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2022
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2021
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2020
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A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome.
Not available
S-EPMC11735868
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biostudies-literature
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Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model.
Not available
S-EPMC9693655
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biostudies-literature
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A normative chart for cognitive development in a genetically selected population.
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S-EPMC9117666
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biostudies-literature
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Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Not available
S-EPMC6986984
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biostudies-literature
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Not available
S-EPMC7396297
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biostudies-literature
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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Not available
S-EPMC7975627
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biostudies-literature
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Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs.
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S-EPMC8675420
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biostudies-literature
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