Curran S - Search Results

1

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

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

QTL association analysis of the DRD4 exon 3 VNTR polymorphism in a population sample of children screened with a parent rating scale for ADHD symptoms.

Curran S, Mill J, Sham P, Rijsdijk F, Marusic K, Taylor E, Asherson P. Curran S, et al. Am J Med Genet. 2001 May 8;105(4):387-93. doi: 10.1002/ajmg.1366. Am J Med Genet. 2001. PMID: 11378855

4

Association study of a SNAP-25 microsatellite and attention deficit hyperactivity disorder.

Mill J, Curran S, Kent L, Gould A, Huckett L, Richards S, Taylor E, Asherson P. Mill J, et al. Among authors: curran s. Am J Med Genet. 2002 Apr 8;114(3):269-71. doi: 10.1002/ajmg.10253. Am J Med Genet. 2002. PMID: 11920846

5

CHIP: Defining a dimension of the vulnerability to attention deficit hyperactivity disorder (ADHD) using sibling and individual data of children in a community-based sample.

Curran S, Rijsdijk F, Martin N, Marusic K, Asherson P, Taylor E, Sham P. Curran S, et al. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):86-97. doi: 10.1002/ajmg.b.20002. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707944

6

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

7

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: curran s. 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

8

The serotonin transporter gene as a QTL for ADHD.

Curran S, Purcell S, Craig I, Asherson P, Sham P. Curran S, et al. 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

9

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

10

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

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