NDA Help Center

Login Dialog

Frequently Asked Questions


NDA Help Center

Filter Cart

The Filter Cart provides a way to query and access data for which you may be interested.  There are multiple places to go query and Add to Filter Cart (Sometimes called Download).  

A few points related to the filter cart are important to understand with the NDA Query/Filter implementation: 

First, the filter cart is populated asyncronously.  So, when you add subjects, sometimes it may take a few minutes to populate.  You can continue to do other things during this time. 

When you are adding your first filter, all data associated with your query will be added to the filter cart (whether it be a collection, a concept, a study, a data structure/elment or subjects). Not all data available for the subjects selected will necessarily be displayed.  For example, if you select the NDA imaging structure image03, and further restrict that query to scan_type fMRI, only fMRI images will appear and only the image03 structure will be available.  However, if you want to see all of the clinical and phenotype, then select, "Find All Subject Data" to see all the data avaialble for those subjects.  

when a secord or third filter is applied, an AND condition is used to determine the subjects that are exist in all filters.  If the subject does not appear in any filter, that subjects data will be excluded from your filter cart. Given the sparcity of data in the NDA, it is possible for no subjects to appear across filters.  If that happens, clear your filter cart, and start over.  

The NDA is looking to enhance query/filtering.  Until additional tools become available, it is best to package more data than you need and then package and download the data and use other tools to further restrict and analyze the data.  If you have any questions on data access, are interested in using avaialble web services or need help accessing data, please contact us for assistance.  

Frequently Asked Questions



Reset Password

NDAR provides a single access to de-identified autism research data. For permission to download data, you will need an NDAR account with approved access to NDAR or a connected repository (AGRE, IAN, or the ATP). For NDAR access, you need to be a research investigator sponsored by an NIH recognized institution with federal wide assurance. See Request Access for more information.

Warning Notice

This is a U.S. Government computer system, which may be accessed and used only for authorized Government business by authorized personnel. Unauthorized access or use of this computer system may subject violators to criminal, civil, and/or administrative action. All information on this computer system may be intercepted, recorded, read, copied, and disclosed by and to authorized personnel for official purposes, including criminal investigations. Such information includes sensitive data encrypted to comply with confidentiality and privacy requirements. Access or use of this computer system by any person, whether authorized or unauthorized, constitutes consent to these terms. There is no right of privacy in this system.

You have logged in with a temporary password. Please update your password. Passwords must contain 8 or more characters and must contain at least 3 of the following types of characters:

Subscribe to our mailing list

Mailing List(s)
Email Format

You are now leaving the National Database for Autism Research (NDAR) web site to go to:

Click on the address above if the page does not change within 10 seconds.


NDAR is not responsible for the content of this external site and does not monitor other web sites for accuracy.

Accept Terms
Selected Filters
No filters selected

The filters you have selected from various query interfaces will be stored here, in the 'Filter Cart'. The database will be queried using filters added to your 'Filter Cart', when multiple filters are defined, each will be executed using 'AND' logic, so with each filter that is applied the result set gets smaller.

From the 'Filter Cart' you can inspect each of the filters that have been defined, and you also have the option to remove filters. The 'Filter Cart' itself will display the number of filters applied along with the number of subjects that are identified by the combination of those filters. For example a GUID filter with two subjects, followed by a GUID filter for just one of those subjects would return only data for the subject that is in both GUID filters.

If you have a question about the filter cart, or underlying filters please contact the help desk at The NDA Help Desk

Value Range
Data Structures with shared data
No filters have been selected
Switch User

1 Numbers reported are subjects by age
New Trial
New Project

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

Please select an experiment type below

SelectExperiment IdExperiment NameExperiment Type
  • Select One
  • EEG
  • EGG
  • Eye Tracking
  • Omics
  • fMRI
Created On
953Shallow EpisodicfMRI06/20/2018
952Semantic EncodingfMRI06/20/2018
951Resting StatefMRI06/20/2018
949Resting StatefMRI06/18/2018
943Emotional Face TaskfMRI06/13/2018
941Meridians localizerfMRI06/07/2018
940V1 localizer movingDotsfMRI06/07/2018
938MT localizer dots movingDotsfMRI06/07/2018
937MT localizer gratings movingDotsfMRI06/07/2018
936V1 localizer peripheryfMRI06/07/2018
935Contrast peripheryfMRI06/07/2018
934MT localizer peripheryfMRI06/07/2018
933Pilot01: Posner Cueing with st-tACSEye Tracking06/06/2018
932Social- Theory of Mind Localizer TaskfMRI06/01/2018
931Faces TaskfMRI05/31/2018
929Moral RatingfMRI05/30/2018
928Pain Detection fMRI05/30/2018
927Reward TaskfMRI05/30/2018
926Go no Go TaskfMRI05/30/2018
924EARLI Placenta WGBSOmics05/24/2018
923Anxiety-CBT fMRI (pre-post) - Version 4 BlockfMRI05/15/2018
922Anxiety-CBT fMRI (pre-post) - Version 3 BlockfMRI05/15/2018
921Anxiety-CBT fMRI (pre-post) - Version 2 BlockfMRI05/15/2018
920Anxiety-CBT fMRI (pre-post) - Version 1 BlockfMRI05/15/2018
919Neural overlap in item representations across episodes impairs context memoryfMRI05/11/2018
918ReferenceTissue: U01MH106892_Brain_Amplicon_SeqOmics05/08/2018
914PFC analysis in bloodOmics04/27/2018
913Task and emotional content driven visual competitionfMRI04/27/2018
912Task and emotional content driven visual competitionEEG04/23/2018
911Resting StatefMRI04/20/2018
910Modified Monetary Incentive Delay fMRI04/20/2018
908Resting State Pre-Stress Visit 1fMRI04/20/2018
907Montreal Imaging Stress Task Visit 1fMRI04/18/2018
9062-back Post-Stress Visit 1fMRI04/18/2018
9051-back Post-Stress Visit 1fMRI04/18/2018
9040-back Post-Stress Visit 1fMRI04/18/2018
9032-back Pre-Stress Visit 1fMRI04/18/2018
9021-back Pre-Stress Visit 1fMRI04/18/2018
9010-back Pre-Stress Visit 1fMRI04/18/2018
899Investigating a Neurobehavioral Mechanism of Paranoia - Resting State ScansfMRI04/06/2018
Collection - Add Experiment
Add Supporting Documentation
Select File

Please enter the name of the data structure to search or if your definition does not exist, please upload that definition so that it can be appropriately defined for submission. Multiple data structures may be associated with a single Data Expected entry. Please add only one data structure per assessment.






You have requested to move the sharing dates for the following assessments:
Data Expected Item Original Sharing Date New Sharing Date

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

Explanation must be between 20 and 200 bytes in length.

Please press Save or Cancel

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


Title, investigators, and Collection Description may be edited along with the Collection Phase. For Collection Phase, the options Pre-enrollment, Enrollment, and Completed can be chosen allowing the Collection Owner to indicate the stage of data collection.

Funding Source

The ability to associate the funding source for the project is provided. For NIH funded grants, linkage to Project Reporter information (e.g. R01MH123456) is supported. Projects funded by others, including the URL of the project, are listed. Non NIH funded projects will become available here to link that data with the appropriate funding agency.

Supporting Documentation

Any documents related to the project may be uploaded clarifying the data or acquisition methods used may be uploaded and made available here. The default is to share these documents to the general public. An option to share only to qualified Researchers is also an option.

Clinical Trials

For clinical trials, the option to link to the clinical trial in clinicaltrials.gov is optionally provided.

Collection Summary Collection Charts
Collection Title Collection Investigators Collection Description
Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study
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 
Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" study
Funding Completed
Loading Chart...
NIH - Extramural None

R56MH097849-01 Population-Based Autism Genetics & Environment Study Not Reported Not Reported ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI $0.00

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


To create a new Omics, eye tracking, fMRI, or EEG experiment, press the "+ New Experiment" button. Once an experiment is created, then raw files for these types of experiments should be provided, associating the experiment – through Experiment_ID – with the metadata defined in the experiments interface.

IDNameCreated DateStatusType
161PAGES study of autism heritability07/31/2014ApprovedOmics

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

Shared Data

Data structures with the number of subjects submitted and shared are provided.

Genomics Sample Genomics 636
Genomics Subject Genomics 548

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


Publications relevant to NDAR 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 IDStudyTitleJournalAuthorsDateStatus
29112194Create StudyGenome-wide association study identifies a novel locus for cannabis dependence.Molecular psychiatryAgrawal A, Chou YL, Carey CE, Baranger DAA, Zhang B, Sherva R, Wetherill L, Kapoor M, Wang JC, Bertelsen S, Anokhin AP, Hesselbrock V, Kramer J, Lynskey MT, Meyers JL, Nurnberger JI, Rice JP, Tischfield J, Bierut LJ, Degenhardt L, Farrer LA, Gelernter J, Hariri AR, Heath AC, Kranzler HR, et al.November 2017Not Determined
29100626Create StudyHeritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden.Biological psychiatryYip BHK, Bai D, Mahjani B, Klei L, Pawitan Y, Hultman CM, Grice DE, Roeder K, Buxbaum JD, Devlin B, Reichenberg A, Sandin SSeptember 2017Not Determined
28569757Create StudyFetal and postnatal metal dysregulation in autism.Nature communicationsArora M, Reichenberg A, Willfors C, Austin C, Gennings C, Berggren S, Lichtenstein P, Anckarsäter H, Tammimies K, Bölte SJune 2017Relevant
28461698Create StudyGenetic risk for schizophrenia and psychosis in Alzheimer disease.Molecular psychiatryDemichele-Sweet MAA, Weamer EA, Klei L, Vrana DT, Hollingshead DJ, Seltman HJ, Sims R, Foroud T, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Ruiz A, Williams J, Mayeux R, Lopez OL, Sibille EL, Kamboh MI, Devlin B, Sweet RAMay 2017Not Determined
28191890Create StudyRefining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.Nature geneticsKosmicki JA, Samocha KE, Howrigan DP, Sanders SJ, Slowikowski K, Lek M, Karczewski KJ, Cutler DJ, Devlin B, Roeder K, Buxbaum JD, Neale BM, Macarthur DG, Wall DP, Robinson EB, Daly MJApril 2017Not Determined
27087321Create StudyA Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.American journal of human geneticsBodea CA, Neale BM, Ripke S, Daly MJ, Devlin B, Roeder KMay 2016Not Determined
26834510Create StudyThe huge Package for High-dimensional Undirected Graph Estimation in R.Journal of machine learning research : JMLRZhao T, Liu H, Roeder K, Lafferty J, Wasserman LApril 2012Not Relevant
26806987Create StudyLocalized Functional Principal Component Analysis.Journal of the American Statistical AssociationChen K, Lei J2015Not Determined
26402605Create StudyInsights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.NeuronSanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF, Klei L, Mandell JD, Moreno-De-Luca D, Poultney CS, Robinson EB, Smith L, Solli-Nowlan T, Su MY, Teran NA, Walker MF, Werling DM, Beaudet AL, et al.September 23, 2015Not Determined
25843333Create StudyDSM-5 and psychiatric genetics - round hole, meet square peg.Biological psychiatryBuxbaum, Joseph DMay 1, 2015Not Relevant
25382957Create StudyPositive 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 AmericaZhao T, Roeder K, Liu HOctober 20, 2014Not Determined
25363760Create StudySynaptic, transcriptional and chromatin genes disrupted in autism.NatureDe Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, et al.November 13, 2014Not Relevant
25152607Create StudyStability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models.Advances in neural information processing systemsLiu H, Roeder K, Wasserman LDecember 31, 2010Not Determined
25086666Create StudyA framework for the interpretation of de novo mutation in human disease.Nature geneticsSamocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A, Wall DP, MacArthur DG, Gabriel SB, DePristo M, Purcell SM, Palotie A, Boerwinkle E, Buxbaum JD, Cook EH, Gibbs RA, Schellenberg GD, Sutcliffe JS, Devlin B, Roeder K, Neale BM, et al.September 2014Not Determined
25038753Study (346)Most genetic risk for autism resides with common variation.Nature geneticsGaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reichert J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, Hultman CM, Devlin B, Roeder K, Buxbaum JDAugust 2014Relevant
24796725Create StudyThe increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison.European child & adolescent psychiatryAtladottir, 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 TFebruary 2015Not Relevant
24794370Create StudyThe familial risk of autism.JAMASandin S, Lichtenstein P, Kuja-Halkola R, Larsson H, Hultman CM, Reichenberg AMay 7, 2014Not Determined
24587841Create StudyREFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.The annals of applied statisticsCrossett A, Lee AB, Klei L, Devlin B, Roeder KJune 27, 2013Not Determined
24094742Create StudyIdentification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.American journal of human geneticsPoultney CS, Goldberg AP, Drapeau E, Kou Y, Harony-Nicolas H, Kajiwara Y, De Rubeis S, Durand S, Stevens C, Rehnström K, Palotie A, Daly MJ, Ma'ayan A, Fromer M, Buxbaum JDOctober 3, 2013Not Determined
23966865Create StudyIntegrated model of de novo and inherited genetic variants yields greater power to identify risk genes.PLoS geneticsHe X, Sanders SJ, Liu L, De Rubeis S, Lim ET, Sutcliffe JS, Schellenberg GD, Gibbs RA, Daly MJ, Buxbaum JD, State MW, Devlin B, Roeder K2013Not Determined
23743231Create StudyWhole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.GenomicsSchafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B, Sutcliffe JS, Buxbaum JD, Roeder KOctober 2013Not Determined
23593035Create StudyAnalysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.PLoS geneticsLiu L, Sabo A, Neale BM, Nagaswamy U, Stevens C, Lim E, Bodea CA, Muzny D, Reid JG, Banks E, Coon H, Depristo M, Dinh H, Fennel T, Flannick J, Gabriel S, Garimella K, Gross S, Hawes A, Lewis L, Makarov V, Maguire J, Newsham I, Poplin R, Ripke S, et al.April 2013Not Determined
23555798Create StudyClustering and alignment of polymorphic sequences for HLA-DRB1 genotyping.PloS oneRingquist S, Bellone G, Lu Y, Roeder K, Trucco M2013Not Determined
23352160Create StudyRare complete knockouts in humans: population distribution and significant role in autism spectrum disorders.NeuronLim 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, 2013Not Determined
23143602Create StudyCommon genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.Nature geneticsWhitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alzheimer's Disease Genetics Consortium, Alkaade S, Amann ST, Anderson MA, Baillie J, Banks PA, Conwell D, Coté GA, Cotton PB, DiSario J, Farrer LA, Forsmark CE, Johnstone M, et al.December 2012Not Determined
22843504Create StudyIndividual common variants exert weak effects on the risk for autism spectrum disorderspi.Human molecular geneticsAnney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, et al.November 1, 2012Not Determined
22511880Create StudyWhole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism.PLoS geneticsChahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR, ARRA Autism Sequencing Collaboration, Greenberg ME, Gabriel SB, Walsh CA2012Not Determined
22499558Create StudyNetwork- 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 geneticsKou Y, Betancur C, Xu H, Buxbaum JD, Ma'ayan AMay 15, 2012Not Determined
22495311Create StudyPatterns and rates of exonic de novo mutations in autism spectrum disorders.NatureNeale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Schafer C, Liu H, Zhao T, Cai G, Lihm J, Dannenfelser R, Jabado O, Peralta Z, et al.May 10, 2012Not Determined
22463983Create StudyGenetic architecture in autism spectrum disorder.Current opinion in genetics & developmentDevlin B, Scherer SWJune 2012Not Determined
22170232Create StudyAmino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis.Genes and immunityAchkar 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 RHApril 2012Not Determined
22005930Create StudyGenome-wide association study of Alzheimer's disease with psychotic symptoms.Molecular psychiatryHollingworth 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 NJ, et al.December 2012Not Determined
21996756Create StudyA novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Human geneticsCasey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, et al.April 2012Not Determined
21982423Create StudyCopy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees.Biological psychiatryMelhem N, Middleton F, McFadden K, Klei L, Faraone SV, Vinogradov S, Tiobech J, Yano V, Kuartei S, Roeder K, Byerley W, Devlin B, Myles-Worsley MDecember 15, 2011Not Determined
21892380Create StudySTRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE.The annals of applied statisticsPercival D, Roeder K, Rosenfeld R, Wasserman LJune 1, 2011Not Determined
21703496Create StudyIdentification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.Journal of the American Academy of Child and Adolescent PsychiatryLiu XQ, Georgiades S, Duku E, Thompson A, Devlin B, Cook EH, Wijsman EM, Paterson AD, Szatmari PJuly 2011Not Determined
21685912Create StudyIdentification of common variants influencing risk of the tauopathy progressive supranuclear palsy.Nature geneticsHöglinger GU, Melhem NM, Dickson DW, Sleiman PM, Wang LS, Klei L, Rademakers R, de Silva R, Litvan I, Riley DE, van Swieten JC, Heutink P, Wszolek ZK, Uitti RJ, Vandrovcova J, Hurtig HI, Gross RG, Maetzler W, Goldwurm S, Tolosa E, Borroni B, Pastor P, PSP Genetics Study Group, Cantwell LB, Han MR, et al.July 2011Not Determined
21658581Create StudyMultiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.NeuronSanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, Davis L, Wright NR, Dhodapkar RM, DiCola M, DiLullo NM, Fernandez TV, Fielding-Singh V, Fishman DO, Frahm S, Garagaloyan R, et al.June 9, 2011Not Determined
21480485Create StudyUsing 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 GeneticsHowrigan DP, Laird NM, Smoller JW, Devlin B, McQueen MBJune 2011Not Determined
21408211Create StudyTesting for an unusual distribution of rare variants.PLoS geneticsNeale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJMarch 2011Not Determined
21078308Create StudyDo common variants play a role in risk for autism? Evidence and theoretical musings.Brain researchDevlin B, Melhem N, Roeder KMarch 22, 2011Not Determined
21067556Create StudyShedding new light on genetic dark matter.Genome medicineMelhem N, Devlin B2010Not Determined
20862653Create StudyUsing ancestry matching to combine family-based and unrelated samples for genome-wide association studies.Statistics in medicineCrossett A, Kent BP, Klei L, Ringquist S, Trucco M, Roeder K, Devlin BDecember 10, 2010Not Determined
20711421Create StudyGenome-Wide Significance Levels and Weighted Hypothesis Testing.Statistical science : a review journal of the Institute of Mathematical StatisticsRoeder K, Wasserman LNovember 2009Not Determined
20689656Create StudyA SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY.The annals of applied statisticsLee AB, Luca D, Roeder K2010Not Determined
20663923Create StudyA genome-wide scan for common alleles affecting risk for autism.Human molecular geneticsAnney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, et al.October 15, 2010Not Determined
20531469Create StudyFunctional impact of global rare copy number variation in autism spectrum disorders.NaturePinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, et al.July 15, 2010Not Determined
20435442Create StudyConsanguinity and increased risk for schizophrenia in Egypt.Schizophrenia researchMansour H, Fathi W, Klei L, Wood J, Chowdari K, Watson A, Eissa A, Elassy M, Ali I, Salah H, Yassin A, Tobar S, El-Boraie H, Gaafar H, Ibrahim NE, Kandil K, El-Bahaei W, El-Boraie O, Alatrouny M, El-Chennawi F, Devlin B, Nimgaonkar VLJuly 2010Not Determined
20088021Create StudyScreen and clean: a tool for identifying interactions in genome-wide association studies.Genetic epidemiologyWu J, Devlin B, Ringquist S, Trucco M, Roeder KApril 2010Not Determined
19784398Create StudyHIGH DIMENSIONAL VARIABLE SELECTION.Annals of statisticsWasserman L, Roeder KJanuary 1, 2009Not Determined
19625980Create StudyNeural correlates of symptom dimensions in pediatric obsessive-compulsive disorder: a functional magnetic resonance imaging study.Journal of the American Academy of Child and Adolescent PsychiatryGilbert AR, Akkal D, Almeida JR, Mataix-Cols D, Kalas C, Devlin B, Birmaher B, Phillips MLSeptember 2009Not Determined
19513023Create StudyPhenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository.The American journal of gastroenterologyBhat 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 2009Not Determined
19455578Create StudyDiscovering genetic ancestry using spectral graph theory.Genetic epidemiologyLee AB, Luca D, Klei L, Devlin B, Roeder KJanuary 2010Not Determined
19404257Create StudyAutism genome-wide copy number variation reveals ubiquitin and neuronal genes.NatureGlessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, et al.May 28, 2009Not Determined
19278733Create StudyReplicable differences in preferred circadian phase between bipolar disorder patients and control individuals.Psychiatry researchWood J, Birmaher B, Axelson D, Ehmann M, Kalas C, Monk K, Turkin S, Kupfer DJ, Brent D, Monk TH, Nimgainkar VLApril 30, 2009Not Determined
19152378Create StudyConsanguinity 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 GeneticsMansour H, Klei L, Wood J, Talkowski M, Chowdari K, Fathi W, Eissa A, Yassin A, Salah H, Tobar S, El-Boraie H, Gaafar H, Elassy M, Ibrahim NE, El-Bahaei W, Elsayed M, Shahda M, El Sheshtawy E, El-Boraie O, El-Chennawi F, Devlin B, Nimgaonkar VLSeptember 5, 2009Not Determined
19122664Create StudyUlcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.Nature geneticsSilverberg 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 2009Not Determined
18519160Create StudySearching for disease susceptibility variants in structured populations.GenomicsRoeder K, Luca DJanuary 2009Not Determined
18252225Create StudyOn the use of general control samples for genome-wide association studies: genetic matching highlights causal variants.American journal of human geneticsLuca D, Ringquist S, Klei L, Lee AB, Gieger C, Wichmann HE, Schreiber S, Krawczak M, Lu Y, Styche A, Devlin B, Roeder K, Trucco MFebruary 2008Not Determined
17922480Create StudyPleiotropy and principal components of heritability combine to increase power for association analysis.Genetic epidemiologyKlei L, Luca D, Devlin B, Roeder KJanuary 2008Not Determined
17561376Create StudyPolymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk.Schizophrenia researchShirts BH, Kim JJ, Reich S, Dickerson FB, Yolken RH, Devlin B, Nimgaonkar VLAugust 2007Not Determined
17549760Create StudyImproving power in genome-wide association studies: weights tip the scale.Genetic epidemiologyRoeder K, Devlin B, Wasserman LNovember 2007Not Determined
17453677Create StudyAre exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?Annals of medicineKim JJ, Shirts BH, Dayal M, Bacanu SA, Wood J, Xie W, Zhang X, Chowdari KV, Yolken R, Devlin B, Nimgaonkar VL2007Not Determined
17436020Create StudyGenetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation.Human geneticsDevlin B, Klei L, Myles-Worsley M, Tiobech J, Otto C, Byerley W, Roeder KJuly 2007Not Determined
17434289Create StudyComprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.GenomicsYu CE, Seltman H, Peskind ER, Galloway N, Zhou PX, Rosenthal E, Wijsman EM, Tsuang DW, Devlin B, Schellenberg GDJune 2007Not Determined
17342507Create StudyTesting for association based on excess allele sharing in a sample of related cases and controls.Human geneticsKlei L, Roeder KJune 2007Not Determined
17322880Create StudyMapping autism risk loci using genetic linkage and chromosomal rearrangements.Nature geneticsAutism Genome Project Consortium, Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, Marshall CR, Scherer SW, Vieland VJ, Bartlett C, Mangin LV, Goedken R, Segre A, Pericak-Vance MA, Cuccaro ML, Gilbert JR, et al.March 2007Not Determined
16893532Create StudyNovel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samples.Biological psychiatryTalkowski ME, Mansour H, Chowdari KV, Wood J, Butler A, Varma PG, Prasad S, Semwal P, Bhatia T, Deshpande S, Devlin B, Thelma BK, Nimgaonkar VLSeptember 15, 2006Not Determined
16631129Create StudyEvaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples.Biological psychiatryTalkowski ME, Seltman H, Bassett AS, Brzustowicz LM, Chen X, Chowdari KV, Collier DA, Cordeiro Q, Corvin AP, Deshpande SN, Egan MF, Gill M, Kendler KS, Kirov G, Heston LL, Levitt P, Lewis DA, Li T, Mirnics K, Morris DW, Norton N, O'Donovan MC, Owen MJ, Richard C, Semwal P, et al.July 15, 2006Not Determined
16507006Create StudyAssociation study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia.Genes, brain, and behaviorMansour HA, Wood J, Logue T, Chowdari KV, Dayal M, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VLMarch 2006Not Determined
16400608Create StudyUsing linkage genome scans to improve power of association in genome scans.American journal of human geneticsRoeder K, Bacanu SA, Wasserman L, Devlin BFebruary 2006Not Determined
16152575Create StudySelection 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 GeneticsBulik CM, Bacanu SA, Klump KL, Fichter MM, Halmi KA, Keel P, Kaplan AS, Mitchell JE, Rotondo A, Strober M, Treasure J, Woodside DB, Sonpar VA, Xie W, Bergen AW, Berrettini WH, Kaye WH, Devlin BNovember 5, 2005Not Determined
16152574Create StudyLinkage 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 GeneticsBacanu SA, Bulik CM, Klump KL, Fichter MM, Halmi KA, Keel P, Kaplan AS, Mitchell JE, Rotondo A, Strober M, Treasure J, Woodside DB, Sonpar VA, Xie W, Bergen AW, Berrettini WH, Kaye WH, Devlin BNovember 5, 2005Not Determined
16103890Create StudyAutism and the serotonin transporter: the long and short of it.Molecular psychiatryDevlin 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 NetworkDecember 2005Not Determined
16094613Create StudyMultipoint linkage analysis for a very dense set of markers.Genetic epidemiologyBacanu SANovember 2005Not Determined
16076655Create StudyCircadian phase variation in bipolar I disorder.Chronobiology internationalMansour HA, Wood J, Chowdari KV, Dayal M, Thase ME, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL2005Not Determined
16027741Create StudyCatechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease.Molecular psychiatrySweet RA, Devlin B, Pollock BG, Sukonick DL, Kastango KB, Bacanu SA, Chowdari KV, DeKosky ST, Ferrell RENovember 2005Not Determined
16009739Create StudyHeritability of psychosis in Alzheimer disease.The American journal of geriatric psychiatry : official journal of the American Association for Geriatric PsychiatryBacanu SA, Devlin B, Chowdari KV, DeKosky ST, Nimgaonkar VL, Sweet RAJuly 2005Not Determined
15920508Create StudyAssociation of multiple DRD2 polymorphisms with anorexia nervosa.Neuropsychopharmacology : official publication of the American College of NeuropsychopharmacologyBergen 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 WHSeptember 2005Not Determined
15915326Create StudyLinkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia.Human geneticsKlei L, Bacanu SA, Myles-Worsley M, Galke B, Xie W, Tiobech J, Otto C, Roeder K, Devlin B, Byerley WAugust 2005Not Determined
15637716Create StudyCharacterization of multilocus linkage disequilibrium.Genetic epidemiologyRinaldo A, Bacanu SA, Devlin B, Sonpar V, Wasserman L, Roeder KApril 2005Not Determined
15637715Create StudyAnalysis of single-locus tests to detect gene/disease associations.Genetic epidemiologyRoeder K, Bacanu SA, Sonpar V, Zhang X, Devlin BApril 2005Not Determined
15601530Create StudyIntegration of association statistics over genomic regions using Bayesian adaptive regression splines.Human genomicsZhang X, Roeder K, Wallstrom G, Devlin BNovember 2003Not Determined
15514657Create StudyGenomic Control to the extreme.Nature geneticsDevlin B, Bacanu SA, Roeder KNovember 2004Not Determined
15498468Create StudyADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.GenomicsYu CE, Devlin B, Galloway N, Loomis E, Schellenberg GDSeptember 2004Not Determined
15372617Create StudyRobust estimation of critical values for genome scans to detect linkage.Genetic epidemiologyBacanu SAJanuary 2005Not Determined
15048647Create StudyAlleles 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 GeneticsDevlin B, Bennett P, Dawson G, Figlewicz DA, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD, CPEA Genetics NetworkApril 1, 2004Not Determined
14755456Create StudyHaplotypes 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 GeneticsVanyukov MM, Maher BS, Devlin B, Tarter RE, Kirillova GP, Yu LM, Ferrell REFebruary 15, 2004Not Determined
14571259Create StudyFalse discovery or missed discovery?HeredityDevlin B, Roeder K, Wasserman LDecember 2003Not Determined
12933562Create StudyGenomic control for association studies: a semiparametric test to detect excess-haplotype sharing.Biostatistics (Oxford, England)Devlin B, Roeder K, Wasserman LDecember 2000Not Relevant
12813726Create StudyEvolutionary-based association analysis using haplotype data.Genetic epidemiologySeltman H, Roeder K, Devlin BJuly 2003Not Determined
12813725Create StudyAnalysis of multilocus models of association.Genetic epidemiologyDevlin B, Roeder K, Wasserman LJuly 2003Not Determined
12675687Create StudyCladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease.Annals of human geneticsWang GQ, DiPietro M, Roeder K, Heng CK, Bunker CH, Hamman RF, Kamboh MIMarch 2003Not Determined
12610778Create StudyOn the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.American journal of human geneticsTzeng JY, Devlin B, Wasserman L, Roeder KApril 2003Not Determined
12476400Create StudySignificant linkage on chromosome 10p in families with bulimia nervosa.American journal of human geneticsBulik CM, Devlin B, Bacanu SA, Thornton L, Klump KL, Fichter MM, Halmi KA, Kaplan AS, Strober M, Woodside DB, Bergen AW, Ganjei JK, Crow S, Mitchell J, Rotondo A, Mauri M, Cassano G, Keel P, Berrettini WH, Kaye WHJanuary 2003Not Determined
12210285Create StudyNo evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.American journal of medical geneticsDevlin 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 NetworkAugust 8, 2002Not Determined
12192612Create StudyGenome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau.Molecular psychiatryDevlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B, Novasad D, Chu A, TCuenco K, Tiobek S, Otto C, Byerley W2002Not Determined
12105318Create StudyLinkage analysis of Alzheimer disease with psychosis.NeurologyBacanu SA, Devlin B, Chowdari KV, DeKosky ST, Nimgaonkar VL, Sweet RAJuly 9, 2002Not Determined
12023979Create StudyAssociation and linkage analyses of RGS4 polymorphisms in schizophrenia.Human molecular geneticsChowdari KV, Mirnics K, Semwal P, Wood J, Lawrence E, Bhatia T, Deshpande SN, B K T, Ferrell RE, Middleton FA, Devlin B, Levitt P, Lewis DA, Nimgaonkar VLJune 1, 2002Not Determined
11914406Create StudyIncreased familial risk of the psychotic phenotype of Alzheimer disease.NeurologySweet RA, Nimgaonkar VL, Devlin B, Lopez OL, DeKosky STMarch 26, 2002Not Determined
11912184Create StudyLinkage analysis of anorexia nervosa incorporating behavioral covariates.Human molecular geneticsDevlin B, Bacanu SA, Klump KL, Bulik CM, Fichter MM, Halmi KA, Kaplan AS, Strober M, Treasure J, Woodside DB, Berrettini WH, Kaye WHMarch 15, 2002Not Determined
11855950Create StudyGenomic control, a new approach to genetic-based association studies.Theoretical population biologyDevlin B, Roeder K, Wasserman LNovember 2001Not Determined
11754475Create StudyAssociation studies for quantitative traits in structured populations.Genetic epidemiologyBacanu SA, Devlin B, Roeder KJanuary 2002Not Determined
11754473Create StudyMixture models for linkage analysis of affected sibling pairs and covariates.Genetic epidemiologyDevlin B, Jones BL, Bacanu SA, Roeder KJanuary 2002Not Determined
11754464Create StudyUnbiased methods for population-based association studies.Genetic epidemiologyDevlin B, Roeder K, Bacanu SADecember 2001Not Determined
11499679Create StudyGenome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania.Human geneticsDevlin B, Roeder K, Otto C, Tiobech S, Byerley WJune 2001Not Determined
11318178Create StudyFlexible parametric measurement error models.BiometricsCarroll RJ, Roeder K, Wasserman LMarch 1999Not Determined
11315092Create StudyGenomic control for association studies.BiometricsDevlin B, Roeder KDecember 1999Not Relevant
11309689Create StudyTransmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes.American journal of human geneticsSeltman H, Roeder K, Devlin BMay 2001Not Determined
11119294Create StudyA Bayesian hierarchical model for allele frequencies.Genetic epidemiologyLockwood JR, Roeder K, Devlin BJanuary 2001Not Determined
10801388Create StudyThe power of genomic control.American journal of human geneticsBacanu SA, Devlin B, Roeder KJune 2000Not Relevant
10677324Create StudyHaplotype fine mapping by evolutionary trees.American journal of human geneticsLam JC, Roeder K, Devlin BFebruary 2000Not Relevant
10657297Create StudyMutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.Science (New York, N.Y.)Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW, Cornelisse CJ, Devilee P, Devlin BFebruary 4, 2000Not Determined

Relevant Publications
PubMed IDStudyTitleJournalAuthorsDate
28569757Create StudyFetal and postnatal metal dysregulation in autism.Nature communicationsArora M, Reichenberg A, Willfors C, Austin C, Gennings C, Berggren S, Lichtenstein P, Anckarsäter H, Tammimies K, Bölte SJune 2017
Data Expected
Data ExpectedTargeted EnrollmentInitial SubmissionSubjects SharedStatus
genomics/omics info iconApproved
Structure not yet defined

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 NameAbstractCollection/Study SubjectsData UsageState
Genotypes of Swedish subjects used in "Most genetic risk for autism resides with common variation" studyA 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.548/548Primary AnalysisShared
* Data not on individual level