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Association of Reelin gene polymorphisms with autism

Data up to Jan 2025

Published2005
Citations124
References47

Total Citations Per Year

Abstract

References (47)

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Reelin-mediated Signaling Locally Regulates Protein Kinase B/Akt and Glycogen Synthase Kinase 3β

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Phosphatidylinositol 3-Kinase Interacts with the Adaptor Protein Dab1 in Response to Reelin Signaling and Is Required for Normal Cortical Lamination

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Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum.

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Analysis of the RELN gene as a genetic risk factor for autism

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Reelin gene alleles and susceptibility to autism spectrum disorders

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A Transmission/Disequilibrium Test That Allows for Genotyping Errors in the Analysis of Single-Nucleotide Polymorphism Data

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Altered levels of Reelin and its isoforms in schizophrenia and mood disorders

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Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism

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Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

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Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

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