methionine has been researched along with Obsessive-Compulsive Disorder in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (45.45) | 29.6817 |
| 2010's | 5 (45.45) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Kumar, P; Rai, V | 1 |
| Baran, B; Büyükgök, D; Direskeneli, GS; Ertekin, BA; Ertekin, E; Gürvit, H; Kalem, ŞA; Özata, B; Öztürk, N; Tükel, R | 2 |
| Cath, DC; Hemmings, SM; Lochner, C; Seedat, S; Stein, DJ; van der Merwe, L | 1 |
| Bochdanovits, Z; Cath, DC; Deforce, DL; den Boer, JA; Denys, DA; Heutink, P; Katerberg, H; Polman, A; van Balkom, AJ; van Nieuwerburgh, FC | 1 |
| Fawzi, MM; Fawzy, N; Hashim, HM; Karam, RA | 1 |
| Barth, N; Fleischhaker, C; Geller, F; Hahn, F; Herpertz-Dahlmann, B; Hinney, A; Lesch, KP; Mössner, R; Remschmidt, H; Schulz, E; Walitza, S; Warnke, A; Wewetzer, C | 1 |
| Amir, I; Buniak, F; Finkel, B; Frisch, A; Hermesh, H; Knoll, G; Michaelovsky, E; Poyurovsky, M; Weizman, R | 1 |
| Bandmann, O; Hebebrand, J; Klaffke, S; König, IR; Poustka, F; Ziegler, A | 1 |
| Apter, A; Aviram-Goldring, A; Burg, M; Frisch, A; Frydman, M; Gothelf, D; Korostishevsky, M; Michaelovsky, E; Presburger, G; Shohat, M; Weizman, A; Yeshaya, J; Zohar, AH | 1 |
| Apter, A; Burg, M; Carmel, M; Frisch, A; Gothelf, D; Inbar, D; Korostishevsky, M; Michaelovsky, E; Steinberg, T; Weizman, A | 1 |
1 review(s) available for methionine and Obsessive-Compulsive Disorder
| Article | Year |
|---|---|
Catechol-O-methyltransferase gene Val158Met polymorphism and obsessive compulsive disorder susceptibility: a meta-analysis.
Topics: Catechol O-Methyltransferase; Genetic Predisposition to Disease; Humans; Methionine; Observational Studies as Topic; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Valine | 2020 |
10 other study(ies) available for methionine and Obsessive-Compulsive Disorder
| Article | Year |
|---|---|
COMT Val158Met polymorphism and executive functions in obsessive-compulsive disorder.
Topics: Adult; Analysis of Variance; Catechol O-Methyltransferase; Cognition Disorders; Executive Function; Female; Gene Frequency; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Valine; Young Adult | 2013 |
BDNF Val66Met modifies the risk of childhood trauma on obsessive-compulsive disorder.
Topics: Adolescent; Adult; Aged; Brain-Derived Neurotrophic Factor; Child; Child Abuse; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Genotype; Humans; Linear Models; Male; Methionine; Middle Aged; Obsessive-Compulsive Disorder; Surveys and Questionnaires; Valine; Young Adult | 2013 |
The role of the COMT Val(158)Met polymorphism in the phenotypic expression of obsessive-compulsive disorder.
Topics: Case-Control Studies; Catechol O-Methyltransferase; Factor Analysis, Statistical; Female; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Phenotype; Polymorphism, Genetic; Valine | 2010 |
Brain-derived neurotrophic factor Val66Met polymorphism and obsessive-compulsive symptoms in Egyptian schizophrenia patients.
Topics: Adult; Brain-Derived Neurotrophic Factor; DNA Mutational Analysis; Egypt; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Schizophrenia; Statistics, Nonparametric; Valine; Young Adult | 2012 |
Brain-derived neurotrophic factor gene Val66Met polymorphism and cognitive function in obsessive-compulsive disorder.
Topics: Adolescent; Adult; Alleles; Brain-Derived Neurotrophic Factor; Cognition; Genetic Predisposition to Disease; Humans; Male; Methionine; Middle Aged; Neuropsychological Tests; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Valine | 2012 |
Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder.
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Anxiety Disorders; Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Child; Comorbidity; Depressive Disorder; Female; Genetic Carrier Screening; Genotype; Hippocampus; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Genetic; Risk Factors; Valine | 2005 |
COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: a case-control study.
Topics: Case-Control Studies; Catechol O-Methyltransferase; Female; Humans; Male; Methionine; Mutation, Missense; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Reference Values; Schizophrenia; Valine | 2005 |
Brain-derived neurotrophic factor: a genetic risk factor for obsessive-compulsive disorder and Tourette syndrome?
Topics: Adolescent; Amino Acid Substitution; Brain-Derived Neurotrophic Factor; Child; DNA; Humans; Linkage Disequilibrium; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single Nucleotide; Risk Factors; Tourette Syndrome; Valine; White People | 2006 |
Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome.
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Cognition; Data Interpretation, Statistical; DiGeorge Syndrome; Female; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Obsessive-Compulsive Disorder; Risk Factors; Schizophrenia | 2007 |
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
Topics: Adolescent; Adult; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, Pair 22; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Obsessive-Compulsive Disorder; Polymorphism, Single-Stranded Conformational; Valine | 2008 |