Similar articles for PMID: 20192879

Year	Number of Results
2005	3
2006	8
2007	6
2008	9
2009	2
2010	5
2011	4
2012	3
2013	8
2014	2
2015	1
2016	1
2017	8
2018	3
2020	1
2024	0

1

UGT2B17 and SULT1A1 gene copy number variation (CNV) detection by LabChip microfluidic technology.

Gaedigk A, Gaedigk R, Leeder JS. Gaedigk A, et al. Clin Chem Lab Med. 2010 May;48(5):627-33. doi: 10.1515/CCLM.2010.128. Clin Chem Lab Med. 2010. PMID: 20192879

2

CYP2D6, SULT1A1 and UGT2B17 copy number variation: quantitative detection by multiplex PCR.

Gaedigk A, Twist GP, Leeder JS. Gaedigk A, et al. Pharmacogenomics. 2012 Jan;13(1):91-111. doi: 10.2217/pgs.11.135. Epub 2011 Nov 23. Pharmacogenomics. 2012. PMID: 22111604

3

UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family.

Uddin M, Maksymowych WP, Inman R, Gladman D, Munn A, Yazdani R, Pellett F, Hamilton S, O'Rielly DD, Rahman P. Uddin M, et al. BMC Genet. 2013 Aug 8;14:67. doi: 10.1186/1471-2156-14-67. BMC Genet. 2013. PMID: 23927372 Free PMC article.

4

Digital PCR for determination of cytochrome P450 2D6 and sulfotransferase 1A1 gene copy number variations.

Motoi Y, Watanabe K, Honma H, Tadano Y, Hashimoto H, Kubota T. Motoi Y, et al. Drug Discov Ther. 2017;11(6):336-341. doi: 10.5582/ddt.2017.01057. Drug Discov Ther. 2017. PMID: 29332892 Free article.

5

Copy-number variations (CNVs) of the human sex steroid metabolizing genes UGT2B17 and UGT2B28 and their associations with a UGT2B15 functional polymorphism.

Ménard V, Eap O, Harvey M, Guillemette C, Lévesque E. Ménard V, et al. Hum Mutat. 2009 Sep;30(9):1310-9. doi: 10.1002/humu.21054. Hum Mutat. 2009. PMID: 19572376

6

Genetic variations in UGT2B28, UGT2B17, UGT2B15 genes and the risk of prostate cancer: A case-control study.

Habibi M, Mirfakhraie R, Khani M, Rakhshan A, Azargashb E, Pouresmaeili F. Habibi M, et al. Gene. 2017 Nov 15;634:47-52. doi: 10.1016/j.gene.2017.08.038. Epub 2017 Sep 4. Gene. 2017. PMID: 28882566

7

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis.

Yang TL, Chen XD, Guo Y, Lei SF, Wang JT, Zhou Q, Pan F, Chen Y, Zhang ZX, Dong SS, Xu XH, Yan H, Liu X, Qiu C, Zhu XZ, Chen T, Li M, Zhang H, Zhang L, Drees BM, Hamilton JJ, Papasian CJ, Recker RR, Song XP, Cheng J, Deng HW. Yang TL, et al. Am J Hum Genet. 2008 Dec;83(6):663-74. doi: 10.1016/j.ajhg.2008.10.006. Epub 2008 Nov 6. Am J Hum Genet. 2008. PMID: 18992858 Free PMC article.

8

Homozygous deletion of the UGT2B17 gene is not associated with osteoporosis risk in elderly Caucasian women.

Chew S, Mullin BH, Lewis JR, Spector TD, Prince RL, Wilson SG. Chew S, et al. Osteoporos Int. 2011 Jun;22(6):1981-6. doi: 10.1007/s00198-010-1405-0. Epub 2010 Sep 29. Osteoporos Int. 2011. PMID: 20878390 Free PMC article.

9

Normalized Testosterone Glucuronide as a Potential Urinary Biomarker for Highly Variable UGT2B17 in Children 7-18 Years.

Zhang H, Basit A, Wolford C, Chen KF, Gaedigk A, Lin YS, Leeder JS, Prasad B. Zhang H, et al. Clin Pharmacol Ther. 2020 May;107(5):1149-1158. doi: 10.1002/cpt.1764. Epub 2020 Feb 12. Clin Pharmacol Ther. 2020. PMID: 31900930 Free PMC article.

10

Relationship of SULT1A1 copy number variation with estrogen metabolism and human health.

Liu J, Zhao R, Ye Z, Frey AJ, Schriver ER, Snyder NW, Hebbring SJ. Liu J, et al. J Steroid Biochem Mol Biol. 2017 Nov;174:169-175. doi: 10.1016/j.jsbmb.2017.08.017. Epub 2017 Sep 1. J Steroid Biochem Mol Biol. 2017. PMID: 28867356 Free PMC article.

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