-
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