Craig IW - Search Results

1

The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression.

Dempster EL, Mill J, Craig IW, Collier DA. Dempster EL, et al. Among authors: craig iw. BMC Med Genet. 2006 Feb 16;7:10. doi: 10.1186/1471-2350-7-10. BMC Med Genet. 2006. PMID: 16483362 Free PMC article.

2

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. BMC Genet. 2005 Jan 31;6:3. doi: 10.1186/1471-2156-6-3. BMC Genet. 2005. PMID: 15683546 Free PMC article.

3

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. 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

4

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. Am J Med Genet. 2002 Dec 8;114(8):975-9. doi: 10.1002/ajmg.b.10948. Am J Med Genet. 2002. PMID: 12457396

5

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. 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

6

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. 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

7

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. Among authors: craig gm. Eur J Hum Genet. 2004 Aug;12(8):639-46. doi: 10.1038/sj.ejhg.5201212. Eur J Hum Genet. 2004. PMID: 15114374

8

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. Among authors: craig iw. Biol Psychiatry. 2004 Nov 1;56(9):691-7. doi: 10.1016/j.biopsych.2004.08.008. Biol Psychiatry. 2004. PMID: 15522254

9

Variable number tandem repeats as agents of functional regulation in the genome.

Breen G, Collier D, Craig I, Quinn J. Breen G, et al. IEEE Eng Med Biol Mag. 2008 Mar-Apr;27(2):103-4, 108. doi: 10.1109/EMB.2008.915501. IEEE Eng Med Biol Mag. 2008. PMID: 18463027 No abstract available.

10

Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain.

Viana J, Pidsley R, Troakes C, Spiers H, Wong CC, Al-Sarraj S, Craig I, Schalkwyk L, Mill J. Viana J, et al. Epigenetics. 2014 Apr;9(4):587-99. doi: 10.4161/epi.27806. Epub 2014 Jan 29. Epigenetics. 2014. PMID: 24476718 Free PMC article.

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