Leventhal BL - Search Results

1

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.

Jacob S, Brune CW, Carter CS, Leventhal BL, Lord C, Cook EH Jr. Jacob S, et al. Among authors: leventhal bl. Neurosci Lett. 2007 Apr 24;417(1):6-9. doi: 10.1016/j.neulet.2007.02.001. Epub 2007 Feb 3. Neurosci Lett. 2007. PMID: 17383819 Free PMC article.

2

Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism.

Veenstra-VanderWeele J, Kim SJ, Lord C, Courchesne R, Akshoomoff N, Leventhal BL, Courchesne E, Cook EH Jr. Veenstra-VanderWeele J, et al. Among authors: leventhal bl. Am J Med Genet. 2002 Apr 8;114(3):277-83. doi: 10.1002/ajmg.10192. Am J Med Genet. 2002. PMID: 11920848

3

5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism.

Brune CW, Kim SJ, Salt J, Leventhal BL, Lord C, Cook EH Jr. Brune CW, et al. Among authors: leventhal bl. Am J Psychiatry. 2006 Dec;163(12):2148-56. doi: 10.1176/ajp.2006.163.12.2148. Am J Psychiatry. 2006. PMID: 17151167

4

Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.

Brune CW, Kim SJ, Hanna GL, Courchesne E, Lord C, Leventhal BL, Cook EH. Brune CW, et al. Among authors: leventhal bl. Autism Res. 2008 Apr;1(2):108-13. doi: 10.1002/aur.11. Autism Res. 2008. PMID: 19360657 Free PMC article.

5

Mutation screening and transmission disequilibrium study of ATP10C in autism.

Kim SJ, Herzing LB, Veenstra-VanderWeele J, Lord C, Courchesne R, Leventhal BL, Ledbetter DH, Courchesne E, Cook EH Jr. Kim SJ, et al. Among authors: leventhal bl. Am J Med Genet. 2002 Mar 8;114(2):137-43. doi: 10.1002/ajmg.10238. Am J Med Genet. 2002. PMID: 11857573

6

Family-based association study of the serotonin transporter gene polymorphisms in Korean ADHD trios.

Kim SJ, Badner J, Cheon KA, Kim BN, Yoo HJ, Kim SJ, Cook E Jr, Leventhal BL, Kim YS. Kim SJ, et al. Among authors: leventhal bl. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):14-8. doi: 10.1002/ajmg.b.30214. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 16082698

7

Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHD.

Kim YS, Leventhal BL, Kim SJ, Kim BN, Cheon KA, Yoo HJ, Kim SJ, Badner J, Cook EH. Kim YS, et al. Among authors: leventhal bl. Neurosci Lett. 2005 Dec 30;390(3):176-81. doi: 10.1016/j.neulet.2005.08.025. Epub 2005 Sep 13. Neurosci Lett. 2005. PMID: 16165273

8

Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder.

Dickel DE, Veenstra-VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL. Dickel DE, et al. Among authors: leventhal bl. Arch Gen Psychiatry. 2006 Jul;63(7):778-85. doi: 10.1001/archpsyc.63.7.778. Arch Gen Psychiatry. 2006. PMID: 16818867

9

Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder.

Dickel DE, Veenstra-VanderWeele J, Bivens NC, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL. Dickel DE, et al. Among authors: leventhal bl. Biol Psychiatry. 2007 Feb 1;61(3):322-9. doi: 10.1016/j.biopsych.2006.09.030. Biol Psychiatry. 2007. PMID: 17241828

10

Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism.

Cross S, Kim SJ, Weiss LA, Delahanty RJ, Sutcliffe JS, Leventhal BL, Cook EH Jr, Veenstra-Vanderweele J. Cross S, et al. Among authors: leventhal bl. Neuropsychopharmacology. 2008 Jan;33(2):353-60. doi: 10.1038/sj.npp.1301406. Epub 2007 Apr 4. Neuropsychopharmacology. 2008. PMID: 17406648 Free PMC article.

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