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Article

The influence of DCDC2 risk genetic variants on reading: Testing main and haplotypic effects.

Neuropsychologia - 1 Jul 2019

Riva Valentina, Mozzi Alessandra, Forni Diego, Trezzi Vittoria, Giorda Roberto, Riva Stefania, Villa Marco, Sironi Manuela, Cagliani Rachele, Mascheretti Sara

Abstract excerpt

Developmental dyslexia (DD) is a complex neurodevelopmental heritable disorder. Among DD candidate genes, DCDC2 is one of the most replicated, with rs793862, READ1 and rs793842 likely contribute to phenotypic variability in reading (dis)ability. In this study, we tested the effects of these genetic variants on DD as a categorical trait and on quantitative reading-related measures in a sample of 555 Italian...

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Identifiers

PMID: 29803723
DOI: 10.1016/j.neuropsychologia.2018.05.021

Genes

DCDC2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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