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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.
Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Griswold AJ, et al. Hum Mol Genet. 2012 Aug 1;21(15):3513-23. doi: 10.1093/hmg/dds164. Epub 2012 Apr 27. Hum Mol Genet. 2012. PMID: 22543975 Free PMC article.
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.
Salyakina D, Cukier HN, Lee JM, Sacharow S, Nations LD, Ma D, Jaworski JM, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Salyakina D, et al. PLoS One. 2011;6(10):e26049. doi: 10.1371/journal.pone.0026049. Epub 2011 Oct 7. PLoS One. 2011. PMID: 22016809 Free PMC article.
Autism in African American families: clinical-phenotypic findings.
Cuccaro ML, Brinkley J, Abramson RK, Hall A, Wright HH, Hussman JP, Gilbert JR, Pericak-Vance MA. Cuccaro ML, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1022-6. doi: 10.1002/ajmg.b.30535. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17671983