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

Examining the Concordance of Detection of Hereditary Cancer Gene Variants Between Blood, Tumour, and Normal Tissue in Patients with High-Grade Serous Ovarian Carcinoma

探讨高级别浆液性卵巢癌患者血液、肿瘤和正常组织中遗传性癌症基因变异检测的一致性

Mui, L; Kerkhof, J; McLachlin, C M; Panabaker, K; McGee, J; Sadikovic, B; Goebel, E A

Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol

安大略省遗传性癌症研究网络的发展:一个统一的登记系统,为患有遗传性癌症综合征的个体提供资源:一项观察性登记系统创建方案

Farncombe, Kirsten M; Hughes, Lauren K; Tuzlali, Elif; Akbari, Mohammad Reza; Andrulis, Irene L; Aronson, Melyssa; Bell, Kathleen; Brazas, Michelle D; Cable-Cibula, Melissa; Chan, Brandon; Courtot, Melanie; Feilotter, Harriet; Harland, Jamie; Lark, Katie; Lerner-Ellis, Jordan; MacDougall, Ellen; Malkin, David; Narod, Steven A; Panabaker, Karen; Radvanyi, Laszlo; Rusnak, Alison; Stein, Lincoln; Kim, Raymond H

Recommendations for the implementation of genetic testing for metastatic prostate cancer patients in Canada

加拿大转移性前列腺癌患者基因检测实施建议

Selvarajah, Shamini; Schrader, Kasmintan A; Kolinsky, Michael P; Rendon, Ricardo A; El Hallani, Soufiane; Fleshner, Neil E; Hotte, Sebastien J; Lorentz, Justin; Panabaker, Karen; Perrier, Renée; Pouliot, Frédéric; Spatz, Alan; Yip, Stephen; Chi, Kim N

Incidental findings from cancer next generation sequencing panels

癌症下一代测序小组的偶然发现

Nika Maani, Karen Panabaker, Jeanna M McCuaig, Kathleen Buckley, Kara Semotiuk, Kirsten M Farncombe, Peter Ainsworth, Seema Panchal, Bekim Sadikovic, Susan Randall Armel, Hanxin Lin #, Raymond H Kim #4

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach

利用独特的基于下一代测序的方法分析加拿大家族性癌症综合征患者队列中的序列和拷贝数变异

Bhai, Pratibha; Levy, Michael A; Rooney, Kathleen; Carere, Deanna Alexis; Reilly, Jack; Kerkhof, Jennifer; Volodarsky, Michael; Stuart, Alan; Kadour, Mike; Panabaker, Karen; Schenkel, Laila C; Lin, Hanxin; Ainsworth, Peter; Sadikovic, Bekim

Direct Genetics Referral Pathway for High-Grade Serous Ovarian Cancer Patients: The "Opt-Out" Process

高级别浆液性卵巢癌患者的直接遗传咨询转诊途径:“选择退出”流程

McGee, Jacob; Peart, Teresa M; Foley, Norine; Bertrand, Monique; Prefontaine, Michel; Sugimoto, Akira; Ettler, Helen; Welch, Stephen; Panabaker, Karen

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap

BRCA相关妇科恶性肿瘤基因检测的演变:加拿大多学会路线图

McCuaig, Jeanna M; Stockley, Tracy L; Shaw, Patricia; Fung-Kee-Fung, Michael; Altman, Alon D; Bentley, James; Bernardini, Marcus Q; Cormier, Beatrice; Hirte, Hal; Kieser, Katharina; MacMillan, Andree; Meschino, Wendy S; Panabaker, Karen; Perrier, Renee; Provencher, Diane; Schrader, Kasmintan A; Serfas, Kimberly; Tomiak, Eva; Wong, Nora; Young, Sean S; Gotlieb, Walter Henri; Hoskins, Paul; Kim, Raymond H

Genetics Consultation Rates Following a Diagnosis of High-Grade Serous Ovarian Carcinoma in the Canadian Province of Ontario

加拿大安大略省高级别浆液性卵巢癌诊断后的遗传咨询率

McGee, Jacob; Panabaker, Karen; Leonard, Sean; Ainsworth, Peter; Elit, Laurie; Shariff, Salimah Z

Performance of BRCA1/2 mutation prediction models in Asian Americans

BRCA1/2 突变预测模型在亚裔美国人中的表现

Kurian, Allison W; Gong, Gail D; Chun, Nicolette M; Mills, Meredith A; Staton, Ashley D; Kingham, Kerry E; Crawford, Beth B; Lee, Robin; Chan, Salina; Donlon, Susan S; Ridge, Yolanda; Panabaker, Karen; West, Dee W; Whittemore, Alice S; Ford, James M