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

Ventilation defect burden predicts lung cancer resection outcomes

通气缺陷负荷可预测肺癌切除术的预后

Radadia, Nisarg; Priel, Eldar; Friedlander, Yonni; Konyer, Norman B; Huang, Chynna; Jamal, Mobin; Farncombe, Troy; Marriott, Christopher; Finley, Christian; Agzarian, John; Noseworthy, Michael D; Nair, Parameswaran; Shargall, Yaron; Svenningsen, Sarah

Clinical integration of germline findings from a tumor testing precision medicine program

将肿瘤检测精准医疗项目中的生殖系结果进行临床整合

Sanabria-Salas, Maria Carolina; Anggala, Nina C; Gillies, Brittany; Farncombe, Kirsten M; Hofstedter, Renee; Peck, Larissa; Purnaghshband, Helia; Redondo, Laura; Thain, Emily; Xu, Wei; Sabatini, Peter; Bedard, Philippe L; Kim, Raymond H

Multi-Platform Curation in the Development of ACMG/AMP Specifications for Von Hippel Lindau (VHL) Disease

在制定冯·希佩尔-林道综合征 (VHL) 的 ACMG/AMP 规范中采用多平台管理

Ritter, D I; Badduke, C; Doonanco, K; Kang, H C; Pesaran, T; Ridd, S; Sheen, C; Farncombe, K M; Giles, R H; Luo, M; Pipko, N; Tsoi, C T; McGoldrick, K; Mighton, C; Abu Kashabeh, R H; Sanabria-Salas, M C; Talab, Y; Deka, K B; Jacobs, M F; Tuzlali, E; Gallinger, B; Griffith, M; Krysiak, K; Machado, J; Maher, E R; Tirosh, A; Kim, R H

Early Cancer Detection in Li-Fraumeni Syndrome with Cell-Free DNA

利用游离DNA对李-弗劳梅尼综合征患者进行早期癌症检测

Wong, Derek; Luo, Ping; Oldfield, Leslie E; Gong, Haifan; Brunga, Ledia; Rabinowicz, Ron; Subasri, Vallijah; Chan, Clarissa; Downs, Tiana; Farncombe, Kirsten M; Luu, Beatrice; Norman, Maia; Sobotka, Julia A; Uju, Precious; Eagles, Jenna; Pedersen, Stephanie; Wellum, Johanna; Danesh, Arnavaz; Prokopec, Stephenie D; Stutheit-Zhao, Eric Y; Znassi, Nadia; Heisler, Lawrence E; Jovelin, Richard; Lam, Bernard; Lujan Toro, Beatriz E; Marsh, Kayla; Sundaravadanam, Yogi; Torti, Dax; Man, Carina; Goldenberg, Anna; Xu, Wei; Veit-Haibach, Patrick; Doria, Andrea S; Malkin, David; Kim, Raymond H; Pugh, Trevor J

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

CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase

CIViCdb 2022:开放获取癌症变异解读知识库的演变

Krysiak, Kilannin; Danos, Arpad M; Saliba, Jason; McMichael, Joshua F; Coffman, Adam C; Kiwala, Susanna; Barnell, Erica K; Sheta, Lana; Grisdale, Cameron J; Kujan, Lynzey; Pema, Shahil; Lever, Jake; Ridd, Sarah; Spies, Nicholas C; Andric, Veronica; Chiorean, Andreea; Rieke, Damian T; Clark, Kaitlin A; Reisle, Caralyn; Venigalla, Ajay C; Evans, Mark; Jani, Payal; Takahashi, Hideaki; Suda, Avila; Horak, Peter; Ritter, Deborah I; Zhou, Xin; Ainscough, Benjamin J; Delong, Sean; Kesserwan, Chimene; Lamping, Mario; Shen, Haolin; Marr, Alex R; Hoang, My H; Singhal, Kartik; Khanfar, Mariam; Li, Brian V; Lin, Wan-Hsin; Terraf, Panieh; Corson, Laura B; Salama, Yasser; Campbell, Katie M; Farncombe, Kirsten M; Ji, Jianling; Zhao, Xiaonan; Xu, Xinjie; Kanagal-Shamanna, Rashmi; King, Ian; Cotto, Kelsy C; Skidmore, Zachary L; Walker, Jason R; Zhang, Jinghui; Milosavljevic, Aleksandar; Patel, Ronak Y; Giles, Rachel H; Kim, Raymond H; Schriml, Lynn M; Mardis, Elaine R; Jones, Steven J M; Raca, Gordana; Rao, Shruti; Madhavan, Subha; Wagner, Alex H; Griffith, Malachi; Griffith, Obi L

Current and new frontiers in hereditary cancer surveillance: Opportunities for liquid biopsy

遗传性癌症监测的现状与新前沿:液体活检的机遇

Farncombe, Kirsten M; Wong, Derek; Norman, Maia L; Oldfield, Leslie E; Sobotka, Julia A; Basik, Mark; Bombard, Yvonne; Carile, Victoria; Dawson, Lesa; Foulkes, William D; Malkin, David; Karsan, Aly; Parkin, Patricia; Penney, Lynette S; Pollett, Aaron; Schrader, Kasmintan A; Pugh, Trevor J; Kim, Raymond H

Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.is

利用 Hypothes.is 开发针对 VHL 基因注释的疾病特异性注释方案

Salehipour, Dena; Farncombe, Kirsten M; Andric, Veronica; Ansar, Safa; Delong, Sean; Li, Eric; Macpherson, Samantha; Ridd, Sarah; Ritter, Deborah I; Thaxton, Courtney; Kim, Raymond H

Comparison of ventilation defects quantified by Technegas SPECT and hyperpolarized (129)Xe MRI

采用 Technegas SPECT 和超极化 (129)Xe MRI 对通气缺陷进行定量分析的比较

Radadia, Nisarg; Friedlander, Yonni; Priel, Eldar; Konyer, Norman B; Huang, Chynna; Jamal, Mobin; Farncombe, Troy; Marriott, Christopher; Finley, Christian; Agzarian, John; Dolovich, Myrna; Noseworthy, Michael D; Nair, Parameswaran; Shargall, Yaron; Svenningsen, Sarah

A community approach to the cancer-variant-interpretation bottleneck

社区方法解决癌症变异解读瓶颈

Krysiak, Kilannin; Danos, Arpad M; Kiwala, Susanna; McMichael, Joshua F; Coffman, Adam C; Barnell, Erica K; Sheta, Lana; Saliba, Jason; Grisdale, Cameron J; Kujan, Lynzey; Pema, Shahil; Lever, Jake; Spies, Nicholas C; Chiorean, Andreea; Rieke, Damian T; Clark, Kaitlin A; Jani, Payal; Takahashi, Hideaki; Horak, Peter; Ritter, Deborah I; Zhou, Xin; Ainscough, Benjamin J; Delong, Sean; Lamping, Mario; Marr, Alex R; Li, Brian V; Lin, Wan-Hsin; Terraf, Panieh; Salama, Yasser; Campbell, Katie M; Farncombe, Kirsten M; Ji, Jianling; Zhao, Xiaonan; Xu, Xinjie; Kanagal-Shamanna, Rashmi; Cotto, Kelsy C; Skidmore, Zachary L; Walker, Jason R; Zhang, Jinghui; Milosavljevic, Aleksandar; Patel, Ronak Y; Giles, Rachel H; Kim, Raymond H; Schriml, Lynn M; Mardis, Elaine R; Jones, Steven J M; Raca, Gordana; Rao, Shruti; Madhavan, Subha; Wagner, Alex H; Griffith, Obi L; Griffith, Malachi