日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services

“遗传导航器”的开发和可用性:面向成人和儿童临床遗传服务的数字解决方案

Saeedi, Saumeh; Hirjikaka, Daena; Clausen, Marc; Luca, Stephanie; Reble, Emma; Kodida, Rita; Assamad, Daniel; Chad, Lauren; Costain, Gregory; Faghfoury, Hanna; Silver, Josh; Shastri-Estrada, Serena; Smith, Maureen; Hayeems, Robin Z; Bombard, Yvonne

Characterization of LED-based hybrid diffuse reflectance spectroscopy method for determination of SPF and UVA-PF in blinded multi-centre study (ALT-SPF)

在盲法多中心研究中,对基于 LED 的混合漫反射光谱法测定 SPF 和 UVA-PF 进行表征 (ALT-SPF)

Reble, Carina; Bayer, Michael; Colson, Bertrand; Emmler, Tanja; Hubaud, Jean-Claude; Seise, Matthias; Perroux-David, Eva; Wiora, Georg; Zamudio Diaz, Daniela F; Meinke, Martina C; Bielfeldt, Stephan

Opportunistic genomic screening has clinical utility: An interventional cohort study

机会性基因组筛查具有临床应用价值:一项干预性队列研究

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

"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screening

“我只是想要更多”:遗传性癌症综合征患者对循环肿瘤DNA检测在癌症筛查中应用价值的看法

Adi-Wauran, Ella; Clausen, Marc; Shickh, Salma; Gagliardi, Anna R; Denburg, Avram; Oldfield, Leslie E; Sam, Jordan; Reble, Emma; Krishnapillai, Suvetha; Regier, Dean A; Baxter, Nancy N; Dawson, Lesa; Penney, Lynette S; Foulkes, William; Basik, Mark; Sun, Sophie; Schrader, Kasmintan A; Karsan, Aly; Pollett, Aaron; Pugh, Trevor J; Kim, Raymond H; Bombard, Yvonne

Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations

遗传导航器:一项混合方法随机对照试验方案,旨在评估一个用于在加拿大儿科和成人人群中提供基因组服务的数字平台

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

Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testing

遗传学顾问:开发并进行一款新型患者数字健康应用程序的可用性测试,以支持临床基因组检测

Clausen, Marc; Krishnapillai, Suvetha; Hirjikaka, Daena; Kodida, Rita; Shickh, Salma; Reble, Emma; Mighton, Chloe; Sam, Jordan; Adi-Wauran, Ella; Baxter, Nancy N; Feldman, Geoff; Glogowski, Emily; Lerner-Ellis, Jordan; Scheer, Adena; Shastri-Estrada, Serena; Shuman, Cheryl; Armel, Susan Randall; Aronson, Melyssa; Graham, Tracy; Panchal, Seema; Thorpe, Kevin E; Carroll, June C; Eisen, Andrea; Elser, Christine; Kim, Raymond H; Faghfoury, Hanna; Schrader, Kasmintan A; Seto, Emily; Bombard, Yvonne

"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

“我不想再让任何未知因素悬在我的头上”:癌症患者对基因组测序中意义未明变异和低/中风险结果的看法

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

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

对智力障碍/自闭症基因测序中常用基因进行临床有效性评估

Riggs, Erin Rooney; Bingaman, Taylor I; Barry, Carrie-Ann; Behlmann, Andrea; Bluske, Krista; Bostwick, Bret; Bright, Alison; Chen, Chun-An; Clause, Amanda R; Dharmadhikari, Avinash V; Ganapathi, Mythily; Gonzaga-Jauregui, Claudia; Grant, Andrew R; Hughes, Madeline Y; Kim, Se Rin; Krause, Amanda; Liao, Jun; Lumaka, Aimé; Mah, Michelle; Maloney, Caitlin M; Mohan, Shruthi; Osei-Owusu, Ikeoluwa A; Reble, Emma; Rennie, Olivia; Savatt, Juliann M; Shimelis, Hermela; Siegert, Rebecca K; Sneddon, Tam P; Thaxton, Courtney; Toner, Kelly A; Tran, Kien Trung; Webb, Ryan; Wilcox, Emma H; Yin, Jiani; Zhuo, Xinming; Znidarsic, Masa; Martin, Christa Lese; Betancur, Catalina; Vorstman, Jacob A S; Miller, David T; Schaaf, Christian P

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

拓宽行动视角:一项关于初级保健提供者对管理次要基因组学发现的观点和经验的定性研究

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

Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery

遗传咨询师:一项评估用于遗传服务提供的数字平台的混合方法随机对照试验方案

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