-
NHLBI TOPMed: San Antonio Family Heart Study (SAFHS)
Study
phs001215
-
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs001217
-
NHLBI TOPMed: Genetic Study of Atherosclerosis Risk (GeneSTAR)
Study
phs001218
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219
-
Centers for Common Disease Genomics (CCDG) - Whole Genome Sequencing in Type 1 Diabetes (T1DGC)
Study
phs001222
-
Regulatory Genomics of Human Embryonic Development
Study
phs001226
-
Washington University Coronary Artery Disease Study
Study
phs001227
-
Gabriella Miller Kids First (GMKF) Pediatric Research Program in Susceptibility to Ewing Sarcoma Based on Germline Risk and Familial History of Cancer
Study
phs001228
-
The Library of Integrated Network-Based Cellular Signatures (LINCS) - NeuroLINCS
Study
phs001231
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
Disease Severity in Familial Dysautonomia
Study
phs001233
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001238
-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Phase 2)
Study
phs001239
-
Genetic Basis of Breast Cancer Resistance in BRCA1 Mutation Carrier
Study
phs001243
-
Genetic Basis of Isolated Arhinia and Bosma Arhinia Microphthalmia Syndrome
Study
phs001246
-
GMKF: Kids First Pediatric Research Program on Congenital Cranial Dysinnervation Disorders and Related Birth Defects
Study
phs001247
-
Chemosensitive Relapse in Small Cell Lung Cancer Patient-Derived Xenografts
Study
phs001249
-
Family-Based Study on Ulcerative Colitis with Whole Exome Sequencing
Study
phs001251
-
Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE)
Study
phs001252
-
Pharmacogenetics of Efavirenz Discontinuation for Reported Central Nervous System Symptoms Appears to Differ by Race
Study
phs001253
-
Molecular Evolution of Cancer
Study
phs001255
-
Genetic Etiology of Hypoplastic Left Heart Syndrome
Study
phs001256
-
CCDG CVD: VIRGO - Variation in Recover-Role of Gender on Outcomes of Young Acute Myocardial Infarction (AMI) Patients
Study
phs001259
-
Metagenomic Epidemiology of Antibiotic Resistance in Infectious Diarrhea
Study
phs001260
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - Genome-Wide Association Study Meta-Analysis
Study
phs001263
-
Oncoarray Consortium - Lung Cancer Studies
Study
phs001273
-
Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) - OncoArray Genotypes
Study
phs001265
-
Genome-Wide Analysis for Addiction Susceptibility Genes
Study
phs001266
-
CIDR/NICHD Genetic Basis of Recessive Pediatric Brain Diseases - Group 2
Study
phs001267
-
Investigating Genetics of Human Natural Short Sleepers (IGHNSS)
Study
phs001270
-
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Study
phs001271
-
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Study
phs001279
-
Response and Resistance to ER-Directed Therapy in Metastatic Breast Cancer
Study
phs001285
-
NHLBI TOPMed: HyperGEN - Genetics of Left Ventricular (LV) Hypertrophy
Study
phs001293
-
NextGen Consortium: The iPSCORE (iPSC Collection for Omic Research) Resource for Studying the Impact of Genetic Variation on Molecular and Physiological Phenotypes - Whole Genome Sequence
Study
phs001325
-
Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis
Study
phs001288
-
Andersen-Tawil Syndrome: Genotype-phenotype correlation and longitudinal study
Study
phs001289
-
CIDR: NCI Genome Wide Predictors of Survival in Colorectal Cancer
Study
phs001290
-
Sleep Abnormalities in Rare Genetic Disorders: Angelman Syndrome, Rett Syndrome, and Prader-Willi Syndrome
Study
phs001292
-
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) - OncoArray Genotypes
Study
phs001321
-
Nicotine Addiction Genetics and Correlates
Study
phs001299
-
Genome-Wide Association Study of Sporadic and Familial Testicular Germ Cell Tumors
Study
phs001303
-
Large Scale Meta-analysis Characterizes Genetic Architecture for Common Psoriasis-associated Variants
Study
phs001306
-
Inherited Genetic Variation and Predisposition to Testicular Germ Cell Tumor: UPenn Local TGCT Study
Study
phs001307
-
Early Onset and Progression of Primary Ciliary Dyskinesia Lung Disease Prior to 10 Years of Age
Study
phs001310
-
National Eye Institute (NEI) Primary Open-Angle African American Glaucoma Genetics (POAAGG) Study
Study
phs001312
-
Modifier Genes in 21-hydroxylase Deficiency
Study
phs001313
-
GECCO: Detecting Common and Rare Genetic Loci and GxE Interactions in Colorectal Cancer
Study
phs001315
-
Glioma International Case Control Study (GICC)
Study
phs001319