Liu X - Search Results

1

Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.

Malenfant P, Liu X, Hudson ML, Qiao Y, Hrynchak M, Riendeau N, Hildebrand MJ, Cohen IL, Chudley AE, Forster-Gibson C, Mickelson EC, Rajcan-Separovic E, Lewis ME, Holden JJ. Malenfant P, et al. Among authors: liu x. J Autism Dev Disord. 2012 Jul;42(7):1459-69. doi: 10.1007/s10803-011-1389-4. J Autism Dev Disord. 2012. PMID: 22048961

2

Reelin gene alleles and susceptibility to autism spectrum disorders.

Zhang H, Liu X, Zhang C, Mundo E, Macciardi F, Grayson DR, Guidotti AR, Holden JJ. Zhang H, et al. Among authors: liu x. Mol Psychiatry. 2002;7(9):1012-7. doi: 10.1038/sj.mp.4001124. Mol Psychiatry. 2002. PMID: 12399956

3

Association of autism severity with a monoamine oxidase A functional polymorphism.

Cohen IL, Liu X, Schutz C, White BN, Jenkins EC, Brown WT, Holden JJ. Cohen IL, et al. Among authors: liu x. Clin Genet. 2003 Sep;64(3):190-7. doi: 10.1034/j.1399-0004.2003.00115.x. Clin Genet. 2003. PMID: 12919132

4

Clinical and molecular cytogenetic characterisation of a newly recognised microdeletion syndrome involving 2p15-16.1.

Rajcan-Separovic E, Harvard C, Liu X, McGillivray B, Hall JG, Qiao Y, Hurlburt J, Hildebrand J, Mickelson EC, Holden JJ, Lewis ME. Rajcan-Separovic E, et al. Among authors: liu x. J Med Genet. 2007 Apr;44(4):269-76. doi: 10.1136/jmg.2006.045013. Epub 2006 Sep 8. J Med Genet. 2007. PMID: 16963482 Free PMC article.

5

The G22A polymorphism of the ADA gene and susceptibility to autism spectrum disorders.

Hettinger JA, Liu X, Holden JJ. Hettinger JA, et al. Among authors: liu x. J Autism Dev Disord. 2008 Jan;38(1):14-9. doi: 10.1007/s10803-006-0354-0. Epub 2007 Mar 6. J Autism Dev Disord. 2008. PMID: 17340203

6

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: liu x. BMC Genomics. 2007 Jun 12;8:167. doi: 10.1186/1471-2164-8-167. BMC Genomics. 2007. PMID: 17565693 Free PMC article.

7

A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.

Hettinger JA, Liu X, Schwartz CE, Michaelis RC, Holden JJ. Hettinger JA, et al. Among authors: liu x. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):628-36. doi: 10.1002/ajmg.b.30655. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18205172

8

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: liu x. 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

9

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders.

Liu X, Novosedlik N, Wang A, Hudson ML, Cohen IL, Chudley AE, Forster-Gibson CJ, Lewis SM, Holden JJ. Liu X, et al. Eur J Hum Genet. 2009 Feb;17(2):228-35. doi: 10.1038/ejhg.2008.148. Epub 2008 Aug 27. Eur J Hum Genet. 2009. PMID: 18728693 Free PMC article.

10

Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH.

Tyson C, Qiao Y, Harvard C, Liu X, Bernier FP, McGillivray B, Farrell SA, Arbour L, Chudley AE, Clarke L, Gibson W, Dyack S, McLeod R, Costa T, Vanallen MI, Yong SL, Graham GE, Macleod P, Patel MS, Hurlburt J, Holden JJ, Lewis SM, Rajcan-Separovic E. Tyson C, et al. Among authors: liu x. Mol Cytogenet. 2008 Nov 11;1:23. doi: 10.1186/1755-8166-1-23. Mol Cytogenet. 2008. PMID: 19000322 Free PMC article.

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