The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists
Boycott, Kym, Hartley, Taila, Adam, Shelin, Bernier, Francois, Chong, Karen, Fernandez, Bridget A, Friedman, Jan M, Geraghty, Michael T, Hume, Stacey, Knoppers, Bartha M, Laberge, Anne-Marie, Majewski, Jacek, Mendoza-Londono, Roberto, Meyn, M Stephen, Michaud, Jacques L, Nelson, Tanya N, Richer, Julie, Sadikovic, Bekim, Skidmore, David L, Stockley, Tracy, Taylor, Sherry, van Karnebeek, Clara, Zawati, Ma'n H, Lauzon, Julie, Armour, Christine M
Published in Journal of medical genetics (01.07.2015)
Published in Journal of medical genetics (01.07.2015)
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Journal Article
Deep learning prediction of renal anomalies for prenatal ultrasound diagnosis
Miguel, Olivier X, Kaczmarek, Emily, Lee, Inok, Ducharme, Robin, Dingwall-Harvey, Alysha L J, Rennicks White, Ruth, Bonin, Brigitte, Aviv, Richard I, Hawken, Steven, Armour, Christine M, Dick, Kevin, Walker, Mark C
Published in Scientific reports (19.04.2024)
Published in Scientific reports (19.04.2024)
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Journal Article
Pregnancies with ‘double-positive’ multiple marker screening results: a population-based study in Ontario, Canada
Bellai-Dussault, Kara, Dougan, Shelley D., Fell, Deshayne B., Hawken, Steven, Huang, Tianhua, Venegas, Carolina Lavin, Little, Julian, Meng, Lynn, Okun, Nan, Walker, Mark, Armour, Christine M., POTTER, Beth K.
Published in BMC pregnancy and childbirth (06.09.2024)
Published in BMC pregnancy and childbirth (06.09.2024)
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Journal Article
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
Lowther, Chelsea, Speevak, Marsha, Armour, Christine M., Goh, Elaine S., Graham, Gail E., Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata J.M., Schultz, Lee-Anne, Morra, Antonella, Nicolson, Rob, Bikangaga, Peter, Samdup, Dawa, Zaazou, Mostafa, Boyd, Kerry, Jung, Jack H., Siu, Victoria, Rajguru, Manjulata, Goobie, Sharan, Tarnopolsky, Mark A., Prasad, Chitra, Dick, Paul T., Hussain, Asmaa S., Walinga, Margreet, Reijenga, Renske G., Gazzellone, Matthew, Lionel, Anath C., Marshall, Christian R., Scherer, Stephen W., Stavropoulos, Dimitri J., McCready, Elizabeth, Bassett, Anne S.
Published in Genetics in medicine (01.01.2017)
Published in Genetics in medicine (01.01.2017)
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Journal Article
Expanding the clinical spectrum of autosomal‐recessive renal tubular dysgenesis: Two siblings with neonatal survival and review of the literature
Vincent, Krista M., Alrajhi, Afrah, Lazier, Joanna, Bonin, Brigitte, Lawrence, Sarah, Weiler, Gabrielle, Armour, Christine M.
Published in Molecular genetics & genomic medicine (01.05.2022)
Published in Molecular genetics & genomic medicine (01.05.2022)
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Journal Article
Cardio-facio-cutaneous syndrome: Does genotype predict phenotype?
Allanson, Judith E., Annerén, Göran, Aoki, Yoki, Armour, Christine M., Bondeson, Marie-Louise, Cave, Helene, Gripp, Karen W., Kerr, Bronwyn, Nystrom, Anna-Maja, Sol-Church, Katia, Verloes, Alain, Zenker, Martin
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2011)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (15.05.2011)
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Journal Article
Joint SOGC–CCMG Opinion for Reproductive Genetic Carrier Screening: An Update for All Canadian Providers of Maternity and Reproductive Healthcare in the Era of Direct-to-Consumer Testing
Wilson, R. Douglas, MD, De Bie, Isabelle, MD, PhD, Armour, Christine M., MD, Brown, Richard N., MD, Campagnolo, Carla, MSc, Carroll, June C., MD, Okun, Nan, MD, Nelson, Tanya, PhD, Zwingerman, Rhonda, MD
Published in Journal of obstetrics and gynaecology Canada (01.08.2016)
Published in Journal of obstetrics and gynaecology Canada (01.08.2016)
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Journal Article
Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada
Armour, Christine M, Dougan, Shelley Danielle, Brock, Jo-Ann, Chari, Radha, Chodirker, Bernie N, DeBie, Isabelle, Evans, Jane A, Gibson, William T, Kolomietz, Elena, Nelson, Tanya N, Tihy, Frédérique, Thomas, Mary Ann, Stavropoulos, Dimitri J
Published in Journal of medical genetics (01.04.2018)
Published in Journal of medical genetics (01.04.2018)
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Journal Article
Application of exome sequencing for prenatal diagnosis: a rapid scoping review
Pratt, Misty, Garritty, Chantelle, Thuku, Micere, Esmaeilisaraji, Leila, Hamel, Candyce, Hartley, Taila, Millar, Kathryn, Skidmore, Becky, Dougan, Shelley, Armour, Christine M
Published in Genetics in medicine (01.12.2020)
Published in Genetics in medicine (01.12.2020)
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Journal Article
Clinical application of fetal genome-wide sequencing during pregnancy: position statement of the Canadian College of Medical Geneticists
Lazier, Joanna, Hartley, Taila, Brock, Jo-Ann, Caluseriu, Oana, Chitayat, David, Laberge, Anne-Marie, Langlois, Sylvie, Lauzon, Julie, Nelson, Tanya N, Parboosingh, Jillian, Stavropoulos, Dimitri J, Boycott, Kym, Armour, Christine M
Published in Journal of medical genetics (01.10.2022)
Published in Journal of medical genetics (01.10.2022)
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Journal Article
Conference Proceeding
Cytogenetic outcomes following a failed cell-free DNA screen: a population-based retrospective cohort study of 35,146 singleton pregnancies
Bellai-Dussault, Kara, Meng, Lynn, Howley, Heather, Reszel, Jessica, Huang, Tianhua, Lanes, Andrea, Walker, Mark C., Okun, Nan, Dougan, Shelley D., Armour, Christine M.
Published in American journal of obstetrics and gynecology (01.08.2023)
Published in American journal of obstetrics and gynecology (01.08.2023)
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Journal Article
Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome
Aref‐Eshghi, Erfan, Bourque, Danielle K., Kerkhof, Jennifer, Carere, Deanna Alexis, Ainsworth, Peter, Sadikovic, Bekim, Armour, Christine M., Lin, Hanxin
Published in Human mutation (01.10.2019)
Published in Human mutation (01.10.2019)
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Journal Article
CAManim: Animating end-to-end network activation maps
Kaczmarek, Emily, Miguel, Olivier X, Bowie, Alexa C, Ducharme, Robin, Dingwall-Harvey, Alysha L. J, Hawken, Steven, Armour, Christine M, Walker, Mark C, Dick, Kevin
Published in PloS one (18.06.2024)
Published in PloS one (18.06.2024)
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Journal Article
First and second trimester maternal serum markers for prenatal aneuploidy screening: An update on the adjustment factors for race, smoking, and insulin dependent diabetes mellitus
Huang, Tianhua, Bellai-Dussault, Kara, Meng, Lynn, Hull, Danna, Howley, Heather, Reszel, Jessica, Lanes, Andrea, Walker, Mark, Armour, Christine M., Okun, Nan, Dougan, Shelley D.
Published in Clinical biochemistry (01.08.2023)
Published in Clinical biochemistry (01.08.2023)
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Journal Article
Performance of a universal prenatal screening program incorporating cell-free fetal DNA analysis in Ontario, Canada
Dougan, Shelley D, Okun, Nan, Bellai-Dussault, Kara, Meng, Lynn, Howley, Heather E, Huang, Tianhua, Reszel, Jessica, Lanes, Andrea, Walker, Mark C, Armour, Christine M
Published in Canadian Medical Association journal (CMAJ) (03.08.2021)
Published in Canadian Medical Association journal (CMAJ) (03.08.2021)
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Journal Article
Survey of Prenatal Counselling Practices Regarding Aneuploidy Risk Modification, Invasive Diagnostic Procedure Risks, and Procedure Eligibility Criteria in Canadian Centres
Hull, Danna, MSc, CCGC, CGC, Davies, Gregory, MD, FRCSC, FACOG, Armour, Christine M., MSc, MD, FRCPC, FCCMG
Published in Journal of obstetrics and gynaecology Canada (01.07.2012)
Published in Journal of obstetrics and gynaecology Canada (01.07.2012)
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Journal Article
The value of diagnostic testing for parents of children with rare genetic diseases
Marshall, Deborah A, MacDonald, Karen V, Heidenreich, Sebastian, Hartley, Taila, Bernier, Francois P, Gillespie, Meredith K, McInnes, Brenda, Innes, A Micheil, Armour, Christine M, Boycott, Kym M
Published in Genetics in medicine (01.12.2019)
Published in Genetics in medicine (01.12.2019)
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Journal Article
Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment
Jiang, Shan, Anis, Aslam H, Cromwell, Ian, Mohammadi, Tima, Schrader, Kasmintan A, Lucas, Janet, Armour, Christine M, Clausen, Marc, Bombard, Yvonne, Regier, Dean A
Published in Genetics in medicine (01.12.2020)
Published in Genetics in medicine (01.12.2020)
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Journal Article