245 related articles for article (PubMed ID: 26068888)
1. 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]
2. 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]
3. Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.
Carmel M; Zarchi O; Michaelovsky E; Frisch A; Patya M; Green T; Gothelf D; Weizman A
J Psychiatr Res; 2014 Sep; 56():28-35. PubMed ID: 24853458
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.
Zinkstok J; Schmitz N; van Amelsvoort T; Moeton M; Baas F; Linszen D
Genes Brain Behav; 2008 Feb; 7(1):61-9. PubMed ID: 17504246
[TBL] [Abstract][Full Text] [Related]
7. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Raux G; Bumsel E; Hecketsweiler B; van Amelsvoort T; Zinkstok J; Manouvrier-Hanu S; Fantini C; Brévière GM; Di Rosa G; Pustorino G; Vogels A; Swillen A; Legallic S; Bou J; Opolczynski G; Drouin-Garraud V; Lemarchand M; Philip N; Gérard-Desplanches A; Carlier M; Philippe A; Nolen MC; Heron D; Sarda P; Lacombe D; Coizet C; Alembik Y; Layet V; Afenjar A; Hannequin D; Demily C; Petit M; Thibaut F; Frebourg T; Campion D
Hum Mol Genet; 2007 Jan; 16(1):83-91. PubMed ID: 17135275
[TBL] [Abstract][Full Text] [Related]
8. Catechol-o-methyltransferase (COMT) and proline dehydrogenase (PRODH) mRNAs in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and major depression.
Tunbridge E; Burnet PW; Sodhi MS; Harrison PJ
Synapse; 2004 Feb; 51(2):112-8. PubMed ID: 14618678
[TBL] [Abstract][Full Text] [Related]
9. Glutamatergic markers, age, intellectual functioning and psychosis in 22q11 deletion syndrome.
Evers LJ; van Amelsvoort TA; Bakker JA; de Koning M; Drukker M; Curfs LM
Psychopharmacology (Berl); 2015 Sep; 232(18):3319-25. PubMed ID: 26055684
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder.
Clelland CL; Drouet V; Rilett KC; Smeed JA; Nadrich RH; Rajparia A; Read LL; Clelland JD
Transl Psychiatry; 2016 Sep; 6(9):e891. PubMed ID: 27622935
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes.
Radoeva PD; Coman IL; Salazar CA; Gentile KL; Higgins AM; Middleton FA; Antshel KM; Fremont W; Shprintzen RJ; Morrow BE; Kates WR
Psychiatr Genet; 2014 Dec; 24(6):269-72. PubMed ID: 25325218
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.
Magnée MJ; Lamme VA; de Sain-van der Velden MG; Vorstman JA; Kemner C
PLoS One; 2011; 6(10):e25882. PubMed ID: 21998713
[TBL] [Abstract][Full Text] [Related]
17. Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response.
Quednow BB; Ejebe K; Wagner M; Giakoumaki SG; Bitsios P; Kumari V; Roussos P
Schizophr Res; 2018 Aug; 198():52-59. PubMed ID: 29287625
[TBL] [Abstract][Full Text] [Related]
18. The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
Hidding E; Swaab H; de Sonneville LM; van Engeland H; Vorstman JA
Clin Genet; 2016 Nov; 90(5):420-427. PubMed ID: 26919535
[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. COMT implication in cognitive and psychiatric symptoms in chromosome 22q11 microdeletion syndrome: a selective review.
Armando M; Papaleo F; Vicari S
CNS Neurol Disord Drug Targets; 2012 May; 11(3):273-81. PubMed ID: 22483289
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
