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Evolutionary trajectories of IDH-mutant astrocytoma identify molecular grading markers related to cell cycling
Study
EGAS00001007527
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Establishment of an iPSC Repository Derived from Healthy Volunteers
Study
phs003649
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Loss of SDHB promotes dysregulated iron homeostasis, oxidative stress and sensitivity to ascorbate
Study
EGAS00001005279
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Fetal Genomics Consortium (FGC)
Study
phs003193
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Aberrant Oligoclonal Hematopoiesis in Remission AML and Relapse from Rare Cells Genomically Resembling Leukemic Blasts
Study
phs001408
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Impact of germline pathogenic variants in 27 cancer-predisposing genes on the risk of lymphoma
Study
JGAS000347
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Myasthenia gravis-specific aberrant neuromuscular gene expression by medullary thymic epithelial cells in thymoma
Study
JGAS000482
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TGF-β signaling mediates microglial resilience to spatiotemporally restricted myelin degeneration
Study
EGAS50000001413
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Advancing fast in the analysis of circulating tumour DNA
Blog
advancing-fast-in-the-analysis-of-circulating-tumour-dna
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The genetic structure of Norway
Study
EGAS00001004826
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DNA methylation atlas of normal human cell types
Study
EGAS00001006791
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CPC-GENE Prostate Cancer Heterogeneity Study
Study
EGAS00001000549
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Mesenchymal inflammation drives genotoxic stress in hematopoietic stem cells and predicts disease evolution in human pre-leukemia
Study
EGAS00001001926
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Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
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Identification_of_the_underlying_causal_variant_in_a_multi_generational_family_with_autosomal_dominant_common_variable_immunodeficiency
Study
EGAS00001000269
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The_genetics_of_thinness_compared_to_obesity
Study
EGAS00001002624
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Genome-wide prediction of human embryos
Study
EGAS00001001020
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Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
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An essential role for MYB in driving oncogenic EVI1 expression in enhancer-rearranged leukemias
Study
EGAS00001004839
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Mapping the breast cancer metastatic cascade onto circulating tumour DNA using genetic and epigenetic clonal tracking
Study
EGAS00001004014
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Epigenomic priming of immune genes implicates oligodendroglia in multiple sclerosissusceptibility
Study
EGAS00001005911
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Tumor-intrinsic expression of the autophagy gene Atg16l1 suppresses anti-tumor immunity in colorectal cancer
Study
EGAS00001005952
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Serum proteomics of aortic diseases
Study
EGAS00001006201
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Upper cortical layer-driven network impairment in schizophrenia
Study
EGAS00001006495
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Human NXPE1 mediates variation in sialic acid O-acetylation in Colon Tissue
Study
EGAS00001007704
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Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Uzbeks (DNA samples from the Institute of Immunology, Uzbek Academy of Sciences, Tashkent, Uzbekistan; Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology, Tashkent, Uzbekistan)
Study
EGAS00001000416
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Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
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NHLBI TOPMed: My Life Our Future (MLOF) Research Repository of Patients with Hemophilia A (Factor VIII Deficiency) or Hemophilia B (Factor IX Deficiency)
Study
phs001515
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Studying Glioblastoma in a Human Organoid Tumor Transplantation Model
Study
phs003936
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Lung Tissue Research Consortium (LTRC-BioLINCC)
Study
phs003913
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A Genome Wide Scan of Lung Cancer and Smoking
Study
phs000093
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Collaborative Study of Genes, Nutrients and Metabolites (CSGNM)
Study
phs000789
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NIH Human Microbiome Project - Core Microbiome Sampling Protocol A (HMP-A)
Study
phs000228
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Cerebrospinal Fluid Analysis of HIV-1 Viral Burden in HIV-1 Infected Subjects: Response to Antiretroviral Therapy
Study
phs001694
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Translational Research Investigating Underlying disparities in acute Myocardial infarction Patients' Health status (TRIUMPH)
Study
phs001518
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Genomic Regions Associated with Susceptibility to Barrett's Esophagus and Esophageal Adenocarcinoma in African Americans: The Cross BETRNet Admixture Study
Study
phs001454
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Pan Cancer Investigation of Human Leukocyte Antigen Loss of Heterozygosity
Study
phs002783
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Genetic Basis of Pulmonary Non-tuberculous Mycobacterial Infections
Study
phs000719
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Next Generation Mendelian Genetics: Malignant Hyperthermia
Study
phs000405
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Exome sequencing of autosomal recessive progressive external ophthalmoplegia (arPEO)
Study
phs000392
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The mutational characterization of adenoid cystic carcinoma
Study
phs000612
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Single Cell Genomic Analysis of Lymphoma
Study
phs002188
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Filtering and Annotation of Variants That Are Rare (FAVR)
Study
phs000601
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Identification of Genomic Markers of Cervical Dystonia and Subtypes
Study
phs001803
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Chromatin Accessibility Landscape of Human Pancreatic Ductal Adenocarcinoma (PDAC)
Study
phs002394
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Transcriptomic Analysis of Pluripotent Stem Cell-Based Model of Human Amniogenesis
Study
phs002184
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Health Effects of Arsenic Longitudinal Study
Study
phs003839
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Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients
Study
EGAS50000000154
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The PRIME-AIR Study: Positive End-Expiratory Pressure, Recruitment, Incentive Spirometry, Muscle Relaxant Optimization, Preoperative Education, Postoperative Early Ambulation, Individualized, and Reinforced
Study
phs003926
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The acute effects of morning bright light on the human white adipose tissue transcriptome: exploratory post hoc analysis
Study
EGAS50000001206