-
Whole Genome Scan for Pancreatic Cancer Risk in the Pancreatic Cancer Cohort Consortium and Pancreatic Cancer Case-Control Consortium (PanScan)
Study
phs000206
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
National Cancer Institute (NCI) TARGET: Therapeutically Applicable Research to Generate Effective Treatments
Study
phs000218
-
National Cancer Institute Cancer Genome Characterization Initiative (CGCI)
Study
phs000235
-
National Eye Institute Glaucoma Human Genetics Collaboration (NEIGHBOR) Consortium Glaucoma Genome-Wide Association Study
Study
phs000238
-
National Eye Institute (NEI) Ocular Hypertension Treatment Study (OHTS)
Study
phs000240
-
Foregut Microbiome in Development of Esophageal Adenocarcinoma
Study
phs000260
-
Genome-Wide Association Study of Celiac Disease
Study
phs000274
-
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
-
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Study
phs000308
-
Towards a Genomic Understanding of Myeloma
Study
phs000348
-
Genome-Wide Analysis of Diffuse Large B-Cell Lymphoma (De Novo and Derived from the High Grade Transformation of Follicular Lymphoma)
Study
phs000328
-
A Genome-Wide Association Study of Lung Cancer Risk
Study
phs000336
-
The genomic complexity of early T-cell progenitor acute lymphoblastic leukemia
Study
phs000340
-
Genome-wide association study for Bladder Cancer Risk
Study
phs000346
-
National Cancer Institute Genome-Wide Association Study of Renal Cell Carcinoma
Study
phs000351
-
The genomic complexity of sporadic and inherited retinoblastoma with a matched orthotopic xenograft
Study
phs000352
-
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
-
The Mutational Landscape of Head and Neck Squamous Cell Carcinoma
Study
phs000370
-
Genentech whole genome and transcriptome sequencing of four hepatocellular carcinoma patients
Study
phs000384
-
Whole Genomic Sequencing of Nine Primary Colorectal Adenocarcinoma Tumor/Germline Pairs
Study
phs000374
-
The Genomic Analysis of Medulloblastoma
Study
phs000409
-
Whole Exome Sequencing for Colorectal Cancer
Study
phs000410
-
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
Study
phs000419
-
Hepatitis C Antiviral Long-term Treatment Against Cirrhosis (HALT-C)
Study
phs000430