S. Christian

发表

Type 8 long QT syndrome: pathogenic variants in CACNA1C-encoded Cav1.2 cluster in STAC protein binding site.

E. Kaufman, C. January, E. Behr, 2019, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Cardiomyopathies and Genetic Testing in Heart Failure: Role in Defining Phenotype-Targeted Approaches and Management.

G. Oudit, Haran Yogasundaram, S. Christian, 2021, The Canadian journal of cardiology.

The Alberta Newborn Screening Approach for Sickle Cell Disease: The Advantages of Molecular Testing

J. Parboosingh, N. Wright, R. Lamont, 2021, International journal of neonatal screening.

Newborn screening for cystic fibrosis in Alberta: Two years of experience.

M. Somerville, F. Bamforth, Stacey Hume, 2010, Paediatrics & child health.

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

J. Atallah, S. Christian, Sherry Taylor, 2018, Circulation. Genomic and precision medicine.

Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy

J. Parboosingh, J. Atallah, S. Christian, 2018, Journal of Genetic Counseling.

Further Defining the Role of the Laboratory Genetic Counselor

Jacquelyn D Riley, McKinsey L Goodenberger, S. Christian, 2016, Journal of Genetic Counseling.

An assessment of Canadian systems for triaging referred out genetic testing

S. Christian, M. Lilley, P. Blumenschein, 2015, Clinical genetics.

Newborn Screening: Current Status in Alberta, Canada

Stacey Hume, S. Christian, Ross Ridsdale, 2019, International journal of neonatal screening.

A rare homozygous missense GDF2 (BMP9) mutation causing PAH in siblings: Does BMP10 status contribute?

N. Morrell, P. Upton, A. Bates, 2022, American journal of medical genetics. Part A.

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

Stacey Hume, G. Maire, M. Yoshimoto, 2017, Prenatal diagnosis.

The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis

J. Natoli, A. Cirino, M. Kelly, 2022, Journal of genetic counseling.

Sickle cell trait newborn screen results: disclosure and management

S. Christian, Ross Ridsdale, Lauren MacNeil, 2020, Journal of community genetics.

Brain tissue oxygen and outcome after severe traumatic brain injury: A systematic review*

Wei Yang, E. Maloney-Wilensky, P. Leroux, 2009, Critical care medicine.

Diagnostic validity and clinical utility of genetic testing for hypertrophic cardiomyopathy: a systematic review and meta-analysis

J. Natoli, M. Kelly, J. Malinowski, 2022, Open Heart.

Exercise and β-blocker therapy recommendations for inherited arrhythmogenic conditions

J. Atallah, S. Christian, Sherry Taylor, 2015, Cardiology in the Young.

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

J. Spence, J. Atallah, S. Christian, 2020, Cardiology in the Young.

Practice Variation among an International Group of Genetic Counselors on when to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy

J. Atallah, S. Christian, C. Huculak, 2018, Journal of Genetic Counseling.

Principles of Genetic Counseling in Inherited Heart Conditions.

S. Christian, Tara Dzwiniel, 2023, Cardiac electrophysiology clinics.

Evaluating stakeholder's perspective on referred out genetic testing in Canada: a discrete choice experiment

J. Bakal, S. Christian, M. Lilley, 2016, Clinical genetics.

Defining the Role of Laboratory Genetic Counselor

Stacey Hume, S. Christian, M. Lilley, 2012, Journal of Genetic Counseling.

Physical activity restriction for children and adolescents diagnosed with an inherited arrhythmia or cardiomyopathy and its impact on body mass index

J. Atallah, S. Christian, M. Giuffre, 2018, Journal of cardiovascular electrophysiology.

Secondary Reporting of G6PD Deficiency on Newborn Screening

N. Wright, S. Christian, M. Lilley, 2023, International journal of neonatal screening.

IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy

F. Bernier, Julia Tagoe, S. Christian, 2021, Journal of community genetics.

IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars—the Alberta experience with hypertrophic cardiomyopathy

Julia Tagoe, S. Christian, R. Ferrier, 2021, Journal of Community Genetics.

A centralized approach to out‐of‐province genetic testing leads to cost savings: the Alberta experience

M Lilley, S Christian, P Blumenschein, 2013, Clinical genetics.

Evaluation of the First Three Years of Treatment of Children with Congenital Hypothyroidism Identified through the Alberta Newborn Screening Program

E. Rosolowsky, S. Christian, I. Sosova, 2024, International Journal of Neonatal Screening.

Characterizing Decision-Making Surrounding Exercise in ARVC: Analysis of Decisional Conflict, Decisional Regret, and Shared Decision-Making

C. James, C. Tichnell, B. Murray, 2023, Circulation. Genomic and precision medicine.