Christina Chrysler

Hamilton, ON, Canada

Last Updated: 09/26/2026

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Found 6 publications

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.

Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.

Journal: Molecular autism

Published: July 28, 2017

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.

Journal: Nature neuroscience

Published: August 08, 2016

Whole-genome sequencing of quartet families with autism spectrum disorder.

Whole-genome sequencing of quartet families with autism spectrum disorder.

Journal: Nature medicine

Published: October 27, 2014

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.

Journal: Human genetics

Published: September 02, 2014

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

Journal: Human molecular genetics

Published: January 02, 2014

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

Rare deletions at the neurexin 3 locus in autism spectrum disorder.

Journal: American journal of human genetics

Published: October 04, 2011

Showing 1-6 of 6

Last Updated: 09/26/2026