methionine has been researched along with 22q11.2 Deletion Syndrome in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 8 (72.73) | 29.6817 |
| 2010's | 3 (27.27) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| 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, O | 1 |
| Carmel, M; Chen, J; Frisch, A; Gothelf, D; Kolachana, B; Law, AJ; Lipska, BK; Michaelovsky, E; Ren-Patterson, R; Weinberger, DR; Weizman, A; Zarchi, O | 1 |
| Schmidt, L; Simon, TJ; Takarae, Y; Tassone, F | 1 |
| Bach Cuadra, M; Debbané, M; Eliez, S; Glaser, B; Ottet, MC; Schaer, M; Thiran, JP | 1 |
| Berry, MN; Howard, TD; Kaczorowski, J; Keshavan, MS; Kwapil, TR; Schoch, K; Shashi, V; Spence, EJ | 1 |
| 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, E | 1 |
| Antonarakis, SE; Dahoun, SP; Debbane, M; Eliez, S; Glaser, B; Hinard, C; Morris, MA | 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 |
| Afenjar, A; Alembik, Y; Bou, J; Brévière, GM; Bumsel, E; Campion, D; Carlier, M; Coizet, C; Demily, C; Di Rosa, G; Drouin-Garraud, V; Fantini, C; Frebourg, T; Gérard-Desplanches, A; Hannequin, D; Hecketsweiler, B; Heron, D; Lacombe, D; Layet, V; Legallic, S; Lemarchand, M; Manouvrier-Hanu, S; Nolen, MC; Opolczynski, G; Petit, M; Philip, N; Philippe, A; Pustorino, G; Raux, G; Sarda, P; Swillen, A; Thibaut, F; van Amelsvoort, T; Vogels, A; Zinkstok, J | 1 |
| De Leeuw, N; Egger, JI; Fekkes, D; Tuinier, S; Van der Heijden, FM; Van Ravenswaaij-Arts, CM; Verhoeven, WM | 1 |
| Daly, E; De Haan, L; Figee, M; Glaser, B; Linszen, DH; Morris, R; Murphy, DG; Murphy, KC; Owen, MJ; van Amelsvoort, T; Zinkstok, J | 1 |
11 other study(ies) available for methionine and 22q11.2 Deletion Syndrome
| Article | Year |
|---|---|
Striatal dopamine release and impaired reinforcement learning in adults with 22q11.2 deletion syndrome.
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.
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.
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.
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.
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.
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.
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 |
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 |
Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.
Topics: Adolescent; Adult; Alleles; Catechol O-Methyltransferase; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Intellectual Disability; Male; Methionine; Middle Aged; Phenotype; Proline; Proline Oxidase; Psychotic Disorders; Risk Factors | 2007 |
Disturbed serine metabolism and psychosis in a patient with a de novo translocation (2;10)(p23;q22.1).
Topics: Adult; Chromosomes, Human, Pair 10; Chromosomes, Human, Pair 2; DiGeorge Syndrome; Female; Humans; Hydro-Lyases; In Situ Hybridization; Karyotyping; Methionine; Psychotic Disorders; Pterins; Serine; Taurine; Translocation, Genetic | 2006 |
Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
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 |