Curran S - Search Results

1

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

2

Mission: not impossible? Candidate gene studies in child psychiatric disorders.

Collier DA, Curran S, Asherson P. Collier DA, et al. Among authors: curran s. Mol Psychiatry. 2000 Sep;5(5):457-60. doi: 10.1038/sj.mp.4000796. Mol Psychiatry. 2000. PMID: 11032375 Review. No abstract available.

3

Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample.

Mill J, Curran S, Kent L, Richards S, Gould A, Virdee V, Huckett L, Sharp J, Batten C, Fernando S, Simanoff E, Thompson M, Zhao J, Sham P, Taylor E, Asherson P. Mill J, et al. Among authors: curran s. Mol Psychiatry. 2001 Jul;6(4):440-4. doi: 10.1038/sj.mp.4000881. Mol Psychiatry. 2001. PMID: 11443530

4

The dopamine transporter gene is associated with attention deficit hyperactivity disorder in a Taiwanese sample.

Chen CK, Chen SL, Mill J, Huang YS, Lin SK, Curran S, Purcell S, Sham P, Asherson P. Chen CK, et al. Among authors: curran s. Mol Psychiatry. 2003 Apr;8(4):393-6. doi: 10.1038/sj.mp.4001238. Mol Psychiatry. 2003. PMID: 12740596

5

An association analysis of microsatellite markers across the Prader-Willi/Angelman critical region on chromosome 15 (q11-13) and autism spectrum disorder.

Curran S, Roberts S, Thomas S, Veltman M, Browne J, Medda E, Pickles A, Sham P, Bolton PF. Curran S, et al. Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):25-8. doi: 10.1002/ajmg.b.30126. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15952184

6

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

7

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

8

An association analysis of candidate genes on chromosome 15 q11-13 and autism spectrum disorder.

Curran S, Powell J, Neale BM, Dworzynski K, Li T, Murphy D, Bolton PF. Curran S, et al. Mol Psychiatry. 2006 Aug;11(8):709-13. doi: 10.1038/sj.mp.4001839. Mol Psychiatry. 2006. PMID: 16868570 No abstract available.

9

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind D, Bolton P, Craig IW. Loat CS, et al. Among authors: curran s. Genes Brain Behav. 2008 Oct;7(7):754-60. doi: 10.1111/j.1601-183X.2008.00414.x. Genes Brain Behav. 2008. PMID: 19125863 Free PMC article.

10

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.

Curran S, Bolton P, Rozsnyai K, Chiocchetti A, Klauck SM, Duketis E, Poustka F, Schlitt S, Freitag CM, Lee I, Muglia P; ITAN; Poot M, Staal W, de Jonge MV, Ophoff RA, Lewis C, Skuse D, Mandy W, Vassos E, Fossdal R, Magnusson P, Hreidarsson S, Saemundsen E, Stefansson H, Stefansson K, Collier D. Curran S, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Sep;156B(6):633-9. doi: 10.1002/ajmg.b.31201. Epub 2011 Jun 8. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21656903

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