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The Journal of Maternal-Fetal & Neonatal Medicine Volume 32, 2019 - Issue 10
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Original Article

Effects of Gly71Arg mutation in UGT1A1 gene on neonatal hyperbilirubinemia: a systematic review and meta-analysis

Hassan Mehrad-MajdClinical Research Unit, Mashhad University of Medical Sciences, Mashhad, Iran; Correspondence[email protected]
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,
Monir Sadat HaerianFaculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; View further author information
,
Javad AkhtariMolecular and Cell Biology Research Center, Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran; View further author information
,
Yalda RavanshadClinical Research Unit, Mashhad University of Medical Sciences, Mashhad, Iran; View further author information
,
Anoush AzarfarDepartment of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranView further author information
&
Gholamali MamouriDepartment of Pediatrics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, IranView further author information
Pages 1575-1585 | Received 15 Oct 2017, Accepted 26 Nov 2017, Published online: 10 Dec 2017

Citations (9)

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Jing Tao, Nana Li, Zhen Liu, Ying Deng, Xiaohong Li, Fangfang Luo, Xiaoyan Li, Ping Yu & Jun Zhu. (2023) Polymorphisms in gene UGT1A1 modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk. The Journal of Maternal-Fetal & Neonatal Medicine 36:1.
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Hongjuan Li & Piqiang Zhang. (2021) UGT1A1*28 gene polymorphism was not associated with the risk of neonatal hyperbilirubinemia: a meta-analysis. The Journal of Maternal-Fetal & Neonatal Medicine 34:24, pages 4064-4071.
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Articles from other publishers (7)

May‐Jen Huang, Pei‐Lain Chen & Ching‐Shan Huang. (2022) Bilirubin metabolism and UDP ‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response . The Kaohsiung Journal of Medical Sciences 38:8, pages 729-738.
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Hong Chen, Danni Zhong, Zongyan Gao & Xiaojing Wu. (2022) Effect of the genetic mutant G71R in uridine diphosphate-glucuronosyltransferase 1A1 on the conjugation of bilirubin. Open Life Sciences 17:1, pages 221-229.
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Zheng Jia, Fan Yang, Xiaoqing Liu, Xiaomeng Zhang, Wanjun Hu & Zunlai Sheng. (2021) The n-butanol fraction of the Xiao-Chai-Hu decoction alleviates the endocrine disturbance in the liver of mice exposed to lead. Journal of Ethnopharmacology 279, pages 114381.
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Zijin Li, Li Song & Lihong Hao. (2020) The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility. BMC Medical Genetics 21:1.
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Tien-Thanh Nguyen, Wei Zhao, Xi Yang & Dan-Ni Zhong. (2020) The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns. Pediatric Research 88:6, pages 940-944.
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May-Jen Huang, Yu-Cheng Lin, Kevin Liu, Pi-Feng Chang & Ching-Shan Huang. (2020) Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia. Pediatrics & Neonatology 61:5, pages 506-512.
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Radhian Amandito, Rinawati Rohsiswatmo, Erica Carolina, Rizka Maulida, Windhi Kresnawati & Amarila Malik. (2019) Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing. Frontiers in Pediatrics 7.
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