Compounds > valine

valine and ADDH

valine has been researched along with ADDH in 23 studies

Research

Studies (23)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's13 (56.52)29.6817
2010's10 (43.48)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blakely, RD; Kovtun, O; Quinlan, MA; Rosenthal, SJ; Thal, LB; Tomlinson, ID1
Ji, N; Li, H; Liu, L; Qian, Q; Tang, Y; Wang, Y; Yang, L1
Biehl, SC; Deckert, J; Gschwendtner, KM; Guhn, A; Herrmann, MJ; Heupel, J; Jacob, CP; Müller, LD; Reichert, S; Reif, A1
Bellingham, J; Goto, Y; Grace, AA; Grizenko, N; Joober, R; Polotskaia, A; Schmitz, N; Schwartz, G; Sengupta, S; Stepanian, MT1
Lachman, HM1
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, C1
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, FC1
Bor, W; Brennan, PA; Hammen, C; Lind, P; Montgomery, G; Najman, J; Smith, AK; Sylvers, P1
Bellgrove, MA; Cho, SC; Chung, US; Cummins, TD; Han, DH; Hong, SB; Kim, BN; Kim, JH; Kim, JW; Shin, MS; Shin, YM; Son, JW; Song, SH1
Chazan, R; Genro, JP; Guimarães, AP; Hutz, MH; Polanczyk, G; Rohde, LA; Roman, T; Salatino-Oliveira, A; Schmitz, M; Zeni, C1
Bau, CH; Belmonte-de-Abreu, P; Bertuzzi, GP; Contini, V; de Lima, LL; Grevet, EH; Kortmann, GL; Mota, NR; Paixão-Côrtes, VR; Rohde, LA; Rovaris, DL; Salgado, CA; Vitola, ES1
Bellgrove, MA; Connolly, A; Cummins, TD; Lockhart, PJ; Matthews, N; Panwar, A; Vance, A; Wagner, J; Wallace, RH; Yamada, J1
Faraone, SV; Glatt, S; Li, J; Qian, Q; Wang, B; Wang, Y; Zhou, R1
Langley, K; Mills, S; O'Donovan, MC; Owen, MJ; Street, E; Thapar, A; Turic, D; Van den Bree, M1
Baron, C; Ben Amor, L; Deguzman, R; Grizenko, N; Joober, R; Lageix, P; Mbekou, V; Taerk, E; Ter Stepanian, M; Torkaman-Zehi, A1
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, C1
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, A1
Blakely, RD; Couch, RS; Mazei-Robison, MS; Shelton, RC; Stein, MA1
Aggleton, J; Fowler, T; Langley, K; O'Donovan, M; Owen, M; Rice, F; Thapar, A; Turic, D; Van den Bree, M; Whittinger, N1
Cheuk, DK; Wong, V1
Dempfle, A; Freitag, C; Friedel, S; Hebebrand, J; Herpertz-Dahlmann, B; Hinney, A; Konrad, K; Lesch, KP; Linder, M; Meyer, J; Palmason, H; Renner, TJ; Romanos, M; Schäfer, H; Schimmelmann, BG; Seitz, C; Walitza, S; Warnke, A1
Apter, A; Burg, M; Carmel, M; Frisch, A; Gothelf, D; Inbar, D; Korostishevsky, M; Michaelovsky, E; Steinberg, T; Weizman, A1
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, B1

Reviews

2 review(s) available for valine and ADDH

ArticleYear
Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2010, Mar-05, Volume: 153B, Issue:2

    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.
    Behavior genetics, 2006, Volume: 36, Issue:5

    Topics: Amino Acid Substitution; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Humans; Methionine; Odds Ratio; Polymorphism, Genetic; Valine

2006

Trials

2 trial(s) available for valine and ADDH

ArticleYear
COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:13

    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
Val/Val genotype of brain-derived neurotrophic factor (BDNF) Val⁶⁶Met polymorphism is associated with a better response to OROS-MPH in Korean ADHD children.
    The international journal of neuropsychopharmacology, 2011, Volume: 14, Issue:10

    Topics: Administration, Oral; Age Factors; Analysis of Variance; Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Central Nervous System Stimulants; Chi-Square Distribution; Child; Child Behavior; Delayed-Action Preparations; Female; Gene Frequency; Genetic Predisposition to Disease; Homozygote; Humans; Male; Methylphenidate; Pharmacogenetics; Phenotype; Polymorphism, Single Nucleotide; Prospective Studies; Psychiatric Status Rating Scales; Regression Analysis; Republic of Korea; Time Factors; Treatment Outcome; Valine

2011

Other Studies

19 other study(ies) available for valine and ADDH

ArticleYear
Single Quantum Dot Imaging Reveals PKCβ-Dependent Alterations in Membrane Diffusion and Clustering of an Attention-Deficit Hyperactivity Disorder/Autism/Bipolar Disorder-Associated Dopamine Transporter Variant.
    ACS chemical neuroscience, 2019, 01-16, Volume: 10, Issue:1

    Topics: Attention Deficit Disorder with Hyperactivity; Autistic Disorder; Bipolar Disorder; Cell Membrane; Diffusion; Dopamine Plasma Membrane Transport Proteins; Genetic Variation; HEK293 Cells; Humans; Protein Kinase C beta; Quantum Dots; Valine

2019
Sex-specific association of brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and plasma BDNF with attention-deficit/hyperactivity disorder in a drug-naïve Han Chinese sample.
    Psychiatry research, 2014, Jul-30, Volume: 217, Issue:3

    Topics: Adolescent; Alleles; Asian People; Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Case-Control Studies; Child; China; Ethnicity; Female; Genotype; Humans; Male; Polymorphism, Genetic; Sex Characteristics; Valine

2014
Does adult ADHD interact with COMT val (158) met genotype to influence working memory performance?
    Attention deficit and hyperactivity disorders, 2015, Volume: 7, Issue:1

    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?
    Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2008, Volume: 33, Issue:13

    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.
    Journal of child psychology and psychiatry, and allied disciplines, 2010, Volume: 51, Issue:11

    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.
    Biological psychology, 2011, Volume: 87, Issue:1

    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
Cathechol-O-methyltransferase Val(158)Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD.
    Journal of neural transmission (Vienna, Austria : 1996), 2012, Volume: 119, Issue:6

    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
The role of a mineralocorticoid receptor gene functional polymorphism in the symptom dimensions of persistent ADHD.
    European archives of psychiatry and clinical neuroscience, 2013, Volume: 263, Issue:3

    Topics: Adult; Attention Deficit Disorder with Hyperactivity; DNA Mutational Analysis; Female; Gene Frequency; Genotype; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Mineralocorticoid; Valine; Young Adult

2013
The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHD.
    Behavioral and brain functions : BBF, 2012, May-28, Volume: 8

    Topics: Adolescent; Alleles; Attention Deficit Disorder with Hyperactivity; Catechol O-Methyltransferase; Child; Female; Genetic Variation; Genotype; Heterozygote; Homozygote; Humans; Male; Memory, Short-Term; Neuropsychological Tests; Pattern Recognition, Visual; Phenotype; Reaction Time; Valine

2012
Family-based and case-control association studies of catechol-O-methyltransferase in attention deficit hyperactivity disorder suggest genetic sexual dimorphism.
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2003, Apr-01, Volume: 118B, Issue:1

    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.
    BMC psychiatry, 2004, Jun-07, Volume: 4

    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.
    BMC medical genetics, 2004, Dec-21, Volume: 5

    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.
    The international journal of neuropsychopharmacology, 2005, Volume: 8, Issue:1

    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
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.
    Molecular psychiatry, 2005, Volume: 10, Issue:10

    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
Sequence variation in the human dopamine transporter gene in children with attention deficit hyperactivity disorder.
    Neuropharmacology, 2005, Volume: 49, Issue:6

    Topics: Adolescent; Alanine; Alleles; Attention Deficit Disorder with Hyperactivity; Child; Cohort Studies; Dopamine Plasma Membrane Transport Proteins; Electrophoresis, Capillary; Exons; Family Health; Female; GABA Plasma Membrane Transport Proteins; Gene Frequency; Genetic Variation; Genotype; Humans; Male; Minisatellite Repeats; Polymorphism, Genetic; Retrospective Studies; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Valine

2005
Catechol O-methyltransferase gene variant and birth weight predict early-onset antisocial behavior in children with attention-deficit/hyperactivity disorder.
    Archives of general psychiatry, 2005, Volume: 62, Issue:11

    Topics: Adolescent; Age Factors; Age of Onset; Antisocial Personality Disorder; Attention Deficit Disorder with Hyperactivity; Birth Weight; Catechol O-Methyltransferase; Child; Child, Preschool; Female; Genetic Variation; Genotype; Humans; Infant, Newborn; Male; Prefrontal Cortex; Pregnancy; Prenatal Exposure Delayed Effects; Psychiatric Status Rating Scales; Regression Analysis; Risk Factors; Valine

2005
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.
    Journal of neural transmission (Vienna, Austria : 1996), 2007, Volume: 114, Issue:4

    Topics: Attention Deficit Disorder with Hyperactivity; Brain-Derived Neurotrophic Factor; Child; Female; Genetic Predisposition to Disease; Humans; Male; Pedigree; Polymorphism, Single Nucleotide; Valine

2007
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
    The international journal of neuropsychopharmacology, 2008, Volume: 11, Issue:3

    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.
    Archives of general psychiatry, 2008, Volume: 65, Issue:2

    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