean; Waisbren, Susan E; Beaudet, Arthur L	December 2011	Relevant
21977908	Create Study	Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.	Genetic testing and molecular biomarkers	Henkhaus RS, Kim SJ, Kimonis VE, Gold JA, Dykens EM, Driscoll DJ, Butler MG	March 2012	Relevant
21831244	Create Study	Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.	Journal of child psychology and psychiatry, and allied disciplines	Peters SU, Horowitz L, Barbieri-Welge R, Taylor JL, Hundley RJ	February 2012	Relevant
21637127	Create Study	Vitamin D deficiency is prevalent in girls and women with Rett syndrome.	Journal of pediatric gastroenterology and nutrition	Motil KJ, Barrish JO, Lane J, Geerts SP, Annese F, Mcnair L, Percy AK, Skinner SA, Neul JL, Glaze DG	November 2011	Relevant
21465655	Create Study	Nutritional phases in Prader-Willi syndrome.	American journal of medical genetics. Part A	Miller, Jennifer L; Lynn, Christy H; Driscoll, Danielle C; Goldstone, Anthony P; Gold, June-Anne; Kimonis, Virginia; Dykens, Elisabeth; Butler, Merlin G; Shuster, Jonathan J; Driscoll, Daniel J	May 2011	Relevant
21418060	Create Study	TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome.	Journal of child psychology and psychiatry, and allied disciplines	Dykens EM, Roof E, Bittel D, Butler MG	May 2011	Relevant
21402637	Create Study	Growth standards of infants with Prader-Willi syndrome.	Pediatrics	Butler MG, Sturich J, Lee J, Myers SE, Whitman BY, Gold JA, Kimonis V, Scheimann A, Terrazas N, Driscoll DJ	April 2011	Relevant
21121904	Create Study	Alterations in white matter pathways in Angelman syndrome.	Developmental medicine and child neurology	Peters SU, Kaufmann WE, Bacino CA, Anderson AW, Adapa P, Chu Z, Yallampalli R, Traipe E, Hunter JV, Wilde EA	April 2011	Relevant
20729760	Create Study	A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlations.	Journal of developmental and behavioral pediatrics : JDBP	Gentile JK, Tan WH, Horowitz LT, Bacino CA, Skinner SA, Barbieri-Welge R, Bauer-Carlin A, Beaudet AL, Bichell TJ, Lee HS, Sahoo T, Waisbren SE, Bird LM, Peters SU	September 2010	Relevant
20032810	Create Study	Profiling scoliosis in Rett syndrome.	Pediatric research	Percy AK, Lee HS, Neul JL, Lane JB, Skinner SA, Geerts SP, Annese F, Graham J, Mcnair L, Motil KJ, Barrish JO, Glaze DG	April 2010	Relevant
19772971	Create Study	Longevity in Rett syndrome: analysis of the North American Database.	The Journal of pediatrics	Kirby RS, Lane JB, Childers J, Skinner SA, Annese F, Barrish JO, Glaze DG, Macleod P, Percy AK	January 2010	Relevant
19225139	Create Study	A study of the treatment of Rett syndrome with folate and betaine.	Journal of child neurology	Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO	May 2009	Relevant

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	1,200	07/15/2016	0	11/15/2016	0	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	1,200	07/15/2016	958	11/15/2016	958	Approved
Demographics	1,200	07/15/2016	0	07/15/2020	0	Approved
SF36 Health QoL	1,200	07/15/2016	847	07/15/2016	847	Approved
Physical Exam	1,200	07/15/2016	955	07/15/2020	955	Approved
Clinical Global Impression of Severity	1,200	07/15/2016	0	07/15/2020	0	Approved
Physical Symptom Checklist	1,200	07/15/2016	0	07/15/2020	0	Approved
Neurological Exam	1,200	07/15/2016	0	07/15/2020	0	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	AbstractFilter by Abstract	Collection/Study SubjectsFilter by Collection/Study Subjects	Data UsageFilter by Data Usage	StateFilter by State
No records found.

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.

Contact NDA Help Desk

Edit

Choose File:	Select File
File Type:
Description:

Exemption Type*
From Date*
To Date*
Reason*	Characters Remaining:

Disclaimer

Filter Cart

Frequently Asked Questions

Glossary