A multi-omics informatics approach for identifying molecular mechanisms and biomarkers in clinical patients with endometriosis
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This study used DNA methylation and RNA sequencing data to identify molecular mechanisms and potential biomarkers for noninvasive endometriosis diagnosis.
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Abstract
Endometriosis is a complex gynecological disorder. The diagnostic process of endometriosis involves an invasive procedure thus delaying the diagnosis for about 10 years on average. Both DNA-methylation data and RNA-seq data has the potential to uncover molecular mechanisms of diseases. The objective of this project is to identify diagnostic molecular mechanisms of endometriosis using a multi-omics approach that will lead to noninvasive diagnostic procedure.
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References (10)
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- Delay in the diagnosis of endometriosis: a survey of women from the USA and the UK via openalex
- Experimental murine endometriosis induces DNA methylation and altered gene expression in eutopic endometrium via openalex
- Promoter methylation regulates estrogen receptor 2 in human endometrium and endometriosis via openalex
- Transcriptional activation of steroidogenic factor-1 by hypomethylation of the 5' CpG island in endometriosis via openalex
- Whole genome deoxyribonucleic acid microarray analysis of gene expression in ectopic versus eutopic endometrium via openalex
- W2574721333 via openalex
- W2044124287 via openalex
- W2116844530 via openalex
- W1968667083 via openalex
Cited by (4)
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- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- unpaywall
- last seen: 2026-10-10T06:25:47.132674+00:00
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