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Marie Bernkopf
Marie Bernkopf
Children's Cancer Research Institute
在 ccri.at 的电子邮件经过验证
标题
引用次数
引用次数
年份
Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden
P Peneder, AM Stütz, D Surdez, M Krumbholz, S Semper, M Chicard, ...
Nature communications 12 (1), 3230, 2021
1322021
The evolutionary dynamics of extrachromosomal DNA in human cancers
JT Lange, JC Rose, CY Chen, Y Pichugin, L Xie, J Tang, KL Hung, ...
Nature genetics 54 (10), 1527-1533, 2022
892022
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR …
A Bellini, U Pötschger, V Bernard, E Lapouble, S Baulande, PF Ambros, ...
Journal of Clinical Oncology 39 (30), 3377-3390, 2021
532021
Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability
M Bernkopf, G Webersinke, C Tongsook, CN Koyani, MA Rafiq, M Ayaz, ...
Human molecular genetics 23 (15), 4015-4023, 2014
472014
High-dose treosulfan and melphalan as consolidation therapy versus standard therapy for high-risk (metastatic) Ewing sarcoma
R Koch, H Gelderblom, L Haveman, B Brichard, H Jürgens, S Cyprova, ...
Journal of Clinical Oncology 40 (21), 2307-2320, 2022
382022
Landscape of bone marrow metastasis in human neuroblastoma unraveled by transcriptomics and deep multiplex imaging
D Lazic, F Kromp, F Rifatbegovic, P Repiscak, M Kirr, F Mivalt, F Halbritter, ...
Cancers 13 (17), 4311, 2021
272021
Single-cell transcriptomics and epigenomics unravel the role of monocytes in neuroblastoma bone marrow metastasis
IS Fetahu, W Esser-Skala, R Dnyansagar, S Sindelar, F Rifatbegovic, ...
Nature Communications 14 (1), 3620, 2023
212023
Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation
M Bernkopf, UB Abdullah, SJ Bush, KA Wood, S Ghaffari, E Giannoulatou, ...
Nature communications 14 (1), 853, 2023
192023
Novel insights into diagnosis, biology, and treatment of primary diffuse leptomeningeal melanomatosis
A Baumgartner, N Stepien, L Mayr, S Madlener, C Dorfer, MT Schmook, ...
Journal of Personalized Medicine 11 (4), 292, 2021
182021
Quantification of transmission risk in a male patient with a FLNB mosaic mutation causing Larsen syndrome: Implications for genetic counseling in postzygotic …
M Bernkopf, D Hunt, N Koelling, T Morgan, AL Collins, J Fairhurst, ...
Human Mutation 38 (10), 1360-1364, 2017
182017
amplimap: a versatile tool to process and analyze targeted NGS data
N Koelling, M Bernkopf, E Calpena, GJ Maher, KA Miller, HK Ralph, ...
Bioinformatics 35 (24), 5349-5350, 2019
142019
Comparison of three different methods to detect bone marrow involvement in patients with neuroblastoma
F Schriegel, S Taschner-Mandl, M Bernkopf, U Grunwald, N Siebert, ...
Journal of cancer research and clinical oncology, 1-8, 2022
82022
The impact of chemo- and radiotherapy treatments on selfish de novo FGFR2 mutations in sperm of cancer survivors
GJ Maher, M Bernkopf, N Koelling, AOM Wilkie, ML Meistrich, A Goriely
Human Reproduction 34 (8), 1404-1415, 2019
82019
A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations
IM Saldana-Guerrero, LF Montano-Gutierrez, K Boswell, C Hafemeister, ...
Nature Communications 15 (1), 3745, 2024
52024
Zoledronic acid add-on therapy for standard-risk Ewing sarcoma patients in the Ewing 2008R1 trial
R Koch, L Haveman, R Ladenstein, B Brichard, H Jürgens, S Cyprova, ...
Clinical Cancer Research 29 (24), 5057-5068, 2023
22023
Identification of a New Methicillin-Resistant Staphylococcus aureus Strain That Cannot Be Assigned to Any Known spa Type
M Reischauer, M Bernkopf, C Webersinke
Journal of clinical microbiology 48 (2), 626-627, 2010
22010
Neuroblastoma-associated chromosomal aberrations drive cell identity loss in human neural crest via disruption of developmental regulators
IM Saldana-Guerrero, LF Montano-Gutierrez, C Hafemeister, D Stavish, ...
Cold Spring Harbor Laboratory, 2022
12022
The PREGCARE study: Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation
M Bernkopf, UB Abdullah, SJ Bush, K Wood, S Ghaffari, E Giannoulatou, ...
BioRxiv, 2022.07. 26.501520, 2022
12022
A stem cell model dissects detrimental effects of neuroblastoma-linked chromosomal aberrations on cell differentiation during neural crest development
IM Saldana-Guerrero, LF Montano-Gutierrez, C Hafemeister, D Stavish, ...
Cancer Research 83 (7_Supplement), 3542-3542, 2023
2023
108P Establishing a multi-modal tissue preparation and imaging workflow to study heterogeneity in neuroblastoma tumors
V Humhal, D Lazic, S Gutwein, E Bozsaky, F Rifatbegovic, M Bernkopf, ...
ESMO Open 8 (1), 2023
2023
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