-
Next-Generation Sequencing of AV Nodal Reentry Tachycardia patients
Study
EGAS00001002745
-
Glioblastoma initiating cells are sensitive to histone demethylase inhibition due to epigenetic deregulation
Study
EGAS00001003750
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
Variation in the Glucose Transporter gene SLC2A2 is associated with glycaemic response to metformin
Study
EGAS00001001875
-
Growth Hormone (GH) -secreting Pituitary Adenoma
Study
EGAS00001003488
-
Kibbutzim Family study
Study
EGAS00001002782
-
Genetic control of the transcriptomic response of monocytes to bacterial and viral stimuli assessed by RNA-seq in Africans and Europeans
Study
EGAS00001001895
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
Knee_OA_Functional_Genomics
Study
EGAS00001001899
-
Whole genome sequencing for novel neuromuscular disease gene discovery
Study
EGAS00001004535
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
-
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Study
EGAS00001003545
-
Genetics and transcriptomes of pediatric B cell precursor leukemia with gain of chromosome 21
Study
EGAS00001003760
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
-
The_contribution_of_POT1_variants_to_sporadic_melanoma_development
Study
EGAS00001001964
-
HipSci___Whole_Exome_sequencing___Battens
Study
EGAS00001001975
-
HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
-
Mapping_genetic_variants_underlying_gene_regulation_in_inflammed_intestinal_cell_types_to_identify_novel_IBD_drug_targets
Study
EGAS00001003770
-
Physiological and genetic adaptations to diving in Sea Nomads
Study
EGAS00001002823
-
HipSci___Whole_Exome_sequencing___Macular_dystrophy
Study
EGAS00001001982
-
HipSci___Whole_Exome_sequencing___PID
Study
EGAS00001001983
-
HipSci HumanExome BeadChip analysis - Hereditary Spastic Paraplegia
Study
EGAS00001002006
-
HipSci HumanExome BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002010
-
HipSci HumanExome BeadChip analysis - Hypertrophic Cardiomyopathy
Study
EGAS00001002011
-
HipSci HumanExome BeadChip analysis - Battens disease
Study
EGAS00001002016