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Unlocking Potential: Harnessing Genetic Insights for Autism

Unlocking Potential: Harnessing Genetic Insights for Autism

Introduction

As a Special Education Director, staying abreast of the latest research is crucial to providing the best possible support for students with autism spectrum disorder (ASD). A recent study titled "Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes" offers groundbreaking insights into the genetic underpinnings of ASD. This research, conducted through the SPARK initiative, highlights the potential of genetic studies to enhance our understanding of autism and improve educational strategies.

Understanding the Study

The study utilized whole exome sequencing (WES) to analyze the genetic data of 457 families with ASD, identifying variants in genes that are significant contributors to autism. This research found clinically recognized genetic causes in 10.4% of families and identified potential associations in an additional 3.4% of families. Notably, the study highlighted BRSK2 as a gene with strong statistical support as a risk factor for ASD.

Implications for Practitioners

For practitioners, these findings underscore the importance of integrating genetic insights into educational and therapeutic approaches. Here are some ways to apply this knowledge:

Encouraging Further Research

This study is a stepping stone towards a deeper understanding of ASD. Practitioners are encouraged to support and participate in ongoing research efforts. By contributing to studies like SPARK, educators can help expand the genetic database, leading to more refined insights and strategies.

Conclusion

The intersection of genetics and education holds promise for unlocking new potentials in supporting students with ASD. By embracing the insights from genetic research, practitioners can enhance their skills and make a significant impact on the lives of students. For those interested in delving deeper into the original research, please follow this link: Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes.


Citation: Feliciano, P., Zhou, X., Astrovskaya, I., Turner, T. N., Wang, T., Brueggeman, L., ... & Chung, W. K. (2019). Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes. NPJ Genomic Medicine. https://doi.org/10.1038/s41525-019-0093-8
Marnee Brick, President, TinyEYE Therapy Services

Author's Note: Marnee Brick, TinyEYE President, and her team collaborate to create our blogs. They share their insights and expertise in the field of Speech-Language Pathology, Online Therapy Services and Academic Research.

Connect with Marnee on LinkedIn to stay updated on the latest in Speech-Language Pathology and Online Therapy Services.

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