Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: 22q11 Deletion Syndrome and COMT[original query] |
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Association of ZNF74 gene genotypes with age-at-onset of schizophrenia. Schizophrenia research 2001 Dec 52 (3): 161-5. Takase K, Ohtsuki T, Migita O, Toru M, Inada T, Yamakawa-Kobayashi K, Arinami |
COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome. Biological psychiatry 2005 Jul 58 (1): 23-31. Baker Kate, Baldeweg Torsten, Sivagnanasundaram Sinthuja, Scambler Peter, Skuse Dav |
Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹°8/¹58Met polymorphism, gender and symptomatology. Journal of psychopharmacology (Oxford, England) 2011 Jul 25 (7): 888-95. Boot Erik, Booij Jan, Abeling Nico, Meijer Julia, da Silva Alves Fabiana, Zinkstok Janneke, Baas Frank, Linszen Don, van Amelsvoort Thérè |
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. Journal of psychopharmacology (Oxford, England) 2012 Dec 26 (12): 1548-60. de Koning Mariken B, Boot Erik, Bloemen Oswald J N, van Duin Esther D A, Abel Kathryn M, de Haan Lieuwe, Linszen Don H, van Amelsvoort Thérèse A M |
PRODH rs450046 and proline x COMT Val¹58 Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome. Psychopharmacology 2015 Sep 232 (17): 3111-22. de Koning Mariken B, van Duin Esther D A, Boot Erik, Bloemen Oswald J N, Bakker Jaap A, Abel Kathryn M, van Amelsvoort Thérèse A M |
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