Skip to main content

previous disabled Page of 4
and
  1. No Access

    Article

    Validation of single nucleotide polymorphism quantification in pooled DNA samples with SNaPIT™

    Association studies using genome scans to identify quantitative trait loci for multifactorial disorders, with anything approaching reasonable power, have been compromised by the need for a very dense array of ...

    Sarah Curran, Linzy Hill, Geraldine O’Grady, Dragana Turic in Molecular Biotechnology (2002)

  2. Article

    Open Access

    Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1)

    The 10-repeat allele of a variable number tandem repeat (VNTR) polymorphism in the 3'-untranslated region of the dopamine transporter gene (DAT1) has been associated with a range of psychiatric phenotypes, most n...

    Jonathan Mill, Philip Asherson, Ian Craig, Ursula M D'Souza in BMC Genetics (2005)

  3. No Access

    Article

    Continuity and Change in Preschool ADHD Symptoms: Longitudinal Genetic Analysis with Contrast Effects

    The genetic and environmental mediation of continuity and change in parent-reported ADHD symptoms were investigated in a cohort of over 6000 twin pairs at 2, 3 and 4 years of age. Genetic analyses of the cross...

    Thomas S. Price, Emily Simonoff, Philip Asherson, Sarah Curran in Behavior Genetics (2005)

  4. Article

    Open Access

    No evidence for the association of DRD4 with ADHD in a Taiwanese population within-family study

    Attention Deficit Hyperactivity Disorder (ADHD) is a prevalent and highly heritable childhood disorder. The dopamine D4 receptor (DRD4) gene has shown a genetic association with ADHD in Caucasian populations w...

    Keeley-Joanne Brookes, **aohui Xu, Chih-Ken Chen, Yu-Shu Huang in BMC Medical Genetics (2005)

  5. Article

    Open Access

    Sequence analysis of Drd2, Drd4, and Dat1 in SHR and WKY rat strains

    The Spontaneously Hypertensive Rat (SHR) shows a number of behaviours that closely parallel those seen in children with attention-deficit hyperactivity disorder. These include motor hyperactivity, excessive re...

    Jonathan Mill, Terje Sagvolden, Philip Asherson in Behavioral and Brain Functions (2005)

  6. Article

    Open Access

    The IMAGE project: methodological issues for the molecular genetic analysis of ADHD

    The genetic mechanisms involved in attention deficit hyperactivity disorder (ADHD) are being studied with considerable success by several centres worldwide. These studies confirm prior hypotheses about the rol...

    Jonna Kuntsi, Benjamin M Neale, Wai Chen in Behavioral and Brain Functions (2006)

  7. No Access

    Article

    Attention deficit hyperactivity disorder

    Attention deficit hyperactivity disorder (ADHD) is a behavioral diagnosis based on the presence of developmentally inappropriate levels of impulsivity, overactivity, and inattentiveness. It is a familial condi...

    Jonna Kuntsi, Gráinne McLoughlin, Philip Asherson in NeuroMolecular Medicine (2006)

  8. No Access

    Article

    Long-acting medications for the hyperkinetic disorders

    A systematic review of published and unpublished data on the use of long-acting medications in ADHD and hyperkinetic disorder is reported, giving effect sizes and numbers-to-treat for extended-release stimulan...

    Priv. Doz. Dr. Tobias Banaschewski, David Coghill in European Child & Adolescent Psychiatry (2006)

  9. Article

    Open Access

    Association study between the monoamine oxidase A gene and attention deficit hyperactivity disorder in Taiwanese samples

    Attention deficit hyperactivity disorder (ADHD) is a common and highly heritable disorder of childhood characterized by inattention, hyperactivity and impulsivity. Molecular genetic and pharmacological studies...

    **aohui Xu, Keeley Brookes, Chih-Ken Chen, Yu-Shu Huang, Yu-Yu Wu in BMC Psychiatry (2007)

  10. No Access

    Article

    Genetic Support for the Dual Nature of Attention Deficit Hyperactivity Disorder: Substantial Genetic Overlap Between the Inattentive and Hyperactive–impulsive Components

    Attention deficit hyperactivity disorder (ADHD) is a common, complex and highly heritable disorder, characterised by inattentive, impulsive and overactive behaviour. Evidence for the heritability of ADHD measu...

    Gráinne McLoughlin, Angelica Ronald, Jonna Kuntsi in Journal of Abnormal Child Psychology (2007)

  11. No Access

    Article

    High Heritability for a Composite Index of Children’s Activity Level Measures

    Despite the high heritability of children’s activity level, which forms part of the core symptom domain of hyperactivity-impulsivity within attention deficit hyperactivity disorder (ADHD), there has only been ...

    Alexis C. Wood, Frühling Rijsdijk, Kimberly J. Saudino in Behavior Genetics (2008)

  12. Article

    Actigraph data are reliable, with functional reliability increasing with aggregation

    Motion sensor devices such as actigraphs are increasingly used in studies that seek to obtain an objective assessment of activity level. They have many advantages, and are useful additions to research in field...

    Alexis C. Wood, Jonna Kuntsi, Philip Asherson in Behavior Research Methods (2008)

  13. Article

    Open Access

    The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis

    Low serotonergic (5-HT) activity correlates with increased impulsive-aggressive behavior, while the opposite association may apply to cognitive impulsiveness. Both types of impulsivity are associated with atte...

    Robert D Oades, Jessica Lasky-Su, Hanna Christiansen in Behavioral and Brain Functions (2008)

  14. Article

    Open Access

    Association study of promoter polymorphisms at the dopamine transporter gene in Attention Deficit Hyperactivity Disorder

    Attention deficit hyperactivity disorder (ADHD) is a complex neurobehavioral disorder. The dopamine transporter gene (DAT1/SLC6A3) has been considered a good candidate for ADHD. Most association studies with ADHD...

    **aohui Xu, Jonathan Mill, Bo Sun, Chih-Ken Chen, Yu-Shu Huang, Yu-Yu Wu in BMC Psychiatry (2009)

  15. Article

    Open Access

    Investigation of the serotonin 2C receptor gene in attention deficit hyperactivity disorder in UK samples

    Attention deficit hyperactivity disorder (ADHD) is a common, childhood-onset neurodevelopmental disorder that is more frequent in males than females. Several genes on the X chromosome have been studied as cand...

    **aohui Xu, Keeley Brookes, Bo Sun, Nicholas Ilott, Philip Asherson in BMC Research Notes (2009)

  16. No Access

    Article

    Hyperactive-Impulsive Symptom Scores and Oppositional Behaviours Reflect Alternate Manifestations of a Single Liability

    Attention deficit hyperactivity disorder and oppositional behaviours frequently co-occur, We aimed to study the etiology of this overlap in a general population–based twin sample, assessing the symptom domains...

    Alexis C. Wood, Frühling Rijsdijk, Philip Asherson, Jonna Kuntsi in Behavior Genetics (2009)

  17. Article

    Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD

    Attention deficit/hyperactivity disorder (ADHD) is one of the most common neuropsychiatric disorders with a worldwide prevalence around 4–5% in children and 1–4% in adults. Although ADHD is highly heritable an...

    Barbara Franke, Alejandro Arias Vasquez, Stefan Johansson in Neuropsychopharmacology (2010)

  18. No Access

    Article

    Exploring the Relationship Between Autistic-Like Traits and ADHD Behaviors in Early Childhood: Findings from a Community Twin Study of 2-Year-Olds

    Behaviors characteristic of autism and ADHD emerge in early childhood, yet research investigating their comorbidity has focused on older children. This study aimed to explore the nature of the relationship bet...

    Angelica Ronald, Lisa R. Edelson, Philip Asherson in Journal of Abnormal Child Psychology (2010)

  19. Article

    Open Access

    Association study between a polymorphism at the 3'-untranslated region of CLOCK gene and attention deficit hyperactivity disorder

    The circadian locomotor output cycles kaput (CLOCK) gene encodes protein regulation circadian rhythm and also plays some roles in neural transmitter systems including the dopamine system. Several lines of evidenc...

    **aohui Xu, Gerome Breen, Chih-Ken Chen, Yu-Shu Huang in Behavioral and Brain Functions (2010)

  20. Article

    Open Access

    European consensus statement on diagnosis and treatment of adult ADHD: The European Network Adult ADHD

    Attention deficit hyperactivity disorder (ADHD) is among the most common psychiatric disorders of childhood that persists into adulthood in the majority of cases. The evidence on persistence poses several diff...

    Sandra JJ Kooij, Susanne Bejerot, Andrew Blackwell, Herve Caci in BMC Psychiatry (2010)

previous disabled Page of 4