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Items: 1 to 20 of 175

1.

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
2.

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
3.

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
4.

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
5.

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
6.

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
7.

Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics.

Schuhmacher A, Becker T, Rujescu D, Quednow BB, Lennertz L, Wagner M, Benninghoff J, Rietschel M, Häfner H, Franke P, Wölwer W, Gaebel W, Maier W, Mössner R.

J Psychiatr Res. 2012 Aug;46(8):1073-80. doi: 10.1016/j.jpsychires.2012.04.021. Epub 2012 May 30.

8.

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
9.

[Association between tryptophan hydroxylase gene polymorphisms and attention deficit hyperactivity disorder with or without learning disorder].

Li J, Wang YF, Zhou RL, Yang L, Zhang HB, Wang B.

Zhonghua Yi Xue Za Zhi. 2003 Dec 25;83(24):2114-8. Chinese.

PMID:
14720417
10.

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
11.

SNP and haplotype analysis of a novel tryptophan hydroxylase isoform (TPH2) gene provide evidence for association with major depression.

Zill P, Baghai TC, Zwanzger P, Schüle C, Eser D, Rupprecht R, Möller HJ, Bondy B, Ackenheil M.

Mol Psychiatry. 2004 Nov;9(11):1030-6.

PMID:
15124006
12.
13.

Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.

Mössner R, Walitza S, Geller F, Scherag A, Gutknecht L, Jacob C, Bogusch L, Remschmidt H, Simons M, Herpertz-Dahlmann B, Fleischhaker C, Schulz E, Warnke A, Hinney A, Wewetzer C, Lesch KP.

Int J Neuropsychopharmacol. 2006 Aug;9(4):437-42. Epub 2005 Sep 7.

PMID:
16146581
14.

Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.

Bhaduri N, Sinha S, Chattopadhyay A, Gangopadhyay PK, Singh M, Mukhopadhyay KK.

Indian Pediatr. 2005 Feb;42(2):123-9.

15.

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.

Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):110-4.

PMID:
15717295
16.

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
17.

Support for tryptophan hydroxylase-2 as a susceptibility gene for bipolar affective disorder.

Roche S, McKeon P.

Psychiatr Genet. 2009 Jun;19(3):142-6. doi: 10.1097/YPG.0b013e32832a4f95.

PMID:
19352219
18.

Serotonin genes and attention deficit/hyperactivity disorder in a Brazilian sample: preferential transmission of the HTR2A 452His allele to affected boys.

Guimarães AP, Zeni C, Polanczyk GV, Genro JP, Roman T, Rohde LA, Hutz MH.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jan 5;144B(1):69-73.

PMID:
16958038
19.

Association of attention-deficit/hyperactivity disorder with serotonin 4 receptor gene polymorphisms in Han Chinese subjects.

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

Neurosci Lett. 2006 Jun 19;401(1-2):6-9. Epub 2006 Mar 23.

PMID:
16563621
20.

Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD).

Quist JF, Barr CL, Schachar R, Roberts W, Malone M, Tannock R, Basile VS, Beitchman J, Kennedy JL.

Mol Psychiatry. 2000 Sep;5(5):537-41.

PMID:
11032388

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