-
Institut Curie Neuroblastoma Whole Genome Sequencing Diagnosis Relapse
Dataset
EGAD00001001356
-
Methylation profiles in blood (controls)
Dataset
EGAD00010002471
-
HPRU in Respiratory Infections DAC
Dac
EGAC50000000307
-
Mutations in ALK signaling pathways conferring resistance to ALK inhibitor treatment lead to collateral vulnerabilities in neuroblastoma cells
Study
EGAS00001005791
-
Molecular determinants of outcomes in relapsed mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial
Study
EGAS00001006342
-
scRNA mCRC PDO
Study
EGAS00001006214
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow-Up Study: BioMe Biobank Program
Study
phs001490
-
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Follow up Study: Pakistan Genomic Resource (PGR)
Study
phs001552
-
Longitudinal Studies of Brain Structure and Function in MPS Disorders
Study
phs001328
-
METSIM (METabolic Syndrome In Men) Study
Study
phs000743
-
Dental Caries: Whole Genome Association and Gene x Environment Studies
Study
phs000095
-
Genetic and Phenotypic Analysis of Multiple Sclerosis in Hispanics
Study
phs003105
-
Natural History and Structural Functional Relationships in Fabry Renal Disease
Study
phs001333
-
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Genetics of Genetic Epidemiology of Metabolic Syndrome in an Island Population
Study
phs000737
-
Phase 2 Study of Nivolumab and Entinostat in Unresectable or Metastatic Cholangiocarcinoma and Pancreatic Adenocarcinoma
Study
phs003615
-
Heterogeneity in Lysosomal Storage Disorders
Study
phs003459
-
Aggressive genomic features in clinicallyindolent primary HHV8-negative effusion-based lymphoma
Study
EGAS00001002743
-
A genomic approach towards an understanding of clonal evolution and disease progression in multiple myeloma
Study
EGAS00001002850
-
Detection of mutational patterns in cell free DNA (cfDNA) of colorectal cancer by custom amplicon sequencing
Study
EGAS00001003382
-
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Study
EGAS00001001606
-
Cerebral organoid model reveals excessive proliferation of human caudal late interneuron progenitors in Tuberous Sclerosis Complex
Study
EGAS00001004586
-
EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION
Study
EGAS00001001645
-
A Multiethnic Genome-wide Scan of Prostate Cancer
Study
phs000306
-
Capturing the Genetic Diversity of the Himba Population
Study
phs001995
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011