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

The New England family study high-risk project: Neurological impairments among offspring of parents with schizophrenia and other psychoses

(2013) Stephen L. Buka et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Genome-Wide Linkage Analyses of 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia

(2013) Tiffany A. Greenwood et al.   AMERICAN JOURNAL OF PSYCHIATRY

Sex Differences in Familiality Effects on Neurocognitive Performance in Schizophrenia

(2013) Monica E. Calkins et al.   BIOLOGICAL PSYCHIATRY

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

(2013) N Hiroi et al.   MOLECULAR PSYCHIATRY

Elevated amygdala response to faces and gaze aversion in autism spectrum disorder

(2013) Nim Tottenham et al.   Social Cognitive and Affective Neuroscience

Cognitive development in children with 22q11.2 deletion syndrome

(2012) Sasja N. Duijff et al.   BRITISH JOURNAL OF PSYCHIATRY

Neuroanatomical Assessment of Biological Maturity

(2012) Timothy T. Brown et al.   CURRENT BIOLOGY

Is there a core neuropsychiatric phenotype in 22q11.2 deletion syndrome?

(2012) Kate Baker et al.   CURRENT OPINION IN NEUROLOGY

Depression and anxiety disorders in children and adolescents with velo-cardio-facial syndrome (VCFS)

(2012) Alice Fabbro et al.   EUROPEAN CHILD & ADOLESCENT PSYCHIATRY

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

Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

(2012) Margarita H Cabaral et al.   Journal of Neurodevelopmental Disorders

Age group and sex differences in performance on a computerized neurocognitive battery in children age 8−21.

(2012) Ruben C. Gur et al.   NEUROPSYCHOLOGY

Neurocognitive Performance Stability in a Multiplex Multigenerational Study of Schizophrenia

(2012) D. R. Roalf et al.   SCHIZOPHRENIA BULLETIN

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

Analysis of 94 Candidate Genes and 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia

(2011) Tiffany A. Greenwood et al.   AMERICAN JOURNAL OF PSYCHIATRY

Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams–Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) Syndromes

(2011) Michèle Carlier et al.   BEHAVIOR 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

Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

(2011) Anne S. Bassett et al.   JOURNAL OF PEDIATRICS

Project Among African-Americans to Explore Risks for Schizophrenia (PAARTNERS): Evidence for Impairment and Heritability of Neurocognitive Functioning in Families of Schizophrenia Patients

(2010) Monica E. Calkins et al.   AMERICAN JOURNAL OF PSYCHIATRY

Abnormal Modulation of Amygdala Activity in Schizophrenia in Response to Direct- and Averted-Gaze Threat-Related Facial Expressions

(2010) Amy E. Pinkham et al.   AMERICAN JOURNAL OF PSYCHIATRY

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

Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: Patterning, proliferation, and mitochondrial functions of 22q11 genes

(2010) D.W. Meechan et al.   INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

(2010) Maria Karayiorgou et al.   NATURE REVIEWS NEUROSCIENCE

Visual scanning of faces in 22q11.2 deletion syndrome: Attention to the mouth or the eyes?

(2010) Linda Campbell et al.   PSYCHIATRY RESEARCH

Prediction of Individual Brain Maturity Using fMRI

(2010) Nico U. F. Dosenbach et al.   SCIENCE

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

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

A cognitive neuroscience-based computerized battery for efficient measurement of individual differences: Standardization and initial construct validation

(2009) Ruben C. Gur et al.   JOURNAL OF NEUROSCIENCE METHODS

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

Phenotypic characterization of cognition and social behavior in mice with heterozygous versus homozygous deletion of catechol-O-methyltransferase

(2008) D. Babovic et al.   NEUROSCIENCE

Impaired Activation of Face Processing Networks Revealed by Functional Magnetic Resonance Imaging in 22q11.2 Deletion Syndrome

(2007) Frédéric Andersson et al.   BIOLOGICAL PSYCHIATRY

Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes

(2007) T.J. Simon et al.   NEUROPSYCHOLOGIA