K02 MH01389/MH/NIMH NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1998	3
1999	3
2000	1
2001	6
2002	5
2003	2
2004	1
2005	3
2006	2
2007	4
2008	2
2009	1
2010	1
2024	0

1

Cook EH Jr. Cook EH Jr. Child Adolesc Psychiatr Clin N Am. 2001 Apr;10(2):333-50. Child Adolesc Psychiatr Clin N Am. 2001. PMID: 11351802 Review.

2

Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder.

Lassig JP, Vachirasomtoon K, Hartzell K, Leventhal M, Courchesne E, Courchesne R, Lord C, Leventhal BL, Cook EH Jr. Lassig JP, et al. Am J Med Genet. 1999 Oct 15;88(5):472-5. doi: 10.1002/(sici)1096-8628(19991015)88:5<472::aid-ajmg7>3.0.co;2-g. Am J Med Genet. 1999. PMID: 10490701

3

Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.

Cook EH Jr, Courchesne RY, Cox NJ, Lord C, Gonen D, Guter SJ, Lincoln A, Nix K, Haas R, Leventhal BL, Courchesne E. Cook EH Jr, et al. Am J Hum Genet. 1998 May;62(5):1077-83. doi: 10.1086/301832. Am J Hum Genet. 1998. PMID: 9545402 Free PMC article.

4

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. Am J Med Genet. 2002 Apr 8;114(3):277-83. doi: 10.1002/ajmg.10192. Am J Med Genet. 2002. PMID: 11920848

5

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. Am J Psychiatry. 2006 Dec;163(12):2148-56. doi: 10.1176/ajp.2006.163.12.2148. Am J Psychiatry. 2006. PMID: 17151167

6

Multisite, double-blind, placebo-controlled trial of porcine secretin in autism.

Owley T, McMahon W, Cook EH, Laulhere T, South M, Mays LZ, Shernoff ES, Lainhart J, Modahl CB, Corsello C, Ozonoff S, Risi S, Lord C, Leventhal BL, Filipek PA. Owley T, et al. J Am Acad Child Adolesc Psychiatry. 2001 Nov;40(11):1293-9. doi: 10.1097/00004583-200111000-00009. J Am Acad Child Adolesc Psychiatry. 2001. PMID: 11699803 Clinical Trial.

7

Strategies for autism candidate gene analysis.

Barnby G, Monaco AP. Barnby G, et al. Novartis Found Symp. 2003;251:48-63; discussion 63-9, 109-11, 281-97. doi: 10.1002/0470869380.ch4. Novartis Found Symp. 2003. PMID: 14521187

8

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E, Blasi F, Maestrini E, Broxholme J, Tzenova J, Weeks D, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium (IMGSAC). Lamb JA, et al. J Med Genet. 2005 Feb;42(2):132-7. doi: 10.1136/jmg.2004.025668. J Med Genet. 2005. PMID: 15689451 Free PMC article.

9

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin.

Weiss LA, Veenstra-Vanderweele J, Newman DL, Kim SJ, Dytch H, McPeek MS, Cheng S, Ober C, Cook EH Jr, Abney M. Weiss LA, et al. Eur J Hum Genet. 2004 Nov;12(11):949-54. doi: 10.1038/sj.ejhg.5201239. Eur J Hum Genet. 2004. PMID: 15292919

10

Mutation screening of the UBE3A/E6-AP gene in autistic disorder.

Veenstra-VanderWeele J, Gonen D, Leventhal BL, Cook EH Jr. Veenstra-VanderWeele J, et al. Mol Psychiatry. 1999 Jan;4(1):64-7. doi: 10.1038/sj.mp.4000472. Mol Psychiatry. 1999. PMID: 10089011

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