-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study
EGAS00001004430
-
Deep MRD profiling defines outcome and unveils different modes of treatment resistance in standard and high risk myeloma
Study
EGAS00001004558
-
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study
EGAS00001004625
-
ATM germline variants in a young adult with chronic lymphocytic leukemia: 8 years of genomic evolution
Study
EGAS00001006268
-
Longitudinal peripheral blood DNA methylation profiling of endoscopic response to tofacitinib in moderate-to-severe ulcerative colitis patients
Study
EGAS00001006968
-
EGFR TARGETING IN GASTRO-ESOPHAGEAL CANCER
Dac
EGAC50000000562
-
Olink CRS DAC
Dac
EGAC50000000547
-
Persister cell phenotypes contribute to poor patient outcomes after neoadjuvant chemotherapy in PDAC (Hipo_015)
Study
EGAS00001007143
-
Genetic drivers define transcriptomic characteristics and clonal hierarchy within intratumoral heterogeneity in adult T-cell leukemia-lymphoma
Study
JGAS000301
-
Exome Sequencing of a family with thrombocytopenia, red cell macrocytosis, and lymphoblastic leukemia predisposition
Study
phs000873
-
Episodic Ataxia Syndrome: Longitudinal Study
Study
phs000521
-
Integrated Genomic Analyses of Cutaneous T Cell Lymphomas Reveal the Molecular Bases for Disease Heterogeneity
Study
phs002456
-
Homozygous Duplication Identified by Whole Genome Sequencing Causes LRBA Deficiency
Study
phs002557
-
Genomics of Brain Metastases
Study
phs000730
-
Single Cell Genomic Analysis of Lymphoma
Study
phs002188
-
Filtering and Annotation of Variants That Are Rare (FAVR)
Study
phs000601
-
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study
Study
phs001624
-
Whole Exome Sequencing for Familial Intracranial Aneurysm (FIA I-II) Study
Study
phs000636
-
NPC Genome Project
Study
phs003214
-
Combined single-cell transcriptomics and T-cell receptor sequencing reveal heterogeneity of mycosis fungoides between and within patients and identify a CD4+ cytotoxic subtype
Study
EGAS50000000226
-
DAC for Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Dac
EGAC50000000332
-
Synchronous patterning of hiPSC-derived CNS progenitors generates comprehensive axial spinal cord organoids (CASCOs) containing diverse motor neuron population
Study
EGAS50000000891
-
DirectHRD Enables Sensitive Scar-Based Classification of Homologous Recombination Deficiency (HRD)
Study
phs003760
-
Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients
Study
EGAS50000000154
-
NHLBI TOPMed: TReating Children to Prevent EXacerbations of Asthma (TREXA)
Study
phs001732