NIMH Data Archive - Data

Genomics

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Phenotype¹

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¹ Numbers reported are subjects by age

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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

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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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Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study #2092

General
Experiments (1)
Shared Data
Publications (126)
Data Expected (1)
Associated Studies (1)

Collection Title	Collection Investigators	Collection Description
Collection Title:	Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study
Collection Investigators:	Joseph D. Buxbaum, Trent Gaugler, Lambertus Klei, Stephan J. Sanders, Corneliu A. Bodea, Arthur P. Goldberg, Ann B. Lee, Yudi Pawitan, Stephan Ripke, Sven Sandin, Pamela Sklar, Oscar Svantesson, Abraham Reichenberg, Christina M. Hultman, Bernie Devlin, Kathryn Roeder
Collection Description:	Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study
Data Repository:	NIMH Data Archive
Permission Group:
Collection Creation Date:	06/29/2014
Collection Phase:	Funding Completed
Collection Sub-Phase:	Close Out
Blinded Clinical Trial:	No
Total Funded Amount:	$1,489,716.00
Subjects Shared:	636

{"values":[["SNP and CNV: microarray",636]]}

{"values":[]}

{"values":[["Not Defined",636]]}

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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
R01MH057881-01	GENETIC ASSOCIATION IN SCHIZOPHRENIA AND OTHER DISORDERS	07/01/1998	06/30/2008	Not Reported	Not Reported	UNIVERSITY OF PITTSBURGH AT PITTSBURGH	$1,489,716.00

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.

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ID	Name	Created Date	Status	Type
161	PAGES study of autism heritability	07/31/2014	Approved	Omics

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
Genomics Sample	Genomics	636
Genomics Subject	Genomics	548

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.

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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
38699304	Create Study	Contribution of autosomal rare and de novo variants to sex differences in autism.	medRxiv : the preprint server for health sciences	Koko, Mahmoud; Kyle Satterstrom, F; Autism Sequencing Consortium; APEX consortium; Warrier, Varun; Martin, Hilary	April 16, 2024	Not Determined
38402414	Create Study	Evaluating and improving health equity and fairness of polygenic scores.	HGG advances	Zhang, Tianyu; Zhou, Geyu; Klei, Lambertus; Liu, Peng; Chouldechova, Alexandra; Zhao, Hongyu; Roeder, Kathryn; G'Sell, Max; Devlin, Bernie	April 11, 2024	Not Determined
35982160	Create Study	Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.	Nature genetics	Fu, Jack M; Satterstrom, F Kyle; Peng, Minshi; Brand, Harrison; Collins, Ryan L; Dong, Shan; Wamsley, Brie; Klei, Lambertus; Wang, Lily; Hao, Stephanie P; Stevens, Christine R; Cusick, Caroline; Babadi, Mehrtash; Banks, Eric; Collins, Brett; Dodge, Sheila; Gabriel, Stacey B; Gauthier, Laura; Lee, Samuel K; Liang, Lindsay; Ljungdahl, Alicia; Mahjani, Behrang; Sloofman, Laura; Smirnov, Andrey N; Barbosa, Mafalda; Betancur, Catalina; Brusco, Alfredo; Chung, Brian H Y; Cook, Edwin H; Cuccaro, Michael L; Domenici, Enrico; Ferrero, Giovanni Battista; Gargus, J Jay; Herman, Gail E; Hertz-Picciotto, Irva; Maciel, Patricia; Manoach, Dara S; Passos-Bueno, Maria Rita; Persico, Antonio M; Renieri, Alessandra; Sutcliffe, James S; Tassone, Flora; Trabetti, Elisabetta; Campos, Gabriele; Cardaropoli, Simona; Carli, Diana; Chan, Marcus C Y; Fallerini, Chiara; Giorgio, Elisa; Girardi, Ana Cristina; Hansen-Kiss, Emily; Lee, So Lun; Lintas, Carla; Ludena, Yunin; Nguyen, Rachel; Pavinato, Lisa; Pericak-Vance, Margaret; Pessah, Isaac N; Schmidt, Rebecca J; Smith, Moyra; Costa, Claudia I S; Trajkova, Slavica; Wang, Jaqueline Y T; Yu, Mullin H C; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler, David J; De Rubeis, Silvia; Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J; Talkowski, Michael E	September 1, 2022	Not Determined
35438146	Create Study	Robust and accurate estimation of cellular fraction from tissue omics data via ensemble deconvolution.	Bioinformatics (Oxford, England)	Cai, Manqi; Yue, Molin; Chen, Tianmeng; Liu, Jinling; Forno, Erick; Lu, Xinghua; Billiar, Timothy; Celedón, Juan; McKennan, Chris; Chen, Wei; Wang, Jiebiao	May 26, 2022	Not Determined
34112972	Create Study	Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.	Molecular psychiatry	DeMichele-Sweet, Mary Ann A; Klei, Lambertus; Creese, Byron; Harwood, Janet C; Weamer, Elise A; McClain, Lora; Sims, Rebecca; Hernandez, Isabel; Moreno-Grau, Sonia; Tárraga, Lluís; Boada, Mercè; Alarcón-Martín, Emilio; Valero, Sergi; NIA-LOAD Family Based Study Consortium, Alzheimer’s Disease Genetics Consortium (ADGC); Liu, Yushi; Hooli, Basavaraj; Aarsland, Dag; Selbaek, Geir; Bergh, Sverre; Rongve, Arvid; Saltvedt, Ingvild; Skjellegrind, Håvard K; Engdahl, Bo; Stordal, Eystein; Andreassen, Ole A; Djurovic, Srdjan; Athanasiu, Lavinia; Seripa, Davide; Borroni, Barbara; Albani, Diego; Forloni, Gianluigi; Mecocci, Patrizia; Serretti, Alessandro; De Ronchi, Diana; Politis, Antonis; Williams, Julie; Mayeux, Richard; Foroud, Tatiana; Ruiz, Agustin; Ballard, Clive; Holmans, Peter; Lopez, Oscar L; Kamboh, M Ilyas; Devlin, Bernie; Sweet, Robert A	October 1, 2021	Not Determined
32268104	Create Study	Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.	Cell reports	Werling, Donna M; Pochareddy, Sirisha; Choi, Jinmyung; An, Joon-Yong; Sheppard, Brooke; Peng, Minshi; Li, Zhen; Dastmalchi, Claudia; Santpere, Gabriel; Sousa, André M M; Tebbenkamp, Andrew T N; Kaur, Navjot; Gulden, Forrest O; Breen, Michael S; Liang, Lindsay; Gilson, Michael C; Zhao, Xuefang; Dong, Shan; Klei, Lambertus; Cicek, A Ercument; Buxbaum, Joseph D; Adle-Biassette, Homa; Thomas, Jean-Leon; Aldinger, Kimberly A; O'Day, Diana R; Glass, Ian A; Zaitlen, Noah A; Talkowski, Michael E; Roeder, Kathryn; State, Matthew W; Devlin, Bernie; Sanders, Stephan J; Sestan, Nenad	April 2020	Not Determined
31981491	Create Study	Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.	Cell	Satterstrom, F Kyle; Kosmicki, Jack A; Wang, Jiebiao; Breen, Michael S; De Rubeis, Silvia; An, Joon-Yong; Peng, Minshi; Collins, Ryan; Grove, Jakob; Klei, Lambertus; Stevens, Christine; Reichert, Jennifer; Mulhern, Maureen S; Artomov, Mykyta; Gerges, Sherif; Sheppard, Brooke; Xu, Xinyi; Bhaduri, Aparna; Norman, Utku; Brand, Harrison; Schwartz, Grace; Nguyen, Rachel; Guerrero, Elizabeth E; Dias, Caroline; Autism Sequencing Consortium; iPSYCH-Broad Consortium; Betancur, Catalina; Cook, Edwin H; Gallagher, Louise; Gill, Michael; Sutcliffe, James S; Thurm, Audrey; Zwick, Michael E; Børglum, Anders D; State, Matthew W; Cicek, A Ercument; Talkowski, Michael E; Cutler, David J; Devlin, Bernie; Sanders, Stephan J; Roeder, Kathryn; Daly, Mark J; Buxbaum, Joseph D	February 2020	Not Determined
31551426	Create Study	CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder.	Scientific data	Hoffman, Gabriel E; Bendl, Jaroslav; Voloudakis, Georgios; Montgomery, Kelsey S; Sloofman, Laura; Wang, Ying-Chih; Shah, Hardik R; Hauberg, Mads E; Johnson, Jessica S; Girdhar, Kiran; Song, Lingyun; Fullard, John F; Kramer, Robin; Hahn, Chang-Gyu; Gur, Raquel; Marenco, Stefano; Lipska, Barbara K; Lewis, David A; Haroutunian, Vahram; Hemby, Scott; Sullivan, Patrick; Akbarian, Schahram; Chess, Andrew; Buxbaum, Joseph D; Crawford, Greg E; Domenici, Enrico; Devlin, Bernie; Sieberts, Solveig K; Peters, Mette A; Roussos, Panos	September 2019	Not Determined
31455887	Create Study	Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia.	Nature neuroscience	Breen, Michael S; Dobbyn, Amanda; Li, Qin; Roussos, Panos; Hoffman, Gabriel E; Stahl, Eli; Chess, Andrew; Sklar, Pamela; Li, Jin Billy; Devlin, Bernie; Buxbaum, Joseph D; CommonMind Consortium	September 2019	Not Determined
31424081	Create Study	Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth.	Schizophrenia bulletin	Jalbrzikowski, Maria; Liu, Fuchen; Foran, William; Roeder, Kathryn; Devlin, Bernie; Luna, Beatriz	February 2020	Not Determined
31400192	Create Study	Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression.	Bioinformatics (Oxford, England)	Wang, Jiebiao; Devlin, Bernie; Roeder, Kathryn	February 2020	Not Determined
30911161	Create Study	Gene expression imputation across multiple brain regions provides insights into schizophrenia risk.	Nature genetics	Huckins, Laura M; Dobbyn, Amanda; Ruderfer, Douglas M; Hoffman, Gabriel; Wang, Weiqing; Pardiñas, Antonio F; Rajagopal, Veera M; Als, Thomas D; T Nguyen, Hoang; Girdhar, Kiran; Boocock, James; Roussos, Panos; Fromer, Menachem; Kramer, Robin; Domenici, Enrico; Gamazon, Eric R; Purcell, Shaun; CommonMind Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium; iPSYCH-GEMS Schizophrenia Working Group; Demontis, Ditte; Børglum, Anders D; Walters, James T R; O'Donovan, Michael C; Sullivan, Patrick; Owen, Michael J; Devlin, Bernie; Sieberts, Solveig K; Cox, Nancy J; Im, Hae Kyung; Sklar, Pamela; Stahl, Eli A	April 2019	Not Determined
29112194	Create Study	Genome-wide association study identifies a novel locus for cannabis dependence.	Molecular psychiatry	Agrawal, A; Chou, Y-L; Carey, C E; Baranger, D A A; Zhang, B; Sherva, R; Wetherill, L; Kapoor, M; Wang, J-C; Bertelsen, S; Anokhin, A P; Hesselbrock, V; Kramer, J; Lynskey, M T; Meyers, J L; Nurnberger, J I; Rice, J P; Tischfield, J; Bierut, L J; Degenhardt, L; Farrer, L A; Gelernter, J; Hariri, A R; Heath, A C; Kranzler, H R; Madden, P A F; Martin, N G; Montgomery, G W; Porjesz, B; Wang, T; Whitfield, J B; Edenberg, H J; Foroud, T; Goate, A M; Bogdan, R; Nelson, E C	May 2018	Not Determined
29100626	Create Study	Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden.	Biological psychiatry	Yip, Benjamin Hon Kei; Bai, Dan; Mahjani, Behrang; Klei, Lambertus; Pawitan, Yudi; Hultman, Christina M; Grice, Dorothy E; Roeder, Kathryn; Buxbaum, Joseph D; Devlin, Bernie; Reichenberg, Abraham; Sandin, Sven	April 2018	Not Determined
28569757	Create Study	Fetal and postnatal metal dysregulation in autism.	Nature communications	Arora, Manish; Reichenberg, Abraham; Willfors, Charlotte; Austin, Christine; Gennings, Chris; Berggren, Steve; Lichtenstein, Paul; Anckarsäter, Henrik; Tammimies, Kristiina; Bölte, Sven	June 2017	Relevant
28461698	Create Study	Genetic risk for schizophrenia and psychosis in Alzheimer disease.	Molecular psychiatry	DeMichele-Sweet, M A A; Weamer, E A; Klei, L; Vrana, D T; Hollingshead, D J; Seltman, H J; Sims, R; Foroud, T; Hernandez, I; Moreno-Grau, S; Tárraga, L; Boada, M; Ruiz, A; Williams, J; Mayeux, R; Lopez, O L; Sibille, E L; Kamboh, M I; Devlin, B; Sweet, R A	April 2018	Not Determined
28191890	Create Study	Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.	Nature genetics	Kosmicki, Jack A; Samocha, Kaitlin E; Howrigan, Daniel P; Sanders, Stephan J; Slowikowski, Kamil; Lek, Monkol; Karczewski, Konrad J; Cutler, David J; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph D; Neale, Benjamin M; MacArthur, Daniel G; Wall, Dennis P; Robinson, Elise B; Daly, Mark J	April 2017	Not Determined
27087321	Create Study	A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.	American journal of human genetics	Bodea, Corneliu A; Neale, Benjamin M; Ripke, Stephan; International IBD Genetics Consortium; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn	May 2016	Not Determined
26834510	Create Study	The huge Package for High-dimensional Undirected Graph Estimation in R.	Journal of machine learning research : JMLR	Zhao, Tuo; Liu, Han; Roeder, Kathryn; Lafferty, John; Wasserman, Larry	April 2012	Not Relevant
26806987	Create Study	Localized Functional Principal Component Analysis.	Journal of the American Statistical Association	Chen, Kehui; Lei, Jing	2015	Not Determined
26402605	Create Study	Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.	Neuron	Sanders, Stephan J; He, Xin; Willsey, A Jeremy; Ercan-Sencicek, A Gulhan; Samocha, Kaitlin E; Cicek, A Ercument; Murtha, Michael T; Bal, Vanessa H; Bishop, Somer L; Dong, Shan; Goldberg, Arthur P; Jinlu, Cai; Keaney 3rd, John F; Klei, Lambertus; Mandell, Jeffrey D; Moreno-De-Luca, Daniel; Poultney, Christopher S; Robinson, Elise B; Smith, Louw; Solli-Nowlan, Tor; Su, Mack Y; Teran, Nicole A; Walker, Michael F; Werling, Donna M; Beaudet, Arthur L; Cantor, Rita M; Fombonne, Eric; Geschwind, Daniel H; Grice, Dorothy E; Lord, Catherine; Lowe, Jennifer K; Mane, Shrikant M; Martin, Donna M; Morrow, Eric M; Talkowski, Michael E; Sutcliffe, James S; Walsh, Christopher A; Yu, Timothy W; Autism Sequencing Consortium; Ledbetter, David H; Martin, Christa Lese; Cook, Edwin H; Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn; State, Matthew W	September 23, 2015	Not Determined
25843333	Create Study	DSM-5 and psychiatric genetics - round hole, meet square peg.	Biological psychiatry	Buxbaum, Joseph D	May 1, 2015	Not Relevant
25382957	Create Study	Positive Semidefinite Rank-based Correlation Matrix Estimation with Application to Semiparametric Graph Estimation.	Journal of computational and graphical statistics : a joint publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America	Zhao, Tuo; Roeder, Kathryn; Liu, Han	October 20, 2014	Not Determined
25363760	Create Study	Synaptic, transcriptional and chromatin genes disrupted in autism.	Nature	De Rubeis, Silvia; He, Xin; Goldberg, Arthur P; Poultney, Christopher S; Samocha, Kaitlin; Cicek, A Erucment; Kou, Yan; Liu, Li; Fromer, Menachem; Walker, Susan; Singh, Tarinder; Klei, Lambertus; Kosmicki, Jack; Shih-Chen, Fu; Aleksic, Branko; Biscaldi, Monica; Bolton, Patrick F; Brownfeld, Jessica M; Cai, Jinlu; Campbell, Nicholas G; Carracedo, Angel; Chahrour, Maria H; Chiocchetti, Andreas G; Coon, Hilary; Crawford, Emily L; Curran, Sarah R; Dawson, Geraldine; Duketis, Eftichia; Fernandez, Bridget A; Gallagher, Louise; Geller, Evan; Guter, Stephen J; Hill, R Sean; Ionita-Laza, Juliana; Jimenz Gonzalez, Patricia; Kilpinen, Helena; Klauck, Sabine M; Kolevzon, Alexander; Lee, Irene; Lei, Irene; Lei, Jing; Lehtimäki, Terho; Lin, Chiao-Feng; Ma'ayan, Avi; Marshall, Christian R; McInnes, Alison L; Neale, Benjamin; Owen, Michael J; Ozaki, Noriio; Parellada, Mara; Parr, Jeremy R; Purcell, Shaun; Puura, Kaija; Rajagopalan, Deepthi; Rehnström, Karola; Reichenberg, Abraham; Sabo, Aniko; Sachse, Michael; Sanders, Stephan J; Schafer, Chad; Schulte-Rüther, Martin; Skuse, David; Stevens, Christine; Szatmari, Peter; Tammimies, Kristiina; Valladares, Otto; Voran, Annette; Li-San, Wang; Weiss, Lauren A; Willsey, A Jeremy; Yu, Timothy W; Yuen, Ryan K C; DDD Study; Homozygosity Mapping Collaborative for Autism; UK10K Consortium; Cook, Edwin H; Freitag, Christine M; Gill, Michael; Hultman, Christina M; Lehner, Thomas; Palotie, Aaarno; Schellenberg, Gerard D; Sklar, Pamela; State, Matthew W; Sutcliffe, James S; Walsh, Christiopher A; Scherer, Stephen W; Zwick, Michael E; Barett, Jeffrey C; Cutler, David J; Roeder, Kathryn; Devlin, Bernie; Daly, Mark J; Buxbaum, Joseph D	November 13, 2014	Not Relevant
25284784	Create Study	De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.	Cell reports	Dong, Shan; Walker, Michael F; Carriero, Nicholas J; DiCola, Michael; Willsey, A Jeremy; Ye, Adam Y; Waqar, Zainulabedin; Gonzalez, Luis E; Overton, John D; Frahm, Stephanie; Keaney 3rd, John F; Teran, Nicole A; Dea, Jeanselle; Mandell, Jeffrey D; Hus Bal, Vanessa; Sullivan, Catherine A; DiLullo, Nicholas M; Khalil, Rehab O; Gockley, Jake; Yuksel, Zafer; Sertel, Sinem M; Ercan-Sencicek, A Gulhan; Gupta, Abha R; Mane, Shrikant M; Sheldon, Michael; Brooks, Andrew I; Roeder, Kathryn; Devlin, Bernie; State, Matthew W; Wei, Liping; Sanders, Stephan J	October 9, 2014	Not Determined
25152607	Create Study	Stability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models.	Advances in neural information processing systems	Liu H, Roeder K, Wasserman L	December 31, 2010	Not Determined
25086666	Create Study	A framework for the interpretation of de novo mutation in human disease.	Nature genetics	Samocha, Kaitlin E; Robinson, Elise B; Sanders, Stephan J; Stevens, Christine; Sabo, Aniko; McGrath, Lauren M; Kosmicki, Jack A; Rehnström, Karola; Mallick, Swapan; Kirby, Andrew; Wall, Dennis P; MacArthur, Daniel G; Gabriel, Stacey B; DePristo, Mark; Purcell, Shaun M; Palotie, Aarno; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Gibbs, Richard A; Schellenberg, Gerard D; Sutcliffe, James S; Devlin, Bernie; Roeder, Kathryn; Neale, Benjamin M; Daly, Mark J	September 2014	Not Determined
25038753	Study (346)	Most genetic risk for autism resides with common variation.	Nature genetics	Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J; Bodea, Corneliu A; Goldberg, Arthur P; Lee, Ann B; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi; Reichert, Jennifer; Ripke, Stephan; Sandin, Sven; Sklar, Pamela; Svantesson, Oscar; Reichenberg, Abraham; Hultman, Christina M; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph D	August 2014	Relevant
24796725	Create Study	The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison.	European child & adolescent psychiatry	Atladottir, Hjordis O; Gyllenberg, David; Langridge, Amanda; Sandin, Sven; Hansen, Stefan N; Leonard, Helen; Gissler, Mika; Reichenberg, Abraham; Schendel, Diana E; Bourke, Jenny; Hultman, Christina M; Grice, Dorothy E; Buxbaum, Joseph D; Parner, Erik T	February 2015	Not Relevant
24794370	Create Study	The familial risk of autism.	JAMA	Sandin, Sven; Lichtenstein, Paul; Kuja-Halkola, Ralf; Larsson, Henrik; Hultman, Christina M; Reichenberg, Abraham	May 7, 2014	Not Determined
24587841	Create Study	REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.	The annals of applied statistics	Crossett, Andrew; Lee, Ann B; Klei, Lambertus; Devlin, Bernie; Roeder, Kathryn	June 27, 2013	Not Determined
24094742	Create Study	Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.	American journal of human genetics	Poultney, Christopher S; Goldberg, Arthur P; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine; Rehnström, Karola; Palotie, Aarno; Daly, Mark J; Ma'ayan, Avi; Fromer, Menachem; Buxbaum, Joseph D	October 3, 2013	Not Determined
23966865	Create Study	Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.	PLoS genetics	He, Xin; Sanders, Stephan J; Liu, Li; De Rubeis, Silvia; Lim, Elaine T; Sutcliffe, James S; Schellenberg, Gerard D; Gibbs, Richard A; Daly, Mark J; Buxbaum, Joseph D; State, Matthew W; Devlin, Bernie; Roeder, Kathryn	2013	Not Determined
23743231	Create Study	Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.	Genomics	Schafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B, Sutcliffe JS, Buxbaum JD, Roeder K	October 2013	Not Determined
23593035	Create Study	Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.	PLoS genetics	Liu, Li; Sabo, Aniko; Neale, Benjamin M; Nagaswamy, Uma; Stevens, Christine; Lim, Elaine; Bodea, Corneliu A; Muzny, Donna; Reid, Jeffrey G; Banks, Eric; Coon, Hillary; Depristo, Mark; Dinh, Huyen; Fennel, Tim; Flannick, Jason; Gabriel, Stacey; Garimella, Kiran; Gross, Shannon; Hawes, Alicia; Lewis, Lora; Makarov, Vladimir; Maguire, Jared; Newsham, Irene; Poplin, Ryan; Ripke, Stephan; Shakir, Khalid; Samocha, Kaitlin E; Wu, Yuanqing; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Devlin, Bernie; Schellenberg, Gerard D; Sutcliffe, James S; Daly, Mark J; Gibbs, Richard A; Roeder, Kathryn	April 2013	Not Determined
23555798	Create Study	Clustering and alignment of polymorphic sequences for HLA-DRB1 genotyping.	PloS one	Ringquist, Steven; Bellone, Gaia; Lu, Ying; Roeder, Kathryn; Trucco, Massimo	2013	Not Determined
23352160	Create Study	Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.	Neuron	Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, et al.	January 23, 2013	Not Determined
23143602	Create Study	Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.	Nature genetics	Whitcomb, David C; LaRusch, Jessica; Krasinskas, Alyssa M; Klei, Lambertus; Smith, Jill P; Brand, Randall E; Neoptolemos, John P; Lerch, Markus M; Tector, Matt; Sandhu, Bimaljit S; Guda, Nalini M; Orlichenko, Lidiya; Alzheimer's Disease Genetics Consortium; Alkaade, Samer; Amann, Stephen T; Anderson, Michelle A; Baillie, John; Banks, Peter A; Conwell, Darwin; Coté, Gregory A; Cotton, Peter B; DiSario, James; Farrer, Lindsay A; Forsmark, Chris E; Johnstone, Marianne; Gardner, Timothy B; Gelrud, Andres; Greenhalf, William; Haines, Jonathan L; Hartman, Douglas J; Hawes, Robert A; Lawrence, Christopher; Lewis, Michele; Mayerle, Julia; Mayeux, Richard; Melhem, Nadine M; Money, Mary E; Muniraj, Thiruvengadam; Papachristou, Georgios I; Pericak-Vance, Margaret A; Romagnuolo, Joseph; Schellenberg, Gerard D; Sherman, Stuart; Simon, Peter; Singh, Vijay P; Slivka, Adam; Stolz, Donna; Sutton, Robert; Weiss, Frank Ulrich; Wilcox, C Mel; Zarnescu, Narcis Octavian; Wisniewski, Stephen R; O'Connell, Michael R; Kienholz, Michelle L; Roeder, Kathryn; Barmada, M Michael; Yadav, Dhiraj; Devlin, Bernie	December 2012	Not Determined
22843504	Create Study	Individual common variants exert weak effects on the risk for autism spectrum disorders.	Human molecular genetics	Anney, Richard; Klei, Lambertus; Pinto, Dalila; Almeida, Joana; Bacchelli, Elena; Baird, Gillian; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Casey, Jillian; Conroy, Judith; Correia, Catarina; Corsello, Christina; Crawford, Emily L; de Jonge, Maretha; Delorme, Richard; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Green, Andrew; Green, Jonathan; Guter, Stephen J; Heron, Elizabeth A; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Jacob, Suma; Kenny, Graham P; Kim, Cecilia; Kolevzon, Alexander; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Law-Smith, Miriam; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Liu, Xiao-Qing; Lombard, Frances; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Magalhaes, Tiago R; Mantoulan, Carine; McDougle, Christopher J; Melhem, Nadine M; Merikangas, Alison; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Noakes, Carolyn; Nygren, Gudrun; Papanikolaou, Katerina; Pagnamenta, Alistair T; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Posey, David J; Poustka, Fritz; Ragoussis, Jiannis; Regan, Regina; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Schlitt, Sabine; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stoppioni, Vera; Sykes, Nuala; Tancredi, Raffaella; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Vorstman, J A S; Wallace, Simon; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Bailey, Anthony J; Battaglia, Agatino; Cantor, Rita M; Coon, Hilary; Cuccaro, Michael L; Dawson, Geraldine; Ennis, Sean; Freitag, Christine M; Geschwind, Daniel H; Haines, Jonathan L; Klauck, Sabine M; McMahon, William M; Maestrini, Elena; Miller, Judith; Monaco, Anthony P; Nelson, Stanley F; Nurnberger Jr, John I; Oliveira, Guiomar; Parr, Jeremy R; Pericak-Vance, Margaret A; Piven, Joseph; Schellenberg, Gerard D; Scherer, Stephen W; Vicente, Astrid M; Wassink, Thomas H; Wijsman, Ellen M; Betancur, Catalina; Buxbaum, Joseph D; Cook, Edwin H; Gallagher, Louise; Gill, Michael; Hallmayer, Joachim; Paterson, Andrew D; Sutcliffe, James S; Szatmari, Peter; Vieland, Veronica J; Hakonarson, Hakon; Devlin, Bernie	November 1, 2012	Not Determined
22511880	Create Study	Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.	PLoS genetics	Chahrour, Maria H; Yu, Timothy W; Lim, Elaine T; Ataman, Bulent; Coulter, Michael E; Hill, R Sean; Stevens, Christine R; Schubert, Christian R; ARRA Autism Sequencing Collaboration; Greenberg, Michael E; Gabriel, Stacey B; Walsh, Christopher A	2012	Not Determined
22499558	Create Study	Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability.	American journal of medical genetics. Part C, Seminars in medical genetics	Kou, Yan; Betancur, Catalina; Xu, Huilei; Buxbaum, Joseph D; Ma'ayan, Avi	May 15, 2012	Not Determined
22495311	Create Study	Patterns and rates of exonic de novo mutations in autism spectrum disorders.	Nature	Neale, Benjamin M; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San; Makarov, Vladimir; Polak, Paz; Yoon, Seungtai; Maguire, Jared; Crawford, Emily L; Campbell, Nicholas G; Geller, Evan T; Valladares, Otto; Schafer, Chad; Liu, Han; Zhao, Tuo; Cai, Guiqing; Lihm, Jayon; Dannenfelser, Ruth; Jabado, Omar; Peralta, Zuleyma; Nagaswamy, Uma; Muzny, Donna; Reid, Jeffrey G; Newsham, Irene; Wu, Yuanqing; Lewis, Lora; Han, Yi; Voight, Benjamin F; Lim, Elaine; Rossin, Elizabeth; Kirby, Andrew; Flannick, Jason; Fromer, Menachem; Shakir, Khalid; Fennell, Tim; Garimella, Kiran; Banks, Eric; Poplin, Ryan; Gabriel, Stacey; DePristo, Mark; Wimbish, Jack R; Boone, Braden E; Levy, Shawn E; Betancur, Catalina; Sunyaev, Shamil; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Devlin, Bernie; Gibbs, Richard A; Roeder, Kathryn; Schellenberg, Gerard D; Sutcliffe, James S; Daly, Mark J	April 4, 2012	Not Determined
22463983	Create Study	Genetic architecture in autism spectrum disorder.	Current opinion in genetics & development	Devlin B, Scherer SW	June 2012	Not Determined
22170232	Create Study	Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis.	Genes and immunity	Achkar JP, Klei L, de Bakker PI, Bellone G, Rebert N, Scott R, Lu Y, Regueiro M, Brzezinski A, Kamboh MI, Fiocchi C, Devlin B, Trucco M, Ringquist S, Roeder K, Duerr RH	April 2012	Not Determined
22005930	Create Study	Genome-wide association study of Alzheimer''s disease with psychotic symptoms.	Molecular psychiatry	Hollingworth, P; Sweet, R; Sims, R; Harold, D; Russo, G; Abraham, R; Stretton, A; Jones, N; Gerrish, A; Chapman, J; Ivanov, D; Moskvina, V; Lovestone, S; Priotsi, P; Lupton, M; Brayne, C; Gill, M; Lawlor, B; Lynch, A; Craig, D; McGuinness, B; Johnston, J; Holmes, C; Livingston, G; Bass, N J; Gurling, H; McQuillin, A; GERAD Consortium; National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group; Holmans, P; Jones, L; Devlin, B; Klei, L; Barmada, M M; Demirci, F Y; DeKosky, S T; Lopez, O L; Passmore, P; Owen, M J; O'Donovan, M C; Mayeux, R; Kamboh, M I; Williams, J	December 2012	Not Determined
21996756	Create Study	A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.	Human genetics	Casey, Jillian P; Magalhaes, Tiago; Conroy, Judith M; Regan, Regina; Shah, Naisha; Anney, Richard; Shields, Denis C; Abrahams, Brett S; Almeida, Joana; Bacchelli, Elena; Bailey, Anthony J; Baird, Gillian; Battaglia, Agatino; Berney, Tom; Bolshakova, Nadia; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Cali, Phil; Correia, Catarina; Corsello, Christina; Coutanche, Marc; Dawson, Geraldine; de Jonge, Maretha; Delorme, Richard; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Foley, Suzanne; Fombonne, Eric; Freitag, Christine M; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Green, Jonathan; Guter, Stephen J; Hakonarson, Hakon; Holt, Richard; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Kim, Cecilia; Klauck, Sabine M; Kolevzon, Alexander; Lamb, Janine A; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Lord, Catherine; Lund, Sabata C; Maestrini, Elena; Mantoulan, Carine; Marshall, Christian R; McConachie, Helen; McDougle, Christopher J; McGrath, Jane; McMahon, William M; Merikangas, Alison; Miller, Judith; Minopoli, Fiorella; Mirza, Ghazala K; Munson, Jeff; Nelson, Stanley F; Nygren, Gudrun; Oliveira, Guiomar; Pagnamenta, Alistair T; Papanikolaou, Katerina; Parr, Jeremy R; Parrini, Barbara; Pickles, Andrew; Pinto, Dalila; Piven, Joseph; Posey, David J; Poustka, Annemarie; Poustka, Fritz; Ragoussis, Jiannis; Roge, Bernadette; Rutter, Michael L; Sequeira, Ana F; Soorya, Latha; Sousa, Inês; Sykes, Nuala; Stoppioni, Vera; Tancredi, Raffaella; Tauber, Maïté; Thompson, Ann P; Thomson, Susanne; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Vorstman, Jacob A S; Wallace, Simon; Wang, Kai; Wassink, Thomas H; White, Kathy; Wing, Kirsty; Wittemeyer, Kerstin; Yaspan, Brian L; Zwaigenbaum, Lonnie; Betancur, Catalina; Buxbaum, Joseph D; Cantor, Rita M; Cook, Edwin H; Coon, Hilary; Cuccaro, Michael L; Geschwind, Daniel H; Haines, Jonathan L; Hallmayer, Joachim; Monaco, Anthony P; Nurnberger Jr, John I; Pericak-Vance, Margaret A; Schellenberg, Gerard D; Scherer, Stephen W; Sutcliffe, James S; Szatmari, Peter; Vieland, Veronica J; Wijsman, Ellen M; Green, Andrew; Gill, Michael; Gallagher, Louise; Vicente, Astrid; Ennis, Sean	April 2012	Not Determined
21982423	Create Study	Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees.	Biological psychiatry	Melhem, Nadine; Middleton, Frank; McFadden, Kathryn; Klei, Lambertus; Faraone, Stephen V; Vinogradov, Sophia; Tiobech, Josepha; Yano, Victor; Kuartei, Stevenson; Roeder, Kathryn; Byerley, William; Devlin, Bernie; Myles-Worsley, Marina	December 15, 2011	Not Determined
21892380	Create Study	STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE.	The annals of applied statistics	Percival, Daniel; Roeder, Kathryn; Rosenfeld, Roni; Wasserman, Larry	June 1, 2011	Not Determined
21703496	Create Study	Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.	Journal of the American Academy of Child and Adolescent Psychiatry	Liu, Xiao-Qing; Georgiades, Stelios; Duku, Eric; Thompson, Ann; Devlin, Bernie; Cook, Edwin H; Wijsman, Ellen M; Paterson, Andrew D; Szatmari, Peter	July 2011	Not Determined
21685912	Create Study	Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.	Nature genetics	Höglinger, Günter U; Melhem, Nadine M; Dickson, Dennis W; Sleiman, Patrick M A; Wang, Li-San; Klei, Lambertus; Rademakers, Rosa; de Silva, Rohan; Litvan, Irene; Riley, David E; van Swieten, John C; Heutink, Peter; Wszolek, Zbigniew K; Uitti, Ryan J; Vandrovcova, Jana; Hurtig, Howard I; Gross, Rachel G; Maetzler, Walter; Goldwurm, Stefano; Tolosa, Eduardo; Borroni, Barbara; Pastor, Pau; PSP Genetics Study Group; Cantwell, Laura B; Han, Mi Ryung; Dillman, Allissa; van der Brug, Marcel P; Gibbs, J Raphael; Cookson, Mark R; Hernandez, Dena G; Singleton, Andrew B; Farrer, Matthew J; Yu, Chang-En; Golbe, Lawrence I; Revesz, Tamas; Hardy, John; Lees, Andrew J; Devlin, Bernie; Hakonarson, Hakon; Müller, Ulrich; Schellenberg, Gerard D	June 2011	Not Determined
21658581	Create Study	Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.	Neuron	Sanders, Stephan J; Ercan-Sencicek, A Gulhan; Hus, Vanessa; Luo, Rui; Murtha, Michael T; Moreno-De-Luca, Daniel; Chu, Su H; Moreau, Michael P; Gupta, Abha R; Thomson, Susanne A; Mason, Christopher E; Bilguvar, Kaya; Celestino-Soper, Patricia B S; Choi, Murim; Crawford, Emily L; Davis, Lea; Wright, Nicole R Davis; Dhodapkar, Rahul M; DiCola, Michael; DiLullo, Nicholas M; Fernandez, Thomas V; Fielding-Singh, Vikram; Fishman, Daniel O; Frahm, Stephanie; Garagaloyan, Rouben; Goh, Gerald S; Kammela, Sindhuja; Klei, Lambertus; Lowe, Jennifer K; Lund, Sabata C; McGrew, Anna D; Meyer, Kyle A; Moffat, William J; Murdoch, John D; O'Roak, Brian J; Ober, Gordon T; Pottenger, Rebecca S; Raubeson, Melanie J; Song, Youeun; Wang, Qi; Yaspan, Brian L; Yu, Timothy W; Yurkiewicz, Ilana R; Beaudet, Arthur L; Cantor, Rita M; Curland, Martin; Grice, Dorothy E; Günel, Murat; Lifton, Richard P; Mane, Shrikant M; Martin, Donna M; Shaw, Chad A; Sheldon, Michael; Tischfield, Jay A; Walsh, Christopher A; Morrow, Eric M; Ledbetter, David H; Fombonne, Eric; Lord, Catherine; Martin, Christa Lese; Brooks, Andrew I; Sutcliffe, James S; Cook Jr, Edwin H; Geschwind, Daniel; Roeder, Kathryn; Devlin, Bernie; State, Matthew W	June 9, 2011	Not Determined
21480485	Create Study	Using linkage information to weight a genome-wide association of bipolar disorder.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Howrigan, D P; Laird, N M; Smoller, J W; Devlin, B; McQueen, M B	June 2011	Not Determined
21408211	Create Study	Testing for an unusual distribution of rare variants.	PLoS genetics	Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ	March 2011	Not Determined
21078308	Create Study	Do common variants play a role in risk for autism? Evidence and theoretical musings.	Brain research	Devlin B, Melhem N, Roeder K	March 22, 2011	Not Determined
21067556	Create Study	Shedding new light on genetic dark matter.	Genome medicine	Melhem N, Devlin B	2010	Not Determined
20862653	Create Study	Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies.	Statistics in medicine	Crossett A, Kent BP, Klei L, Ringquist S, Trucco M, Roeder K, Devlin B	December 10, 2010	Not Determined
20711421	Create Study	Genome-Wide Significance Levels and Weighted Hypothesis Testing.	Statistical science : a review journal of the Institute of Mathematical Statistics	Roeder K, Wasserman L	November 2009	Not Determined
20689656	Create Study	A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY.	The annals of applied statistics	Lee, Ann B; Luca, Diana; Roeder, Kathryn	2010	Not Determined
20663923	Create Study	A genome-wide scan for common alleles affecting risk for autism.	Human molecular genetics	Anney, Richard; Klei, Lambertus; Pinto, Dalila; Regan, Regina; Conroy, Judith; Magalhaes, Tiago R; Correia, Catarina; Abrahams, Brett S; Sykes, Nuala; Pagnamenta, Alistair T; Almeida, Joana; Bacchelli, Elena; Bailey, Anthony J; Baird, Gillian; Battaglia, Agatino; Berney, Tom; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Carson, Andrew R; Casallo, Guillermo; Casey, Jillian; Chu, Su H; Cochrane, Lynne; Corsello, Christina; Crawford, Emily L; Crossett, Andrew; Dawson, Geraldine; de Jonge, Maretha; Delorme, Richard; Drmic, Irene; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Freitag, Christine M; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Goldberg, Jeremy; Green, Jonathan; Guter, Stephen J; Hakonarson, Hakon; Heron, Elizabeth A; Hill, Matthew; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Kim, Cecilia; Klauck, Sabine M; Kolevzon, Alexander; Korvatska, Olena; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Laskawiec, Magdalena; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Lionel, Anath C; Liu, Xiao-Qing; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Maestrini, Elena; Mahoney, William; Mantoulan, Carine; Marshall, Christian R; McConachie, Helen; McDougle, Christopher J; McGrath, Jane; McMahon, William M; Melhem, Nadine M; Merikangas, Alison; Migita, Ohsuke; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Nelson, Stanley F; Noakes, Carolyn; Noor, Abdul; Nygren, Gudrun; Oliveira, Guiomar; Papanikolaou, Katerina; Parr, Jeremy R; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Piven, Joseph; Posey, David J; Poustka, Annemarie; Poustka, Fritz; Prasad, Aparna; Ragoussis, Jiannis; Renshaw, Katy; Rickaby, Jessica; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Bierut, Laura J; Rice, John P; Salt, Jeff; Sansom, Katherine; Sato, Daisuke; Segurado, Ricardo; Senman, Lili; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stoppioni, Vera; Strawbridge, Christina; Tancredi, Raffaella; Tansey, Katherine; Thiruvahindrapduram, Bhooma; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Wallace, Simon; Wang, Kai; Wang, Zhouzhi; Wassink, Thomas H; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Yaspan, Brian L; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Betancur, Catalina; Buxbaum, Joseph D; Cantor, Rita M; Cook, Edwin H; Coon, Hilary; Cuccaro, Michael L; Gallagher, Louise; Geschwind, Daniel H; Gill, Michael; Haines, Jonathan L; Miller, Judith; Monaco, Anthony P; Nurnberger Jr, John I; Paterson, Andrew D; Pericak-Vance, Margaret A; Schellenberg, Gerard D; Scherer, Stephen W; Sutcliffe, James S; Szatmari, Peter; Vicente, Astrid M; Vieland, Veronica J; Wijsman, Ellen M; Devlin, Bernie; Ennis, Sean; Hallmayer, Joachim	October 15, 2010	Not Determined
20531469	Create Study	Functional impact of global rare copy number variation in autism spectrum disorders.	Nature	Pinto, Dalila; Pagnamenta, Alistair T; Klei, Lambertus; Anney, Richard; Merico, Daniele; Regan, Regina; Conroy, Judith; Magalhaes, Tiago R; Correia, Catarina; Abrahams, Brett S; Almeida, Joana; Bacchelli, Elena; Bader, Gary D; Bailey, Anthony J; Baird, Gillian; Battaglia, Agatino; Berney, Tom; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Bryson, Susan E; Carson, Andrew R; Casallo, Guillermo; Casey, Jillian; Chung, Brian H Y; Cochrane, Lynne; Corsello, Christina; Crawford, Emily L; Crossett, Andrew; Cytrynbaum, Cheryl; Dawson, Geraldine; de Jonge, Maretha; Delorme, Richard; Drmic, Irene; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Freitag, Christine M; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Goldberg, Jeremy; Green, Andrew; Green, Jonathan; Guter, Stephen J; Hakonarson, Hakon; Heron, Elizabeth A; Hill, Matthew; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Kim, Cecilia; Klauck, Sabine M; Kolevzon, Alexander; Korvatska, Olena; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Laskawiec, Magdalena; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Lionel, Anath C; Liu, Xiao-Qing; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Maestrini, Elena; Mahoney, William; Mantoulan, Carine; Marshall, Christian R; McConachie, Helen; McDougle, Christopher J; McGrath, Jane; McMahon, William M; Merikangas, Alison; Migita, Ohsuke; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Nelson, Stanley F; Noakes, Carolyn; Noor, Abdul; Nygren, Gudrun; Oliveira, Guiomar; Papanikolaou, Katerina; Parr, Jeremy R; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Pilorge, Marion; Piven, Joseph; Ponting, Chris P; Posey, David J; Poustka, Annemarie; Poustka, Fritz; Prasad, Aparna; Ragoussis, Jiannis; Renshaw, Katy; Rickaby, Jessica; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Bierut, Laura J; Rice, John P; Salt, Jeff; Sansom, Katherine; Sato, Daisuke; Segurado, Ricardo; Sequeira, Ana F; Senman, Lili; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stein, Olaf; Sykes, Nuala; Stoppioni, Vera; Strawbridge, Christina; Tancredi, Raffaella; Tansey, Katherine; Thiruvahindrapduram, Bhooma; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Wallace, Simon; Wang, Kai; Wang, Zhouzhi; Wassink, Thomas H; Webber, Caleb; Weksberg, Rosanna; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Wu, Jing; Yaspan, Brian L; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Buxbaum, Joseph D; Cantor, Rita M; Cook, Edwin H; Coon, Hilary; Cuccaro, Michael L; Devlin, Bernie; Ennis, Sean; Gallagher, Louise; Geschwind, Daniel H; Gill, Michael; Haines, Jonathan L; Hallmayer, Joachim; Miller, Judith; Monaco, Anthony P; Nurnberger Jr, John I; Paterson, Andrew D; Pericak-Vance, Margaret A; Schellenberg, Gerard D; Szatmari, Peter; Vicente, Astrid M; Vieland, Veronica J; Wijsman, Ellen M; Scherer, Stephen W; Sutcliffe, James S; Betancur, Catalina	July 15, 2010	Not Determined
20435442	Create Study	Consanguinity and increased risk for schizophrenia in Egypt.	Schizophrenia research	Mansour, Hader; Fathi, Warda; Klei, Lambertus; Wood, Joel; Chowdari, Kodavali; Watson, Annie; Eissa, Ahmed; Elassy, Mai; Ali, Ibtihal; Salah, Hala; Yassin, Amal; Tobar, Salwa; El-Boraie, Hala; Gaafar, Hanan; Ibrahim, Nahed E; Kandil, Kareem; El-Bahaei, Wafaa; El-Boraie, Osama; Alatrouny, Mohamed; El-Chennawi, Farha; Devlin, Bernie; Nimgaonkar, Vishwajit L	July 2010	Not Determined
20088021	Create Study	Screen and clean: a tool for identifying interactions in genome-wide association studies.	Genetic epidemiology	Wu J, Devlin B, Ringquist S, Trucco M, Roeder K	April 2010	Not Determined
19784398	Create Study	HIGH DIMENSIONAL VARIABLE SELECTION.	Annals of statistics	Wasserman, Larry; Roeder, Kathryn	January 1, 2009	Not Determined
19625980	Create Study	Neural correlates of symptom dimensions in pediatric obsessive-compulsive disorder: a functional magnetic resonance imaging study.	Journal of the American Academy of Child and Adolescent Psychiatry	Gilbert AR, Akkal D, Almeida JR, Mataix-Cols D, Kalas C, Devlin B, Birmaher B, Phillips ML	September 2009	Not Determined
19513023	Create Study	Phenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository.	The American journal of gastroenterology	Bhat M, Nguyen GC, Pare P, Lahaie R, Deslandres C, Bernard EJ, Aumais G, Jobin G, Wild G, Cohen A, Langelier D, Brant S, Dassopoulos T, McGovern D, Torres E, Duerr R, Regueiro M, Silverberg MS, Steinhart H, Griffiths AM, Elkadri A, Cho J, Proctor D, Goyette P, Rioux J, et al.	September 2009	Not Determined
19455578	Create Study	Discovering genetic ancestry using spectral graph theory.	Genetic epidemiology	Lee AB, Luca D, Klei L, Devlin B, Roeder K	January 2010	Not Determined
19404257	Create Study	Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.	Nature	Glessner, Joseph T; Wang, Kai; Cai, Guiqing; Korvatska, Olena; Kim, Cecilia E; Wood, Shawn; Zhang, Haitao; Estes, Annette; Brune, Camille W; Bradfield, Jonathan P; Imielinski, Marcin; Frackelton, Edward C; Reichert, Jennifer; Crawford, Emily L; Munson, Jeffrey; Sleiman, Patrick M A; Chiavacci, Rosetta; Annaiah, Kiran; Thomas, Kelly; Hou, Cuiping; Glaberson, Wendy; Flory, James; Otieno, Frederick; Garris, Maria; Soorya, Latha; Klei, Lambertus; Piven, Joseph; Meyer, Kacie J; Anagnostou, Evdokia; Sakurai, Takeshi; Game, Rachel M; Rudd, Danielle S; Zurawiecki, Danielle; McDougle, Christopher J; Davis, Lea K; Miller, Judith; Posey, David J; Michaels, Shana; Kolevzon, Alexander; Silverman, Jeremy M; Bernier, Raphael; Levy, Susan E; Schultz, Robert T; Dawson, Geraldine; Owley, Thomas; McMahon, William M; Wassink, Thomas H; Sweeney, John A; Nurnberger, John I; Coon, Hilary; Sutcliffe, James S; Minshew, Nancy J; Grant, Struan F A; Bucan, Maja; Cook, Edwin H; Buxbaum, Joseph D; Devlin, Bernie; Schellenberg, Gerard D; Hakonarson, Hakon	May 28, 2009	Not Determined
19278733	Create Study	Replicable differences in preferred circadian phase between bipolar disorder patients and control individuals.	Psychiatry research	Wood, Joel; Birmaher, Boris; Axelson, David; Ehmann, Mary; Kalas, Catherine; Monk, Kelly; Turkin, Scott; Kupfer, David J; Brent, David; Monk, Timothy H; Nimgainkar, Vishwajit L	April 30, 2009	Not Determined
19152378	Create Study	Consanguinity associated with increased risk for bipolar I disorder in Egypt.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Mansour, Hader; Klei, Lambertus; Wood, Joel; Talkowski, Michael; Chowdari, Kodavali; Fathi, Warda; Eissa, Ahmed; Yassin, Amal; Salah, Hala; Tobar, Salwa; El-Boraie, Hala; Gaafar, Hanan; Elassy, Mai; Ibrahim, Nahed E; El-Bahaei, Wafaa; Elsayed, Mohamed; Shahda, Mohamed; El Sheshtawy, Eman; El-Boraie, Osama; El-Chennawi, Farha; Devlin, Bernie; Nimgaonkar, Vishwajit L	September 5, 2009	Not Determined
19122664	Create Study	Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.	Nature genetics	Silverberg MS, Cho JH, Rioux JD, McGovern DP, Wu J, Annese V, Achkar JP, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, Bossa F, Griffiths AM, Ippoliti AF, Lahaie RG, Latiano A, Paré P, Proctor DD, Regueiro MD, Steinhart AH, Targan SR, et al.	February 2009	Not Determined
18519160	Create Study	Searching for disease susceptibility variants in structured populations.	Genomics	Roeder K, Luca D	January 2009	Not Determined
18252225	Create Study	On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.	American journal of human genetics	Luca, Diana; Ringquist, Steven; Klei, Lambertus; Lee, Ann B; Gieger, Christian; Wichmann, H-Erich; Schreiber, Stefan; Krawczak, Michael; Lu, Ying; Styche, Alexis; Devlin, Bernie; Roeder, Kathryn; Trucco, Massimo	February 2008	Not Determined
17922480	Create Study	Pleiotropy and principal components of heritability combine to increase power for association analysis.	Genetic epidemiology	Klei L, Luca D, Devlin B, Roeder K	January 2008	Not Determined
17561376	Create Study	Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk.	Schizophrenia research	Shirts BH, Kim JJ, Reich S, Dickerson FB, Yolken RH, Devlin B, Nimgaonkar VL	August 2007	Not Determined
17549760	Create Study	Improving power in genome-wide association studies: weights tip the scale.	Genetic epidemiology	Roeder K, Devlin B, Wasserman L	November 2007	Not Determined
17453677	Create Study	Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?	Annals of medicine	Kim JJ, Shirts BH, Dayal M, Bacanu SA, Wood J, Xie W, Zhang X, Chowdari KV, Yolken R, Devlin B, Nimgaonkar VL	2007	Not Determined
17436020	Create Study	Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation.	Human genetics	Devlin, Bernie; Klei, Lambertus; Myles-Worsley, Marina; Tiobech, Josepha; Otto, Caleb; Byerley, William; Roeder, Kathryn	July 2007	Not Determined
17434289	Create Study	Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.	Genomics	Yu CE, Seltman H, Peskind ER, Galloway N, Zhou PX, Rosenthal E, Wijsman EM, Tsuang DW, Devlin B, Schellenberg GD	June 2007	Not Determined
17342507	Create Study	Testing for association based on excess allele sharing in a sample of related cases and controls.	Human genetics	Klei, Lambertus; Roeder, Kathyrn	June 2007	Not Determined
17322880	Create Study	Mapping autism risk loci using genetic linkage and chromosomal rearrangements.	Nature genetics	Autism Genome Project Consortium; Szatmari, Peter; Paterson, Andrew D; Zwaigenbaum, Lonnie; Roberts, Wendy; Brian, Jessica; Liu, Xiao-Qing; Vincent, John B; Skaug, Jennifer L; Thompson, Ann P; Senman, Lili; Feuk, Lars; Qian, Cheng; Bryson, Susan E; Jones, Marshall B; Marshall, Christian R; Scherer, Stephen W; Vieland, Veronica J; Bartlett, Christopher; Mangin, La Vonne; Goedken, Rhinda; Segre, Alberto; Pericak-Vance, Margaret A; Cuccaro, Michael L; Gilbert, John R; Wright, Harry H; Abramson, Ruth K; Betancur, Catalina; Bourgeron, Thomas; Gillberg, Christopher; Leboyer, Marion; Buxbaum, Joseph D; Davis, Kenneth L; Hollander, Eric; Silverman, Jeremy M; Hallmayer, Joachim; Lotspeich, Linda; Sutcliffe, James S; Haines, Jonathan L; Folstein, Susan E; Piven, Joseph; Wassink, Thomas H; Sheffield, Val; Geschwind, Daniel H; Bucan, Maja; Brown, W Ted; Cantor, Rita M; Constantino, John N; Gilliam, T Conrad; Herbert, Martha; Lajonchere, Clara; Ledbetter, David H; Lese-Martin, Christa; Miller, Janet; Nelson, Stan; Samango-Sprouse, Carol A; Spence, Sarah; State, Matthew; Tanzi, Rudolph E; Coon, Hilary; Dawson, Geraldine; Devlin, Bernie; Estes, Annette; Flodman, Pamela; Klei, Lambertus; McMahon, William M; Minshew, Nancy; Munson, Jeff; Korvatska, Elena; Rodier, Patricia M; Schellenberg, Gerard D; Smith, Moyra; Spence, M Anne; Stodgell, Chris; Tepper, Ping Guo; Wijsman, Ellen M; Yu, Chang-En; Rogé, Bernadette; Mantoulan, Carine; Wittemeyer, Kerstin; Poustka, Annemarie; Felder, Bärbel; Klauck, Sabine M; Schuster, Claudia; Poustka, Fritz; Bölte, Sven; Feineis-Matthews, Sabine; Herbrecht, Evelyn; Schmötzer, Gabi; Tsiantis, John; Papanikolaou, Katerina; Maestrini, Elena; Bacchelli, Elena; Blasi, Francesca; Carone, Simona; Toma, Claudio; Van Engeland, Herman; de Jonge, Maretha; Kemner, Chantal; Koop, Frederieke; Koop, Frederike; Langemeijer, Marjolein; Langemeijer, Marjolijn; Hijmans, Channa; Hijimans, Channa; Staal, Wouter G; Baird, Gillian; Bolton, Patrick F; Rutter, Michael L; Weisblatt, Emma; Green, Jonathan; Aldred, Catherine; Wilkinson, Julie-Anne; Pickles, Andrew; Le Couteur, Ann; Berney, Tom; McConachie, Helen; Bailey, Anthony J; Francis, Kostas; Honeyman, Gemma; Hutchinson, Aislinn; Parr, Jeremy R; Wallace, Simon; Monaco, Anthony P; Barnby, Gabrielle; Kobayashi, Kazuhiro; Lamb, Janine A; Sousa, Ines; Sykes, Nuala; Cook, Edwin H; Guter, Stephen J; Leventhal, Bennett L; Salt, Jeff; Lord, Catherine; Corsello, Christina; Hus, Vanessa; Weeks, Daniel E; Volkmar, Fred; Tauber, Maïté; Fombonne, Eric; Shih, Andy; Meyer, Kacie J	March 2007	Not Determined
16893532	Create Study	Novel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samples.	Biological psychiatry	Talkowski ME, Mansour H, Chowdari KV, Wood J, Butler A, Varma PG, Prasad S, Semwal P, Bhatia T, Deshpande S, Devlin B, Thelma BK, Nimgaonkar VL	September 15, 2006	Not Determined
16631129	Create Study	Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples.	Biological psychiatry	Talkowski, Michael E; Seltman, Howard; Bassett, Anne S; Brzustowicz, Linda M; Chen, Xiangning; Chowdari, Kodavali V; Collier, David A; Cordeiro, Quirino; Corvin, Aiden P; Deshpande, Smita N; Egan, Michael F; Gill, Michael; Kendler, Kenneth S; Kirov, George; Heston, Leonard L; Levitt, Pat; Lewis, David A; Li, Tao; Mirnics, Karoly; Morris, Derek W; Norton, Nadine; O'Donovan, Michael C; Owen, Michael J; Richard, Christian; Semwal, Prachi; Sobell, Janet L; St Clair, David; Straub, Richard E; Thelma, B K; Vallada, Homero; Weinberger, Daniel R; Williams, Nigel M; Wood, Joel; Zhang, Feng; Devlin, Bernie; Nimgaonkar, Vishwajit L	July 15, 2006	Not Determined
16507006	Create Study	Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia.	Genes, brain, and behavior	Mansour HA, Wood J, Logue T, Chowdari KV, Dayal M, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL	March 2006	Not Determined
16400608	Create Study	Using linkage genome scans to improve power of association in genome scans.	American journal of human genetics	Roeder, Kathryn; Bacanu, Silvi-Alin; Wasserman, Larry; Devlin, B	February 2006	Not Determined
16152575	Create Study	Selection of eating-disorder phenotypes for linkage analysis.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Bulik, Cynthia M; Bacanu, Silviu-Alin; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Keel, Pamela; Kaplan, Allan S; Mitchell, James E; Rotondo, Alessandro; Strober, Michael; Treasure, Janet; Woodside, D Blake; Sonpar, Vibhor A; Xie, Weiting; Bergen, Andrew W; Berrettini, Wade H; Kaye, Walter H; Devlin, Bernie	November 5, 2005	Not Determined
16152574	Create Study	Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Bacanu, Silviu-Alin; Bulik, Cynthia M; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Keel, Pamela; Kaplan, Allan S; Mitchell, James E; Rotondo, Alessandro; Strober, Michael; Treasure, Janet; Woodside, D Blake; Sonpar, Vibhor A; Xie, Weiting; Bergen, Andrew W; Berrettini, Wade H; Kaye, Walter H; Devlin, Bernie	November 5, 2005	Not Determined
16103890	Create Study	Autism and the serotonin transporter: the long and short of it.	Molecular psychiatry	Devlin B, Cook EH, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD, CPEA Genetics Network	December 2005	Not Determined
16094613	Create Study	Multipoint linkage analysis for a very dense set of markers.	Genetic epidemiology	Bacanu SA	November 2005	Not Determined
16076655	Create Study	Circadian phase variation in bipolar I disorder.	Chronobiology international	Mansour HA, Wood J, Chowdari KV, Dayal M, Thase ME, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL	2005	Not Determined
16027741	Create Study	Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease.	Molecular psychiatry	Sweet RA, Devlin B, Pollock BG, Sukonick DL, Kastango KB, Bacanu SA, Chowdari KV, DeKosky ST, Ferrell RE	November 2005	Not Determined
16009739	Create Study	Heritability of psychosis in Alzheimer disease.	The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry	Bacanu, Silviu-Alin; Devlin, Bernie; Chowdari, Kodavali V; DeKosky, Steven T; Nimgaonkar, Vishwajit L; Sweet, Robert A	July 2005	Not Determined
15920508	Create Study	Association of multiple DRD2 polymorphisms with anorexia nervosa.	Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology	Bergen AW, Yeager M, Welch RA, Haque K, Ganjei JK, van den Bree MB, Mazzanti C, Nardi I, Fichter MM, Halmi KA, Kaplan AS, Strober M, Treasure J, Woodside DB, Bulik CM, Bacanu SA, Devlin B, Berrettini WH, Goldman D, Kaye WH	September 2005	Not Determined
15915326	Create Study	Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia.	Human genetics	Klei, Lambertus; Bacanu, Silviu-Alin; Myles-Worsley, Marina; Galke, Brandi; Xie, Weiting; Tiobech, Josepha; Otto, Caleb; Roeder, Kathyrn; Devlin, Bernie; Byerley, William	August 2005	Not Determined
15637716	Create Study	Characterization of multilocus linkage disequilibrium.	Genetic epidemiology	Rinaldo A, Bacanu SA, Devlin B, Sonpar V, Wasserman L, Roeder K	April 2005	Not Determined
15637715	Create Study	Analysis of single-locus tests to detect gene/disease associations.	Genetic epidemiology	Roeder K, Bacanu SA, Sonpar V, Zhang X, Devlin B	April 2005	Not Determined
15601530	Create Study	Integration of association statistics over genomic regions using Bayesian adaptive regression splines.	Human genomics	Zhang X, Roeder K, Wallstrom G, Devlin B	November 2003	Not Determined
15514657	Create Study	Genomic Control to the extreme.	Nature genetics	Devlin B, Bacanu SA, Roeder K	November 2004	Not Determined
15498468	Create Study	ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.	Genomics	Yu CE, Devlin B, Galloway N, Loomis E, Schellenberg GD	September 2004	Not Determined
15372617	Create Study	Robust estimation of critical values for genome scans to detect linkage.	Genetic epidemiology	Bacanu SA	January 2005	Not Determined
15048647	Create Study	Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Devlin, Bernie; Bennett, Pamela; Dawson, Geraldine; Figlewicz, Denise A; Grigorenko, Elena L; McMahon, William; Minshew, Nancy; Pauls, David; Smith, Moyra; Spence, M Anne; Rodier, Patricia M; Stodgell, Chris; Schellenberg, Gerard D; CPEA Genetics Network	April 1, 2004	Not Determined
14755456	Create Study	Haplotypes of the monoamine oxidase genes and the risk for substance use disorders.	American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics	Vanyukov, Michael M; Maher, Brion S; Devlin, Bernie; Tarter, Ralph E; Kirillova, Galina P; Yu, Ling-Mei; Ferrell, Robert E	February 15, 2004	Not Determined
14571259	Create Study	False discovery or missed discovery?	Heredity	Devlin B, Roeder K, Wasserman L	December 2003	Not Determined
12933562	Create Study	Genomic control for association studies: a semiparametric test to detect excess-haplotype sharing.	Biostatistics (Oxford, England)	Devlin B, Roeder K, Wasserman L	December 2000	Not Relevant
12813726	Create Study	Evolutionary-based association analysis using haplotype data.	Genetic epidemiology	Seltman H, Roeder K, Devlin B	July 2003	Not Determined
12813725	Create Study	Analysis of multilocus models of association.	Genetic epidemiology	Devlin B, Roeder K, Wasserman L	July 2003	Not Determined
12675687	Create Study	Cladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease.	Annals of human genetics	Wang, G Q; DiPietro, M; Roeder, K; Heng, C-K; Bunker, C H; Hamman, R F; Kamboh, M I	March 2003	Not Determined
12610778	Create Study	On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.	American journal of human genetics	Tzeng, Jung-Ying; Devlin, B; Wasserman, Larry; Roeder, Kathryn	April 2003	Not Determined
12476400	Create Study	Significant linkage on chromosome 10p in families with bulimia nervosa.	American journal of human genetics	Bulik, Cynthia M; Devlin, B; Bacanu, Silviu-Alin; Thornton, Laura; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Kaplan, Allan S; Strober, Michael; Woodside, D Blake; Bergen, Andrew W; Ganjei, J Kelly; Crow, Scott; Mitchell, James; Rotondo, Alessandro; Mauri, Mauro; Cassano, Giovanni; Keel, Pamela; Berrettini, Wade H; Kaye, Walter H	January 2003	Not Determined
12210285	Create Study	No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.	American journal of medical genetics	Devlin B, Bennett P, Cook EH, Dawson G, Gonen D, Grigorenko EL, McMahon W, Pauls D, Smith M, Spence MA, Schellenberg GD, Collaborative Programs of Excellence in Autism (CPEA) Genetics Network	August 8, 2002	Not Determined
12192612	Create Study	Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau.	Molecular psychiatry	Devlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B, Novasad D, Chu A, TCuenco K, Tiobek S, Otto C, Byerley W	2002	Not Determined
12105318	Create Study	Linkage analysis of Alzheimer disease with psychosis.	Neurology	Bacanu, S A; Devlin, B; Chowdari, K V; DeKosky, S T; Nimgaonkar, V L; Sweet, R A	July 9, 2002	Not Determined
12023979	Create Study	Association and linkage analyses of RGS4 polymorphisms in schizophrenia.	Human molecular genetics	Chowdari, Kodavali V; Mirnics, Karoly; Semwal, Prachi; Wood, Joel; Lawrence, Elizabeth; Bhatia, Triptish; Deshpande, Smita N; B K, Thelma; Ferrell, Robert E; Middleton, Frank A; Devlin, Bernie; Levitt, Pat; Lewis, David A; Nimgaonkar, Vishwajit L	June 1, 2002	Not Determined
11914406	Create Study	Increased familial risk of the psychotic phenotype of Alzheimer disease.	Neurology	Sweet, R A; Nimgaonkar, V L; Devlin, B; Lopez, O L; DeKosky, S T	March 26, 2002	Not Determined
11912184	Create Study	Linkage analysis of anorexia nervosa incorporating behavioral covariates.	Human molecular genetics	Devlin, Bernie; Bacanu, Silviu-Alin; Klump, Kelly L; Bulik, Cynthia M; Fichter, Manfred M; Halmi, Katherine A; Kaplan, Allan S; Strober, Michael; Treasure, Janet; Woodside, D Blake; Berrettini, Wade H; Kaye, Walter H	March 15, 2002	Not Determined
11855950	Create Study	Genomic control, a new approach to genetic-based association studies.	Theoretical population biology	Devlin, B; Roeder, K; Wasserman, L	November 2001	Not Determined
11754475	Create Study	Association studies for quantitative traits in structured populations.	Genetic epidemiology	Bacanu SA, Devlin B, Roeder K	January 2002	Not Determined
11754473	Create Study	Mixture models for linkage analysis of affected sibling pairs and covariates.	Genetic epidemiology	Devlin B, Jones BL, Bacanu SA, Roeder K	January 2002	Not Determined
11754464	Create Study	Unbiased methods for population-based association studies.	Genetic epidemiology	Devlin, B; Roeder, K; Bacanu, S A	December 2001	Not Determined
11499679	Create Study	Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania.	Human genetics	Devlin, B; Roeder, K; Otto, C; Tiobech, S; Byerley, W	June 2001	Not Determined
11318178	Create Study	Flexible parametric measurement error models.	Biometrics	Carroll RJ, Roeder K, Wasserman L	March 1999	Not Determined
11315092	Create Study	Genomic control for association studies.	Biometrics	Devlin, B; Roeder, K	December 1999	Not Relevant
11309689	Create Study	Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes.	American journal of human genetics	Seltman, H; Roeder, K; Devlin, B	May 2001	Not Determined
11119294	Create Study	A Bayesian hierarchical model for allele frequencies.	Genetic epidemiology	Lockwood JR, Roeder K, Devlin B	January 2001	Not Determined
10801388	Create Study	The power of genomic control.	American journal of human genetics	Bacanu, S A; Devlin, B; Roeder, K	June 2000	Not Relevant
10677324	Create Study	Haplotype fine mapping by evolutionary trees.	American journal of human genetics	Lam, J C; Roeder, K; Devlin, B	February 2000	Not Relevant
10657297	Create Study	Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.	Science (New York, N.Y.)	Baysal, B E; Ferrell, R E; Willett-Brozick, J E; Lawrence, E C; Myssiorek, D; Bosch, A; van der Mey, A; Taschner, P E; Rubinstein, W S; Myers, E N; Richard 3rd, C W; Cornelisse, C J; Devilee, P; Devlin, B	February 4, 2000	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
No Mandatory Data Expected

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
Genomics/omics	41	07/15/2013	636	11/15/2013	636	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
Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study	A key component of genetic architecture is the allelic spectrum influencing trait variability. For autism spectrum disorder (herein termed autism), the nature of the allelic spectrum is uncertain. Individual risk-associated genes have been identified from rare variation, especially de novo mutations. From this evidence, one might conclude that rare variation dominates the allelic spectrum in autism, yet recent studies show that common variation, individually of small effect, has substantial impact en masse. At issue is how much of an impact relative to rare variation this common variation has. Using a unique epidemiological sample from Sweden, new methods that distinguish total narrow-sense heritability from that due to common variation and synthesis of results from other studies, we reach several conclusions about autism's genetic architecture: its narrow-sense heritability is ~52.4%, with most due to common variation, and rare de novo mutations contribute substantially to individual liability, yet their contribution to variance in liability, 2.6%, is modest compared to that for heritable variation.	548/548	Primary 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.

Contact NDA Help Desk

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Glossary