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

Long read nanopore DNA sequencing with adaptive sampling to identify tyrosine kinase fusion genes

利用自适应采样进行长读长纳米孔DNA测序,以鉴定酪氨酸激酶融合基因

Salmon, Matthew; Naumann, Nicole; Rinke, Jenny; Meggendorfer, Manja; Radia, Deepti; Pomfret, Mark; Ernst, Thomas; Hochhaus, Andreas; Reiter, Andreas; Tapper, William J; White, Helen; Cross, Nicholas C P

Solving Riddles Through Sequencing (SIRIUS): unlocking hematologic diagnoses by whole genome and transcriptome sequencing

通过测序解谜(SIRIUS):利用全基因组和转录组测序破解血液学诊断难题

Truger, Marietta; Meggendorfer, Manja; Walter, Wencke; Hutter, Stephan; Alsdorf, Winfried; Massenkeil, Gero; Martens, Uwe M; Kern, Wolfgang; Hörst, Katharina; Kühn, Constanze; Reiter, Andreas; Hochhaus, Andreas; Haferlach, Torsten

The FGFR1 N546K mutation confers resistance to pemigatinib in MLN-ZMYM2::FGFR1

FGFR1 N546K 突变赋予 MLN-ZMYM2::FGFR1 对 pemigatinib 的耐药性

Shoumariyeh, Khalid; Haug, Stefan; Schwaab, Juliana; Pfeil, Julie K; Stappenbeck, Jannis; Schmitt-Graeff, Annette; Naumann, Nicole; Waltemode, Greta; Zeiser, Robert; Miething, Cornelius; Hofmann, Wolf-Karsten; Meggendorfer, Manja; Diederichs, Sven; Duyster, Justus; Reiter, Andreas

Primary asciminib resistance in a chronic myeloid leukemia patient with the atypical BCR::ABL1 e13a3 transcript: a case study

一例伴有非典型 BCR::ABL1 e13a3 转录本的慢性粒细胞白血病患者出现原发性 asciminib 耐药:病例研究

Jung, Birte Kristin; Weißmann, Sandra; Schock, Caroline; Meggendorfer, Manja; Haferlach, Torsten; Dicker, Frank

Clonal haematopoiesis of indeterminate potential and mortality in coronary artery disease

克隆性造血(潜能未定)与冠状动脉疾病死亡率

von Scheidt, Moritz; Adkar, Shaunak S; Krefting, Johannes; Hoermann, Gregor; Meggendorfer, Manja; Bauer, Sabine; Mitchell, Shaneice; Pugach, Irina; Friess, Christian; Ma, Angela; Hao, Ke; Steigerwald, Sophia; Wahle, Maria; Kessler, Thorsten; Schwab, Marius; Voll, Felix; Mokry, Michal; Sofokleous, Charalampos; Palm, Kaylin C A; Bongiovanni, Dario; Fleig, Julia; Oldenbuettel, Lilith; Chen, Zhifen; Hecker, Judith S; Bassermann, Florian; Maegdefessel, Lars; Graw, Matthias; Ruusalepp, Arno; Hilgendorf, Ingo; Leuschner, Florian; Sager, Hendrik B; Heimlich, J Brett; Koenig, Wolfgang; Cremer, Sebastian; Leistner, David M; Abplanalp, Wesley T; Dimmeler, Stefanie; Zeiher, Andreas M; van der Laan, Sander W; Pasterkamp, Gerard; Braun, Christian; Jaiswal, Siddhartha; Kovacic, Jason C; Kern, Wolfgang; Haferlach, Claudia; Mann, Matthias; Cassese, Salvatore; Kastrati, Adnan; Haferlach, Torsten; Leeper, Nicholas J; Björkegren, Johan L M; Schunkert, Heribert

A novel prognostic risk model for patients with refractory/relapsed acute myeloid leukemia receiving venetoclax plus hypomethylating agents

一种用于接受维奈托克联合去甲基化药物治疗的难治性/复发性急性髓系白血病患者的新型预后风险模型

Shahswar, Rabia; Gabdoulline, Razif; Krueger, Katja; Wichmann, Martin; Götze, Katharina S; Braitsch, Krischan; Meggendorfer, Manja; Schmalbrock, Laura; Bullinger, Lars; Modemann, Franziska; Fiedler, Walter; Krauter, Juergen; Kaun, Stephan; Rotermund, Susanne; Voß, Andreas; Behrens, Yvonne Lisa; Bergmann, Anke Katharina; Koller, Elisabeth; Beutel, Gernot; Thol, Felicitas; Heidel, Florian; Heuser, Michael

ATM aberrations in chronic lymphocytic leukemia: del(11q) rather than ATM mutations is an adverse-prognostic biomarker

慢性淋巴细胞白血病中的ATM异常:del(11q)而非ATM突变是不良预后生物标志物

Thorvaldsdottir, Birna; Mansouri, Larry; Sutton, Lesley-Ann; Nadeu, Ferran; Meggendorfer, Manja; Parker, Helen; Brieghel, Christian; Laidou, Stamatia; Moia, Riccardo; Rossi, Davide; Kotaskova, Jana; Delgado, Julio; Rodríguez-Vicente, Ana E; Benito, Rocío; Rigolin, Gian Matteo; Bonfiglio, Silvia; Scarfò, Lydia; Mattsson, Mattias; Davis, Zadie; Baliakas, Panagiotis; Rapado, Inmaculada; Miras, Fatima; Martinez-Lopez, Joaquín; de la Serna, Javier; Hernández Rivas, Jesús María; Larráyoz, María José; Calasanz, María José; Smedby, Karin E; Espinet, Blanca; Puiggros, Anna; Bullinger, Lars; Bosch, Francesc; Tazón-Vega, Bárbara; Baran-Marszak, Fanny; Oscier, David; Nguyen-Khac, Florence; Zenz, Thorsten; Terol, Maria Jose; Cuneo, Antonio; Hernández-Sánchez, María; Pospisilova, Sarka; Gaidano, Gianluca; Niemann, Carsten U; Campo, Elias; Strefford, Jonathan C; Ghia, Paolo; Stamatopoulos, Kostas; Rosenquist, Richard

Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutations

VEXAS致病性UBA1 M41突变和复发性功能性非M41突变的独特特征

Sakuma, Maki; Wang, Amy K; Magaziner, Samuel J; Keane, Sachiko P; Meggendorfer, Manja; Kern, Wolfgang; Haferlach, Claudia; Haferlach, Torsten; Beck, David B; Walter, Wencke

Myeloid neoplasms with MYC-positive double minutes: towards recognition as a distinct entity

MYC阳性双微体髓系肿瘤:迈向一种独立实体的认知

Summerer, Isolde; Walter, Wencke; Meggendorfer, Manja; Haferlach, Torsten; Dicker, Frank; Hutter, Stephan; Nadarajah, Niroshan; Stengel, Anna; Kuehn, Constanze; Kern, Wolfgang; Bennett, John M; Haferlach, Claudia; Pohlkamp, Christian

Two ways to complex karyotype in MDS-the role of del(5q) and TP53

MDS中复杂核型的两种解释——del(5q)和TP53的作用

Huber, Sandra; Hutter, Stephan; Baer, Constance; Meggendorfer, Manja; Hoermann, Gregor; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia