-
Pharmacogenomics of HIV Therapy - Atazanavir Bilirubin-related Side Effects
Study
phs001484
-
Somatic Mutations and Cell Lineage in the Human Brain
Study
phs001485
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Epilepsy: Epi25 Consortium
Study
phs001489
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: BioMe Biobank Program
Study
phs001490
-
Genetics of Disorders Affecting Tooth Structure, Number, Morphology and Eruption
Study
phs001491
-
A Genomic Approach to Warfarin Dose Prescription in Admixed Caribbean Hispanics
Study
phs001496
-
UCSF Adult Glioma Study
Study
phs001497
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Meta-analysis
Study
phs001499
-
Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure
Study
phs001501
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: Research Studies in Hong Kong
Study
phs001504
-
Host Genetic Determinants of the Outcome of Staphylococcus Aureus Bacteremia by Whole Exome Sequencing
Study
phs001505
-
Columbia-Yale-Bilkent Study: Genetics Study of Essential Tremor
Study
phs001507
-
Genetic Analysis of Metopic Nonsyndromic Craniosynostosis
Study
phs001508
-
Progress in Diabetes Genetics in Youth (ProDIGY) Exome Sequencing Study: SEARCH for Diabetes in Youth
Study
phs001511
-
Gene Expression Signatures Characterized by Longitudinal Stability and Inter-Individual Variability Delineate Baseline Phenotypic Groups with Distinct Responses to Immune Stimulation
Study
phs001512
-
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
-
Genetics of Human Inherited Retinal Diseases (GHIRD)
Study
phs001517
-
Translational Research Investigating Underlying disparities in acute Myocardial infarction Patients' Health status (TRIUMPH)
Study
phs001518
-
Genome and Transcriptome Assembly Reveals SVA-Mediated Aberrant Splicing in X-Linked Dystonia Parkinsonism
Study
phs001525
-
Germline
Study
phs001522
-
The Genetic Basis of Aggressive Prostate Cancer, The Role of Rare Variation
Study
phs001524
-
Genetic Study of Inflammatory Bowel Disease (IBD) in African Americans
Study
phs001571
-
Gene Expression of Small Cell Carcinoma of the Ovary-Hypercalcemic Type (SCCOHT)
Study
phs001528
-
Whole exome sequencing to discover genetic variation associated with aortopathy in Turner Syndrome
Study
phs001531
-
The epigenetic landscape controlled by p63 in epidermal development
Study
phs001737