methionine has been researched along with Diseases in Twins in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, J; Li, X; McGue, M | 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 |
| Gupta, VJ; Reddy, SG; Wilcken, DE | 1 |
3 other study(ies) available for methionine and Diseases in Twins
| Article | Year |
|---|---|
Interacting effect of BDNF Val66Met polymorphism and stressful life events on adolescent depression.
Topics: Adolescent; Alleles; Brain-Derived Neurotrophic Factor; Child; China; Depressive Disorder; Diseases in Twins; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; Humans; Life Change Events; Male; Methionine; Neuronal Plasticity; Polymorphism, Genetic; Random Allocation; Valine | 2012 |
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 |
Homocysteinemia, ischemic heart disease, and the carrier state for homocystinuria.
Topics: Adult; Amino Acids, Sulfur; Aminobutyrates; Coronary Disease; Diseases in Twins; Female; Heterozygote; Homocysteine; Homocystinuria; Humans; Male; Methionine; Middle Aged; Myocardial Infarction; Pregnancy; Twins, Monozygotic | 1983 |