To view a list of NINDS Repository samples used in dbGaP studies, please click on the link 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 |
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 |
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 | 936 | 800 | Illumina HumanHap550 |
| phs001103 | National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease | 618 | 0 | whole exome sequencing |
| phs000654 | Epi4K: Gene Discovery in 4,000 Epilepsy Genomes | 329 | 664 | whole exome sequencing |
| phs001380.v1.p1 | Genomic Studies of Gilles de la Tourette Syndrome | 15 | 0 | Illumina Human610_Quadv1_B |
| phs001380.v1.p1 | Genomic Studies of Gilles de la Tourette Syndrome | 1880 | 0 | Illumina Infinium OmniExpressExome-8v1-1_A |
| phs001380.v1.p1 | Genomic Studies of Gilles de la Tourette Syndrome | 378 | 0 | whole exome sequencing |
| phs001585.v3.p1 | Identification of ALS Associated Genes Using Whole Genome Sequencing | 70 | 0 | whole genome sequencing |
| phs001004.v1.p1 | Genetic Analysis of Parkinson's Disease | 362 | 0 | whole exome sequencing |
