Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.pdf (1.61 MB)

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2020

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Article

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Artículos Medicina y Ciencias de la Salud

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43

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3
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https://doi.org/10.1038/s41591-020-1103-1
 http://hdl.handle.net/11447/4226

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13 p.

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Abstract

The 22q11.2 deletion syndrome (22q11DS) is associated with a 20-25% risk of schizophrenia. In a cohort of 962 individuals with 22q11DS, we examined the shared genetic basis between schizophrenia and s...

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Citation

Nature Medicine. 2020 Dec;26(12):1912-1918

Keywords

Genetic variation , Phenotypic expression , 22q11DS , 22q11.2 deletion syndrome , Schizophrenia

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