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

Using artificial intelligence (AI) to model clinical variant reporting for next generation sequencing (NGS) oncology assays

利用人工智能(AI)对下一代测序(NGS)肿瘤检测的临床变异报告进行建模

Doig, Kenneth D; Perera, Rashindrie; Kankanige, Yamuna; Fellowes, Andrew; Li, Jason; Lupat, Richard; Thompson, Ella R; Blombery, Piers; Fox, Stephen B

Adjuvant rituximab and elevated intratumoural CD8 expression are associated with sustained disease control after radiotherapy in a randomised trial of systemic therapy in early-stage follicular lymphoma

在早期滤泡性淋巴瘤的一项系统治疗随机试验中,辅助利妥昔单抗治疗和肿瘤内CD8表达升高与放疗后疾病的持续控制相关。

MacManus, Michael P; Seymour, John F; Tsang, Hennes; Fisher, Richard; Keane, Colm; Sabdia, Muhammed B; Law, Soi C; Gunawardana, Jay; Nath, Karthik; Kazakoff, Stephen H; Marques-Piubelli, Mario L; Duenas, Daniela E; Green, Michael R; Roos, Daniel; O'Brien, Peter; McCann, Andrew; Tsang, Richard; Davis, Sidney; Christie, David; Cheah, Chan; Amanuel, Benhur; Cochrane, Tara; Butler, Jason; Johnston, Anna; Shanavas, Mohamed; Li, Li; Vajdic, Claire; Kridel, Robert; Shelton, Victoria; Hershenfield, Samantha; Baetz, Tara; Lebrun, David; Johnson, Nathalie; Brodtkorb, Marianne; Ludvigsen, Maja; d'Amore, Francesco; Thompson, Ella R; Blombery, Piers; Gandhi, Maher K; Tobin, Joshua W D

Erratum to: Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes

勘误:临床综合基因组特征分析在低细胞性骨髓衰竭综合征患者诊断分类中的应用

Blombery, Piers; Fox, Lucy; Ryland, Georgina L; Thompson, Ella R; Lickiss, Jennifer; McBean, Michelle; Yerneni, Satwica; Trainer, Alison; Hughes, David; Greenway, Anthea; Mechinaud, Francoise; Wood, Erica M; Lieschke, Graham J; Szer, Jeff; Barbaro, Pasquale; Roy, John; Wight, Joel; Lynch, Elly; Martyn, Melissa; Gaff, Clara; Ritchie, David

Cost Effectiveness of Molecular Diagnostic Testing Algorithms for the Treatment Selection of Frontline Ibrutinib for Patients with Chronic Lymphocytic Leukemia in Australia

澳大利亚慢性淋巴细胞白血病患者一线伊布替尼治疗方案选择中分子诊断检测算法的成本效益分析

Vu, Martin; Degeling, Koen; Thompson, Ella R; Blombery, Piers; Westerman, David; IJzerman, Maarten J

Acquired mutations in BAX confer resistance to BH3-mimetic therapy in acute myeloid leukemia.

BAX 基因的获得性突变可使急性髓系白血病对 BH3 模拟疗法产生耐药性

Moujalled Donia M, Brown Fiona C, Chua Chong Chyn, Dengler Michael A, Pomilio Giovanna, Anstee Natasha S, Litalien Veronique, Thompson Ella, Morley Thomas, MacRaild Sarah, Tiong Ing S, Morris Rhiannon, Dun Karen, Zordan Adrian, Shah Jaynish, Banquet Sebastien, Halilovic Ensar, Morris Erick, Herold Marco J, Lessene Guillaume, Adams Jerry M, Huang David C S, Roberts Andrew W, Blombery Piers, Wei Andrew H

Patient Pathway to Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Findings from a Multinational Survey of 204 Patients

髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)患者的诊断路径:一项包含204名患者的多国调查结果

Santoro, Jonathan D; Gould, Jennifer; Panahloo, Zoya; Thompson, Ella; Lefelar, Julia; Palace, Jacqueline

A patient-centered nurse-supported primary care-based collaborative care program to treat opioid use disorder and depression: Design and protocol for the MI-CARE randomized controlled trial

以患者为中心、护士支持的、以初级保健为基础的协作护理项目,用于治疗阿片类药物使用障碍和抑郁症:MI-CARE随机对照试验的设计和方案

DeBar, Lynn L; Bushey, Michael A; Kroenke, Kurt; Bobb, Jennifer F; Schoenbaum, Michael; Thompson, Ella E; Justice, Morgan; Zatzick, Douglas; Hamilton, Leah K; McMullen, Carmit K; Hallgren, Kevin A; Benes, Lindsay L; Forman, David P; Caldeiro, Ryan M; Brown, Ryan P; Campbell, Noll L; Anderson, Melissa L; Son, Sungtaek; Haggstrom, David A; Whiteside, Lauren; Schleyer, Titus K L; Bradley, Katharine A

Biallelic deleterious germline SH2B3 variants cause a novel syndrome of myeloproliferation and multi-organ autoimmunity

双等位基因有害的生殖系SH2B3变异会导致一种新的骨髓增生和多器官自身免疫综合征。

Blombery, Piers; Pazhakh, Vahid; Albuquerque, Adriana S; Maimaris, Jesmeen; Tu, Lingge; Briones Miranda, Brenda; Evans, Florence; Thompson, Ella R; Carpenter, Ben; Proctor, Ian; Curtin, Julie A; Lambert, Jonathan; Burns, Siobhan O; Lieschke, Graham J

Integration of tumour sequencing and case-control data to assess pathogenicity of RAD51C missense variants in familial breast cancer

整合肿瘤测序和病例对照数据以评估RAD51C错义变异在家族性乳腺癌中的致病性

Lim, Belle W X; Li, Na; Rowley, Simone M; Thompson, Ella R; McInerny, Simone; Zethoven, Magnus; Scott, Rodney J; Devereux, Lisa; Sloan, Erica K; James, Paul A; Campbell, Ian G

Health economic evidence for the use of molecular biomarker tests in hematological malignancies: A systematic review

血液系统恶性肿瘤分子生物标志物检测的卫生经济学证据:系统评价

Vu, Martin; Degeling, Koen; Thompson, Ella R; Blombery, Piers; Westerman, David; IJzerman, Maarten J