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

Frequent and clinically relevant germline DNA repair gene variants in young and familial myeloproliferative neoplasms

年轻和家族性骨髓增生性肿瘤中常见且具有临床意义的种系DNA修复基因变异

Meyer, Robert; Rodriguez, Maria Jimena; Caduc, Madeline; Kricheldorf, Kim; Begemann, Matthias; Kraft, Florian; Spier, Isabel; Dey, Daniela; Güzel, Nergis; Becker, Kerstin; Baumeister, Julian; S de Toledo, Marcelo A; Isfort, Susanne; Germing, Ulrich; Aretz, Stefan; Brümmendorf, Tim H; Kurth, Ingo; Elbracht, Miriam; Teichmann, Lino L; Koschmieder, Steffen

Mitigation of atrial fibrillation-related complications with antithrombotic and cytoreductive therapy in patients with Myeloproliferative Neoplasms: Implications from the GSG-MPN bioregistry

抗血栓和细胞减灭疗法减轻骨髓增生性肿瘤患者房颤相关并发症:来自 GSG-MPN 生物注册研究的启示

Cho, Hyunyee Rosa; Isfort, Susanne; Kricheldorf, Kim; Stegelmann, Frank; Klausmann, Martine; Heidel, Florian H; Griesshammer, Martin; Schulz, Holger; Hochhaus, Andreas; Göthert, Joachim; Schlag, Rudolf; Hollburg, Wiebke; Teichmann, Lino; Sockel, Katja; Wilop, Stefan; Gezer, Deniz; Kirschner, Martin; Döhner, Konstanze; Brümmendorf, Tim H; Koschmieder, Steffen

Comparison of recognition of symptom burden in MPN between patient- and physician-reported assessment - an intraindividual analysis by the German Study Group for MPN (GSG-MPN)

德国骨髓增生性肿瘤研究组 (GSG-MPN) 对 MPN 症状负担的识别进行了比较,比较了患者报告评估和医生报告评估的结果——一项个体内部分析

Manz, Kirsi; Heidel, Florian H; Koschmieder, Steffen; Schlag, Rudolf; Lipke, Jörg; Stegelmann, Frank; Griesshammer, Martin; Klausmann, Martine; Crodel, Carl; Hochhaus, Andreas; Schulz, Holger; Göthert, Joachim R; Al-Ali, Haifa; Becker, Heiko; Reiter, Andreas; Beutel, Gernot; Kricheldorf, Kim; Brümmendorf, Tim H; Hoffmann, Wolfgang; Döhner, Konstanze; Isfort, Susanne

Allogeneic stem cell transplantation from variant-carrying family donors leads to long-term engraftment in Telomere Biology Disorders

来自携带变异基因的家族供体的异基因干细胞移植可导致端粒生物学疾病患者的长期植入。

Güzel, Nergis; Schumacher, Yannic; Kricheldorf, Kim; Vieri, Margherita; Kirschner, Martin; Gerhard-le Gars, Anne-Claire; Panse, Jens; Tometten, Mareike; Walter, Jeanette; Gehrig, Andrea; Kunstmann, Erdmute; Holthöfer, Laura; Schweiger, Susann; Wolff, Daniel; Kraft, Florian; Elbracht, Miriam; Kurth, Ingo; Brümmendorf, Tim H; Meyer, Robert; Beier, Fabian

Late-onset telomere biology disorders in adults: clinical insights and treatment outcomes from a retrospective registry cohort

成人迟发性端粒生物学疾病:来自回顾性登记队列的临床见解和治疗结果

Tometten, Mareike; Beier, Fabian; Kirschner, Martin; Schumacher, Yannic; Walter, Jeanette; Vieri, Margherita; Kricheldorf, Kim; Röth, Alexander; Platzbecker, Uwe; Radsak, Markus; Schafhausen, Philippe; Corbacioglu, Selim; Höchsmann, Britta; Balabanov, Stefan; Hinze, Claas; Chromik, Jörg; Heuser, Michael; Kreuter, Michael; Wlodarski, Marcin W; Elbracht, Miriam; Kurth, Ingo; Koschmieder, Steffen; Panse, Jens; Isfort, Susanne; Meyer, Robert; Brümmendorf, Tim H

DNA methylation in primary myelofibrosis is partly associated with driver mutations and distinct from other myeloid malignancies

原发性骨髓纤维化中的DNA甲基化部分与驱动基因突变相关,并且与其他髓系恶性肿瘤不同。

Dursun Torlak, Esra; Tharmapalan, Vithurithra; Kricheldorf, Kim; Schifflers, Joelle; Caduc, Madeline; Zenke, Martin; Koschmieder, Steffen; Wagner, Wolfgang

SIngle cell level Genotyping Using scRna Data (SIGURD)

利用scRNA数据进行单细胞水平基因分型(SIGURD)

Grasshoff, Martin; Kalmer, Milena; Chatain, Nicolas; Kricheldorf, Kim; Maurer, Angela; Weiskirchen, Ralf; Koschmieder, Steffen; Costa, Ivan G

Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria

利用年龄修正标准进行端粒长度筛查,识别患有经典型先天性角化不良或隐匿性端粒生物学疾病的成年患者

Tometten, Mareike; Kirschner, Martin; Meyer, Robert; Begemann, Matthias; Halfmeyer, Insa; Vieri, Margherita; Kricheldorf, Kim; Maurer, Angela; Platzbecker, Uwe; Radsak, Markus; Schafhausen, Philippe; Corbacioglu, Selim; Höchsmann, Britta; Matthias Wilk, C; Hinze, Claas; Chromik, Jörg; Heuser, Michael; Kreuter, Michael; Koschmieder, Steffen; Panse, Jens; Isfort, Susanne; Kurth, Ingo; Brümmendorf, Tim H; Beier, Fabian

Clinicohematologic and molecular response of essential thrombocythemia patients treated with pegylated interferon-α: a multi-center study of the German Study Group-Myeloproliferative Neoplasms (GSG-MPN)

聚乙二醇干扰素-α治疗原发性血小板增多症患者的临床血液学和分子反应:德国骨髓增生性肿瘤研究组(GSG-MPN)的多中心研究

Stegelmann, Frank; Teichmann, Lino L; Heidel, Florian H; Crodel, Carl C; Ernst, Thomas; Kreil, Sebastian; Reiter, Andreas; Otten, Sara; Schauer, Stefanie; Körber, Ruth-Miriam; Kricheldorf, Kim; Isfort, Susanne; Döhner, Hartmut; Brümmendorf, Tim H; Griesshammer, Martin; Döhner, Konstanze; Koschmieder, Steffen

Impaired Overall Survival in Young Patients With Acute Myeloid Leukemia and Variants in Genes Predisposing for Myeloid Malignancies

年轻急性髓系白血病患者总体生存率降低,且存在易患髓系恶性肿瘤的基因变异

Kirschner, Martin; Rolles, Benjamin; Crysandt, Martina; Röllig, Christoph; Stölzel, Friedrich; Kramer, Michael; Bornhäuser, Martin; Serve, Hubert; Platzbecker, Uwe; Müller-Tidow, Carsten; Kricheldorf, Kim; Vieri, Margherita; Begemann, Matthias; Maurer, Angela; Wlodarski, Marcin W; Sahoo, Sushree S; Brümmendorf, Tim H; Jost, Edgar; Beier, Fabian