-
Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
-
Genetic heritage of the Baphuthi highlights an over-ethnicised notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
Study
EGAS00001007080
-
IL7-receptor expression is frequent in T-cell acute lymphoblastic leukemia and predicts sensitivity to JAK-inhibition
Study
EGAS00001007144
-
Genome-Wide Association Studies of Prematurity and Its Complications
Study
phs000103
-
Trial of Late Surfactant for Prevention of Bronchopulmonary Dysplasia: A Study in Ventilated Preterm Infants Receiving Inhaled Nitric Oxide (TOLSURF-BioLINCC)
Study
phs003899
-
Genomics Define Malignant Transformation in Myeloma Precursor Conditions
Dataset
EGAD00001015768
-
Genome-Wide Association Study of HIV-1 Host Genetics Among Injection Drug Users
Study
phs000454
-
Phenotypic and Genotypic Study of Keratoconus
Study
phs003168
-
Integrative analysis reveals a macrophage-predominant, immunosuppressive immune microenvironment and subtype-specific therapeutic vulnerabilities in advanced salivary gland cancer
Study
EGAS50000000809
-
Single-Gene vs. Panel Sequencing in Advanced HR+/HER2− Breast Cancer
Study
EGAS00001008200
-
Probabilistic modeling of personalized drug combinations from integrated chemical screen and molecular data in sarcoma
Study
EGAS00001003564
-
Bulk-RNA Sequencing of high-grade pancreatic and non-pancreatic Neuroendocrine Neoplasms
Study
EGAS00001004861
-
Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
-
Angelman, Rett, Prader-Willi Syndrome Consortium (ARP) Rett Syndrome Natural History Protocol
Study
phs000574
-
Add Health: Longitudinal Study of a Nationally Representative Sample of Adolescents in Grades 7-12 in the United States during the 1994-95 School Year, Followed into Adulthood with Five Interviews/Surveys in 1995, 1996, 2001-02, 2008, and 2016-18
Study
phs001367
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Exome Sequencing of Statin-Induced Myopathy Cases
Study
phs001342
-
Exploring the Genetic Variants Associated with Brain Growth in Children
Study
phs000962
-
NSIGHT North Carolina Newborn Exome Sequencing for Universal Screening (NC NEXUS)
Study
phs002095
-
NRG-GY017: Atezolizumab before and/or with Chemoradiotherapy in Immune System Activation in Patients with Node Positive Stage IB2, II, IIIB, or IVA Cervical Cancer
Study
phs003833
-
Clinical and Genetic Evaluation of Individuals with Undiagnosed Disorders through the Undiagnosed Diseases Network (UDN)
Study
phs001232
-
Profiling Genome-Wide Circulating ncRNAs for the Early Detection of Lung Cancer
Study
phs004166
-
Acute Respiratory Distress Syndrome Clinical Network: Fluid and Catheter Treatment Trial (ARDSNet FACTT-BioLINCC)
Study
phs004165
-
Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
Study
JGAS000052
-
Implementation, Adoption, and Utility of Family History in Diverse Care Settings
Study
phs001641