Wu BL - Search Results

1

Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study.

Chen X, Guo J, Lei Y, Zou J, Lu X, Bao Y, Wu L, Wu J, Zheng X, Shen Y, Wu BL, Zhang T. Chen X, et al. Among authors: wu l, wu bl, wu j. Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):575-81. doi: 10.1002/bdra.20670. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20641100

2

Detection of copy number variants reveals association of cilia genes with neural tube defects.

Chen X, Shen Y, Gao Y, Zhao H, Sheng X, Zou J, Lip V, Xie H, Guo J, Shao H, Bao Y, Shen J, Niu B, Gusella JF, Wu BL, Zhang T. Chen X, et al. Among authors: wu bl. PLoS One. 2013;8(1):e54492. doi: 10.1371/journal.pone.0054492. Epub 2013 Jan 17. PLoS One. 2013. PMID: 23349908 Free PMC article.

3

Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.

Chen X, An Y, Gao Y, Guo L, Rui L, Xie H, Sun M, Lam Hung S, Sheng X, Zou J, Bao Y, Guan H, Niu B, Li Z, Finnell RH, Gusella JF, Wu BL, Zhang T. Chen X, et al. Among authors: wu bl. Hum Mutat. 2017 Apr;38(4):378-389. doi: 10.1002/humu.23153. Epub 2017 Feb 15. Hum Mutat. 2017. PMID: 27925688 Free PMC article.

4

Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.

Chen X, Shen Y, Zhang F, Chiang C, Pillalamarri V, Blumenthal I, Talkowski M, Wu BL, Gusella JF. Chen X, et al. Among authors: wu bl. Am J Hum Genet. 2013 Mar 7;92(3):375-86. doi: 10.1016/j.ajhg.2013.02.006. Am J Hum Genet. 2013. PMID: 23472757 Free PMC article.

5

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.

6

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.

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

VANGL2 mutations in human cranial neural-tube defects.

Lei YP, Zhang T, Li H, Wu BL, Jin L, Wang HY. Lei YP, et al. Among authors: wu bl. N Engl J Med. 2010 Jun 10;362(23):2232-5. doi: 10.1056/NEJMc0910820. N Engl J Med. 2010. PMID: 20558380 No abstract available.

10

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

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