Cook EH - Search Results

1

A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.

Chen R, Wei Q, Zhan X, Zhong X, Sutcliffe JS, Cox NJ, Cook EH, Li C, Chen W, Li B. Chen R, et al. Among authors: cook eh. Bioinformatics. 2015 May 1;31(9):1452-9. doi: 10.1093/bioinformatics/btu860. Epub 2015 Jan 6. Bioinformatics. 2015. PMID: 25568282 Free PMC article.

2

Association of attention-deficit disorder and the dopamine transporter gene.

Cook EH Jr, Stein MA, Krasowski MD, Cox NJ, Olkon DM, Kieffer JE, Leventhal BL. Cook EH Jr, et al. Am J Hum Genet. 1995 Apr;56(4):993-8. Am J Hum Genet. 1995. PMID: 7717410 Free PMC article.

3

Evidence of linkage between the serotonin transporter and autistic disorder.

Cook EH Jr, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal BL. Cook EH Jr, et al. Mol Psychiatry. 1997 May;2(3):247-50. doi: 10.1038/sj.mp.4000266. Mol Psychiatry. 1997. PMID: 9152989

4

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.

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: cook eh jr. Am J Med Genet. 2002 Mar 8;114(2):137-43. doi: 10.1002/ajmg.10238. Am J Med Genet. 2002. PMID: 11857573

6

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.

Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH Jr. Kim SJ, et al. Among authors: cook eh jr. Mol Psychiatry. 2002;7(3):278-88. doi: 10.1038/sj.mp.4001033. Mol Psychiatry. 2002. PMID: 11920155

7

Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.

Hanna GL, Veenstra-VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC, Leventhal BL, Cook EH Jr. Hanna GL, et al. Among authors: cook eh jr. Am J Med Genet. 2002 Jul 8;114(5):541-52. doi: 10.1002/ajmg.10519. Am J Med Genet. 2002. PMID: 12116192 Free article.

8

Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS. Weiss LA, et al. Among authors: cook eh. Eur J Hum Genet. 2006 Aug;14(8):923-31. doi: 10.1038/sj.ejhg.5201644. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724005

9

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: cook eh jr. Arch Gen Psychiatry. 2006 Jul;63(7):778-85. doi: 10.1001/archpsyc.63.7.778. Arch Gen Psychiatry. 2006. PMID: 16818867

10

Genetic studies of stuttering in a founder population.

Wittke-Thompson JK, Ambrose N, Yairi E, Roe C, Cook EH, Ober C, Cox NJ. Wittke-Thompson JK, et al. Among authors: cook eh. J Fluency Disord. 2007;32(1):33-50. doi: 10.1016/j.jfludis.2006.12.002. Epub 2006 Dec 30. J Fluency Disord. 2007. PMID: 17276504 Free PMC article.

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