Comparison of autism domains across thirty rare variant genotypesResearch in context

Comparison of autism domains across thirty rare variant genotypesResearch in context

Summary: Background: A number of Neurodevelopmental risk Copy Number Variants (ND-CNVs) and Single Gene Variants (SGVs) are strongly linked to elevated likelihood of autism. However, few studies have examined the impact on autism phenotypes across a wide range of rare variant genotypes. Methods: Th...

Full description

Saved in:
Bibliographic Details
Main Authors: Nabila M.H. Ali, Samuel J.R.A. Chawner, Leila Kushan-Wells, Carrie E. Bearden, Jennifer Gladys Mulle, Rebecca M. Pollak, Raquel E. Gur, Wendy K. Chung, Michael J. Owen, Marianne B.M. van den Bree, Harriet Housby, Irene Lee, David Skuse, Jeanne Wolstencroft, William Mandy, Spiros Denaxas, Kate Baker, Lucy Raymond, Marianne van den Bree, Samuel Chawner, Jeremy Hall, Peter Holmans, Josh Hope-Bell, Danielle Le Roux, Sally Morrin, Michael Owen, Shreeya Sivakumar
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:EBioMedicine
Subjects:
Autism
Rare genetic variants
Copy number variants (CNVs)
Single gene variants (SGVs)
Online Access:http://www.sciencedirect.com/science/article/pii/S2352396424005577
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items