Search Results - "Kodida, Rita"

Widening the lens of actionability: A qualitative study of primary care providers' views and experiences of managing secondary genomic findings by 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

“…Most secondary genomic findings (SFs) fall in the scope of primary care practice. However, primary care providers' (PCPs) capacity to manage these findings is…”
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Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings by 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

“…Genomic sequencing advances have increased the potential to identify secondary findings (SFs). Current guidelines recommend the analysis of 59 medically…”
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The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care by 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.

“…Alternative models of genetic counseling are needed to meet the rising demand for genomic sequencing. Digital tools have been proposed as a method to augment…”
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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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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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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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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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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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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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P523: Returning all clinically relevant findings from genomic sequencing: Preliminary results from the incidental genomics RCT by Bombard, Yvonne, Mighton, Chloe, Shickh, Salma, Clausen, Marc, Kodida, Rita, 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, Lerner-Ellis, Jordan, Kim, Raymond, Thorpe, Kevin

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P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review by Shickh, Salma, Mighton, Chloe, Clausen, Marc, Kodida, Rita, Sam, Jordan, Hirjikaka, Daena, Reble, Emma, Graham, Tracy, Panchal, Seema, Eisen, Andrea, Elser, Christine, Schrader, Kasmintan, Baxter, Nancy N., Laupacis, Andreas, Lerner-Ellis, Jordan, Kim, Raymond, Bombard, Yvonne

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“Doctors shouldn’t have to cheat the system”: Clinicians’ real-world experiences of the utility of genomic sequencing by Shickh, Salma, Mighton, Chloe, Clausen, Marc, Adi-Wauran, Ella, Hirjikaka, Daena, Kodida, Rita, Krishnapillai, Suvetha, Reble, Emma, Sam, Jordan, Shaw, Angela, Lerner-Ellis, Jordan, Baxter, Nancy N., Laupacis, Andreas, Bombard, Yvonne

“…Emerging genetic tests such as genomic sequencing (GS) can generate a broad range of benefits, but funding criteria only prioritize diagnosis and clinical…”
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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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Finding the sweet spot: a qualitative study exploring patients’ acceptability of chatbots in genetic service delivery by Luca, Stephanie, Clausen, Marc, Shaw, Angela, Lee, Whiwon, Krishnapillai, Suvetha, Adi-Wauran, Ella, Faghfoury, Hanna, Costain, Gregory, Jobling, Rebekah, Aronson, Melyssa, Liston, Eriskay, Silver, Josh, Shuman, Cheryl, Chad, Lauren, Hayeems, Robin Z., Bombard, Yvonne

“…Chatbots, web-based artificial intelligence tools that simulate human conversation, are increasingly in use to support many areas of genomic medicine. However,…”
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Opportunistic genomic screening has clinical utility: An interventional cohort study by 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., Bombard, Yvonne

“…Practice is shifting toward genome-first approaches, such as opportunistic screening for secondary findings (SFs). Analysis of SFs could be extended beyond…”
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A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findings by Sam, Jordan, Reble, Emma, Kodida, Rita, Shaw, Angela, Clausen, Marc, Salazar, Mariana Gutierrez, Shickh, Salma, Mighton, Chloe, Carroll, June C., Armel, Susan Randall, Aronson, Melyssa, Capo-Chichi, José-Mario, Cohn, Iris, Eisen, Andrea, Elser, Christine, Graham, Tracy, Ott, Karen, Panchal, Seema, Piccinin, Carolyn, Schrader, Kasmintan A., Kim, Raymond H., Lerner-Ellis, Jordan, Bombard, Yvonne

“…Genomic sequencing (GS) can reveal secondary findings (SFs), findings unrelated to the reason for testing, that can be overwhelming to both patients and…”
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Genetics providers’ perspectives on the use of digital tools in clinical practice by 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.

“…Digital tools are increasingly incorporated into genetics practice to address challenges with the current model of care. Yet, genetics providers’ perspectives…”
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“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 by Shickh, Salma, Mighton, Chloe, Clausen, Marc, Kodida, Rita, Adi-Wauran, Ella, Hirjikaka, Daena, Krishnapillai, Suvetha, Reble, Emma, Sam, Jordan, Baxter, Nancy N., Baxter, Nancy N., Laupacis, Andreas, Bombard, Yvonne, Bombard, Yvonne, Armel, Susan Randall, Aronson, Melyssa, Bond, Kenneth, Capo-Chichi, José-Mario, Carroll, June C., Caulfield, Timothy, 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.

“…We sought to explore patient-reported utility of all types of cancer results from genomic sequencing (GS). Qualitative study, using semi-structured interviews…”
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A model for the return and referral of all clinically significant secondary findings of genomic sequencing by Kodida, Rita, Reble, Emma, Clausen, Marc, Shickh, Salma, Mighton, Chloe, Sam, Jordan, Forster, Nicole, Panchal, Seema, Aronson, Melyssa, Semotiuk, Kara, Graham, Tracy, Silberman, Yael, Randall Armel, Susan, McCuaig, Jeanna M, Cohn, Iris, Morel, Chantal F, Elser, Christine, Eisen, Andrea, Carroll, June C, Glogowski, Emily, Schrader, Kasmintan A, Di Gioacchino, Vanessa, Lerner-Ellis, Jordan, Kim, Raymond H, Bombard, Yvonne

“…Secondary findings (SFs) identified through genomic sequencing (GS) can offer a wide range of health benefits to patients. Resource and capacity constraints…”
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Challenges and practical solutions for managing secondary genomic findings in primary care by 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

“…Primary care providers will increasingly be tasked with managing most secondary findings from genomic sequencing, but literature exploring their capacity to…”
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