-
ALS Compute
Study
phs003184
-
Joslin Study on the Genetics of Type 2 Diabetes
Study
phs002959
-
Genome-Wide Association Study of Anorexia Nervosa (Price Foundation, Klarman Family Foundation, Center for Applied Genomics at the Children's Hospital of Philadelphia, Scripps Translational Sciences Institute Clinical Translational Science Award)
Study
phs000679
-
Genetic Components of Knee Osteoarthritis (GeCKO) Study: The Osteoarthritis Initiative
Study
phs000955
-
Discovering the Genetic Basis of Cleft Palate: CIDR
Study
phs002220
-
Genome wide association study for early onset coronary disease and related phenotypes (ADVANCE)
Study
phs000423
-
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Study
phs001091
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011
-
NHLBI and NIA The New England Centenarian Study (NECS)
Study
phs000451
-
Female Infertility: Primary Ovarian Insufficiency
Study
phs001174
-
Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea
Study
phs001260
-
Brain Arteriovenous Malformation Genetics Study
Study
phs002069
-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Study
phs000893
-
NINDS-Genome-Wide Genotyping in Parkinson's Disease: First Stage Analysis and Public Release of Data
Study
phs000089
-
Genetic Discovery and Application in a Clinical Setting: Continuing a Partnership (eMERGE Phase II)
Study
phs000948
-
Center for Craniofacial and Dental Genetics: Study of Dental Caries and Cleft Lip/Palate in Guatemala
Study
phs000440
-
Germ Cell Tumor Molecular Heterogeneity Revealed through Analysis of Primary and Metastasis Pairs
Study
phs002229
-
3/7 Psychiatric Genomics Consortium: Finding Actionable Variation
Study
phs003138
-
NHLBI Recipient Epidemiology Donor Evaluation Study (REDS)-III - Red Blood Cell Omics (RBC-Omics) Study
Study
phs001955
-
Sequencing of Cervical Cancer
Study
phs000723
-
Natural History and Structural Functional Relationships in Fabry Renal Disease
Study
phs001333
-
A Study of the Genetic Causes of Complex Pediatric Disorders
Study
phs000490
-
Zostavax vaccination-induced changes in the T cell receptor repertoire to varicella zoster virus
Study
phs001082
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219