Curran S - Search Results

1

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

2

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

3

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

4

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

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. 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

6

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

7

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.

8

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

9

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

10

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.

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