Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.

BMC pregnancy and childbirth - 29 Jun 2012

Zhao Linlu, Triche Elizabeth W, Walsh Kyle M, Bracken Michael B, Saftlas Audrey F, Hoh Josephine, Dewan Andrew T

Abstract excerpt

BACKGROUND: Specific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS) aims to identify maternal single nucleotide polymorphisms (SNPs) and copy-number variants (CNVs) involved in the etiology of PE. METHODS: A genome-wide scan was performed on 177 PE cases (diagnosed according to National Heart, Lung and Blood Institute guidelines) and 116 normotensive...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Deletion

Share to Genome-Wide Association Study

Share to Pre-Eclampsia

Share to Pregnancy

Share to Protein Array Analysis

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 22748001
DOI: 10.1186/1471-2393-12-61
PMCID: PMC3476390

Genes

PSG11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.PMID 22748001Read ↗

Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.Semantic proximity Read ↗

The genetic component of preeclampsia: A whole-exome sequencing study.Semantic proximity Read ↗

Gene-Centric Analysis of Preeclampsia Identifies Maternal Association at PLEKHG1.Semantic proximity Read ↗

Endometriosis is associated with rare copy number variants.Semantic proximity Read ↗

Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA.Semantic proximity Read ↗

Common deletion polymorphisms in the human genome.Semantic proximity Read ↗

Candidate-gene association study of mothers with pre-eclampsia, and their infants, analyzing 775 SNPs in 190 genes.Semantic proximity Read ↗

A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13.Semantic proximity Read ↗

Targeted sequencing analysis of ACVR2A gene identifies novel risk variants associated with preeclampsia.Semantic proximity Read ↗

Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies.Semantic proximity Read ↗

Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnanciesSemantic proximity Read ↗

Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.