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A balanced t(10;15) translocation in a male patient with developmental language disorder.
Ercan-Sencicek AG, Davis Wright NR, Sanders SJ, Oakman N, Valdes L, Bakkaloglu B, Doyle N, Yrigollen CM, Morgan TM, Grigorenko EL. Ercan-Sencicek AG, et al. Among authors: grigorenko el. Eur J Med Genet. 2012 Feb;55(2):128-31. doi: 10.1016/j.ejmg.2011.12.005. Epub 2011 Dec 29. Eur J Med Genet. 2012. PMID: 22266071 Free PMC article.
Genes controlling affiliative behavior as candidate genes for autism.
Yrigollen CM, Han SS, Kochetkova A, Babitz T, Chang JT, Volkmar FR, Leckman JF, Grigorenko EL. Yrigollen CM, et al. Among authors: grigorenko el. Biol Psychiatry. 2008 May 15;63(10):911-6. doi: 10.1016/j.biopsych.2007.11.015. Epub 2008 Jan 22. Biol Psychiatry. 2008. PMID: 18207134 Free PMC article.
Macrophage migration inhibitory factor and autism spectrum disorders.
Grigorenko EL, Han SS, Yrigollen CM, Leng L, Mizue Y, Anderson GM, Mulder EJ, de Bildt A, Minderaa RB, Volkmar FR, Chang JT, Bucala R. Grigorenko EL, et al. Pediatrics. 2008 Aug;122(2):e438-45. doi: 10.1542/peds.2007-3604. Pediatrics. 2008. PMID: 18676531 Free PMC article.
Twenty-one-base-pair insertion polymorphism creates an enhancer element and potentiates SLC6A1 GABA transporter promoter activity.
Hirunsatit R, George ED, Lipska BK, Elwafi HM, Sander L, Yrigollen CM, Gelernter J, Grigorenko EL, Lappalainen J, Mane S, Nairn AC, Kleinman JE, Simen AA. Hirunsatit R, et al. Among authors: grigorenko el. Pharmacogenet Genomics. 2009 Jan;19(1):53-65. doi: 10.1097/FPC.0b013e328318b21a. Pharmacogenet Genomics. 2009. PMID: 19077666 Free PMC article.
Variation in the catechol-O-methyltransferase Val 158 Met polymorphism associated with conduct disorder and ADHD symptoms, among adolescent male delinquents.
DeYoung CG, Getchell M, Koposov RA, Yrigollen CM, Haeffel GJ, af Klinteberg B, Oreland L, Ruchkin VV, Pakstis AJ, Grigorenko EL. DeYoung CG, et al. Among authors: grigorenko el. Psychiatr Genet. 2010 Feb;20(1):20-4. doi: 10.1097/YPG.0b013e32833511e4. Psychiatr Genet. 2010. PMID: 19997043 Free PMC article.
The distribution and most recent common ancestor of the 17q21 inversion in humans.
Donnelly MP, Paschou P, Grigorenko E, Gurwitz D, Mehdi SQ, Kajuna SL, Barta C, Kungulilo S, Karoma NJ, Lu RB, Zhukova OV, Kim JJ, Comas D, Siniscalco M, New M, Li P, Li H, Manolopoulos VG, Speed WC, Rajeevan H, Pakstis AJ, Kidd JR, Kidd KK. Donnelly MP, et al. Am J Hum Genet. 2010 Feb 12;86(2):161-71. doi: 10.1016/j.ajhg.2010.01.007. Epub 2010 Jan 28. Am J Hum Genet. 2010. PMID: 20116045 Free PMC article.
218 results