Craig I - Search Results

1

Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR.

Mill J, Asherson P, Browes C, D'Souza U, Craig I. Mill J, et al. Among authors: craig i. Am J Med Genet. 2002 Dec 8;114(8):975-9. doi: 10.1002/ajmg.b.10948. Am J Med Genet. 2002. PMID: 12457396

2

Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP-25, and 5HT1B.

Mill J, Xu X, Ronald A, Curran S, Price T, Knight J, Craig I, Sham P, Plomin R, Asherson P. Mill J, et al. Among authors: craig i. Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):68-73. doi: 10.1002/ajmg.b.30107. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15578613

3

Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1).

Mill J, Asherson P, Craig I, D'Souza UM. Mill J, et al. Among authors: craig i. BMC Genet. 2005 Jan 31;6:3. doi: 10.1186/1471-2156-6-3. BMC Genet. 2005. PMID: 15683546 Free PMC article.

4

The serotonin transporter gene as a QTL for ADHD.

Curran S, Purcell S, Craig I, Asherson P, Sham P. Curran S, et al. Among authors: craig i. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):42-7. doi: 10.1002/ajmg.b.30118. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15719397

5

DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: no evidence for association.

Xu X, Knight J, Brookes K, Mill J, Sham P, Craig I, Taylor E, Asherson P. Xu X, et al. Among authors: craig i. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):115-8. doi: 10.1002/ajmg.b.30160. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15719398

6

Functional effects of a tandem duplication polymorphism in the 5'flanking region of the DRD4 gene.

D'Souza UM, Russ C, Tahir E, Mill J, McGuffin P, Asherson PJ, Craig IW. D'Souza UM, et al. Biol Psychiatry. 2004 Nov 1;56(9):691-7. doi: 10.1016/j.biopsych.2004.08.008. Biol Psychiatry. 2004. PMID: 15522254

7

Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene.

Mill J, Dempster E, Caspi A, Williams B, Moffitt T, Craig I. Mill J, et al. Among authors: craig i. Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):421-5. doi: 10.1002/ajmg.b.30316. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16583437

8

Prediction of heterogeneity in intelligence and adult prognosis by genetic polymorphisms in the dopamine system among children with attention-deficit/hyperactivity disorder: evidence from 2 birth cohorts.

Mill J, Caspi A, Williams BS, Craig I, Taylor A, Polo-Tomas M, Berridge CW, Poulton R, Moffitt TE. Mill J, et al. Among authors: craig i. Arch Gen Psychiatry. 2006 Apr;63(4):462-9. doi: 10.1001/archpsyc.63.4.462. Arch Gen Psychiatry. 2006. PMID: 16585476

9

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene.

Caspi A, Sugden K, Moffitt TE, Taylor A, Craig IW, Harrington H, McClay J, Mill J, Martin J, Braithwaite A, Poulton R. Caspi A, et al. Science. 2003 Jul 18;301(5631):386-9. doi: 10.1126/science.1083968. Science. 2003. PMID: 12869766

10

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes.

Craig IW, Mill J, Craig GM, Loat C, Schalkwyk LC. Craig IW, et al. Eur J Hum Genet. 2004 Aug;12(8):639-46. doi: 10.1038/sj.ejhg.5201212. Eur J Hum Genet. 2004. PMID: 15114374

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