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

Developing an advanced risk stratification model for pediatric intracranial ependymoma based on the prospective trial E-HIT2000 and subsequent registries

基于前瞻性试验 E-HIT2000 和后续注册研究,开发儿童颅内室管膜瘤的高级风险分层模型

von Hoff, Katja; Obrecht-Sturm, Denise; Ghasemi, David R; Wenning, Janna; Mynarek, Martin; Gerber, Nicolas U; Benesch, Martin; Juhnke, Björn O; Bison, Brigitte; Warmuth-Metz, Monika; Timmermann, Beate; Faldum, Andreas; Tippelt, Stephan; Fleischhack, Gudrun; Grotzer, Michael; Hernáiz Driever, Pablo; Beilken, Andreas; Ebinger, Martin; Graf, Norbert; Frühwald, Michael C; Schmid, Irene; Slavc, Irene; Koch, Arend; Bergmann, Markus; Hagel, Christian; Coras, Roland; Blümcke, Ingmar; Reifenberger, Guido; Felsberg, Jörg; Keyvani, Kathy; Harter, Patrick N; Prinz, Marco; Staszewski, Ori; Acker, Till; Stadelmann-Nessler, Christine; Hartmann, Christian; von Deimling, Andreas; Sommer, Clemens; Hasselblatt, Martin; Riemenschneider, Markus J; Monoranu, Camelia-Maria; Rushing, Elisabeth; Haberler, Christine; Kool, Marcel; Sill, Martin; Pfister, Stefan M; Schüller, Ulrich; Pietsch, Torsten; Kortmann, Rolf D; Kwiecien, Robert; Witt, Hendrik; Pajtler, Kristian W; Rutkowski, Stefan

Detection of Copy-Number Variations in CNS Tumours From Off-Target Reads of Hybrid-Capture Sequencing

利用杂交捕获测序的非靶向读段检测中枢神经系统肿瘤中的拷贝数变异

Schnorrenberg, Jan; Adrian, Yannis Luca; Schlathölter, Judith; Ruckert, Christian; Horvath, Judit; Paulus, Werner; Hasselblatt, Martin; Thomas, Christian

Characteristic immune cell interactions in livers of children with acute hepatitis revealed by spatial single-cell analysis identify a possible postacute sequel of COVID-19

通过空间单细胞分析揭示急性肝炎患儿肝脏中特征性的免疫细胞相互作用,可识别出新冠肺炎可能的急性后遗症。

Röttele, Felix; Zollner, Andreas; Mogler, Carolin; Yuksel, Muhammed; Arikan, Cigdem; Karl, Vivien; Aberle, Judith Helene; Aberle, Stephan W; Kogler, Hubert; Vécsei, Andreas; Vodopiutz, Julia; Salié, Henrike; Gräser, Anne; Krimmel, Laurenz; Martin, Pius; Lurz, Eberhard; Maier, Felix Immanuel; Woelfle, Lena; Nobre, Susana; Goncalves, Isabel; Kern, Lisa; Schwemmle, Martin; Boettler, Tobias; Hofmann, Maike; Hasselblatt, Peter; Thimme, Robert; Tilg, Herbert; Müller, Thomas; Vogel, Georg Friedrich; Bengsch, Bertram

Activation of Wnt/β-catenin signaling is critical for the tumorigenesis of choroid plexus

Wnt/β-catenin信号通路的激活对脉络丛肿瘤的发生至关重要

Ho, Kim Hoa; Trapp, Marleen; Guida, Catello; Ivanova, Ekaterina L; De Jaime-Soguero, Anchel; Jabali, Ammar; Thomas, Christian; Salasova, Alena; Bernatík, Ondřej; Salio, Chiara; Horschitz, Sandra; Hasselblatt, Martin; Sassoè-Pognetto, Marco; Čajánek, Lukáš; Ishikawa, Hiroshi; Schroten, Horst; Schwerk, Christian; Acebrón, Sergio P; Angel, Peter; Koch, Philipp; Patrizi, Annarita

Constitutional mosaicism of pathogenic variants in SMARCB1 in a subset of patients with sporadic rhabdoid tumors

散发性横纹肌样瘤患者亚群中SMARCB1致病变异的体质嵌合现象

Fleischmann, Lara S; Nemes, Karolina; Glaser, Selina; Kouroukli, Alexandra G; Boros, Matej; Bens, Susanne; Dahlum, Sonja; Kretzmer, Helene; Oyen, Florian; Gerss, Joachim; Hasselblatt, Martin; Frühwald, Michael C; Siebert, Reiner

VGLL fusions define a new class of intraparenchymal central nervous system schwannoma.

VGLL 融合定义了一类新的实质内中枢神经系统神经鞘瘤

Schmid Simone, Mirchia Kanish, Tietze Anna, Liu Ilon, Siewert Christin, Nückles Jakob, Schittenhelm Jens, Behling Felix, Snuderl Matija, Hartmann Christian, Brandner Sebastian, Paine Simon M L, Korshunov Andrey, Hasselblatt Martin, Coras Roland, Epari Sridhar, Stadelmann Christine, Zechel Sabrina, Simon Michèle, Wilson Yelena, Gianno Francesca, Lucas Calixto-Hope G Jr, Zherebitskiy Viktor, Kaimaktchiev Vassil B, Robinson Lorraina, Aldape Kenneth, Hoving Eelco W, Tops Bastiaan B J, Perera Ashwyn Augustine, Göller Pauline, Hernáiz Driever Pablo, Wesseling Pieter, Koch Arend, Perry Arie, Sahm Felix, Jones David T W, Capper David

PLAG1 fusions define a third subtype of CNS embryonal tumor with PLAG family gene alteration

PLAG1融合定义了第三种具有PLAG家族基因改变的中枢神经系统胚胎性肿瘤亚型。

Keck, Michaela-Kristina; Al-Hussaini, Maysa; Amayiri, Nisreen; Yiadom, Akosua Adoma Boakye; Chamyan, Gabriel; Cheesman, Edmund; Faure-Conter, Cécile; Garcia-Ariza, Miguel; Gauchotte, Guillaume; Hasselblatt, Martin; Jorgensen, Mette; Kilday, John-Paul; Lamas, Gabriela; Lavarino, Cinzia; Li, Marilyn M; Lubieniecki, Fabiana; Maher, Ossama M; Meyronet, David; Mueller, Jan; Santi, Mariarita; Schüller, Ulrich; Seidinger, Ana Luiza; Sill, Martin; Sudhakar, Sniya; García, María Tallón; Tauziede-Espariat, Arnault; Varlet, Pascale; Vasiljevic, Alexandre; Wittmann, Andrea; von Deimling, Andreas; Solomon, David A; Sahm, Felix; Tietze, Anna; von Hoff, Katja; Sievers, Philipp; Jones, David T W

IDH-mutant astrocytomas with primitive neuronal component have a distinct methylation profile and a higher risk of leptomeningeal spread

具有原始神经元成分的IDH突变型星形细胞瘤具有独特的甲基化谱,且发生软脑膜扩散的风险更高。

Hinz, Felix; Friedel, Dennis; Korshunov, Andrey; Ippen, Franziska M; Bogumil, Henri; Banan, Rouzbeh; Brandner, Sebastian; Hasselblatt, Martin; Boldt, Henning B; Dirse, Vaidas; Dohmen, Hildegard; Aronica, Eleonora; Brodhun, Michael; Broekman, Marike L D; Capper, David; Cherkezov, Asan; Deng, Maximilian Y; van Dis, Vera; Felsberg, Jörg; Frank, Stephan; French, Pim J; Gerlach, Rüdiger; Göbel, Kirsten; Goold, Eric; Hench, Jürgen; Kantelhardt, Sven; Kohlhof-Meinecke, Patricia; Krieg, Sandro; Mawrin, Christian; Morrison, Gillian; Mühlebner, Angelika; Ozduman, Koray; Pfister, Stefan M; Poliani, Pietro Luigi; Prinz, Marco; Reifenberger, Guido; Riemenschneider, Markus J; Sankowski, Roman; Schrimpf, Daniel; Sill, Martin; Snuderl, Matija; Verdijk, Robert M; Voisin, Mathew R; Wesseling, Pieter; Wick, Wolfgang; Reuss, David E; von Deimling, Andreas; Sahm, Felix; Maas, Sybren L N; Suwala, Abigail K

Concurrence of FGFR1 mutations modulates oncogenesis in glioneuronal tumors.

FGFR1 突变的并发会调节神经胶质肿瘤的发生。

Boni Jacopo, Fernández-González Míriam, Han HyeRim, Roca Carla, Wong Cassandra J, Rioja Cristina, Nogué Clara, Manen-Freixa Leticia, Boulais Jonathan, Torres-Urtizberea Endika, Gomez Antonio, Hasselblatt Martin, Estrada-Tejedor Roger, Antolin Albert A, Elkholi Islam E, Jabado Nada, Côté Jean-François, Gingras Anne-Claude, Rivera Barbara

A rare case of atypical teratoid rhabdoid tumor (AT/RT) with homozygous SMARCB1 loss and one concurrent somatic heterozygous SMARCA4 variant

一例罕见的非典型畸胎瘤样横纹肌瘤(AT/RT),伴有SMARCB1纯合缺失和一处同时存在的体细胞杂合SMARCA4变异。

Müller, Ylvi; Bühner, Sebastian; Fincke, Victoria; Mauch-Mücke, Katrin; Riemenschneider, Markus J; Manea, Selma; Liesche-Starnecker, Friederike; Hasselblatt, Martin; Dahlum, Sonja; Boros, Matej; Siebert, Reiner; Frühwald, Michael C; Johann, Pascal