Cox NJ - 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: cox nj. 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

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: cox nj. 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.

3

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

4

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: cox nj. 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.

5

Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder.

Hanna GL, Veenstra-Vanderweele J, Cox NJ, Van Etten M, Fischer DJ, Himle JA, Bivens NC, Wu X, Roe CA, Hennessy KA, Dickel DE, Leventhal BL, Cook EH Jr. Hanna GL, et al. Among authors: cox nj. Biol Psychiatry. 2007 Oct 15;62(8):856-62. doi: 10.1016/j.biopsych.2007.01.008. Epub 2007 Jun 4. Biol Psychiatry. 2007. PMID: 17544380 Free PMC article.

6

Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines.

Liu W, Wu X, Zhang W, Montenegro RC, Fackenthal DL, Spitz JA, Huff LM, Innocenti F, Das S, Cook EH Jr, Cox NJ, Bates SE, Ratain MJ. Liu W, et al. Among authors: cox nj. Clin Cancer Res. 2007 Nov 15;13(22 Pt 1):6788-95. doi: 10.1158/1078-0432.CCR-07-0547. Clin Cancer Res. 2007. PMID: 18006781

7

Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.

Kim SJ, Brune CW, Kistner EO, Christian SL, Courchesne EH, Cox NJ, Cook EH. Kim SJ, et al. Among authors: cox nj. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1116-25. doi: 10.1002/ajmg.b.30733. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18361419 Free PMC article.

8

Population-specific GSTM1 copy number variation.

Huang RS, Chen P, Wisel S, Duan S, Zhang W, Cook EH, Das S, Cox NJ, Dolan ME. Huang RS, et al. Among authors: cox nj. Hum Mol Genet. 2009 Jan 15;18(2):366-72. doi: 10.1093/hmg/ddn345. Epub 2008 Oct 23. Hum Mol Genet. 2009. PMID: 18948376 Free PMC article.

9

SCAN: SNP and copy number annotation.

Gamazon ER, Zhang W, Konkashbaev A, Duan S, Kistner EO, Nicolae DL, Dolan ME, Cox NJ. Gamazon ER, et al. Among authors: cox nj. Bioinformatics. 2010 Jan 15;26(2):259-62. doi: 10.1093/bioinformatics/btp644. Epub 2009 Nov 17. Bioinformatics. 2010. PMID: 19933162 Free PMC article.

10

Parent-of-origin effects of the serotonin transporter gene associated with autism.

Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH Jr. Kistner-Griffin E, et al. Among authors: cox nj. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):139-44. doi: 10.1002/ajmg.b.31146. Epub 2010 Dec 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302342 Free PMC article.

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