Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder

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Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder

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Elsevier statement on Research4Life

(2011) Alicia Wise   LANCET

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

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A genome-wide scan for common alleles affecting risk for autism

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Astn2, A Novel Member of the Astrotactin Gene Family, Regulates the Trafficking of ASTN1 during Glial-Guided Neuronal Migration

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Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients

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Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

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Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree

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Functional impact of global rare copy number variation in autism spectrum disorders

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Williams–Beuren Syndrome

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Strong synaptic transmission impact by copy number variations in schizophrenia

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A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder

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Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability

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Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation

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Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders

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Diffuse subcortical band heterotopia, periodic limb movements during sleep and a novel “de novo” mutation in the DCX gene

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The TRIM-NHL Protein TRIM32 Activates MicroRNAs and Prevents Self-Renewal in Mouse Neural Progenitors

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High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?

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Educational and Occupational Underattainment in Adults With Attention-Deficit/Hyperactivity Disorder

(2009) Joseph Biederman et al.   JOURNAL OF CLINICAL PSYCHIATRY

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

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Kinesin Family Member 6 Variant Trp719Arg Does Not Associate With Angiographically Defined Coronary Artery Disease in the Ottawa Heart Genomics Study

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Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism

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Mice lacking doublecortin and doublecortin-like kinase 2 display altered hippocampal neuronal maturation and spontaneous seizures

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Comparative genomics of autism and schizophrenia

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Contact in the genetics of autism and schizophrenia

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Genetic overlap between autism, schizophrenia and bipolar disorder

(2009) Liam S Carroll et al.   Genome Medicine

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients

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Genome-wide association scan of attention deficit hyperactivity disorder

(2008) Benjamin M. Neale et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations

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Evidence for overlapping genetic influences on autistic and ADHD behaviours in a community twin sample

(2008) Angelica Ronald et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

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Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

(2008) Klaus-Peter Lesch et al.   JOURNAL OF NEURAL TRANSMISSION

Singleton deletions throughout the genome increase risk of bipolar disorder

(2008) D Zhang et al.   MOLECULAR PSYCHIATRY

Genome-wide linkage analysis of ADHD using high-density SNP arrays: novel loci at 5q13.1 and 14q12

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Copy-number variations associated with neuropsychiatric conditions

(2008) Edwin H. Cook Jr et al.   NATURE

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

The prevalence and workplace costs of adult attention deficit hyperactivity disorder in a large manufacturing firm

(2008) R. C. Kessler et al.   PSYCHOLOGICAL MEDICINE

Phenome connections

(2008) Martin Oti et al.   TRENDS IN GENETICS

Predictive validity of DSM-IV and ICD-10 criteria for ADHD and hyperkinetic disorder

(2007) Soyoung I. Lee et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY