Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 183 Records) |
| Query Trace: Hyperbilirubinemia and UGT1A1[original query] |
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| Gilbert syndrome with systemic lupus erythematosus presenting with persistent unconjugated hyperbilirubinemia: A case report. Experimental and therapeutic medicine 2020 9 20 (5): 91. Ye Naifang, Zhou Zhuochao, Gong Huiyun, Teng Jialing, Han Yue, Yang Chengde, Ye Jun |
| A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent ?-thalassemia. Annals of hematology 2020 7 99 (9): 2019-2026. Shrestha Oshan, Khadwal Alka Rani, Singhal Manphool, Trehan Amita, Bansal Deepak, Jain Richa, Pal Arnab, Hira Jasbir Kaur, Chhabra Sanjeev, Malhotra Pankaj, Das Reena, Sharma Prasha |
| Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy. Journal of tropical pediatrics 2020 6 66 (6): 569-582. Boo Nem-Yun, Sin Shwe, Chee Seok-Chiong, Mohamed Maslina, Ahluwalia Anita Kaur, Ling Michelle Min-Min, Ong Han-Ki |
| Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia. Pediatrics and neonatology 2020 6 61 (5): 506-512. Huang May-Jen, Lin Yu-Cheng, Liu Kevin, Chang Pi-Feng, Huang Ching-Sh |
| The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns. Pediatric research 2020 Mar . Nguyen Tien-Thanh, Zhao Wei, Yang Xi, Zhong Dan- |
| Roles of UGT1A1 Gly71Arg and TATA promoter polymorphisms in neonatal hyperbilirubinemia: A meta-analysis. Gene 2020 Jan 144409. Wang Jing, Yin Jiansong, Xue Mei, Lyu Jun, Wan |
| Carbon monoxide breath test assessment of mild hemolysis in Gilbert's syndrome. Medicine 2020 2 99 (7): e19109. Kang Ling-Ling, Ma Yong-Jian, Zhang Hou- |
| The role of UGT1A1 (c.-3279?T?>?G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility. BMC medical genetics 2020 Nov 21 (1): 218. Li Zijin, Song Li, Hao Liho |
| Pharmacogenetic Associations Between Atazanavir/UGT1A1*28 and Efavirenz/rs3745274 (CYP2B6) Account for Specific Adverse Reactions in Chilean Patients Undergoing Antiretroviral Therapy. Frontiers in pharmacology 2021 6 12 660965. Poblete Daniela, Bernal Fernando, Llull Gabriel, Archiles Sebastian, Vasquez Patricia, Chanqueo Leonardo, Soto Nicole, Lavanderos María A, Quiñones Luis A, Varela Nelson |
| UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China. BMC pediatrics 2021 06 21 (1): 259. Yang Hui, Lin Fen, Chen Zi-Kai, Zhang Lin, Xu Jia-Xin, Wu Yong-Hao, Gu Jing-Ying, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
| Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people. Gene 2021 2 781 145526. Zhang Meng, Wang Hongwu, Huang Yuancheng, Xu Xin, Liu Wei, Ning Qin, Chen Tao, Qi Junyi |
| Influence of UGT1A1 promoter polymorphism, ?-thalassemia and ? haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort. Annals of hematology 2021 Feb . Batista Jéssica V G F, Arcanjo Gabriela S, Batista Thais H C, Sobreira Marcondes J, Santana Rodrigo M, Domingos Igor F, Hatzlhofer Betânia L, Falcão Diego A, Pereira-Martins Diego A, Oliveira Jéssica M, Araujo Amanda S, Laranjeira Luana P M, Medeiros Fernanda S, Albuquerque Flávia P, Albuquerque Dulcinéia M, Santos Magnun N, Hazin Manuela F, Dos Anjos Ana C, Costa Fernando F, Araujo Aderson S, Lucena-Araujo Antonio R, Bezerra Marcos |
| Co-inheritance of G6PD deficiency and 211?G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong. BMC pediatrics 2021 12 21 (1): 564. Xu Jia-Xin, Lin Fen, Chen Zi-Kai, Luo Zhao-Yun, Zhan Xiao-Fen, Wu Jiao-Ren, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
| [Gilbert's syndrome: hyperbilirubinemia enemy or friend]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2021 11 29 (10): 1024-1027. Xiang G Q, Sun F R, Wang B |
| Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response. The Kaohsiung journal of medical sciences 2022 8 38 (8): 729-738. Huang May-Jen, Chen Pei-Lain, Huang Ching-Sh |
| [UGT1A1 gene mutations in Chinese Dong neonates in Sanjiang, Guangxi]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2022 7 24 (7): 792-796. Yao Xuan, Zhong Dan-Ni, Peng Yun-Co |
| Serum Bilirubin Concentrations and the Prevalence of Gilbert Syndrome in Elite Athletes. Sports medicine - open 2022 Jun 8 (1): 84. Woronyczová Jana, Nováková Miroslava, Lení?ek Martin, Bátovský Miloš, Bolek Emil, Cífková Renata, Vítek Lib |
| Associations between UGT1A1 and SLCO1B1 polymorphisms and susceptibility to neonatal hyperbilirubinemia in Thai population. BMC pediatrics 2022 05 22 (1): 243. Atasilp Chalirmporn, Kanjanapipak Janjira, Vichayaprasertkul Jaratdao, Jinda Pimonpan, Tiyasirichokchai Rawiporn, Srisawasdi Pornpen, Prempunpong Chatchay, Chamnanphon Monpat, Puangpetch Apichaya, Vanwong Natchaya, Klongthalay Suwit, Jantararoungtong Thawinee, Sukasem Chonlaph |
| Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity. Italian journal of pediatrics 2022 4 48 (1): 59. Cozzi Laura, Nuti Federica, Degrassi Irene, Civeriati Daniela, Paolella Giulia, Nebbia Gabriel |
| Genetic testing of UGT1A1 in the diagnosis of Gilbert syndrome: The discovery of seven novel variants in the Chinese population. Molecular genetics & genomic medicine 2022 4 10 (7): e1958. Gu Leilei, Han Yue, Zhang Donghua, Gong Qiming, Zhang Xinx |
| Association of Inherited Genetic Factors With Drug-Induced Hepatic Damage Among Children With Acute Lymphoblastic Leukemia. JAMA network open 2022 12 5 (12): e2248803. Yang Wenjian, Karol Seth E, Hoshitsuki Keito, Lee Shawn, Larsen Eric C, Winick Naomi, Carroll William L, Loh Mignon L, Raetz Elizabeth A, Hunger Stephen P, Winter Stuart S, Dunsmore Kimberly P, Devidas Meenakshi, Relling Mary V, Yang Jun |
| UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia. PloS one 2022 12 17 (12): e0279059. Yang Hui, Li Huijun, Xia Qingyao, Dai Wencheng, Li Xin, Liu Yan, Nie Jie, Yang Fei, Sun Yunfeng, Feng Lei, Yang Li |
| Influence of UGT1A1 Genetic Variants on Free Bilirubin Levels in Japanese Newborns: A Preliminary Study. International journal of environmental research and public health 2022 10 19 (20): . Hanafusa Hiroaki, Abe Shinya, Ohyama Shohei, Kyono Yuki, Kido Takumi, Nakasone Ruka, Ashina Mariko, Tanimura Kenji, Nozu Kandai, Fujioka Kazumic |
| The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia. Children (Basel, Switzerland) 2023 7 10 (7): . Arieh Riskin, Yulia Bravdo, Clair Habib, Irit Maor, Julnar Mousa, Sizett Shahbarat, Elena Shahak, Adel Shala |
| Red Blood Cell Membrane-Related Gene Variants and Clinical Risk Factors in Chinese Neonates with Hyperbilirubinemia. Neonatology 2023 4 1-10. Lin Fen, Xu Jia-Xin, Wu Yong-Hao, Chen Zi-Kai, Chen Man-Tong, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
| UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice. Frontiers in pediatrics 2023 1 10 1080212. Yang Zhe, Lin Fen, Xu Jia-Xin, Yang Hui, Wu Yong-Hao, Chen Zi-Kai, Xie He, Huang Bin, Lin Wei-Hao, Wu Jian-Peng, Ma Yu-Bin, Li Jian-Dong, Yang Li- |
| Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group. Journal of experimental & clinical cancer research : CR 2023 1 42 (1): 21. Junk Stefanie V, Schaeffeler Elke, Zimmermann Martin, Möricke Anja, Beier Rita, Schütte Peter, Fedders Birthe, Alten Julia, Hinze Laura, Klein Norman, Kulozik Andreas, Muckenthaler Martina U, Koehler Rolf, Borkhardt Arndt, Vijayakrishnan Jayaram, Ellinghaus David, Forster Michael, Franke Andre, Wintering Astrid, Kratz Christian P, Schrappe Martin, Schwab Matthias, Houlston Richard S, Cario Gunnar, Stanulla Mart |
| Cabozantinib Induces Isolated Hyperbilirubinemia in Renal Cell Carcinoma Patients carrying the UGT1A1*28 Polymorphism. Clinical genitourinary cancer 2024 8 102180. Sajedeh Mobaraki, Peter Henrik Nissen, Frede Donskov, Agnieszka Wozniak, Yannick Van Herck, Lina Coosemans, Tine van Nieuwenhuyse, Diether Lambrechts, Oliver Bechter, Marcella Baldewijns, Eduard Roussel, Annouschka Laenen, Benoit Beuselin |
| Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population. BMC pediatrics 2024 1 24 (1): 82. Juan Fan, Hua-Yun He, Huan-Huan Li, Pi-Liu Wu, Lei Tang, Bo-Yin Deng, Wen-Hui Dong, Jian-Hui Wa |
| 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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