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Georgina L. Ryland

peter maccallum cancer center

24H指数
81论文数
2.4K被引数
收录论文 19
发表时间
Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes (vol 106, pg 64, 2021)
err2024-04-01
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errBlombery, 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
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JAFFAL: detecting fusion genes with long-read transcriptome sequencingJAFFAL: 利用长读段转录组测序检测融合基因
err2022-01-06
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errOAAI
errDavidson, Nadia M.; Chen, Ying; Sadras, Teresa; Ryland, Georgina L.; Blombery, Piers; Ekert, Paul G.; Goke, Jonathan; Oshlack, Alicia
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HIGH DOSE-RATE BRACHYTHERAPY OF LOCALIZED PROSTATE CANCER CONVERTS TUMORS FROM COLD TO HOT
err2020-12-10
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errKeam, Simon; Halse, Heloise; ThuNgoc Nguyen; Wang, Minyu; Losio, Nicolas Van Kooten; Mitchell, Catherine; Caramia, Franco; Byrne, David; Haupt, Sue; Ryland, Georgina; Darcy, Phillip; Sandhu, Shahneen; Blombery, Piers; Haupt, Ygal; Williams, Scott; Neeson, Paul
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High dose-rate brachytherapy of localized prostate cancer converts tumors from cold to hot
err2020-06-24
err54
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errKeam, Simon P.; Halse, Heloise; Nguyen, Thu; Wang, Minyu; Van Kooten Losio, Nicolas; Mitchell, Catherine; Caramia, Franco; Byrne, David J.; Haupt, Sue; Ryland, Georgina; Darcy, Phillip K.; Sandhu, Shahneen; Blombery, Piers; Haupt, Ygal; Williams, Scott G.; Neeson, Paul J.
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CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing (vol 9, 6426, 2019)
err2020-06-23
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errMarkham, John F.; Yerneni, Satwica; Ryland, Georgina L.; Leong, Huei San; Fellowes, Andrew; Thompson, Ella R.; De Silva, Wasanthi; Kumar, Amit; Lupat, Richard; Li, Jason; Ellul, Jason; Fox, Stephen; Dickinson, Michael; Papenfuss, Anthony T.; Blombery, Piers
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Utility of clinical comprehensive genomic characterization for diagnostic categorization in patients presenting with hypocellular bone marrow failure syndromes
err2020-02-13
err19
errOAAI
errBlombery, Piers; Fox, Lucy C.; Ryland, Georgina L.; Thompson, Ella R.; Lickiss, Jennifer; McBean, Michelle; Yerneni, Satwica; 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
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CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing
err2019-04-23
err21
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errMarkham, John F.; Yerneni, Satwica; Ryland, Georgina L.; San Leong, Huei; Fellowes, Andrew; Thompson, Ella R.; De Silva, Wasanthi; Kumar, Amit; Lupat, Richard; Li, Jason; Ellul, Jason; Fox, Stephen; Dickinson, Michael; Papenfuss, Anthony T.; Blombery, Piers
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Sensitive NPM1 Mutation Quantitation in Acute Myeloid Leukemia Using Ultradeep Next-Generation Sequencing in the Diagnostic Laboratory
err2018-02-09
err8
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errBlombery, Piers; Jones, Kate; Doig, Ken; Ryland, Georgina; McBean, Michelle; Thompson, Ella; Yannakou, Costas K.; Westerman, David
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ASXL1 c.1934dup;p.Gly646Trpfs*12-a true somatic alteration requiring a new approach
err2017-12-20
err21
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errYannakou, Costas K.; Jones, Kate; McBean, Michelle; Thompson, Ella R.; Ryland, Georgina L.; Doig, Ken; Markham, John; Westerman, David; Blombery, Piers
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Prevalence and timing of TP53 mutations in del(17p) myeloma and effect on survival
err2017-09-15
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errChin, M.; Sive, J. I.; Allen, C.; Roddie, C.; Chavda, S. J.; Smith, D.; Blombery, P.; Jones, K.; Ryland, G. L.; Popat, R.; Rismani, A.; D'Sa, S.; Rabin, N.; Gale, R. E.; Yong, K. L.
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Multiplexed transcriptome analysis to detect ALK, ROS1 and RET rearrangements in lung cancer多重转录组分析检测肺癌中ALK,ROS1和RET重排
err2017-02-09
err48
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errRogers, Toni-Maree; Arnau, Gisela Mir; Ryland, Georgina L.; Huang, Stephen; Lira, Maruja E.; Emmanuel, Yvette; Perez, Omar D.; Irwin, Darryl; Fellowes, Andrew P.; Wong, Stephen Q.; Fox, Stephen B.
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Genomics analyses of less common epithelial ovarian cancer subtypes.
err2016-01-15
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PREAI
errGorringe, Kylie L.; Wakefield, Matthew; Hunter, Sally M.; Ryland, Georgina L.; Cheasley, Dane; Anglesio, Michael S.; Christie, Michael; Sharma, Raghwa; Yoland, Antill; Rowley, Simone M.; Li, Jason; Gilks, Blake; Allan, Prue E.; Stephens, Andrew N.; Ananda, Sumi; Pyman, Jan; Koebel, Martin; McAlpine, Jessica; Gourley, Charlie; Huntsman, David G.; deFazio, Anna; Bowtell, David D. L.; Campbell, Ian G.; Scott, Clare
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Inferring copy number and genotype in tumour exome data
err2014-08-28
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errAmarasinghe, Kaushalya C.; Li, Jason; Hunter, Sally M.; Ryland, Georgina L.; Cowin, Prue A.; Campbell, Ian G.; Halgamuge, Saman K.
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A simple consensus approach improves somatic mutation prediction accuracy
err2013-09-30
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errGoode, David L.; Hunter, Sally M.; Doyle, Maria A.; Ma, Tao; Rowley, Simone M.; Choong, David; Ryland, Georgina L.; Campbell, Ian G.
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RNF43 is a tumour suppressor gene mutated in mucinous tumours of the ovary
err2013-01-25
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errRyland, Georgina L.; Hunter, Sally M.; Doyle, Maria A.; Rowley, Simone M.; Christie, Michael; Allan, Prue E.; Bowtell, David D. L.; Gorringe, Kylie L.; Campbell, Ian G.
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Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles
err2012-09-27
err180
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errThompson, Ella R.; Doyle, Maria A.; Ryland, Georgina L.; Rowley, Simone M.; Choong, David Y. H.; Tothill, Richard W.; Thorne, Heather; Barnes, Daniel R.; Li, Jason; Ellul, Jason; Philip, Gayle K.; Antill, Yoland C.; James, Paul A.; Trainer, Alison H.; Mitchell, Gillian; Campbell, Ian G.
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An activating Pik3ca mutation coupled with Pten loss is sufficient to initiate ovarian tumorigenesis in mice
err2012-02-01
err198
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errKinross, Kathryn M.; Montgomery, Karen G.; Kleinschmidt, Margarete; Waring, Paul; Ivetac, Ivan; Tikoo, Anjali; Saad, Mirette; Hare, Lauren; Roh, Vincent; Mantamadiotis, Theo; Sheppard, Karen E.; Ryland, Georgina L.; Campbell, Ian G.; Gorringe, Kylie L.; Christensen, James G.; Cullinane, Carleen; Hicks, Rodney J.; Pearson, Richard B.; Johnstone, Ricky W.; McArthur, Grant A.; Phillips, Wayne A.
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Analysis of RAD51C Germline Mutations in High-Risk Breast and Ovarian Cancer Families and Ovarian Cancer Patients
err2011-11-04
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errThompson, Ella R.; Boyle, Samantha E.; Johnson, Julie; Ryland, Georgina L.; Sawyer, Sarah; Choong, David Y. H.; Chenevix-Trench, Georgia; Trainer, Alison H.; Lindeman, Geoffrey J.; Mitchell, Gillian; James, Paul A.; Campbell, Ian G.
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Analysis of the Mitogen-activated protein kinase kinase 4 (MAP2K4) tumor suppressor gene in ovarian cancer
err2011-05-17
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errDavis, Sally J.; Choong, David Y. H.; Ramakrishna, Manasa; Ryland, Georgina L.; Campbell, Ian G.; Gorringe, Kylie L.
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