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Genesis of Two Most Prevalent Variants Causing Combined Pituitary Hormone Deficiency in 21 Populations
Study
EGAS00001001165
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GWAS study on arsenic-exposed population
Study
EGAS00001001168
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Sequencing of heritable Bleeding and Platelet Disorders
Study
EGAS00001001172
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Prediction of pigmentation phenotypes by SNP typing in a Northern German population
Study
EGAS00001001174
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Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
Study
EGAS00001001179
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Neuroblastoma relapse trio series from the AMC
Study
EGAS00001001183
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Genome-wide DNA-methylation assessment by MethylCap-seq and Infinium HumanMethylation450 BeadChips: an independent large-scale comparison
Study
EGAS00001001191
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Associations between APOE status and cognitive ability across the lifecourse
Study
EGAS00001001235
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Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Study
EGAS00001001244
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Engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus
Study
EGAS00001001252
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Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
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Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
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BLUEPRINT DNA methylation profiles of graft donors in allogenic hematopoietic stem cell transplantation
Study
EGAS00001001287
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The Genomic Landscape of Response to EGFR Blockade in Colorectal Cancer
Study
EGAS00001001305
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Genetic landscape of pediatric high hyperdiploid acute lymphoblastic leukemia
Study
EGAS00001001316
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JMML targeted sequencing (2013)
Study
EGAS00001001324
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Carcinoma of the oral tongue (OTSCC) genomic landscape characterisation
Study
EGAS00001001329
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Independent development of lymphoid and histiocytic malignancies from a shared early precursor
Study
EGAS00001001353
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Genomes of Relapsing Neuroblastoma
Study
EGAS00001001387
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Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
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Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis
Study
EGAS00001001418
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Trans-ethnic genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Study
EGAS00001001427
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GENETIC HISTORY OF ITALY
Study
EGAS00001001458
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GoT2D: Genetics of Type 2 Diabetes, a study of the the genetic architecture of type 2 diabetes using low pass whole genome sequencing and high density SNP genotyping in 2,657 individuals.
Study
EGAS00001001459
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T2D-GENES: Exome sequencing
Study
EGAS00001001460
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Inherited damaging mutations in immune-related genes favour the development of genetically heterogeneous synchronous colorectal cancer.
Study
EGAS00001001461
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Second hit rare genetic variants in families with seemingly GBA gene associated Parkinson’s disease
Study
EGAS00001004777
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Genotype and exome data for an Australian Aboriginal population: a reference panel for health-based research
Study
EGAS00001001585
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Genetic history of the Comorian populations.
Study
EGAS00001002565
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Genetic history of the Swahili population
Study
EGAS00001002569
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The multifaceted genomic history of Ashaninka from Amazonian Peru
Study
EGAS00001006958
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MeDALL epigenetics study
Study
EGAS00001002169
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Integrative analysis of whole genome sequencing, RNA sequencing and methylome array of 20 carcinosarcomas.
Study
EGAS00001002271
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This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
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TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfism
Study
EGAS00001001501
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Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
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Malignant pheochromocytomas/paragangliomas harbor mutations in transport and cell adhesion genes
Study
EGAS00001001601
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Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
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Conjunctival fibrosis and the innate barriers to Chlamydia trachomatis intracellular infection: a genome wide association study
Study
EGAS00001001516
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Whole exome sequencing of germline DNA was performed and subsequent polymorphisms in genes known and putatively involved in the innate immune response to fungi were identified
Study
EGAS00001001542
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Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
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Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
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Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation
Study
EGAS00001001575
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A genetic compendium of human brains from the UK Medical Research Council brain tissue resource
Study
EGAS00001001599
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The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
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Long-term organoid culture of a small intestinal neuroendocrine tumor
Study
EGAS00001007093
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UK10K NEURO FSZ
Study
EGAS00001000118
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Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
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Sequencing_component_for_the_whole_genome_methylation_analysis_in_PBMCs_and_cell_subsets__pilot_study_
Study
EGAS00001000490
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Next Generation Children project - WGS study of patients in NICU and PICU and their families
Study
EGAS00001003002