Enhancing DLG2 Implications in Neuropsychiatric Disorders: Analysis of a Cohort of Eight Patients with 11q14.1 Imbalances

Selective behavioural impairments in mice heterozygous for the cross disorder psychiatric risk gene DLG2

(2022) Rachel Pass et al.   GENES BRAIN AND BEHAVIOR

A DLG2 deficiency in mice leads to reduced sociability and increased repetitive behavior accompanied by aberrant synaptic transmission in the dorsal striatum

(2020) Taesun Yoo et al.   Molecular Autism

Mood‐Stabilizing Antiepileptic Treatment Response in Bipolar Disorder: A Genome‐Wide Association Study

(2020) Ada Man‐Choi Ho et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Synapse Formation: From Cellular and Molecular Mechanisms to Neurodevelopmental and Neurodegenerative Disorders

(2019) Shadab Batool et al.   JOURNAL OF NEUROPHYSIOLOGY

Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies CAPG as a Functionally Relevant Candidate Gene

(2019) Elena Bacchelli et al.   Journal of Clinical Medicine

Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

(2019) Elizabeth K. Ruzzo et al.   CELL

Development of bipolar disorder and other comorbidity among youth with attention‐deficit/hyperactivity disorder

(2019) L. Eugene Arnold et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Jmy regulates oligodendrocyte differentiation via modulation of actin cytoskeleton dynamics

(2018) Maria M. Azevedo et al.   GLIA

Neurodevelopmental disorders: prevalence and comorbidity in children referred to mental health services

(2018) Berit Hjelde Hansen et al.   NORDIC JOURNAL OF PSYCHIATRY

Differentiating between bipolar and unipolar depression in functional and structural MRI studies

(2018) Kyu-Man Han et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

European guidelines for constitutional cytogenomic analysis

(2018) Marisa Silva et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Synaptopathology Involved in Autism Spectrum Disorder

(2018) Shiqi Guang et al.   Frontiers in Cellular Neuroscience

Altered resting-state cerebral blood flow and functional connectivity of striatum in bipolar disorder and major depressive disorder

(2018) Zongling He et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability

(2017) Claudio Reggiani et al.   Genome Medicine

Human GRIN2B variants in neurodevelopmental disorders

(2016) Chun Hu et al.   JOURNAL OF PHARMACOLOGICAL SCIENCES

Mechanistic basis of MAGUK-organized complexes in synaptic development and signalling

(2016) Jinwei Zhu et al.   NATURE REVIEWS NEUROSCIENCE

A Systematic Review and Meta-analysis of Neuroimaging in Oppositional Defiant Disorder (ODD) and Conduct Disorder (CD) Taking Attention-Deficit Hyperactivity Disorder (ADHD) Into Account

(2016) Siri D. S. Noordermeer et al.   NEUROPSYCHOLOGY REVIEW

Neuroanatomical correlates of childhood apraxia of speech: A connectomic approach

(2016) Simona Fiori et al.   NeuroImage-Clinical

Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy

(2016) Federico Sicca et al.   Scientific Reports

New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder

(2015) Silvia Alemany et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Autism Spectrum Disorder and Epilepsy

(2015) Shafali Spurling Jeste et al.   JOURNAL OF CHILD NEUROLOGY

Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics

(2015) Zhiqiang Hu et al.   Scientific Reports

Neuroimaging and neuromodulation approaches to study eating behavior and prevent and treat eating disorders and obesity

(2015) D. Val-Laillet et al.   NeuroImage-Clinical

Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes

(2014) Abdul Noor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families

(2014) Gerald Egger et al.   NEUROGENETICS

Clinical Significance of De Novo and Inherited Copy-Number Variation

(2013) Anneke T. Vulto-van Silfhout et al.   HUMAN MUTATION

Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses

(2013) Hyejung Won et al.   Frontiers in Molecular Neuroscience

Synaptic scaffold evolution generated components of vertebrate cognitive complexity

(2012) Jess Nithianantharajah et al.   NATURE NEUROSCIENCE

Synaptic Dysfunction in Neurodevelopmental Disorders Associated with Autism and Intellectual Disabilities

(2012) H. Y. Zoghbi et al.   Cold Spring Harbor Perspectives in Biology

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

(2011) Hutton M Kearney et al.   GENETICS IN MEDICINE

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

(2011) G Kirov et al.   MOLECULAR PSYCHIATRY

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

(2010) Feng Li et al.   European Journal of Medical Genetics

Adult ADHD and its comorbidities, with a focus on bipolar disorder

(2009) Larry J. Klassen et al.   JOURNAL OF AFFECTIVE DISORDERS

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

Clathrin Assembly Protein AP180 and CALM Differentially Control Axogenesis and Dendrite Outgrowth in Embryonic Hippocampal Neurons

(2008) I. Bushlin et al.   JOURNAL OF NEUROSCIENCE