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Browse curated datasets across OpenNeuro, HCP, ABCD, NDA, and more. Use search and filters to narrow down quickly.
Multi-site datasets with extensive participant counts for population-level analyses.
Massive midlife/aging population imaging within UK Biobank
National US clinical dataset with neuropsych, diagnoses, and imaging subsets
Longitudinal US cohort on child/adolescent brain development, behavior, and environment
Multimodal biomarker study in early Parkinson’s disease
Handpicked datasets focused on psychiatric, neurological, and developmental conditions.
National US clinical dataset with neuropsych, diagnoses, and imaging subsets
Multimodal biomarker study in early Parkinson’s disease
Italian memory clinic cohort with MRI, EEG, and biomarkers for dementia research
Multi-site ASD vs control resting-state fMRI and structural MRI
Datasets featuring resting-state paradigms, movies, or naturalistic stimuli.
Multi-site ASD vs control resting-state fMRI and structural MRI
Young-adult structural and resting fMRI with behavioral and some genetic data
Multi-site aggregation of resting-state fMRI datasets for mapping intrinsic connectivity
Multi-site resting-state fMRI meta-dataset for major depressive disorder
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Massive midlife/aging population imaging within UK Biobank
National US clinical dataset with neuropsych, diagnoses, and imaging subsets
Longitudinal US cohort on child/adolescent brain development, behavior, and environment
Multimodal biomarker study in early Parkinson’s disease
Pediatric mental health biobank with MRI, EEG, behavior, and genomics
Italian memory clinic cohort with MRI, EEG, and biomarkers for dementia research
Multi-site ASD vs control resting-state fMRI and structural MRI
Longitudinal adolescent imaging-genetics study of mental health and addiction
No description available.
Twin adolescent neuroimaging cohort, with microbiome and phenotyping
Open MRI (and PET in OASIS-3) datasets for aging & Alzheimer’s research
Young-adult structural and resting fMRI with behavioral and some genetic data
Multi-site aggregation of resting-state fMRI datasets for mapping intrinsic connectivity
Community-based lifespan sample with deep phenotyping and multimodal MRI
Longitudinal multi-center imaging and biomarker study of Alzheimer’s disease
Pediatric multi-site normative cohort linking brain, cognition, genetics
Youth cohort linking clinical risk, cognition, and MRI
Three multimodal MRI datasets (ID1000, PIOP1, PIOP2) for individual-differences research
Structural and functional connectivity in children and adolescents
Multi-site resting-state fMRI meta-dataset for major depressive disorder
Lifespan connectome data for midlife to very old adults
Flagship young-adult connectome dataset with high-res multi-modal MRI
No description available.
Neonatal and fetal MRI to characterize early structural and functional connectivity
No description available.
Longitudinal Australian cohort on aging and AD with MRI, PiB-PET, and biomarkers
Federated portal aggregating MRI datasets for schizophrenia
No description available.
No description available.
No description available.
Multi-site ADHD vs control resting-state fMRI along with phenotypic data
No description available.
Lifespan cohort with MRI/MEG and cognitive tests for healthy aging
Multi-scanner structural MRI dataset for normal adult brains
Longitudinal twin study of male aging with MRI and cognition
Structural and functional MRI of infants/toddlers for early brain connectivity mapping
Healthy adult lifespan MRI dataset from Chinese cohort
No description available.
No description available.
Longitudinal MRI and clinical study of FTD and controls
No description available.
fMRI responses to naturalistic spoken stories with aligned transcripts
Young adult twin neuroimaging cohort for heritability of brain structure
No description available.
Longitudinal imaging of 4-repeat tauopathies (PSP/CBD) with MRI and tau PET
No description available.
No description available.
The Consortium for Neuropsychiatric Phenomics (CNP) is a large study funded by the NIH Roadmap Initiative that aims to facilitate discovery of the genetic and environmental bases of variation in psychological and neural system phenotypes, to elucidate the mechanisms that link the human genome to complex psychological syndromes, and to foster breakthroughs in the development of novel treatments for neuropsychiatric disorders. The study includes imaging of a large group of healthy individuals from the community (138 subjects), as well as samples of individuals diagnosed with schizoprenia (58), bipolar disorder (49), and ADHD (45). The participants, ages 21-50, were recruited by community advertisements from the Los Angeles area and completed extensive neuropsychogical testing, in addition to fMRI scanning. To be included individuals had to be either 'White, Not of Hispanic or Latino Origin' or 'Hispanic or Latino, of Any Race' following NIH designations of racial and ethnic minority groups, and have completed at least 8 years of education (other racial and ethnic minority groups were excluded because this was thought to increase risk of confounding planned genetic studies). For participants who spoke both English and Spanish, language for testing was determined by a verbal fluency test. Participants were screened for neurological disease, history of head injury with loss of consciousness or cognitive sequelae, use of psychoactive medications, substance dependence within past 6 months, history of major mental illness or ADHD, and current mood or anxiety disorder. Self-reported history of psychopathology was verified with the SCID-IV (First, Spitzer, Gibbon, & Williams, 1995). Urinalysis was used to screen for drugs of abuse (cannabis, amphetamine, opioids, cocaine, benzodiazepines) on the day of testing and excluded if results were positive. A portion of this large sample took part in two separate fMRI sessions, which each included one-hour of behavioral testing and a one-hour scan on the same day. Participants were recruited from the parent study to participate in the fMRI portion if they successfully completed all previous testing sessions, and did not meet the following additional exclusion criteria: history of significant medical illness, contraindications for MRI (including pregnancy), any mood-altering medication on scan day (based on self-report), vision that was insufficient to see task stimuli, and left-handedness. After receiving a thorough explanation, all participants gave written informed consent according to the procedures approved by the University of California Los Angeles Institutional Review Board. Modalities Include: T1-weighted Anatomical MPRAGE, 64 Direction DWI, BOLD contrast fMRI, Resting State (with physiological monitoring), Breath Hold fMRI (with physiological monitoring), Balloon Analog Risk Task (BART) fMRI, Stopsignal Task fMRI, Taskswitching fMRI, Spatial Working Memory Capacity Tasks (SCAP) fMRI, Paired Associates Memory Task - Encoding/Retrieval (PAMenc/PAMret)
No description available.
No description available.
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No description available.