Barbara Kellam
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 9 publications
Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome.
Journal: International journal of molecular sciences
Published: December 16, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family.
Journal: Molecular genetics & genomic medicine
Published: February 14, 2020
A large data resource of genomic copy number variation across neurodevelopmental disorders.
Journal: NPJ genomic medicine
Published: May 06, 2019
Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.
Journal: Brain : a journal of neurology
Published: October 08, 2018
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Journal: Journal of neurodevelopmental disorders
Published: May 11, 2018
Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
Journal: European journal of human genetics : EJHG
Published: August 21, 2017
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.
Journal: American journal of medical genetics. Part A
Published: December 15, 2016
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Journal: Nature neuroscience
Published: August 08, 2016
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Journal: Human genetics
Published: September 02, 2014
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Last Updated: 09/26/2026