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

Prolonged Trapping of Adeno-Associated Virus Capsids Reveals that Genome Packaging Affects Single-Ion Mass Spectrometry Measurements

腺相关病毒衣壳的长期滞留揭示基因组包装影响单离子质谱测量

期刊:Journal of the American Chemical Society
影响因子:15.6
doi:10.1021/jacs.4c13393
Ebberink, Eduard H T M; Yin, Victor C; Deslignière, Evolène; Barendregt, Arjan; Wörner, Tobias P; Fort, Kyle L; Makarov, Alexander A; Heck, Albert J R
微生物学
发表日期：2025
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Isotype conversion of Staphylococcal-specific IgG into IgM broadens the reactivity to other bacterial pathogens

葡萄球菌特异性IgG向IgM的同型转化会拓宽对其他细菌病原体的反应性。

期刊:Cell Reports Medicine
影响因子:11.7
doi:10.1016/j.xcrm.2025.102414
Remy M Muts ，Astrid Hendriks ，Josefien W Hommes ，Max L B Grönloh ，Douwe J Dijkstra ，Carla J C de Haas ，Piet C Aerts ，Eduard H T M Ebberink ，Albert J R Heck ，Zhen Wang ，Haoru Zhuang ，Jeroen D C Codée ，Bas G J Surewaard ，Dani A C Heesterbeek ，Nina M van Sorge ，Suzan H M Rooijakkers
微生物学
IgG
IgM
发表日期：2025
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Probing recombinant AAV capsid integrity and genome release after thermal stress by mass photometry

通过质谱法探测重组 AAV 衣壳的完整性和热应激后基因组的释放

期刊:Molecular Therapy-Methods & Clinical Development
影响因子:
doi:10.1016/j.omtm.2024.101293
Eduard H T M Ebberink, Alisa Ruisinger, Markus Nuebel, Helena Meyer-Berg, Irene R S Ferreira, Marco Thomann, Albert J R Heck
信号转导
发表日期：2024
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Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene

由 PEX14 基因新生变异引起的常染色体显性泽尔韦格综合征

期刊:Genetics in Medicine
影响因子:6.6
doi:10.1016/j.gim.2023.100944
Hans R Waterham, Janet Koster, Merel S Ebberink, Pavel Ješina, Jiri Zeman, Lenka Nosková, Stanislav Kmoch, Perrine Devic, David Cheillan, Ronald J A Wanders, Sacha Ferdinandusse
信号转导
发表日期：2023
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Sex-specific newborn screening for X-linked adrenoleukodystrophy

针对X连锁肾上腺脑白质营养不良症的性别特异性新生儿筛查

期刊:Journal of Inherited Metabolic Disease
影响因子:3.8
doi:10.1002/jimd.12571
Albersen, Monique; van der Beek, Samantha L; Dijkstra, Inge M E; Alders, Mariëlle; Barendsen, Rinse W; Bliek, Jet; Boelen, Anita; Ebberink, Merel S; Ferdinandusse, Sacha; Goorden, Susan M I; Heijboer, Annemieke C; Jansen, Mandy; Jaspers, Yorrick R J; Metgod, Ingrid; Salomons, Gajja S; Vaz, Frédéric M; Verschoof-Puite, Rendelien K; Visser, Wouter F; Dekkers, Eugènie; Engelen, Marc; Kemp, Stephan
神经科学
免疫/内分泌
发表日期：2023
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Assessing production variability in empty and filled adeno-associated viruses by single molecule mass analyses

利用单分子质量分析评估空载和填充腺相关病毒的生产变异性

期刊:Molecular Therapy-Methods & Clinical Development
影响因子:4.7
doi:10.1016/j.omtm.2022.11.003
Ebberink, Eduard H T M; Ruisinger, Alisa; Nuebel, Markus; Thomann, Marco; Heck, Albert J R
微生物学
发表日期：2022
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Thermo-sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy

表现为发作性肌病的热敏性线粒体三功能蛋白缺乏症

期刊:Journal of Inherited Metabolic Disease
影响因子:4.2
doi:10.1002/jimd.12503
Marit Schwantje, Merel S Ebberink, Mirjam Doolaard, Jos P N Ruiter, Sabine A Fuchs, Niklas Darin, Carola Hedberg-Oldfors, Luc Régal, Laura Donker Kaat, Hidde H Huidekoper, Simon Olpin, Duncan Cole, Stuart J Moat, Gepke Visser, Sacha Ferdinandusse
细胞生物学
发表日期：2022
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Probing activation-driven changes in coagulation factor IX by mass spectrometry

通过质谱法探测凝血因子 IX 的活化驱动变化

期刊:Journal of Thrombosis and Haemostasis
影响因子:5.5
doi:10.1111/jth.15288
Nadia Freato, Floris P J van Alphen, Mariëtte Boon-Spijker, Maartje van den Biggelaar, Alexander B Meijer, Koen Mertens, Eduard H T M Ebberink
信号转导
发表日期：2021
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Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the ABCD1 Gene

利用成纤维细胞的生化研究来解读ABCD1基因中意义不明的变异

期刊:Genes
影响因子:2.8
doi:10.3390/genes12121930
van de Stadt, Stephanie I W; Mooyer, Petra A W; Dijkstra, Inge M E; Dekker, Conny J M; Vats, Divya; Vera, Moin; Ruzhnikov, Maura R Z; van Haren, Keith; Tang, Nelson; Koop, Klaas; Willemsen, Michel A; Hui, Joannie; Vaz, Frédéric M; Ebberink, Merel S; Engelen, Marc; Kemp, Stephan; Ferdinandusse, Sacha
成纤维细胞
细胞生物学
发表日期：2021
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Abnormal VLCADD newborn screening resembling MADD in four neonates with decreased riboflavin levels and VLCAD activity

四名新生儿出现异常的VLCADD新生儿筛查结果，类似于MADD，表现为核黄素水平和VLCAD活性降低。

期刊:JIMD Reports
影响因子:1.8
doi:10.1002/jmd2.12223
Hagemeijer, Marne C; Oussoren, Esmee; Ruijter, George J G; Onkenhout, Willem; Huidekoper, Hidde H; Ebberink, Merel S; Waterham, Hans R; Ferdinandusse, Sacha; de Vries, Maaike C; Huigen, Marleen C D G; Kluijtmans, Leo A J; Coene, Karlien L M; Blom, Henk J
发表日期：2021
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