Search Results - "Clausen, Marc"

Patient-facing digital tools for delivering genetic services: a systematic review by Whiwon, Lee, Salma, Shickh, Daniel, Assamad, Stephanie, Luca, Marc, Clausen, Cherith, Somerville, Abby, Tafler, Angela, Shaw, Robin, Hayeems, Yvonne, Bombard

“…This study systematically reviewed the literature on the impact of digital genetics tools on patient care and system efficiencies. MEDLINE and Embase were…”
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Greenotyper: Image-Based Plant Phenotyping Using Distributed Computing and Deep Learning by Tausen, Marni, Clausen, Marc, Moeskjær, Sara, Shihavuddin, Asm, Dahl, Anders Bjorholm, Janss, Luc, Andersen, Stig Uggerhøj

“…Image-based phenotype data with high temporal resolution offers advantages over end-point measurements in plant quantitative genetics experiments, because…”
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P564: Doing no harm: Exploring the psychosocial impacts of receiving secondary findings from whole exome sequencing by Rokoszak, Vanessa, Hirjikaka, Daena, Clausen, Marc, Shickh, Salma, Cheung, Keven, Bombard, Yvonne

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Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol by Bouffler, Sophie E, Lee, Ling, Lynch, Fiona, Martyn, Melissa, Lynch, Elly, Macciocca, Ivan, Curnow, Lisette, McCorkell, Giulia, Lunke, Sebastian, Chong, Belinda, Marum, Justine E, Delatycki, Martin, Downie, Lilian, Goranitis, Ilias, Vears, Danya F, Best, Stephanie, Clausen, Marc, Bombard, Yvonne, Stark, Zornitza, Gaff, Clara L

“…IntroductionAs routine genomic testing expands, so too does the opportunity to look for additional health information unrelated to the original reason for…”
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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 by 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

“…IntroductionGenetic testing is used across medical disciplines leading to unprecedented demand for genetic services. This has resulted in excessive waitlists…”
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Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol by Lunke, Sebastian, Bouffler, Sophie E, Downie, Lilian, Caruana, Jade, Amor, David J, Archibald, Alison, Bombard, Yvonne, Christodoulou, John, Clausen, Marc, De Fazio, Paul, Greaves, Ronda F, Hollizeck, Sebastian, Kanga-Parabia, Anaita, Lang, Nitzan, Lynch, Fiona, Peters, Riccarda, Sadedin, Simon, Tutty, Erin, Eggers, Stefanie, Lee, Crystle, Wall, Meaghan, Yeung, Alison, Gaff, Clara, Gyngell, Christopher, Vears, Danya F, Best, Stephanie, Goranitis, Ilias, Stark, Zornitza

“…IntroductionNewborn bloodspot screening (NBS) is a highly successful public health programme that uses biochemical and other assays to screen for severe but…”
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Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery by 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

“…IntroductionThe high demand for genetic tests and limited supply of genetics professionals has created a need for alternative service delivery models. Digital…”
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O54: Reimagining genetics service delivery: Genetics providers’ perspectives on the integration of digital tools into clinical practice by Lee, Whiwon, Hirjikaka, Daena, Grewal, Sonya, Clausen, Marc, Luca, Stephanie, Shaw, Angela, Bombard, Yvonne, Hayeems, Robin

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P516: The Genetics Navigator: The development and usability testing of a new patient-facing digital health application to support clinical genetic testing by Clausen, Marc, Luca, Stephanie, Reble, Emma, Kodida, Rita, Saeedi, Saumeh, Hirjikaka, Daena, Chad, Lauren, Costain, Gregory, Faghfoury, Hanna, Silver, Josh, Shastri-Estrada, Serena, Smith, Maureen, Hayeems, Robin, Bombard, Yvonne

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Implementation of serological and molecular tools to inform COVID-19 patient management: protocol for the GENCOV prospective cohort study by Taher, Jennifer, Mighton, Chloe, Chowdhary, Sunakshi, Casalino, Selina, Frangione, Erika, Arnoldo, Saranya, Bearss, Erin, Binnie, Alexandra, Bombard, Yvonne, Borgundvaag, Bjug, Chertkow, Howard, Clausen, Marc, Devine, Luke, Faghfoury, Hanna, Friedman, Steven Marc, Gingras, Anne-Claude, Khan, Zeeshan, Mazzulli, Tony, McGeer, Allison, McLeod, Shelley L, Pugh, Trevor J, Richardson, David, Simpson, Jared, Stern, Seth, Strug, Lisa, Taher, Ahmed, Lerner-Ellis, Jordan

“…IntroductionThere is considerable variability in symptoms and severity of COVID-19 among patients infected by the SARS-CoV-2 virus. Linking host and virus…”
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P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results by Shickh, Salma, Kodida, Rita, Mighton, Chloe, Clausen, Marc, Reble, Emma, Sam, Jordan, Grewal, Sonya, Panchal, Seema, Aronson, Melyssa, Armel, Susan, Graham, Tracy, Elser, Christine, Eisen, Andrea, Carroll, June, Glogowski, Emily, Schrader, Kasmintan, Thorpe, Kevin, Lerner-Ellis, Jordan, Kim, Raymond, Bombard, Yvonne

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P373: Patients’ and parents’ perspectives on the use of digital tools to deliver genetic services by Assamad, Daniel, Saeedi, Saumeh, Grewal, Sonya, Jha, Vedika, Luca, Stephanie, Clausen, Marc, Shaw, Angela, Lee, Whiwon, Bombard, Yvonne, Hayeems, Robin, Study Team, Genetics Navigator

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P391: What are patients’ perspectives on the privacy and security of digital genomic tools? A qualitative study by Jha, Vedika, Saeedi, Saumeh, Assamad, Daniel, Grewal, Sonya, Hirjikaka, Daena, Lee, Whiwon, Luca, Stephanie, Shaw, Angela, Hayeems, Robin, Clausen, Marc, Bombard, Yvonne, Study Team, Genetics Navigator

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P382: Professionals’ perspectives on the use of digital tools to support patient recontact in clinical genetics by D'Amours, Guylaine, Reble, Emma, Aguda, Vernie, Clausen, Marc, Shickh, Salma, Mighton, Chloe, Carroll, June, Lerner-Ellis, Jordan, Nelson, Tanya, Richer, Julie, Schrader, Kasmintan, Seto, Emily, Shastri-Estrada, Serena, Thorpe, Kevin, Bombard, Yvonne

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P543: Comparing the analytical performance of exome sequencing and traditional panel testing in a cancer population by Reble, Emma, Sam, Jordan, Kodida, Rita, Clausen, Marc, Shickh, Salma, Mighton, Chloe, Capo-Chichi, Jose-Mario, Greenfeld, Elena, Noor, Abdul, Kim, Raymond, Lerner-Ellis, Jordan, Bombard, Yvonne

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

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

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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 Gopalakrishnan, Ridhi, Reble, Emma, Sam, Jordan, Butkowsky, Carly, Clausen, Marc, Rajeziesfahani, Sepideh, Sparkes, Brooklyn, Aguda, Vernie, Aronson, Melyssa, Bishop, Derrick, Dawson, Lesa, Eisen, Andrea, Graham, Tracy, Green, Jane, Mighton, Chloe, Pauling, Julee, Pavao, Claudia, Pechlivanoglou, Petros, Remocker, Catriona, Savas, Sevtap, Sun, Sophie, Tiano, Teresa, Tilley, Angelina, Thorpe, Kevin, Schrader, Kasmintan, Etchegary, Holly, Bombard, Yvonne

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

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

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