<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(11)</volume><submitter>Vaiman D</submitter><pubmed_abstract>Preeclampsia (PE) is a pregnancy disorder defined by hypertension and proteinuria. This disease remains a major cause of maternal and fetal morbidity and mortality. Defective placentation is generally described as being at the root of the disease. The characterization of the transcriptome signature of the preeclamptic placenta has allowed to identify differentially expressed genes (DEGs). However, we still lack a detailed knowledge on how these DEGs impact the function of the placenta. The tools of network biology offer a methodology to explore complex diseases at a systems level. In this study we performed a cross-platform meta-analysis of seven publically available gene expression datasets comparing non-pathological and preeclamptic placentas. Using the rank product algorithm we identifi</pubmed_abstract><journal>PloS one</journal><pagination>e0165849</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5089765</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An Integrative Analysis of Preeclampsia Based on the Construction of an Extended Composite Network Featuring Protein-Protein Physical Interactions and Transcriptional Relationships.</pubmed_title><pmcid>PMC5089765</pmcid><pubmed_authors>Miralles F</pubmed_authors><pubmed_authors>Vaiman D</pubmed_authors></additional><is_claimable>false</is_claimable><name>An Integrative Analysis of Preeclampsia Based on the Construction of an Extended Composite Network Featuring Protein-Protein Physical Interactions and Transcriptional Relationships.</name><description>Preeclampsia (PE) is a pregnancy disorder defined by hypertension and proteinuria. This disease remains a major cause of maternal and fetal morbidity and mortality. Defective placentation is generally described as being at the root of the disease. The characterization of the transcriptome signature of the preeclamptic placenta has allowed to identify differentially expressed genes (DEGs). However, we still lack a detailed knowledge on how these DEGs impact the function of the placenta. The tools of network biology offer a methodology to explore complex diseases at a systems level. In this study we performed a cross-platform meta-analysis of seven publically available gene expression datasets comparing non-pathological and preeclamptic placentas. Using the rank product algorithm we identifi</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2026-04-30T18:42:42.375Z</modification><creation>2025-05-18T12:27:32.788Z</creation></dates><accession>S-EPMC5089765</accession><cross_references><pubmed>27802351</pubmed><doi>10.1371/journal.pone.0165849</doi></cross_references></HashMap>