-
T2D-GENES Consortium: San Antonio Mexican American Family Studies (SAMAFS)
Study
phs000847
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Precocious Coronary Artery Disease Study
Study
phs000883
-
Autosomal recessive
Study
phs000848
-
Resistance studies in Lung Cancer
Study
phs000855
-
Chromothripsis in Patient WHIM-09
Study
phs000856
-
National Cancer Institute (NCI) Genome-Wide Association Study (GWAS) of Renal Cell Carcinoma in African Americans
Study
phs000863
-
Genomic Predictors of Combat Stress Vulnerability and Resilience
Study
phs000864
-
Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
Study
phs000869
-
High-Risk Breast Cancer GWAS
Study
phs000929
-
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Study
phs000873
-
Genetic and Environmental Risk Factors for Hemorrhagic Stroke (GERFHS)
Study
phs000874
-
Transdisciplinary Research Into Cancer of the Lung (TRICL) - Exome Plus Targeted Sequencing
Study
phs000876
-
Substance Dependence GWAS in European- and African - Americans
Study
phs000952
-
An Omics View of Asthma through Monozygotic Twins
Study
phs000886
-
eMERGE Network Imputed GWAS for 41 Phenotypes
Study
phs000888
-
Genome-Wide Association Study of Endometrial Cancer in the Epidemiology of Endometrial Cancer Consortium (E2C2)
Study
phs000893
-
National Institute of Mental Health (NIMH) Amish Mennonite Bipolar Genetics Study (AmBiGen)
Study
phs000899
-
Myocardial Infarction Genetics Exome Sequencing Consortium: Registre Gironi del Cor
Study
phs000902
-
OCD Collaborative Genetic Association Study (OCGAS)
Study
phs000903
-
eMERGE Network's Multi-Center Pilot of Pharmacogenetic Sequencing in Clinical Practice
Study
phs000906
-
Next Generation Sequencing of Stage IV Squamous Cell Lung Cancers Reveals an Association of PI3K Aberrations and Evidence of Clonal Heterogeneity in Patients with Brain Metastases
Study
phs000907
-
University of Miami Udall Center of Excellence Identification of Rare Variants in PD through Whole Exome Sequencing
Study
phs000908
-
Type 1 Diabetes Genetics Consortium (T1DGC): Copy Number Variant (CNV) Study
Study
phs000910
-
Type 1 Diabetes Genetics Consortium (T1DGC): ImmunoChip Study
Study
phs000911
-
San Francisco Bay Area Latina Breast Cancer Study
Study
phs000912