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Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld‐Rieger Syndrome

Human mutation, 2017-02, Vol.38 (2), p.169-179

2017

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Glioblastoma-derived Tumor Cells Induce Vasculogenic Mimicry through Flk-1 Protein Activation

The Journal of biological chemistry, 2012-07, Vol.287 (29), p.24821-24831

2012

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Role of YKL-40 in the Angiogenesis, Radioresistance, and Progression of Glioblastoma

The Journal of biological chemistry, 2011-04, Vol.286 (17), p.15332-15343

2011

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Sirenomelia: An anatomical assessment and genetic sex determination of two cases

Journal of anatomy, 2024-06, Vol.244 (6), p.1093-1101

2024

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Transdifferentiation of glioblastoma stem-like cells into mural cells drives vasculogenic mimicry in glioblastomas

The Journal of neuroscience, 2012-09, Vol.32 (37), p.12950-12960

2012

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Vascular heterogeneity and targeting: the role of YKL-40 in glioblastoma vascularization

Oncotarget, 2015-12, Vol.6 (38), p.40507-40518

2015

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Novel PITX2 gene mutations in patients with Axenfeld‐Rieger syndrome

Acta ophthalmologica (Oxford, England), 2016-11, Vol.94 (7), p.e571-e579

2016

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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

Journal of medical genetics, 2015-07, Vol.52 (7), p.431-437

2015

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Anti-YKL-40 antibody and ionizing irradiation synergistically inhibit tumor vascularization and malignancy in glioblastoma

Carcinogenesis (New York), 2014-02, Vol.35 (2), p.373-382

2014

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A refined, rapid and reproducible high resolution melt (HRM)-based method suitable for quantification of global LINE-1 repetitive element methylation

BMC research notes, 2011-12, Vol.4 (1), p.565-565, Article 565

2011

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Genetic education for primary care providers Improving attitudes, knowledge, and confidence

Canadian family physician, 2009-12, Vol.55 (12), p.e92-e99

2009

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Postpartum granulomatous hypophysitis with sphenoid sinus involvement: a case study

Endocrine practice, 2010-03, Vol.16 (2), p.264-269

2010

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Maternal age–based prenatal screening for chromosomal disorders Attitudes of women and health care providers toward changes

Canadian family physician, 2013-01, Vol.59 (1), p.e39-e47

2013

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The WHO genomics program of work for equitable implementation of human genomics for global health

Nature medicine, 2024-09

2024

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The impact of physical activity modification on the well-being of a cohort of children with an inherited arrhythmia or cardiomyopathy

Cardiology in the young, 2020-05, Vol.30 (5), p.692-697

2020

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Contract Negotiation for Neurosurgeons: A Practical Guide

Neurosurgery, 2020-10, Vol.87 (4), p.614-619

2020

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Cover Image, Volume 38, Issue 2

Human mutation, 2017-02, Vol.38 (2), p.i-i

2017

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Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies

Prenatal diagnosis, 2017-09, Vol.37 (9), p.916-923

2017

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Exercise and β-blocker therapy recommendations for inherited arrhythmogenic conditions

Cardiology in the young, 2016-08, Vol.26 (6), p.1123-1129

2016

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Commentary: Impact of Hospital and Health System Mergers and Acquisitions on the Practicing Neurosurgeon: Survey and Analysis from the Council of State Neurosurgical Societies Medical Director's Ad Hoc Representative Section

Neurosurgery, 2018-06, Vol.82 (6), p.157-163

2018

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When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy: The Family Perspective

Circulation. Genomic and precision medicine, 2018-08, Vol.11 (8)

2018

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When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy

Circulation. Genomic and precision medicine, 2018-08, Vol.11 (8), p.e002300-e002300

2018

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Exercise and[...]-blocker therapy recommendations for inherited arrhythmogenic conditions

Cardiology in the young, 2016-08, Vol.26 (6), p.1123

2016

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Novel PITX 2 gene mutations in patients with Axenfeld‐Rieger syndrome

Acta ophthalmologica (Oxford, England), 2016-11, Vol.94 (7)

2016

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Retrospective testing of respiratory specimens for COVID-19 to assess for earlier SARS-CoV-2 infections in Alberta, Canada

Journal of the Association of Medical Microbiology and Infectious Disease Canada = Journal officiel de l'Association pour la microbiologie médicale et l'infectiologie Canada, 2021-03, Vol.6 (1), p.10-15

2021

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Comparison of Bioinformatics Prediction, Molecular Modeling, and Functional Analyses of FOXC1 Mutations in Patients with Axenfeld‐Rieger Syndrome

Glioblastoma-derived Tumor Cells Induce Vasculogenic Mimicry through Flk-1 Protein Activation

Role of YKL-40 in the Angiogenesis, Radioresistance, and Progression of Glioblastoma

Sirenomelia: An anatomical assessment and genetic sex determination of two cases

Transdifferentiation of glioblastoma stem-like cells into mural cells drives vasculogenic mimicry in glioblastomas

Vascular heterogeneity and targeting: the role of YKL-40 in glioblastoma vascularization

Novel PITX2 gene mutations in patients with Axenfeld‐Rieger syndrome

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists

Anti-YKL-40 antibody and ionizing irradiation synergistically inhibit tumor vascularization and malignancy in glioblastoma

A refined, rapid and reproducible high resolution melt (HRM)-based method suitable for quantification of global LINE-1 repetitive element methylation

Genetic education for primary care providers Improving attitudes, knowledge, and confidence

Postpartum granulomatous hypophysitis with sphenoid sinus involvement: a case study

Maternal age–based prenatal screening for chromosomal disorders Attitudes of women and health care providers toward changes

The WHO genomics program of work for equitable implementation of human genomics for global health

The impact of physical activity modification on the well-being of a cohort of children with an inherited arrhythmia or cardiomyopathy

Contract Negotiation for Neurosurgeons: A Practical Guide

Cover Image, Volume 38, Issue 2

Assessing the cost of implementing the 2011 Society of Obstetricians and Gynecologists of Canada and Canadian College of Medical Genetics practice guidelines on the detection of fetal aneuploidies

Exercise and β-blocker therapy recommendations for inherited arrhythmogenic conditions

Commentary: Impact of Hospital and Health System Mergers and Acquisitions on the Practicing Neurosurgeon: Survey and Analysis from the Council of State Neurosurgical Societies Medical Director's Ad Hoc Representative Section

When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy: The Family Perspective

When to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy

Exercise and[...]-blocker therapy recommendations for inherited arrhythmogenic conditions

Novel PITX 2 gene mutations in patients with Axenfeld‐Rieger syndrome

Retrospective testing of respiratory specimens for COVID-19 to assess for earlier SARS-CoV-2 infections in Alberta, Canada

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