Christian R. Marshall - The Hospital for Sick Children and Department of Molecular Genetics, University of Toronto

Nicole Si Yan Liang,Gregory Costain, Alissa D'Gama,Amy McTague, Katherine Howell,Vann Chau, Sarah Mulhern,Annapurna Poduri,Ingrid Scheffer, Beth Sheidley, Meredith Curtis, Edward Higginbotham,

Genetics in Medicine Open (2024): 101201

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A Study on the Incidence and Prevalence of 5q Spinal Muscular Atrophy in Canada Using Multiple Data Sources

Tiffany R. Price,Victoria Hodgkinson, Grace Westbury,Lawrence Korngut,Micheil A. Innes,Christian R. Marshall,Tanya N. Nelson,Lijia Huang,Jillian Parboosingh,Jean K. Mah

CANADIAN JOURNAL OF NEUROLOGICAL SCIENCESpp.1-12, (2024)

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P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service

Meredith Gillespie,Robin Hayeems,Christian Marshall,Anna Szuto,Caitlin Chisholm, James Stavropoulos,Lijia Huang,Lynette Lau,Wilson Sung,Melanie Beaulieu Bergeron, Ted Higginbotham,Meredith Curtis,

Genetics in Medicine Open (2024): 101439

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P597: All for One Clinical Genomics Network: Linking Canadian diagnostic laboratories to share genome-wide sequencing data to support rare disease diagnosis

E. Magda Price,Meredith Gillespie, Caitlin Chisholm, Ruben Attali, Talia Silver,Anna Szuto, GSO Study Team, Jacques Michaud, Dennis Bulman,Jordan Lerner-Ellis, Ma'n Zawati, Vincent Ferretti,

Genetics in Medicine Open (2024): 101503

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P873: “If you look for a problem, you’ll find one”: A qualitative study to understand why parents/adult patients decline secondary findings

Abigail Hansen,Stephanie Luca, Olivia Moran, Riyana Babul-Hirji, Joyce Yan, Katharine Fooks, Viji Venkataramanan,Wendy Ungar,Robin Hayeems, Secondary Findings Study Team, Elise Poole, Daniel Assamad,

Genetics in Medicine Open (2024): 101787

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P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing

Katharine Fooks, Lydia Vermeer, Elise Poole,Stephanie Luca,Riyana Babul-Hirji,Lauren Chad,David Chitayat, Michael Mackley,Marci Schwartz,Wendy Ungar,Robin Hayeems, Secondary Findings Study Team,

Genetics in Medicine Open (2024): 101780

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P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape

Meredith Gillespie,Robin Hayeems,Christian Marshall,Anna Szuto,Caitlin Chisholm,Wendy Ungar, James Stavropoulos,Lijia Huang,Viji Venkataramanan,Lynette Lau,Wilson Sung,Melanie Beaulieu Bergeron,

Genetics in Medicine Open (2024): 101522

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