Mullins C - Search Results

1

Association of the 480 bp DAT1 allele with methylphenidate response in a sample of Irish children with ADHD.

Kirley A, Lowe N, Hawi Z, Mullins C, Daly G, Waldman I, McCarron M, O'Donnell D, Fitzgerald M, Gill M. Kirley A, et al. Among authors: mullins c. Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):50-4. doi: 10.1002/ajmg.b.20071. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12898575

2

Tryptophan hydroxylase 2 (TPH2) gene variants associated with ADHD.

Sheehan K, Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. Sheehan K, et al. Among authors: mullins c. Mol Psychiatry. 2005 Oct;10(10):944-9. doi: 10.1038/sj.mp.4001698. Mol Psychiatry. 2005. PMID: 15940290

3

Dopaminergic system genes in ADHD: toward a biological hypothesis.

Kirley A, Hawi Z, Daly G, McCarron M, Mullins C, Millar N, Waldman I, Fitzgerald M, Gill M. Kirley A, et al. Among authors: mullins c. Neuropsychopharmacology. 2002 Oct;27(4):607-19. doi: 10.1016/S0893-133X(02)00315-9. Neuropsychopharmacology. 2002. PMID: 12377397

4

Phenotype studies of the DRD4 gene polymorphisms in ADHD: association with oppositional defiant disorder and positive family history.

Kirley A, Lowe N, Mullins C, McCarron M, Daly G, Waldman I, Fitzgerald M, Gill M, Hawi Z. Kirley A, et al. Among authors: mullins c. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):38-42. doi: 10.1002/ajmg.b.30072. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389763

5

Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: evidence of linkage and association with the SNP -616.

Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z. Lowe N, et al. Among authors: mullins c. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):33-7. doi: 10.1002/ajmg.b.30071. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389764

6

The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.

Bellgrove MA, Domschke K, Hawi Z, Kirley A, Mullins C, Robertson IH, Gill M. Bellgrove MA, et al. Among authors: mullins c. Exp Brain Res. 2005 Jun;163(3):352-60. doi: 10.1007/s00221-004-2180-y. Epub 2005 Jan 15. Exp Brain Res. 2005. PMID: 15654584

7

Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected children.

Domschke K, Sheehan K, Lowe N, Kirley A, Mullins C, O'sullivan R, Freitag C, Becker T, Conroy J, Fitzgerald M, Gill M, Hawi Z. Domschke K, et al. Among authors: mullins c. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):110-4. doi: 10.1002/ajmg.b.30158. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15717295

8

Variability in time reproduction: difference in ADHD combined and inattentive subtypes.

Mullins C, Bellgrove MA, Gill M, Robertson IH. Mullins C, et al. J Am Acad Child Adolesc Psychiatry. 2005 Feb;44(2):169-76. doi: 10.1097/00004583-200502000-00009. J Am Acad Child Adolesc Psychiatry. 2005. PMID: 15689730

9

Impaired temporal resolution of visual attention and dopamine beta hydroxylase genotype in attention-deficit/hyperactivity disorder.

Bellgrove MA, Mattingley JB, Hawi Z, Mullins C, Kirley A, Gill M, Robertson IH. Bellgrove MA, et al. Among authors: mullins c. Biol Psychiatry. 2006 Nov 15;60(10):1039-45. doi: 10.1016/j.biopsych.2006.03.062. Epub 2006 Jul 28. Biol Psychiatry. 2006. PMID: 16876143

10

D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13.

Krebs CJ, Horton JH, Mullins CM, Paradee WJ, Taggart RT. Krebs CJ, et al. Among authors: mullins cm. Hum Mol Genet. 1993 Jun;2(6):825. doi: 10.1093/hmg/2.6.825-a. Hum Mol Genet. 1993. PMID: 8353510 No abstract available.

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