-
SardiNIA Medical Sequencing Discovery Project
Study
phs000313
-
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Study
phs000433
-
ARRA - NHLBI Lung Cohorts Sequencing Project: Genetic modifiers of
Study
phs000254
-
NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
-
Genomics of Pediatric Renal Medullary Carcinomas
Study
phs001800
-
Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi
Study
phs001320
-
The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN)
Study
phs000615
-
Genetic Association Studies in the Solomon Islanders
Study
phs000493
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
Genomic Variation in Diffuse Large B Cell Lymphomas
Study
phs001444
-
Nature and Contribution of Noncoding, Regulatory Mutations in Neurodevelopmental Disorders
Study
phs001874
-
Next Generation Mendelian Genetics: Muscle Hypertrophy
Study
phs000541
-
Exome Sequencing of Schizophrenia Cases and Controls in the South African Xhosa Population
Study
phs000959
-
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Study
phs001246
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Advanced Genetic and Molecular Analysis of Solid Tumors
Study
phs001999
-
Genomics of Brain Metastases
Study
phs000730
-
Genetic Study of Vascular Anomalies
Study
phs003197
-
NHLBI GO-ESP Family Studies: Idiopathic Bronchiectasis of unknown etiology that is not related to cystic fibrosis or classic primary ciliary dyskinesia or immune deficiency or any other known causes
Study
phs000518
-
Washington University Coronary Artery Disease Study
Study
phs001227
-
Pharmacogenomics of HIV Therapy - Atazanavir Bilirubin-related Side Effects
Study
phs001484
-
Gabriella Miller Kids First Pediatric Research Program in Craniofacial Microsomia
Study
phs002130
-
PGRN-Leducq: Identification of the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
Study
phs000617
-
NHLBI: Genetic modifiers of sickle cell anemia severity and fetal hemoglobin expression in the Cooperative Study of Sickle Cell Disease (CSSCD)
Study
phs000366
-
NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001468