Similar articles for PMID: 21412181

Year	Number of Results
1951	1
1962	1
1976	1
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1997	1
1998	2
1999	7
2000	4
2001	5
2002	3
2003	3
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2005	9
2006	6
2007	8
2008	6
2009	9
2010	8
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2013	18
2014	12
2015	8
2016	10
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2018	10
2019	14
2020	12
2021	16
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2023	2
2024	1

1

Genetic variation in UGT1A1 typical of Gilbert syndrome is associated with unconjugated hyperbilirubinemia in patients receiving tocilizumab.

Lee JS, Wang J, Martin M, Germer S, Kenwright A, Benayed R, Spleiss O, Platt A, Pilson R, Hemmings A, Weinblatt ME, Kaplowitz N, Krasnow J. Lee JS, et al. Pharmacogenet Genomics. 2011 Jul;21(7):365-74. doi: 10.1097/FPC.0b013e32834592fe. Pharmacogenet Genomics. 2011. PMID: 21412181

2

Tocilizumab-induced hyperbilirubinemia in Japanese patients with rheumatoid arthritis: its association with UDP glucuronosyltransferase 1A1 gene polymorphisms.

Mori S, Terada K, Ueki Y. Mori S, et al. Mod Rheumatol. 2012 Aug;22(4):515-23. doi: 10.1007/s10165-011-0537-1. Epub 2011 Oct 13. Mod Rheumatol. 2012. PMID: 21993917

3

Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome.

Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y. Maruo Y, et al. J Gastroenterol Hepatol. 2016 Feb;31(2):403-8. doi: 10.1111/jgh.13071. J Gastroenterol Hepatol. 2016. PMID: 26250421

4

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.

Dabke PS, Colah RB, Ghosh KK, Nadkarni AH. Dabke PS, et al. Hematology. 2014 Oct;19(7):388-92. doi: 10.1179/1607845413Y.0000000142. Epub 2013 Nov 30. Hematology. 2014. PMID: 24620945

5

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.

Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR. Kadakol A, et al. Hum Mutat. 2000 Oct;16(4):297-306. doi: 10.1002/1098-1004(200010)16:4<297::AID-HUMU2>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 11013440 Review.

6

Influence of UGT1A1 promoter polymorphism, α-thalassemia and β^s haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.

Batista JVGF, Arcanjo GS, Batista THC, Sobreira MJ, Santana RM, Domingos IF, Hatzlhofer BL, Falcão DA, Pereira-Martins DA, Oliveira JM, Araujo AS, Laranjeira LPM, Medeiros FS, Albuquerque FP, Albuquerque DM, Santos MN, Hazin MF, Dos Anjos AC, Costa FF, Araujo AS, Lucena-Araujo AR, Bezerra MA. Batista JVGF, et al. Ann Hematol. 2021 Apr;100(4):903-911. doi: 10.1007/s00277-021-04422-1. Epub 2021 Feb 1. Ann Hematol. 2021. PMID: 33523291

7

A functional polymorphism in UGT1A1 related to hyperbilirubinemia is associated with a decreased risk for Crohn's disease.

de Vries HS, Te Morsche RH, Jenniskens K, Peters WH, de Jong DJ. de Vries HS, et al. J Crohns Colitis. 2012 Jun;6(5):597-602. doi: 10.1016/j.crohns.2011.11.010. Epub 2011 Dec 16. J Crohns Colitis. 2012. PMID: 22398043

8

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.

Rodrigues C, Vieira E, Santos R, de Carvalho J, Santos-Silva A, Costa E, Bronze-da-Rocha E. Rodrigues C, et al. Blood Cells Mol Dis. 2012 Mar 15;48(3):166-72. doi: 10.1016/j.bcmd.2012.01.004. Epub 2012 Feb 9. Blood Cells Mol Dis. 2012. PMID: 22325916 Free article.

9

A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.

Nakagawa T, Mure T, Yusoff S, Ono E, Kusuma Harahap IS, Morikawa S, Morioka I, Takeshima Y, Nishio H, Matsuo M. Nakagawa T, et al. Kobe J Med Sci. 2011 Jul 20;57(1):E26-31. Kobe J Med Sci. 2011. PMID: 22169899 Free article.

10

Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism.

Xu CF, Reck BH, Xue Z, Huang L, Baker KL, Chen M, Chen EP, Ellens HE, Mooser VE, Cardon LR, Spraggs CF, Pandite L. Xu CF, et al. Br J Cancer. 2010 Apr 27;102(9):1371-7. doi: 10.1038/sj.bjc.6605653. Epub 2010 Apr 13. Br J Cancer. 2010. PMID: 20389299 Free PMC article.

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