-
Oncogenic Ectodomain deletion of FGFR1 caused by Breakage-Fusion-Bridges in Squamous Cell lung Cancer
Study
EGAS00001005059
-
Knoll et al Identification of drug candidates targeting monocyte reprogramming in people living with HIV
Study
EGAS00001007460
-
Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma
Study
EGAS00001002443
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Study
EGAS00001001606
-
Comprehensive Genomic Characterization of Gene Therapy-Induced T-cell Acute Lymphoblastic Leukemia (H007)
Study
EGAS00001003870
-
ctDNA monitoring using patient-specific sequencing and integration of variant reads - Lung cohort
Study
EGAS00001004447
-
Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
-
UK10K_NEURO_ASD_FI
Study
EGAS00001000110
-
Identification of a Fumarate-Hydratase Deficient-like RCC Subtype with Convergent Pathway Alterations
Study
EGAS00001002646
-
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Study
EGAS00001004145
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
-
Platelet RNAseq data for SLFN14 K219N patients
Study
EGAS00001006339
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
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Single-cell atlas of penile cancer reveals TP53 mutations as driver for an aggressive phenotype, irrespective of HPV status, and provides clues for treatment personalization
Study
EGAS50000000217
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Pharmacological improvement of CFTR function rescues airway epithelial homeostasis and host defense in cystic fibrosis children
Study
EGAS50000000128
-
Nanopore sequencing of blood, saliva, buccal mucosa samples of patients with inherited retinal disorders
Study
EGAS50000000440
-
Transcriptional_reprogramming_from_innate_immune_functions_to_a_pro_thrombotic_signature_upon_SARS_CoV_2_sensing_by_monocytes_in_COVID_19
Study
EGAS00001006788
-
DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
-
Breast cancer DNA repair
Study
EGAS00001002792
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Study
EGAS00001003656
-
A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
Study
EGAS00001002840
-
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Study
EGAS00001003177
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Bone marrow breakout lesions act as key sites for tumor-immune cell diversification and exhaustion in multiple myeloma
Study
EGAS50000000304
-
RNAseq: Acquired non-permissive bone marrow microenvironment impairs hematopoietic stem cell proliferation and maintenance and B-cell development post-HSCT
Study
EGAS50000001437
-
ATAC-seq: Acquired non-permissive bone marrow microenvironment impairs hematopoietic stem cell proliferation and maintenance and B-cell development post-HSCT
Study
EGAS50000001438
-
Influence of age on molecular changes and treatment stratification in multimodal glioblastoma therapy
Study
EGAS00001008246
-
Monocyte and macrophage lipid accumulation results in downregulated type-I interferon responses
Study
EGAS00001005955
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
-
Whole genome sequencing of 108 epileptic patients from CENet cohort
Study
EGAS00001007507
-
Tubulointerstitial fibrosis is the histological hallmark of chronic kidney disease (CKD). Hypoxia and inflammation (i.e., interleukin (IL)-1β signalling) are independent mediators of tubulointerstitial fibrosis. However, the physiological response of human kidney tubular cells to IL-1β/IL-1RI signalling under the hypoxic conditions of CKD is poorly understood and remains a clinical imperative for therapeutic targeting. This study reports that hypoxia and IL-1β act in synergy to trigger cell cycle arrest/cellular senescence of ex vivo patient-derived primary proximal tubular epithelial cells (PTECs).
Study
EGAS00001007904
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
UK10K_OBESITY_SCOOP
Study
EGAS00001000124
-
Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
-
Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
-
ImmunAID
Study
EGAS50000001393
-
Successful immune checkpoint blockade in a patient with advanced stage microsatellite unstable biliary tract cancer (H021)
Study
EGAS00001002441
-
Genomic profiling of paediatric high grade gliomas from the HERBY clinical trial
Study
EGAS00001002328
-
Liver biopsy derived induced pluripotent stem cells provide an unlimited supply for the generation of patient-specific hepatocyte-like cells
Study
EGAS00001002676
-
Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
-
Clinical and Molecular Investigation of Familial CEBPA-mutated Acute Myeloid Leukaemia
Study
EGAS00001000949
-
Control sets genotyped with Dynal RELI SSO and Roche Molecular Systems platfroms
Study
EGAS00000000032
-
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Study
EGAS00000000129
-
Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis
Study
EGAS00001007008
-
Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
Study
EGAS00000000119
-
NGS on cardiac samples in Hungarian patients of dilated cardiomyopathy
Study
EGAS50000000049
-
Exceptional Outcomes in a Phase Ib Study Combining PARP and MEK Inhibition, With or Without Anti-PD-L1, for BRCA-Wildtype Platinum-Sensitive Recurrent Ovarian Cancer
Study
EGAS00001007496
-
300BCG study: human population variation of trained immunity
Study
EGAS50000000090
-
Progressive multifocal leukoencephalopathy (PML)
Study
EGAS50000000139
-
Multi-omic characterisation of PBMCs in IBD
Study
EGAS50000000140
-
Single cell RNA sequencing of cerebrospinal fluid
Study
EGAS00001007478
-
Immunomodulatory effects and improved outcomes with cisplatin- vs carboplatin-based chemotherapy plus atezolizumab in urothelial cancer
Study
EGAS50000000104
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Lifelines NEXT
Study
EGAS50000000133
-
Investigating differential diagnostic and prognostic biomarkers in primary cutaneous follicle center lymphoma and follicular lymphoma using low-coverage whole-genome sequencing
Study
EGAS50000000141
-
Transcriptional profiling and clonality analysis of peripheral blood B cells and small intestinal plasma cells in celiac disease
Study
EGAS50000000229
-
Targeted sequencing of genomic regions of interest in depression and obesity
Study
EGAS50000000330
-
Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell ATAC-seq
Study
EGAS00001007380
-
A comprehensive genetic map of cytokine responses in Lyme borreliosis
Study
EGAS50000000024
-
Toxigenic Clostridium perfringens isolated from at-risk pediatric inflammatory bowel disease patients
Study
EGAS50000000334
-
"BaTwa" populations from Zambia retain ancestry of past hunter-gatherer groups
Study
EGAS50000000378
-
METABRIC
Study
EGAS00000000098
-
Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositis
Study
EGAS50000000310
-
Efficacy and safety of entrectinib in patients with ROS1-positive advanced/metastatic non-small cell lung cancer (NSCLC) from the Blood First Assay Screening Trial (BFAST)
Study
EGAS50000000105
-
The effects of inhaled corticosteroids on healthy airways
Study
EGAS00001007538
-
Full AfricanNeo ModernDNA Study
Study
EGAS50000000006
-
Circulating tumor DNA dynamics reveal KRAS G12C mutation heterogeneity and response to treatment with the KRAS G12C inhibitor divarasib in solid tumors
Study
EGAS50000000315
-
Spatially resolved transcriptomics reveals profound subclonal heterogeneity and T cell dysfunction in extramedullary myeloma
Study
EGAS50000000227
-
Tumor Evolution Analysis Uncovered Immune-Escape Related Mutations in Relapsed Diffuse Large B-Cell Lymphoma
Study
EGAS50000000032
-
Variables of mass cytometry (CyTOF) innate immune cell counts
Study
EGAS50000000588
-
snRNA-seq of subcortical MS
Study
EGAS50000000354
-
ICARUS-BREAST01-RNAseq
Study
EGAS50000000543
-
Characterizing the cell-free transcriptome in a humanized DLBCL patient-derived tumor xenograft model for RNA-based liquid biopsy in a preclinical setting
Study
EGAS50000000566
-
Non-invasive prediction of immunotherapy response (NIPIT) project
Study
EGAS50000000266
-
IL-17B uses IL-17RA and IL-17RB to induce Type-2 inflammation from human lymphocytes
Study
EGAS50000000579
-
Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Study
EGAS50000000484
-
Full genome sequencing of a monozygotic twin discordant for schizophrenia
Study
EGAS00001000152
-
Whole Genome Sequencing of Neuroblastoma
Study
EGAS00001000222
-
The Cardiogenics study
Study
EGAS00001000411
-
Somatic mutations increase hepatic clonal fitness and regeneration in chronic liver disease
Study
EGAS00001003496
-
The Sys4MS cohort: a prospective cohort of patients with Multiple Sclerosis and omics
Study
EGAS00001007145
-
Enhanced detection of MRD with cfDNA Fragmentomics.
Study
EGAS00001007192
-
Small molecule screen reveals synergy of cell cycle checkpoint kinase inhibitors with DNA-damaging chemotherapies in medulloblastoma (RNAseq dataset)
Study
EGAS00001004748
-
Archaeogenomic distinctiveness of the Isthmo-Colombian area
Study
EGAS00001007131
-
The transition from normal lung anatomy to minimal and established fibrosis in Idiopathic Pulmonary Fibrosis
Study
EGAS00001004758
-
The impact of urbanization and diet on innate immune responses in healthy Tanzanians
Study
EGAS00001004284
-
Candidate Gene Case Control Study of Human African Trypanosomiasis in the Democratic Republic of Congo
Study
EGAS00001004365
-
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study
EGAS00001004625
-
Integration of metabolomics, genomics and immune phenotypes reveals the causal roles of metabolites in disease
Study
EGAS00001005348
-
The Xq22.3 contiguous gene deletion syndrome (ATS-ID)
Study
EGAS00001005354
-
Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features
Study
EGAS00001005355