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16 results on '"Carroll, June C."'

1. Genetics providers’ perspectives on the use of digital tools in clinical practice

Author

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., Lee, Whiwon, Hirjikaka, Daena, Grewal, Sonya, and Shaw, Angela

Published
2024
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2. Opportunistic genomic screening has clinical utility: An interventional cohort study

Author

Bombard, Yvonne, Armel, Susan Randall, Aronson, Melyssa, Baxter, Nancy N., Bond, Kenneth, Capo-Chichi, José-Mario, Carroll, June C., Caulfield, Timothy, Clausen, Marc, Clifford, Tammy J., Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Eisen, Andrea, Elser, Christine, Evans, Michael, Glogowski, Emily, Graham, Tracy, Greenfeld, Elena, Hamilton, Jada G., Isaranuwatchai, Wanrudee, Kastner, Monika, Kim, Raymond H., Lerner-Ellis, Jordan, Morel, Chantal F., Mujoomdar, Michelle, Noor, Abdul, Offit, Kenneth, Panchal, Seema, Robson, Mark E., Scherer, Stephen W., Scheer, Adena, Schrader, Kasmintan A., Sullivan, Terrence, Thorpe, Kevin E., Mighton, Chloe, Kodida, Rita, Shickh, Salma, Reble, Emma, Sam, Jordan, Grewal, Sonya, Hirjikaka, Daena, Piccinin, Carolyn, Ward, Thomas, Hofstedter, Renee, Mancuso, Talia, Forster, Nicole, Glogowksi, Emily, and Chan, Kelvin K.W.

Published
2024
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3. “I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing

Author

Bombard, Yvonne, Armel, Susan Randall, Aronson, Melyssa, Baxter, Nancy N., Bond, Kenneth, Capo-Chichi, José-Mario, Carroll, June C., Caulfield, Timothy, Clausen, Marc, Clifford, Tammy J., Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Eisen, Andrea, Elser, Christine, Evans, Michael, Glogowski, Emily, Graham, Tracy, Greenfeld, Elena, Hamilton, Jada G., Isaranuwatchai, Wanrudee, Kastner, Monika, Kim, Raymond H., Laupacis, Andreas, Lerner-Ellis, Jordan, Morel, Chantal F., Mujoomdar, Michelle, Noor, Abdul, Offit, Kenneth, Panchal, Seema, Robson, Mark E., Scherer, Stephen W., Scheer, Adena, Schrader, Kasmintan A., Sullivan, Terrence, Thorpe, Kevin E., Shickh, Salma, Mighton, Chloe, Kodida, Rita, Adi-Wauran, Ella, Hirjikaka, Daena, Krishnapillai, Suvetha, Reble, Emma, and Sam, Jordan

Published
2023
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4. The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care

Author

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, 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, and Thorpe, Kevin E.

Published
2021
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6. Effectiveness of the Genomics ADvISER decision aid for the selection of secondary findings from genomic sequencing: a randomized clinical trial

Author

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, Armel, Susan, Bayoumi, Ahmed, Bond, Ken, Caulfield, Timothy, Clifford, Tammy, Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Isaranuwatchai, Wanrudee, Kastner, Monika, Mujoomdar, Michelle, Robson, Mark E., Scherer, Stephen W., and Sullivan, Terrence

Published
2020
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8. “I don’t need any more unknowns hanging over my head”: Cancer patients’ views on variants of uncertain significance and low/moderate risk results from genomic sequencing

Author

Shickh, Salma, primary, Mighton, Chloe, additional, Clausen, Marc, additional, Kodida, Rita, additional, Adi-Wauran, Ella, additional, Hirjikaka, Daena, additional, Krishnapillai, Suvetha, additional, Reble, Emma, additional, Sam, Jordan, additional, Baxter, Nancy N., additional, Laupacis, Andreas, additional, Bombard, Yvonne, additional, Armel, Susan Randall, additional, Aronson, Melyssa, additional, Bond, Kenneth, additional, Capo-Chichi, José-Mario, additional, Carroll, June C., additional, Caulfield, Timothy, additional, Clifford, Tammy J., additional, Cohn, Iris, additional, Dhalla, Irfan, additional, Earle, Craig C., additional, Eisen, Andrea, additional, Elser, Christine, additional, Evans, Michael, additional, Glogowski, Emily, additional, Graham, Tracy, additional, Greenfeld, Elena, additional, Hamilton, Jada G., additional, Isaranuwatchai, Wanrudee, additional, Kastner, Monika, additional, Kim, Raymond H., additional, Lerner-Ellis, Jordan, additional, Morel, Chantal F., additional, Mujoomdar, Michelle, additional, Noor, Abdul, additional, Offit, Kenneth, additional, Panchal, Seema, additional, Robson, Mark E., additional, Scherer, Stephen W., additional, Scheer, Adena, additional, Schrader, Kasmintan A., additional, Sullivan, Terrence, additional, and Thorpe, Kevin E., additional

Published
2023
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11. Use of eConsult to enhance genetics service delivery in primary care: A multimethod study

Author

Carroll, June C., primary, Liddy, Clare, additional, Afkham, Amir, additional, Keely, Erin, additional, Goh, Elaine S., additional, Graham, Gail E., additional, Permaul, Joanne A., additional, Allanson, Judith, additional, Heisey, Ruth, additional, Makuwaza, Tutsirai, additional, Manca, Donna P., additional, O’Brien, Mary Ann, additional, and Grunfeld, Eva, additional

Published
2022
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13. Ensuring best practice in genomics education and evaluation: reporting item standards for education and its evaluation in genomics (RISE2 Genomics)

Author

Nisselle, Amy, primary, Janinski, Monika, additional, Martyn, Melissa, additional, McClaren, Belinda, additional, Kaunein, Nadia, additional, Maguire, Jane, additional, Riggs, Erin Rooney, additional, Barlow-Stewart, Kristine, additional, Belcher, Andrea, additional, Bernat, John A., additional, Best, Stephanie, additional, Bishop, Michelle, additional, Carroll, June C., additional, Cornel, Martina, additional, Dissanayake, Vajira H.W., additional, Dodds, Agnes, additional, Dunlop, Kate, additional, Garg, Gunjan, additional, Gear, Russell, additional, Graves, Debra, additional, Knight, Ken, additional, Korf, Bruce, additional, Kumar, Dhavendra, additional, Laurino, Mercy, additional, Ma, Alan, additional, Mallett, Andrew, additional, McCarthy, Maria, additional, McEwen, Alison, additional, Mulder, Nicola, additional, Patel, Chirag, additional, Quinlan, Catherine, additional, Reed, Kate, additional, Sinnerbrink, Ingrid, additional, Slavotinek, Anne, additional, Suppiah, Vijayaprakash, additional, Terrill, Bronwyn, additional, Tobias, Edward S., additional, Tonkin, Emma, additional, Trumble, Steve, additional, Wessels, Tina-Marie, additional, Metcalfe, Sylvia, additional, Jordan, Helen, additional, and Gaff, Clara, additional

Published
2021
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14. Opportunistic genomic screening has clinical utility: An interventional cohort study

Author

Mighton, Chloe, Kodida, Rita, Shickh, Salma, Clausen, Marc, Reble, Emma, Sam, Jordan, Grewal, Sonya, Hirjikaka, Daena, Panchal, Seema, Piccinin, Carolyn, Aronson, Melyssa, Ward, Thomas, Armel, Susan Randall, Hofstedter, Renee, Graham, Tracy, Mancuso, Talia, Forster, Nicole, Capo-Chichi, José-Mario, Greenfeld, Elena, Noor, Abdul, Cohn, Iris, Morel, Chantal F., Elser, Christine, Eisen, Andrea, Carroll, June C., Glogowksi, Emily, Schrader, Kasmintan A., Chan, Kelvin K.W., Thorpe, Kevin E., Lerner-Ellis, Jordan, Kim, Raymond H., and Bombard, Yvonne

Abstract

Practice is shifting toward genome-first approaches, such as opportunistic screening for secondary findings (SFs). Analysis of SFs could be extended beyond medically actionable results to include non-medically actionable monogenic disease risks, carrier status, pharmacogenomic variants, and risk variants for common complex disease. However, evidence on the clinical utility of returning these results is lacking. We assessed the outcomes of opportunistic screening for a broad spectrum of SFs by evaluating the yield, impact on clinical management, and consistency between SFs and participants’ clinical features and family history.

Published
2024
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15. Genetics providers’ perspectives on the use of digital tools in clinical practice

Author

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, and Ungar, Wendy J.

Abstract

Digital tools are increasingly incorporated into genetics practice to address challenges with the current model of care. Yet, genetics providers’ perspectives on digital tool use are not well characterized.

Published
2024
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16. “I don’t need any more unknowns hanging over my head”: Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing

Author

Shickh, Salma, Mighton, Chloe, Clausen, Marc, Kodida, Rita, Adi-Wauran, Ella, Hirjikaka, Daena, Krishnapillai, Suvetha, Reble, Emma, Sam, Jordan, Baxter, Nancy N., Laupacis, Andreas, Bombard, Yvonne, Bombard, Yvonne, Armel, Susan Randall, Aronson, Melyssa, Baxter, Nancy N., Bond, Kenneth, Capo-Chichi, José-Mario, Carroll, June C., Caulfield, Timothy, Clausen, Marc, Clifford, Tammy J., Cohn, Iris, Dhalla, Irfan, Earle, Craig C., Eisen, Andrea, Elser, Christine, Evans, Michael, Glogowski, Emily, Graham, Tracy, Greenfeld, Elena, Hamilton, Jada G., Isaranuwatchai, Wanrudee, Kastner, Monika, Kim, Raymond H., Laupacis, Andreas, Lerner-Ellis, Jordan, Morel, Chantal F., Mujoomdar, Michelle, Noor, Abdul, Offit, Kenneth, Panchal, Seema, Robson, Mark E., Scherer, Stephen W., Scheer, Adena, Schrader, Kasmintan A., Sullivan, Terrence, and Thorpe, Kevin E.

Abstract

We sought to explore patient-reported utility of all types of cancer results from genomic sequencing (GS).

Published
2023
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