Compounds > valine

valine and DiGeorge Syndrome

valine has been researched along with DiGeorge Syndrome in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (62.50)29.6817
2010's3 (37.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Beck, MCH; Booij, J; Ceccarini, J; Frank, M; Heinzel, A; Hernaus, D; Kasanova, Z; Mohammadkhani-Shali, S; Mottaghy, F; Myin-Germeys, I; van Amelsvoort, T; van Duin, EDA; Winz, O1
Carmel, M; Chen, J; Frisch, A; Gothelf, D; Kolachana, B; Law, AJ; Lipska, BK; Michaelovsky, E; Ren-Patterson, R; Weinberger, DR; Weizman, A; Zarchi, O1
Schmidt, L; Simon, TJ; Takarae, Y; Tassone, F1
Bach Cuadra, M; Debbané, M; Eliez, S; Glaser, B; Ottet, MC; Schaer, M; Thiran, JP1
Berry, MN; Howard, TD; Kaczorowski, J; Keshavan, MS; Kwapil, TR; Schoch, K; Shashi, V; Spence, EJ1
Bearden, CE; Emanuel, BS; Harris, SE; Jawad, AF; Kanes, SJ; Lynch, DR; McDonald-McGinn, DM; Moss, E; Saitta, SC; Simon, TJ; Sokol, S; Wang, PP; Zackai, E1
Antonarakis, SE; Dahoun, SP; Debbane, M; Eliez, S; Glaser, B; Hinard, C; Morris, MA1
Daly, E; De Haan, L; Figee, M; Glaser, B; Linszen, DH; Morris, R; Murphy, DG; Murphy, KC; Owen, MJ; van Amelsvoort, T; Zinkstok, J1

Other Studies

8 other study(ies) available for valine and DiGeorge Syndrome

ArticleYear
Striatal dopamine release and impaired reinforcement learning in adults with 22q11.2 deletion syndrome.
    European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2018, Volume: 28, Issue:6

    Topics: Adult; Benzamides; Brain Mapping; Catechol O-Methyltransferase; Corpus Striatum; DiGeorge Syndrome; Dopamine; Dopamine D2 Receptor Antagonists; Female; Fluorodeoxyglucose F18; Humans; Intelligence Tests; Learning Disabilities; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Mutation; Positron-Emission Tomography; Reinforcement, Psychology; Task Performance and Analysis; Valine

2018
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
    Biological psychiatry, 2014, Mar-01, Volume: 75, Issue:5

    Topics: Adolescent; Adult; Catechol O-Methyltransferase; Chi-Square Distribution; Child; Chromosome Deletion; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Male; Methionine; Psychiatric Status Rating Scales; Psychotic Disorders; Valine; Young Adult

2014
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome.
    Cognitive, affective & behavioral neuroscience, 2009, Volume: 9, Issue:1

    Topics: Adolescent; Analysis of Variance; Attention; Case-Control Studies; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition Disorders; DiGeorge Syndrome; DNA Mutational Analysis; Female; Humans; Intelligence Tests; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Reaction Time; Valine

2009
Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
    Schizophrenia research, 2009, Volume: 115, Issue:2-3

    Topics: Adolescent; Age Factors; Analysis of Variance; Brain Mapping; Case-Control Studies; Catechol O-Methyltransferase; Cerebral Cortex; Child; Cross-Sectional Studies; DiGeorge Syndrome; Female; Humans; Image Processing, Computer-Assisted; Intelligence; Longitudinal Studies; Magnetic Resonance Imaging; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Schizophrenia; Valine; Young Adult

2009
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.
    Psychiatry research, 2010, Jul-30, Volume: 178, Issue:2

    Topics: Adolescent; Anxiety; Catechol O-Methyltransferase; Child; Cognition Disorders; DiGeorge Syndrome; Executive Function; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Valine

2010
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.
    The American journal of psychiatry, 2004, Volume: 161, Issue:9

    Topics: Alleles; Catechol O-Methyltransferase; Child; Chromosomes, Human, Pair 22; Cognition; DiGeorge Syndrome; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Prefrontal Cortex; Valine

2004
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.
    The American journal of psychiatry, 2006, Volume: 163, Issue:3

    Topics: Adolescent; Adult; Catechol O-Methyltransferase; Child; Cognition Disorders; DiGeorge Syndrome; Female; Frontal Lobe; Gene Expression; Genetic Predisposition to Disease; Genotype; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Valine

2006
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
    Psychological medicine, 2008, Volume: 38, Issue:1

    Topics: Adult; Brain; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition Disorders; DiGeorge Syndrome; Female; Gene Frequency; Humans; Hypertrophy; Male; Methionine; Neuropsychological Tests; Polymorphism, Genetic; Psychotic Disorders; Valine

2008