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Query Trace: 22q11 Deletion Syndrome and PRODH[original query]

PRODH rs450046 and proline x COMT Val(158)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 Similar articles in PubMed
Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma. Molecular psychiatry 2015 Feb . Luykx J J, Bakker S C, Visser W F, Verhoeven-Duif N, Buizer-Voskamp J E, den Heijer J M, Boks M P M, Sul J H, Eskin E, Ori A P, Cantor R M, Vorstman J, Strengman E, DeYoung J, Kappen T H, Pariama E, van Dongen E P A, Borgdorff P, Bruins P, de Koning T J, Kahn R S, Ophoff R Similar articles in PubMed
Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and function. PLoS genetics 2008 Nov 4 (11): e1000252. Kempf Lucas, Nicodemus Kristin K, Kolachana Bhaskar, Vakkalanka Radhakrishna, Verchinski Beth A, Egan Michael F, Straub Richard E, Mattay Venkata A, Callicott Joseph H, Weinberger Daniel R, Meyer-Lindenberg Andre Similar articles in PubMed