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Article

A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Mar 2013

Tran C, Gagnon F, Wigg K G, Feng Y, Gomez L, Cate-Carter T D, Kerr E N, Field L L, Kaplan B J, Lovett M W, Barr C L

Abstract excerpt

Reading disabilities (RD) have a significant genetic basis and have shown linkage to multiple regions including chromosome 15q. Dyslexia susceptibility 1 candidate gene 1 (DYX1C1) on chromosome 15q21 was originally proposed as a candidate gene with two potentially functional polymorphisms at the -3G/A and 1249G/T positions showing association with RD. However, subsequent studies have yielded mixed results. We...

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PMID: 23341075
DOI: 10.1002/ajmg.b.32123
PMCID: PMC5381964

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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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