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Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdb.
Tan PP, Rogic S, Zoubarev A, McDonald C, Lui F, Charathsandran G, Jacobson M, Belmadani M, Leong J, Van Rossum T, Portales-Casamar E, Qiao Y, Calli K, Liu X, Hudson M, Rajcan-Separovic E, Lewis MS, Pavlidis P. Tan PP, et al. Among authors: liu x. Hum Mutat. 2016 Aug;37(8):719-26. doi: 10.1002/humu.23011. Epub 2016 May 20. Hum Mutat. 2016. PMID: 27158917 Free PMC article.
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
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.
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.
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: liu x. 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
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