Patient-physician relationships, health self-efficacy, and gynecologic cancer screening among women with Lynch syndrome by Kaitlin M. McGarragle, Melyssa Aronson, Kara Semotiuk, Spring Holter, Crystal J. Hare, Sarah E. Ferguson, Zane Cohen, Tae L. Hart

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P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results by Salma Shickh, Rita Kodida, Chloe Mighton, Marc Clausen, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Kevin Thorpe, Jordan Lerner-Ellis, Raymond Kim, Yvonne Bombard

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P862: How to conduct equitable genetics research to include underserved populations: A systematic review of best practices by Vernie Aguda, Sonya Grewal, Arielle Nsenga, Daena Hirjikaka, Saumeh Saeedi, Emma Reble, Marc Clausen, Charles Law, Francine Holness, Kristal John, Tracy Reece, Aaron Pollett, Aisha Lofters, Ambreen Sayani, Andrea Eisen, David Lightfoot, Harriet Feilotter, Jordan Lerner-Ellis, Melyssa Aronson, Nav Persaud, Yvonne Bombard

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P406: Partnering with patients to explore the psychosocial and socioeconomic impacts of hereditary cancer syndromes by Jordan Sam, Holly Etchegary, Marc Clausen, Derrick Bishop, Julee Pauling, Claudia Pavao, Catriona Remocker, Teresa Tiano, Angelina Tilley, Chloe Mighton, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Melyssa Aronson, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Sevtap Savas, Sophie Sun, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard

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P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN) by Lauren Hughes, Kirsten Farncombe, Michelle Brazas, Melyssa Aronson, Kathleen Bell, Brandon Chan, Andrea Eisen, Harriet Feilotter, Bailey Gallinger, Jordan Lerner-Ellis, David Malkin, Ellen MacDougall, Steven Narod, Karen Panabaker, Trevor Pugh, Sarah Sawyer, Alison Rusnak, Andrea Vaags, Laszlo Radvanyi, Lincoln Stein, Raymond Kim

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Additional germline findings from a tumor profiling program by Neda Stjepanovic, Tracy L. Stockley, Philippe L. Bedard, Jeanna M. McCuaig, Melyssa Aronson, Spring Holter, Kara Semotiuk, Natasha B. Leighl, Raymond Jang, Monika K. Krzyzanowska, Amit M. Oza, Abha Gupta, Christine Elser, Lailah Ahmed, Lisa Wang, Suzanne Kamel-Reid, Lillian L. Siu, Raymond H. Kim

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P375: Fragmented systems of care: An overview of Canadian health system care models for hereditary cancer syndromes by Jordan Sam, Carly Butkowsky, Marc Clausen, Chloe Mighton, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Julee Pauling, Claudia Pavao, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

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P892: “Should I let them know I have this?”: Concerns and experiences of genetic discrimination amongst individuals with hereditary cancer syndromes by Ridhi Gopalakrishnan, Emma Reble, Jordan Sam, Carly Butkowsky, Marc Clausen, Sepideh Rajeziesfahani, Brooklyn Sparkes, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

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P881: Revealing the hidden costs: Exploring the financial toxicity of hereditary cancer syndromes by Sepideh Rajeziesfahani, Jordan Sam, Carly Butkowsky, Emma Reble, Marc Clausen, Brooklyn Sparkes, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard, Holly Etchegary

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P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT by Yvonne Bombard, Chloe Mighton, Salma Shickh, Marc Clausen, Rita Kodida, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Nicole Forster, Jose-Mario Capo-Chichi, Elena Greenfeld, Abdul Noor, Iris Cohn, Chantal Morel, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Jordan Lerner-Ellis, Raymond Kim, Kevin Thorpe

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P867: “I worry I don’t have control”: The psychosocial impacts of living with a hereditary cancer syndrome by Jordan Sam, Brooklyn Sparkes, Marc Clausen, Carly Butkowsky, Emma Reble, Sepideh Rajeziesfahani, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Yvonne Bombard, Holly Etchegary

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P555: Clinical utility returning of all types of medically relevant genomic sequencing findings: An observational study by Chloe Mighton, Rita Kodida, Salma Shickh, Marc Clausen, Emma Reble, Jordan Sam, Sonya Grewal, Seema Panchal, Melyssa Aronson, Susan Armel, Tracy Graham, Nicole Forster, Jose-Mario Capo-Chichi, Elena Greenfeld, Abdul Noor, Iris Cohn, Chantal Morel, Christine Elser, Andrea Eisen, June Carroll, Emily Glogowski, Kasmintan Schrader, Kelvin Chan, Kevin Thorpe, Jordan Lerner-Ellis, Raymond Kim, Yvonne Bombard

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P553: How do patients with hereditary cancer syndromes navigate the healthcare system? A qualitative comparative study across Canada by Carly Butkowsky, Jordan Sam, Emma Reble, Marc Clausen, Sepideh Rajeziesfahani, Brooklyn Sparkes, Ridhi Gopalakrishnan, Vernie Aguda, Melyssa Aronson, June Carroll, Derrick Bishop, Lesa Dawson, Andrea Eisen, Tracy Graham, Jane Green, Chloe Mighton, Julee Pauling, Claudia Pavao, Petros Pechlivanoglou, Catriona Remocker, Sevtap Savas, Sophie Sun, Teresa Tiano, Angelina Tilley, Kevin Thorpe, Kasmintan Schrader, Holly Etchegary, Yvonne Bombard

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Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium by Pål Møller, Toni Seppälä, James G. Dowty, Saskia Haupt, Mev Dominguez-Valentin, Lone Sunde, Inge Bernstein, Christoph Engel, Stefan Aretz, Maartje Nielsen, Gabriel Capella, Dafydd Gareth Evans, John Burn, Elke Holinski-Feder, Lucio Bertario, Bernardo Bonanni, Annika Lindblom, Zohar Levi, Finlay Macrae, Ingrid Winship, John-Paul Plazzer, Rolf Sijmons, Luigi Laghi, Adriana Della Valle, Karl Heinimann, Elizabeth Half, Francisco Lopez-Koestner, Karin Alvarez-Valenzuela, Rodney J. Scott, Lior Katz, Ido Laish, Elez Vainer, Carlos Alberto Vaccaro, Dirce Maria Carraro, Nathan Gluck, Naim Abu-Freha, Aine Stakelum, Rory Kennelly, Des Winter, Benedito Mauro Rossi, Marc Greenblatt, Mabel Bohorquez, Harsh Sheth, Maria Grazia Tibiletti, Leonardo S. Lino-Silva, Karoline Horisberger, Carmen Portenkirchner, Ivana Nascimento, Norma Teresa Rossi, Leandro Apolinário da Silva, Huw Thomas, Attila Zaránd, Jukka-Pekka Mecklin, Kirsi Pylvänäinen, Laura Renkonen-Sinisalo, Anna Lepisto, Päivi Peltomäki, Christina Therkildsen, Lars Joachim Lindberg, Ole Thorlacius-Ussing, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Verena Steinke-Lange, Wolff Schmiegel, Deepak Vangala, Claudia Perne, Robert Hüneburg, Aída Falcón de Vargas, Andrew Latchford, Anne-Marie Gerdes, Ann-Sofie Backman, Carmen Guillén-Ponce, Carrie Snyder, Charlotte K. Lautrup, David Amor, Edenir Palmero, Elena Stoffel, Floor Duijkers, Michael J. Hall, Heather Hampel, Heinric Williams, Henrik Okkels, Jan Lubiński, Jeanette Reece, Joanne Ngeow, Jose G. Guillem, Julie Arnold, Karin Wadt, Kevin Monahan, Leigha Senter, Lene J. Rasmussen, Liselotte P. van Hest, Luigi Ricciardiello, Maija R. J. Kohonen-Corish, Marjolijn J. L. Ligtenberg, Melissa Southey, Melyssa Aronson, Mohd N. Zahary, N. Jewel Samadder, Nicola Poplawski, Nicoline Hoogerbrugge, Patrick J. Morrison, Paul James, Grant Lee, Rakefet Chen-Shtoyerman, Ravindran Ankathil, Rish Pai, Robyn Ward, Susan Parry, Tadeusz Dębniak, Thomas John, Thomas van Overeem Hansen, Trinidad Caldés, Tatsuro Yamaguchi, Verónica Barca-Tierno, Pilar Garre, Giulia Martina Cavestro, Jürgen Weitz, Silke Redler, Reinhard Büttner, Vincent Heuveline, John L. Hopper, Aung Ko Win, Noralane Lindor, Steven Gallinger, Loïc Le Marchand, Polly A. Newcomb, Jane Figueiredo, Daniel D. Buchanan, Stephen N. Thibodeau, Sanne W. ten Broeke, Eivind Hovig, Sigve Nakken, Marta Pineda, Nuria Dueñas, Joan Brunet, Kate Green, Fiona Lalloo, Katie Newton, Emma J. Crosbie, Miriam Mints, Douglas Tjandra, Florencia Neffa, Patricia Esperon, Revital Kariv, Guy Rosner, Walter Hernán Pavicic, Pablo Kalfayan, Giovana Tardin Torrezan, Thiago Bassaneze, Claudia Martin, Gabriela Moslein, Aysel Ahadova, Matthias Kloor, Julian R. Sampson, Mark A. Jenkins, The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC)

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