-
Autism Sequencing Consortium (ASC)
Study
phs000298
-
Genetic Study on Nephropathy in Type-2 Diabetes
Study
phs000302
-
Genetic Epidemiology of Refractive Error in the KORA (Kooperative Gesundheitsforschung in der Region Augsburg) Study
Study
phs000303
-
Genes and Blood Clotting Study (GABC)
Study
phs000304
-
A Genome-Wide Association Study in Participants Experiencing Breast Cancer Events in High-Risk Postmenopausal Women Receiving Selective Estrogen Receptor Modulators on NSABP Trials P-1 and P-2. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000305
-
A Multiethnic Genome-wide Scan of Prostate Cancer
Study
phs000306
-
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Study
phs000308
-
Coronary Artery Risk Development in Young Adults (CARDIA) Study - Gene Environment Association Studies Initiative (GENEVA)
Study
phs000309
-
Towards a Genomic Understanding of Myeloma
Study
phs000348
-
SardiNIA Medical Sequencing Discovery Project
Study
phs000313
-
Genetic Associations in Idiopathic Talipes Equinovarus (Clubfoot) - GAIT
Study
phs000314
-
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Siblings with Ischemic Stroke Study, SWISS)
Study
phs000327
-
Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma)
Study
phs000328
-
A Genome-Wide Association Study in Patients Experiencing Drug-Induced Long-QT Syndrome and/or Torsades de Pointes; A Collaboration Between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000331
-
Genome-Wide Association Study of Preterm Birth
Study
phs000332
-
Family Investigation of Nephropathy and Diabetes (FIND) Study
Study
phs000333
-
Genome-Wide associations of Lung Health Study (LHS)
Study
phs000335
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
Genetic Basis of Developmental Disabilities
Study
phs000337
-
National Institute on Aging (NIA) SardiNIA Study
Study
phs000338
-
Targeted MitoExome Sequencing of Mitochondrial OXPHOS Diseases (Massachusetts General Hospital)
Study
phs000339
-
SNPs and Extent of Atherosclerosis (SEA) Study
Study
phs000349
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
The Genetic Basis of Hypodiploid ALL
Study
phs000341
-
The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) Trial
Study
phs000343
-
Genome-Wide Association Study of Amyotrophic Lateral Sclerosis in Finland
Study
phs000344
-
NIDDK IBD Genetics Consortium Ulcerative Colitis Genome-Wide Association Study
Study
phs000345
-
Genome-wide association study for Bladder Cancer Risk
Study
phs000346
-
NHLBI GO-ESP: Family Studies (Thoracic aortic aneurysms leading to acute aortic dissections)
Study
phs000347
-
Fred Hutchinson Cancer Research Center - Whole-Exome Sequencing of Hereditary Prostate Cancer Families
Study
phs000350
-
National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs000351
-
The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft
Study
phs000352
-
Genome-Wide Association Studies of Prematurity and Its Complications (African American)
Study
phs000353
-
NHLBI GO-ESP Family Studies: Pulmonary Arterial Hypertension
Study
phs000354
-
Genome-Wide Association Studies in Upper Gastrointestinal Cancers (Asian)
Study
phs000361
-
Genome Wide Association for Asthma and Lung Function
Study
phs000355
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
Autopsy-Confirmed Parkinson Disease GWAS Consortium (APDGC)
Study
phs000394
-
Genome-Wide Association Study in Systemic Sclerosis
Study
phs000357
-
eMERGE Network Genome-Wide Association Study of Red Cell Indices, White Blood Count (WBC) Differential, Diabetic Retinopathy, Height, Serum Lipid Levels, Specifically Total Cholesterol, HDL (High Density Lipoprotein), LDL (Low Density Lipoprotein), and Triglycerides, and Autoimmune Hypothyroidism.
Study
phs000360
-
NIDDK⁄CIDR Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease
Study
phs000367
-
NHLBI GO-ESP: Family Studies (Familial Atrial Fibrillation)
Study
phs000362
-
High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases
Study
phs000364
-
Exome Sequencing for Diseases of the Immune System: X-linked Immunodeficiency with Magnesium Defect, EBV Infection, and Neoplasia (XMEN)
Study
phs000365
-
NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD)
Study
phs000366
-
Polycystic Ovary Syndrome (PCOS) Genetics
Study
phs000368
-
Genetic Modifiers of Huntington's Disease
Study
phs000371
-
Alzheimer's Disease Genetics Consortium (ADGC) Genome Wide Association Study -NIA Alzheimer's Disease Centers Cohort
Study
phs000372
-
Osteoporotic Fractures in Men (MrOS)
Study
phs000373
-
Genome-Wide Association of Native and Post Aspirin Platelet Function Phenotypes
Study
phs000375