Tbx1, a gene encoded in 22q11.2 copy number variant, is a link between alterations in fimbria myelination and cognitive speed in mice

Patterns of de novo tandem repeat mutations and their role in autism

(2021) Ileena Mitra et al.   NATURE

Can MRI measure myelin? Systematic review, qualitative assessment, and meta-analysis of studies validating microstructural imaging with myelin histology

(2021) Alberto Lazari et al.   NEUROIMAGE

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

(2020) F. Kyle Satterstrom et al.   CELL

Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice

(2020) Atsuki Kawamura et al.   HUMAN MOLECULAR GENETICS

Anatomy and function of the fornix in the context of its potential as a therapeutic target

(2020) Suhan Senova et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

A myelin-related transcriptomic profile is shared by Pitt–Hopkins syndrome models and human autism spectrum disorder

(2020) BaDoi N. Phan et al.   NATURE NEUROSCIENCE

Cognition- and circuit-based dysfunction in a mouse model of 22q11.2 microdeletion syndrome: effects of stress

(2020) Anushree Tripathi et al.   Translational Psychiatry

ENIGMA‐DTI: Translating reproducible white matter deficits into personalized vulnerability metrics in cross‐diagnostic psychiatric research

(2020) Peter Kochunov et al.   HUMAN BRAIN MAPPING

Memory in autism spectrum disorder: A meta-analysis of experimental studies.

(2020) Pierre Desaunay et al.   PSYCHOLOGICAL BULLETIN

ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries

(2020) Paul M. Thompson et al.   Translational Psychiatry

Maternal approach behaviors toward neonatal calls are impaired by mother's experiences of raising pups with a risk gene variant for autism

(2020) Risa Kato et al.   DEVELOPMENTAL PSYCHOBIOLOGY

Rare copy number variations are associated with poorer cognition in schizophrenia

(2020) Leon Hubbard et al.   BIOLOGICAL PSYCHIATRY

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

Modeling and predicting developmental trajectories of neuropsychiatric dimensions associated with copy number variations

(2019) Noboru Hiroi et al.   INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY

Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study

(2019) Julio E. Villalón-Reina et al.   MOLECULAR PSYCHIATRY

White matter microstructural alterations across four major psychiatric disorders: mega-analysis study in 2937 individuals

(2019) Daisuke Koshiyama et al.   MOLECULAR PSYCHIATRY

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia

(2018) Femke M. de Vrij et al.   MOLECULAR PSYCHIATRY

Critical reappraisal of mechanistic links of copy number variants to dimensional constructs of neuropsychiatric disorders in mouse models

(2018) Noboru Hiroi   PSYCHIATRY AND CLINICAL NEUROSCIENCES

Oligodendrocyte precursor survival and differentiation requires chromatin remodeling by Chd7 and Chd8

(2018) Corentine Marie et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis

(2017) S Boku et al.   MOLECULAR PSYCHIATRY

Widespread white matter microstructural differences in schizophrenia across 4322 individuals: results from the ENIGMA Schizophrenia DTI Working Group

(2017) S Kelly et al.   MOLECULAR PSYCHIATRY

The role of myelination in measures of white matter integrity: Combination of diffusion tensor imaging and two-photon microscopy of CLARITY intact brains

(2017) Eric H. Chang et al.   NEUROIMAGE

Oligodendroglial excitability mediated by glutamatergic inputs and Nav1.2 activation

(2017) Emmanuelle Berret et al.   Nature Communications

Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts

(2016) James J. Yi et al.   BRAIN AND COGNITION

Assessing the Cognitive Translational Potential of a Mouse Model of the 22q11.2 Microdeletion Syndrome

(2016) Simon RO. Nilsson et al.   CEREBRAL CORTEX

Myelination

(2016) J.L. Salzer et al.   CURRENT BIOLOGY

Behavioral flexibility in rats and mice: contributions of distinct frontocortical regions

(2015) D. A. Hamilton et al.   GENES BRAIN AND BEHAVIOR

Structure and function of neonatal social communication in a genetic mouse model of autism

(2015) T Takahashi et al.   MOLECULAR PSYCHIATRY

Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome

(2015) Yi Deng et al.   PSYCHIATRY RESEARCH-NEUROIMAGING

Neurocognitive performance in family-based and case-control studies of schizophrenia

(2015) Ruben C. Gur et al.   SCHIZOPHRENIA RESEARCH

Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome

(2015) Jacob A. S. Vorstman et al.   JAMA Psychiatry

The Longitudinal Course of Cognitive Impairment in Schizophrenia

(2014) Richard S. E. Keefe   JOURNAL OF CLINICAL PSYCHIATRY

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities

(2014) R E Gur et al.   MOLECULAR PSYCHIATRY

A High-Resolution Spatiotemporal Atlas of Gene Expression of the Developing Mouse Brain

(2014) Carol L. Thompson et al.   NEURON

TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

(2014) Tsutomu Ogata et al.   PLoS One

Neurocognitive Growth Charting in Psychosis Spectrum Youths

(2014) Ruben C. Gur et al.   JAMA Psychiatry

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

(2013) George Kirov et al.   BIOLOGICAL PSYCHIATRY

Cognitive Ability is Associated with Altered Medial Frontal Cortical Circuits in the LgDel Mouse Model of 22q11.2DS

(2013) D. W. Meechan et al.   CEREBRAL CORTEX

The role of myelin and oligodendrocytes in axonal energy metabolism

(2013) Aiman S Saab et al.   CURRENT OPINION IN NEUROBIOLOGY

Motor Skill Learning Induces Changes in White Matter Microstructure and Myelination

(2013) C. Sampaio-Baptista et al.   JOURNAL OF NEUROSCIENCE

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders

(2013) N Hiroi et al.   MOLECULAR PSYCHIATRY

CNVs conferring risk of autism or schizophrenia affect cognition in controls

(2013) Hreinn Stefansson et al.   NATURE

Oligodendrogliogenic and neurogenic adult subependymal zone neural stem cells constitute distinct lineages and exhibit differential responsiveness to Wnt signalling

(2013) Felipe Ortega et al.   NATURE CELL BIOLOGY

Longitudinal processing speed impairments in males with autism and the effects of white matter microstructure

(2013) Brittany G. Travers et al.   NEUROPSYCHOLOGIA

The Development of Myelin in the Brain of the Juvenile Rat

(2013) Noel Downes et al.   TOXICOLOGIC PATHOLOGY

A hitchhiker's guide to diffusion tensor imaging

(2013) José M. Soares et al.   Frontiers in Neuroscience

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

(2012) Dheeraj Malhotra et al.   CELL

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain

(2012) Kathryn M. Harper et al.   HUMAN MOLECULAR GENETICS

Oligodendroglia metabolically support axons and contribute to neurodegeneration

(2012) Youngjin Lee et al.   NATURE

Neuroprotection and repair in multiple sclerosis

(2012) Robin J. M. Franklin et al.   Nature Reviews Neurology

Social cognition in 22q11.2 microdeletion syndrome: Relevance to psychosis?

(2012) Maria Jalbrzikowski et al.   SCHIZOPHRENIA RESEARCH

Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and At-Risk for psychosis

(2011) Paula C. Goldenberg et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Tbx1: identification of a 22q11.2 gene as a risk factor for autism spectrum disorder in a mouse model

(2011) Takeshi Hiramoto et al.   HUMAN MOLECULAR GENETICS

Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion

(2011) Liam J. Drew et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

Changes in Prefrontal Axons May Disrupt the Network in Autism

(2010) B. Zikopoulos et al.   JOURNAL OF NEUROSCIENCE

Twenty-five pitfalls in the analysis of diffusion MRI data

(2010) Derek K. Jones et al.   NMR IN BIOMEDICINE

Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice

(2009) G. Suzuki et al.   HUMAN MOLECULAR GENETICS

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice

(2009) G. Suzuki et al.   HUMAN MOLECULAR GENETICS

What Is the Optimal Value of the g-Ratio for Myelinated Fibers in the Rat CNS? A Theoretical Approach

(2009) Taylor Chomiak et al.   PLoS One

Introducing Black-Gold II, a highly soluble gold phosphate complex with several unique advantages for the histochemical localization of myelin

(2008) Larry Schmued et al.   BRAIN RESEARCH