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

Genomic Therapy Matching in Rare and Refractory Cancers

罕见和难治性癌症的基因组治疗匹配

Lin, Frank P; Thavaneswaran, Subotheni; Grady, John P; Napier, Christine E; Kansara, Maya; Sebastian, Lucille; Kee, Damien; Desai, Jayesh; Zaheed, Milita; Chinchen, Sarah; Oakes, Samantha R; Blackburn, James; Scott, Hamish S; Glover, Anthony; Fox, Stephen B; Goldstein, David; Leo, Paul; Amanuel, Benhur; Mersiades, Antony; Millward, Michael; Brown, Michael P; Charakidis, Michail; Pokorny, Adrian M J; Craft, Paul; Espinoza, David; Grimison, Peter; Harrup, Rosemary; Joshua, Anthony M; O'Byrne, Ken; Lee, Chee Khoon; Cowley, Mark J; Ballinger, Mandy L; Simes, John; Thomas, David M

Impact of Spiritual Wellbeing in Advanced Cancer Patients Receiving Genomic Test Results

精神健康对接受基因组检测结果的晚期癌症患者的影响

Best, Megan C; Descallar, Joseph; Simpson, Grahame; Napier, Christine E; Bartley, Nicci; Ballinger, Mandy L; Goldstein, David; Thomas, David M; Tucker, Katherine M; Butow, Phyllis

Implementation of precision medicine in treating non-communicable diseases: a systematic review

精准医疗在非传染性疾病治疗中的应用:系统评价

Liang, Shuang; Kennedy, Elizabeth; Gale, Nyree; Watson, Paul; Ramanathan, Mahitha; Shinde, Arya; McKay, Skye; Torres-Robles, Andrea; Li, Zhicheng; Chan, Jeffery; Jones, Helen; Ballinger, Mandy L; Butow, Phyllis; Goldstein, David; Leaney, Kathryn; Middleton, Sandy; Morrow, April; Thomas, David M; Tucker, Kathy M; Zaheed, Milita; Parkinson, Bonny; Lin, Frank; Taylor, Natalie

SMARCAL1 is a new osteosarcoma predisposition gene

SMARCAL1 是一种新的骨肉瘤易感基因

Rafati, Maryam; Guenther, Lillian M; Egolf, Laura E; Gianferante, D Matthew; Kim, Jung; Wang, Kevin; Zhu, Bin; Spector, Logan G; Anderson, Nathan; Janeway, Katherine A; Barkauskas, Donald A; Hawkins, Douglas S; Patiño-Garcia, Ana; Lupo, Philip J; Scheurer, Michael E; Morton, Lindsay; Armstrong, Gregory T; Sapkota, Yadav; Gramatges, M Monica; Serra, Massimo; Hattinger, Claudia; Scotlandi, Katia; Andrulis, Irene L; Wunder, Jay S; Ballinger, Mandy L; Thomas, David M; Yeager, Meredith; Dean, Michael; Stewart, Douglas R; Vogt, Aurelie; Liu, Jia; Hicks, Belynda D; Huang, Wen-Yi; Landi, Maria Teresa; Lori, Adriana; Diver, W Ryan; Savage, Sharon A; Chanock, Stephen J; Mirabello, Lisa

POT1 clinical risk management is an open question

POT1临床风险管理仍是一个悬而未决的问题。

Ballinger, Mandy L; Thomas, David M

Low & Anaplastic Grade Glioma Umbrella Study of MOlecular Guided TherapieS (LUMOS-2): study protocol for a phase 2, prospective, multicentre, open-label, multiarm, biomarker-directed, signal-seeking, umbrella, clinical trial for recurrent IDH mutant, grade 2/3 glioma

低级别和间变性胶质瘤分子靶向治疗伞式研究 (LUMOS-2):一项针对复发性 IDH 突变型 2/3 级胶质瘤的 II 期前瞻性、多中心、开放标签、多组、生物标志物导向、信号探索性伞式临床试验的研究方案

McParland, Kristen; Koh, Eng-Siew; Kong, Benjamin; Sim, Hao-Wen; Thavaneswaran, Subotheni; Yip, Sonia; Barnes, Elizabeth H; Ballinger, Mandy L; Thomas, David M; De Abreu Lourenco, Richard; Simes, John; Sebastian, Lucille; Wheeler, Patrick J; Spyridopoulos, Desma; Hawkins, Cynthia; Pitz, Marshall; O'Callaghan, Christopher; Gan, Hui K

Integration of precision medicine into routine cancer care-protocol for the Precision Care Initiative: a research programme of effectiveness-implementation hybrid trials

将精准医疗整合到常规癌症治疗方案中——精准医疗计划:一项有效性-实施混合试验研究项目

Liang, Shuang; McKay, Skye; Lin, Frank; Zaheed, Milita; Morrow, April; Douglas, Bridget; Chan, Jeffery; Monaghan, Helen; Chan, Priscilla; Kennedy, Elizabeth; Tyedmers, Elijah; Walker, Stephanie; Leaney, Kathryn; Napier, Christine E; Middleton, Sandy; Butow, Phyllis; Williams, Rachel; Parkinson, Bonny; Ballinger, Mandy L; Tucker, Katherine; Goldstein, David; Thomas, David; Taylor, Natalie

Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum

TP53致病变异相关的癌症风险:基于扩展家系的最大似然分析,用于诊断超出李-弗劳梅尼综合征谱系的首发癌症

Fortuno, Cristina; Feng, Bing-Jian; Carroll, Courtney; Innella, Giovanni; Kohlmann, Wendy; Lázaro, Conxi; Brunet, Joan; Feliubadaló, Lidia; Iglesias, Silvia; Menéndez, Mireia; Teulé, Alex; Ballinger, Mandy L; Thomas, David M; Campbell, Ainsley; Field, Mike; Harris, Marion; Kirk, Judy; Pachter, Nicholas; Poplawski, Nicola; Susman, Rachel; Tucker, Kathy; Wallis, Mathew; Williams, Rachel; Cops, Elisa; Goldgar, David; James, Paul A; Spurdle, Amanda B

From ownership to custodianship of tumor biopsy tissue in genomic testing: a mixed methods study of patient views

从基因组检测中肿瘤活检组织的拥有权到保管权:一项基于患者观点的混合方法研究

Best, Megan C; Butow, Phyllis; Savard, Jacqueline; Newson, Ainsley J; Campbell, Rachel; Vatter, Sabina; Napier, Christine E; Bartley, Nicci; Tucker, Katherine; Ballinger, Mandy L; Thomas, David M

Genetically inferred birthweight, height, and puberty timing and risk of osteosarcoma

基因推断的出生体重、身高和青春期发育时间与骨肉瘤风险

Gianferante, D Matthew; Moore, Amy; Spector, Logan G; Wheeler, William; Yang, Tianzhong; Hubbard, Aubrey; Gorlick, Richard; Patiño-Garcia, Ana; Lecanda, Fernando; Flanagan, Adrienne M; Amary, Fernanda; Andrulis, Irene L; Wunder, Jay S; Thomas, David M; Ballinger, Mandy L; Serra, Massimo; Hattinger, Claudia; Demerath, Ellen; Johnson, Will; Birmann, Brenda M; De Vivo, Immaculata; Giles, Graham; Teras, Lauren R; Arslan, Alan; Vermeulen, Roel; Sample, Jeannette; Freedman, Neal D; Huang, Wen-Yi; Chanock, Stephen J; Savage, Sharon A; Berndt, Sonja I; Mirabello, Lisa