NINDS Samples in dbGaP

Several thousand samples from the NINDS repository have been used in studies reported in the database of phenotypes and genotypes (dbGaP). The file available for download lists all NINDS repository samples included in one or more dbGaP submissions. 

To view a list of NINDS Repository samples used in dbGaP studies, please click on the link below: 

To view a searchable list of dbGaP submissions, please click on the link below:

dbGaP study search


dbGaP submissions containing NINDS Repository samples are outlined below:

Study Accession Study Title # NINDS Repository Case Samples # NINDS Repository Control Samples Genomic Assay
phs000126 CIDR: Genome Wide Association Study in Familial Parkinson Disease (PD) 0 895

Illumina HumanCNV370v1

phs000101.v5.p1

NIH Genome-Wide Association Studies of Amyotrophic Lateral Sclerosis

580 786

Illumina HumanOmniExpress-24 v1.0

phs000101.v4.p1

NIH Genome-Wide Association Studies of Amyotrophic Lateral Sclerosis

97 0

whole exome sequencing

phs000102

Ischemic Stroke Genetics Study (ISGS)

71 266

Illumina HumanHap300v1 and Illumina Infinium Human-1

phs000636

CIDR_Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study

27 0

whole exome sequencing

phs000089

National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease

259 779

Illumina HumanHap550

phs001103

National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease

27
0

whole exome sequencing

phs000654

Epi4K: Gene Discovery in 4,000 Epilepsy Genomes

329
664

whole exome sequencing