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Times Co-cited
Similarity
Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
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Practical guidelines for managing patients with 22q11.2 deletion syndrome.
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Practical guidelines for managing adults with 22q11.2 deletion syndrome.
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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
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Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening.
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
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Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
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Neurobiological perspective of 22q11.2 deletion syndrome.
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Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.
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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
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Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.
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Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model.
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Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia.
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
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Analysis of copy number variations at 15 schizophrenia-associated loci.
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Reciprocal Copy Number Variations at 22q11.2 Produce Distinct and Convergent Neurobehavioral Impairments Relevant for Schizophrenia and Autism Spectrum Disorder.
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Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome.
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A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
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Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.
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Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.
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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.