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

Outcomes of second-line axicabtagene ciloleucel for large B-cell lymphoma in the UK

英国二线治疗大B细胞淋巴瘤的axicabtagene ciloleucel疗效

Kuhnl, Andrea; Kirkwood, Amy A; Northend, Michael; Besley, Caroline; Uttenthal, Ben; Norman, Jane; Hiew, Hwai; Seymour, Frances; Maybury, Bernard; Osborne, Wendy; Sillito, Francesca; Abdulgawad, Ahmed; Jones, Ceri; McCarthy, Pierre; Panopoulou, Aikaterini; Gribben, John G; Bataillard, Edward; Martinez-Calle, Nicolas; Gajendran, Lavanya; O'Reilly, Maeve; Kumar, Emil; Wilson, Robert P; Kasivisvanathan, Shenbagaram; Fadlelmula, Nada; Pryce, Angharad; Awofisayo, Olateni; Maraj, Adrian; Townsend, William; Cwynarski, Kate; Paneesha, Shankara; Mathew, Amrith; Dulobdas, Vaishali; El-Sharkawi, Dima; Creasey, Thomas; Warren, Mary; Malladi, Ram; Owen, Mary; Waraich, Muddeha; Ediriwickrema, Kushani; Froggatt, Joseph; Delaney, Alison; Davies, Andrew J; Alajangi, Rajesh; Collins, Graham P; Sanderson, Robin; Roddie, Claire; Menne, Tobias; Chaganti, Sridhar

LncRNA SLNCR phenocopies the E2F1 DNA binding site to promote melanoma progression

长链非编码RNA SLNCR通过模拟E2F1 DNA结合位点促进黑色素瘤进展

Kushani Shah ,Eleni Anastasakou ,Leinal Sejour ,Yufei Wang ,Leon Wert-Lamas ,Christopher Rauchet ,Sabine Studer ,Simon Goller ,Robert J Distel ,Wayne Marasco ,Lalith Perera ,Ioannis S Vlachos ,Carl D Novina

Genomic sequencing technologies for rare disease in mainstream healthcare: the current state of implementation

基因组测序技术在罕见病主流医疗保健中的应用现状

Mackley, Michael P; Agrawal, Pankaj B; Ali, Sara S; Archibald, Alison D; Dawson-McClaren, Belinda; Ellard, Holly; Freeman, Lucinda; Gu, Yuanyuan; Jayasinghe, Kushani; Jiang, Shan; Kirk, Edwin P; Lewis, Celine; McEwen, Alison; Nisselle, Amy; Quinlan, Catherine; Terrill, Bronwyn; Tutty, Erin; McNeill, Alisdair

Optimising the mainstreaming of renal genomics: Complementing empirical and theoretical strategies for implementation

优化肾脏基因组学主流化:补充经验和理论实施策略

Cheng, Lin; Kugenthiran, Nathasha; Quinlan, Catherine; Stark, Zornitza; Jayasinghe, Kushani; Best, Stephanie

Atypical presentations of fetal polycystic kidney disease demonstrates the utility of a genomic autopsy for accurate post-mortem diagnoses

胎儿多囊肾病的非典型表现表明基因组尸检对于准确的死后诊断具有实用价值。

Frank, Mahalia S B; Bennett, Melissa K; Ha, Thuong T; Moore, Lynette; Arts, Peer; Byrne, Alicia B; Babic, Milena; Arriola-Martinez, Luis; Toubia, John; Brautigan, Peter J; Feng, Jinghua; Schwarz, Quenten; Thomas, Paul Q; Piltz, Sandra G; White, Melissa A; Moghimi, Ali; Strachan, Kate; Kwan, Edward; Springer, Amanda; Lewit-Mendes, Miranda; Dearman, Jarrad; Davis, Tenielle; Kevin, Lucy; McCarthy, Hugh J; Liebelt, Jan; Krzesinski, Emma; Regan, Matthew; Verma, Kunal; McGillivray, George; Jayasinghe, Kushani; Jackson, Matilda R; Barnett, Christopher P; Scott, Hamish S

Next-generation nephrology: part 1-an aid for genetic and genomic testing in pediatric nephrology

下一代肾脏病学:第一部分——儿科肾脏病学中基因和基因组检测的辅助工具

Gupta, Asheeta; Jayasinghe, Kushani; Majmundar, Amar; Mann, Nina; Sinha, Rajiv; Sampson, Matthew G; Quinlan, Catherine

Next-generation nephrology: part 2-mainstreaming genomics in nephrology, a global perspective

下一代肾脏病学:第二部分——肾脏病学基因组学主流化:全球视角

Gupta, Asheeta; Jayasinghe, Kushani; Majmundar, Amar; Mann, Nina; Sinha, Rajiv; Sampson, Matthew G; Quinlan, Catherine

Enhancing diagnostic outcomes in kidney genetic disorders: the KidGen national kidney genomics study protocol

提高肾脏遗传疾病的诊断结果:KidGen 国家肾脏基因组学研究方案

Mallawaarachchi, Amali; McCarthy, Hugh; Forbes, Thomas A; Jayasinghe, Kushani; Patel, Chirag; Alexander, Stephen I; Boughtwood, Tiffany; Braithwaite, Jeffrey; Chakera, Aron; Crafter, Sam; Deveson, Ira W; Faull, Randall; Harris, Trudie; Johnstone, Lilian; Jose, Matthew; Leaver, Anna; Little, Melissa H; MacArthur, Daniel; Mattiske, Tessa; Mincham, Christine; Nicholls, Kathy; Quinlan, Catherine; Quinn, Michael C J; Rangan, Gopala; Ryan, Jessica; Simons, Cas; Smyth, Ian; Sundaram, Madhivanan; Trnka, Peter; Wedd, Laura; Biros, Erik; Stark, Zornitza; Mallett, Andrew

Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study

针对病因不明的肾衰竭患者的基因组检测:一项澳大利亚全国性研究

Mallawaarachchi, Amali C; Fowles, Lindsay; Wardrop, Louise; Wood, Alasdair; O'Shea, Rosie; Biros, Erik; Harris, Trudie; Alexander, Stephen I; Bodek, Simon; Boudville, Neil; Burke, Jo; Burnett, Leslie; Casauria, Sarah; Chadban, Steve; Chakera, Aron; Crafter, Sam; Dai, Pei; De Fazio, Paul; Faull, Randall; Honda, Andrew; Huntley, Vanessa; Jahan, Sadia; Jayasinghe, Kushani; Jose, Matthew; Leaver, Anna; MacShane, Mandi; Madelli, Evanthia Olympia; Nicholls, Kathy; Pawlowski, Rhonda; Rangan, Gopi; Snelling, Paul; Soraru, Jacqueline; Sundaram, Madhivanan; Tchan, Michel; Valente, Giulia; Wallis, Mathew; Wedd, Laura; Welland, Matthew; Whitlam, John; Wilkins, Ella J; McCarthy, Hugh; Simons, Cas; Quinlan, Catherine; Patel, Chirag; Stark, Zornitza; Mallett, Andrew J

Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years

国家多学科肾脏遗传学诊疗网络的实施与评估(历时10年)

Jayasinghe, Kushani; Biros, Erik; Harris, Trudie; Wood, Alasdair; O'Shea, Rosie; Hill, Lauren; Fowles, Lindsay; Wardrop, Louise; Shalhoub, Carolyn; Hahn, Deirdre; Rangan, Gopala; Kevin, Lucy; Tchan, Michel; Snelling, Paul; Sandow, Rhiannon; Sundaram, Madhivan; Chaturvedi, Swasti; Trnka, Peter; Faull, Randall; Poplawski, Nicola K; Huntley, Vanessa; Garza, Denisse; Wallis, Mathew; Jose, Matthew; Leaver, Anna; Trainer, Alison H; Wilkins, Ella J; White, Sue; Elbaum, Yoni; Prawer, Yael; Krzesinski, Emma; Valente, Giulia; Winship, Ingrid; Ryan, Jessica; Whitlam, John; Nicholls, Kathy; West, Kirsty; Donaldson, Liz; Johnstone, Lilian; Lewit-Mendes, Miranda; Kerr, Peter G; Bodek, Simon; Chakera, Aron; MacShane, Mandi; Mincham, Christine; Stackpoole, Elaine; Willis, Francis; Soraru, Jacqueline; Pachter, Nick; Bennetts, Bruce; Forbes, Thomas A; Mallawaarachchi, Amali; Quinlan, Catherine; Patel, Chirag; McCarthy, Hugh; Goranitis, Illias; Best, Stephanie; Alexander, Stephen; Stark, Zornitza; Mallett, Andrew J