Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Weight Loss and UGT1A1[original query] |
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| 211 G to a variation of UDP-glucuronosyl transferase 1A1 gene and neonatal breastfeeding jaundice. Pediatric research 2011 Feb 69 (2): 170-4. Chou Hung-Chieh, Chen Mei-Huei, Yang Hwai-I, Su Yi-Ning, Hsieh Wu-Shiun, Chen Chien-Yi, Chen Huey-Ling, Chang Mei-Hwei, Tsao Po-Ni |
| Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding. Journal of human genetics 2013 Jan 58 (1): 7-10. Sato Hiroko, Uchida Toshihiko, Toyota Kentaro, Kanno Miyako, Hashimoto Taeko, Watanabe Masashi, Nakamura Tomohiro, Tamiya Gen, Aoki Kuraaki, Hayasaka Kiyos |
| Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns. European journal of pediatrics 2013 Dec 172 (12): 1627-32. Tiwari Pankaj Kumar, Sethi Amanpreet, Basu Sriparna, Raman Rajiva, Kumar Ash |
| UGT1A1 gene variants and clinical risk factors modulate hyperbilirubinemia risk in newborns. Journal of perinatology : official journal of the California Perinatal Association 2014 Feb 34 (2): 120-4. Tiwari P K, Bhutada A, Agarwal R, Basu S, Raman R, Kumar |
| Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms. Journal of human genetics 2015 Jan 60 (1): 35-40. Sato Hiroko, Uchida Toshihiko, Toyota Kentaro, Nakamura Tomohiro, Tamiya Gen, Kanno Miyako, Hashimoto Taeko, Watanabe Masashi, Aoki Kuraaki, Hayasaka Kiyos |
| Case-controlled study on indirect hyperbilirubinemia in exclusively breast fed neonates and mutations of the bilirubin Uridine Diphosphate-Glucuronyl transferase gene 1A1. Annals of medicine and surgery (2012) 2017 Jan 13 6-12. Mohammed Amal E, Behiry Eman G, El-Sadek Akram E, Abdulghany Waleed E, Mahmoud Dalia M, Elkholy Abdelfattah |
| The frequency, clinical course, and health related quality of life in adults with Gilbert's syndrome: a longitudinal study. BMC gastroenterology 2019 2 19 (1): 22. Kamal Sanaa, Abdelhakam Sara, Ghoraba Dalia, Massoud Yasmin, Aziz Kareem Abdel, Hassan Huda, Hafez Tamer, Abdel Sallam Ahm |
| Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case-control study based on the China Neonatal Genomes Project. Frontiers in genetics 2024 1 14 1292921. Xiao Wang, Tiantian Xiao, Jin Wang, Bingbing Wu, Huijun Wang, Yulan Lu, Yaqiong Wang, Bin Chen, Liyuan Hu, Yun Cao, Rong Zhang, Guoqiang Cheng, Laishuan Wang, Zhihua Li, Xinran Dong, Lin Yang, Wenhao Zh |
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