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 | 132 | 2021 |
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 | 89 | 2022 |
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 | 53 | 2021 |
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 | 47 | 2014 |
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 | 38 | 2022 |
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 | 27 | 2021 |
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 | 21 | 2023 |
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 | 19 | 2023 |
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 | 18 | 2021 |
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 | 18 | 2017 |
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 | 14 | 2019 |
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 | 8 | 2022 |
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 | 8 | 2019 |
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 | 5 | 2024 |
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 | 2 | 2023 |
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 | 2 | 2010 |
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 | 1 | 2022 |
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 | 1 | 2022 |
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 |