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Peter Priestley

Utrecht University Medical Center

15H指数
36论文数
2.7K被引数
收录论文 10
发表时间
Whole genome sequencing improves tissue-of-origin diagnosis and treatment options for cancer of unknown primary全基因组测序提高了未知原发灶癌症的组织来源诊断和治疗选择。
err2025-05-20
err0
errOAAI
errRebello, Richard J.; Posner, Atara; Dong, Ruining; Prall, Owen W. J.; Sivakumaran, Tharani; Mitchell, Camilla B.; Flynn, Aidan; Caneborg, Alex; Mitchell, Catherine; Kanwal, Sehrish; Fedele, Clare; Webb, Samantha; Fisher, Krista; Wong, Hui-Li; Balachander, Shiva; Zhu, Wenying; Nicolson, Shannon; Dimitriadis, Voula; Wilcken, Nicholas; Defazio, Anna; Gao, Bo; Singh, Madhu; Collins, Ian M.; Steer, Christopher; Warren, Mark; Karanth, Narayan; Xu, Huiling; Fellowes, Andrew; Hicks, Rodney J.; Stewart, Kym Pham; Shale, Charles; Priestley, Peter; Dawson, Sarah-Jane; Vissers, Joseph H. A.; Fox, Stephen B.; Schofield, Penelope; Bowtell, David; Hofmann, Oliver; Grimmond, Sean M.; Mileshkin, Linda; Tothill, Richard W.
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Implementing ultra-sensitive, ctDNA-based liquid biopsy for disease monitoring in paediatric tumours
err2024-09-05
err0
PREAI
errSalomon, Robert; Chen, Wenhan; Shale, Charles; Toumari, Mojgan; Lowe, Aileen; Li, Wenyan; Chen, Jingwei; Bazaz, Sajad Razavi; Barahona, Paulette; Cui, Louise; Mayoh, Chelsea; El-Kamand, Sam; Tryell, Vanessa; Wong-Erasmus, Marie; Lau, Loretta M. S.; Bolanos, Noemi Fuentes; Cuppen, Edwin; Dong Anh Khuong Quang; Staunton, Jordan; Mateos, Marion K.; Trahair, Toby; Haber, Michelle; Ziegler, David S.; Ekert, Paul G.; Priestley, Peter; Cowley, Mark J.
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Complete genomic characterization in patients with cancer of unknown primary origin in routine diagnostics在常规诊断中,原发性未知癌症患者的完整基因组表征
err2022-12-01
err15
errOAAI
errSchipper, L. J.; Samsom, K. G.; Snaebjornsson, P.; Battaglia, T.; Bosch, L. J. W.; Lalezari, F.; Priestley, P.; Shale, C.; van den Broek, A. J.; Jacobs, N.; Roepman, P.; van der Hoeven, J. J. M.; Steeghs, N.; Vollebergh, M. A.; Marchetti, S.; Cuppen, E.; Meijer, G. A.; Voest, E. E.; Monkhorst, K.
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Recurrent exon-deleting activating mutations in AHR act as drivers of urinary tract cancer
err2022-06-16
err3
errOAAI
errVlaar, Judith M.; Borgman, Anouska; Kalkhoven, Eric; Westland, Denise; Besselink, Nicolle; Shale, Charles; Faltas, Bishoy M.; Priestley, Peter; Kuijk, Ewart; Cuppen, Edwin
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A multi-platform reference for somatic structural variation detection
err2022-06-01
err7
errOAAI
errValle-Inclan, Jose Espejo; Besselink, Nicolle J. M.; de Bruijn, Ewart; Cameron, Daniel L.; Ebler, Jana; Kutzera, Joachim; van Lieshout, Stef; Marschall, Tobias; Nelen, Marcel; Priestley, Peter; Renkens, Ivo; Roemer, Margaretha G. M.; Roosmalen, Markus J. van; Wenger, Aaron M.; Ylstra, Bauke; Fijneman, Remond J. A.; Kloosterman, Wigard P.; Cuppen, Edwin
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Unscrambling cancer genomes via integrated analysis of structural variation and copy number通过结构变异和拷贝数的整合分析来解读癌症基因组
err2022-04-01
err25
errOAAI
errShale, Charles; Cameron, Daniel L.; Baber, Jonathan; Wong, Marie; Cowley, Mark J.; Papenfuss, Anthony T.; Cuppen, Edwin; Priestley, Peter
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Whole genome sequencing can classify diagnostically challenging tumors
err2021-09-01
err1
errOAAI
errSchipper, L. J.; Snaebjornsson, P.; Samsom, K. G.; Bosch, L. J. W.; Lalezari, F.; Priestley, P.; Shale, C.; Jacobs, N.; van den Broek, A. J.; Roepman, P.; van der Hoeven, J. J. M.; Steeghs, N.; Cuppen, E.; Meijer, G.; Voest, E. E.; Monkhorst, K.
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GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing
err2021-07-12
err77
errOAAI
errCameron, Daniel L.; Baber, Jonathan; Shale, Charles; Valle-Inclan, Jose Espejo; Besselink, Nicolle; van Hoeck, Arne; Janssen, Roel; Cuppen, Edwin; Priestley, Peter; Papenfuss, Anthony T.
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Whole genome, transcriptome and methylome profiling enhances actionable target discovery in high-risk pediatric cancer全基因组,转录组和甲基化分析可增强高风险儿科癌症的可操作靶标发现
err2020-10-05
err229
PREAI
errWong, Marie; Mayoh, Chelsea; Lau, Loretta M. S.; Khuong-Quang, Dong-Anh; Pinese, Mark; Kumar, Amit; Barahona, Paulette; Wilkie, Emilie E.; Sullivan, Patricia; Bowen-James, Rachel; Syed, Mustafa; Martincorena, Inigo; Abascal, Federico; Sherstyuk, Alexandra; Bolanos, Noemi A.; Baber, Jonathan; Priestley, Peter; Dolman, M. Emmy M.; Fleuren, Emmy D. G.; Gauthier, Marie-Emilie; Mould, Emily V. A.; Gayevskiy, Velimir; Gifford, Andrew J.; Grebert-Wade, Dylan; Strong, Patrick A.; Manouvrier, Elodie; Warby, Meera; Thomas, David M.; Kirk, Judy; Tucker, Katherine; O'Brien, Tracey; Alvaro, Frank; McCowage, Geoffry B.; Dalla-Pozza, Luciano; Gottardo, Nicholas G.; Tapp, Heather; Wood, Paul; Khaw, Seong-Lin; Hansford, Jordan R.; Moore, Andrew S.; Norris, Murray D.; Trahair, Toby N.; Lock, Richard B.; Tyrrell, Vanessa; Haber, Michelle; Marshall, Glenn M.; Ziegler, David S.; Ekert, Paul G.; Cowley, Mark J.
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5-Fluorouracil treatment induces characteristic T>G mutations in human cancer
err2019-10-08
err141
errOAAI
errChristenser, Sharon; Van Der Roest, Bastiaan; Besselink, Nicolle; Janssen, Roel; Boymans, Sander; Martens, John W. M.; Yaspo, Marie-Laure; Priestley, Peter; Kuijk, Ewart; Cuppen, Edwin; Van Hoeck, Arne
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