Eric I. Campos

1 King's College Circle
Toronto, ON M5S1A8, Canada

Last Updated: 09/26/2026

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Found 16 publications

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

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

Replisome Proximal Protein Associations and Dynamic Proteomic Changes at Stalled Replication Forks.

Replisome Proximal Protein Associations and Dynamic Proteomic Changes at Stalled Replication Forks.

Journal: Molecular & cellular proteomics : MCP

Published: August 16, 2023

CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.

CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence.

Journal: Human genetics

Published: July 05, 2023

Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.

Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.

Journal: Cell

Published: June 30, 2022

Oncohistone interactome profiling uncovers contrasting oncogenic mechanisms and identifies potential therapeutic targets in high grade glioma.

Oncohistone interactome profiling uncovers contrasting oncogenic mechanisms and identifies potential therapeutic targets in high grade glioma.

Journal: Acta neuropathologica

Published: June 07, 2022

Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration.

Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration.

Journal: Cell

Published: April 04, 2022

The in vivo Interaction Landscape of Histones H3.1 and H3.3.

The in vivo Interaction Landscape of Histones H3.1 and H3.3.

Journal: Molecular & cellular proteomics : MCP

Published: February 08, 2022

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.

Journal: JCI insight

Published: October 22, 2021

ATRX proximal protein associations boast roles beyond histone deposition.

ATRX proximal protein associations boast roles beyond histone deposition.

Journal: PLoS genetics

Published: October 07, 2021

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing.

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing.

Journal: Nucleic acids research

Published: May 18, 2021

Comprehensive interactome profiling of the human Hsp70 network highlights functional differentiation of J domains.

Comprehensive interactome profiling of the human Hsp70 network highlights functional differentiation of J domains.

Journal: Molecular cell

Published: January 21, 2021

Showing 1-12 of 16

Last Updated: 09/26/2026