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Clinical Epigenetics|February 20, 2018
Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in <i>KDM5C</i>Laila C Schenkel, Erfan Aref-Eshghi, Cindy Skinner, et al.
The Journal of Molecular Diagnostics : JMD|August 16, 2017
Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting DisordersErfan Aref-Eshghi, Laila C Schenkel, Hanxin Lin, et al.
Scientific Reports|December 10, 2016
The defining DNA methylation signature of Floating-Harbor SyndromeRebecca L Hood, Laila C Schenkel, Sarah M Nikkel, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2014
Mechanism of choline deficiency and membrane alteration in postural orthostatic tachycardia syndrome primary skin fibroblastsLaila C Schenkel, Ratnesh K Singh, Vera Michel, et al.
Frontiers in Genetics|July 30, 2021
Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based ApproachPratibha Bhai, Michael A Levy, Kathleen Rooney, et al.
Epigenetics & Chromatin|March 16, 2017
Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndromeLaila C Schenkel, Kristin D Kernohan, Arran McBride, et al.
The Journal of Molecular Diagnostics : JMD|July 5, 2016
Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel AnalysisLaila C Schenkel, Jennifer Kerkhof, Alan Stuart, et al.
The Journal of Molecular Diagnostics : JMD|August 19, 2017
Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing PanelsJennifer Kerkhof, Laila C Schenkel, Jack Reilly, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 13, 2025
Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing ProgramTugce B Balci, Laila C Schenkel, Cassandra Rastin, et al.
Molecular Diagnosis & Therapy|April 6, 2022
Clinical Utility of Implementing a Frontline NGS-Based DNA and RNA Fusion Panel Test for Patients with Suspected Myeloid MalignanciesPratibha Bhai, Cyrus C Hsia, Laila C Schenkel, et al.
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