-
Somatic mutation burden and copy-number variation analysis in neurofibromatosis type 1-associated plexiform neurofibromas
Study
phs001403
-
The Environmental Determinants of Diabetes in the Young Study (TEDDY)
Study
phs001037
-
Genomic Origins and Admixture in Latinos (GOAL)
Study
phs000750
-
Molecular Biomarkers in Glioma (Mechanisms and Therapeutic Implications of Hypermutation in Gliomas)
Study
phs001967
-
Genetic Analysis of Metopic Nonsyndromic Craniosynostosis
Study
phs001508
-
A Joint Linkage/Association Strategy to Interrogate AMD Genetic Susceptibility
Study
phs001379
-
Slim Initiative in Genomic Medicine for the Americas (SIGMA): Diabetes in Mexico Study (DMS)
Study
phs001388
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
Integrated Epigenetic Maps of Human Embryonic, Extraembryonic and Adult Cells
Study
phs000791
-
Whole Exome Sequencing of Congenital Diaphragmatic Hernia Patients and Trios
Study
phs000783
-
CIDR: Collaborative Study on the Genetics of Alcoholism Case Control Study
Study
phs000125
-
Genetic Studies of Chronic Kidney Disease (CKD)
Study
phs001828
-
Viral Respiratory Pathogens Genetics
Study
phs001030
-
PGRN/PAT: The genomic basis for susceptibility to drug-induced long QT syndrome (diLQTS)
Study
phs000808
-
Cross-Sectional Characterization of Idiopathic Bronchiectasis
Study
phs001279
-
Developmental Mechanisms of Human Congenital Heart Disease in Subjects with 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
Study
phs001339
-
NHLBI GO-ESP Family Studies: Pulmonary Arterial Hypertension
Study
phs000354
-
Genome-Wide Association Study of Breast Cancer in the African Diaspora - the ROOT study
Study
phs000383
-
Environmental Arsenic and Diabetes Mellitus (Chihuahua Cohort)
Study
phs002139
-
Mutations in GNAI2 Cause Developmental and Immune Dysregulation
Study
phs002817
-
Common Variant GWAS, Genetics & Epidemiology of Colorectal Cancer Consortium (GECCO)
Study
phs001078
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Discovering the Genetic Basis of Human Neuroblastoma: A Gabriella Miller Kids First Pediatric Research Program (Kids First) Project
Study
phs001436
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: KARE
Study
phs001096
-
HuBMAP: KULMAP - Human Kidney, Urinary Tract, and Lung Mapping Center
Study
phs002249