Role of CNTN6 in neurodevelopment and neuropathology
gene have shown impaired spatial orientation and memory patterns. In humans, copy number variation (CNV) analysis and genome-wide association studies (GWAS) found allele-phenotype relationship of this gene with autism spectrum disorder (ASD), intellectual disability (ID), Tourette syndrome (TS), schizophrenia (SCZ), anorexia, and other mental and neurodevelopmental diseases.
Authors
- А. А. Кашеварова (ORCID: https://orcid.org/0000-0002-0716-4302)
- И. Н. Лебедев (ORCID: https://orcid.org/0000-0002-0482-8046)
- Marina Khodanovich (ORCID: https://orcid.org/0000-0003-1856-0674)
- Maria M. Shadrina
- Ariuna T. Ranzaeva
- Yana A. Tyumentceva
Institutions
- National Research Tomsk State University (RU)
- Research Institute of Medical Genetics of Russian Academy of Medical Sciences (RU)
- Tomsk National Research Medical Center (RU)
Publication Details
- Journal
- Frontiers in Neuroscience
- Published
- 2026-04-22
- DOI
- https://doi.org/10.3389/fnins.2026.1726979
- Primary Topic
- Wnt/β-catenin signaling in development and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00