Liu MY - Search Results

1

Further evidence of no association between Ser9Gly polymorphism of dopamine D3 receptor gene and schizophrenia.

Chen CH, Liu MY, Wei FC, Koong FJ, Hwu HG, Hsiao KJ. Chen CH, et al. Among authors: liu my. Am J Med Genet. 1997 Feb 21;74(1):40-3. doi: 10.1002/(sici)1096-8628(19970221)74:1<40::aid-ajmg9>3.0.co;2-z. Am J Med Genet. 1997. PMID: 9034004

2

Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophrenia.

Chen CH, Lee YR, Liu MY, Wei FC, Koong FJ, Hwu HG, Hsiao KJ. Chen CH, et al. Among authors: liu my. Am J Med Genet. 1996 Nov 22;67(6):556-9. doi: 10.1002/(SICI)1096-8628(19961122)67:6<556::AID-AJMG8>3.0.CO;2-F. Am J Med Genet. 1996. PMID: 8950414

3

Mutation analysis of synapsin III gene in schizophrenia.

Tsai MT, Hung CC, Tsai CY, Liu MY, Su YC, Chen YH, Hsiao KJ, Chen CH. Tsai MT, et al. Among authors: liu my. Am J Med Genet. 2002 Jan 8;114(1):79-83. doi: 10.1002/ajmg.10116. Am J Med Genet. 2002. PMID: 11840510

4

Growth hormone therapy in neonatal patients with methylmalonic acidemia.

Kao CH, Liu MY, Liu TT, Hsiao KJ, Cheng KH, Huang CH, Lin HY, Niu DM. Kao CH, et al. Among authors: liu tt, liu my. J Chin Med Assoc. 2009 Sep;72(9):462-7. doi: 10.1016/S1726-4901(09)70408-3. J Chin Med Assoc. 2009. PMID: 19762313 Free article.

5

Newborn screening for methylmalonic aciduria by tandem mass spectrometry: 7 years' experience from two centers in Taiwan.

Cheng KH, Liu MY, Kao CH, Chen YJ, Hsiao KJ, Liu TT, Lin HY, Huang CH, Chiang CC, Ho HJ, Lin SP, Lee NC, Hwu WL, Lin JL, Hung PY, Niu DM. Cheng KH, et al. Among authors: liu tt, liu my. J Chin Med Assoc. 2010 Jun;73(6):314-8. doi: 10.1016/S1726-4901(10)70067-8. J Chin Med Assoc. 2010. PMID: 20603089 Free article.

6

Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria.

Liu MY, Yang YL, Chang YC, Chiang SH, Lin SP, Han LS, Qi Y, Hsiao KJ, Liu TT. Liu MY, et al. Among authors: liu tt. J Hum Genet. 2010 Sep;55(9):621-6. doi: 10.1038/jhg.2010.81. Epub 2010 Jul 15. J Hum Genet. 2010. PMID: 20631720

7

Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients.

Liu MY, Liu TT, Yang YL, Chang YC, Fan YL, Lee SF, Teng YT, Chiang SH, Niu DM, Lin SJ, Chao MC, Lin SP, Han LS, Qi Y, Hsiao KJ. Liu MY, et al. Among authors: liu tt. JIMD Rep. 2012;6:55-64. doi: 10.1007/8904_2011_117. Epub 2012 Jan 31. JIMD Rep. 2012. PMID: 23430940 Free PMC article.

8

Applying a multiplexed primer extension method on dried blood spots increased the detection of carriers at risk of glucose-6-phosphate dehydrogenase deficiency in newborn screening program.

Chiu YH, Chen HJ, Chang YC, Liu YN, Kao SM, Liu MY, Weng YY, Hsiao KJ, Liu TT. Chiu YH, et al. Among authors: liu tt, liu yn, liu my. Clin Chim Acta. 2019 Aug;495:271-277. doi: 10.1016/j.cca.2019.04.074. Epub 2019 Apr 22. Clin Chim Acta. 2019. PMID: 31022393

9

Prediction of functional consequences of the five newly discovered G6PD variations in Taiwan.

Chiu YH, Liu YN, Chen HJ, Chang YC, Kao SM, Liu MY, Weng YY, Hsiao KJ, Liu TT. Chiu YH, et al. Among authors: liu tt, liu yn, liu my. Data Brief. 2019 Jun 11;25:104129. doi: 10.1016/j.dib.2019.104129. eCollection 2019 Aug. Data Brief. 2019. PMID: 31294066 Free PMC article.

10

Implementation of newborn screening for mucopolysaccharidosis type IVA and long-term monitoring in Taiwan.

Lin HY, Lee CL, Chang YH, Tu YR, Lo YT, Wu JY, Niu DM, Liu MY, Liu HY, Chen HJ, Kao SM, Wang LY, Ho HJ, Chuang CK, Lin SP. Lin HY, et al. Among authors: liu hy, liu my. Genet Med. 2024 Dec;26(12):101286. doi: 10.1016/j.gim.2024.101286. Epub 2024 Oct 4. Genet Med. 2024. PMID: 39375993

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