Erika S. Tavares

Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 34 publications

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies.

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies.

Journal: Science advances

Published: October 17, 2025

A novel phenotype-guided genome analysis pipeline for variant discovery.

A novel phenotype-guided genome analysis pipeline for variant discovery.

Journal: NPJ genomic medicine

Published: October 06, 2025

Retinal Pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 -Related Phenotype.

Retinal Pigment Epitheliopathy due to Sub-Optimal Recycling of Vitamin A (RESORVA): A Novel RDH11 -Related Phenotype.

Journal: Clinical genetics

Published: October 03, 2025

Gene therapy outcomes in young patients with RPE65-retinal degeneration.

Gene therapy outcomes in young patients with RPE65-retinal degeneration.

Journal: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie

Published: October 03, 2025

Epigenomic alterations and neural development anomalies in induced pluripotent stem cells from sporadic Alzheimer's disease.

Epigenomic alterations and neural development anomalies in induced pluripotent stem cells from sporadic Alzheimer's disease.

Journal: Development (Cambridge, England)

Published: May 02, 2025

Loss of RPGR disrupts motile cilia and causes primary ciliary dyskinesia by affecting F-actin dynamics.

Loss of RPGR disrupts motile cilia and causes primary ciliary dyskinesia by affecting F-actin dynamics.

Journal: The Journal of clinical investigation

Published: March 13, 2025

Defective IFT57 underlies a novel cause of Bardet-Biedl syndrome.

Defective IFT57 underlies a novel cause of Bardet-Biedl syndrome.

Journal: Human molecular genetics

Published: February 25, 2025

Novel BBS1 deletion and BBS9 nonsense pathogenic variant in Bardet-Biedl syndrome.

Novel BBS1 deletion and BBS9 nonsense pathogenic variant in Bardet-Biedl syndrome.

Journal: Ophthalmic genetics

Published: December 02, 2024

Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.

Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplication.

Journal: JCI insight

Published: December 21, 2023

Factors associated with research participation in a large primary care practice-based pediatric cohort: Results from the TARGet Kids! longitudinal cohort study.

Factors associated with research participation in a large primary care practice-based pediatric cohort: Results from the TARGet Kids! longitudinal cohort study.

Journal: PloS one

Published: September 22, 2022

Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non-syndromic retinitis pigmentosa.

Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non-syndromic retinitis pigmentosa.

Journal: Clinical genetics

Published: May 07, 2022

Randomized controlled trial evaluating a virtual parenting intervention for young children at risk of obesity: study protocol for Parenting Addressing Early Years Intervention with Coaching Visits in Toronto (PARENT) trial.

Randomized controlled trial evaluating a virtual parenting intervention for young children at risk of obesity: study protocol for Parenting Addressing Early Years Intervention with Coaching Visits in Toronto (PARENT) trial.

Journal: Trials

Published: April 12, 2022

Showing 1-12 of 34

Last Updated: 09/26/2026