valine has been researched along with Conduct Disorder in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chazan, R; Genro, JP; Guimarães, AP; Hutz, MH; Polanczyk, G; Rohde, LA; Roman, T; Salatino-Oliveira, A; Schmitz, M; Zeni, C | 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 other study(ies) available for valine and Conduct Disorder
| Article | Year |
|---|---|
Cathechol-O-methyltransferase Val(158)Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD.
Topics: Adolescent; Alleles; Amino Acid Substitution; Attention Deficit and Disruptive Behavior Disorders; Attention Deficit Disorder with Hyperactivity; Brazil; Catechol O-Methyltransferase; Child; Comorbidity; Conduct Disorder; Diagnostic and Statistical Manual of Mental Disorders; DNA; Female; Gene Frequency; Genotype; Humans; Male; Neuropsychological Tests; Polymorphism, Genetic; 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 |