Compounds > methionine
Page last updated: 2024-08-17

methionine and Psychoses

methionine has been researched along with Psychoses in 49 studies

Research

Studies (49)

TimeframeStudies, this research(%)All Research%
pre-19906 (12.24)18.7374
1990's3 (6.12)18.2507
2000's15 (30.61)29.6817
2010's24 (48.98)24.3611
2020's1 (2.04)2.80

Authors

AuthorsStudies
Ito, Y; Nishikubo, T; Nishimoto, E; Sakakibara, T1
Bouvier, D; Brailova, M; Minet-Quinard, R; Regnier, A; Sapin, V; Szymanowski, M1
Damen, T; de Jong, L; Drukker, M; Ermiş, A; Kennedy, JL; Krolinski, P; Nieman, DH; Nwosu, CV; Pinckaers, FME; Rotee, ILM; Schäfer, AT; Smeets, APW; Tiwari, A; Uittenboogaard, A; Vaessen, TSJ; van Os, J1
Grayson, DR; Guidotti, A1
Barić, I; Bártl, J; Baumgartner, MR; Ben-Omran, T; Blasco-Alonso, J; Blom, HJ; Bueno Delgado, MA; Carducci, C; Cassanello, M; Cerone, R; Chrastina, P; Couce, ML; Crushell, E; Delgado Pecellin, C; Dionisi-Vici, C; Dulin, E; Espada, M; Ferino, G; Fingerhut, R; Garcia Jimenez, I; Gleich, F; Gonzalez Gallego, I; González-Irazabal, Y; Gouveia, S; Gramer, G; Huemer, M; Juan Fita, MJ; Karg, E; Keller, R; Klein, J; Kölker, S; Konstantopoulou, V; Kožich, V; la Marca, G; Leão Teles, E; Leuzzi, V; Lilliu, F; Lopez, RM; Lund, AM; Mayne, P; Meavilla, S; Moat, SJ; Morris, AA; Okun, JG; Pasquini, E; Pavlíková, M; Pedron-Giner, CC; Racz, GZ; Ribes, A; Ruiz Gomez, MA; Vilarinho, L; Yahyaoui, R; Zerjav Tansek, M; Zetterström, RH; Zeyda, M1
Apud, J; Berman, KF; Eisenberg, DP; Ianni, AM; Kohn, PD; Kolachana, B; Wei, SM; Weinberger, DR1
Aas, M; Agartz, I; Andreassen, OA; Athanasiu, L; Bergmann, Ø; Djurovic, S; Haukvik, UK; Hellvin, T; Lorentzen, S; Melle, I; Steen, NE; Sundet, K; Tesli, MS1
Boks, MP; Bruggeman, R; Cahn, W; de Haan, L; Joëls, M; Kahn, RS; Luykx, JJ; Meijer, CJ; Myin-Germeys, I; Ophoff, RA; Schubart, CD; Van Eijk, KR; Van Gastel, WA; van Os, J; Van Winkel, R; Vinkers, CH; Wiersma, D1
Carmel, M; Chen, J; Frisch, A; Gothelf, D; Kolachana, B; Law, AJ; Lipska, BK; Michaelovsky, E; Ren-Patterson, R; Weinberger, DR; Weizman, A; Zarchi, O1
Cushnie, DW; Garner, JL; Hermo, L; McGraw, S; Nagano, MC; Niles, KM; Trasler, JM; Yeh, JR1
Bearden, D; D'Aco, KE; Ficicioglu, C; Hyland, K; Rosenblatt, DS; Watkins, D1
Berry, SA; Bishop, L; Fair, AL; Gallant, N; Gavrilov, D; Hopkin, RJ; Leslie, ND; Matern, D; Oglesbee, D; Prada, CE; Raymond, K; Rinaldo, P; Rosenblatt, DS; Schimmenti, LA; Sellars, EA; Tortorelli, S; Wong, D1
Baumgartner, MR; Burda, P; Chinnery, PF; Demirkol, M; Dionisi-Vici, C; Dobbelaere, D; Fowler, B; Froese, DS; Gökcay, G; Häberle, J; Huemer, M; Lossos, A; Mengel, E; Morris, AA; Mulder-Bleile, R; Niezen-Koning, KE; Parini, R; Plecko, B; Rokicki, D; Schiff, M; Schimmel, M; Sewell, AC; Sperl, W; Spiekerkoetter, U; Steinmann, B; Suormala, T; Taddeucci, G; Trefz, F; Trejo-Gabriel-Galán, JM; Tsuji, M; Vilaseca, MA; von Kleist-Retzow, JC; Walker, V; Zeev, BB; Zeman, J1
Gogos, JA; Hill, RA; Notaras, MJ; van den Buuse, M1
Haring, L; Janno, S; Koido, K; Kriisa, K; Vasar, E; Vasar, V; Zilmer, K; Zilmer, M1
Barrantes-Vidal, N; Cristóbal-Narváez, P; de Castro-Catala, M; Derom, C; Jacobs, N; Kwapil, TR; Peña, E; Rosa, A; Sheinbaum, T; Thiery, E; van Nierop, M; van Os, J; van Winkel, R1
Asayama, S; Iida, S; Kaneko, S; Kunieda, T; Kusaka, H; Nakamura, M; Osaka, H1
Arango, C; Arias, B; Bernardo, M; Bioque, M; Bulbena, A; Cabrera, B; Castro-Fornieles, J; Corripio, I; Cuesta, MJ; Díaz-Caneja, CM; Fraguas, D; González-Pinto, A; Lobo, A; Parellada, M; Rodríguez-Toscano, E; Sanjuán, J; Sarró, S; Vieta, E1
Docherty, AR; Sponheim, SR1
Carrasco-Marín, E; Crespo-Facorro, B; Mata, I; Pelayo-Terán, JM; Pérez-Iglesias, R; Vázquez-Barquero, JL; Vázquez-Bourgon, J1
Bernabeu, C; Campanera, S; Estrada, G; Fañanás, L; Fatjó-Vilas, M; Illa, JM; Martín, M; Miñano, MJ; Miralles, ML; Miret, S; Muñoz, MJ; Navarro, ME; Pulido, G; Toledo, E1
Aguilera, M; Alemany, S; Arias, B; Fañanás, L; Gastó, C; Ibáñez, MI; Moya, J; Ortet, G; Villa, H; Vossen, H1
Evans, J; Heron, J; Lewis, G; Owen, MJ; Zammit, S1
Ehmann, TS; Honer, WG; Kennedy, JL; Kopala, LC; Lang, DJ; Macewan, GW; Shiau, G; Smith, GN; Tee, K; Thornton, AE; Voineskos, AN1
Dean, DJ; Lunsford-Avery, J; Mittal, VA; Pelletier, AL; Smith, A; Smolen, A1
Basili, S; Cerasa, L; Ciabattoni, G; Davì, G; Dragani, A; Falco, A; Lattanzio, S; Patrono, C; Rolandi, G; Santilli, F1
RYSANEK, K; VITEK, V; VOJTECHOVSKY, M1
BALDESSARINI, RJ; KETY, SS; PARK, LC1
Abrahamsson, L; Blennow, K; Gottfries, CG; Grenfeldt, B; Regland, B1
Archetti, S; Borroni, B; Caimi, L; Costanzi, C; Franzoni, S; Grassi, M; Padovani, A; Zanetti, M1
Cortés, MJ; Gutiérrez-Zotes, A; Jariod, M; Labad, A; Martorell, L; Mulet, B; Pérez, M; Valero, J; Vilella, E1
Borroni, B; Di Luca, M; Padovani, A1
Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J1
De Leeuw, N; Egger, JI; Fekkes, D; Tuinier, S; Van der Heijden, FM; Van Ravenswaaij-Arts, CM; Verhoeven, WM1
Daly, E; De Haan, L; Figee, M; Glaser, B; Linszen, DH; Morris, R; Murphy, DG; Murphy, KC; Owen, MJ; van Amelsvoort, T; Zinkstok, J1
Hokoishi, K; Iga, J; Kinouchi, S; Nakataki, M; Numata, S; Ohmori, T; Sano, A; Song, H; Tanabe, H; Tayoshi-Shibuya, S; Ueno, S; Yamauchi, K1
De Hert, M; Fananás, L; Henquet, C; Myin-Germeys, I; Papiol, S; Peuskens, J; Rosa, A; van Os, J; van Winkel, R1
Arranz, MJ; Carrasco-Marín, E; Crespo-Facorro, B; Leyva-Cobián, F; Mata, I; Pelayo-Terán, JM; Pérez-Iglesias, R; Vázquez-Barquero, JL1
Bilbao, JR; Castaño, L; Echevarria, E; Galdos, P; Isusi, P; Krabbendam, L; Martin-Pagola, A; Mengelers, R; Myin-Germeys, I; Papiol, S; van Os, J; van Winkel, R1
Giraudier, S; Michot, JM; Papo, T; Sedel, F; Smiejan, JM1
Carrasco-Marin, E; Crespo-Facorro, B; Gonzalez-Blanch, C; Mata, I; Pelayo-Teran, JM; Perez-Iglesias, R; Rodríguez-Sanchez, JM; Vazquez-Barquero, JL1
Bath, K; Chen, ZY; Hempstead, B; Lee, F; McEwen, B1
Bruinvels, J; Fekkes, D; Pepplinkhuizen, L; Verheij, R1
Bode, WT; Fekkes, D; Pepplinkhuizen, L; Zijlstra, FJ1
Chari, S; Deth, RC; DuRand, CJ; Kotb, M; Kramer, ML; Liu, D; Nagata, M; Ouellette, D; Sharma, A; Shim, S; Tan, W; Wick, PF1
Baldessarini, RJ1
Kanig, K; Oesterle, W1
Kanig, K1
Bradley, RJ; Johnston, VS1

Reviews

5 review(s) available for methionine and Psychoses

ArticleYear
The interaction between cannabis use and the Val158Met polymorphism of the COMT gene in psychosis: A transdiagnostic meta - analysis.
    PloS one, 2018, Volume: 13, Issue:2

    Topics: Cannabis; Catechol O-Methyltransferase; Humans; Methionine; Polymorphism, Single Nucleotide; Psychotic Disorders; Valine

2018
DNA Methylation in Animal Models of Psychosis.
    Progress in molecular biology and translational science, 2018, Volume: 157

    Topics: Animals; Disease Models, Animal; DNA Methylation; Epigenesis, Genetic; Methionine; Psychotic Disorders; Stress, Psychological

2018
Impact of genetic variant BDNF (Val66Met) on brain structure and function.
    Novartis Foundation symposium, 2008, Volume: 289

    Topics: Amino Acid Substitution; Animals; Anxiety Disorders; Brain; Brain-Derived Neurotrophic Factor; Depressive Disorder; Genetic Predisposition to Disease; Genetic Variation; Growth Substances; Humans; Mental Disorders; Methionine; Mice; Mice, Transgenic; Polymorphism, Single Nucleotide; Psychotic Disorders; Valine

2008
[Biochemical treatment possibilities in psychoses].
    Die Medizinische Welt, 1969, Sep-06, Volume: 36

    Topics: Amino Acids; Ascorbic Acid; Dihydroxyphenylalanine; Humans; Methionine; Niacinamide; Nicotinic Acids; Phenylalanine; Psychotic Disorders; Pyridoxine; Schizophrenia; Tryptophan; Tyrosine

1969
Molecular pharmacology of hallucinogens.
    Recent advances in biological psychiatry, 1968, Volume: 10

    Topics: Amphetamine; Animals; Avoidance Learning; Brain; Conditioning, Operant; Emotions; Hallucinogens; Humans; Lysergic Acid Diethylamide; Melatonin; Mescaline; Methionine; Methods; Models, Chemical; Psychoses, Substance-Induced; Psychotic Disorders; Rats; Reaction Time; Schizophrenia; Serotonin; Stress, Physiological; Tryptamines

1968

Trials

2 trial(s) available for methionine and Psychoses

ArticleYear
Catechol-O-methyltransferase Val158Met polymorphism and negative symptoms after acute antipsychotic treatment in first-episode non-affective psychosis.
    Psychiatry research, 2011, Jan-30, Volume: 185, Issue:1-2

    Topics: Adolescent; Adult; Analysis of Variance; Antipsychotic Agents; Catechol O-Methyltransferase; DNA Mutational Analysis; Double-Blind Method; Female; Gene Frequency; Genotype; Humans; Longitudinal Studies; Male; Methionine; Middle Aged; Pharmacogenetics; Polymorphism, Genetic; Psychiatric Status Rating Scales; Psychotic Disorders; Regression Analysis; Treatment Outcome; Valine; Young Adult

2011
Lack of influence of COMT Val158Met genotype on cognition in first-episode non-affective psychosis.
    Schizophrenia research, 2008, Volume: 102, Issue:1-3

    Topics: Adult; Antipsychotic Agents; Catechol O-Methyltransferase; Cognition Disorders; Diagnostic and Statistical Manual of Mental Disorders; Female; Genetic Predisposition to Disease; Genotype; Humans; Longitudinal Studies; Male; Methionine; Neuropsychological Tests; Phenotype; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Schizophrenic Psychology; Valine

2008

Other Studies

42 other study(ies) available for methionine and Psychoses

ArticleYear
Early treatment using betaine and methionine for a neonate with MTHFR deficiency.
    Pediatrics international : official journal of the Japan Pediatric Society, 2019, Volume: 61, Issue:12

    Topics: Betaine; Homocysteine; Homocystinuria; Humans; Infant; Infant, Newborn; Japan; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Psychotic Disorders; Treatment Outcome

2019
[Remethylation disorders: about two cases].
    Annales de biologie clinique, 2020, Dec-01, Volume: 78, Issue:6

    Topics: Alcoholism; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Female; Folic Acid; Folic Acid Deficiency; Homocysteine; Homocystinuria; Humans; Infant, Newborn; Metabolic Networks and Pathways; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Muscle Spasticity; Psychotic Disorders; Vitamin B 12

2020
Newborn screening for homocystinurias: Recent recommendations versus current practice.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:1

    Topics: Acetylcarnitine; Amino Acid Metabolism, Inborn Errors; Carnitine; Female; Glycine N-Methyltransferase; Homocysteine; Homocystinuria; Humans; Infant, Newborn; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Methylmalonic Acid; Muscle Spasticity; Neonatal Screening; Phenylalanine; Psychotic Disorders

2019
Hippocampal dysfunction in schizophrenia: association with brain-derived neurotrophic factor genotype.
    Molecular psychiatry, 2013, Volume: 18, Issue:6

    Topics: Brain-Derived Neurotrophic Factor; Cohort Studies; Female; Genetic Association Studies; Genotype; Hippocampus; Humans; Male; Memory, Short-Term; Methionine; Polymorphism, Single Nucleotide; Positron-Emission Tomography; Psychotic Disorders; Schizophrenia; Valine

2013
BDNF val66met modulates the association between childhood trauma, cognitive and brain abnormalities in psychoses.
    Progress in neuro-psychopharmacology & biological psychiatry, 2013, Oct-01, Volume: 46

    Topics: Adolescent; Adult; Bipolar Disorder; Brain; Brain-Derived Neurotrophic Factor; Child Abuse; Cognition Disorders; Hippocampus; Humans; Lateral Ventricles; Methionine; Psychotic Disorders; Valine; Young Adult

2013
The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val¹⁵⁸Met polymorphism.
    Schizophrenia research, 2013, Volume: 150, Issue:1

    Topics: Adolescent; Adult; Catechol O-Methyltransferase; Child; Child Abuse; Cross-Sectional Studies; Female; Genetic Predisposition to Disease; Humans; Male; Marijuana Abuse; Methionine; Multivariate Analysis; Polymorphism, Single Nucleotide; Psychotic Disorders; Surveys and Questionnaires; Valine; Young Adult

2013
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
    Biological psychiatry, 2014, Mar-01, Volume: 75, Issue:5

    Topics: Adolescent; Adult; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Chromosome Deletion; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult

2014
Stability of DNA methylation patterns in mouse spermatogonia under conditions of MTHFR deficiency and methionine supplementation.
    Biology of reproduction, 2013, Volume: 89, Issue:5

    Topics: Adult Stem Cells; Animals; Animals, Newborn; Cells, Cultured; Dietary Supplements; DNA Methylation; Female; Genomic Instability; Homocystinuria; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Transgenic; Muscle Spasticity; Psychotic Disorders; Spermatogonia

2013
Severe 5,10-methylenetetrahydrofolate reductase deficiency and two MTHFR variants in an adolescent with progressive myoclonic epilepsy.
    Pediatric neurology, 2014, Volume: 51, Issue:2

    Topics: Adolescent; Betaine; Female; Folic Acid; Homocystinuria; Humans; Lipotropic Agents; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Mutation; Myoclonic Epilepsies, Progressive; Psychotic Disorders; Vitamin B Complex

2014
Outcomes of four patients with homocysteine remethylation disorders detected by newborn screening.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2016, Volume: 18, Issue:2

    Topics: Amino Acid Metabolism, Inborn Errors; Female; Homocysteine; Homocystinuria; Humans; Infant, Newborn; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Neonatal Screening; Psychotic Disorders; Treatment Outcome

2016
Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency.
    Journal of inherited metabolic disease, 2016, Volume: 39, Issue:1

    Topics: Ataxia; Betaine; Child; Female; Folic Acid; Genetic Association Studies; Homocystinuria; Humans; Intellectual Disability; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Mutation; Phenotype; Psychotic Disorders; Retrospective Studies; Spinal Cord Diseases; Vitamin B 12

2016
BDNF Val66Met Genotype Interacts With a History of Simulated Stress Exposure to Regulate Sensorimotor Gating and Startle Reactivity.
    Schizophrenia bulletin, 2017, 05-01, Volume: 43, Issue:3

    Topics: Animals; Brain-Derived Neurotrophic Factor; Corticosterone; Disease Models, Animal; Female; Male; Methionine; Mice, Inbred C57BL; Prepulse Inhibition; Psychotic Disorders; Reflex, Startle; Schizophrenia; Sensory Gating; Steroids; Stress, Psychological; Valine

2017
Antipsychotic Treatment Reduces Indices of Oxidative Stress in First-Episode Psychosis Patients.
    Oxidative medicine and cellular longevity, 2016, Volume: 2016

    Topics: Adult; Antioxidants; Antipsychotic Agents; Biomarkers; Case-Control Studies; Cytokines; Enzyme-Linked Immunosorbent Assay; Female; Humans; Male; Methionine; Oxidative Stress; Peroxides; Psychotic Disorders; Young Adult

2016
Childhood trauma, BDNF Val66Met and subclinical psychotic experiences. Attempt at replication in two independent samples.
    Journal of psychiatric research, 2016, Volume: 83

    Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Surveys and Questionnaires; Valine; Young Adult

2016
Rapidly progressive psychotic symptoms triggered by infection in a patient with methylenetetrahydrofolate reductase deficiency: a case report.
    BMC neurology, 2017, Feb-28, Volume: 17, Issue:1

    Topics: Adolescent; Base Sequence; Homocystinuria; Humans; Leukoencephalopathies; Magnetic Resonance Imaging; Male; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Mutation; Psychotic Disorders

2017
Gene-environment interaction as a predictor of early adjustment in first episode psychosis.
    Schizophrenia research, 2017, Volume: 189

    Topics: Adult; Catechol O-Methyltransferase; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Parents; Polymorphism, Single Nucleotide; Psychotic Disorders; Retrospective Studies; Statistics, Nonparametric; Valine; Young Adult

2017
Anhedonia as a phenotype for the Val158Met COMT polymorphism in relatives of patients with schizophrenia.
    Journal of abnormal psychology, 2008, Volume: 117, Issue:4

    Topics: Adult; Affective Symptoms; Aged; Alleles; Bipolar Disorder; Catechol O-Methyltransferase; Female; Genotype; Homozygote; Humans; Male; Methionine; Middle Aged; Phenotype; Polymorphism, Genetic; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Schizophrenic Psychology; Schizotypal Personality Disorder; Valine

2008
Cannabis use and age at onset of psychosis: further evidence of interaction with COMT Val158Met polymorphism.
    Acta psychiatrica Scandinavica, 2011, Volume: 123, Issue:6

    Topics: Adolescent; Age of Onset; Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Male; Marijuana Abuse; Marijuana Smoking; Methionine; Polymorphism, Genetic; Psychotic Disorders; Schizophrenia; Valine

2011
Childhood abuse, the BDNF-Val66Met polymorphism and adult psychotic-like experiences.
    The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:1

    Topics: Adult; Adult Survivors of Child Abuse; Alleles; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Linear Models; Male; Methionine; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult

2011
Cannabis, COMT and psychotic experiences.
    The British journal of psychiatry : the journal of mental science, 2011, Volume: 199, Issue:5

    Topics: Adolescent; Catechol O-Methyltransferase; Child; Dose-Response Relationship, Drug; Genetic Predisposition to Disease; Genotype; Hallucinations; Haplotypes; Humans; Longitudinal Studies; Male; Marijuana Abuse; Methionine; Polymorphism, Single Nucleotide; Psychotic Disorders; Risk; Self Report; Valine

2011
Hippocampal volume and the brain-derived neurotrophic factor Val66Met polymorphism in first episode psychosis.
    Schizophrenia research, 2012, Volume: 134, Issue:2-3

    Topics: Adolescent; Adult; Age Factors; Analysis of Variance; Brain-Derived Neurotrophic Factor; Cognition Disorders; Female; Genetic Association Studies; Genetic Predisposition to Disease; Genotype; Hippocampus; Humans; Magnetic Resonance Imaging; Male; Memory; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychotic Disorders; Valine; Young Adult

2012
BDNF Val66Met and spontaneous dyskinesias in non-clinical psychosis.
    Schizophrenia research, 2012, Volume: 140, Issue:1-3

    Topics: Adolescent; Adult; Analysis of Variance; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Dyskinesias; Female; Genetic Predisposition to Disease; Genotype; Humans; Logistic Models; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult

2012
Oxidative stress and platelet activation in subjects with moderate hyperhomocysteinaemia due to MTHFR 677 C→T polymorphism.
    Thrombosis and haemostasis, 2012, Volume: 108, Issue:3

    Topics: Biomarkers; Cardiovascular Diseases; Comorbidity; Cross-Sectional Studies; Diabetes Mellitus; Dinoprost; Dyslipidemias; Folic Acid; Homocystinuria; Humans; Hyperhomocysteinemia; Lipid Peroxidation; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Muscle Spasticity; Oxidative Stress; Platelet Activation; Polymorphism, Single Nucleotide; Psychotic Disorders; Smoking; Thromboxane B2

2012
[Effect of neurohormone precursors from the amino acid group on experimental psychoses induced with Psilocybine].
    Activitas nervosa superior, 1962, Volume: 4

    Topics: Amino Acids; Hallucinogens; Methionine; Neurotransmitter Agents; Psilocybin; Psychotic Disorders; Serotonin

1962
METHIONINE EFFECTS ON CHRONIC SCHIZOPHRENICS: PATIENTS TREATED WITH MONOAMINE OXIDASE INHIBITORS.
    Archives of general psychiatry, 1965, Volume: 12

    Topics: Biomedical Research; Drug Synergism; Drug Therapy; Glycine; Iproniazid; Isocarboxazid; Mental Disorders; Methionine; Monoamine Oxidase Inhibitors; Placebos; Psychoses, Substance-Induced; Psychotic Disorders; Schizophrenia; Toxicology

1965
CSF-methionine is elevated in psychotic patients.
    Journal of neural transmission (Vienna, Austria : 1996), 2004, Volume: 111, Issue:5

    Topics: Adult; Biomarkers; Cystathionine; Female; Homocysteine; Humans; Male; Methionine; Middle Aged; Psychotic Disorders; Sex Factors

2004
Haplotypes in cathechol-O-methyltransferase gene confer increased risk for psychosis in Alzheimer disease.
    Neurobiology of aging, 2007, Volume: 28, Issue:8

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Catechol O-Methyltransferase; Chi-Square Distribution; Cognition; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Humans; Linkage Disequilibrium; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Psychotic Disorders; Risk; Valine

2007
M129V variation in the prion protein gene and psychotic disorders: relationship to neuropsychological and psychopathological measures.
    Journal of psychiatric research, 2007, Volume: 41, Issue:10

    Topics: Adult; Aged; Alleles; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Genotype; Homozygote; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Phenotype; Polymorphism, Genetic; Prion Proteins; Prions; Psychiatric Status Rating Scales; Psychotic Disorders; Schizophrenia; Schizophrenic Psychology; Valine; Wechsler Scales

2007
Catechol-o-methyltransferase gene polymorphism in dementia with Lewy bodies-related psychosis: evidence for a genetic predisposition.
    International psychogeriatrics, 2006, Volume: 18, Issue:4

    Topics: Aged; Alleles; Catechol O-Methyltransferase; Corpus Striatum; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Humans; Lewy Body Disease; Methionine; Polymorphism, Genetic; Psychotic Disorders; Risk Factors; Valine

2006
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
    Human molecular genetics, 2007, Jan-01, Volume: 16, Issue:1

    Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors

2007
Disturbed serine metabolism and psychosis in a patient with a de novo translocation (2;10)(p23;q22.1).
    Genetic counseling (Geneva, Switzerland), 2006, Volume: 17, Issue:4

    Topics: Adult; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 2; DiGeorge Syndrome; Female; Humans; Hydro-Lyases; In Situ Hybridization; Karyotyping; Methionine; Psychotic Disorders; Pterins; Serine; Taurine; Translocation, Genetic

2006
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
    Psychological medicine, 2008, Volume: 38, Issue:1

    Topics: Adult; Brain; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition Disorders; DiGeorge Syndrome; Female; Gene Frequency; Humans; Hypertrophy; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Psychotic Disorders; Valine

2008
The Val66Met polymorphism of the brain-derived neurotrophic factor gene is associated with psychotic feature and suicidal behavior in Japanese major depressive patients.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2007, Dec-05, Volume: 144B, Issue:8

    Topics: Adult; Age Distribution; Age of Onset; Brain-Derived Neurotrophic Factor; Case-Control Studies; Depressive Disorder, Major; Diagnostic and Statistical Manual of Mental Disorders; Female; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Psychotic Disorders; Sex Distribution; Suicide; Valine

2007
Evidence that the COMT(Val158Met) polymorphism moderates sensitivity to stress in psychosis: an experience-sampling study.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008, Jan-05, Volume: 147B, Issue:1

    Topics: Adult; Catechol O-Methyltransferase; Female; Genotype; Humans; Male; Marijuana Abuse; Methionine; Middle Aged; Polymorphism, Genetic; Psychotic Disorders; Stress, Physiological; Valine

2008
Catechol-O-methyltransferase Val158Met polymorphism and clinical characteristics in first episode non-affective psychosis.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008, Jul-05, Volume: 147B, Issue:5

    Topics: Adolescent; Adult; Affective Disorders, Psychotic; Age of Onset; Amino Acid Substitution; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Psychotic Disorders; Schizophrenia; Valine

2008
Evidence that the COMTVal158Met polymorphism moderates subclinical psychotic and affective symptoms in unaffected first-degree relatives of patients with schizophrenia.
    European psychiatry : the journal of the Association of European Psychiatrists, 2008, Volume: 23, Issue:3

    Topics: Adult; Brief Psychiatric Rating Scale; Catechol O-Methyltransferase; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Methionine; Middle Aged; Polymorphism, Genetic; Psychiatric Status Rating Scales; Psychotic Disorders; Risk Factors; Schizophrenia; Valine

2008
Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman.
    Journal of neurology, neurosurgery, and psychiatry, 2008, Volume: 79, Issue:8

    Topics: Brain; Brain Diseases, Metabolic, Inborn; Catatonia; Chromosome Aberrations; Chromosomes, Human, Pair 1; Coma; Dementia; Exons; Folic Acid; Genes, Recessive; Homocysteine; Humans; Magnetic Resonance Imaging; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Neurologic Examination; Paraplegia; Polymorphism, Genetic; Psychotic Disorders

2008
Abnormal plasma levels of serine, methionine, and taurine in transient acute polymorphic psychosis.
    Psychiatry research, 1994, Volume: 51, Issue:1

    Topics: Adult; Bipolar Disorder; Diagnosis, Differential; Female; Humans; Male; Methionine; Middle Aged; Psychotic Disorders; Schizophrenia; Serine; Taurine

1994
Eicosanoid and amino acid metabolism in transient acute psychoses with psychedelic symptoms.
    Prostaglandins, leukotrienes, and essential fatty acids, 1996, Volume: 54, Issue:4

    Topics: Adult; Female; Glutathione; Humans; Male; Methionine; Prostaglandins E; Psychotic Disorders; Serine; Taurine; Thromboxane B2

1996
D4 dopamine receptor-mediated phospholipid methylation and its implications for mental illnesses such as schizophrenia.
    Molecular psychiatry, 1999, Volume: 4, Issue:3

    Topics: Amino Acid Sequence; Aminopyridines; Animals; Benzazepines; Binding Sites; Carbon Radioisotopes; CHO Cells; Clozapine; Cricetinae; Dopamine Agonists; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Formates; Guanosine 5'-O-(3-Thiotriphosphate); Humans; Methionine; Mutagenesis, Site-Directed; Neuroblastoma; Phospholipids; Phosphorylation; Piperidines; Psychotic Disorders; Pyridines; Pyrroles; Raclopride; Receptors, Dopamine D2; Receptors, Dopamine D4; Recombinant Proteins; S-Adenosylmethionine; Salicylamides; Schizophrenia; Transfection; Tumor Cells, Cultured

1999
Editorial: Metabolic hypotheses in schizophrenia.
    The New England journal of medicine, 1975, Mar-06, Volume: 292, Issue:10

    Topics: Folic Acid; Homocystine; Homocystinuria; Humans; Methionine; Methylation; Psychotic Disorders; Schizophrenia

1975
[Biochemical mechanism of action of nicotinic acid, nicotinamide, methionine and D-penicillamine in treatment of psychoses].
    Arzneimittel-Forschung, 1970, Volume: 20, Issue:7

    Topics: Amines; Amino Acids; Biochemical Phenomena; Biochemistry; Humans; Methionine; Methylation; Niacinamide; Nicotinic Acids; Penicillamine; Psychopharmacology; Psychotic Disorders; Serotonin; Sulfhydryl Compounds; Tryptamines; Tryptophan

1970