Sun M - Search Results

1

Mitochondrial haplogroups and hypervariable region polymorphisms in schizophrenia: a case-control study.

Wang GX, Zhang Y, Zhang YT, Dong YS, Lv ZW, Sun M, Wu D, Wu YM. Wang GX, et al. Among authors: sun m. Psychiatry Res. 2013 Oct 30;209(3):279-83. doi: 10.1016/j.psychres.2013.01.001. Epub 2013 Jan 29. Psychiatry Res. 2013. PMID: 23374981

2

Hypervariable region polymorphism of mtDNA of recurrent oral ulceration in Chinese.

Sun M, Fu SM, Wang LF, Dong GY, Wu D, Wang GX, Wu Y. Sun M, et al. PLoS One. 2012;7(9):e45359. doi: 10.1371/journal.pone.0045359. Epub 2012 Sep 19. PLoS One. 2012. PMID: 23028959 Free PMC article.

3

Inflammatory factors gene polymorphism in recurrent oral ulceration.

Sun M, Fu SM, Dong GY, Wu D, Wang GX, Wu Y. Sun M, et al. J Oral Pathol Med. 2013 Aug;42(7):528-34. doi: 10.1111/jop.12048. Epub 2013 Feb 14. J Oral Pathol Med. 2013. PMID: 23406059

4

CIITA rs4774 and rs6498122 polymorphisms are associated with oral lichen planus in Chinese people: a case-control study.

Wu D, Wang L, Sun M, Wang G, Fu S, Dong G, Wu Y. Wu D, et al. Among authors: sun m. Eur J Oral Sci. 2013 Apr;121(2):69-75. doi: 10.1111/eos.12029. Epub 2013 Mar 4. Eur J Oral Sci. 2013. PMID: 23489895

5

Female specific association between NNMT gene and schizophrenia in a Han Chinese population.

Wang GX, Zhang Y, Lv ZW, Sun M, Wu D, Chen XY, Wu YM. Wang GX, et al. Among authors: sun m. Int J Med Sci. 2014 Sep 19;11(12):1234-9. doi: 10.7150/ijms.9426. eCollection 2014. Int J Med Sci. 2014. PMID: 25317069 Free PMC article.

6

Population genetic data of 15 STR loci in Gansu Han population from China.

Sun M, Zhang X, Wu D, Shen Q, Wu Y. Sun M, et al. Int J Legal Med. 2015 Jul;129(4):735-6. doi: 10.1007/s00414-014-1132-8. Epub 2014 Dec 12. Int J Legal Med. 2015. PMID: 25504110

7

Mutations of short tandem repeat loci in cases of paternity testing in Chinese.

Sun M, Zhang X, Wu D, Shen Q, Wu Y, Fu S. Sun M, et al. Int J Legal Med. 2016 Sep;130(5):1203-4. doi: 10.1007/s00414-015-1229-8. Epub 2015 Jul 30. Int J Legal Med. 2016. PMID: 26223683

8

Two novel mutations in ERCC6 cause Cockayne syndrome B in a Chinese family.

He C, Sun M, Wang G, Yang Y, Yao L, Wu Y. He C, et al. Among authors: sun m. Mol Med Rep. 2017 Jun;15(6):3957-3962. doi: 10.3892/mmr.2017.6487. Epub 2017 Apr 20. Mol Med Rep. 2017. PMID: 28440418 Free PMC article.

9

Genetic polymorphisms of 12 X STR loci in Shaanxi Han population from China.

Sun M, Zhang Y, Zhang X, Fu S, Wu Y. Sun M, et al. Leg Med (Tokyo). 2017 May;26:76-78. doi: 10.1016/j.legalmed.2017.01.007. Epub 2017 Jan 21. Leg Med (Tokyo). 2017. PMID: 28549553

10

Two novel CPS1 mutations in a case of carbamoyl phosphate synthetase 1 deficiency causing hyperammonemia and leukodystrophy.

Chen X, Yuan L, Sun M, Liu Q, Wu Y. Chen X, et al. Among authors: sun m. J Clin Lab Anal. 2018 Jun;32(5):e22375. doi: 10.1002/jcla.22375. Epub 2018 Jan 4. J Clin Lab Anal. 2018. PMID: 29314318 Free PMC article.

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