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Article

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.

Translational psychiatry - 29 Nov 2022

Price Kaitlyn M, Wigg Karen G, Eising Else, Feng Yu, Blokland Kirsten, Wilkinson Margaret, Kerr Elizabeth N, Guger Sharon L, Fisher Simon E, Lovett Maureen W, Strug Lisa J, Barr Cathy L

Abstract excerpt

Reading Disability (RD) is often characterized by difficulties in the phonology of the language. While the molecular mechanisms underlying it are largely undetermined, loci are being revealed by genome-wide association studies (GWAS). In a previous GWAS for word reading (Price, 2020), we observed that top single-nucleotide polymorphisms (SNPs) were located near to or in genes involved in neuronal migration/axon...

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Identifiers

PMID: 36446759
DOI: 10.1038/s41398-022-02250-z
PMCID: PMC9709072

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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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