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

Canadian Recommendations for Germline Genetic Testing of Patients with Breast Cancer: A Call to Action

加拿大关于乳腺癌患者生殖系基因检测的建议:行动呼吁

Weber, Evan; Carmona-Gonzalez, Carlos A; Boucher, Melanie; Eisen, Andrea; Laing, Kara; Melvin, Jennifer; Schrader, Kasmintan A; Sehdev, Sandeep; Wong, Stephanie M; Gelmon, Karen A

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

The Pancreatic Cancer Early Detection (PRECEDE) Study is a Global Effort to Drive Early Detection: Baseline Imaging Findings in High-Risk Individuals

胰腺癌早期检测(PRECEDE)研究是一项旨在推动早期检测的全球性研究:高危人群的基线影像学检查结果

Zogopoulos, George; Haimi, Ido; Sanoba, Shenin A; Everett, Jessica N; Wang, Yifan; Katona, Bryson W; Farrell, James J; Grossberg, Aaron J; Paiella, Salvatore; Klute, Kelsey A; Bi, Yan; Wallace, Michael B; Kwon, Richard S; Stoffel, Elena M; Wadlow, Raymond C; Sussman, Daniel A; Merchant, Nipun B; Permuth, Jennifer B; Golan, Talia; Raitses-Gurevich, Maria; Lowy, Andrew M; Liau, Joy; Jeter, Joanne M; Lindberg, James M; Chung, Daniel C; Earl, Julie; Brentnall, Teresa A; Schrader, Kasmintan A; Kaul, Vivek; Huang, Chenchan; Chandarana, Hersh; Smerdon, Caroline; Graff, John J; Kastrinos, Fay; Kupfer, Sonia S; Lucas, Aimee L; Sears, Rosalie C; Brand, Randall E; Parmigiani, Giovanni; Simeone, Diane M

Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers

全基因组和转录组整合分析指导儿童预后不良癌症的临床治疗

Deyell, Rebecca J; Shen, Yaoqing; Titmuss, Emma; Dixon, Katherine; Williamson, Laura M; Pleasance, Erin; Nelson, Jessica M T; Abbasi, Sanna; Krzywinski, Martin; Armstrong, Linlea; Bonakdar, Melika; Ch'ng, Carolyn; Chuah, Eric; Dunham, Chris; Fok, Alexandra; Jones, Martin; Lee, Anna F; Ma, Yussanne; Moore, Richard A; Mungall, Andrew J; Mungall, Karen L; Rogers, Paul C; Schrader, Kasmintan A; Virani, Alice; Wee, Kathleen; Young, Sean S; Zhao, Yongjun; Jones, Steven J M; Laskin, Janessa; Marra, Marco A; Rassekh, Shahrad R

Consensus Statement: Recommendations on Actionable Biomarker Testing for Thyroid Cancer Management

共识声明:关于甲状腺癌管理中可操作生物标志物检测的建议

Mete, Ozgur; Boucher, Andrée; Schrader, Kasmintan A; Abdel-Rahman, Omar; Bahig, Houda; Ho, Cheryl; Hasan, Olfat Kamel; Lemieux, Bernard; Winquist, Eric; Wong, Ralph; Wu, Jonn; Chau, Nicole; Ezzat, Shereen

Economic Evaluation of Population-Based BRCA1 and BRCA2 Testing in Canada

加拿大基于人群的BRCA1和BRCA2基因检测的经济评估

Sun, Li; Wei, Xia; Fierheller, Caitlin T; Dawson, Lesa; Oxley, Samuel; Kalra, Ashwin; Sia, Jacqueline; Feldman, Fabio; Peacock, Stuart; Schrader, Kasmintan A; Legood, Rosa; Kwon, Janice S; Manchanda, Ranjit

Improving Access to Hereditary Testing in Pancreatic Ductal Carcinoma

改善胰腺导管癌基因检测的可及性

Cremin, Carol; Bedard, Angela C; Hong, Quan; Mung, Sze Wing; Nuk, Jennifer; Wong, Andrew; Akbar, Husain; Cheung, Eugene; Renouf, Daniel; Schaeffer, David; Sun, Sophie; Schrader, Kasmintan A

"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 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

Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq

利用长读长DNA甲基化测序和Strand-seq进行亲本来源检测和染色体尺度单倍型分析

Akbari, Vahid; Hanlon, Vincent C T; O'Neill, Kieran; Lefebvre, Louis; Schrader, Kasmintan A; Lansdorp, Peter M; Jones, Steven J M