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Annemieke Aartsma‐Rus

leiden university medical center

67H指数
426论文数
1.9W被引数
收录论文 179
发表时间
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Individualized antisense oligonucleotide treatment eligibility of patients living with neurodevelopmental diseases神经发育障碍患者个体化反义寡核苷酸治疗的适用性
errCell Reports Medicine
IF10.6
err2026-08-13
err0
errOAAI
errAnnemieke Aartsma-Rus; Claudio Melo de Gusmao; Scott Demarest; Willeke van Roon-Mom; Holm Graessner; Lynn Wein Bush; Charlotte Kogel; Timothy Wei-Wen Yu; Matthis Synofzik; Rebecca Schuele
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err收藏
Guidance on communication and informed consent with patients and their families for experimental individualized treatments与患者及其家属就实验性个体化治疗进行沟通和知情同意的指导
errThe American Journal of Human Genetics
IF0
err2026-05-26
err0
errOAAI
errAnnemieke Aartsma-Rus; Claudio M. de Gusmao; Scott Demarest; Matias Wagner; Georg Marckmann; Charlotte Kogel; Roseline Favresse; Rebecca Schuele; Matthis Synofzik; Holm Graessner; Lynn Bush; Timothy W. Yu
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Unraveling the spatial landscape of dystrophinopathies: a transcriptomic approach to Becker and Duchenne muscular dystrophies揭开肌营养不良症的时空景观：一种针对贝克和杜氏肌营养不良症的转录组学方法
errThe Journal of Pathology
IF0
err2026-05-01
err0
errOAAI
errLaura GM Heezen; Qirong Mao; Stefan Nicolau; Claudio Novella Rausell; Julia van der Weerd; Jan Kueckelhaus; Rasya Gokul Nath; Jordi Diaz- Manera; Hermien E Kan; Erik H Niks; Maaike van Putten; Annemieke Aartsma-Rus; Kevin M Flanigan; Ahmed Mahfouz; Pietro Spitali
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TREAT-NMD advisory committee for therapeutics: Preclinical and clinical learnings from 15 years of TACTTREAT-NMD治疗建议委员会：15年TACT的预临床与临床经验
errJournal of Neuromuscular Diseases
IF3.4
err2026-04-24
err0
PREAI
errAnnemieke Aartsma-Rus; Laura Robertson; Lindsay N. Alfano; Anna Mayhew; Heather Gordish-Dressman; Mike Kelly; Carl Morris; Volker Straub; Conrad C. Weihl; Colin Werth; Olivier M. Dorchies; Amanda Riviere; Kanneboyina Nagaraju; Kathryn R. Wagner
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Myonuclear Domain-Associated and Central Nucleation-Dependent Spatial Restriction of Dystrophin Protein Expression肌核域相关及中心核化依赖的 dystrophin 蛋白表达的空域限制
errjournal of cachexia, sarcopenia and muscle
IF0
err2026-04-07
err0
errOAAI
errKatarzyna Chwalenia; Vivi-Yun Feng; Nicole Hemmer; John C. W. Hildyard; Liberty E. Roskrow; Richard J. Piercy; Eric T. Wang; Annemieke Aartsma-Rus; Maaike van Putten; Matthew J. A. Wood; Thomas C. Roberts
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The complexity of dystrophin transcription and processing: implications of transcript imbalance on dystrophin gene targeting strategies
errNEUROMUSCULAR DISORDERS
IF2.8
err2026-01-21
err0
PREAI
errRossi, Rachele; Aartsma-Rus, Annemieke; Muntoni, Francesco; Goyenvalle, Aurelie; Spitali, Pietro
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err收藏
Report of the multistakeholder drug development round table meeting of the World Duchenne Organization focusing on challenges for clinical development of therapies世界杜氏肌营养不良组织多方利益相关者药物研发圆桌会议报告，重点关注疗法临床开发的挑战
errJournal of Neuromuscular Diseases
IF3.4
err2025-12-04
err0
errOAAI
errAnnemieke Aartsma-Rus
err分享
err收藏
RNA therapies are delivering as therapies for neuromuscular dystrophy patients: Editorial for the special issue on RNA therapies in Journal of Neuromuscular DiseasesRNA疗法正成为神经肌肉营养不良患者的有效治疗手段：载于《神经肌肉疾病杂志》RNA疗法特刊的社论
errJournal of Neuromuscular Diseases
IF3.4
err2025-12-04
err0
errOAAI
errAnnemieke Aartsma-Rus; Shin’ichi Takeda
err分享
err收藏
Antisense-mediated exon skipping therapy improves neuromuscular junction deficits in a Duchenne muscular dystrophy mouse model反义寡核苷酸介导的外显子跳跃疗法改善了杜氏肌营养不良小鼠模型的神经肌肉接头缺陷
errNeuromuscular Disorders
IF2.8
err2025-10-24
err0
PREAI
errElizabeth M. van der Pijl; Svetlana Pasteuning-Vuhman; Johanna Boertje-van der Meulen; Erik H. Niks; Jan J.G.M. Verschuuren; Annemieke Aartsma-Rus; Jaap J. Plomp; Maaike van Putten
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Screening rare genetic diagnoses for amenability to bespoke antisense oligonucleotide therapy development: a retrospective cohort study筛查罕见遗传诊断以评估其是否适合定制反义寡核苷酸疗法的开发：一项回顾性队列研究
errGenetics in Medicine
IF6.2
err2025-10-11
err0
PREAI
errDavid Cheerie; Marlen C. Lauffer; Logan Newton; Kimberly Amburgey; Danique Beijer; Bushra Haque; Brian T. Kalish; Margaret Meserve; Rachel Y. Oh; Amy Y. Pan; Miriam S. Reuter; Michael J. Szego; Anna Szuto; Annemieke Aartsma-Rus; Michelle M. Axford; Ashish R. Deshwar; James J. Dowling; Christian R. Marshall; Zhenya Ivakine; Matthis Synofzik; Timothy W. Yu; Gregory Costain
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Applying the International Rare Disease Research Consortium (IRDIRC) N=1 Therapy Task Force Eligibility Criteria for individualised therapies Use case: Duchenne muscular dystrophy应用国际罕见病研究联盟（IRDIRC）N=1疗法工作组个体化疗法的入组标准 用例：杜氏肌营养不良症
errNeuromuscular Disorders
IF2.8
err2025-09-25
err0
errOAAI
errAnnemieke Aartsma-Rus; Anneliene Jonker; Daniel O’Connor
err分享
err收藏
In Vivo Phage Display for the Identification of Muscle Homing Peptides to Improve the Delivery of Phosphorodiamidate Morpholino Oligomers for Duchenne Muscular Dystrophy Therapy体内噬菌体展示技术用于鉴定靶向肌肉的归巢肽，以改善磷酸二酰胺类吗啉寡聚体在杜氏肌营养不良症治疗中的递送。
errnucleic acid therapeutics
IF4.7
err2025-08-29
err0
PREAI
errAnne-Fleur E. Schneider; Christa L. Tanganyika-de Winter; Hailiang Mei; Silvana M. G. Jirka; Xuyu Tan; Emily G. Thompson; Kristin Ha; Anindita Mitra; Stephanie Garcia; Marleen Luimes; Ryan Oliver; Kathy Y. Morgan; Vincent Guerlavais; Annemieke Aartsma-Rus
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Using muscle homing peptide CyPep10 to deliver phosphorodiamidate morpholino oligomers in the mdx mouse使用肌肉归巢肽CyPep10递送磷酸二酰胺类吗啉寡聚体至mdx小鼠
errMolecular Therapy Nucleic Acids
IF6.1
err2025-07-17
err0
errOAAI
errAnne-Fleur E. Schneider; Christa L. Tanganyika-de Winter; Silvana M.G. Jirka; Xuyu Tan; Emily G. Thompson; Kristen Ha; Anindita Mitra; Stephanie Garcia; Marleen Luimes; Ryan A. Oliver; Vincent Guerlavais; Annemieke Aartsma-Rus
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Tailored antisense oligonucleotides for ultrarare CNS diseases: An experience-based best practice framework for individual patient evaluation针对超罕见CNS疾病的定制反义寡核苷酸：基于经验的最佳实践框架用于个体患者评估
errMolecular Therapy Nucleic Acids
IF6.1
err2025-07-01
err0
errOAAI
errRebecca Schüle; Holm Graessner; Annemieke Aartsma-Rus; Willeke M.C. van Roon-Mom; Matthis Synofzik
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err收藏
Design and In Vitro Evaluation of a Novel Antisense Oligonucleotide for Treatment of BK Virus Infection新型反义寡核苷酸的设计及其对BK病毒感染治疗的体外评价
errnucleic acid therapeutics
IF4.7
err2025-06-04
err0
PREAI
errJurriën Prins; Janneke Kouwenberg; Anouk Spruit; Lizanne Daleman; Iris van Wissen; Bianca Matthee; Angela Koudijs; Caroline de Brouwer; Ellen Lievers; Franca Witjas; Vita Dauksaite; Carla van Alem; Roel Bijkerk; Annemieke Aartsma-Rus; Jessica Sipkens; Ton Rabelink; Mariet Feltkamp; Tamara Pfaff; Holger Zimmermann; Anton Jan van Zonneveld; Peter Lischka; Eric van der Veer
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Antisense RNA therapies for muscular dystrophies反义RNA疗法治疗肌营养不良症
errJOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
err2025-03-27
err0
PREAI
errVirginia Arechavala-Gomeza; Andrea López-Martínez; Annemieke Aartsma-Rus
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err收藏
A historical perspective on the development of antisense oligonucleotide treatments for Duchenne muscular dystrophy and spinal muscular atrophy从历史角度探讨反义寡核苷酸疗法在杜氏肌营养不良症和脊髓性肌萎缩症治疗中的发展
errJOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
err2025-03-04
err0
PREAI
errAnnemieke Aartsma-Rus; Shin'ichi Takeda
err分享
err收藏
Identification of suitable qPCR reference genes for the normalization of gene expression in the BL10-mdx and D2-mdx mouse models of Duchenne muscular dystrophy筛选适合BL10-mdx和D2-mdx杜氏肌营养不良小鼠模型基因表达量标准化分析的qPCR参考基因
errPLOS ONE
IF2.6
err2025-02-25
err0
errOAAI
errPutker, Kayleigh; Schneider, Anne-Fleur; van de Vijver, Davy; Hildyard, John; Aartsma-Rus, Annemieke; van Putten, Maaike
err分享
err收藏
Histone deacetylase inhibition with givinostat: a multi-targeted mode of action with the potential to halt the pathological cascade of Duchenne muscular dystrophygivinostat组蛋白去乙酰化酶抑制：一种具有阻断杜氏肌营养不良病理级联反应潜力的多靶点作用机制
errFRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
IF4.3
err2025-01-06
err2
errOAAI
errAartsma-Rus, A.
err分享
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A Guide to Chemical Considerations for the Pre-Clinical Development of Oligonucleotides
errNUCLEIC ACID THERAPEUTICS
IF4.7
err2024-12-01
err0
PREAI
errO'Reilly, Daniel; van Roon-Mom, Willeke; Aartsma-Rus, Annemieke
err分享
err收藏

研究方向

暂无研究方向
合作学者
合作期刊
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Cornelia M. van Duijn
H 指数: 238 · 论文数: 1.9K
A
Albert Hofman
H 指数: 195 · 论文数: 1.4K
M
M. Arfan Ikram
H 指数: 167 · 论文数: 1.8K
J
James M. Wilson
H 指数: 155 · 论文数: 1.4K
P
Peter ten Dijke
H 指数: 147 · 论文数: 794
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