Wu BL - Search Results

1

Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics.

Shen Y, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2009 Apr;55(4):659-69. doi: 10.1373/clinchem.2008.112821. Epub 2009 Feb 20. Clin Chem. 2009. PMID: 19233918 Review.

2

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2007 Dec;53(12):2051-9. doi: 10.1373/clinchem.2007.090290. Epub 2007 Sep 27. Clin Chem. 2007. PMID: 17901113

3

Oligonucleotide microarrays for clinical diagnosis of copy number variation.

Miller DT, Shen Y, Wu BL. Miller DT, et al. Among authors: wu bl. Curr Protoc Hum Genet. 2008 Jul;Chapter 8:Unit 8.12. doi: 10.1002/0471142905.hg0812s58. Curr Protoc Hum Genet. 2008. PMID: 18633976

4

Genetic testing for developmental delay: keep searching for an answer.

Miller DT, Shen Y, Harris DJ, Wu BL, Sobeih MM. Miller DT, et al. Among authors: wu bl. Clin Chem. 2009 Apr;55(4):827-30; discussion 830-2. doi: 10.1373/clinchem.2008.119438. Clin Chem. 2009. PMID: 19325017 No abstract available.

5

Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome.

Shen Y, Wu BL. Shen Y, et al. Among authors: wu bl. J Genet Genomics. 2009 Apr;36(4):257-65. doi: 10.1016/S1673-8527(08)60113-7. J Genet Genomics. 2009. PMID: 19376486

6

Large-scale medical resequencing for X-linked mental retardation.

Shen Y, Wu BL, Gusella JF. Shen Y, et al. Among authors: wu bl. Clin Chem. 2010 Mar;56(3):339-41. doi: 10.1373/clinchem.2009.135020. Epub 2009 Dec 29. Clin Chem. 2010. PMID: 20040618 No abstract available.

7

Standardization and diversification of copy number microarray testing for clinical diagnostics--implications of the cross-platform/algorithm study on clinical diagnostic chromosomal microarray analysis.

Shen Y, An Y, Wu BL. Shen Y, et al. Among authors: wu bl. Clin Chem. 2011 Oct;57(10):1354-6. doi: 10.1373/clinchem.2011.171769. Clin Chem. 2011. PMID: 21852392 No abstract available.

8

Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status.

Miller DT, Shen Y, Wu BL. Miller DT, et al. Among authors: wu bl. Curr Protoc Hum Genet. 2012 Jul;Chapter 8:Unit8.12. doi: 10.1002/0471142905.hg0812s74. Curr Protoc Hum Genet. 2012. PMID: 22786613

9

Exome and whole-genome sequencing as clinical tests: a transformative practice in molecular diagnostics.

Yu Y, Wu BL, Wu J, Shen Y. Yu Y, et al. Among authors: wu bl, wu j. Clin Chem. 2012 Nov;58(11):1507-9. doi: 10.1373/clinchem.2012.193128. Epub 2012 Oct 11. Clin Chem. 2012. PMID: 23065473 Review. No abstract available.

10

Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population.

An Y, Duan W, Huang G, Chen X, Li L, Nie C, Hou J, Gui Y, Wu Y, Zhang F, Shen Y, Wu B, Wang H. An Y, et al. BMC Med Genomics. 2016 Jan 8;9:2. doi: 10.1186/s12920-015-0163-4. BMC Med Genomics. 2016. PMID: 26742958 Free PMC article.

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