-
Center for Education and Drug Abuse Research (CEDAR)
Study
phs001649
-
Mechanisms of Restoring T Cell Immunity after Cure of Chronic Viral Infection
Study
phs002510
-
Relapsed Acute Lymphoblastic Leukemia (ALL): Mutational Landscape
Study
phs001951
-
A Genome-Wide Association Study in Participants Experiencing Breast Cancer Events in High-Risk Postmenopausal Women Receiving Selective Estrogen Receptor Modulators on NSABP Trials P-1 and P-2. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine
Study
phs000305
-
A Phenotypic and Genomics Approach in a Multi-Ethnic Cohort to Subtype Systemic Lupus Erythematosus
Study
phs001850
-
NIDDM-Atherosclerosis Study (NIDDM-Athero)
Study
phs001130
-
Performance Characteristics of Selective Targeted Enrichment in Genetic Diagnostic Testing
Study
phs000798
-
Comparative Sequence Analysis Between Primary and Metastatic Colorectal Cancer Lesions
Study
phs000790
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Study
phs000902
-
CIDR: NCI Genome Wide Predictors of Survival in Colorectal Cancer
Study
phs001290
-
Pancreatitis after Treatment for Acute Lymphoblastic Leukemia (SJIRB XPD04-123 and XPD05-078)
Study
phs001350
-
Genome-Wide Association Study of Relapse of Childhood Acute Lymphoblastic Leukemia
Study
phs000638
-
TOPDECC-Trans-omics for Precision Dentistry and Early Childhood Caries: Genome-Wide Genotyping (CIDR) and Microbiome in the ZOE 2.0 Study
Study
phs002232
-
INCLUDE: The Epidemiology of Transient Leukemia in Newborns with Down Syndrome
Study
phs002982
-
Whole Genome Bisulfite Sequencing of Circulating Cell-Free (CCF) DNA and its Cellular Contributors
Study
phs000846
-
International Consortium on the Genetics of Systemic Lupus Erythematosus (SLEGEN)
Study
phs000216
-
National Eye Institute (NEI) Genetic Epidemiology of Age-Related Macular Degeneration in the Old Order Amish
Study
phs001361
-
RNA Expression in Diverse Donor Derived Dermal Fibroblasts Correlates with Reprogramming to Pluripotency
Study
phs002341
-
NEI CIDR Methylation Profiling of Primary Open Angle Glaucoma in GLAUGEN Samples
Study
phs000461
-
Rare Disease Susceptibility Alleles in Children with Crohn Disease
Study
phs000926
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
Center for Common Disease Genomics [CCDG] - Neuropsychiatric: Genomics of Autism Spectrum Disorder (GASD)
Study
phs002509
-
Genetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS)
Study
phs000244
-
Exome Sequencing in Schizophrenia Families
Study
phs000738
-
Genetic Heterogeneity of Diffuse Large B Cell Lymphoma
Study
phs000573
-
Alzheimer's Disease Sequencing Project (ADSP)
Study
phs000572
-
Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs000784
-
Early Onset and Progression of Primary Ciliary Dyskinesia Lung Disease Prior to 10 Years of Age
Study
phs001310
-
The Research Institute at Nationwide Children's Hospital Genetics of Congenital Heart Disease (CHD)
Study
phs002010
-
Genetic defects in familial renal disorders
Study
phs000477
-
Pharmacogenomic Analysis of Microtubule Targeting Agent Response and Toxicity
Study
phs002060
-
The Longevity Genes Project
Study
phs000584
-
High density copy number analysis and whole exome sequencing of unselected chronic lymphocytic leukemia cases and of paired chronic lymphocytic leukemia and Richter Syndrome cases
Study
phs000364
-
Deletion of FUNDC2 and CMC4 on chromosome Xq28 is sufficient to cause hypergonadotropic hypogonadism in men
Study
phs002234
-
Genetic Epidemiology of Chronic Lymphocytic Leukemia
Study
phs001568
-
Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome
Study
phs000701
-
Kids First: Genomics of Orofacial Cleft Birth Defects in Latin American Families
Study
phs001420
-
Hyperdiploid Acute Lymphoblastic Leukemia RNA-Seq
Study
phs000522
-
Genetic Study of Northern Kenya Pastoral Populations
Study
phs002654
-
Impact of Race and Genetic Factors on Beta Blocker Effectiveness in Heart Failure
Study
phs001501
-
Genomic Characterization of Head and Neck Squamous Cell Carcinoma Cell Lines
Study
phs001581
-
Genetic Analysis of Normal Human Facial Variation
Study
phs000949
-
Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS)
Study
phs001119
-
Genetics of Mammographic Density in Ashkenazi Jews
Study
phs001857
-
Molecular defects in pseudohypoparathyroidism or related disorders
Study
phs000476
-
NHLBI TOPMed: Genetic Epidemiology Network of Salt Sensitivity (GenSalt)
Study
phs001217
-
OncoArray: Prostate Cancer
Study
phs001391
-
Molecular Genetic Studies of Developmental Brain Disorders
Study
phs000455
-
The Genomics and Randomized Trials Network (GARNET) Vitamin Intervention Stroke Prevention (VISP) Trial
Study
phs000343
-
The Mood and Methylation Study (MMS)
Study
phs002858
-
The International Consortium for Prostate Cancer Genetics Genome Wide Association Study of Familial Prostate Cancer
Study
phs000733
-
Whole-Exome Sequencing and Targeted DNA Sequencing of Matched Ocular Melanocytosis and Uveal Melanoma
Study
phs001835
-
National Eye Institute (NEI) Exfoliation Genotyping Study
Study
phs001053
-
NIDA Genetic Epidemiology of Opioid Dependence in Bulgaria (GEODB)
Study
phs001804
-
STAMPEED: Northern Finland Birth Cohort 1966 (NFBC1966)
Study
phs000276
-
Regulatory Genomics of Human Embryonic Development
Study
phs001226
-
Molecular Genetics of Heroin Dependence in China
Study
phs001213
-
National Cancer Institute (NCI) Genome Wide Association Study (GWAS) of Lung Cancer in Never Smokers
Study
phs000634
-
Genetic Model of MS Severity Predicts Future Accumulation of Disability
Study
phs001833
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Age related Macular Degeneration (AMD)-- Michigan, Mayo, AREDS, Pennsylvania (MMAP) Cohort Study: A Joint Genome Wide Association Study
Study
phs000182
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Singapore
Study
phs001097
-
Center for Common Disease Genomics (CCDG) Neuropsychiatric: Homozygosity Mapping Consortium for Autism (HMCA)
Study
phs001894
-
The Genetic Architecture of Smoking and Smoking Cessation
Study
phs000404
-
Glioma International Case Control Study (GICC)
Study
phs001319
-
Breast Cancer Genome Guided Therapy Study (BEAUTY)
Study
phs001050
-
OICR: Molecular Pathological Epidemiology of Colorectal Cancer
Study
phs002050
-
Molecular Genetics of Secondary Histiocytic/Dendritic Sarcoma
Study
phs001942
-
Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) - OncoArray Genotypes
Study
phs001321
-
Kids First: Congenital Heart Defects and Laterality Birth Defects
Study
phs002589
-
National Cancer Institute (NCI) Adding Hispanics to Ongoing GWAS in Colorectal Cancer
Study
phs001193
-
Whole exome sequencing and methylation profiling of uveal melanoma
Study
phs001421
-
Center for Common Disease Genomics [CCDG] - Inflammatory Bowel Disease (IBD) - Global Microbiome Conservancy Host Exomes
Study
phs002205
-
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
-
Palindromic Amplification of The ERBB2 Oncogene in HER2-Positive Breast Cancer
Study
phs001261
-
Gene-Environment Interactions (GxE) and Complex Traits
Study
phs001176
-
NIDDK⁄CIDR Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease
Study
phs000367
-
Melanoma and Cancer-Associated Fibroblast Short-Term Cultures Derived from Patient Metastases
Study
phs001115
-
Genetic Epidemiology of Lung Cancer Consortium GWAS of Familial Lung Cancer
Study
phs000629
-
OCD Collaborative Genetic Association Study (OCGAS)
Study
phs000903
-
Natural History of and Genetic Modifiers in Spinocerebellar Ataxias
Study
phs001332
-
NHLBI TOPMed: Defining the Time-Dependent Genetic and Transcriptomic Responses to Cardiac Injury Among Patients with Arrhythmias
Study
phs001434
-
Genetic analysis of Hirschsprung disease
Study
phs000497
-
Pilot Sequencing Study: DNA Hydroxymethylation and Gene Expression in Peripheral Blood Mononuclear Cells in Healthy Human Aging
Study
phs001916
-
Molecular Evolution of Cancer
Study
phs001255
-
Blepharospasm in a Multiplex African-American Pedigree
Study
phs001206
-
Genetics of Congenital Anomalies of the Kidney and Urinary Tract
Study
phs001749
-
Gabriella Miller Kids First Pediatric Research Program: An Integrated Clinical and Genomic Analysis of Treatment Failure in Pediatric Osteosarcoma
Study
phs001714
-
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
-
Exome sequencing of autosomal recessive progressive external ophthalmoplegia (arPEO)
Study
phs000392
-
Genetic Effects on miRNA Expression During Mid-Gestation Neocortical Development
Study
phs003106
-
An APOBEC Cytidine Deaminase Mutagenesis in Human Cancers
Study
phs000677
-
Phenotyping and Therapeutic Approaches for Patients with Sellar/Suprasellar Disorders
Study
phs003245
-
Epidemiological study comparing rates and risk factors for dementia in African Americans in Indianapolis and Yoruba living in Ibadan, Nigeria
Study
phs000378
-
National Institute on Aging - Late Onset Alzheimer's Disease Family Study: Genome-Wide Association Study for Susceptibility Loci
Study
phs000168
-
Genomics of Hepatocellular Carcinoma
Study
phs001106
-
Neurogenetic Investigations of Obsessive-Compulsive Disorder
Study
phs001929
-
MP2PRT: Identification of Genetic Changes Associated with Relapse and/or Adaptive Resistance in Patients Registered as Favorable Histology Wilms Tumor on AREN03B2
Study
phs001965
-
Genetic Epidemiology of Refractive Error in the KORA (Kooperative Gesundheitsforschung in der Region Augsburg) Study
Study
phs000303
-
The Role of CDX2 in Controlling ABCB1 Expression and Chemosensitivity in Human Colon Cancer
Study
phs002903