-
Integrative Analysis of Lung Adenocarcinoma in EAGLE (Version 2)
Study
phs001169
-
National Institute of Neurological Disorders and Stroke (NINDS) Parkinson's Disease
Study
phs001172
-
National Cancer Institute (NCI) Head and Neck Cancer Study
Study
phs001173
-
Female Infertility: Primary Ovarian Insufficiency
Study
phs001174
-
CTSP: Clinical Trial Sequencing Project
Study
phs001175
-
Gene-Environment Interactions (GxE) and Complex Traits
Study
phs001176
-
Rare germline sequence variants, copy number variations, expression alterations, methylation variations and disease susceptibility in familial melanoma
Study
phs001177
-
Disorders/Differences of Sex Development (DSD) Study Performed at UCLA in Collaboration with the DSD-Translational Research Network (DSD-TRN), with the Support of the Gabriella Miller Kids First Pediatric Research Program
Study
phs001178
-
Genes-Environments and Admixture in Latino Asthmatics (GALA II) Study
Study
phs001180
-
National Institute of Environmental Health (NIEHS) Sciences Study of Somatic Mutation Load in Clones of Single Human Cells
Study
phs001182
-
Genome-Wide Scan for Genetic Variants Associated with Early-Onset Prostate Cancer
Study
phs001185
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Study - Islet Expression and Regulation by RNAseq and ATACseq
Study
phs001188
-
NHLBI TOPMed: Cleveland Clinic Atrial Fibrillation (CCAF) Study
Study
phs001189
-
eMERGE: Northwestern (NUgene) WGS
Study
phs001191
-
National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer
Study
phs001193
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Pediatric Cardiac Genetics Consortium (PCGC) Study
Study
phs001194
-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
National Eye Institute (NEI) Genetic Epidemiology of Age-Related Macular Degeneration in the Old Order Amish
Study
phs001361
-
OncoArray: Oral and Pharynx Cancer
Study
phs001202
-
Stockholm-Tartu Atherosclerosis Reverse Network Engineering Task (STARNET)
Study
phs001203
-
Blepharospasm in a Multiplex African-American Pedigree
Study
phs001206
-
NHLBI TOPMed: African American Sarcoidosis Genetics Resource
Study
phs001207
-
Study on the Genetics of Alcoholism (COGA): Smoke screen and exome sequencing
Study
phs001208
-
National Cancer Institute (NCI) Study of Lung Cancer and Smoking Phenotypes in African-American Cases and Controls
Study
phs001210
-
NextGen Consortium: Globin Gene Expression in Sickle Cell Genotype-Specific iPS Cells
Study
phs001212
-
Molecular Genetics of Heroin Dependence in China
Study
phs001213
-
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
-
Investigating Human Placentation and Pregnancy Using First Trimester Chorionic Villi
Study
phs001320
-
Childhood Cancer Survivor Study (CCSS)
Study
phs001327
-
Natural History and Structural Functional Relationships in Fabry Renal Disease
Study
phs001333
-
A whole-genome sequencing study for evolutionary history of Tibetans and their genetic adaptations to high altitude
Study
phs001338
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
The National Heart, Lung, and Blood Institute (NHLBI)-funded Next Generation Genetic Association Studies (NextGen) Consortium: Phenotyping Lipid traits in iPS derived hepatocytes Study (PhLiPS Study)
Study
phs001341
-
Exome Sequencing of Statin-Induced Myopathy Cases
Study
phs001342
-
Whole Exome Sequences of Human Embryonic Stem Cell Lines
Study
phs001343
-
The National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) Consortium for the Longitudinal Evaluation of African-Americans with Early Rheumatoid Arthritis (CLEAR)
Study
phs001360
-
NHLBI TOPMed: Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs001345
-
Identification of 22 Novel Loci Associated with Susceptibility to Testicular Germ Cell Tumors
Study
phs001349
-
Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)
Study
phs001350
-
Research Study into The Molecular Genetics of Hereditary Neuropathies
Study
phs001351
-
Metagenomics-Guided Pathogen Discovery in Travelers' Diarrhea
Study
phs001352
-
The Genomic Landscape of Tuberous Sclerosis Complex (TSC)
Study
phs001357
-
NHLBI TOPMed: GOLDN Epigenetic Determinants of Lipid Response to Dietary Fat and Fenofibrate
Study
phs001359
-
Mapping the Human Connectome - Structure, Function, and Heritability: Healthy Young Adults (Age 22-35 Years) Including Twins and their Non-Twin Siblings
Study
phs001364
-
Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab on NSABP B-40
Study
phs001365
-
Add Health: Longitudinal Study of a Nationally Representative Sample of Adolescents in Grades 7-12 in the United States during the 1994-95 School Year, Followed into Adulthood with Five Interviews/Surveys in 1995, 1996, 2001-02, 2008, and 2016-18.
Study
phs001367
-
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study
Study
phs001624
-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Integrated Single-Cell Genetic and Transcriptional Analysis Suggests Novel Drivers of Chronic Lymphocytic Leukemia
Study
phs001372
-
Brain cell type-specific enhancer-promoter connectivity maps and disease risk association
Study
phs001373
-
VA APOLLO Project - Research for Precision Oncology (RePOP)
Study
phs001374