-
Inherited Defect in ST6GalNAc1 Reveals Roles of Sialylation in Intestinal Homeostasis
Study
phs002598
-
RB1 Loss Triggers Dependence on ESRRG in Retinoblastoma
Study
phs002859
-
Combined Targeting of CDK4/6 and HER2 Signaling in Orthotopic Patient-Derived Xenografts of HER2-Positive Breast Cancer Brain Metastases
Study
phs002482
-
Lineage Plasticity and Immune Cell Heterogeneity Are Coordinately Dysregulated Through Changes in FOXA1 Expression in Bladder Cancers with Squamous Differentiation
Study
phs002357
-
Germline and Somatic Genetic Landscape of Pediatric Rhabdomyosarcoma
Study
phs002304
-
Novel Gene-Environment Regulatory Circuit in Chamber-Specific Growth of Perinatal Heart
Study
phs002725
-
Intercepting Progression from Pre-Invasive to Invasive Lung Adenocarcinoma
Study
phs002818
-
Genetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS)
Study
phs000244
-
Dissecting Cell Composition and Drug Sensitivity in Human Adenoid Cystic Carcinomas (ACCs)
Study
phs002764
-
Longitudinal Studies of Patients with Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)
Study
phs003075
-
Exome sequencing of autosomal recessive progressive external ophthalmoplegia (arPEO)
Study
phs000392
-
Very Low Tumor Mutation Burden Identifies Inflamed Recurrent Glioblastomas Responsive to Cancer Immunotherapy
Study
phs002270
-
Genetics of Male Infertility Initiative (GEMINI)
Study
phs003115
-
Immunogenomics of Malignant Brain Tumors
Study
phs002612
-
Genetic Diseases of Immune Homeostasis and Autoimmunity Caused by GIMAP Deficiency
Study
phs002816
-
Inherited T Cell Defects: Diagnosis, Mechanisms and Treatments
Study
phs002968
-
International Cancer Proteogenomics Consortium (ICPC): Proteogenomics of East-Asian Breast Cancer
Study
phs003150
-
Leveraging Extended Families for Cardiovascular Disease Genomic Discovery
Study
phs002464
-
Next Generation Mendelian Genetics: Kabuki Syndrome
Study
phs000295
-
Ameloblastoma Cell Line Resource
Study
phs002753
-
Investigation of the Causal Etiology in a Patient with T-B+NK+ Immunodeficiency
Study
phs002990
-
Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line
Study
phs002440
-
Genetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS)
Study
phs000204
-
Genomic Analysis of Extra-Nodal Natural Killer/T-Cell Lymphoma (ENKTCL)
Study
phs002925
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
Personalized Breast Cancer Vaccines Based on Genome Sequencing
Study
phs002787
-
Reference Standards for Mosaic Variant Detection
Study
phs003399
-
The Genomic Landscape of Interval Colorectal Cancers
Study
phs003093
-
PIEZO1 Loss of Function Compound Heterozygous Mutation in the Rare Congenital Human Disorder Prune Belly Syndrome
Study
phs003475
-
The Genetic Evolution of Acral Melanoma
Study
phs003451
-
The Role of GPD1L in the Pathogenesis of Brugada Syndrome
Study
phs003468
-
Multi-Omic Profiling of Glioma Patient Tumors and Patient-Derived Model Systems
Study
phs003286