214 related articles for article (PubMed ID: 22952320)
1. Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol-O-methyl-transferase Val(158) Met polymorphism in adults with 22q11 deletion syndrome.
de Koning MB; Boot E; Bloemen OJ; van Duin ED; Abel KM; de Haan L; Linszen DH; van Amelsvoort TA
J Psychopharmacol; 2012 Dec; 26(12):1548-60. PubMed ID: 22952320
[TBL] [Abstract][Full Text] [Related]
2. Prepulse inhibition of the startle reflex depends on the catechol O-methyltransferase Val158Met gene polymorphism.
Roussos P; Giakoumaki SG; Rogdaki M; Pavlakis S; Frangou S; Bitsios P
Psychol Med; 2008 Nov; 38(11):1651-8. PubMed ID: 18261249
[TBL] [Abstract][Full Text] [Related]
3. PRODH rs450046 and proline x COMT Val¹⁵⁸ Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome.
de Koning MB; van Duin ED; Boot E; Bloemen OJ; Bakker JA; Abel KM; van Amelsvoort TA
Psychopharmacology (Berl); 2015 Sep; 232(17):3111-22. PubMed ID: 26068888
[TBL] [Abstract][Full Text] [Related]
4. Improvement of prepulse inhibition and executive function by the COMT inhibitor tolcapone depends on COMT Val158Met polymorphism.
Giakoumaki SG; Roussos P; Bitsios P
Neuropsychopharmacology; 2008 Dec; 33(13):3058-68. PubMed ID: 18536698
[TBL] [Abstract][Full Text] [Related]
5. Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.
Boot E; Booij J; Abeling N; Meijer J; da Silva Alves F; Zinkstok J; Baas F; Linszen D; van Amelsvoort T
J Psychopharmacol; 2011 Jul; 25(7):888-95. PubMed ID: 21447540
[TBL] [Abstract][Full Text] [Related]
6. IQ and hemizygosity for the Val
Franconi CP; McDonald-McGinn D; Zackai EH; McNamara MA; Salmons H; Moss E; Gur RE; Devoto M; Emanuel BS
Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1112-1115. PubMed ID: 27619075
[TBL] [Abstract][Full Text] [Related]
7. Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
Shashi V; Keshavan MS; Howard TD; Berry MN; Basehore MJ; Lewandowski E; Kwapil TR
Clin Genet; 2006 Mar; 69(3):234-8. PubMed ID: 16542388
[TBL] [Abstract][Full Text] [Related]
8. COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.
Baker K; Baldeweg T; Sivagnanasundaram S; Scambler P; Skuse D
Biol Psychiatry; 2005 Jul; 58(1):23-31. PubMed ID: 15935994
[TBL] [Abstract][Full Text] [Related]
9. Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.
Zarchi O; Carmel M; Avni C; Attias J; Frisch A; Michaelovsky E; Patya M; Green T; Weinberger R; Weizman A; Gothelf D
J Psychiatr Res; 2013 Nov; 47(11):1623-9. PubMed ID: 23910792
[TBL] [Abstract][Full Text] [Related]
10. Influence of catechol-O-methyltransferase Val158Met polymorphism on startle response in the presence of high estradiol levels.
Comasco E; Hellgren C; Sundström-Poromaa I
Eur Neuropsychopharmacol; 2013 Jul; 23(7):629-35. PubMed ID: 22831878
[TBL] [Abstract][Full Text] [Related]
11. Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.
Vorstman JA; Turetsky BI; Sijmens-Morcus ME; de Sain MG; Dorland B; Sprong M; Rappaport EF; Beemer FA; Emanuel BS; Kahn RS; van Engeland H; Kemner C
Neuropsychopharmacology; 2009 Feb; 34(3):739-46. PubMed ID: 18769474
[TBL] [Abstract][Full Text] [Related]
12. Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome.
Bassett AS; Caluseriu O; Weksberg R; Young DA; Chow EW
Biol Psychiatry; 2007 May; 61(10):1135-40. PubMed ID: 17217925
[TBL] [Abstract][Full Text] [Related]
13. Striatal dopamine release and impaired reinforcement learning in adults with 22q11.2 deletion syndrome.
van Duin EDA; Kasanova Z; Hernaus D; Ceccarini J; Heinzel A; Mottaghy F; Mohammadkhani-Shali S; Winz O; Frank M; Beck MCH; Booij J; Myin-Germeys I; van Amelsvoort T
Eur Neuropsychopharmacol; 2018 Jun; 28(6):732-742. PubMed ID: 29703646
[TBL] [Abstract][Full Text] [Related]
14. The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.
Ohnishi T; Hashimoto R; Mori T; Nemoto K; Moriguchi Y; Iida H; Noguchi H; Nakabayashi T; Hori H; Ohmori M; Tsukue R; Anami K; Hirabayashi N; Harada S; Arima K; Saitoh O; Kunugi H
Brain; 2006 Feb; 129(Pt 2):399-410. PubMed ID: 16330500
[TBL] [Abstract][Full Text] [Related]
15. Catechol-O-methyltransferase val108/158met genotype predicts working memory response to antipsychotic medications.
Weickert TW; Goldberg TE; Mishara A; Apud JA; Kolachana BS; Egan MF; Weinberger DR
Biol Psychiatry; 2004 Nov; 56(9):677-82. PubMed ID: 15522252
[TBL] [Abstract][Full Text] [Related]
16. Catechol-O-methyltransferase gene and obsessive-compulsive symptoms in patients with recent-onset schizophrenia: preliminary results.
Zinkstok J; van Nimwegen L; van Amelsvoort T; de Haan L; Yusuf MA; Baas F; Linszen D
Psychiatry Res; 2008 Jan; 157(1-3):1-8. PubMed ID: 17850881
[TBL] [Abstract][Full Text] [Related]
17. Genetic association of catechol-O-methyltransferase val(158)met polymorphism in Saudi schizophrenia patients.
Al-Asmary S; Kadasah S; Arfin M; Tariq M; Al-Asmari A
Genet Mol Res; 2014 Apr; 13(2):3079-88. PubMed ID: 24782165
[TBL] [Abstract][Full Text] [Related]
18. COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.
Boot E; Booij J; Zinkstok JR; Baas F; Swillen A; Owen MJ; Murphy DG; Murphy KC; Linszen DH; Van Amelsvoort TA
Synapse; 2011 Sep; 65(9):967-70. PubMed ID: 21465565
[TBL] [Abstract][Full Text] [Related]
19. Sensorimotor gating of schizophrenia patients depends on Catechol O-methyltransferase Val158Met polymorphism.
Quednow BB; Wagner M; Mössner R; Maier W; Kühn KU
Schizophr Bull; 2010 Mar; 36(2):341-6. PubMed ID: 18635674
[TBL] [Abstract][Full Text] [Related]
20. No association found between 158 Val/Met polymorphism of the COMT gene and schizophrenia with minor physical anomalies.
Joo EJ; Jeong SH; Ahn YM; Lee KY; Chang Yoon S; Kim EJ; Kim SU; Cho SC; Sik Kim Y
Psychiatry Res; 2005 Sep; 136(2-3):83-91. PubMed ID: 16109444
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]