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Items: 1 to 20 of 178

1.

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
2.

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
3.

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
4.

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
5.

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
6.

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
7.

A gene-environment investigation on personality traits in two independent clinical sets of adult patients with personality disorder and attention deficit/hyperactive disorder.

Jacob CP, Nguyen TT, Dempfle A, Heine M, Windemuth-Kieselbach C, Baumann K, Jacob F, Prechtl J, Wittlich M, Herrmann MJ, Gross-Lesch S, Lesch KP, Reif A.

Eur Arch Psychiatry Clin Neurosci. 2010 Jun;260(4):317-26. doi: 10.1007/s00406-009-0079-0. Epub 2009 Nov 6.

PMID:
19894072
8.

[ADHD and attachment processes: are they related?].

Franc N, Maury M, Purper-Ouakil D.

Encephale. 2009 Jun;35(3):256-61. doi: 10.1016/j.encep.2008.04.007. Epub 2008 Sep 20. Review. French.

PMID:
19540412
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.

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
11.

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.

Ribasés M, Ramos-Quiroga JA, Hervás A, Bosch R, Bielsa A, Gastaminza X, Artigas J, Rodriguez-Ben S, Estivill X, Casas M, Cormand B, Bayés M.

Mol Psychiatry. 2009 Jan;14(1):71-85. Epub 2007 Oct 16.

PMID:
17938636
12.

Predominant expression of tryptophan hydroxylase 1 mRNA in the pituitary: a postmortem study in human brain.

Zill P, Büttner A, Eisenmenger W, Müller J, Möller HJ, Bondy B.

Neuroscience. 2009 Apr 10;159(4):1274-82. doi: 10.1016/j.neuroscience.2009.01.006. Epub 2009 Jan 10.

PMID:
19233335
13.

Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victims.

Perroud N, Neidhart E, Petit B, Vessaz M, Laforge T, Relecom C, La Harpe R, Malafosse A, Guipponi M.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):909-18. doi: 10.1002/ajmg.b.31059.

PMID:
20052688
14.

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
15.
16.

Tryptophan hydroxylase 1 gene (TPH1) moderates the influence of social support on depressive symptoms in adults.

Jokela M, Räikkönen K, Lehtimäki T, Rontu R, Keltikangas-Järvinen L.

J Affect Disord. 2007 Jun;100(1-3):191-7. Epub 2006 Nov 28.

PMID:
17134762
17.

Late developmental stage-specific role of tryptophan hydroxylase 1 in brain serotonin levels.

Nakamura K, Sugawara Y, Sawabe K, Ohashi A, Tsurui H, Xiu Y, Ohtsuji M, Lin QS, Nishimura H, Hasegawa H, Hirose S.

J Neurosci. 2006 Jan 11;26(2):530-4.

18.

Maternal alcohol use disorder and offspring ADHD: disentangling genetic and environmental effects using a children-of-twins design.

Knopik VS, Heath AC, Jacob T, Slutske WS, Bucholz KK, Madden PA, Waldron M, Martin NG.

Psychol Med. 2006 Oct;36(10):1461-71. Epub 2006 May 31.

PMID:
16734942
19.

Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism.

Qian Q, Wang Y, Zhou R, Li J, Wang B, Glatt S, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):103-9.

PMID:
12627475
20.

The tryptophan hydroxylase 1 (TPH1) gene and risk of schizophrenia: a moderate-scale case-control study and meta-analysis.

Watanabe Y, Nunokawa A, Kaneko N, Someya T.

Neurosci Res. 2007 Nov;59(3):322-6. Epub 2007 Aug 15.

PMID:
17870198
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