Catechol-O-methyltransferase Gene Polymorphism (Val158Met) and Development of Pre-eclampsia
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference33 articles.
1. Association of COMT G675A and MTHFR C677T polymorphisms with hypertensive disorders of pregnancy in Mexican mestizo population;Vazquez-Alaniz;Pregnancy Hypertens,2014
2. Association Between Val158Met Functional Polymorphism in the COMT Gene and Risk of Preeclampsia in a Chinese Population;Liang;Arch Med Res,2012
3. Molecular genetics of preeclampsia and HELLP syndrome — A review;Jebbink;Biochim Biophys Acta,2012
4. A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2);Roten;Mol Hum Reprod,2011
5. Epistasis between COMT and MTHFR in Maternal-Fetal Dyads Increases Risk for Preeclampsia;Hill;PLoS One,2011
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1. Association of catechol-o-methyltransferase gene polymorphism with preeclampsia and biomarkers of oxidative stress: Study protocol for a prospective case-control study in Pakistan;PLOS ONE;2024-06-11
2. The impact of female sex hormones on cardiovascular disease: from mechanisms to hormone therapy;Journal of Geriatric Cardiology;2024-06
3. The COMT Val158Met Polymorphism is Significantly Associated with Early Onset Preeclampsia in Both African American and Caucasian Mothers;2024-05-03
4. Association between Vitamin D receptor (VDR) gene polymorphisms and hypertensive disorders of pregnancy: a systematic review and meta-analysis;PeerJ;2023-04-25
5. Associations of FOXP3 gene polymorphisms with susceptibility and severity of preeclampsia: A meta‐analysis;American Journal of Reproductive Immunology;2022-04-29
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