Cathy L. Barr

Toronto, ON, Canada

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 42 publications

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology.

Distinct patterns of de novo coding variants contribute to Tourette Syndrome etiology.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

MIR1255A regulates pathways critical for brain development, risk genes for depression and neurodevelopmental disorders.

MIR1255A regulates pathways critical for brain development, risk genes for depression and neurodevelopmental disorders.

Journal: Translational psychiatry

Published: October 16, 2025

Overexpression of OTX2 in human neural cells links depression risk genes.

Overexpression of OTX2 in human neural cells links depression risk genes.

Journal: Translational psychiatry

Published: September 20, 2024

Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts.

Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts.

Journal: PloS one

Published: January 17, 2024

The Dyslexia-associated gene KIAA0319L is involved in neuronal migration in the developing chick visual system.

The Dyslexia-associated gene KIAA0319L is involved in neuronal migration in the developing chick visual system.

Journal: The International journal of developmental biology

Published: July 06, 2023

Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneity.

Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneity.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: May 08, 2023

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.

Journal: Translational psychiatry

Published: October 10, 2022

Identification of brain cell types underlying genetic association with word reading and correlated traits.

Identification of brain cell types underlying genetic association with word reading and correlated traits.

Journal: Molecular psychiatry

Published: August 24, 2022

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 23, 2022

Language and reading impairments are associated with increased prevalence of non-right-handedness.

Language and reading impairments are associated with increased prevalence of non-right-handedness.

Journal: Child development

Published: March 19, 2022

Language Difficulties in School-Age Children With Developmental Dyslexia.

Language Difficulties in School-Age Children With Developmental Dyslexia.

Journal: Journal of learning disabilities

Published: April 23, 2021

Synaptic processes and immune-related pathways implicated in Tourette syndrome.

Synaptic processes and immune-related pathways implicated in Tourette syndrome.

Journal: Translational psychiatry

Published: April 27, 2020

Showing 1-12 of 42

Last Updated: 09/26/2026