scholarly article | Q13442814 |
P50 | author | Kenneth Blum | Q6389872 |
Marlene Oscar-Berman | Q30001940 | ||
P2093 | author name string | Trevor Archer | |
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Perinatal risk factors interacting with catechol O-methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD | Q34268180 | ||
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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 | Q34309797 | ||
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The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes | Q34555115 | ||
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Confirmation that a specific haplotype of the dopamine transporter gene is associated with combined-type ADHD. | Q51990055 | ||
The influence of four serotonin-related genes on decision-making in suicide attempters. | Q51997036 | ||
Heritability of attention problems in children: longitudinal results from a study of twins, age 3 to 12. | Q52000373 | ||
Prenatal exposure to polychlorinated biphenyls and attention at school age. | Q52003875 | ||
A 2-year prospective follow-up study of children and adolescents with disruptive behavior disorders. Prediction by cerebrospinal fluid 5-hydroxyindoleacetic acid, homovanillic acid, and autonomic measures? | Q52043522 | ||
Deficient response inhibition as a cognitive endophenotype of ADHD. | Q52099095 | ||
Bilateral inheritance as evidence for polygenicity in the hyperactive child syndrome | Q52116640 | ||
Exploring and explaining epigenetic effects. | Q52193311 | ||
Parent-of-origin effects in attention-deficit hyperactivity disorder. | Q53013785 | ||
Association study of the brain-derived neurotropic factor (BDNF) gene in attention deficit hyperactivity disorder. | Q53028419 | ||
Gene for the serotonin transporter and ADHD: no association with two functional polymorphisms. | Q53610175 | ||
The D2 dopamine receptor gene as a determinant of reward deficiency syndrome. | Q55331780 | ||
Association of 4-repeat allele of the dopamine D4 receptor gene exon III polymorphism and response to methylphenidate treatment in Korean ADHD children | Q57215652 | ||
Mutation screen of the brain derived neurotrophic factor gene (BDNF): Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder | Q57285564 | ||
Serotonergic function in aggressive and nonaggressive boys with attention deficit hyperactivity disorder | Q72747073 | ||
Impulsive aggression in personality disorder correlates with platelet 5-HT2A receptor binding | Q73313661 | ||
Use and costs of medical care for children and adolescents with and without attention-deficit/hyperactivity disorder | Q73376032 | ||
Platelet serotonin measures in adolescents with conduct disorder | Q73894326 | ||
SNP- and haplotype analysis of the tryptophan hydroxylase 2 gene in alcohol-dependent patients and alcohol-related suicide | Q79656767 | ||
Relationship between motor proficiency, attention, impulse, and activity in children with ADHD | Q80154325 | ||
Effect of ADRA2A and BDNF gene-gene interaction on the continuous performance test phenotype | Q82383966 | ||
Characterization of impulsivity in suicide completers: clinical, behavioral and psychosocial dimensions | Q82869700 | ||
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) | Q83049439 | ||
Lack of significant association between -1021C-->T polymorphism in the dopamine beta hydroxylase gene and attention deficit hyperactivity disorder | Q83158731 | ||
Polymorphism of DRD2 gene and ADHD | Q83223138 | ||
P433 | issue | 104 | |
P921 | main subject | epigenetics | Q26939 |
endophenotype | Q2032061 | ||
developmental disorder | Q3087172 | ||
P577 | publication date | 2011-06-01 | |
P1433 | published in | Journal of genetic syndromes & gene therapy | Q27723954 |
P1476 | title | Epigenetics in Developmental Disorder: ADHD and Endophenotypes | |
P478 | volume | 2 |
Q38153339 | A network medicine approach to psychiatric genetics |
Q92432113 | Association of norepinephrine transporter methylation with in vivo NET expression and hyperactivity-impulsivity symptoms in ADHD measured with PET |
Q26781527 | Attention Deficit Hyperactivity Disorder in the Light of the Epigenetic Paradigm |
Q38030489 | Attention-deficit/hyperactivity disorder genomics: update for clinicians |
Q22242325 | Does perinatal exposure to endocrine disruptors induce autism spectrum and attention deficit hyperactivity disorders? Review |
Q90327659 | Early Postnatal Manganese Exposure Reduces Rat Cortical and Striatal Biogenic Amine Activity in Adulthood |
Q26748876 | Epigenetic Mechanisms in Developmental Alcohol-Induced Neurobehavioral Deficits |
Q28731615 | Generational association studies of dopaminergic genes in reward deficiency syndrome (RDS) subjects: selecting appropriate phenotypes for reward dependence behaviors |
Q28652508 | Genetic Addiction Risk Score (GARS): molecular neurogenetic evidence for predisposition to Reward Deficiency Syndrome (RDS) |
Q36166867 | Insights into multimodal imaging classification of ADHD. |
Q27026214 | Low dopamine function in attention deficit/hyperactivity disorder: should genotyping signify early diagnosis in children? |
Q36476979 | Neurogenetic Impairments of Brain Reward Circuitry Links to Reward Deficiency Syndrome (RDS): Potential Nutrigenomic Induced Dopaminergic Activation |
Q36477153 | Neurogenetics and Epigenetics in Impulsive Behaviour: Impact on Reward Circuitry |
Q48944467 | Physical exercise alleviates ADHD symptoms: regional deficits and development trajectory |
Q34490946 | The Molecular Neurobiology of Twelve Steps Program & Fellowship: Connecting the Dots for Recovery |
Q38249952 | Tourette syndrome and comorbid ADHD: causes and consequences. |
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