-
Genetics of Cerebral Hemorrhage with Anticoagulation (GOCHA)
Study
phs000416
-
BrainCloud: Data from human postmortem brain procurement for the neuropathology section
Study
phs000417
-
Temporal Dissection of Tumorigenesis in Primary Cancers
Study
phs000418
-
A Genome-Wide Association Study of Fuchs' Endothelial Corneal Dystrophy (FECD)
Study
phs000421
-
NHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Asthma): Genetic variants affecting susceptibility and severity
Study
phs000422
-
Genome wide association study for early onset coronary disease and related phenotypes (ADVANCE)
Study
phs000423
-
Common Fund (CF) Genotype-Tissue Expression Project (GTEx)
Study
phs000424
-
Alcohol Dependence GWAS in European- and African Americans
Study
phs000425
-
SLCO1B1 Variants and Methotrexate Clearance
Study
phs000426
-
Health and Retirement Study (HRS)
Study
phs000428
-
GWAS for IgA Nephropathy
Study
phs000431
-
The Sea Islands Genetic Network (SIGNET): Identifying genetic contributors to diabetes and dyslipidemia in African Americans
Study
phs000433
-
Next Generation Mendelian Genetics: Atypical Werner Syndrome
Study
phs000434
-
Whole Exome Sequencing of Chronic Lymphocytic Leukemia
Study
phs000435
-
University of Miami Study on Genetics of Autism and Related Disorders (AutismDisorders)
Study
phs000436
-
Next Generation Mendelian Genetics: Auriculocondylar syndrome (ACS)
Study
phs000437
-
A Genome-Wide Association Analysis in Angiotensin-Converting Enzyme (ACE) Inhibitor-Associated Angioedema and ACE Inhibitor-Exposed Controls; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Center for Genomic Medicine
Study
phs000438
-
A Genome-Wide Association Comparative Analysis of Response of AF Patients to Rate Control Therapy; A Collaboration between the NIH Pharmacogenomics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000439
-
Center for Craniofacial and Dental Genetics: Study of Dental Caries and Cleft Lip/Palate in Guatemala
Study
phs000440
-
Drug Resistant Hypertension in African Americans' Exome
Study
phs000442
-
Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort
Study
phs000448
-
Genetic Variation and Signatures of Natural Selection in Diverse Africans
Study
phs000449
-
Whole Exome Sequencing of Primary Mediastinal B-cell Lymphoma
Study
phs000450
-
NHLBI and NIA The New England Centenarian Study (NECS)
Study
phs000451
-
Genome-Wide Association Study of HIV-1 Host Genetics Among Injection Drug Users
Study
phs000454
-
Molecular Genetic Studies of Developmental Brain Disorders
Study
phs000455
-
Risk Assessment of Cerebrovascular Events (RACE) Study
Study
phs000456
-
Estrogen Receptor Positive Breast Cancer: Aromatase Inhibitor Response Study
Study
phs000472
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in NEIGHBOR Samples
Study
phs000458
-
Genetics of 24 hour urine composition
Study
phs000460
-
Identification of Cancer Predisposition Genes in Breast Cancer Families
Study
phs000480
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Study
phs000461
-
T2D-GENES Project 2: San Antonio Mexican American Family Studies
Study
phs000462
-
Sweden-Schizophrenia Population-Based Case-Control Exome Sequencing
Study
phs000473
-
Biology and Molecular Analysis of Human Hematopoiesis Genetics
Study
phs000474
-
The molecular basis of inherited reproductive disorders
Study
phs000475
-
Molecular defects in pseudohypoparathyroidism or related disorders
Study
phs000476
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Study
phs000482
-
Genetic defects in familial renal disorders
Study
phs000477
-
Strabismus, CCDD and other anomalies
Study
phs000478
-
Genome-Wide Analysis of Splenic Marginal Zone Lymphoma
Study
phs000502
-
Cholesterol and Pharmacogenetics (CAP) Study
Study
phs000481
-
Massachusetts General Hospital/Eisai National Institute of Mental Health (NIMH) Genetics Initiative Alzheimer's Disease GWAS - Affymetrix GeneChip Human Mapping 500K Array Set
Study
phs000483
-
Molecular genetic analysis of inherited kidney dysfunction
Study
phs000484
-
Integration of Genomics and Transcriptomics in unselected Twins and in Major Depression
Study
phs000486
-
A Study of the Genetic Causes of Complex Pediatric Disorders
Study
phs000490
-
Whole-Genome and Exome Sequencing in clear-cell Renal Cell Carcinoma (ccRCC)
Study
phs000491
-
Genetics of Human Developmental Brain Disorders
Study
phs000492
-
Genetic Association Studies in the Solomon Islanders
Study
phs000493
-
Better Outcomes for Children: GWAS from Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase II data - (dbGaP Deposit 1)
Study
phs000494
-
The Gene Partnership (TGP) - eMERGE Data
Study
phs000495
-
Columbia University Study of Caribbean Hispanics with Familial and Sporadic Late Onset Alzheimer's disease
Study
phs000496
-
Genetic analysis of Hirschsprung disease
Study
phs000497
-
Medulloblastoma exome sequence analysis
Study
phs000504
-
NHLBI and NIDDK Sponsored GWAS in Benign Ethnic Neutropenia/Leukopenia (BEN) in African-Americans (age >45 yrs old) from the REGARDS
Study
phs000507
-
Study of Osteoporotic Fractures (SOF)
Study
phs000510
-
Treatment of genetic screening of hypertriglyceridemia type I, III, and V - HTG Amsterdam
Study
phs000511
-
GWAS in African Americans, Latinos and Japanese
Study
phs000517
-
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
-
Study of Melanoma Risk in Australia and the United Kingdom
Study
phs000519
-
Episodic Ataxia Syndrome: Longitudinal Study
Study
phs000521
-
Hyperdiploid Acute Lymphoblastic Leukemia RNA-Seq
Study
phs000522
-
Whole Genome and Exon Capture Sequencing of Bladder Cancers
Study
phs000535
-
Next Generation Mendelian Genetics: Familial Hemophagocytic Lymphohistiocytosis
Study
phs000537
-
Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
Study
phs000538
-
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Study
phs000539
-
Next Generation Mendelian Genetics: Ehlers-Danlos Syndrome Type VIII
Study
phs000540
-
Next Generation Mendelian Genetics: Muscle Hypertrophy
Study
phs000541
-
Next Generation Mendelian Genetics: Neonatal Diabetes
Study
phs000542
-
Predicting Chemotherapy-Induced Mucositis with Genetic and Clinical Factors
Study
phs000545
-
NHLBI GO-ESP: Heart Cohorts Exome Sequencing Project (Ischemic Stroke Genetic Study, ISGS)
Study
phs000546
-
A Genome-Wide Association Study in Breast Cancer Patients from the Prospectively Randomized SUCCESS Trial
Study
phs000547
-
Genomic Characterization of Meningiomas
Study
phs000552
-
NHLBI GO-ESP: Family Studies (JHMI-Molecular Genetics of Atypical Cystic Fibrosis (CF) Study)
Study
phs000556
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study: Whole Exome Resequencing in Glaucoma
Study
phs000558
-
Population Architecture Using Genomics and Epidemiology (PAGE): Epidemiologic Architecture for Genes Linked to Environment (EAGLE) - BioVU Cancer Project
Study
phs000559
-
Ecological Stressors, PTSD, and Drug Use in Detroit: The Detroit Neighborhood Health Study (DNHS)
Study
phs000560
-
Metabolism and Genetics of Hypobetalipoproteinemia
Study
phs000561
-
The Genetic Landscape of Mutations in Burkitt Lymphoma
Study
phs000562
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs000571
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Genetic Heterogeneity of Diffuse Large B Cell Lymphoma
Study
phs000573
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Study
phs000575
-
Non Dystrophic Myotonias: Genotype-Phenotype Correlation and Longitudinal
Study
phs000578
-
Small Intestine Neuroendocrine Tumors (Carcinoid Tumors)
Study
phs000579
-
Population Architecture using Genomics and Epidemiology (PAGE): Causal Variants Across the Life Course (CALiCo): Strong Heart Study (SHS) and Strong Heart Family Study (SHFS)
Study
phs000580
-
NHLBI GO-ESP: Family Studies (Dilated Cardiomyopathy)
Study
phs000581
-
NHLBI GO-ESP: Family Studies (Familial Interstitial Pneumonia)
Study
phs000582
-
Asian Indian Diabetic Heart Study (AIDHS) /Sikh Diabetes Study (SDS)
Study
phs000583
-
The Longevity Genes Project
Study
phs000584
-
International Consortium for Blood Pressure (ICBP)
Study
phs000585
-
NHLBI GO-ESP: Family Studies (Mendelian Lipid Disorders)
Study
phs000587
-
Screening Protocol and Longitudinal Study of Bone Marrow Failure Syndromes and Cytopenias
Study
phs000592
-
Mucociliary Clearance Consortium (MCC) Rare Genetic Disorders of the Airways: Cross-section Comparison of Clinical Features, and Development of Novel Screening and Genetic Test
Study
phs000595
-
Mucociliary Clearance Consortium (MCC) Longitudinal Study of Primary Ciliary Dyskinesia: Participants 5-18 Years of Age
Study
phs000596
-
DNA Methylation Analysis of Prostate Cancer Cell Lines and Tissues Using Next Generation Sequencing
Study
phs000597
-
Exome Sequencing of Esophageal Adenocarcinoma
Study
phs000598
-
Filtering and Annotation of Variants That Are Rare (FAVR)
Study
phs000601