Genetics

Open Access
Secondary causes of elevated hemoglobin in patients undergoing molecular testing for suspected polycythemia vera in southwestern Ontario: a chart review
Benjamin Chin-Yee, Maxim Matyashin, Ian Cheong, Pratibha Bhai, Alejandro Lazo-Langner, Ala Almanaseer, Eri Kawata, Michael A. Levy, Alan Stuart, Hanxin Lin, Ian Chin-Yee, Bekim Sadikovic and Cyrus Hsia

November 08, 2022 10 (4) E988-E992; DOI: https://doi.org/10.9778/cmajo.20210322
Open Access
Determinants of guideline-concordant breast cancer screening by family physicians for women aged 40–49 years: a qualitative analysis
Michelle B. Nadler, Ann Marie Corrado, Laura Desveaux, Sarah E. Neil-Sztramko, Brooke E. Wilson, Alexandra Desnoyers, Eitan Amir and Noah Ivers

October 18, 2022 10 (4) E900-E910; DOI: https://doi.org/10.9778/cmajo.20210266
Open Access
Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario
Robin Z. Hayeems, Christian R. Marshall, Meredith K. Gillespie, Anna Szuto, Caitlin Chisholm, Dimitri J. Stavropoulos, Viji Venkataramanan, Kate Tsiplova, Sarah Sawyer, E. Magda Price, Lynette Lau, Reem Khan, Whiwon Lee, Lijia Huang, Olga Jarinova, Wendy J. Ungar, Roberto Mendoza-Londono, Martin J. Somerville and Kym M. Boycott

May 24, 2022 10 (2) E460-E465; DOI: https://doi.org/10.9778/cmajo.20210272
Open Access
Building the What Comes Next Cohort for BRCA1 and BRCA2 testing: a descriptive analysis
Fahima Dossa, Kelly Metcalfe, Rinku Sutradhar, Tari Little, Andrea Eisen, Kathy Chun, Wendy S. Meschino, Lea Velsher, Jordan Lerner Ellis and Nancy N. Baxter

September 21, 2021 9 (3) E874-E885; DOI: https://doi.org/10.9778/cmajo.20200228
Open Access
Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening
Christina Blagojevic, Tracy Heung, Mylene Theriault, Aoy Tomita-Mitchell, Pranesh Chakraborty, Kristin Kernohan, Dennis E. Bulman and Anne S. Bassett

August 17, 2021 9 (3) E802-E809; DOI: https://doi.org/10.9778/cmajo.20200294
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Genetic testing in families with hereditary colorectal cancer in British Columbia and Yukon: a retrospective cross-sectional analysis
Vivienne K. Beard, Angela C. Bedard, Jennifer Nuk, Petra W.C. Lee, Quan Hong, James E.J. Bedard, Sophie Sun and Kasmintan A. Schrader

October 19, 2020 8 (4) E637-E642; DOI: https://doi.org/10.9778/cmajo.20190167
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Benefits, challenges and ethical principles associated with implementing noninvasive prenatal testing: a Delphi study
Charles Dupras, Stanislav Birko, Aliya Affdal, Hazar Haidar, Marie-Eve Lemoine and Vardit Ravitsky

October 31, 2018 6 (4) E513-E519; DOI: https://doi.org/10.9778/cmajo.20180083
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Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive study
Tianhua Huang, Shelley Dougan, Mark Walker, Christine M. Armour and Nan Okun

October 05, 2018 6 (4) E436-E444; DOI: https://doi.org/10.9778/cmajo.20180046
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Introducing pharmacogenetic testing with clinical decision support into primary care: a feasibility study
Martin Dawes, Martin N. Aloise, J. Sidney Ang, Pieter Cullis, Diana Dawes, Robert Fraser, Gideon Liknaitzky, Andrea Paterson, Paul Stanley, Adriana Suarez-Gonzalez and Hagit Katzov-Eckert

September 22, 2016 4 (3) E528-E534; DOI: https://doi.org/10.9778/cmajo.20150070

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