Laila C. Schenkel

London, ON, Canada

Last Updated: 09/26/2026

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Found 39 publications

Segmental Copy Number Variant Detection Using an Amplicon-Based Next-Generation Sequencing Panel for Integrated Glioma Classification.

Segmental Copy Number Variant Detection Using an Amplicon-Based Next-Generation Sequencing Panel for Integrated Glioma Classification.

Journal: The Journal of molecular diagnostics : JMD

Published: October 22, 2025

Segmental Copy Number Variant Detection Using an Amplicon-based NGS Panel for Integrated Glioma Classification.

Segmental Copy Number Variant Detection Using an Amplicon-based NGS Panel for Integrated Glioma Classification.

Journal: The Journal of molecular diagnostics : JMD

Published: October 22, 2025

Patient-Centered Genomic Diagnostic Testing for AML: A Quality Improvement Project.

Patient-Centered Genomic Diagnostic Testing for AML: A Quality Improvement Project.

Journal: JCO oncology practice

Published: June 03, 2025

Health Care Impact of Comprehensive Genomic Profiling of Solid Tumors in Patient Management Using POWER (Precision Oncology at Western University).

Health Care Impact of Comprehensive Genomic Profiling of Solid Tumors in Patient Management Using POWER (Precision Oncology at Western University).

Journal: The Journal of molecular diagnostics : JMD

Published: May 28, 2025

Health Care Impact of Comprehensive Genomic Profiling of Solid Tumors in Patient Management Using POWER (Precision Oncology at Western University).

Health Care Impact of Comprehensive Genomic Profiling of Solid Tumors in Patient Management Using POWER (Precision Oncology at Western University).

Journal: The Journal of molecular diagnostics : JMD

Published: May 28, 2025

Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program.

Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing Program.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: April 13, 2025

Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario.

Framework for standardized genetic testing recommendations for chronic kidney disease in Ontario.

Journal: Genetics in medicine open

Published: April 07, 2025

Homeostatic response of phospholipid pathways to PCYT2 deficiency and impaired de Novo synthesis of phosphatidylethanolamine.

Homeostatic response of phospholipid pathways to PCYT2 deficiency and impaired de Novo synthesis of phosphatidylethanolamine.

Journal: Scientific reports

Published: October 12, 2024

A Novel and Rare Pathogenic Gene Variant in 2 Patients With Multiple Endocrine Neoplasia Type 1 (MEN-1) Syndrome.

A Novel and Rare Pathogenic Gene Variant in 2 Patients With Multiple Endocrine Neoplasia Type 1 (MEN-1) Syndrome.

Journal: JCEM case reports

Published: August 29, 2024

Myelodysplastic Neoplasms (MDS) with Ring Sideroblasts or SF3B1 Mutations: The Improved Clinical Utility of World Health Organization and International Consensus Classification 2022 Definitions, a Single-Centre Retrospective Chart Review.

Myelodysplastic Neoplasms (MDS) with Ring Sideroblasts or SF3B1 Mutations: The Improved Clinical Utility of World Health Organization and International Consensus Classification 2022 Definitions, a Single-Centre Retrospective Chart Review.

Journal: Current oncology (Toronto, Ont.)

Published: February 13, 2024

An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis.

An Approach to the Investigation of Thrombocytosis: Differentiating between Essential Thrombocythemia and Secondary Thrombocytosis.

Journal: Advances in hematology

Published: December 06, 2023

Clinical validation of a single NGS targeted panel pipeline using the KAPA HyperChoice system for detection of germline, somatic and mitochondrial sequence and copy number variants.

Clinical validation of a single NGS targeted panel pipeline using the KAPA HyperChoice system for detection of germline, somatic and mitochondrial sequence and copy number variants.

Journal: Expert review of molecular diagnostics

Published: August 05, 2023

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Last Updated: 09/26/2026