methionine has been researched along with ADDH in 16 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 12 (75.00) | 29.6817 |
| 2010's | 4 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Biehl, SC; Deckert, J; Gschwendtner, KM; Guhn, A; Herrmann, MJ; Heupel, J; Jacob, CP; Müller, LD; Reichert, S; Reif, A | 1 |
| Bellingham, J; Goto, Y; Grace, AA; Grizenko, N; Joober, R; Polotskaia, A; Schmitz, N; Schwartz, G; Sengupta, S; Stepanian, MT | 1 |
| Lachman, HM | 1 |
| Asherson, P; Bayés, M; Boreatti-Hümmer, A; Bosch, R; Buitelaar, JK; Casas, M; Cormand, B; Faraone, SV; Fasmer, OB; Franke, B; Haavik, J; Heine, M; Jacob, CP; Johansson, S; Kan, C; Knappskog, PM; Kooij, JJS; Lesch, KP; Mick, E; Ramos-Quiroga, JA; Reif, A; Ribasés, M; Sánchez-Mora, C | 1 |
| Altink, ME; Buitelaar, JK; Buschgens, CJ; Fliers, EA; Franke, B; Hartman, CA; Hoekstra, PJ; Minderaa, RB; Nijmeijer, JS; Ormel, J; Rommelse, NN; Sergeant, JA; Verhulst, FC | 1 |
| Bor, W; Brennan, PA; Hammen, C; Lind, P; Montgomery, G; Najman, J; Smith, AK; Sylvers, P | 1 |
| Faraone, SV; Glatt, S; Li, J; Qian, Q; Wang, B; Wang, Y; Zhou, R | 1 |
| Langley, K; Mills, S; O'Donovan, MC; Owen, MJ; Street, E; Thapar, A; Turic, D; Van den Bree, M | 1 |
| Baron, C; Ben Amor, L; Deguzman, R; Grizenko, N; Joober, R; Lageix, P; Mbekou, V; Taerk, E; Ter Stepanian, M; Torkaman-Zehi, A | 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 |
| Bellgrove, MA; Domschke, K; Gill, M; Hawi, Z; Kirley, A; Mullins, C; Robertson, IH | 1 |
| Bray, N; Craddock, N; Dudbridge, F; Fitzgerald, M; Gill, M; Green, E; Hawi, Z; Kent, L; Kirley, A; Langley, K; Lowe, N; O'Donovan, MC; Owen, MJ; Raybould, R; Thapar, A | 1 |
| Cheuk, DK; Wong, V | 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 |
| Caspi, A; Langley, K; Milne, B; Moffitt, TE; O'Donovan, M; Owen, MJ; Polo Tomas, M; Poulton, R; Rutter, M; Taylor, A; Thapar, A; Williams, B | 1 |
2 review(s) available for methionine and ADDH
| Article | Year |
|---|---|
Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.
Topics: Adult; Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Case-Control Studies; Europe; Female; Genetics, Population; Genotype; Humans; Male; Mental Disorders; Methionine; Models, Genetic; Models, Neurological; Polymorphism, Single Nucleotide; Retrospective Studies; Sex Factors; Valine | 2010 |
Meta-analysis of association between a catechol-O-methyltransferase gene polymorphism and attention deficit hyperactivity disorder.
Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Humans; Methionine; Odds Ratio; Polymorphism, Genetic; Valine | 2006 |
1 trial(s) available for methionine and ADDH
| Article | Year |
|---|---|
COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.
Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Central Nervous System Stimulants; Child; Cognition Disorders; Cross-Over Studies; DNA Mutational Analysis; Double-Blind Method; Female; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Mental Processes; Methionine; Methylphenidate; Placebo Effect; Polymorphism, Genetic; Thinking; Valine | 2008 |
13 other study(ies) available for methionine and ADDH
| Article | Year |
|---|---|
Does adult ADHD interact with COMT val (158) met genotype to influence working memory performance?
Topics: Adult; Attention Deficit Disorder with Hyperactivity; Case-Control Studies; Catechol O-Methyltransferase; Executive Function; Female; Genotype; Humans; Male; Memory, Short-Term; Methionine; Neuropsychological Tests; Valine; Young Adult | 2015 |
Does COMT val158met affect behavioral phenotypes: yes, no, maybe?
Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Behavior; Brain Chemistry; Catechol O-Methyltransferase; Catecholamines; Cocaine-Related Disorders; Genetic Predisposition to Disease; Humans; Methionine; Neurocognitive Disorders; Phenotype; Polymorphism, Genetic; Reward; Valine | 2008 |
Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD.
Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Birth Weight; Catechol O-Methyltransferase; Child; Child Development Disorders, Pervasive; Female; Genetic Predisposition to Disease; Genotype; Humans; INDEL Mutation; Interpersonal Relations; Linear Models; Male; Maternal Behavior; Methionine; Netherlands; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors; Sampling Studies; Serotonin Plasma Membrane Transport Proteins; Smoking; Stereotyped Behavior; Surveys and Questionnaires; Valine | 2010 |
Interactions between the COMT Val108/158Met polymorphism and maternal prenatal smoking predict aggressive behavior outcomes.
Topics: Adolescent; Adult; Age Factors; Aggression; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Cohort Studies; Female; Humans; Male; Methionine; Models, Biological; Polymorphism, Single Nucleotide; Pregnancy; Prenatal Exposure Delayed Effects; Smoking; Valine; Young Adult | 2011 |
Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism.
Topics: Adolescent; Adult; Alleles; Attention Deficit Disorder with Hyperactivity; Case-Control Studies; Catechol O-Methyltransferase; Chi-Square Distribution; Child; DNA; Family Health; Female; Gene Frequency; Genotype; Haplotypes; Humans; Linkage Disequilibrium; Male; Methionine; Mutation, Missense; Nuclear Family; Phenotype; Polymorphism, Genetic; Sex Factors; Valine | 2003 |
No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control study.
Topics: Adolescent; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Female; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Regression Analysis; Task Performance and Analysis; Valine | 2004 |
Catechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHD.
Topics: Amino Acid Substitution; Analysis of Variance; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Dopamine; Female; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Prefrontal Cortex; Valine | 2004 |
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 |
The methionine allele of the COMT polymorphism impairs prefrontal cognition in children and adolescents with ADHD.
Topics: Adolescent; Alleles; Attention; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Cognition Disorders; Dopamine; Female; Genotype; Humans; Male; Methionine; Polymorphism, Genetic; Prefrontal Cortex; Psychomotor Performance | 2005 |
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD.
Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Base Sequence; Brain-Derived Neurotrophic Factor; DNA Primers; Female; Genetic Predisposition to Disease; Humans; Male; Methionine; Molecular Sequence Data; Nuclear Family; Polymorphism, Single Nucleotide; Valine | 2005 |
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 |
A replicated molecular genetic basis for subtyping antisocial behavior in children with attention-deficit/hyperactivity disorder.
Topics: Adolescent; Adult; Aggression; Antisocial Personality Disorder; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Child, Preschool; Codon; Cohort Studies; Conduct Disorder; Crime; Diseases in Twins; England; Female; Genetic Carrier Screening; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Longitudinal Studies; Male; Methionine; New Zealand; Phenotype; Polymorphism, Genetic; Reproducibility of Results; Valine; Wales | 2008 |