Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 30 Records) |
| Query Trace: Schizophrenia 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 |
| Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia research 2006 Oct 87 (1-3): 21-7. Glaser Beate, Moskvina Valentina, Kirov George, Murphy Kieran C, Williams Hywel, Williams Nigel, Owen Michael J, O'Donovan Michael |
| Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis. European journal of human genetics : EJHG 2006 Oct 14 (10): 1130-5. Li Dawei, He L |
| Bipolar 1 disorder is not associated with the RGS4, PRODH, COMT and GRK3 genes. Psychiatric genetics 2006 Dec 16 (6): 229-30. Prata Diana Pinto, Breen Gerome, Munro Janet, Sinclair Maggie, Osborne Sarah, Li Tao, Kerwin Robert, St Clair David, Collier David |
| Hyperprolinemia is not associated with childhood onset schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006 1 141B (2): 192. Jacquet Hélène, Rapoport Judith L, Hecketsweiler Bernadette, Bobb Aaron, Thibaut Florence, Frébourg Thierry, Campion Dominiq |
| A quantitative association study between schizotypal traits and COMT, PRODH and BDNF genes in a healthy Chinese population. Psychiatry research 2007 Sep 153 (1): 7-15. Ma Xiaohong, Sun Jinhua, Yao Jing, Wang Qiang, Hu Xun, Deng Wei, Sun Xueli, Liu Xiehe, Murray Robin M, Collier David A, Li T |
| Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia. Genes, brain, and behavior 2008 Feb 7 (1): 61-9. Zinkstok J, Schmitz N, van Amelsvoort T, Moeton M, Baas F, Linszen |
| 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 |
| PRODH gene is associated with executive function in schizophrenic families. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jul 147B (5): 654-7. Li Tao, Ma Xiaohong, Hu Xun, Wang Yingcheng, Yan Chengying, Meng Huaqing, Liu Xiehe, Toulopoulou Timothea, Murray Robin M, Collier David |
| Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation. Archives of general psychiatry 2009 Sep 66 (9): 947-56. Guilmatre Audrey, Dubourg Christèle, Mosca Anne-Laure, Legallic Solenn, Goldenberg Alice, Drouin-Garraud Valérie, Layet Valérie, Rosier Antoine, Briault Sylvain, Bonnet-Brilhault Frédérique, Laumonnier Frédéric, Odent Sylvie, Le Vacon Gael, Joly-Helas Géraldine, David Véronique, Bendavid Claude, Pinoit Jean-Michel, Henry Céline, Impallomeni Caterina, Germano Eva, Tortorella Gaetano, Di Rosa Gabriella, Barthelemy Catherine, Andres Christian, Faivre Laurence, Frébourg Thierry, Saugier Veber Pascale, Campion Dominiq |
| A risk PRODH haplotype affects sensorimotor gating, memory, schizotypy, and anxiety in healthy male subjects. Biological psychiatry 2009 Jun 65 (12): 1063-70. Roussos Panos, Giakoumaki Stella G, Bitsios Pan |
DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2012 May 15 (4): 459-69. Alkelai Anna, Lupoli Sara, Greenbaum Lior, Kohn Yoav, Kanyas-Sarner Kyra, Ben-Asher Edna, Lancet Doron, Macciardi Fabio, Lerer Berna |
| 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 |
| 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 |
| Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia risk. Genetics and molecular research : GMR 2015 14 (4): 11681-91. Ghasemvand F, Omidinia E, Salehi Z, Rahmanzadeh |
| Evidence that COMT genotype and proline interact on negative-symptom outcomes in schizophrenia and bipolar disorder. Translational psychiatry 2016 6 (9): e891. Clelland C L, Drouet V, Rilett K C, Smeed J A, Nadrich R H, Rajparia A, Read L L, Clelland J |
| Linkage and Association Analyses of Schizophrenia with Genetic Variations on Chromosome 22q11 in Koreans. Psychiatry investigation 2016 Nov 13 (6): 630-636. Yoon Se Chang, Jang Yong Lee, Kim Jong-Won, Cho Eun-Young, Park Dong Yeon, Hong Kyung Sue, Lee Yu Sa |
| 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 |
| Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response. Schizophrenia research 2017 Dec . Quednow Boris B, Ejebe Kenechi, Wagner Michael, Giakoumaki Stella G, Bitsios Panos, Kumari Veena, Roussos Pan |
| Proline dehydrogenase gene (PRODH) polymorphisms and schizophrenia susceptibility: a meta-analysis. Metabolic brain disease 2017 Oct . Guo Xingzhi, Tang Peng, Yang Caiping, Li R |
| Association of Candidate Single Nucleotide Polymorphisms Related to Candidate Genes in Patients With Schizophrenia. Basic and clinical neuroscience 0 11 (5): 595-608. Karimian Seyedeh Sara, Akbari Mohammad Taghi, Sadr Seyed Saeed, Javadi Gholamre |
| 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 |
| Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia. Archives of medical research 2022 4 53 (4): 388-398. Fricke-Galindo Ingrid, Pérez-Aldana Blanca E, Macías-Kauffer Luis R, González-Arredondo Susana, Dávila-Ortiz de Montellano David, Aviña-Cervantes Carlos L, López-López Marisol, Rodríguez-Agudelo Yaneth, Monroy-Jaramillo Nan |
| Prognostic and immunomodulatory roles of schizophrenia-associated genes HTR2A, COMT, and PRODH in pan-cancer analysis and glioma survival prediction model. Frontiers in immunology 2023 8 14 1201252. Jing Shen, Qiang Wang, Fengquan Lu, Hua Xu, Peng Wang, Yu Fe |
- Page last reviewed:Feb 1, 2024
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