Increasing SARS-CoV-2 testing capacity through specimen pooling: An acute care center experience by Cabrera, Ana, Al Mutawah, Fatimah, Kadour, Mike, Schofield, Shannon, Conkey, Beverley, Fuller, Jeffrey, Payne, Michael, Elsayed, Sameer, Delport, Johan

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Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach by Bhai, Pratibha, Levy, Michael A., Rooney, Kathleen, Carere, Deanna Alexis, Reilly, Jack, Kerkhof, Jennifer, Volodarsky, Michael, Stuart, Alan, Kadour, Mike, Panabaker, Karen, Schenkel, Laila C., Lin, Hanxin, Ainsworth, Peter, Sadikovic, Bekim

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A Prediction Rule to Guide JAK2 Testing in Patients with Suspected Polycythemia Vera by Chin-Yee, Benjamin, Bhai, Pratibha, Cheong, Ian, Matyashin, Maxim, Hsia, Cyrus C., Kawata, Eri, Ho, Jenny, Lin, Hanxin, Chin-Yee, Ian, Kadour, Mike, Sadikovic, Bekim, Lazo-Langner, Alejandro

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Using pathology data to evaluate surgical backlogs: considerations for resource planning by Tran, Christopher, Kadour, Mike, Cecchini, Matthew J, Leslie, Ken A, Driman, David K

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A Rational Approach to JAK2 Mutation Testing in Patients with Elevated Hemoglobin: Results from the JAK2 Prediction Cohort (JAKPOT) Study by Chin-Yee, Benjamin, Bhai, Pratibha, Cheong, Ian, Matyashin, Maxim, Hsia, Cyrus C., Kawata, Eri, Ho, Jenny M., Levy, Michael A., Stuart, Alan, Lin, Hanxin, Chin-Yee, Ian, Kadour, Mike, Sadikovic, Bekim, Lazo-Langner, Alejandro

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Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders by Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., France, Groupe DI, Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christéle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer, Takano, Kyoko, Kleefstra, Tjitske, de Leeuw, Nicole, Field, Michael, Shaw, Marie, Gecz, Jozef, Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Friez, Michael J., Tedder, Matt, Lee, Jennifer A., DuPont, Barbara R., Stevenson, Roger E., Skinner, Steven A., Schwartz, Charles E., Genevieve, David, Sadikovic, Bekim

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Reducing cytogenetic testing in the era of next generation sequencing: Are we choosing wisely? by Kawata, Eri, Hedley, Benjamin D., Chin‐Yee, Benjamin, Xenocostas, Anargyros, Lazo‐Langner, Alejandro, Hsia, Cyrus C., Howson‐Jan, Kang, Yang, Ping, Levy, Michael A., Santos, Stephanie, Bhai, Pratibha, Howlett, Christopher, Lin, Hanxin, Kadour, Mike, Sadikovic, Bekim, Chin‐Yee, Ian

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