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Plasma pQTLs in INTERVAL cohort
Study
EGAS00001002555
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Etiology of congenital thyroid dysfunction in Down Syndrome: a multi-omics investigation
Study
EGAS50000000264
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RNA-sequencing on thyroid samples from fetuses with Down syndrome and fetuses with no genetic/developmental abnormality
Dataset
EGAD50000000387
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Enhanced resolution profiling in twins reveals differential methylation signatures of Type 2 Diabetes with links to its complications
Study
EGAS50000000197
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Whole Exome Sequencing
Study
EGAS50000000259
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Childhood Cancer Data Initiative (CCDI): Enhancement of Data Sharing in Pediatric, Adolescent and Young Adult Cancers
Study
phs002431
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Colorectal cancer functional annotation - ChIP
Study
EGAS50000000207
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Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
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The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
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Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases
Study
EGAS00001007783