-
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