Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 52 Records) |
| Query Trace: Jaundice and UGT1A1[original query] |
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| 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 |
| Relation between Neonatal Icter and Gilbert Syndrome in Gloucose-6-Phosphate Dehydrogenase Deficient Subjects. Journal of clinical and diagnostic research : JCDR 2014 Mar 8 (3): 63-5. Zahedpasha Yadollah, Ahmadpour Mousa, Niaki Haleh Akhavan, Alaee Ehs |
| Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice. The Journal of pediatrics 2014 Jul 165 (1): 36-41.e1. Maruo Yoshihiro, Morioka Yoriko, Fujito Hiroshi, Nakahara Sayuri, Yanagi Takahide, Matsui Katsuyuki, Mori Asami, Sato Hiroshi, Tukey Robert H, Takeuchi Yoshihi |
| High prevalence of the UGT1A1*28 variant in HIV-infected individuals in Greece. International journal of STD & AIDS 2014 Oct 25 (12): 860-5. Panagopoulos P, Paraskevis D, Katsarolis I, Sypsa V, Detsika M, Protopapas K, Antoniadou A, Papadopoulos A, Petrikkos G, Hatzakis |
| Clinical significance of the UGT1A1*28 allele detection in HIV-infected patients. Journal of the International AIDS Society 2014 17 (4 Suppl 3): 19579. Kanestri Veronika, Mironov Konstantin, Kravchenko Alexey, Pokrovskaya Anastasiya, Dribnohodova Olga, Dunayeva Elena, Tsiganova Galina, Harbutly Marina, Goliusova Marina, Konnov Vladislav, Kozirina Nadezhda, Shahgildyan Vasiliy, Kuimova Ulyana, Popova Anna, Efremova Oksana, Konnov Dani |
| Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2. European journal of human genetics : EJHG 2015 Sep . Slachtova Lenka, Seda Ondrej, Behunova Jana, Mistrik Martin, Martasek Pav |
| Screening for UGT1A1 Genotype in Study A5257 Would Have Markedly Reduced Premature Discontinuation of Atazanavir for Hyperbilirubinemia. Open forum infectious diseases 2015 Sep 2 (3): ofv085. Vardhanabhuti Saran, Ribaudo Heather J, Landovitz Raphael J, Ofotokun Ighovwerha, Lennox Jeffrey L, Currier Judith S, Olson Lana M, Haas David |
| Gene Mutation in Neonatal Jaundice - Mutations in UGT1A1 and OATP2 Genes. Indian journal of pediatrics 2016 Mar . Min Jiang, Jie Luo, Caiyun Yang, Ying Lin, Xuefang Ya |
| The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2016 Nov 1-21. Halis Hülya, Ergin Hacer, Köseler Aylin, Atalay Erol Öm |
| The Association between Prolonged Jaundice and TATA Box Dinucleotide Repeats in Gilbert's Syndrome. Journal of clinical and diagnostic research : JCDR 2017 12 11 (9): GC05-GC07. Pasha Yadollah Zahed, Kacho Mousa Ahmadpor, Niaki Haleh Akhavan, Tarighati Mehdi, Alaee Ehs |
| Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan. Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2017 Oct 37 (5): 740-743. Liu Wei, Chang Li-Wen, Xie Min, Li Wen-Bin, Rong Zhi-Hui, Wu Li, Chen Li |
| The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome. Journal of clinical and diagnostic research : JCDR 2016 Nov 10 (11): GC05-GC08. Alaee Ehsan, Bazrafshan Behnaz, Azaminejad Ali Reza, Fouladinejad Mahnaz, Shahbazi Maj |
| Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population. Journal of clinical and experimental hepatology 2018 Dec 8 (4): 362-366. Bale Govardhan, Avanthi Urmila S, Padaki N Rao, Sharma Mithun, Duvvur N Reddy, Vishnubhotla V Ravi Kan |
| Identification of Genetic Risk Factors for Neonatal Hyperbilirubinemia in Fujian Province, Southeastern China: A Case-Control Study. BioMed research international 2018 2018 7803175. Zhou Jinfu, Yang Changyi, Zhu Wenbin, Chen Shuwei, Zeng Yinglin, Wang Jing, Zhao Hong, Chen Yao, Lin Fe |
| Profiling of UGT1A16, UGT1A160, UGT1A193, and UGT1A128 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing. Frontiers in pediatrics 2019 8 7 328. Amandito Radhian, Rohsiswatmo Rinawati, Carolina Erica, Maulida Rizka, Kresnawati Windhi, Malik Amari |
| 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 |
Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population.
Nutrients 2019 Jan 11 (1): . Coltell Oscar, Asensio Eva M, Sorlí José V, Barragán Rocio, Fernández-Carrión Rebeca, Portolés Olga, Ortega-Azorín Carolina, Martínez-LaCruz Raul, González José I, Zanón-Moreno Vicente, Gimenez-Alba Ignacio, Fitó Montserrat, Ros Emilio, Ordovas Jose M, Corella Dolor |
| 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 |
| 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- |
| 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- |
| [Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2021 3 29 (2): 143-149. Zhang M, Li W N, Chen G, Xu X, Qi J |
| Genetic Analysis of UGT1A1 Polymorphisms Using Preserved Dried Umbilical Cord for Assessing the Potential of Neonatal Jaundice as a Risk Factor for Autism Spectrum Disorder in Children. Journal of autism and developmental disorders 2021 Mar . Horinouchi Tomoko, Maeyama Kaori, Nagai Masashi, Mizobuchi Masami, Takagi Yasuko, Okada Yuka, Kato Takeshi, Nishimura Mio, Kawasaki Yoko, Yoshioka Mieko, Takada Satoshi, Matsumoto Hisayuki, Nakamachi Yuji, Saegusa Jun, Fukushima Sachiyo, Fujioka Kazumichi, Tomioka Kazumi, Nagase Hiroaki, Nozu Kandai, Iijima Kazumoto, Nishimura Noriyu |
| Prevalence of UGT1A1 (TA)n promoter polymorphism in Panamanians neonates with G6PD deficiency. Journal of genetics 2021 2 99 . Chávez-Peña Teresa, Martínez-Camberos Alejandra, Cossio-Gurrola Gladys, Arámbula-Meraz Eliakym, Herrera-Rodríguez Indira, Romo-Martínez Enrique, García-Magallanes Noe |
| Gilbert's Syndrome, Bilirubin Level and UGT1A1?28 Genotype in Men of North-West Region of Russia. Journal of clinical and experimental hepatology 2021 12 11 (6): 691-699. Ivanov Andrei, Semenova Ele |
| Identifying Potential Therapeutic Applications and Diagnostic Harms of Increased Bilirubin Concentrations: A Clinical and Genetic Approach. Clinical pharmacology and therapeutics 2021 10 111 (2): 435-443. Zanussi Jacy T, Zhao Juan, Dorn Chad A, Liu Ge, Feng QiPing, Wei WeiQi, Mosley Jonathan D, Stein C Michael, Kawai Vivian |
| 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 |
| 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 |
| 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- |
| Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism. Nature communications 2024 8 15 (1): 7550. Pol Solé-Navais, Julius Juodakis, Karin Ytterberg, Xiaoping Wu, Jonathan P Bradfield, Marc Vaudel, Abigail L LaBella, Øyvind Helgeland, Christopher Flatley, Frank Geller, Moshe Finel, Mengqi Zhao, Philip Lazarus, Hakon Hakonarson, Per Magnus, Ole A Andreassen, Pål R Njølstad, Struan F A Grant, Bjarke Feenstra, Louis J Muglia, Stefan Johansson, Ge Zhang, Bo Jacobss |
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