Faculty profile

Laila Schenkel

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Professor EmeritusDepartment of Pathology and Laboratory MedicineWestern University

Signals and details

Research

Read how they describe their research on their Western University profile.

Latest papers

Patient-Centered Genomic Diagnostic Testing for AML: A Quality Improvement Project.
JCO oncology practice · 2026
Health Care Impact of Comprehensive Genomic Profiling of Solid Tumors in Patient Management Using POWER (Precision Oncology at Western University).
The Journal of molecular diagnostics : JMD · 2026
Segmental Copy Number Variant Detection Using an Amplicon-Based Next-Generation Sequencing Panel for Integrated Glioma Classification.
The Journal of molecular diagnostics : JMD · 2026

All 10 publications

10 publications.

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

Ho JM, Deotare U, Qureshi A, Schenkel L, Chin-Yee B, Mohseni Meybodi A, Lalonde E, Saini L, Gob A, Lam S, Hsia C, Sadikovic B, Hedley B, Chin-Yee I

JCO oncology practice20261 citationsOpen Access

DOI: 10.1200/op-24-00776 PMID: 40460323

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

Bhai P, Turowec JP, Pickard LA, Haghshenas S, Karim K, McConkey H, Santos S, Kerkhof J, Black M, Breadner D, Cecchini M, Howlett C, Schenkel L, Lalonde E, Panuganty V, Raphael J, Lohmann AE, Winquist E, Lenehan J, Stewart P, Tsvetkova E, Vincent M, Fernandes R, Bauman G, Welch S, Sadikovic B

The Journal of molecular diagnostics : JMD2026

DOI: 10.1016/j.jmoldx.2025.12.007 PMID: 41654253

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

Sarvananthan K, Santos S, Saylor B, Khanderooy P, Banwait T, Sadikovic B, Schenkel L, Mohseni Meybodi A, Lalonde E

The Journal of molecular diagnostics : JMD2026Open Access

DOI: 10.1016/j.jmoldx.2026.06.003 PMID: 42386144

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

Du A, Lemay K, Bagga A, Bhola PT, Brown PA, Colaiacovo S, Charames GS, Lemaire M, Lanktree MB, Schenkel L

Genetics in Medicine Open20258 citationsOpen Access

DOI: 10.1016/j.gimo.2025.103442

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

Almanaseer A, Chin-Yee B, Ho J, Lazo-Langner A, Schenkel L, Bhai P, Sadikovic B, Chin-Yee IH, Hsia CC

Advances in hematology202414 citationsOpen Access

DOI: 10.1155/2024/3056216 PMID: 38375212

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.

Mortuza S, Chin-Yee B, James TE, Chin-Yee IH, Hedley BD, Ho JM, Saini L, Lazo-Langner A, Schenkel L, Bhai P, Sadikovic B, Keow J, Sangle N, Hsia CC

Current oncology (Toronto, Ont.)20247 citationsOpen Access

DOI: 10.3390/curroncol31040134 PMID: 38668037

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.

Kerkhof J, Rastin C, Schenkel L, Lin H, Sadikovic B

Expert review of molecular diagnostics20231 citationsOpen Access

DOI: 10.1080/14737159.2023.2245747 PMID: 37542410

Double Duty: Complete Pathologic Response of Two Colonic Primaries with Mosaicism of a Novel MLH1 Mutation to Neoadjuvant Pembrolizumab.

Preti B, Schenkel L, Cecchini M, Romagnoli T, Sanatani MS, French K, Colquhoun P, Vincent MD

Current oncology (Toronto, Ont.)20231 citationsOpen Access

DOI: 10.3390/curroncol30100653 PMID: 37887553

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.

Sadikovic B, Levy MA, Kerkhof J, Aref-Eshghi E, Schenkel L, Stuart A, McConkey H, Henneman P, Venema A, Schwartz CE, Stevenson RE, Skinner SA, DuPont BR, Fletcher RS, Balci TB, Siu VM, Granadillo JL, Masters J, Kadour M, Friez MJ, van Haelst MM, Mannens MMAM, Louie RJ, Lee JA, Tedder ML, Alders M

Genetics in medicine : official journal of the American College of Medical Genetics2021210 citationsOpen Access

DOI: 10.1038/s41436-020-01096-4 PMID: 33547396

Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.

Genetics in medicine : official journal of the American College of Medical Genetics20215 citationsOpen Access

DOI: 10.1038/s41436-021-01130-z PMID: 33637969

Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.

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Laila Schenkel

Research

Latest papers

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

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

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

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

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

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.

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.

Double Duty: Complete Pathologic Response of Two Colonic Primaries with Mosaicism of a Novel MLH1 Mutation to Neoadjuvant Pembrolizumab.

Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.

Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disorders.

Frequent collaborators

Bekim Sadikovic

Emilie Lalonde

Benjamin Chin-Yee

Matthew Cecchini

Anahita Mohseni Meybodi

Alejandro Lazo-Langner

Mark Vincent

Christopher Howlett

Nikhil Sangle

Matthew Lanktree

Ted Young

Glenn Bauman

Mathieu Lemaire

Raymond Kim

Stephen Welch

Eric Winquist

George Charames