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Items: 1 to 20 of 177

1.

Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations.

Johansson S, Halmøy A, Mavroconstanti T, Jacobsen KK, Landaas ET, Reif A, Jacob C, Boreatti-Hümmer A, Kreiker S, Lesch KP, Kan CC, Kooij JJ, Kiemeney LA, Buitelaar JK, Franke B, Ribasés M, Bosch R, Bayés M, Casas M, Ramos-Quiroga JA, Cormand B, Knappskog P, Haavik J.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jul;153B(5):1008-15. doi: 10.1002/ajmg.b.31067.

PMID:
20213726
2.

Attention-deficit/hyperactivity disorder symptoms in offspring of mothers with impaired serotonin production.

Halmøy A, Johansson S, Winge I, McKinney JA, Knappskog PM, Haavik J.

Arch Gen Psychiatry. 2010 Oct;67(10):1033-43. doi: 10.1001/archgenpsychiatry.2010.124.

PMID:
20921119
3.

No association between TPH2 gene polymorphisms and ADHD in a UK sample.

Sheehan K, Hawi Z, Gill M, Kent L.

Neurosci Lett. 2007 Jan 29;412(2):105-7. Epub 2006 Nov 22.

PMID:
17123708
4.

An international multicenter association study of the serotonin transporter gene in persistent ADHD.

Landaas ET, Johansson S, Jacobsen KK, Ribasés M, Bosch R, Sánchez-Mora C, Jacob CP, Boreatti-Hümmer A, Kreiker S, Lesch KP, Kiemeney LA, Kooij JJ, Kan C, Buitelaar JK, Faraone SV, Halmøy A, Ramos-Quiroga JA, Cormand B, Reif A, Franke B, Mick E, Knappskog PM, Haavik J.

Genes Brain Behav. 2010 Jul;9(5):449-58. doi: 10.1111/j.1601-183X.2010.00567.x. Epub 2010 Jan 25.

5.

Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese.

Lin YM, Chao SC, Chen TM, Lai TJ, Chen JS, Sun HS.

Arch Gen Psychiatry. 2007 Sep;64(9):1015-24.

PMID:
17768266
6.

A case-control association study of serotonin 1A receptor gene and tryptophan hydroxylase 2 gene in attention deficit hyperactivity disorder.

Shim SH, Hwangbo Y, Kwon YJ, Jeong HY, Lee BH, Hwang JA, Kim YK.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Aug 16;34(6):974-9. doi: 10.1016/j.pnpbp.2010.05.006. Epub 2010 May 11.

PMID:
20470849
7.

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

Sheehan K, Lowe N, Kirley A, Mullins C, Fitzgerald M, Gill M, Hawi Z.

Mol Psychiatry. 2005 Oct;10(10):944-9. Erratum in: Mol Psychiatry. 2006 Feb;11(2):221.

PMID:
15940290
8.

Association between tryptophan hydroxylase 2, performance on a continuance performance test and response to methylphenidate in ADHD participants.

Manor I, Laiba E, Eisenberg J, Meidad S, Lerer E, Israel S, Gritsenko I, Tyano S, Faraone SV, Ebstein RP.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1501-8. doi: 10.1002/ajmg.b.30702.

PMID:
18213624
9.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in attention-deficit/hyperactivity disorder.

Walitza S, Renner TJ, Dempfle A, Konrad K, Wewetzer Ch, Halbach A, Herpertz-Dahlmann B, Remschmidt H, Smidt J, Linder M, Flierl L, Knölker U, Friedel S, Schäfer H, Gross C, Hebebrand J, Warnke A, Lesch KP.

Mol Psychiatry. 2005 Dec;10(12):1126-32.

PMID:
16116490
10.

Tph2 gene variants modulate response control processes in adult ADHD patients and healthy individuals.

Baehne CG, Ehlis AC, Plichta MM, Conzelmann A, Pauli P, Jacob C, Gutknecht L, Lesch KP, Fallgatter AJ.

Mol Psychiatry. 2009 Nov;14(11):1032-9. doi: 10.1038/mp.2008.39. Epub 2008 Apr 22.

PMID:
18427560
11.

Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder in Chinese Han population.

Li J, Wang Y, Zhou R, Zhang H, Yang L, Wang B, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):126-9.

PMID:
16389593
12.

A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han population.

Guan L, Wang B, Chen Y, Yang L, Li J, Qian Q, Wang Z, Faraone SV, Wang Y.

Mol Psychiatry. 2009 May;14(5):546-54. doi: 10.1038/sj.mp.4002139. Epub 2008 Jan 8.

PMID:
18180757
13.

Association between catechol O-methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in adults.

Halleland H, Lundervold AJ, Halmøy A, Haavik J, Johansson S.

Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):403-10. doi: 10.1002/ajmg.b.30831.

PMID:
18802928
14.

Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population.

Van Den Bogaert A, Sleegers K, De Zutter S, Heyrman L, Norrback KF, Adolfsson R, Van Broeckhoven C, Del-Favero J.

Arch Gen Psychiatry. 2006 Oct;63(10):1103-10.

PMID:
17015812
15.

TPH2 and TPH1: association of variants and interactions with heroin addiction.

Nielsen DA, Barral S, Proudnikov D, Kellogg S, Ho A, Ott J, Kreek MJ.

Behav Genet. 2008 Mar;38(2):133-50. doi: 10.1007/s10519-007-9187-7. Epub 2008 Jan 8.

PMID:
18181017
16.

An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples.

Ribasés M, Sánchez-Mora C, Ramos-Quiroga JA, Bosch R, Gómez N, Nogueira M, Corrales M, Palomar G, Jacob CP, Gross-Lesch S, Kreiker S, Reif A, Lesch KP, Cormand B, Casas M, Bayés M.

Psychiatr Genet. 2012 Aug;22(4):155-60. doi: 10.1097/YPG.0b013e328353957e.

PMID:
22504457
17.

Haplotype-based linkage of tryptophan hydroxylase 2 to suicide attempt, major depression, and cerebrospinal fluid 5-hydroxyindoleacetic acid in 4 populations.

Zhou Z, Roy A, Lipsky R, Kuchipudi K, Zhu G, Taubman J, Enoch MA, Virkkunen M, Goldman D.

Arch Gen Psychiatry. 2005 Oct;62(10):1109-18.

PMID:
16203956
18.
19.

Common genetic variations in TPH1/TPH2 genes are not associated with schizophrenia in Japanese population.

Shiroiwa K, Hishimoto A, Mouri K, Fukutake M, Supriyanto I, Nishiguchi N, Shirakawa O.

Neurosci Lett. 2010 Mar 26;472(3):194-8. doi: 10.1016/j.neulet.2010.02.003. Epub 2010 Feb 6.

PMID:
20144688
20.

Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum.

Lantieri F, Glessner JT, Hakonarson H, Elia J, Devoto M.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1127-33. doi: 10.1002/ajmg.b.31110.

PMID:
20607790
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