Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder

Identification of common genetic risk variants for autism spectrum disorder

(2019) Jakob Grove et al.   NATURE GENETICS

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

(2019) Kimberley M. Kendall et al.   BRITISH JOURNAL OF PSYCHIATRY

Genetics of attention deficit hyperactivity disorder

(2018) Stephen V. Faraone et al.   MOLECULAR PSYCHIATRY

Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan

(2018) Barbara Franke et al.   EUROPEAN NEUROPSYCHOPHARMACOLOGY

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

(2018) Ditte Demontis et al.   NATURE GENETICS

Genomic Disorders in Psychiatry—What Does the Clinician Need to Know?

(2017) Chelsea Lowther et al.   Current Psychiatry Reports

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication

(2017) Louise K. Hoeffding et al.   JAMA Psychiatry

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

(2017) M O Ulfarsson et al.   Translational Psychiatry

Genetics of attention-deficit/hyperactivity disorder: an update

(2016) Glaucia Chiyoko Akutagava-Martins et al.   Expert Review of Neurotherapeutics

The complex behavioral phenotype of 15q13.3 microdeletion syndrome

(2016) Mark N. Ziats et al.   GENETICS IN MEDICINE

Cohort Profile Update: The Norwegian Mother and Child Cohort Study (MoBa)

(2016) Per Magnus et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Whole-Exome Sequencing Reveals Increased Burden of Rare Functional and Disruptive Variants in Candidate Risk Genes in Individuals With Persistent Attention-Deficit/Hyperactivity Disorder

(2016) Ditte Demontis et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

(2016) Christian R Marshall et al.   NATURE GENETICS

Genetics of attention-deficit/hyperactivity disorder: an update

(2016) Glaucia Chiyoko Akutagava-Martins et al.   Expert Review of Neurotherapeutics

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

(2016) Tara L. Wenger et al.   Molecular Autism

Clinical phenotype of the recurrent 1q21.1 copy-number variant

(2015) Raphael Bernier et al.   GENETICS IN MEDICINE

The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review

(2015) Devin Cox et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

(2015) Brendan K Bulik-Sullivan et al.   NATURE GENETICS

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

(2014) Dalila Pinto et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome

(2014) Maude Schneider et al.   AMERICAN JOURNAL OF PSYCHIATRY

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature

(2014) Chelsea Lowther et al.   GENETICS IN MEDICINE

Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants

(2014) Joanna Martin et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice

(2014) Joanne L Doherty et al.   Genome Medicine

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome-wide association study of both common and rare variants

(2013) Li Yang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

(2013) Marian L. Hamshere et al.   BRITISH JOURNAL OF PSYCHIATRY

Risk of bipolar disorder and schizophrenia in relatives of people with attention-deficit hyperactivity disorder

(2013) Henrik Larsson et al.   BRITISH JOURNAL OF PSYCHIATRY

Evidence that duplications of 22q11.2 protect against schizophrenia

(2013) E Rees et al.   MOLECULAR PSYCHIATRY

CNVs conferring risk of autism or schizophrenia affect cognition in controls

(2013) Hreinn Stefansson et al.   NATURE

Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders

(2013) Maria Tropeano et al.   PLoS One

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

(2011) Nigel M. Williams et al.   AMERICAN JOURNAL OF PSYCHIATRY

16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders

(2011) Arivudainambi Ramalingam et al.   JOURNAL OF HUMAN GENETICS

Developmental and Behavioral Disorders Through the Life Span

(2011) D. S. Stein et al.   PEDIATRICS

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

(2011) A. C. Lionel et al.   Science Translational Medicine

Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder

(2010) Nanda N. J. Rommelse et al.   EUROPEAN CHILD & ADOLESCENT PSYCHIATRY

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

(2010) Nigel M Williams et al.   LANCET

Shared and Nonshared Symptoms in Youth-Onset Psychosis and ADHD

(2009) Canan Karatekin et al.   Journal of Attention Disorders

Occupational Outcome in Adult ADHD: Impact of Symptom Profile, Comorbid Psychiatric Problems, and Treatment

(2009) Anne Halmøy et al.   Journal of Attention Disorders

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders

(2009) S Ben-Shachar et al.   JOURNAL OF MEDICAL GENETICS

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

(2009) M. Shinawi et al.   JOURNAL OF MEDICAL GENETICS

Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

(2008) Anna Brunet et al.   Behavioral and Brain Functions

Disruption of the neurexin 1 gene is associated with schizophrenia

(2008) Dan Rujescu et al.   HUMAN MOLECULAR GENETICS