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2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.
Liu X, Malenfant P, Reesor C, Lee A, Hudson ML, Harvard C, Qiao Y, Persico AM, Cohen IL, Chudley AE, Forster-Gibson C, Rajcan-Separovic E, Lewis ME, Holden JJ. Liu X, et al. Among authors: cohen il. Eur J Hum Genet. 2011 Dec;19(12):1264-70. doi: 10.1038/ejhg.2011.112. Epub 2011 Jul 13. Eur J Hum Genet. 2011. PMID: 21750575 Free PMC article.
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. Among authors: cohen il. 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.
18-month predictors of later outcomes in younger siblings of children with autism spectrum disorder: a baby siblings research consortium study.
Chawarska K, Shic F, Macari S, Campbell DJ, Brian J, Landa R, Hutman T, Nelson CA, Ozonoff S, Tager-Flusberg H, Young GS, Zwaigenbaum L, Cohen IL, Charman T, Messinger DS, Klin A, Johnson S, Bryson S. Chawarska K, et al. Among authors: cohen il. J Am Acad Child Adolesc Psychiatry. 2014 Dec;53(12):1317-1327.e1. doi: 10.1016/j.jaac.2014.09.015. Epub 2014 Oct 2. J Am Acad Child Adolesc Psychiatry. 2014. PMID: 25457930 Free PMC article.
106 results