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

Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

欧洲神经母细胞瘤研究组(SIOPEN)高危神经母细胞瘤试验(HR-NBL1)中ALK扩增和突变的频率及预后影响

Bellini, Angela; Pötschger, Ulrike; Bernard, Virginie; Lapouble, Eve; Baulande, Sylvain; Ambros, Peter F; Auger, Nathalie; Beiske, Klaus; Bernkopf, Marie; Betts, David R; Bhalshankar, Jaydutt; Bown, Nick; de Preter, Katleen; Clément, Nathalie; Combaret, Valérie; Font de Mora, Jaime; George, Sally L; Jiménez, Irene; Jeison, Marta; Marques, Barbara; Martinsson, Tommy; Mazzocco, Katia; Morini, Martina; Mühlethaler-Mottet, Annick; Noguera, Rosa; Pierron, Gaelle; Rossing, Maria; Taschner-Mandl, Sabine; Van Roy, Nadine; Vicha, Ales; Chesler, Louis; Balwierz, Walentyna; Castel, Victoria; Elliott, Martin; Kogner, Per; Laureys, Geneviève; Luksch, Roberto; Malis, Josef; Popovic-Beck, Maja; Ash, Shifra; Delattre, Olivier; Valteau-Couanet, Dominique; Tweddle, Deborah A; Ladenstein, Ruth; Schleiermacher, Gudrun

Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden

对低突变负荷的儿童癌症进行无细胞DNA全基因组测序的多模式分析

Peneder, Peter; Stütz, Adrian M; Surdez, Didier; Krumbholz, Manuela; Semper, Sabine; Chicard, Mathieu; Sheffield, Nathan C; Pierron, Gaelle; Lapouble, Eve; Tötzl, Marcus; Ergüner, Bekir; Barreca, Daniele; Rendeiro, André F; Agaimy, Abbas; Boztug, Heidrun; Engstler, Gernot; Dworzak, Michael; Bernkopf, Marie; Taschner-Mandl, Sabine; Ambros, Inge M; Myklebost, Ola; Marec-Bérard, Perrine; Burchill, Susan Ann; Brennan, Bernadette; Strauss, Sandra J; Whelan, Jeremy; Schleiermacher, Gudrun; Schaefer, Christiane; Dirksen, Uta; Hutter, Caroline; Boye, Kjetil; Ambros, Peter F; Delattre, Olivier; Metzler, Markus; Bock, Christoph; Tomazou, Eleni M

Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

常见种系易感基因位点附近的低频变异与尤文氏肉瘤的风险相关。

Lin, Shu-Hong; Sampson, Joshua N; Grünewald, Thomas G P; Surdez, Didier; Reynaud, Stephanie; Mirabeau, Olivier; Karlins, Eric; Rubio, Rebeca Alba; Zaidi, Sakina; Grossetête-Lalami, Sandrine; Ballet, Stelly; Lapouble, Eve; Laurence, Valérie; Michon, Jean; Pierron, Gaelle; Kovar, Heinrich; Kontny, Udo; González-Neira, Anna; Alonso, Javier; Patino-Garcia, Ana; Corradini, Nadège; Bérard, Perrine Marec; Miller, Jeremy; Freedman, Neal D; Rothman, Nathaniel; Carter, Brian D; Dagnall, Casey L; Burdett, Laurie; Jones, Kristine; Manning, Michelle; Wyatt, Kathleen; Zhou, Weiyin; Yeager, Meredith; Cox, David G; Hoover, Robert N; Khan, Javed; Armstrong, Gregory T; Leisenring, Wendy M; Bhatia, Smita; Robison, Leslie L; Kulozik, Andreas E; Kriebel, Jennifer; Meitinger, Thomas; Metzler, Markus; Krumbholz, Manuela; Hartmann, Wolfgang; Strauch, Konstantin; Kirchner, Thomas; Dirksen, Uta; Mirabello, Lisa; Tucker, Margaret A; Tirode, Franck; Morton, Lindsay M; Chanock, Stephen J; Delattre, Olivier; Machiela, Mitchell J

Study of chromatin remodeling genes implicates SMARCA4 as a putative player in oncogenesis in neuroblastoma.

染色质重塑基因的研究表明,SMARCA4 可能是神经母细胞瘤发生过程中的一个潜在因素

Bellini Angela, Bessoltane-Bentahar Nadia, Bhalshankar Jaydutt, Clement Nathalie, Raynal Virginie, Baulande Sylvain, Bernard Virginie, Danzon Adrien, Chicard Mathieu, Colmet-Daage Léo, Pierron Gaelle, Le Roux Laura, Planchon Julien M, Combaret Valérie, Lapouble Eve, Corradini Nadège, Thebaud Estelle, Gambart Marion, Valteau-Couanet Dominique, Michon Jean, Louis-Brennetot Caroline, Janoueix-Lerosey Isabelle, Defachelles Anne-Sophie, Bourdeaut Franck, Delattre Olivier, Schleiermacher Gudrun

Genomic Amplifications and Distal 6q Loss: Novel Markers for Poor Survival in High-risk Neuroblastoma Patients

基因组扩增和远端6q缺失:高危神经母细胞瘤患者预后不良的新型标志物

Depuydt, Pauline; Boeva, Valentina; Hocking, Toby D; Cannoodt, Robrecht; Ambros, Inge M; Ambros, Peter F; Asgharzadeh, Shahab; Attiyeh, Edward F; Combaret, Valérie; Defferrari, Raffaella; Fischer, Matthias; Hero, Barbara; Hogarty, Michael D; Irwin, Meredith S; Koster, Jan; Kreissman, Susan; Ladenstein, Ruth; Lapouble, Eve; Laureys, Geneviève; London, Wendy B; Mazzocco, Katia; Nakagawara, Akira; Noguera, Rosa; Ohira, Miki; Park, Julie R; Pötschger, Ulrike; Theissen, Jessica; Tonini, Gian Paolo; Valteau-Couanet, Dominique; Varesio, Luigi; Versteeg, Rogier; Speleman, Frank; Maris, John M; Schleiermacher, Gudrun; De Preter, Katleen

QuantumClone: clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction

QuantumClone:基于基因型感知克隆重建方法的癌症功能突变克隆评估

Deveau, Paul; Colmet Daage, Leo; Oldridge, Derek; Bernard, Virginie; Bellini, Angela; Chicard, Mathieu; Clement, Nathalie; Lapouble, Eve; Combaret, Valerie; Boland, Anne; Meyer, Vincent; Deleuze, Jean-Francois; Janoueix-Lerosey, Isabelle; Barillot, Emmanuel; Delattre, Olivier; Maris, John M; Schleiermacher, Gudrun; Boeva, Valentina

DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma

DNA甲基化异质性定义了尤文氏肉瘤的疾病谱

Sheffield, Nathan C; Pierron, Gaelle; Klughammer, Johanna; Datlinger, Paul; Schönegger, Andreas; Schuster, Michael; Hadler, Johanna; Surdez, Didier; Guillemot, Delphine; Lapouble, Eve; Freneaux, Paul; Champigneulle, Jacqueline; Bouvier, Raymonde; Walder, Diana; Ambros, Ingeborg M; Hutter, Caroline; Sorz, Eva; Amaral, Ana T; de Álava, Enrique; Schallmoser, Katharina; Strunk, Dirk; Rinner, Beate; Liegl-Atzwanger, Bernadette; Huppertz, Berthold; Leithner, Andreas; de Pinieux, Gonzague; Terrier, Philippe; Laurence, Valérie; Michon, Jean; Ladenstein, Ruth; Holter, Wolfgang; Windhager, Reinhard; Dirksen, Uta; Ambros, Peter F; Delattre, Olivier; Kovar, Heinrich; Bock, Christoph; Tomazou, Eleni M

Segmental Chromosomal Aberrations in Localized Neuroblastoma Can be Detected in Formalin-Fixed Paraffin-Embedded Tissue Samples and Are Associated With Recurrence

局限性神经母细胞瘤的节段性染色体畸变可在福尔马林固定石蜡包埋组织样本中检测到,且与复发相关。

Pinto, Navin; Mayfield, Jodi R; Raca, Gordana; Applebaum, Mark A; Chlenski, Alexandre; Sukhanova, Madina; Bagatell, Rochelle; Irwin, Meredith S; Little, Anthony; Rawwas, Jawhar; Gosiengfiao, Yasmin; Delattre, Olivier; Janoueix-Lerosey, Isabelle; Lapouble, Eve; Schleiermacher, Gudrun; Cohn, Susan L

Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite

嵌合体 EWSR1-FLI1 通过 GGAA 微卫星调控尤文氏肉瘤易感基因 EGR2

Grünewald, Thomas G P; Bernard, Virginie; Gilardi-Hebenstreit, Pascale; Raynal, Virginie; Surdez, Didier; Aynaud, Marie-Ming; Mirabeau, Olivier; Cidre-Aranaz, Florencia; Tirode, Franck; Zaidi, Sakina; Perot, Gaëlle; Jonker, Anneliene H; Lucchesi, Carlo; Le Deley, Marie-Cécile; Oberlin, Odile; Marec-Bérard, Perrine; Véron, Amélie S; Reynaud, Stephanie; Lapouble, Eve; Boeva, Valentina; Rio Frio, Thomas; Alonso, Javier; Bhatia, Smita; Pierron, Gaëlle; Cancel-Tassin, Geraldine; Cussenot, Olivier; Cox, David G; Morton, Lindsay M; Machiela, Mitchell J; Chanock, Stephen J; Charnay, Patrick; Delattre, Olivier

Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations

尤文氏肉瘤的基因组图谱定义了一种侵袭性亚型,该亚型与STAG2和TP53突变的共存有关。

Tirode, Franck; Surdez, Didier; Ma, Xiaotu; Parker, Matthew; Le Deley, Marie Cécile; Bahrami, Armita; Zhang, Zhaojie; Lapouble, Eve; Grossetête-Lalami, Sandrine; Rusch, Michael; Reynaud, Stéphanie; Rio-Frio, Thomas; Hedlund, Erin; Wu, Gang; Chen, Xiang; Pierron, Gaelle; Oberlin, Odile; Zaidi, Sakina; Lemmon, Gordon; Gupta, Pankaj; Vadodaria, Bhavin; Easton, John; Gut, Marta; Ding, Li; Mardis, Elaine R; Wilson, Richard K; Shurtleff, Sheila; Laurence, Valérie; Michon, Jean; Marec-Bérard, Perrine; Gut, Ivo; Downing, James; Dyer, Michael; Zhang, Jinghui; Delattre, Olivier