Attention deficit hyperactivity disorder: June 2-9, 2016 || Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)






Last Updated: Jun 02, 2016

• Testing for the mediating role of endophenotypes using molecular genetic data in a twin study of ADHD traits.
  Pinto Rebecca, et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 5
• Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.
  Bonvicini C, et al. Molecular psychiatry 2016 5
• Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications.
  Chang Yi Shin, et al. Human brain mapping 2016 5
• BDNF Val66Met polymorphism and peripheral protein levels in pediatric bipolar disorder and attention-deficit/hyperactivity disorder.
  Zeni C P, et al. Acta psychiatrica Scandinavica 2016 5
• A Review and Update on Tourette Syndrome: Where Is the Field Headed?
  Gunduz Aysegul et al. Current neurology and neuroscience reports 2016 Apr 16(4) 37
• Parental Serotonin Transporter Polymorphism (5-HTTLPR) Moderates Associations of Stress and Child Behavior With Parenting Behavior.
  Morgan Julia E, et al. Journal of clinical child and adolescent psychology : the official journal for the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53 2016 5 1-12
• Testing differential susceptibility: Plasticity genes, the social environment, and their interplay in adolescent response inhibition.
  Richards Jennifer S, et al. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2016 5 1-14
• CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
  Mercati O, et al. Molecular psychiatry 2016 5
• White matter alterations related to attention-deficit hyperactivity disorder and COMT val(158)met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (cingulate gyrus).
  Kabukcu Basay Burge, et al. Neuropsychiatric disease and treatment 2016 0 969-81
• The role of ASTN2 variants in childhood and adult ADHD, comorbid disorders and associated personality traits.
  Freitag Christine M, et al. Journal of neural transmission (Vienna, Austria : 1996) 2016 4
• Altered structural connectivity is related to attention deficit/hyperactivity subtypes: A DTI study.
  Ercan Eyup Sabri, et al. Psychiatry research 2016 4
• The 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 Spectroscopy.
  Ozturk Onder, et al. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2016 5 (2) 184-93
• Relationship between the DAT1 gene and the effects of methylphenidate administration in adult attention deficit hyperactivity disorder: a magnetic resonance spectroscopy study.
  Inci Kenar A N, et al. European review for medical and pharmacological sciences 2016 4 (7) 1373-8
• A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study.
  Hegvik Tor-Arne, et al. Journal of neural transmission (Vienna, Austria : 1996) 2016 4
• Association between RELN Gene Polymorphisms and Attention Deficit Hyperactivity Disorder in Korean Children.
  Kwon Ho Jang, et al. Psychiatry investigation 2016 3 (2) 210-6
• Increased risk of attention-deficit/hyperactivity disorder associated with exposure to organophosphate pesticide in Taiwanese children.
  Yu C-J, et al. Andrology 2016 4
• ADHD risk alleles associated with opiate addiction: study of addicted parents and their children.
  Ornoy Asher, et al. Pediatric research 2016 4
• Neuropsychological performance measures as intermediate phenotypes for attention-deficit/hyperactivity disorder: A multiple mediation analysis.
  Kamradt Jaclyn M, et al. Development and psychopathology 2016 4 1-14
• Adolescent behavioral and neural reward sensitivity: a test of the differential susceptibility theory.
  Richards J S, et al. Translational psychiatry 2016 0 e771
• Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
  Mooney Michael A, et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 3
• Psychopathic traits mediate the association of serotonin transporter genotype and child externalizing behavior.
  Brammer Whitney A, et al. Aggressive behavior 2016 3
• An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder.
  de Araújo Lima Leandro, et al. Scientific reports 2016 0 22851
• Enlarged striatal volume in adults with ADHD carrying the 9-6 haplotype of the dopamine transporter gene DAT1.
  Onnink A Marten H, et al. Journal of neural transmission (Vienna, Austria : 1996) 2016 3
• Patterns of Nonrandom Mating Within and Across 11 Major Psychiatric Disorders.
  Nordsletten Ashley E, et al. JAMA psychiatry 2016 2
• Attention Deficit/Hyperactivity Disorder and Urinary Nonylphenol Levels: A Case-Control Study in Taiwanese Children.
  Yu Ching-Jung, et al. PloS one 2016 0 (2) e0149558
• Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports.
  Brownstein Catherine A, et al. American journal of medical genetics. Part A 2016 2
• NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children.
  Salatino-Oliveira Angélica, et al. Journal of psychiatric research 2016 1 75-81
• [Influence of ODD diagnosis on the association between NET1 and attention-deficit/hyperactivity disorder].
  Liu Lu, et al. Zhonghua yi xue za zhi 2015 11 (41) 3351-6
• Pharmacogenetics of methylphenidate response and tolerability in attention-deficit/hyperactivity disorder.
  Pagerols M, et al. The pharmacogenomics journal 2016 1
• Association between the 5-HTTLPR Genotype and Childhood Characteristics in Mood Disorders.
  Eun Tae Kyung, et al. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology 2016 2 (1) 88-95

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Relevant Resources

• Cancer Genomics and Epidemiology Navigator (CGEN)
• Genetics and Genomics Competencies Center (G2C2)
• NIH Genetic Testing Registry
• NIH MedGen Database
• Online Mendelian Inheritance in Man (OMIM)
• PharmGKB