-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307
-
Whole Exome Sequencing of Colorectal Cancer Patients from the Nurses' Health Study (NHS) and Health Professionals Follow-up Study (HPFS)
Study
phs000722
-
GUARDIAN: The Insulin Resistance Atherosclerosis Family Study (IRASFS)
Study
phs001008
-
Pediatric Investigation for Genetic Factors Linked with Renal Progression (PediGFR)
Study
phs000842
-
New England-Based Case-Control Study of Ovarian Cancer
Study
phs001034
-
Addictions: Genotypes, Polymorphisms, and Function/Human Genetic Correlates of Addictive Diseases
Study
phs001109
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections
Study
phs000719
-
Next Generation Mendelian Genetics: Malignant Hyperthermia
Study
phs000405
-
Biological Determinants of Peritoneal Dialysis Outcomes
Study
phs002996
-
Peripheral Blood Transcriptome Analysis of ALS Patients
Study
phs002055
-
Maternal Plasma Folate and DNA Methylation in Epigenome-Wide Meta-Analysis of Newborns
Study
phs001059
-
Population Architecture using Genomics and Epidemiology (PAGE)
Study
phs000356
-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Study
phs001644
-
Towards a Genomic Understanding of Myeloma
Study
phs000348
-
Intervention with Micronutrients and Long-Term Impact in Brazil-RECODISA
Study
phs003174
-
Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
Study
phs001687
-
Clinical and genetic analysis of retinopathy of prematurity - GWAS
Study
phs002020
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs000799
-
Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study - Maternal Glycemia and Birthweight GEI Study
Study
phs000096
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
A Genome-Wide Association Study of Heroin Dependence
Study
phs000277
-
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