-
A Genome-Wide Association Study in Patients Experiencing Breast Events While Receiving Adjuvant Aromatase Inhibitors for Early Breast Cancer on NCIC CTG Trial MA.27
Study
phs001043
-
Genomic Architecture of Progression and Treatment Response in AMD
Study
phs001046
-
The Finland-United States Investigation of NIDDM Genetics (FUSION) Tissue Biopsy Study
Study
phs001048
-
Breast Cancer Genome Guided Therapy Study (BEAUTY)
Study
phs001050
-
National Eye Institute (NEI) Exfoliation Genotyping Study
Study
phs001053
-
Population Genetics Analysis Program: Immunity to Vaccines/Infections - Smallpox Vaccination (NIAID/NIH)
Study
phs001057
-
Myocardial Infarction Genetics Exome Sequencing Consortium: BioImage Study
Study
phs001058
-
Maternal Plasma Folate and DNA Methylation in Epigenome-Wide Meta-Analysis of Newborns
Study
phs001059
-
NINDS Family-Based Whole-Genome Sequencing to Find Modifiers of Age of Onset in Huntington's Disease
Study
phs001071
-
Epigenetic Analysis of Malnutrition
Study
phs001073
-
GeneSTAR (Genetic Study of Atherosclerosis Risk) NextGen Consortium: Functional Genomics of Platelet Aggregation Using iPS and Derived Megakaryocytes
Study
phs001074
-
Sequencing to Guide Cancer Care (CanSeq)
Study
phs001075
-
Inflammatory Bowel Disease Exome Sequencing Study
Study
phs001076
-
Common Variant GWAS, Genetics & Epidemiology of Colorectal Cancer Consortium (GECCO)
Study
phs001078
-
Genome Studies in Hereditary Spastic Paraplegia
Study
phs001080
-
Zostavax vaccination-induced changes in the T cell receptor repertoire to varicella zoster virus
Study
phs001082
-
99 Cases of Small Cell Lung Cancer Study
Study
phs001083
-
Differential Mutations in Matched Primary and Metastatic Colorectal Cancers
Study
phs001084
-
Genetic History of Neandertal and Denisovan Introgression into Melanesian Individuals
Study
phs001085
-
Shanghai Breast Cancer Genetics Study (SBCGS)
Study
phs001088
-
HudsonAlpha Institute for Biotechnology Clinical Sequencing Exploratory Research (CSER): Genomic Diagnosis in Children with Developmental Delay
Study
phs001089
-
Genome-wide Association Study for Non-syndromic Clefts in the African Population: CIDR
Study
phs001090
-
Clonal Evolution in Patients with Chronic Lymphocytic Leukemia
Study
phs001091
-
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: London Life Sciences Population Study (LOLIPOP) UK South Asian
Study
phs001093
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Ashkenazi
Study
phs001095
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: KARE
Study
phs001096
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Singapore
Study
phs001097
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Malmo Diet and Cancer Study
Study
phs001101
-
Genomics of Hepatocellular Carcinoma
Study
phs001106
-
Patient-Specific Factors Influence Somatic Variation Patterns in Von Hippel-Lindau Disease Renal Tumors
Study
phs001107
-
Addictions: Genotypes, Polymorphisms, and Function/Human Genetic Correlates of Addictive Diseases
Study
phs001109
-
Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia
Study
phs001110
-
Melanoma and Cancer-Associated Fibroblast Short-Term Cultures Derived from Patient Metastases
Study
phs001115
-
Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS)
Study
phs001119
-
ELLIPSE Prostate Cancer Meta-Analysis and Genotyping
Study
phs001120
-
Integrated Genetic and Pharmacologic Interrogation of Rare Cancers
Study
phs001121
-
Genome-wide Identification of Variants Affecting Early Human Brain Development
Study
phs001122
-
Mechanisms of Risk for Sulfonamide Hypersensitivity
Study
phs001124
-
Genomic Analysis of Paired Endometrial Cancer Primaries and Metastases
Study
phs001127
-
NIDDM-Atherosclerosis Study (NIDDM-Athero)
Study
phs001130
-
Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Study
phs001133
-
National Heart, Lung, and Blood Institute (NHLBI) Bench to Bassinet Program: The Gabriella Miller Kids First Pediatric Research Program of the Pediatric Cardiac Genetics Consortium (PCGC)
Study
phs001138
-
NextGen Consortium: GENESiPS Study: Identifying the Gene Networks of Insulin Resistance
Study
phs001139
-
ALCHEMIST Study
Study
phs001140
-
PROstate Cancer Medically Optimized Genome Enhanced ThErapy (PROMOTE) of Castration Resistant Prostate Cancer (CRPC) Patients Treated with Abiraterone Acetate
Study
phs001141
-
NHLBI TOPMed: The Genetics and Epidemiology of Asthma in Barbados
Study
phs001143
-
The EVE Asthma Genetics Consortium: Building Upon GWAS
Study
phs001156
-
Wisconsin Longitudinal Study on Aging
Study
phs001157
-
CRU-Ukrainian National Research Center for Radiation Medicine Trio Study
Study
phs001163
-
The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders
Study
phs001164
-
Genomic Changes in Breast Cancer Among Chinese Women in Hong Kong
Study
phs001870
-
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Study
phs001165
-
Kids First: Genomic Studies of Orofacial Cleft Birth Defects
Study
phs001168
-
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