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Stephan Hütter

mll munich leukemia laboratory

27H指数
198论文数
2.4K被引数
收录论文 64
发表时间
Functional Classification of Monoallelic TP53 Mutations Refines Prognostic Stratification in Myelodysplastic Neoplasms单等位基因TP53突变的功能分类细化了骨髓增生异常性肿瘤的预后分层
errBlood
IF23.1
err2026-10-06
err0
PREAI
errAlexander Streuer; Yotaro Ochi; Stephan Hutter; Vladimir Riabov; Yasuhito Nannya; Laurenz Steiner; Mohammed Abba; Georgia Metzgeroth; Eva Altrock; Felicitas Rapp; Verena Nowak; Edin Hepgülüm; Steffen Boettcher; Torsten Haferlach; Daniel Nowak; Wolf-Karsten Hofmann; Seishi Ogawa; Nanni Schmitt
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Two cases of an imatinib-sensitive PRKG2::PDGFRA-positive chronic myeloid neoplasm with basophilia两例对伊马替尼敏感的PRKG2::PDGFRA阳性伴嗜碱性粒细胞增多慢性髓系肿瘤
errLeukemia
IF13.4
err2026-09-28
err0
errOAAI
errJohannes Lübke; Olaposi Yomade; Manja Meggendorfer; Jan-Hendrik Kozik; Marietta Truger; Wencke Walter; Stephan Hutter; Uwe Martens; Martina Rudelius; Nicole Naumann; Alice Fabarius; Matthew Salmon; Carl Crodel; Jenny Rinke; Hans-Peter Horny; Florian H. Heidel; Jan Hinrich Bräsen; Hans-H. Kreipe; Georgia Metzgeroth; Wolf-Karsten Hofmann; Nicholas C. P. Cross; Torsten Haferlach; Juliana Schwaab; Andreas Hochhaus; Andreas Reiter
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MDS without clonal marker: when depth outperforms breadth无克隆标记的MDS:当深度优于广度时
errLeukemia
IF13.4
err2026-08-10
err0
PREAI
errSandra Huber; Marietta Truger; Stephan Hutter; Heiko Mueller; Veronika Ecker; Gregor Hoermann; Torsten Haferlach; Manja Meggendorfer
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Not Missing the Notch: Detection Challenges of Juxtamembrane NOTCH1 Variant Detection in T-Cell Acute Lymphoblastic Leukemia不应遗漏“Notch”:T细胞急性淋巴细胞白血病中近膜区域NOTCH1变异检测的挑战
err2026-06-08
err0
errOAAI
errFrancisco Beas; Stephan Hutter; Ferran Balbastre-Úbeda; Sandra Novoa-Jáuregui; Maria Gabarrós-Subirà; Eulalia Genescà; Petri Pölönen; Torsten Haferlach; Andrés Jerez
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Comprehensive landscape of secondary cytogenetic and molecular genetic events in multiple myeloma patients at diagnosis多发性骨髓瘤患者诊断时继发性细胞遗传学和分子遗传学事件的全面景观
errLeukemia
IF13.4
err2026-06-08
err0
PREAI
errJana Wobst; Marietta Truger; Natalie Wossidlo; Stephan Hutter; Manja Meggendorfer; Wolfgang Kern; Torsten Haferlach; Claudia Haferlach
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The clinical relevance of sole loss of chromosome Y in myeloid neoplasms纯染色体Y缺失在髓系肿瘤中的临床相关性
err2026-05-09
err0
errOAAI
errSandra Huber; Stephan Hutter; Manja Meggendorfer; Christian Pohlkamp; Torsten Haferlach; Isolde Summerer
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Prevalence and characterization of germline RAS pathway variants in children with chronic myeloid leukemia
errLeukemia
IF13.4
err2026-04-24
err0
errOAAI
errTabita Ghete; Laura Gaschler; Manuela Krumbholz; Stephanie Sembill; Yvonne Lisa Behrens; Axel Karow; Matthias Wölfl; Franziska Auer; Julia Hauer; Maria Giulia Carta; Fulvia Ferrazzi; Stephan Hutter; Anselm H. C. Horn; Heinrich Sticht; Paul-Gerhardt Schlegel; Markus Metzler
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IntegrateALL: An end-to-end RNA-seq analysis pipeline for multilevel data extraction and interpretable subtype classification in B-precursor ALLIntegrateALL:一种用于多层级数据提取和可解释亚型分类的B-前体ALL端到端RNA-seq分析流程
err2026-04-16
err0
errOAAI
errNadine Wolgast; Thomas Beder; Mayukh Mondal; Wencke Walter; Stephan Hutter; Sonja Bendig; Jan Kässens; Björn-Thore Hansen; Katharina Iben; Sebastian Wolf; Anjali Cremer; Malwine Barz; Martin Neumann; Nicola Gökbuget; Claudia Haferlach; Monika Brüggemann; Claudia D. Baldus; Alina M. Hartmann; Lorenz Bastian
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Genetic characterization of AML defined by differentiation shows a high frequency of DDX41 mutationsAML以分化为特征的遗传学表征显示DDX41突变频率较高
err2026-04-14
err0
PREAI
errSandra Huber; Christoph Kornauth; Stephan Hutter; Manja Meggendorfer; Isolde Summerer; Wolfgang Kern; Torsten Haferlach; Christian Pohlkamp; Gregor Hoermann
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The evolution to hepta-refractory myeloma involves sequential loss of CD38, BCMA and GPRC5D演进至七难治性骨髓瘤涉及CD38、BCMA和GPRC5D的顺序性丢失
errLeukemia
IF13.4
err2026-02-17
err0
errOAAI
errC. Riedhammer; M. Truger; H. Lee; LB Leypoldt; M. Meggendorfer; S. Hutter; H. Müller; J. Mersi; SK Kadel; T. Buchwald; R. Kosch; M. Helal; N. Afrin; A. Rosenwald; E. Gerhard-Hartmann; A. Brioli; J. Krönke; T. Haferlach; C. Haferlach; KC Weisel; P. Neri; H. Einsele; KM Kortüm; JM Waldschmidt; N. Bahlis; N. Weinhold; L. Rasche
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Solving Riddles Through Sequencing (SIRIUS): unlocking hematologic diagnoses by whole genome and transcriptome sequencing通过测序解谜(SIRIUS):利用全基因组测序和转录组测序解锁血液学诊断
errLeukemia
IF13.4
err2025-12-19
err0
errOAAI
errMarietta Truger; Manja Meggendorfer; Wencke Walter; Stephan Hutter; Winfried Alsdorf; Gero Massenkeil; Uwe M. Martens; Wolfgang Kern; Katharina Hörst; Constanze Kühn; Andreas Reiter; Andreas Hochhaus; Torsten Haferlach
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Telomere content and genomics of myeloid neoplasia by WGS端粒含量和髓系肿瘤的全基因组测序(WGS)基因组学
errBlood
IF23.1
err2025-09-24
err0
errOAAI
errLuca Guarnera; Adam Wahida; Carmelo Gurnari; Stephan Hutter; Sabine A. Stainczyk; Nakisha D. Williams; Arda Durmaz; Yasuo Kubota; Carlos Bravo-Perez; Naomi Kawashima; Mark Orland; Simona Pagliuca; Yimin Huang; Thomas LaFramboise; Valeria Visconte; Wencke Walter; Manja Meggendorfer; Wolfgang Kern; Frank Westermann; Lars Feuerbach; Torsten Haferlach; Jaroslaw P. Maciejewski
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TELOMERE CONTENT IN MYELOID NEOPLASIA COULD INFORM ON DIFFERENTIAL SENSITIVITY TO TELOMERASE INHIBITORS髓系肿瘤中的端粒含量可能提示对端粒酶抑制剂的差异性敏感性
err2025-09-01
err0
PREAI
errGuarnera, Luca; Wahida, Adam; Gurnari, Carmelo; Hutter, Stephan; Stainczyk, Sabine; Williams, Nakisha; Durmaz, Arda; Kubota, Yasuo; Bravo-Perez, Carlos; Kawashima, Naomi; Pagliuca, Simona; Huang, Yimin; Laframboise, Thomas; Visconte, Valeria; Walter, Wencke; Meggendorfer, Manja; Kern, Wolfgang; Westermann, Frank; Feuerbach, Lars; Haferlach, Torsten; Maciejewski, Jaroslaw
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Two ways to complex karyotype in MDS-the role of del(5q) and TP53MDS中复杂核型形成的两种方式——del(5q)和TP53的作用
err2025-05-19
err0
errOAAI
errHuber, Sandra; Hutter, Stephan; Baer, Constance; Meggendorfer, Manja; Hoermann, Gregor; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia
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Relevance of blast counts for genetic subclassification in MDS
errLEUKEMIA
IF13.4
err2024-11-27
err0
errOAAI
errHuber, Sandra; Haferlach, Torsten; Hutter, Stephan; Hoermann, Gregor; Kern, Wolfgang; Haferlach, Claudia
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Similarities and Differences of DNMT3A, TET2 and ASXL1 Mutations across Ccus, MDS and AMLDNMT3A、TET2和ASXL1基因突变在CCUS、MDS和AML中的相似性与差异性
errBLOOD
IF23.1
err2024-11-05
err0
PREAI
errHuber, Sandra; Hutter, Stephan; Baer, Constance Regina; Meggendorfer, Manja; Hoermann, Gregor; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia
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A Unified Post-Transcriptional Mechanism Regulates Intron Retention in Splicing Factor-Mutant MDS统一的后转录机制调控剪接因子突变型MDS中的内含子滞留
errBLOOD
IF23.1
err2024-11-05
err0
PREAI
errBoddu, Prajwal; Roy, Rahul; Baumgartner, Francis; Hutter, Stephan; Haferlach, Torsten; Pillai, Manoj
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Clonal Hematopoiesis Can Precede AML with Defining Cytogenetic Abnormalities- the Frequencies Vary克隆性造血可先于具有特征性细胞遗传学异常的急性髓系白血病发生——其频率各不相同
errBLOOD
IF23.1
err2024-11-05
err0
PREAI
errMarcinek, Anetta; Baer, Constance Regina; Hutter, Stephan; Meggendorfer, Manja; Haferlach, Torsten; Kern, Wolfgang; Haferlach, Claudia
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Phenotypic and Genetic Heterogeneity of NPM1 Mutated AML at Diagnosis and during Course of DiseaseNPM1突变急性髓系白血病(AML)在诊断时及疾病过程中的表型和遗传异质性
errBLOOD
IF23.1
err2024-11-05
err0
PREAI
errEcker, Veronika; Huber, Sandra; Walter, Wencke; Hutter, Stephan; Mueller, Martha-Lena; Meggendorfer, Manja; Baer, Constance Regina; Haferlach, Claudia; Haferlach, Torsten; Kern, Wolfgang
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