Chen M - Search Results

1

Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays.

Liu W, Zhang R, Wei J, Zhang H, Yu G, Li Z, Chen M, Sun X. Liu W, et al. Among authors: chen m. Cytogenet Genome Res. 2015;146(1):9-18. doi: 10.1159/000435847. Epub 2015 Jul 16. Cytogenet Genome Res. 2015. PMID: 26184742

2

Modification of PCR conditions and design of exon-specific primers for the efficient molecular diagnosis of PKD1 mutations.

Liu W, Chen M, Wei J, He W, Li Z, Sun X, Shi Y. Liu W, et al. Among authors: chen m. Kidney Blood Press Res. 2014;39(6):536-45. doi: 10.1159/000368464. Epub 2014 Nov 30. Kidney Blood Press Res. 2014. PMID: 25531466 Free article.

3

Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.

Wei J, Xie Y, He W, Liu W, Jian W, Chen M, Wang D, Wang X, Sun X. Wei J, et al. Among authors: chen m. Cytogenet Genome Res. 2014;144(4):294-8. doi: 10.1159/000371461. Epub 2015 Jan 28. Cytogenet Genome Res. 2014. PMID: 25634515

4

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations.

Liu W, Zhang H, Wang J, Yu G, Qiu W, Li Z, Chen M, Choy KW, Sun X. Liu W, et al. Among authors: chen m. Mol Cytogenet. 2015 Nov 4;8:85. doi: 10.1186/s13039-015-0190-z. eCollection 2015. Mol Cytogenet. 2015. PMID: 26539248 Free PMC article.

5

Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study.

Cao Y, Li Z, Rosenfeld JA, Pursley AN, Patel A, Huang J, Wang H, Chen M, Sun X, Leung TY, Cheung SW, Choy KW. Cao Y, et al. Among authors: chen m. Genet Med. 2016 Oct;18(10):1052-5. doi: 10.1038/gim.2015.216. Epub 2016 Feb 25. Genet Med. 2016. PMID: 26913922 Free article.

6

Prenatal diagnosis of hemivertebrae--A likely association with 7q deletion.

Song YQ, Chen M, Yang ZL, He WY, Liu WQ, Li Y, Gong YF, Wang JY, Sun XF, Chen XJ. Song YQ, et al. Among authors: chen m, chen xj. Taiwan J Obstet Gynecol. 2016 Feb;55(1):112-6. doi: 10.1016/j.tjog.2015.05.004. Taiwan J Obstet Gynecol. 2016. PMID: 26927261 Free article. Review.

7

Implementation of a High-Resolution Single-Nucleotide Polymorphism Array in Analyzing the Products of Conception.

Zhang H, Liu W, Chen M, Li Z, Sun X, Wang C. Zhang H, et al. Among authors: chen m. Genet Test Mol Biomarkers. 2016 Jul;20(7):352-8. doi: 10.1089/gtmb.2016.0035. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27228077

8

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.

Ji X, Li J, Huang Y, Sung PL, Yuan Y, Liu Q, Chen Y, Ju J, Zhou Y, Huang S, Chen F, Han Y, Yuan W, Fan C, Zhao Q, Wu H, Feng S, Liu W, Li Z, Chen J, Chen M, Yao H, Zeng L, Ma T, Fan S, Zhang J, Yuen KY, Cheng SH, Chik IWS, Liu NT, Zhu J, Lin S, Cao J, Tong S, Shan Z, Li W, Hekmat MR, Garshasbi M, Suela J, Torres Y, Cigudosa JC, Ruiz FJP, Rodríguez L, García M, Bernik J, Traven E, Reš U, Tul N, Tseng CF, Zhao D, Sun L, Pan Q, Shen L, Dai M, Wang Y, Wang J, Yang H, Yin Y, Duan T, Zhu B, Choolani M, Jin X, Chen Y, Mao M. Ji X, et al. Among authors: chen j, chen m, chen f, chen y. Genet Med. 2019 Oct;21(10):2293-2302. doi: 10.1038/s41436-019-0510-5. Epub 2019 Apr 12. Genet Med. 2019. PMID: 30976098 Free article.

9

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.

Choy KW, Wang H, Shi M, Chen J, Yang Z, Zhang R, Yan H, Wang Y, Chen S, Chau MHK, Cao Y, Chan OYM, Kwok YK, Zhu Y, Chen M, Leung TY, Dong Z. Choy KW, et al. Among authors: chen j, chen m, chen s. Front Genet. 2019 Aug 16;10:761. doi: 10.3389/fgene.2019.00761. eCollection 2019. Front Genet. 2019. PMID: 31475041 Free PMC article.

10

Noninvasive prenatal diagnosis of β-thalassemia by relative haplotype dosage without analyzing proband.

Li H, Du B, Jiang F, Guo Y, Wang Y, Zhang C, Zeng X, Xie Y, Ouyang S, Xian Y, Chen M, Liu W, Sun X. Li H, et al. Among authors: chen m. Mol Genet Genomic Med. 2019 Nov;7(11):e963. doi: 10.1002/mgg3.963. Epub 2019 Sep 30. Mol Genet Genomic Med. 2019. PMID: 31566929 Free PMC article.

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