Clinical and psychological outcomes of receiving a variant of uncertain significance from multigene panel testing or genomic sequencing: a systematic review and meta-analysis von Mighton, Chloe, Shickh, Salma, Uleryk, Elizabeth, Pechlivanoglou, Petros, Bombard, Yvonne

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The clinical utility of exome and genome sequencing across clinical indications: a systematic review von Shickh, Salma, Mighton, Chloe, Uleryk, Elizabeth, Pechlivanoglou, Petros, Bombard, Yvonne

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Heath policy guiding the identification, analysis and management of secondary findings for individuals undergoing genomic sequencing: a systematic review protocol von Majeed, Safa, Mighton, Chloe, Malkin, David, Bombard, Yvonne

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Effect of genetics clinical decision support tools on health-care providers’ decision making: a mixed-methods systematic review von Sebastian, Agnes, Carroll, June C., Oldfield, Leslie E., Mighton, Chloe, Shickh, Salma, Uleryk, Elizabeth, Bombard, Yvonne

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Variant classification changes over time in BRCA1 and BRCA2 von Mighton, Chloe, Charames, George S., Wang, Marina, Zakoor, Kathleen-Rose, Wong, Andrew, Shickh, Salma, Watkins, Nicholas, Lebo, Matthew S., Bombard, Yvonne, Lerner-Ellis, Jordan

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From the patient to the population: Use of genomics for population screening von Mighton, Chloe, Shickh, Salma, Aguda, Vernie, Krishnapillai, Suvetha, Adi-Wauran, Ella, Bombard, Yvonne

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Widening the lens of actionability: A qualitative study of primary care providers' views and experiences of managing secondary genomic findings von Sebastian, Agnes, Carroll, June C, Vanstone, Meredith, Clausen, Marc, Kodida, Rita, Reble, Emma, Mighton, Chloe, Shickh, Salma, Aronson, Melyssa, Eisen, Andrea, Elser, Christine, Lerner-Ellis, Jordan, Kim, Raymond H, Bombard, Yvonne

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Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings von Reble, Emma, Gutierrez Salazar, Mariana, Zakoor, Kathleen-Rose, Khalouei, Sam, Clausen, Marc, Kodida, Rita, Shickh, Salma, Mighton, Chloe, Cohn, Iris, Schrader, Kasmintan A., Kim, Raymond H., Lerner-Ellis, Jordan, Bombard, Yvonne

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Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario von Lerner-Ellis, Jordan, Mighton, Chloe, Lazaro, Conxi, Watkins, Nicholas, Di Gioacchino, Vanessa, Wong, Andrew, Chang, Martin C., Charames, George S.

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Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial von Bombard, Yvonne, Clausen, Marc, Shickh, Salma, Mighton, Chloe, Casalino, Selina, Kim, Theresa H.M., Muir, Sarah M., Carlsson, Lindsay, Baxter, Nancy, Scheer, Adena, Elser, Christine, Eisen, Andrea, Panchal, Seema, Graham, Tracy, Aronson, Melyssa, Piccinin, Carolyn, Mancuso, Talia, Semotiuk, Kara, Evans, Michael, Carroll, June C., Offit, Kenneth, Robson, Mark, Hamilton, Jada G., Glogowski, Emily, Schrader, Kasmintan, Kim, Raymond H., Lerner-Ellis, Jordan, Thorpe, Kevin E., Laupacis, Andreas, Bombard, Yvonne, Armel, Susan, Aronson, Melyssa, Bayoumi, Ahmed, Bond, Ken, Caulfield, Timothy, Clausen, Marc, Clifford, Tammy, Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Elser, Christine, Isaranuwatchai, Wanrudee, Kastner, Monika, Kim, Raymond H., Mujoomdar, Michelle, Robson, Mark E., Scheer, Adena, Scherer, Stephen W., Schrader, Kasmintan, Sullivan, Terrence, Thorpe, Kevin E.

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Patient and public preferences for being recontacted with updated genomic results: a mixed methods study von Mighton, Chloe, Clausen, Marc, Sebastian, Agnes, Muir, Sarah M., Shickh, Salma, Baxter, Nancy N., Scheer, Adena, Glogowski, Emily, Schrader, Kasmintan A., Thorpe, Kevin E., Kim, Theresa H. M., Lerner-Ellis, Jordan, Kim, Raymond H., Regier, Dean A., Bayoumi, Ahmed M., Bombard, Yvonne

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The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care von Shickh, Salma, Rafferty, Sara A., Clausen, Marc, Kodida, Rita, Mighton, Chloe, Panchal, Seema, Lorentz, Justin, Ward, Thomas, Watkins, Nicholas, Elser, Christine, Eisen, Andrea, Carroll, June C., Glogowski, Emily, Schrader, Kasmintan A., Lerner-Ellis, Jordan, Kim, Raymond H., Chitayat, David, Shuman, Cheryl, Bombard, Yvonne, Bombard, Yvonne, Armel, Susan, Aronson, Melyssa, Baxter, Nancy, Bond, Kenneth, Capo-Chichi, José-Mario, Caulfield, Timothy, Clifford, Tammy, Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Evans, Mike, Graham, Tracy, Hamilton, Jada G., Isaranuwatchai, Wanrudee, Kastner, Monika, Laupacis, Andreas, Morel, Chantal F., Mujoomdar, Michelle, Offit, Kenneth, Robson, Mark E., Scheer, Adena, Scherer, Stephen W., Sullivan, Terrence, Thorpe, Kevin E.

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Correction to: Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario von Lerner-Ellis, Jordan, Mighton, Chloe, Lazaro, Conxi, Watkins, Nicholas, Di Gioacchino, Vanessa, Wong, Andrew, Chang, Martin C., Charames, George S.

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Quality of life drives patients' preferences for secondary findings from genomic sequencing von Mighton, Chloe, Carlsson, Lindsay, Clausen, Marc, Casalino, Selina, Shickh, Salma, McCuaig, Laura, Joshi, Esha, Panchal, Seema, Semotiuk, Kara, Ott, Karen, Elser, Christine, Eisen, Andrea, Kim, Raymond H, Lerner-Ellis, Jordan, Carroll, June C, Glogowski, Emily, Schrader, Kasmintan, Bombard, Yvonne

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Primary care provider perspectives on using genomic sequencing in the care of healthy children von Joshi, Esha, Mighton, Chloe, Clausen, Marc, Casalino, Selina, Kim, Theresa H M, Kowal, Christine, Birken, Catherine, Maguire, Jonathon L, Bombard, Yvonne

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Development of patient "profiles" to tailor counseling for incidental genomic sequencing results von Mighton, Chloe, Carlsson, Lindsay, Clausen, Marc, Casalino, Selina, Shickh, Salma, McCuaig, Laura, Joshi, Esha, Panchal, Seema, Graham, Tracy, Aronson, Melyssa, Piccinin, Carolyn, Winter-Paquette, Laura, Semotiuk, Kara, Lorentz, Justin, Mancuso, Talia, Ott, Karen, Silberman, Yael, Elser, Christine, Eisen, Andrea, Kim, Raymond H, Lerner-Ellis, Jordan, Carroll, June C, Glogowski, Emily, Schrader, Kasmintan, Bombard, Yvonne

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Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery von Shickh, Salma, Hirjikaka, Daena, Clausen, Marc, Kodida, Rita, Mighton, Chloe, Reble, Emma, Sam, Jordan, Panchal, Seema, Aronson, Melyssa, Graham, Tracy, Armel, Susan Randall, Glogowski, Emily, Elser, Christine, Eisen, Andrea, Carroll, June C, Shuman, Cheryl, Seto, Emily, Baxter, Nancy N, Scheer, Adena, Shastri-Estrada, Serena, Feldman, Geoff, Thorpe, Kevin E, Schrader, Kasmintan A, Lerner-Ellis, Jordan, Kim, Raymond H, Faghfoury, Hanna, Bombard, Yvonne

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P782: Validation of low-pass genome sequencing for prenatal diagnosis von Mighton, Chloe, Noor, Abdul, Watkins, Nicholas, Di Gioacchino, Vanessa, Lerner-Ellis, Jordan, Wong, Andrew, Anggala, Nina, Chitayat, David, Greenfeld, Elena

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P539: International policies guiding the identification, analysis, and management of secondary findings from genomic sequencing: Results from a systematic review von Majeed, Safa, Johnston, Christine, Saeedi, Saumeh, Mighton, Chloe, Rokoszak, Vanessa, Abbasi, Ilham, Grewal, Sonya, Aguda, Vernie, Malkin, David, Bombard, Yvonne

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Recontacting clinical genetics patients with reclassified results: equity and policy challenges von Bombard, Yvonne, Mighton, Chloe

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