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Human Molecular Genetics
|
January 10, 2014
Recurrent genomic alterations in sequential progressive leukoplakia and oral cancer: drivers of oral tumorigenesis?
Nilva K Cervigne, Jerry Machado, Rashmi S Goswami, et al.
The Journal of Molecular Diagnostics : JMD
|
August 19, 2017
Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels
Jennifer Kerkhof, Laila C Schenkel, Jack Reilly, et al.
Epigenetics & Chromatin
|
July 24, 2025
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans
Francesco Cecere, Raissa Relator, Michael Levy, et al.
Journal of Human Genetics
|
October 23, 2020
Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario
Erfan Aref-Eshghi, Jennifer Kerkhof, Deana Alexis Carere, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
October 8, 2019
Implementation of Epilepsy Multigene Panel Testing in Ontario, Canada
David A Dyment, Asuri N Prasad, Kym M Boycott, et al.
Journal of General Internal Medicine
|
November 30, 2022
A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study
Benjamin Chin-Yee, Pratibha Bhai, Ian Cheong, 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 Program
Tugce B Balci, Laila C Schenkel, Cassandra Rastin, et al.
Plos One
|
October 1, 2021
Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours
John Bartlett, Yutaka Amemiya, Heleen Arts, 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 Malignancies
Pratibha Bhai, Cyrus C Hsia, Laila C Schenkel, et al.
European Journal of Medical Genetics
|
May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris Syndrome
Sarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
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of 22
Search research articles
Search
Showing results (101-110 of 218) with videos related to
Sort By:
Page
of 22
Human Molecular Genetics
|
January 10, 2014
Recurrent genomic alterations in sequential progressive leukoplakia and oral cancer: drivers of oral tumorigenesis?
Nilva K Cervigne, Jerry Machado, Rashmi S Goswami, et al.
The Journal of Molecular Diagnostics : JMD
|
August 19, 2017
Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels
Jennifer Kerkhof, Laila C Schenkel, Jack Reilly, et al.
Epigenetics & Chromatin
|
July 24, 2025
Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans
Francesco Cecere, Raissa Relator, Michael Levy, et al.
Journal of Human Genetics
|
October 23, 2020
Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario
Erfan Aref-Eshghi, Jennifer Kerkhof, Deana Alexis Carere, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
October 8, 2019
Implementation of Epilepsy Multigene Panel Testing in Ontario, Canada
David A Dyment, Asuri N Prasad, Kym M Boycott, et al.
Journal of General Internal Medicine
|
November 30, 2022
A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study
Benjamin Chin-Yee, Pratibha Bhai, Ian Cheong, 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 Program
Tugce B Balci, Laila C Schenkel, Cassandra Rastin, et al.
Plos One
|
October 1, 2021
Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours
John Bartlett, Yutaka Amemiya, Heleen Arts, 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 Malignancies
Pratibha Bhai, Cyrus C Hsia, Laila C Schenkel, et al.
European Journal of Medical Genetics
|
May 22, 2026
A multi-omics approach to characterize a deep intronic ARID1A deletion in Coffin-Siris Syndrome
Sarah Schuhmann, Elisabeth Bosch, Andreas Fink, et al.
Page
of 22