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

Enriched environment and physical activity reduce microglia and influence the fate of NG2 cells in the amygdala of adult mice

(2011) Dan Ehninger et al.   CELL AND TISSUE RESEARCH

Solving the Autism Puzzle a Few Pieces at a Time

(2011) Christian P. Schaaf et al.   NEURON

Patterns of cardiac and extracardiac anomalies in adults with tetralogy of Fallot

(2010) Sara Piran et al.   AMERICAN HEART JOURNAL

Executive Functions and Memory Abilities in Children With 22q11.2 Deletion Syndrome

(2010) Linda E. Campbell et al.   AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY

Changes in molecular composition of rat medial prefrontal cortex synapses during adolescent development

(2010) Danielle S. Counotte et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?

(2010) Elliott A. Beaton et al.   Journal of Neurodevelopmental Disorders

Disruption of Adult Neurogenesis in the Olfactory Bulb Affects Social Interaction but not Maternal Behavior

(2010) Claudia E. Feierstein et al.   Frontiers in Behavioral Neuroscience

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

Environmental enrichment stimulates progenitor cell proliferation in the amygdala

(2009) Hiroaki Okuda et al.   JOURNAL OF NEUROSCIENCE RESEARCH

Psychiatric Disorders and Intellectual Functioning Throughout Development in Velocardiofacial (22q11.2 Deletion) Syndrome

(2009) Tamar Green et al.   JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY

Constitutional mechanisms of vulnerability and resilience to nicotine dependence

(2009) N Hiroi et al.   MOLECULAR PSYCHIATRY

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

(2008) Susan L. Christian et al.   BIOLOGICAL PSYCHIATRY

Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT

(2008) Guiqing Cai et al.   BMC Medical Genomics

Mechanisms and Functional Implications of Adult Neurogenesis

(2008) Chunmei Zhao et al.   CELL

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

(2008) Anne S. Bassett et al.   HUMAN MOLECULAR GENETICS

Inhibition of adult hippocampal neurogenesis disrupts contextual learning but spares spatial working memory, long-term conditional rule retention and spatial reversal

(2008) V. Hernández-Rabaza et al.   NEUROSCIENCE

Ultrasonic vocalizations: A tool for behavioural phenotyping of mouse models of neurodevelopmental disorders

(2008) Maria Luisa Scattoni et al.   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Unusual Repertoire of Vocalizations in the BTBR T+tf/J Mouse Model of Autism

(2008) Maria Luisa Scattoni et al.   PLoS One