-
Deregulation of FOXF1/FENDRR from t(14;16)(q32;q24) defines a subtype of high risk lineage ambiguous leukemia
Study
EGAS50000001255
-
Analysis of a cohort of familial ademomatous polyposis patients bearing APC gene mutation
Study
EGAS00001007237
-
H3K27ac ChIP-seq in a selected group of AML patients
Dataset
EGAD00001007582
-
Epithelial, fibroblast, myeloid, T cell, primary prostate cancer
Dataset
EGAD00001004948
-
RNA-seq as a tool for evaluating human embryo competence
Dataset
EGAD00001005044
-
NHLBI TOPMed - NHGRI CCDG: The BioMe Biobank at Mount Sinai
Study
phs001644
-
Cambridge Neoadjuvant Cancer of the Prostate (CANCAP03): A Window Study into the Effects of Olaparib ± Degarelix in Primary Prostate Cancer.
Study
EGAS50000000880
-
NCI COVID-19 in Cancer Patients Study (NCCAPS): A Longitudinal Natural History Study
Study
phs004178
-
A Therapeutic Vaccine for Fibrolamellar Hepatocellular Carcinoma
Study
phs003970
-
Cross-tissue transcriptomic analysis of human secondary lymphoid organ residing ILC3 reveals a default quiescent state in the absence of inflammation
Study
EGAS00001002636
-
Rucaparib in patients presenting a metastatic breast cancer with Homologous Recombination Deficiency, without germline BRCA1/2 mutation, pronostic value of high LOH genomic score and predictive value of HRDetect (microarray)
Study
EGAS00001004755
-
Familial psychosis associated with a missense mutation at MACF1 gene combined with the rare duplications DUP3p26.3 and DUP16p23.3, affecting the CNTN6 and CDH13 genes
Study
EGAS00001004791
-
A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia
Study
EGAS00001005509
-
Health and Retirement Study (HRS)
Study
phs000428
-
Diagnostic Genomic Analysis is Prognostic in AYA ALL Patients Treated on a MRD-Stratified Paediatric Protocol
Study
EGAS50000000752
-
Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
Study
JGAS000057
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
Genomic stratification and liquid biopsy in a rare adrenocortical carcinoma (ACC) case, with dual lung metastases
Study
EGAS00001003497
-
Expanding the SPTBN1 Spectrum: A Case of Neurodevelopmental Disorder with GI and Musculoskeletal Involvement
Study
EGAS50000001213
-
Submitter Portal
Documentation
submission/metadata/submission/sequencing-phenotype/submitter-portal
-
COLO-829/COLO-829BL
Dataset
EGAD00000000055
-
EGAS00001001311_MalariaGEN_GWAS_summary_statistics_2015
Dataset
EGAD00010001081
-
Homozygous IL37 mutation leads to infantile inflammatory bowel disease
Study
phs002040
-
WTCCC2 Schizophrenia study
Study
EGAS00000000118
-
WTCCC2 Ischaemic Stroke study
Study
EGAS00000000103