Wu BL - Search Results

1

Age- and gender-dependent obesity in individuals with 16p11.2 deletion.

Yu Y, Zhu H, Miller DT, Gusella JF, Platt OS, Wu BL, Shen Y; Children's Hospital Boston Genotype Phenotype Study Group. Yu Y, et al. Among authors: wu bl. J Genet Genomics. 2011 Sep 20;38(9):403-9. doi: 10.1016/j.jgg.2011.08.003. Epub 2011 Aug 17. J Genet Genomics. 2011. PMID: 21930099

2

Association between microdeletion and microduplication at 16p11.2 and autism.

Weiss LA, Shen Y, Korn JM, Arking DE, Miller DT, Fossdal R, Saemundsen E, Stefansson H, Ferreira MA, Green T, Platt OS, Ruderfer DM, Walsh CA, Altshuler D, Chakravarti A, Tanzi RE, Stefansson K, Santangelo SL, Gusella JF, Sklar P, Wu BL, Daly MJ; Autism Consortium. Weiss LA, et al. Among authors: wu bl. N Engl J Med. 2008 Feb 14;358(7):667-75. doi: 10.1056/NEJMoa075974. Epub 2008 Jan 9. N Engl J Med. 2008. PMID: 18184952 Free article.

3

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

4

Cognitive and behavioral characterization of 16p11.2 deletion syndrome.

Hanson E, Nasir RH, Fong A, Lian A, Hundley R, Shen Y, Wu BL, Holm IA, Miller DT; 16p11.2 Study Group Clinicians. Hanson E, et al. Among authors: wu bl. J Dev Behav Pediatr. 2010 Oct;31(8):649-57. doi: 10.1097/DBP.0b013e3181ea50ed. J Dev Behav Pediatr. 2010. PMID: 20613623

5

Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.

Shen Y, Chen X, Wang L, Guo J, Shen J, An Y, Zhu H, Zhu Y, Xin R, Bao Y, Gusella JF, Zhang T, Wu BL. Shen Y, et al. Among authors: wu bl. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):225-32. doi: 10.1002/ajmg.b.31147. Epub 2010 Dec 28. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302351

6

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

7

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

8

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.

9

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.

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

240 results

Search Page

Filters