Compounds > methionine
Page last updated: 2024-08-17

methionine and 22q11 Deletion Syndrome

methionine has been researched along with 22q11 Deletion Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Devoto, M; Emanuel, BS; Franconi, CP; Gur, RE; McDonald-McGinn, D; McNamara, MA; Moss, E; Salmons, H; Zackai, EH1
Baas, F; Booij, J; Boot, E; Linszen, DH; Murphy, DG; Murphy, KC; Owen, MJ; Swillen, A; Van Amelsvoort, TA; Zinkstok, JR1
Simon, TJ; Stoddard, J; Takarae, Y1

Other Studies

3 other study(ies) available for methionine and 22q11 Deletion Syndrome

ArticleYear
IQ and hemizygosity for the Val
    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2016, Volume: 171, Issue:8

    Topics: 22q11 Deletion Syndrome; Adolescent; Catechol O-Methyltransferase; Child; Chromosome Deletion; Chromosomes, Human, Pair 22; Cognition; Cognition Disorders; Female; Genetic Association Studies; Genetic Predisposition to Disease; Hemizygote; Humans; Intelligence Tests; Male; Methionine; Polymorphism, Single Nucleotide; Valine; Young Adult

2016
COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.
    Synapse (New York, N.Y.), 2011, Volume: 65, Issue:9

    Topics: 22q11 Deletion Syndrome; Adolescent; Adult; Catechol O-Methyltransferase; Corpus Striatum; Female; Genotype; Humans; Male; Methionine; Protein Binding; Receptors, Dopamine D2; Receptors, Dopamine D3; Tomography, Emission-Computed, Single-Photon; Valine; Young Adult

2011
A second look: no effect of the COMT Val158Met polymorphism on conflict adaptation in youth with chromosome 22q11.2 deletion syndrome.
    Schizophrenia research, 2012, Volume: 135, Issue:1-3

    Topics: 22q11 Deletion Syndrome; Adaptation, Psychological; Adolescent; Catechol O-Methyltransferase; Child; Cognition Disorders; Conflict, Psychological; Female; Genetic Association Studies; Humans; Male; Methionine; Neuropsychological Tests; Polymorphism, Single Nucleotide; Valine

2012