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The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism
Rena J Vanzo1, Aparna Prasad1, Lauren Staunch1
1Lineagen, Inc., Salt Lake City, UT 84109, USA.
Journal of Personalized Medicine
|January 1, 2021
Summary
Genomic analysis of Temple Grandin identified genetic variants in SHANK2, ALX1, and RELN associated with autism spectrum disorder (ASD). Additional variants may explain other clinical features, highlighting the complexity of ASD genetics.
Area of Science:
- Genetics
- Neurodevelopmental Disorders
- Personalized Medicine
Background:
- Autism spectrum disorder (ASD) presents a complex genetic basis, influencing phenotype and clinical features.
- Understanding the genetic underpinnings of ASD is crucial for medical management, personalized treatments, and identifying associated health risks.
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