-
Center Common Disease Genomics [CCDG] - CVD - TAICHI
Study
phs001487
-
Evaluating genetic ancestry and self-reported ethnicity in the context of carrier screening
Study
phs001482
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - germline whole genome sequencing
Study
phs001483
-
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
-
Nicotine dependence GWAS meta-analysis across European and African American ancestries
Study
phs001532
-
Offspring Sex Impacts DNA Methylation and Gene Expression in Placentae from Women with Diabetes during Pregnancy
Study
phs001535
-
North American Mitochondrial Disease Consortium Patient Registry and Biorepository
Study
phs001538
-
Anorexia Nervosa Genetics Initiative (ANGI)
Study
phs001541
-
NHLBI TOPMed: Genetics of Asthma in Latino Americans (GALA)
Study
phs001542
-
NHLBI TOPMed - NHGRI CCDG: AF Biobank LMU in the context of the MED Biobank LMU
Study
phs001543
-
NHLBI TOPMed: Determining the Association of Chromosomal Variants with Non-PV Triggers and Ablation-Outcome in AF (DECAF)
Study
phs001546
-
NHLBI TOPMed - NHGRI CCDG: The GENetics in Atrial Fibrillation (GENAF) Study
Study
phs001547
-
The Genetic and Transcriptomic Evolution of Melanoma
Study
phs001550
-
Epilepsy Genetics Initiative
Study
phs001551
-
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow up Study: Pakistan Genomic Resource (PGR)
Study
phs001552
-
Detection of Colorectal Cancer Susceptibility Loci Using Genome-Wide Sequencing
Study
phs001554
-
BRAIN Cell EncyclOpeDia of Transcribed Elements (BRAINcode)
Study
phs001556
-
Contribution of Genetic Polymorphisms to the Abuse Liability of Oxycodone
Study
phs001559
-
Novel Factors for Unexplained Phenotypes of Subclinical Carotid Atherosclerosis
Study
phs001560
-
WES Elucidation of Pathogenetic Mechanisms for Immune System Disorders and NIAID Pilot of Genetic Incidental Finding Management
Study
phs001561
-
Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity
Study
phs001566
-
Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines
Study
phs001581
-
eMERGE Network Phase III: HRC SNV and 1000 Genomes SV Imputed Array Data of 105,000 Participants
Study
phs001584
-
Identification of ALS Associated Genes Using Whole Genome Sequencing
Study
phs001585
-
Characterization of prostate cancer organoids
Study
phs001587
-
Relationship between low LDL cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: a US-based cross-sectional observational study using electronic medical records
Study
phs001588