Curran S - Search Results

1

Polymorphisms in the dopamine D5 receptor (DRD5) gene and ADHD.

Mill J, Curran S, Richards S, Taylor E, Asherson P. Mill J, et al. Among authors: curran s. Am J Med Genet B Neuropsychiatr Genet. 2004 Feb 15;125B(1):38-42. doi: 10.1002/ajmg.b.20127. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14755441

2

Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders.

Tropeano M, Ahn JW, Dobson RJ, Breen G, Rucker J, Dixit A, Pal DK, McGuffin P, Farmer A, White PS, Andrieux J, Vassos E, Ogilvie CM, Curran S, Collier DA. Tropeano M, et al. Among authors: curran s. PLoS One. 2013 Apr 18;8(4):e61365. doi: 10.1371/journal.pone.0061365. Print 2013. PLoS One. 2013. PMID: 23637818 Free PMC article.

3

Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.

Milner KM, Craig EE, Thompson RJ, Veltman MW, Thomas NS, Roberts S, Bellamy M, Curran SR, Sporikou CM, Bolton PF. Milner KM, et al. Among authors: curran sr. J Child Psychol Psychiatry. 2005 Oct;46(10):1089-96. doi: 10.1111/j.1469-7610.2005.01520.x. J Child Psychol Psychiatry. 2005. PMID: 16178933

4

Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis.

de Jong S, Newhouse SJ, Patel H, Lee S, Dempster D, Curtis C, Paya-Cano J, Murphy D, Wilson CE, Horder J, Mendez MA, Asherson P, Rivera M, Costello H, Maltezos S, Whitwell S, Pitts M, Tye C, Ashwood KL, Bolton P, Curran S, McGuffin P, Dobson R, Breen G. de Jong S, et al. Among authors: curran s. Br J Psychiatry. 2016 Sep;209(3):202-8. doi: 10.1192/bjp.bp.115.175471. Epub 2016 May 5. Br J Psychiatry. 2016. PMID: 27151072 Free PMC article.

5

Cortical serotonin 5-HT2A receptor binding and social communication in adults with Asperger's syndrome: an in vivo SPECT study.

Murphy DG, Daly E, Schmitz N, Toal F, Murphy K, Curran S, Erlandsson K, Eersels J, Kerwin R, Ell P, Travis M. Murphy DG, et al. Among authors: curran s. Am J Psychiatry. 2006 May;163(5):934-6. doi: 10.1176/ajp.2006.163.5.934. Am J Psychiatry. 2006. PMID: 16648340

6

A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy.

Brookes KJ, Mill J, Guindalini C, Curran S, Xu X, Knight J, Chen CK, Huang YS, Sethna V, Taylor E, Chen W, Breen G, Asherson P. Brookes KJ, et al. Among authors: curran s. Arch Gen Psychiatry. 2006 Jan;63(1):74-81. doi: 10.1001/archpsyc.63.1.74. Arch Gen Psychiatry. 2006. PMID: 16389200

7

A common variant in DRD3 receptor is associated with autism spectrum disorder.

de Krom M, Staal WG, Ophoff RA, Hendriks J, Buitelaar J, Franke B, de Jonge MV, Bolton P, Collier D, Curran S, van Engeland H, van Ree JM. de Krom M, et al. Among authors: curran s. Biol Psychiatry. 2009 Apr 1;65(7):625-30. doi: 10.1016/j.biopsych.2008.09.035. Epub 2008 Dec 5. Biol Psychiatry. 2009. PMID: 19058789

8

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series - further understanding of the relevance of NRXN1 to neurodevelopmental disorders.

Curran S, Ahn JW, Grayton H, Collier DA, Ogilvie CM. Curran S, et al. J Mol Psychiatry. 2013 Apr 23;1(1):4. doi: 10.1186/2049-9256-1-4. eCollection 2013. J Mol Psychiatry. 2013. PMID: 25408897 Free PMC article.

9

No major effect of twinning on autistic traits.

Curran S, Dworzynski K, Happé F, Ronald A, Allison C, Baron-Cohen S, Brayne C, Bolton PF. Curran S, et al. Autism Res. 2011 Oct;4(5):377-82. doi: 10.1002/aur.207. Epub 2011 Jul 15. Autism Res. 2011. PMID: 21766464

10

Continuity and change in preschool ADHD symptoms: longitudinal genetic analysis with contrast effects.

Price TS, Simonoff E, Asherson P, Curran S, Kuntsi J, Waldman I, Plomin R. Price TS, et al. Among authors: curran s. Behav Genet. 2005 Mar;35(2):121-32. doi: 10.1007/s10519-004-1013-x. Behav Genet. 2005. PMID: 15685426

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