Behrendtz相关文献与解析，生知库 | 链接生命科学的每一步

Harant, Anne; Zanuzdana, Arina; Tomczyk, Sara; Eckmanns, Tim; Kong, Insik; Lahra, Monica; Gill, Savannah; Hendriksen, Rene; Perovic, Olga; Corso, Alejandra; Löfmark Behrendtz, Sonja; Kreienbrock, Lothar; Alshamrani, Majid; Harbarth, Stephan; de Kraker, Marlieke; Ekelund, Oskar; Karatuna, Onur; Ruesen, Carolien; Bertagnolio, Silvia; Hutin, Yvan

发表日期：2026

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Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia

近单倍体急性淋巴细胞白血病中单体染色体的亲本来源

期刊:Blood Cancer Journal

影响因子:11.6

doi:10.1038/s41408-020-0317-2

Lundin-Ström, Kristina B; Ström, Kristoffer; Biloglav, Andrea; Barbany, Gisela; Behrendtz, Mikael; Castor, Anders; Olsson-Arvidsson, Linda; Johansson, Bertil

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

儿童 B 细胞前体急性淋巴细胞白血病中 ETV6-RUNX1 样和 DUX4 重排亚型的鉴定

期刊:Nature Communications

影响因子:14.7

doi:10.1038/ncomms11790

Henrik Lilljebjörn, Rasmus Henningsson, Axel Hyrenius-Wittsten, Linda Olsson, Christina Orsmark-Pietras, Sofia von Palffy, Maria Askmyr, Marianne Rissler, Martin Schrappe, Gunnar Cario, Anders Castor, Cornelis J H Pronk, Mikael Behrendtz, Felix Mitelman, Bertil Johansson, Kajsa Paulsson, Anna K Ande

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A

对儿童T细胞急性淋巴细胞白血病进行深度测序和SNP芯片分析，发现少数亚克隆中存在NOTCH1突变，且CDKN2A单亲二体性发生率较高。

期刊:Journal of Hematology & Oncology

影响因子:40.4

doi:10.1186/s13045-015-0138-0

Karrman, Kristina; Castor, Anders; Behrendtz, Mikael; Forestier, Erik; Olsson, Linda; Ehinger, Mats; Biloglav, Andrea; Fioretos, Thoas; Paulsson, Kajsa; Johansson, Bertil

Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

启动子 DNA 甲基化模式可识别儿童 T 细胞急性淋巴细胞白血病的预后亚群

期刊:PLoS One

影响因子:2.9

doi:10.1371/journal.pone.0065373

Magnus Borssén, Lars Palmqvist, Kristina Karrman, Jonas Abrahamsson, Mikael Behrendtz, Jesper Heldrup, Erik Forestier, Göran Roos, Sofie Degerman

Digital gene expression profiling of primary acute lymphoblastic leukemia cells

原发性急性淋巴细胞白血病细胞的数字基因表达谱分析

期刊:Leukemia

影响因子:13.4

doi:10.1038/leu.2011.358

Nordlund, J; Kiialainen, A; Karlberg, O; Berglund, E C; Göransson-Kultima, H; Sønderkær, M; Nielsen, K L; Gustafsson, M G; Behrendtz, M; Forestier, E; Perkkiö, M; Söderhäll, S; Lönnerholm, G; Syvänen, A-C

The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias

164例ETV6/RUNX1阳性儿童急性淋巴细胞白血病获得性拷贝数改变的相关模式

期刊:Human Molecular Genetics

影响因子:3.2

doi:10.1093/hmg/ddq224

Lilljebjörn, Henrik; Soneson, Charlotte; Andersson, Anna; Heldrup, Jesper; Behrendtz, Mikael; Kawamata, Norihiko; Ogawa, Seishi; Koeffler, H Phillip; Mitelman, Felix; Johansson, Bertil; Fontes, Magnus; Fioretos, Thoas

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

甲氨蝶呤/6-巯基嘌呤维持治疗会影响儿童急性淋巴细胞白血病后发生第二原发性恶性肿瘤的风险：来自NOPHO ALL-92研究的结果

期刊:Blood

影响因子:23.1

doi:10.1182/blood-2008-11-187880

Schmiegelow, Kjeld; Al-Modhwahi, Ibrahim; Andersen, Mette Klarskov; Behrendtz, Mikael; Forestier, Erik; Hasle, Henrik; Heyman, Mats; Kristinsson, Jon; Nersting, Jacob; Nygaard, Randi; Svendsen, Anne Louise; Vettenranta, Kim; Weinshilboum, Richard

Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations

儿童急性白血病的分子特征及其与正常造血亚群表达模式的相关性

期刊:Proceedings of the National Academy of Sciences of the United States of America

影响因子:9.1

doi:10.1073/pnas.0506637102

Andersson, Anna; Olofsson, Tor; Lindgren, David; Nilsson, Björn; Ritz, Cecilia; Edén, Patrik; Lassen, Carin; Råde, Johan; Fontes, Magnus; Mörse, Helena; Heldrup, Jesper; Behrendtz, Mikael; Mitelman, Felix; Höglund, Mattias; Johansson, Bertil; Fioretos, Thoas

白血病

发表日期：2005

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Surveillance of antimicrobial resistance by a global network of WHO collaborating centres

世界卫生组织合作中心全球网络开展抗菌素耐药性监测

Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia

近单倍体急性淋巴细胞白血病中单体染色体的亲本来源

Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

儿童 B 细胞前体急性淋巴细胞白血病中 ETV6-RUNX1 样和 DUX4 重排亚型的鉴定

Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A

对儿童T细胞急性淋巴细胞白血病进行深度测序和SNP芯片分析，发现少数亚克隆中存在NOTCH1突变，且CDKN2A单亲二体性发生率较高。

Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

启动子 DNA 甲基化模式可识别儿童 T 细胞急性淋巴细胞白血病的预后亚群

Digital gene expression profiling of primary acute lymphoblastic leukemia cells

原发性急性淋巴细胞白血病细胞的数字基因表达谱分析

The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias

164例ETV6/RUNX1阳性儿童急性淋巴细胞白血病获得性拷贝数改变的相关模式

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

甲氨蝶呤/6-巯基嘌呤维持治疗会影响儿童急性淋巴细胞白血病后发生第二原发性恶性肿瘤的风险：来自NOPHO ALL-92研究的结果

Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations

儿童急性白血病的分子特征及其与正常造血亚群表达模式的相关性