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Open access Oct 2026

Neural Cell Models of Specific Reading Disabilities: Identification of Cellular and Transcriptome Alterations

ABSTRACT Based on post‐mortem studies, a long‐standing hypothesis on the biological bases of specific reading disabilities (RD) has been that alterations in neuronal migration alter language neural circuits. However, there are questions concerning the original studies (small sample size, comorbidities). Further, this i...

Cathy L. Barr, K. Wigg, Yu Feng et al. · 0 citations
Open access Sep 2026

The spectrum of copy number variation in the Pan-Canadian HostSeq databank

The integration of copy number variant (CNV) workflows into genome sequencing (GS) analysis pipelines allows for the identification of CNVs implicated in disease. Here, we generated a novel resource of CNVs identified in the HostSeq population cohort from Canada, identified the prevalence of recurrent CNVs associated w...

Navneet Aujla, B. Thiruvahindrapuram, S. Casalino et al. · 0 citations

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