Association of FCRL3 −169T/C polymorphism with endometriosis and identification of a protective haplotype against the development of the disease in Brazilian population
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This study investigated the FCRL3 -169T/C polymorphism and identified a protective haplotype associated with a reduced risk of endometriosis in the Brazilian population.
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References (31)
- Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis via openalex
- Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis via openalex
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Cited by (11)
- Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort 2023
- Single nucleotide polymorphisms of Interleukin − 4, Interleukin-18, FCRL3 and sPLA2IIa genes and their association in pathogenesis of endometriosis 2023
- Increased risk of rheumatoid arthritis in patients with endometriosis: genetic aspects 2022
- Auto-immunity and endometriosis 2021
- The link between immunity, autoimmunity and endometriosis: a literature update 2018
- Association of FCRL3 Genetic Polymorphisms With Endometriosis-Related Infertility Risk 2015
- Understanding the role of epigenomic, genomic and genetic alterations in the development of endometriosis (Review) 2014
- The FCRL3 −169T>C polymorphism and the risk of endometriosis-related infertility in a Polish population 2013
- The nuclear factor-kB functional promoter polymorphism is associated with endometriosis and infertility 2012
- TYK2 rs34536443 polymorphism is associated with a decreased susceptibility to endometriosis-related infertility 2012
- Genetic association study of polymorphisms FOXP3 and FCRL3 in women with endometriosis 2012
Source provenance
- europepmc
- last seen: 2026-06-11T06:19:48.454388+00:00
- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-05-13T22:16:42.478857+00:00
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