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Items: 1 to 20 of 190

1.

Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22.

Hamilton SP, Slager SL, Heiman GA, Deng Z, Haghighi F, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA.

Biol Psychiatry. 2002 Apr 1;51(7):591-601.

PMID:
11950461
2.

Investigation of polymorphisms in the CREM gene in panic disorder.

Hamilton SP, Slager SL, Mayo D, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA.

Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):111-5.

PMID:
15048659
3.

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia.

Handoko HY, Nyholt DR, Hayward NK, Nertney DA, Hannah DE, Windus LC, McCormack CM, Smith HJ, Filippich C, James MR, Mowry BJ.

Mol Psychiatry. 2005 Jun;10(6):589-97.

PMID:
15505638
5.

The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study.

Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I.

Int Clin Psychopharmacol. 2010 Jul;25(4):218-27. doi: 10.1097/YIC.0b013e328338b884.

PMID:
20531207
6.

Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.

Borroni B, Grassi M, Costanzi C, Zanetti M, Archetti S, Franzoni S, Caimi L, Padovani A.

Neurobiol Aging. 2007 Aug;28(8):1231-8.

PMID:
16837108
7.

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
8.

Is 472G/A catechol-O-methyl-transferase gene polymorphism related to panic disorder?

Zintzaras E, Sakelaridis N.

Psychiatr Genet. 2007 Oct;17(5):267-73.

PMID:
17728665
9.

Haplotype analysis of the COMT-ARVCF gene region in Israeli anorexia nervosa family trios.

Michaelovsky E, Frisch A, Leor S, Stein D, Danziger Y, Carel C, Fennig S, Mimouni M, Klauck SM, Benner A, Poustka A, Apter A, Weizman A.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):45-50.

PMID:
16118784
10.

Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder.

Hamilton SP, Slager SL, De Leon AB, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA.

Neuropsychopharmacology. 2004 Mar;29(3):558-65.

11.

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11.

Li T, Ball D, Zhao J, Murray RM, Liu X, Sham PC, Collier DA.

Mol Psychiatry. 2000 Jan;5(1):77-84. Erratum in: Mol Psychiatry 2000 Jul;5(4):452.

PMID:
10673772
12.

Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families.

Chen X, Wang X, O'Neill AF, Walsh D, Kendler KS.

Mol Psychiatry. 2004 Oct;9(10):962-7.

PMID:
15124004
13.

The corticotropin-releasing hormone gene and behavioral inhibition in children at risk for panic disorder.

Smoller JW, Yamaki LH, Fagerness JA, Biederman J, Racette S, Laird NM, Kagan J, Snidman N, Faraone SV, Hirshfeld-Becker D, Tsuang MT, Slaugenhaupt SA, Rosenbaum JF, Sklar PB.

Biol Psychiatry. 2005 Jun 15;57(12):1485-92.

PMID:
15953484
14.

Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease.

Sweet RA, Devlin B, Pollock BG, Sukonick DL, Kastango KB, Bacanu SA, Chowdari KV, DeKosky ST, Ferrell RE.

Mol Psychiatry. 2005 Nov;10(11):1026-36.

PMID:
16027741
15.

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia.

Sanders AR, Rusu I, Duan J, Vander Molen JE, Hou C, Schwab SG, Wildenauer DB, Martinez M, Gejman PV.

Mol Psychiatry. 2005 Apr;10(4):353-65.

PMID:
15340358
16.

A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population.

Ma X, Sun J, Yao J, Wang Q, Hu X, Deng W, Sun X, Liu X, Murray RM, Collier DA, Li T.

Psychiatry Res. 2007 Sep 30;153(1):7-15.

PMID:
17604122
17.

No association or linkage between polymorphisms in the genes encoding cholecystokinin and the cholecystokinin B receptor and panic disorder.

Hamilton SP, Slager SL, Helleby L, Heiman GA, Klein DF, Hodge SE, Weissman MM, Fyer AJ, Knowles JA.

Mol Psychiatry. 2001 Jan;6(1):59-65.

PMID:
11244486
18.

Investigation of dopamine receptor (DRD4) and dopamine transporter (DAT) polymorphisms for genetic linkage or association to panic disorder.

Hamilton SP, Haghighi F, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA.

Am J Med Genet. 2000 Jun 12;96(3):324-30.

PMID:
10898909
19.

The association of functional catechol-O-methyltransferase haplotypes with risk of Parkinson's disease, levodopa treatment response, and complications.

Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Tan EK, Drozdzik M.

Pharmacogenet Genomics. 2008 Sep;18(9):815-21. doi: 10.1097/FPC.0b013e328306c2f2.

PMID:
18698234
20.

Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders.

Erhardt A, Lucae S, Unschuld PG, Ising M, Kern N, Salyakina D, Lieb R, Uhr M, Binder EB, Keck ME, Müller-Myhsok B, Holsboer F.

J Affect Disord. 2007 Aug;101(1-3):159-68.

PMID:
17197037
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