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Potassium Channels: Newly Found Players in Synaptic Plasticity

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Informative phenotypes for genetic studies of psychiatric disorders

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A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16

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Meta-analysis of Association Between a Catechol-O-Methyltransferase Gene Polymorphism and Attention Deficit Hyperactivity Disorder

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Preferential Transmission of Paternal Alleles at Risk Genes in Attention-Deficit/Hyperactivity Disorder

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Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD

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Association between alpha-2a-adrenergic receptor gene and ADHD inattentive type.

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SNPs in Dopamine D2 Receptor Gene (DRD2) and Norepinephrine Transporter Gene (NET) Are Associated with Continuous Performance Task (CPT) Phenotypes in ADHD children and their families

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Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11

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Genotypic interaction between DRD4 and DAT1 loci is a high risk factor for attention‐deficit/hyperactivity disorder in Chilean families

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Linkage Analysis of Attention Deficit Hyperactivity Disorder

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Genetic Risk for Conduct Disorder Symptom Subtypes in an ADHD Sample: Specificity to Aggressive Symptoms

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Meta‐analysis of brain‐derived neurotrophic factor p.Val66Met in adult ADHD in four European populations

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Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region

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The −1021 C/T DBH polymorphism is associated with neuropsychological performance among children and adolescents with ADHD

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A common haplotype at the dopamine transporter gene 5′ region is associated with attention‐deficit/hyperactivity disorder

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A review and analysis of the relationship between neuropsychological measures and DAT1 in ADHD

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<i>MAOA</i> promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children

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Association between Catechol O‐methyltransferase (COMT) haplotypes and severity of hyperactivity symptoms in Adults

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DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association

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The adrenergic receptor α-2A gene (ADRA2A) and neuropsychological executive functions as putative endophenotypes for childhood ADHD

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A psycho-genetic study of associations between the symptoms of binge eating disorder and those of attention deficit (hyperactivity) disorder

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The future of genetics in psychology and psychiatry: microarrays, genome‐wide association, and non‐coding RNA

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Association between cannabinoid receptor gene (CNR1) and childhood attention deficit/hyperactivity disorder in Spanish male alcoholic patients

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Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

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Report from the 4th International Meeting of the Attention Deficit Hyperactivity Disorder Molecular Genetics Network

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Further evidence of association between two NET single-nucleotide polymorphisms with ADHD

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No evidence of linkage or association between the norepinephrine transporter (NET) gene polymorphisms and ADHD in the Irish population.

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Association between polymorphisms in serotonin transporter gene and attention deficit hyperactivity disorder in Chinese Han subjects

Li, J., Wang, Y.-F., Zhou, R., Zhang, H.-B., Yang, L., Wang, B., & Faraone, S. (2007) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30373 · Cited by 55 · see citing works

Relationship between endophenotype and phenotype in ADHD

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A family‐based study of Indian subjects from Kolkata reveals allelic association of the serotonin transporter intron‐2 (STin2) polymorphism and attention‐deficit‐hyperactivity disorder (ADHD)

Banerjee, E., Sinha, S., Chatterjee, A., Gangopadhyay, P., Singh, M., & Nandagopal, K. (2006) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30296 · Cited by 52 · see citing works

Association of ADHD with genetic variants in the 5′‐region of the dopamine transporter gene: Evidence for allelic heterogeneity

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Some ADHD polymorphisms (in genes DAT1, DRD2, DRD3, DBH, 5-HTT) in case-control study of 100 subjects 6-10 age.

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Cognitive functioning in affected sibling pairs with ADHD: familial clustering and dopamine genes.

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Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder

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Spatial Attentional Bias as a Marker of Genetic Risk, Symptom Severity, and Stimulant Response in ADHD

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Gene for the serotonin transporter and ADHD: No association with two functional polymorphisms

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Serotonin 5‐HT1B receptor gene and attention deficit hyperactivity disorder in Chinese Han subjects

Li, J., Wang, Y.-F., Zhou, R., Zhang, H.-B., Yang, L., Wang, B., Khan, S., & Faraone, S. (2005) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30075 · Cited by 46 · see citing works

Serotonin genes and attention deficit/hyperactivity disorder in a Brazilian sample: Preferential transmission of the HTR2A 452His allele to affected boys

Guimarães, A. P., Zeni, C., Polanczyk, G. V., Genro, J., Román, T., Rohde, L., & Hutz, M. (2007) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30400 · Cited by 45 · see citing works

Polymorphisms TaqI A of the DRD2, BalI of the DRD3, exon III repeat of the DRD4, and 3′ UTR VNTR of the DAT: Association with childhood ADHD in male African‐Caribbean cocaine dependents?

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