Viji Venkataramanan

Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 21 publications

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study.

Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study.

Journal: BMJ open

Published: March 27, 2026

Clinical utility of exome sequencing: Post-exome testing decision changes in the management of children with suspected rare genetic disease.

Clinical utility of exome sequencing: Post-exome testing decision changes in the management of children with suspected rare genetic disease.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 30, 2025

Clinical Utility of Exome Sequencing: Post-Exome Testing Decision Changes in the Management of Children with Suspected Rare Genetic Disease.

Clinical Utility of Exome Sequencing: Post-Exome Testing Decision Changes in the Management of Children with Suspected Rare Genetic Disease.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 30, 2025

TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticist.

TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticist.

Journal: BMJ open

Published: August 10, 2025

A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohort.

A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 01, 2025

Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.

Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.

Journal: Journal of genetic counseling

Published: July 11, 2025

A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis.

A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 24, 2025

Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial.

Comparing the performance of exome and genome sequencing for rare disease diagnostics: A randomized implementation effectiveness trial.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 10, 2025

Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?

Exome Sequencing in the Diagnostic Pathway for Suspected Rare Genetic Diseases: Does the Order of Testing Affect its Cost-Effectiveness?

Journal: Applied health economics and health policy

Published: December 01, 2024

Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.

Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions.

Journal: Clinical therapeutics

Published: January 17, 2023

Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario.

Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario.

Journal: CMAJ open

Published: May 24, 2022

The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidence.

The complexity of diagnosing rare disease: An organizing framework for outcomes research and health economics based on real-world evidence.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 14, 2021

Showing 1-12 of 21

Last Updated: 09/26/2026