Publication: Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities
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Price, K. M., Wigg, K. G., Eising, E., et al, & Brandeis, D. (2022). Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry, 12, 495. https://doi.org/10.1038/s41398-022-02250-z
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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 guidance (NM/AG) or loci implicated in autism spectrum disorder (ASD). A prominent theory of RD etiology posits that it invol
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- Price, Kaitlyn M
- Wigg, Karen G
- Eising, Else
- Brandeis, Daniel
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Price, K. M., Wigg, K. G., Eising, E., et al, & Brandeis, D. (2022). Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. Translational Psychiatry, 12, 495. https://doi.org/10.1038/s41398-022-02250-z
