Harvard C - Search Results

1

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.

Qiao Y, Tyson C, Hrynchak M, Lopez-Rangel E, Hildebrand J, Martell S, Fawcett C, Kasmara L, Calli K, Harvard C, Liu X, Holden JJ, Lewis SM, Rajcan-Separovic E. Qiao Y, et al. Among authors: harvard c. Clin Genet. 2013 Feb;83(2):145-54. doi: 10.1111/j.1399-0004.2012.01860.x. Epub 2012 Apr 9. Clin Genet. 2013. PMID: 22369279

2

Phenomic determinants of genomic variation in autism spectrum disorders.

Qiao Y, Riendeau N, Koochek M, Liu X, Harvard C, Hildebrand MJ, Holden JJ, Rajcan-Separovic E, Lewis ME. Qiao Y, et al. Among authors: harvard c. J Med Genet. 2009 Oct;46(10):680-8. doi: 10.1136/jmg.2009.066795. Epub 2009 Jul 21. J Med Genet. 2009. PMID: 19625284

3

Submicroscopic deletions and duplications in individuals with intellectual disability detected by array-CGH.

Tyson C, Harvard C, Locker R, Friedman JM, Langlois S, Lewis ME, Van Allen M, Somerville M, Arbour L, Clarke L, McGilivray B, Yong SL, Siegel-Bartel J, Rajcan-Separovic E. Tyson C, et al. Among authors: harvard c. Am J Med Genet A. 2005 Dec 15;139(3):173-85. doi: 10.1002/ajmg.a.31015. Am J Med Genet A. 2005. PMID: 16283669

4

15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.

Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME. Koochek M, et al. Among authors: harvard c. Clin Genet. 2006 Feb;69(2):124-34. doi: 10.1111/j.1399-0004.2005.00560.x. Clin Genet. 2006. PMID: 16433693

5

Autism-associated familial microdeletion of Xp11.22.

Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, Lewis ME. Qiao Y, et al. Among authors: harvard c. Clin Genet. 2008 Aug;74(2):134-44. doi: 10.1111/j.1399-0004.2008.01028.x. Epub 2008 May 21. Clin Genet. 2008. PMID: 18498374

6

Putatively benign copy number variants in subjects with idiopathic autism spectrum disorder and/or intellectual disability.

Qiao Y, Harvard C, Riendeau N, Fawcett C, Liu X, Holden JJ, Lewis ME, Rajcan-Separovic E. Qiao Y, et al. Among authors: harvard c. Cytogenet Genome Res. 2008;123(1-4):79-87. doi: 10.1159/000184694. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287141

7

Genomic changes detected by array CGH in human embryos with developmental defects.

Rajcan-Separovic E, Qiao Y, Tyson C, Harvard C, Fawcett C, Kalousek D, Stephenson M, Philipp T. Rajcan-Separovic E, et al. Among authors: harvard c. Mol Hum Reprod. 2010 Feb;16(2):125-34. doi: 10.1093/molehr/gap083. Epub 2009 Sep 23. Mol Hum Reprod. 2010. PMID: 19778950

8

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.

Qiao Y, Harvard C, Tyson C, Liu X, Fawcett C, Pavlidis P, Holden JJ, Lewis ME, Rajcan-Separovic E. Qiao Y, et al. Among authors: harvard c. Hum Genet. 2010 Aug;128(2):179-94. doi: 10.1007/s00439-010-0837-0. Epub 2010 May 29. Hum Genet. 2010. PMID: 20512354

9

Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.

Qiao Y, Liu X, Harvard C, Nolin SL, Brown WT, Koochek M, Holden JJ, Lewis ME, Rajcan-Separovic E. Qiao Y, et al. Among authors: harvard c. BMC Genomics. 2007 Jun 12;8:167. doi: 10.1186/1471-2164-8-167. BMC Genomics. 2007. PMID: 17565693 Free PMC article.

10

Phenotype-genotype characterization of alpha-thalassemia mental retardation syndrome due to isolated monosomy of 16p13.3.

Gibson WT, Harvard C, Qiao Y, Somerville MJ, Lewis ME, Rajcan-Separovic E. Gibson WT, et al. Among authors: harvard c. Am J Med Genet A. 2008 Jan 15;146A(2):225-32. doi: 10.1002/ajmg.a.32056. Am J Med Genet A. 2008. PMID: 18076105

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