-
NHLBI TOPMed: Genetic Epidemiology of COPD (COPDGene)
Study
phs000951
-
Genetic Components of Knee Osteoarthritis (GeCKO) Study: The Osteoarthritis Initiative
Study
phs000955
-
NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish
Study
phs000956
-
National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500)
Study
phs000958
-
Exome Sequencing of Schizophrenia Cases and Controls in the South African Xhosa Population
Study
phs000959
-
eMERGE III: Columbia GENIE (Genomic Integration with EHR)
Study
phs000961
-
Exploring the Genetic Variants Associated with Brain Growth in Children
Study
phs000962
-
PGRN-RIKEN: Genetic Determinants of Clinical Cardiovascular Events in Patients Receiving Statins
Study
phs000963
-
National Institute of Neurological Disorders and Stroke (NINDS), Family Study of Essential Tremor (FASET), Identification of Susceptibility Genes for Essential Tremor
Study
phs000966
-
The ClinSeq Project: Piloting Large-Scale Genome Sequencing for Research in Genomic Medicine
Study
phs000971
-
NHLBI TOPMed: Genome-Wide Association Study of Adiposity in Samoans
Study
phs000972
-
NHLBI TOPMed: Genomic Activities such as Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study
Study
phs000974
-
Study on the Genetics of Alcoholism (COGA): African American Family GWAS
Study
phs000976
-
Genetic Analysis of Desmoplastic Melanoma
Study
phs000977
-
HBCC Postmortem Psychiatric Molecular Studies
Study
phs000979
-
Genetic Analysis of Psoriasis and Psoriatic Arthritis: GWAS of Psoriatic Arthritis
Study
phs000982
-
Pharmacogenomics of Rheumatoid Arthritis Therapy
Study
phs000983
-
Functional Significance of Prostate Cancer Risk-SNPs
Study
phs000985
-
Genetic Basis of Cryptorchidism
Study
phs000986
-
Whole exome sequencing of 184 unrelated subjects with 22q11.2 deletion syndrome (DiGeorge syndrome/velo-cardio-facial syndrome)
Study
phs000987
-
NHLBI TOPMed: The Genetic Epidemiology of Asthma in Costa Rica
Study
phs000988
-
Cellular Diversity of the Developing Human Cerebral Cortex
Study
phs000989
-
Myocardial Infarction Genetics Exome Sequencing Consortium: University of Lubeck
Study
phs000990
-
Breast Cancer Susceptibility
Study
phs001017
-
NHLBI TOPMed: Heart and Vascular Health Study (HVH)
Study
phs000993
-
The Mutational Landscape of CTCL and Sezary Syndrome
Study
phs000994
-
Clinical Sequencing Exploratory Research (CSER): Clinical sequencing in cancer: Clinical, ethical, and technological studies
Study
phs000999
-
Myocardial Infarction Genetics Exome Sequencing Consortium: U. of Leicester
Study
phs001000
-
Genetic Analysis of Parkinson's Disease
Study
phs001004
-
Lobular Carcinomas In Situ Display Intra-Lesion Genetic Heterogeneity and Clonal Evolution in the Progression to Invasive Disease
Study
phs001006
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
GUARDIAN: The Insulin Resistance Atherosclerosis Family Study (IRASFS)
Study
phs001008
-
Determinants of Asthma Following RSV Bronchiolitis in Early Life
Study
phs001009
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011
-
The Diabetes Heart Study (DHS)
Study
phs001012
-
Heart and Vascular Health Study (HVH)
Study
phs001013
-
Genomic Psychiatry Cohort (GPC) Whole Genome Sequencing and Genotyping Study
Study
phs001020
-
PsychENCODE Consortium: Epigenetic and Transcriptional Dysregulation in Autism Spectrum
Study
phs001022
-
Male Infertility: Genetics of Spermatogenic Failure
Study
phs001023
-
NHLBI TOPMed: Partners HealthCare Biobank
Study
phs001024
-
Viral Respiratory Pathogens Genetics
Study
phs001030
-
New England-Based Case-Control Study of Ovarian Cancer
Study
phs001034
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001037
-
Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses
Study
phs001038
-
International Age-Related Macular Degeneration Genomics Consortium - Exome Chip Experiment
Study
phs001039
-
Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA)
Study
phs001123
-
Genetic Basis for Clinical Response to CTLA-4 Blockade in Melanoma
Study
phs001041
-
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