Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Syndrome and PRODH[original query] |
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PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Human molecular genetics 2002 Sep 11 (19): 2243-9. Jacquet Hélène, Raux Grégory, Thibaut Florence, Hecketsweiler Bernadette, Houy Emmanuelle, Demilly Caroline, Haouzir Sadeq, Allio Gabrielle, Fouldrin Gael, Drouin Valérie, Bou Jacqueline, Petit Michel, Campion Dominique, Frébourg Thier |
Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jul 120B (1): 42-6. Williams H J, Williams N, Spurlock G, Norton N, Zammit S, Kirov G, Owen M J, O'Donovan M |
Functional consequences of PRODH missense mutations. American journal of human genetics 2005 1 76 (3): 409-20. Bender Hans-Ulrich, Almashanu Shlomo, Steel Gary, Hu Chien-An, Lin Wei-Wen, Willis Alecia, Pulver Ann, Valle Dav |
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 |
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes. Journal of psychiatric research 2013 Aug . Zarchi O, Carmel M, Avni C, Attias J, Frisch A, Michaelovsky E, Patya M, Green T, Weinberger R, Weizman A, Gothelf D |
Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects. Journal of psychiatric research 2014 Sep 56 28-35. Carmel Miri, Zarchi Omer, Michaelovsky Elena, Frisch Amos, Patya Miriam, Green Tamar, Gothelf Doron, Weizman Abrah |
PRODH polymorphisms, cortical volumes and thickness in schizophrenia. PloS one 2014 9 (2): e87686. Ota Vanessa K, Bellucco Fernanda T, Gadelha Ary, Santoro Marcos L, Noto Cristiano, Christofolini Denise M, Assunção Idaiane B, Yamada Karen M, Ribeiro-dos-Santos Andrea K, Santos Sidney, Mari Jair J, Smith Marília A C, Melaragno Maria I, Bressan Rodrigo A, Sato João R, Jackowski Andrea P, Belangero Sintia |
Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes. Psychiatric genetics 2014 Dec 24 (6): 269-72. Radoeva Petya D, Coman Ioana L, Salazar Cynthia A, Gentile Karen L, Higgins Anne Marie, Middleton Frank A, Antshel Kevin M, Fremont Wanda, Shprintzen Robert J, Morrow Bernice E, Kates Wendy |
Mitochondrial Citrate Transporter-dependent Metabolic Signature in the 22q11.2 Deletion Syndrome. The Journal of biological chemistry 2015 Sep 290 (38): 23240-53. Napoli Eleonora, Tassone Flora, Wong Sarah, Angkustsiri Kathleen, Simon Tony J, Song Gyu, Giulivi Cecil |
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 |
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 |
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan . Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy |
CNVs and Chromosomal Aneuploidy in Patients With Early-Onset Schizophrenia and Bipolar Disorder: Genotype-Phenotype Associations. Frontiers in psychiatry 2021 1 11 606372. Gregoric Kumperscak Hojka, Krgovic Danijela, Drobnic Radobuljac Maja, Senica Nina, Zagorac Andreja, Kokalj Vokac Nad |
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- Page last updated:Apr 22, 2024
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