Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder

Clinically relevant copy number variations detected in cerebral palsy

(2015) Maryam Oskoui et al.   Nature Communications

Molecular Convergence of Neurodevelopmental Disorders

(2014) Elizabeth S. Chen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Transmission Disequilibrium of Small CNVs in Simplex Autism

(2013) Niklas Krumm et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Refinement and Discovery of New Hotspots of Copy-Number Variation Associated with Autism Spectrum Disorder

(2013) Santhosh Girirajan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

What have we learned from recent twin studies about the etiology of neurodevelopmental disorders?

(2013) Danielle Posthuma et al.   CURRENT OPINION IN NEUROLOGY

Recurrent HERV-H-Mediated 3q13.2-q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays

(2013) Andrey Shuvarikov et al.   HUMAN MUTATION

Different neurodevelopmental symptoms have a common genetic etiology

(2013) Erik Pettersson et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

High rate of disease-related copy number variations in childhood onset schizophrenia

(2013) K Ahn et al.   MOLECULAR PSYCHIATRY

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system

(2013) A S Cristino et al.   MOLECULAR PSYCHIATRY

SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties

(2013) Kihoon Han et al.   NATURE

Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders

(2013) Wei-Hsien Chien et al.   Molecular Autism

Motor imagery skills of children with Attention Deficit Hyperactivity Disorder and Developmental Coordination Disorder

(2012) Jacqueline Williams et al.   HUMAN MOVEMENT SCIENCE

GAP-43 dependency defines distinct effects of netrin-1 on cortical and spinal neurite outgrowth and directional guidance

(2012) Yiping Shen et al.   INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE

Phenotypic variability of distal 22q11.2 copy number abnormalities

(2011) Tiong Yang Tan et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

De Novo SYNGAP1 Mutations in Nonsyndromic Intellectual Disability and Autism

(2011) Fadi F. Hamdan et al.   BIOLOGICAL PSYCHIATRY

European Academy for Childhood Disability (EACD): Recommendations on the definition, diagnosis and intervention of developmental coordination disorder (long version)*

(2011) RAINER BLANK et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

(2011) Vladimir Vacic et al.   NATURE

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

(2011) Josephine Elia et al.   NATURE GENETICS

Genetic and functional analysis of the gene encoding GAP-43 in schizophrenia

(2011) Yu-Chih Shen et al.   SCHIZOPHRENIA RESEARCH

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

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

Temporal phasing of locomotor activity, heart rate rhythmicity, and core body temperature is disrupted in VIP receptor 2-deficient mice

(2010) Jens Hannibal et al.   AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY

The Genetics of Autism Spectrum Disorders and Related Neuropsychiatric Disorders in Childhood

(2010) Paul Lichtenstein et al.   AMERICAN JOURNAL OF PSYCHIATRY

Resistance to change and vulnerability to stress: autistic-like features of GAP43-deficient mice

(2010) K. J. Zaccaria et al.   GENES BRAIN AND BEHAVIOR

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

(2010) Nigel M Williams et al.   LANCET

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

(2010) Dalila Pinto et al.   NATURE

Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function

(2010) Soumya Raychaudhuri et al.   PLoS Genetics

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

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

Microduplications of 16p11.2 are associated with schizophrenia

(2009) Shane E McCarthy et al.   NATURE GENETICS

Psychometric Properties of the Revised Developmental Coordination Disorder Questionnaire

(2009) Brenda N. Wilson et al.   PHYSICAL & OCCUPATIONAL THERAPY IN PEDIATRICS

Race differences in nicotine dependence in the Collaborative Genetic study of Nicotine Dependence (COGEND)

(2008) Zhehui Luo et al.   NICOTINE & TOBACCO RESEARCH