Similar articles for PMID: 20053576

Year	Number of Results
1991	1
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2002	4
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2010	17
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2013	6
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2017	12
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2023	9
2024	1

1

Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.

Tong Y, Sun YH, Zhou X, Zhao F, Mao Y, Wei QP, Yang L, Qu J, Guan MX. Tong Y, et al. Mol Genet Metab. 2010 Apr;99(4):417-24. doi: 10.1016/j.ymgme.2009.12.004. Epub 2010 Jan 6. Mol Genet Metab. 2010. PMID: 20053576 Free PMC article.

2

Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.

Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, Yuan M, Liu Q, Tong Y, Wei QP, Yang L, Guan MX. Qu J, et al. Biochim Biophys Acta. 2010 Mar;1800(3):305-12. doi: 10.1016/j.bbagen.2009.08.010. Epub 2009 Sep 3. Biochim Biophys Acta. 2010. PMID: 19733221 Free PMC article.

3

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX. Qu J, et al. Ophthalmology. 2009 Mar;116(3):558-564.e3. doi: 10.1016/j.ophtha.2008.10.022. Epub 2009 Jan 22. Ophthalmology. 2009. PMID: 19167085 Free PMC article.

4

Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.

Ji Y, Liang M, Zhang J, Zhang M, Zhu J, Meng X, Zhang S, Gao M, Zhao F, Wei QP, Jiang P, Tong Y, Liu X, Qin Mo J, Guan MX. Ji Y, et al. J Hum Genet. 2014 Mar;59(3):134-40. doi: 10.1038/jhg.2013.134. Epub 2014 Jan 16. J Hum Genet. 2014. PMID: 24430572

5

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.

Zhou X, Zhang H, Zhao F, Ji Y, Tong Y, Zhang J, Zhang Y, Yang L, Qian Y, Lu F, Qu J, Guan MX. Zhou X, et al. Mol Genet Metab. 2010 Aug;100(4):379-84. doi: 10.1016/j.ymgme.2010.04.013. Epub 2010 Apr 29. Mol Genet Metab. 2010. PMID: 20627642 Free PMC article.

6

Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.

Zhang M, Zhou X, Li C, Zhao F, Zhang J, Yuan M, Sun YH, Wang J, Tong Y, Liang M, Yang L, Cai W, Wang L, Qu J, Guan MX. Zhang M, et al. Mol Genet Metab. 2010 Oct-Nov;101(2-3):192-9. doi: 10.1016/j.ymgme.2010.07.014. Epub 2010 Aug 3. Mol Genet Metab. 2010. PMID: 20728388

7

Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.

Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX. Qu J, et al. Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4906-12. doi: 10.1167/iovs.09-5027. Epub 2010 Apr 30. Invest Ophthalmol Vis Sci. 2010. PMID: 20435583 Free PMC article.

8

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.

Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX. Qian Y, et al. Biochem Biophys Res Commun. 2005 Jul 1;332(2):614-21. doi: 10.1016/j.bbrc.2005.05.003. Biochem Biophys Res Commun. 2005. PMID: 15896721

9

Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees.

Xie S, Zhang J, Sun J, Zhang M, Zhao F, Wei QP, Tong Y, Liu X, Zhou X, Jiang P, Ji Y, Guan MX. Xie S, et al. Mitochondrial DNA A DNA Mapp Seq Anal. 2017 May;28(3):434-441. doi: 10.3109/19401736.2015.1136304. Epub 2016 Jan 22. Mitochondrial DNA A DNA Mapp Seq Anal. 2017. PMID: 27159682

10

Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.

Liu XL, Zhou X, Zhou J, Zhao F, Zhang J, Li C, Ji Y, Zhang Y, Wei QP, Sun YH, Yang L, Lin B, Yuan Y, Li Y, Qu J, Guan MX. Liu XL, et al. Ophthalmology. 2011 May;118(5):978-85. doi: 10.1016/j.ophtha.2010.09.003. Epub 2010 Dec 4. Ophthalmology. 2011. PMID: 21131053

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