Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.
about
No evidence of association between Catechol-O-Methyltransferase (COMT) Val158Met genotype and performance on neuropsychological tasks in children with ADHD: a case-control studyCatechol-O-methyltransferase (COMT) Val108/158 Met polymorphism does not modulate executive function in children with ADHDAttention deficit/hyperactivity disorder (ADHD): complex phenotype, simple genotype?Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderAttention-deficit hyperactivity disorder and the adrenergic receptors alpha 1C and alpha 2CThe Effect of Single Dose Methylphenidate on Neurometabolites according to COMT Gene Val158Met Polymorphism in the Patient with Attention Deficit Hyperactivity Disorder: A Study Using Magnetic Resonance SpectroscopyAttention-deficit hyperactivity disorder (ADHD).COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD.Investigating the relationship between COMT polymorphisms and working memory performance among childhood brain tumor survivors.Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes.Dopamine genes and attention-deficit hyperactivity disorder: a review.The policy and ethical implications of genetic research on attention deficit hyperactivity disorder.The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes.Attention-deficit/hyperactivity disorder: advancing on pharmacogenomics.Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.Neural phenotypes of common and rare genetic variants.Genetic contributions to age-related decline in executive function: a 10-year longitudinal study of COMT and BDNF polymorphisms.Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant CasesAssociation of the dopamine transporter (DAT1) 10/10-repeat genotype with ADHD symptoms and response inhibition in a general population sample.Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study.Lack of association between the tryptophan hydroxylase gene A218C polymorphism and attention-deficit hyperactivity disorder in Chinese Han population.The norepinephrine transporter gene and attention-deficit hyperactivity disorder.Linkage of the dopamine receptor D1 gene to attention-deficit/hyperactivity disorder.Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.Attention deficit disorder: not just for children.Association of genetic risk severity with ADHD clinical characteristics.Multicenter linkage study of schizophrenia loci on chromosome 22q.Failure to replicate an association between the catechol-O-methyltransferase polymorphism and attention deficit hyperactivity disorder in a second, independently recruited Israeli cohort.Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor.Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.
P2860
Q24794008-4748B2D2-1635-425A-8FDF-097F397713A5Q24802440-73864EE4-2593-40FA-9D46-4113CB940CD4Q28239000-4EF2532B-EF4F-40EA-9C28-D953B939495CQ28266092-D676FE80-6AD9-46DB-9185-F44254E457BDQ28363902-B4A89B40-617D-4665-A612-37BCEA4E1672Q28833475-52136D9A-126E-454F-8D0A-D91B9573EBC8Q30976949-D97A7C36-0A98-4A6C-9876-B6E0A38E4108Q33911088-17EFD1D4-4543-4CBA-B769-041A5799AEDFQ33914593-FC4FB56D-A3C3-405F-9A93-7A8396FA598CQ34142470-C5DE317E-7C17-4185-939D-3058613C4804Q35066854-09017229-5083-4A03-A922-ADB614D3785AQ35632783-78FED823-A4C3-423C-AD97-418BBEBFF938Q35860569-D90A8193-E951-4050-92A0-7D1749726BAAQ36192663-4CC667E5-6030-46FC-B71A-FE5083DCC89CQ36803173-82AEF155-7E63-4E01-AC87-BDE832E2C45CQ36874111-64A70D9F-8E27-404F-9D79-3876C9FABD51Q36947139-A577B2B8-D246-4344-A4B7-6A6D4C02AFFCQ38835434-266B5203-610D-4B6D-81D5-79836F4641A3Q43479612-721B443C-CFDF-4A93-976B-C77F8F63C4FAQ43671198-1C438249-0BC5-4C66-89C4-FC4CA1ABA296Q43701977-7876612A-B8C1-4D32-999D-476BA8C74A8AQ43938267-37D04639-7527-4B97-8C9E-D8456E2B30F9Q44625523-643B1D02-338B-44F2-977D-FD6ED20A1018Q44709351-AF2C9B25-250B-4FAA-93C2-74AC6CADABFEQ45935735-E2A3F7C8-7C25-40D3-8EAC-89AC8B71FB1DQ46824390-8564E40B-F119-4147-A290-B13677526AD7Q47967896-77D1A195-E6CA-424C-B6E8-8F73FC55DE56Q51942673-4A307BFD-A329-40B9-8831-DE7CE7CEE1C6Q51971354-2B9571EE-E514-4C7E-9202-4433267A6D16Q52926125-E261E398-EBA8-4798-99A2-1C1439B36D5DQ52931373-549AB972-A45F-4069-9720-B15E28D66D1D
P2860
Linkage study of catechol-O-methyltransferase and attention-deficit hyperactivity disorder.
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@ast
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@en
type
label
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@ast
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@en
prefLabel
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@ast
Linkage study of catechol-O-me ...... eficit hyperactivity disorder.
@en
P2093
P2860
P1476
Linkage study of catechol-O-me ...... deficit hyperactivity disorder
@en
P2093
P2860
P304
P356
10.1002/(SICI)1096-8628(19991215)88:6<710::AID-AJMG23>3.0.CO;2-Q
P577
1999-12-01T00:00:00Z