Comparing Copy Number Variations in a Danish Case Cohort of Individuals With Psychiatric Disorders

Psychiatric disorders in children with 16p11.2 deletion and duplication

(2019) Maria Niarchou et al.   Translational Psychiatry

Association of Rare Copy Number Variants With Risk of Depression

(2019) Kimberley Marie Kendall et al.   JAMA Psychiatry

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

(2019) Olafur O. Gudmundsson et al.   Translational Psychiatry

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

(2019) Ron Nudel et al.   Translational Psychiatry

Unknown

(2018)   ANNALS OF HUMAN GENETICS

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

(2018) Karen Crawford et al.   JOURNAL OF MEDICAL GENETICS

The iPSYCH2012 case–cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders

(2017) C B Pedersen et al.   MOLECULAR PSYCHIATRY

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

(2017) Chelsea Lowther et al.   Current Psychiatry Reports

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

(2016) Christian R Marshall et al.   NATURE GENETICS

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

(2015) Raphael Bernier et al.   GENETICS IN MEDICINE

CNVs in neuropsychiatric disorders

(2015) George Kirov   HUMAN MOLECULAR GENETICS

Copy number variation in bipolar disorder

(2015) E K Green et al.   MOLECULAR PSYCHIATRY

The Danish National Patient Registry: a review of content, data quality, and research potential

(2015) Morten Schmidt et al.   Clinical Epidemiology

22q11.2 deletion syndrome

(2015) Donna M. McDonald-McGinn et al.   Nature Reviews Disease Primers

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

(2014) Chelsea Lowther et al.   GENETICS IN MEDICINE

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

(2014) Eva M. Reinthaler et al.   HUMAN MOLECULAR GENETICS

Copy number variation in schizophrenia in Sweden

(2014) J P Szatkiewicz et al.   MOLECULAR PSYCHIATRY

CNVs conferring risk of autism or schizophrenia affect cognition in controls

(2013) Hreinn Stefansson et al.   NATURE

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

The UK Biobank and selection bias

(2012) James M Swanson   LANCET

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

(2010) Daniel Moreno-De-Luca et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Penetrance for copy number variants associated with schizophrenia

(2010) E. Vassos et al.   HUMAN MOLECULAR GENETICS

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

(2009) George Kirov et al.   HUMAN MOLECULAR GENETICS

Microduplications of 16p11.2 are associated with schizophrenia

(2009) Shane E McCarthy et al.   NATURE GENETICS

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE