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Article

Copy number variation analysis reveals additional variants contributing to endometriosis development.

Journal of assisted reproduction and genetics - 1 Jan 2017

Mafra Fernanda, Mazzotti Diego, Pellegrino Renata, Bianco Bianca, Barbosa Caio Parente, Hakonarson Hakon, Christofolini Denise

Abstract excerpt

PURPOSE: Endometriosis is a gynecological disease influenced by multiple genetic and environmental factors. The aim of the current study was to use SNP-array technology to identify genomic aberrations that may possibly contribute to the development of endometriosis. METHODS: We performed an SNP-array genotyping of pooled DNA samples from both patients (n = 100) and controls (n = 50). Copy number variation (CNV)...

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Share to Chromosomes, Human, Pair 19
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Genetic Predisposition to Disease

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Share to Genome-Wide Association Study

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Share to Polymorphism, Single Nucleotide

Source

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Identifiers

PMID: 27817035
DOI: 10.1007/s10815-016-0822-1
PMCID: PMC5330977

Genes

FCGBP

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.

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