-
Slim Initiative in Genomic Medicine for the Americas (SIGMA): Mexico City Diabetes Study (MCDS)
Study
phs001375
-
Epigenetics of Cocaine and Nicotine Addiction
Study
phs001377
-
A Joint Linkage/Association Strategy to Interrogate AMD Genetic Susceptibility
Study
phs001379
-
Genomic Studies of Gilles de la Tourette Syndrome
Study
phs001380
-
Birth Defects: Moebius Syndrome and Related Congenital Facial Weakness Disorders
Study
phs001383
-
Time Lapse to Cancer-Defining the Transition from Polyp to Cancer
Study
phs001384
-
Slim Initiative in Genomic Medicine for the Americas (SIGMA): Diabetes in Mexico Study (DMS)
Study
phs001388
-
OncoArray: Prostate Cancer
Study
phs001391
-
The Hypertension-Insulin Resistance Family Study (HTN-IR)
Study
phs001394
-
Genetics of Pigmentation in Eastern and Southern African Populations Study
Study
phs001396
-
The Mexican-American Coronary Artery Disease Study (MACAD)
Study
phs001397
-
Center for Common Disease Genomics [CCDG] - Cardiovascular: The Bangladesh Risk of Acute Vascular Events (BRAVE) Study
Study
phs001398
-
Deep Sequencing Studies for Cannabis and Stimulant Dependence
Study
phs001458
-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
Molecular Profiling of Gallbladder Cancer (MPOG)
Study
phs001404
-
LCCC1122: Defining the Triple Negative Breast Cancer Kinome Response to GSK1120212
Study
phs001405
-
Large Scale Genotyping of Psychiatric Disorders
Study
phs001413
-
Uncovering the Genetic Architecture of Colorectal Cancer with Focus of Rare and Less Frequent Variants
Study
phs001415
-
National Institute of Mental Health (NIMH) Duke Cognition Cohort
Study
phs001406
-
Understanding the genetic risk underlying racial disparities in uterine fibroids
Study
phs001409
-
Kids First: Pediatric Research Project on Adolescent Idiopathic Scoliosis
Study
phs001410
-
Action to Control Cardiovascular Risk in Diabetes (ACCORD) Clinical Trial
Study
phs001411
-
NHLBI TOPMed: MESA and MESA Family AA-CAC
Study
phs001416
-
Interpreting molecular role of DNA variants associated with Crohn's Disease through integrative analysis of open chromatin, epigenome and transcriptome data in diverse and relevant tissues and cells
Study
phs001418
-
Kids First: Genomics of Orofacial Cleft Birth Defects in Latin American Families
Study
phs001420
-
Whole exome sequencing and methylation profiling of uveal melanoma
Study
phs001421
-
GEnomics and Transcriptomics of Human INsulinoma (GETHIN)
Study
phs001422
-
Tourette International Collaborative Genetics (TIC Genetics) Study - NJCTS and NIMH
Study
phs001423
-
NHLBI TOPMed: Australian Familial Atrial Fibrillation Study
Study
phs001435
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
Genomic Analysis of Pre-Treatment and Autopsy Glioblastoma Specimens
Study
phs001424
-
Type 1 Diabetes Genetics Consortium (T1DGC): Case-only RNA-Seq Study
Study
phs001426
-
Genome-Wide Predictors of Treatment-Related Toxicities in SWOG S0221 Trial
Study
phs001428
-
Pediatric Preclinical Testing Consortium (PPTC)
Study
phs001437
-
Non-coding RNAs Activated by the Wnt/Beta-catenin Signaling Pathway in Hepatoblastoma
Study
phs001433
-
NHLBI TOPMed: Defining the Time-Dependent Genetic and Transcriptomic Responses to Cardiac Injury Among Patients with Arrhythmias
Study
phs001434
-
NHLBI TOPMed: Study of Asthma Phenotypes and Pharmacogenomic Interactions by Race-Ethnicity (SAPPHIRE)
Study
phs001467
-
University of Utah Pelvic Organ Prolapse Disorder Study
Study
phs001439
-
Admixture Mapping of Staphylococcus aureus Bacteremia
Study
phs001441
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001442
-
Genomic Variation in Diffuse Large B Cell Lymphomas
Study
phs001444
-
Genomic Resistance Patterns to Second Generation Androgen Blockade in Paired Tumor Biopsies of Metastatic Castrate-Resistant Prostate Cancer
Study
phs001447
-
Multiregion Sequencing of Localized Prostate Cancer
Study
phs001465
-
NHLBI TOPMed: Pharmacogenomics of Hydroxyurea in Sickle Cell Disease (PharmHU)
Study
phs001466
-
NHLBI TOPMed: Recipient Epidemiology and Donor Evaluation Study-III Brazil Sickle Cell Disease Cohort (REDS-BSCDC)
Study
phs001468
-
NHLBI TOPMed: Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Study
phs001472
-
Clonal Evolution and Transcriptomic Analysis of Chronic Lymphocytic Leukemia Treated with Ibrutinib
Study
phs001473
-
Field Studies of Human Immunity to Amebiasis in Bangladesh (NIH Birth Cohort) and Exploration of the Biologic Basis for Underperformance of Oral Polio and Rotavirus Vaccines in Bangladesh (PROVIDE)
Study
phs001475
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
Etiological Investigation of Cancer Susceptibility in Inherited Bone Marrow Failure Syndromes: A Natural History Study
Study
phs001481
-
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