Attitudes Regarding Predictive Testing for Retinitis Pigmentosa von Mezer, Eedy, Babul-Hirji, Riyana, Wise, Richard, Chipman, Mary, DaSilva, Lisa, Rowell, Mary, Thackray, Robin, Shuman, Cheryl T., Levin, Alex V.

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Genetics providers’ perspectives on the use of digital tools in clinical practice von Lee, Whiwon, Hirjikaka, Daena, Grewal, Sonya, Shaw, Angela, Luca, Stephanie, Clausen, Marc, Bombard, Yvonne, Hayeems, Robin Z., Bombard, Yvonne, Hayeems, Robin Z., Aronson, Melyssa, Bernier, Francois, Brudno, Michael, Carroll, June C., Chad, Lauren, Clausen, Marc, Cohn, Ronald, Costain, Gregory, Dhalla, Irfan, Faghfoury, Hanna, Friedman, Jan, Hewson, Stacy, Jamieson, Trevor, Jobling, Rebekah, Kodida, Rita, Laberge, Anne-Marie, Lerner-Ellis, Jordan, Liston, Eriskay, Luca, Stephanie, Mamdani, Muhammad, Marshall, Christian R., Osmond, Matthew, Pham, Quynh, Reble, Emma, Rudzicz, Frank, Seto, Emily, Shastri-Estrada, Serena, Shuman, Cheryl, Silver, Josh, Smith, Maureen, Thorpe, Kevin, Ungar, Wendy J.

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Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR) von Lebo, Matthew S, Zakoor, Kathleen-Rose, Chun, Kathy, Speevak, Marsha D, Waye, John S, McCready, Elizabeth, Parboosingh, Jillian S, Lamont, Ryan E, Feilotter, Harriet, Bosdet, Ian, Tucker, Tracy, Young, Sean, Karsan, Aly, Charames, George S, Agatep, Ronald, Spriggs, Elizabeth L, Chisholm, Caitlin, Vasli, Nasim, Daoud, Hussein, Jarinova, Olga, Tomaszewski, Robert, Hume, Stacey, Taylor, Sherryl, Akbari, Mohammad R, Lerner-Ellis, Jordan

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Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations von Lerner-Ellis, Jordan, Wang, Marina, White, Shana, Lebo, Matthew S

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Natural history of Alström syndrome in early childhood: Onset with dilated cardiomyopathy von Michaud, Jacques L., Héon, Elise, Guilbert, Françoise, Weill, Jacques, Puech, Bernard, Benson, Lee, Smallhorn, Jeffrey F., Shuman, Cheryl T., Buncic, J.Raymond, Levin, Alex V., Weksberg, Rosanna, Brevière, Georges-Marie

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Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions von Fitzpatrick, Jennifer L., Hutton, Elaine M., Babul, Riyana, Cytrynbaum, Cheryl S., Sutherland, Joanne E., Shuman, Cheryl T.

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The Rickettsial Ankyrin Repeat Protein 2 Is a Type IV Secreted Effector That Associates with the Endoplasmic Reticulum von Lehman, Stephanie S, Noriea, Nicholas F, Aistleitner, Karin, Clark, Tina R, Dooley, Cheryl A, Nair, Vinod, Kaur, Simran Jeet, Rahman, M Sayeedur, Gillespie, Joseph J, Azad, Abdu F, Hackstadt, Ted

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Postreplication Roles of the Brucella VirB Type IV Secretion System Uncovered via Conditional Expression of the VirB11 ATPase von Smith, Erin P, Miller, Cheryl N, Child, Robert, Cundiff, Jennifer A, Celli, Jean

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Beckwith-Wiedemann syndrome von WEKSBERG, Rosanna, SHUMAN, Cheryl, BECKWITH, J. Bruce

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Chlamydia Hijacks ARF GTPases To Coordinate Microtubule Posttranslational Modifications and Golgi Complex Positioning von Wesolowski, Jordan, Weber, Mary M, Nawrotek, Agata, Dooley, Cheryl A, Calderon, Mike, St Croix, Claudette M, Hackstadt, Ted, Cherfils, Jacqueline, Paumet, Fabienne

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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test von Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Walker, Susan, Reuter, Miriam S, Hosseini, S Mohsen, Thiruvahindrapuram, Bhooma, Merico, Daniele, Jobling, Rebekah, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Sung, Wilson W L, Wang, Zhuozhi, Bikangaga, Peter, Boelman, Cyrus, Carter, Melissa T, Cordeiro, Dawn, Cytrynbaum, Cheryl, Dell, Sharon D, Dhir, Priya, Dowling, James J, Heon, Elise, Hewson, Stacy, Hiraki, Linda, Inbar-Feigenberg, Michal, Klatt, Regan, Kronick, Jonathan, Laxer, Ronald M, Licht, Christoph, MacDonald, Heather, Mercimek-Andrews, Saadet, Mendoza-Londono, Roberto, Piscione, Tino, Schneider, Rayfel, Schulze, Andreas, Silverman, Earl, Siriwardena, Komudi, Snead, O Carter, Sondheimer, Neal, Sutherland, Joanne, Vincent, Ajoy, Wasserman, Jonathan D, Weksberg, Rosanna, Shuman, Cheryl, Carew, Chris, Szego, Michael J, Hayeems, Robin Z, Basran, Raveen, Stavropoulos, Dimitri J, Ray, Peter N, Bowdin, Sarah, Meyn, M Stephen, Cohn, Ronald D, Scherer, Stephen W, Marshall, Christian R

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Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 2... von Bogatan, Simina, Shugar, Andrea, Wasim, Syed, Ball, Susan, Schmidt, Cathryn, Chitayat, David, Shuman, Cheryl, Cytrynbaum, Cheryl

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Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae von Guo, Lin, Choufani, Sanaa, Ferreira, Jose, Smith, Adam, Chitayat, David, Shuman, Cheryl, Uxa, Ruchita, Keating, Sarah, Kingdom, John, Weksberg, Rosanna

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Prenatally diagnosed omphaloceles: Report of 92 cases and association with Beckwith‐Wiedemann syndrome von Abbasi, Nimrah, Moore, Aideen, Chiu, Priscilla, Ryan, Greg, Weksberg, Rosanna, Shuman, Cheryl, Steele, Leslie, Chitayat, David

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Encystation of Entamoeba histolytica in Axenic Culture von Wesel, Jordan, Shuman, Jennifer, Bastuzel, Item, Dickerson, Julie, Ingram-Smith, Cheryl

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Abstract B04: Three distinct subgroups of Wilms’ tumors with novel molecular features and important clinical implications are defined by genome-wide DNA methylation profiles von Brzezinski, Jack, Choufani, Sanaa, Romao, Rodrigo, Shuman, Cheryl, Chen, Haiying, Grant, Ronald, Lorenzo, Armando, Weksberg, Rosanna

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Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing von Costain, Gregory, Jobling, Rebekah, Walker, Susan, Reuter, Miriam S, Snell, Meaghan, Bowdin, Sarah, Cohn, Ronald D, Dupuis, Lucie, Hewson, Stacy, Mercimek-Andrews, Saadet, Shuman, Cheryl, Sondheimer, Neal, Weksberg, Rosanna, Yoon, Grace, Meyn, M Stephen, Stavropoulos, Dimitri J, Scherer, Stephen W, Mendoza-Londono, Roberto, Marshall, Christian R

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Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome von Cytrynbaum, Cheryl, Chong, Karen, Hannig, Vickie, Choufani, Sanaa, Shuman, Cheryl, Steele, Leslie, Morgan, Thomas, Scherer, Stephen W., Stavropoulos, Dimitri J., Basran, Raveen K., Weksberg, Rosanna

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Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment von Patai, E Zita, Javadi, Amir-Homayoun, Ozubko, Jason D, O’Callaghan, Andrew, Ji, Shuman, Robin, Jessica, Grady, Cheryl, Winocur, Gordon, Rosenbaum, R Shayna, Moscovitch, Morris, Spiers, Hugo J

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Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations von D'Amours, Guylaine, Clausen, Marc, Luca, Stephanie, Reble, Emma, Kodida, Rita, Assamad, Daniel, Bernier, Francois, Chad, Lauren, Costain, Gregory, Dhalla, Irfan, Faghfoury, Hanna, Friedman, Jan M, Hewson, Stacy, Jamieson, Trevor, Silver, Josh, Shuman, Cheryl, Osmond, Matthew, Carroll, June C, Jobling, Rebekah, Laberge, Anne-Marie, Aronson, Melyssa, Liston, Eriskay, Lerner-Ellis, Jordan, Marshall, Christian, Brudno, Michael, Pham, Quynh, Rudzicz, Frank, Cohn, Ronald, Mamdani, Muhammad, Smith, Maureen, Shastri-Estrada, Serena, Seto, Emily, Thorpe, Kevin, Ungar, Wendy, Hayeems, Robin Z, Bombard, Yvonne

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