-
Geographical structure and differential natural selection among North European populations
Study
EGAS00000000033
-
Carbamazepine-induced hypersensitivity reactions in Europeans
Study
EGAS00000000037
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Study
EGAS00000000097
-
Identification of genetic etiology of CAMRQ2
Study
EGAS00000000099
-
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Study
EGAS00000000129
-
DAC_for_study___Screening_for_human_epigenetic_variation_at_CpG_islands
Dac
EGAC00001000043
-
MRCA and MRCE SNP genotypes
Study
EGAS00000000137
-
Genetic_variation_in_Kuusamo
Study
EGAS00001000020
-
An exome sequencing pilot study of HIV elite-long term non progressors and rapid progressors
Study
EGAS00001000057
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Determination of the molecular nature of the Vel blood group by exome sequencing
Study
EGAS00001000069
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Functional_characterisation_of_CpG_islands_in_human_and_mouse_tissues
Study
EGAS00001000075
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Dilgom_Exome
Study
EGAS00001000086
-
Unraveling_the_genetic_basis_of_a_collagen_migration_defect_in_patients_with_a_combined__platelet_dysfunction_and_reduced_bone_density
Study
EGAS00001000093
-
Exome sequencing
Study
EGAS00001005761
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
ENGAGE___Amendment__500_genes_exon_sequencing_
Study
EGAS00001000137
-
Genetic_background_for_the_major_psychiatric_disorders_in_the_general_Finnish_population
Study
EGAS00001000162
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299