Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.
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The genetics of attention deficit/hyperactivity disorder in adults, a reviewAdenomatous polyposis coli (APC) membrane recruitment 3, a member of the APC membrane recruitment family of APC-binding proteins, is a positive regulator of Wnt-β-catenin signallingShared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorderThe neurobiological link between OCD and ADHDGenetic association of left ventricular mass assessed by M-mode and two-dimensional echocardiography.Multivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder.Brain electrophysiological endophenotypes for externalizing psychopathology: a multivariate approachMolecular genetics of attention deficit hyperactivity disorder.The path to open-angle glaucoma gene discovery: endophenotypic status of intraocular pressure, cup-to-disc ratio, and central corneal thickness.Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate.Rank-based inverse normal transformations are increasingly used, but are they merited?Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.Genome-wide linkage analysis in a Dutch multigenerational family with attention deficit hyperactivity disorder.Twin studies and their implications for molecular genetic studies: endophenotypes integrate quantitative and molecular genetics in ADHD research.Choline transporter gene variation is associated with attention-deficit hyperactivity disorder.Interval timing deficits assessed by time reproduction dual tasks as cognitive endophenotypes for attention-deficit/hyperactivity disorder.Neuropsychological and dimensional behavioral trait profiles in Costa Rican ADHD sib pairs: Potential intermediate phenotypes for genetic studiesLow serum sphingolipids in children with attention deficit-hyperactivity disorder.Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148GWAS for executive function and processing speed suggests involvement of the CADM2 gene.Glutamatergic medication in the treatment of obsessive compulsive disorder (OCD) and autism spectrum disorder (ASD) - study protocol for a randomised controlled trial.Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate.Genome-wide association studies in ADHD.Resting heart rate and the development of antisocial behavior from age 9 to 14: genetic and environmental influencesBehavioral, neurocognitive and treatment overlap between attention-deficit/hyperactivity disorder and mood instability.Molecular genetics of attention-deficit/hyperactivity disorder: an overviewNeurobiology of attention deficit/hyperactivity disorder.Neuropsychological endophenotypes in attention-deficit/hyperactivity disorder: a review of genetic association studies.The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells.Recognition of facial emotion and affective prosody in children with ASD (+ADHD) and their unaffected siblings.A marginal rank-based inverse normal transformation approach to comparing multiple clinical trial endpoints.Searching for the true genetic vulnerability for schizophrenia.Genetic dissection of behavioral flexibility: reversal learning in mice.Neuropsychological intra-individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17.The NeuroIMAGE study: a prospective phenotypic, cognitive, genetic and MRI study in children with attention-deficit/hyperactivity disorder. Design and descriptives.ADHD in Dutch adults: heritability and linkage study.When Is EEG Indicated in Attention-Deficit/Hyperactivity Disorder?Association analyses of MAOA in Chinese Han subjects with attention-deficit/hyperactivity disorder: family-based association test, case-control study, and quantitative traits of impulsivity.Heritability of response inhibition in children.
P2860
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P2860
Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@ast
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@en
type
label
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@ast
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@en
prefLabel
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@ast
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@en
P2093
P2860
P50
P1476
Neuropsychological endophenoty ...... r ADHD on 2q21.1 and 13q12.11.
@en
P2093
Cathelijne J M Buschgens
Ellen Fliers
Joseph A Sergeant
Marieke E Altink
Nanda N J Rommelse
P2860
P304
P356
10.1016/J.AJHG.2008.06.006
P407
P577
2008-07-01T00:00:00Z