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Barry Eng

Hamilton Health Sciences
McMaster University Medical Centre
McMaster University

103

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1738

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Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours

2021 PLOS ONE
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Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G]

2020 Hemoglobin
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Microcytosis in patients with haemoglobin C trait: is α-thalassaemia trait to blame?

2020 British Journal of Haematology
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ATM Whole Gene Deletion in an Italian Family with Hereditary Pancreatic Cancer: Challenges to cancer risk prediction associated with an 11q22.3 microdeletion

2019 Cancer Genetics and Cytogenetics
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Multiplex Allele-Specific PCR for Simultaneous Detection of H63D and C282Y HFE Mutations in Hereditary Hemochromatosis

2018
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Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene

2017 Hemoglobin
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α0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD)

2017 Hemoglobin
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Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)

2016 Hemoglobin
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Comparison of Three Commercially Available Platforms for Somatic Mutation Profiling in Solid Tumors

2016 Cancer Genetics and Cytogenetics
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Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis

2016 The Journal of Molecular Diagnostics
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Citations (33)