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

The PreGen Research Program: Implementing Prenatal Genomic Testing in Australia-A Commentary

PreGen研究项目:在澳大利亚实施产前基因组检测——评述

Long, Sarah; Schofield, Deborah; Kraindler, Josh; Vink, Rebecca; Ross, Kate; Hart, Natalie; Evans, Holly; Wilson, Alyssa; Hyett, Jon; Wakefield, Claire E; Kelada, Lauren; Scott, Hamish; Lunke, Sebastian; Wall, Meaghan; Buckley, Michael F; Fernihough, Gemma; McGillivray, George; Roscioli, Tony

Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study

BabyScreen+ 基因组新生儿筛查研究的可行性、可接受性和临床结果

Lunke, Sebastian; Downie, Lilian; Caruana, Jade; Kugenthiran, Nathasha; De Fazio, Paul; Hollizeck, Sebastian; Bouffler, Sophie E; Amor, David J; Archibald, Alison D; Bombard, Yvonne; Christodoulou, John; Clausen, Marc; Fagan, Wendy; Gaff, Clara; Greaves, Ronda F; Gyngell, Christopher; Kanga-Parabia, Anaita; Lang, Nitzan; Lee, Crystle; Lynch, Fiona; Marty, Anthony; Marty, Melanie; McGregor, Candice; Riseley, Jessica; Sadedin, Simon; Scarff, Katrina; da Cunha Torres, Michelle; Tutty, Erin; Vang, Ching; Wall, Meaghan; Wong, Ee Ming; Yeung, Alison; Goranitis, Ilias; Best, Stephanie; Vears, Danya F; Stark, Zornitza

How comparable are patient outcomes in the "real-world" with populations studied in pivotal AML trials?

真实世界中患者的治疗结果与关键性 AML 试验中研究人群的治疗结果有多大可比性?

Tiong, Ing Soo; Wall, Meaghan; Bajel, Ashish; Kalro, Akash; Fleming, Shaun; Roberts, Andrew W; Thiagarajah, Nisha; Chua, Chong Chyn; Latimer, Maya; Yeung, David; Marlton, Paula; Johnston, Amanda; Enjeti, Anoop; Fong, Chun Yew; Cull, Gavin; Larsen, Stephen; Kennedy, Glen; Schwarer, Anthony; Kipp, David; Ramanathan, Sundra; Verner, Emma; Tiley, Campbell; Morris, Edward; Hahn, Uwe; Moore, John; Taper, John; Purtill, Duncan; Warburton, Pauline; Stevenson, William; Murphy, Nicholas; Tan, Peter; Beligaswatte, Ashanka; Mutsando, Howard; Hertzberg, Mark; Shortt, Jake; Szabo, Ferenc; Dunne, Karin; Wei, Andrew H

Prospective cohort study of genomic newborn screening: BabyScreen+ pilot study protocol

前瞻性队列研究:新生儿基因组筛查:BabyScreen+试点研究方案

Lunke, Sebastian; Bouffler, Sophie E; Downie, Lilian; Caruana, Jade; Amor, David J; Archibald, Alison; Bombard, Yvonne; Christodoulou, John; Clausen, Marc; De Fazio, Paul; Greaves, Ronda F; Hollizeck, Sebastian; Kanga-Parabia, Anaita; Lang, Nitzan; Lynch, Fiona; Peters, Riccarda; Sadedin, Simon; Tutty, Erin; Eggers, Stefanie; Lee, Crystle; Wall, Meaghan; Yeung, Alison; Gaff, Clara; Gyngell, Christopher; Vears, Danya F; Best, Stephanie; Goranitis, Ilias; Stark, Zornitza

Sorafenib plus intensive chemotherapy in newly diagnosed FLT3-ITD AML: a randomized, placebo-controlled study by the ALLG

索拉非尼联合强化化疗治疗新诊断的FLT3-ITD AML:ALLG的一项随机、安慰剂对照研究

Loo, Sun; Roberts, Andrew W; Anstee, Natasha S; Kennedy, Glen A; He, Simon; Schwarer, Anthony P; Enjeti, Anoop K; D'Rozario, James; Marlton, Paula; Bilmon, Ian A; Taper, John; Cull, Gavin; Tiley, Campbell; Verner, Emma; Hahn, Uwe; Hiwase, Devendra K; Iland, Harry J; Murphy, Nick; Ramanathan, Sundra; Reynolds, John; Ong, Doen Ming; Tiong, Ing Soo; Wall, Meaghan; Murray, Michael; Rawling, Tristan; Leadbetter, Joanna; Rowley, Leesa; Latimer, Maya; Yuen, Sam; Ting, Stephen B; Fong, Chun Yew; Morris, Kirk; Bajel, Ashish; Seymour, John F; Levis, Mark J; Wei, Andrew H

Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability

比较唾液和血液样本以检测导致综合征性智力障碍的嵌合型基因组异常

Francis, David I; Stark, Zornitza; Scheffer, Ingrid E; Tan, Tiong Yang; Murali, Krithika; Gallacher, Lyndon; Amor, David J; Goel, Himanshu; Downie, Lilian; Stutterd, Chloe A; Krzesinski, Emma I; Vasudevan, Anand; Oertel, Ralph; Petrovic, Vida; Boys, Amber; Wei, Vivian; Burgess, Trent; Dun, Karen; Oliver, Karen L; Baxter, Anne; Hackett, Anna; Ayres, Samantha; Lunke, Sebastian; Kalitsis, Paul; Wall, Meaghan

Are We Ready for Whole Population Genomic Sequencing of Asymptomatic Newborns?

我们是否已准备好对无症状新生儿进行全人群基因组测序?

Vears, Danya F; Savulescu, Julian; Christodoulou, John; Wall, Meaghan; Newson, Ainsley J

Favorable outcomes of DDX41-mutated myelodysplastic syndrome and low blast count acute myeloid leukemia treated with azacitidine ± lenalidomide

采用阿扎胞苷±来那度胺治疗DDX41突变型骨髓增生异常综合征和低原始细胞计数急性髓系白血病可获得良好疗效。

Tiong, Ing S; Stevenson, William S; Wall, Meaghan; Yap, Yan Zhuang; Seymour, John F; Kenealy, Melita; Blombery, Piers

Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multi-center study

基因组芯片可识别具有基因组复杂性的高危慢性淋巴细胞白血病:一项多中心研究

Leeksma, Alexander C; Baliakas, Panagiotis; Moysiadis, Theodoros; Puiggros, Anna; Plevova, Karla; Van der Kevie-Kersemaekers, Anne-Marie; Posthuma, Hidde; Rodriguez-Vicente, Ana E; Tran, Anh Nhi; Barbany, Gisela; Mansouri, Larry; Gunnarsson, Rebeqa; Parker, Helen; Van den Berg, Eva; Bellido, Mar; Davis, Zadie; Wall, Meaghan; Scarpelli, Ilaria; Österborg, Anders; Hansson, Lotta; Jarosova, Marie; Ghia, Paolo; Poddighe, Pino; Espinet, Blanca; Pospisilova, Sarka; Tam, Constantine; Ysebaert, Loïc; Nguyen-Khac, Florence; Oscier, David; Haferlach, Claudia; Schoumans, Jacqueline; Stevens-Kroef, Marian; Eldering, Eric; Stamatopoulos, Kostas; Rosenquist, Richard; Strefford, Jonathan C; Mellink, Clemens; Kater, Arnon P

Newborn bloodspot screening in the time of COVID-19

新冠疫情期间的新生儿血斑筛查

Greaves, Ronda F; Pitt, James; McGregor, Candice; Wall, Meaghan; Christodoulou, John