-
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Study
EGAS00001004145
-
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Association of DNA-methylation profiles with immune responses in breast cancer patients
Study
EGAS00001004211
-
single-stranded DNA study
Study
EGAS00001005093
-
Analysis of exonic somatic variants in light-chain amyloidosis (ALA) and ALA concomitant with multiple myeloma
Study
EGAS00001004214
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
Genetic characterization of a Unique Neuroendocrine Transdifferentiation Prostate Circulating Tumor Cell - Derived eXplant (CDX) Model
Study
EGAS00001004272
-
RUNX1 mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
Study
EGAS00001004273
-
Whole genome sequencing of 76 tumor and normal samples from 11 SI-NET patients
Study
EGAS00001005096
-
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma (arrays set)
Study
EGAS00001004314
-
Multiregion Whole-Exome Sequencing Uncovers the Genetic Evolution and Mutational Heterogeneity of Early-Stage Metastatic Melanoma.
Study
EGAS00001004320
-
Overrepresentation of genetic variation in the AnkyrinG interactome is related to a range of neurological disorders
Study
EGAS00001004326
-
METABRIC: Data from Batra et al (2021); DNA methylation landscapes of 1538 breast cancers reveal a replication-linked clock, epigenomic instability and cis-regulation
Study
EGAS00001004327
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
MeDALL Epigenetics group
Dac
EGAC00001000578
-
Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
-
Sequencing of an adolescent patient with germline RET mutant alveolar rhabdomyosarcoma
Study
EGAS00001004359
-
Genetic diversity and continuity of the population of the UAE
Study
EGAS00001004362
-
Whole-genome sequencing of rare disease patients in a national healthcare system
Study
EGAS00001004364
-
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
-
Genomic study of an AT-AML
Study
EGAS00001004392
-
Search for genetic variants influencing gestational weight gain in type 1 diabetes patients by genome wide association method
Study
EGAS00001004408
-
Genome-wide associations of human gut microbiota variation and implications for causal inference analyses
Study
EGAS00001004420
-
Impact of genetic variants in clinical outcome of a cohort of patients with oropharyngeal squamous cell carcinoma
Study
EGAS00001004430
-
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: Defining a Healthy Volunteer Cohort
Study
EGAS00001004434
-
DO NOT USE - Whole genome sequencing of SI-NETs from five patients
Study
EGAS00001004435
-
Modulation of macrophage inflammatory function through selective inhibition of the epigenetic reader protein SP140
Study
EGAS00001004460
-
Collection of Genotypic and Ethnographic Information from Individuals of South African Ethnic Groups
Study
EGAS00001004472
-
Versatile workflow for cell-type resolved transcriptional and epigenetic profiles from cryopreserved human lung
Study
EGAS00001004477
-
Identifying the role of ID3 in DNA repair and maintenance of genome integrity
Study
EGAS00001004478
-
Targets of MEK inhibition in DIPG
Study
EGAS00001004495
-
Uterine leiomyoma: DNA methylation, chromatin activity and gene expression
Study
EGAS00001004499
-
A reference map of potential determinants for the human serum metabolome
Study
EGAS00001004512
-
An epigenetic single-cell atlas of IDH-mutant glioma reveals the role of ATRX in shaping tumor composition
Study
EGAS00001004523
-
Whole genome sequencing for novel neuromuscular disease gene discovery
Study
EGAS00001004535
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma
Study
EGAS00001004551
-
Whole Genome Sequencing of 317 individuals from the Pacific region
Study
EGAS00001004540
-
Super enhancers define regulatory subtypes and cell identity in neuroblastoma - RNA-seq
Study
EGAS00001004552
-
Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
Study
EGAS00001004559
-
The Genetic Basis of Preeclampsia in an Andean Population Adapted to High Altitude
Study
EGAS00001004625
-
Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial
Study
EGAS00001004574
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
-
A Universal Gut Metagenomic-Derived Signature Predicts Cirrhosis
Study
EGAS00001004600
-
The endometrial transcription landscape of MRKH syndrome
Study
EGAS00001004601
-
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Study
EGAS00001004624
-
The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
-
International consensus definition of DNA methylation subgroups in juvenile myelomonocytic leukemia
Study
EGAS00001004682
-
Mechanisms of active DNA demethylation in human monocytes
Study
EGAS00001004784
-
Chromosomal copy number heterogeneity predicts survival rates across cancers
Study
EGAS00001004702
-
Methylation analysis for plasma DNA of patients with organ transplantation
Study
EGAS00001004788
-
A novel orthotopic patient-derived xenograft model of radiation-induced glioma following medulloblastoma
Study
EGAS00001004709
-
STAT5 is a therapeutically targetable vulnerability in cutaneous T-cell lymphoma
Study
EGAS00001004719
-
Mutational Landscape and Tumor Burden Assessed by Cell-Free DNA in Diffuse Large B-Cell Lymphoma: a Population-based Study
Study
EGAS00001004733
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
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
-
Epigenome-wide association study of asthma remission in whole blood and nasal epithelium
Study
EGAS00001004766
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
The genetic structure of Norway
Study
EGAS00001004826
-
AGECAN - Interespecies conservation of brain specific DNA methylation in aging and cancer
Study
EGAS00001004851
-
Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
-
Targeted de-methylation of the FOXP3-TSDR
Study
EGAS00001004867
-
Genetic makeup of agnospheres
Study
EGAS00001004868
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Targeted sequencing DDR genes in cancer stem cells
Study
EGAS00001004892
-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
-
Breast tissue methylation analysis
Study
EGAS00001005070
-
Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Study
EGAS00001005005
-
DO NOT USE - Whole genome sequencing of SI-NETs from six patients
Study
EGAS00001005009
-
Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry
Study
EGAS00001005022
-
The WID-EC test for the detection and risk prediction of endometrial cancer
Study
EGAS00001005033
-
The DNA methylome of cervical cells and risk of ovarian cancer
Study
EGAS00001005045
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Study
EGAS00001005064
-
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Study
EGAS00001005104
-
Chronic myelomonocytic leukemia
Study
EGAS00001005107
-
Sequencing of cancer autopsies and ctDNA
Study
EGAS00001005109
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
Epigenomic profiling and transcriptomic profiling of LUAD patients tumor tissues and tumor adjacent tissues
Study
EGAS00001005132
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
Bulk-tissue RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Study
EGAS00001005305
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Study
EGAS00001005430
-
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
-
Analysis of RAD51C promoter methylation using targeted bisulfite sequencing (amplicon sequencing) in ovarian cancer pre-clinical models and patient samples.
Study
EGAS00001005395
-
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Study
EGAS00001005402
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005408
-
Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Study
EGAS00001005444
-
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442