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Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (2019)
Paramasivam, Nagarajan ; Hübschmann, Daniel ; Toprak, Umut H ; Ishaque, Naveed ; Neidert, Marian ; Schrimpf, Daniel ; Stichel, Damian ; Reuss, David ; Sievers, Philipp ; Reinhardt, Annekathrin ; Wefers, Annika K. ; Jones, David T. W. ; Gu, Zuguang ; Werner, Johannes ; Uhrig, Sebastian ; Wirsching, Hans-Georg ; Schick, Matthias ; Bewerunge-Hudler, Melanie ; Beck, Katja ; Brehmer, Stephanie ; Urbschat, Steffi ; Seiz-Rosenhagen, Marcel ; Hänggi, Daniel ; Herold-Mende, Christel ; Ketter, Ralf ; Eils, Roland ; Ram, Zvi ; Pfister, Stefan M. ; Wick, Wolfgang ; Weller, Michael ; Grossmann, Rachel ; Deimling, Andreas von ; Schlesner, Matthias ; Sahm, Felix
YAP1-fusions in pediatric NF2-wildtype meningioma (2020)
Sievers, Philipp ; Chiang, Jason ; Schrimpf, Daniel ; Stichel, Damian ; Paramasivam, Nagarajan ; Sill, Martin ; Gayden, Tenzin ; Casalini, Belen ; Reuss, David E. ; Dalton, James ; Pajtler, Kristian W. ; Hänggi, Daniel ; Herold-Mende, Christel ; Rushing, Elisabeth ; Korshunov, Andrey ; Mawrin, Christian ; Weller, Michael ; Schlesner, Matthias ; Wick, Wolfgang ; Jabado, Nada ; Jones, David T. W. ; Pfister, Stefan M. ; Deimling, Andreas von ; Ellison, David W. ; Sahm, Felix
Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature (2017)
Sahm, Felix ; Toprak, Umut H. ; Hübschmann, Daniel ; Kleinheinz, Kortine ; Buchhalter, Ivo ; Sill, Martin ; Stichel, Damian ; Schick, Matthias ; Bewerunge-Hudler, Melanie ; Schrimpf, Daniel ; Zadeh, Gelareh ; Aldape, Ken ; Herold-Mende, Christel ; Beck, Katja ; Staszewski, Ori ; Prinz, Marco ; Harosh, Carmit Ben ; Eils, Roland ; Sturm, Dominik ; Jones, David T. W. ; Pfister, Stefan M. ; Paulus, Werner ; Ram, Zvi ; Schlesner, Matthias ; Grossman, Rachel ; Deimling, Andreas von
AT-10: atypical teratoid rhabdoid tumors and poorly differentiated chordomas: distinct molecular entities with SMARCB1/INI1 loss and dismal prognosis (2016)
Thomas, Christian ; Hovestadt, Volker ; Schrimpf, Daniel ; Johann, Pascal-David ; Bens, Susanne ; Oyen, Florian ; Vogel, Hannes ; Giangaspero, Felice ; Antonelli, Manila ; Riemenschneider, Markus ; Bernardo, Marie Christine ; Giannini, Caterina ; Din, Nasir Ud ; Perry, Arie ; Keyvani, Kathy ; van Landeghem, Frank ; Sumerauer, David ; Hauser, Peter ; Capper, David ; Korshunov, Andrey ; Jones, David T. W. ; Pfister, Stefan ; Schneppenheim, Reinhard ; Siebert, Reiner ; Frühwald, Michael C. ; Kool, Marcel ; Hasselblatt, Martin
Poorly differentiated chordoma with SMARCB1/INI1 loss: a distinct molecular entity with dismal prognosis (2016)
Hasselblatt, Martin ; Thomas, Christian ; Hovestadt, Volker ; Schrimpf, Daniel ; Johann, Pascal-David ; Bens, Susanne ; Oyen, Florian ; Peetz-Dienhart, Susanne ; Crede, Yvonne ; Wefers, Annika ; Vogel, Hannes ; Riemenschneider, Markus J. ; Antonelli, Manila ; Giangaspero, Felice ; Bernardo, Marie Christine ; Giannini, Caterina ; Ud Din, Nasir ; Perry, Arie ; Keyvani, Kathy ; van Landeghem, Frank ; Sumerauer, David ; Hauser, Peter ; Capper, David ; Korshunov, Andrey ; Jones, David T. W. ; Pfister, Stefan M. ; Schneppenheim, Reinhard ; Siebert, Reiner ; Frühwald, Michael C. ; Kool, Marcel
Molecular profiling of pediatric meningiomas shows tumor characteristics distinct from adult meningiomas (2021)
Kirches, Elmar ; Sahm, Felix ; Korshunov, Andrey ; Bluecher, Christina ; Waldt, Natalie ; Kropf, Siegfried ; Schrimpf, Daniel ; Sievers, Philipp ; Stichel, Damian ; Schüller, Ulrich ; Schittenhelm, Jens ; Riemenschneider, Markus J. ; Karajannis, Matthias A. ; Perry, Arie ; Pietsch, Torsten ; Boekhoff, Svenja ; Capper, David ; Beck, Katja ; Paramasivam, Nagarajan ; Schlesner, Matthias ; Brastianos, Priscilla K. ; Müller, Hermann L. ; Pfister, Stefan M. ; Mawrin, Christian
Accurate calling of KIAA1549‐BRAF fusions from DNA of human brain tumours using methylation array‐based copy number and gene panel sequencing data (2021)
Stichel, Damian ; Schrimpf, Daniel ; Sievers, Philipp ; Reinhardt, Annekathrin ; Suwala, Abigail K. ; Sill, Martin ; Reuss, David E. ; Korshunov, Andrey ; Casalini, Belén M. ; Sommerkamp, Alexander C. ; Ecker, Jonas ; Selt, Florian ; Sturm, Dominik ; Gnekow, Astrid ; Koch, Arend ; Simon, Michèle ; Hernáiz Driever, Pablo ; Schüller, Ulrich ; Capper, David ; Tilburg, Cornelis M. ; Witt, Olaf ; Milde, Till ; Pfister, Stefan M. ; Jones, David T. W. ; Deimling, Andreas ; Sahm, Felix ; Wefers, Annika K.
A subset of pediatric-type thalamic gliomas share a distinct DNA methylation profile, H3K27me3 loss and frequent alteration of EGFR (2020)
Sievers, Philipp ; Sill, Martin ; Schrimpf, Daniel ; Stichel, Damian ; Reuss, David E ; Sturm, Dominik ; Hench, Jürgen ; Frank, Stephan ; Krskova, Lenka ; Vicha, Ales ; Zapotocky, Michal ; Bison, Brigitte ; Castel, David ; Grill, Jacques ; Debily, Marie-Anne ; Harter, Patrick N ; Snuderl, Matija ; Kramm, Christof M ; Reifenberger, Guido ; Korshunov, Andrey ; Jabado, Nada ; Wesseling, Pieter ; Wick, Wolfgang ; Solomon, David A ; Perry, Arie ; Jacques, Thomas S ; Jones, Chris ; Witt, Olaf ; Pfister, Stefan M ; von Deimling, Andreas ; Jones, David T W ; Sahm, Felix
Epigenetic profiling reveals a subset of pediatric-type glioneuronal tumors characterized by oncogenic gene fusions involving several targetable kinases (2022)
Sievers, Philipp ; Sill, Martin ; Schrimpf, Daniel ; Friedel, Dennis ; Sturm, Dominik ; Gardberg, Maria ; Kurian, Kathreena M. ; Krskova, Lenka ; Vicha, Ales ; Schaller, Tina ; Hagel, Christian ; Abdullaev, Zied ; Aldape, Kenneth ; Jacques, Thomas S. ; Korshunov, Andrey ; Wick, Wolfgang ; Pfister, Stefan M. ; von Deimling, Andreas ; Jones, David T. W. ; Sahm, Felix
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology (2023)
Sturm, Dominik ; Capper, David ; Andreiuolo, Felipe ; Gessi, Marco ; Kölsche, Christian ; Reinhardt, Annekathrin ; Sievers, Philipp ; Wefers, Annika K. ; Ebrahimi, Azadeh ; Suwala, Abigail K. ; Gielen, Gerrit H. ; Sill, Martin ; Schrimpf, Daniel ; Stichel, Damian ; Hovestadt, Volker ; Daenekas, Bjarne ; Rode, Agata ; Hamelmann, Stefan ; Previti, Christopher ; Jäger, Natalie ; Buchhalter, Ivo ; Blattner-Johnson, Mirjam ; Jones, Barbara C. ; Warmuth-Metz, Monika ; Bison, Brigitte ; Grund, Kerstin ; Sutter, Christian ; Hirsch, Steffen ; Dikow, Nicola ; Hasselblatt, Martin ; Schüller, Ulrich ; Gerber, Nicolas U. ; White, Christine L. ; Buntine, Molly K. ; Kinross, Kathryn ; Algar, Elizabeth M. ; Hansford, Jordan R. ; Gottardo, Nicholas G. ; Hernáiz Driever, Pablo ; Gnekow, Astrid ; Witt, Olaf ; Müller, Hermann L. ; Calaminus, Gabriele ; Fleischhack, Gudrun ; Kordes, Uwe ; Mynarek, Martin ; Rutkowski, Stefan ; Frühwald, Michael C. ; Kramm, Christof M. ; von Deimling, Andreas ; Pietsch, Torsten ; Sahm, Felix ; Pfister, Stefan M. ; Jones, David. T. W.
PATH-10. Accelerating comprehensive CNS tumor molecular diagnostics with Rapid-CNS2 and MNP-flex: a prospective multi-center validation [Abstract] (2024)
Patel, Areeba J. ; Göbel, Kirsten ; Hinz, Felix ; Dogan, Helin ; Schrimpf, Daniel ; Göller, Pauline ; Leske, Henning ; Halldórsson, Skarphéðinn ; Fox, Graeme ; Deacon, Simon ; Paine, Simon ; Smith, Stuart ; Jäger, Natalie ; Herold-Mende, Christel ; Wick, Wolfgang ; Pfister, Stefan M. ; Vik-Mo, Einar ; von Deimling, Andreas ; Schlesner, Matthias ; Jones, David T. W. ; Loose, Matthew ; Sill, Martin ; Sahm, Felix
BACKGROUND The 2021 WHO classification update highlights the necessity of integrating molecular alterations for precise central nervous system (CNS) tumor diagnoses. However, current molecular reporting methods are hindered by significant initial investment, labor-intensive protocols, and lengthy turnaround times. Methylation-based classification has emerged as a pivotal diagnostic tool but is currently limited to array-based techniques. This necessitates exploration of novel technologies to streamline molecular analysis. METHODS We implemented Rapid-CNS2 - our adaptive sampling-based nanopore sequencing workflow- on 190 adult and pediatric samples at University Hospital Heidelberg and University of Nottingham. Intraoperative potential was assessed through real-time analysis followed by 24-hour sequencing for comprehensive genomic insights. Additionally, we developed MNP-Flex, a platform-agnostic version of the Heidelberg methylation classifier covering 184 CNS tumor classes. We evaluated MNP-flex on a global cohort of over 78,000 samples from methylation arrays, whole genome bisulfite sequencing, nanopore whole genome sequencing, methylation panels and Rapid-CNS2. RESULTS Rapid-CNS2 validation yielded accurate integrated diagnoses in all 190 samples. Within a crucial 30-minute timeframe, we reported accurate methylation families and arm-level copy number profiles followed by next-day reporting of fine-grained methylation classification, SNVs, focal CNVs, MGMT status, fusions and novel structural variants. Moreover, MNP-Flex achieved 92% accuracy over the validation dataset spanning over 78,000 samples from five different technologies. CONCLUSIONS The adoption of Rapid-CNS2 and MNP-Flex enables rapid intraoperative broad methylation classification and copy number alteration reporting within 30 minutes, with additional clinically relevant, fine-grained molecular insights available the following day. It offers clinicians rapid access to comprehensive molecular information critical for treatment decisions. Furthermore, MNP-Flex extends the utility of the Heidelberg methylation classifier to diverse sequencing-based data. By overcoming the limitations of currently available methods, our workflow represents a paradigm shift in the field, promising improved management of CNS tumor patients. Rapid-CNS2 can be executed with a single command, while MNP-Flex is publicly available as a web service, enhancing accessibility and usability for clinical applications.
Rapid-CNS2 combined with MNP-Flex enables next-day comprehensive molecular diagnostic profiling of CNS tumors in a global cohort [Abstract] (2024)
Patel, Areeba ; Göbel, Kirsten ; Hinz, Felix ; Dogan, Helin ; Schrimpf, Daniel ; Göller, Pauline ; Leske, Henning ; Halldórsson, Skarpheoinn ; Fox, Graeme ; Deacon, Simon ; Paine, Simon ; Smith, Stuart ; Jäger, Natalie ; Herold-Mende, Christel ; Wick, Wolfgang ; Pfister, Stefan ; Vik-Mo, Einar ; von Deimling, Andreas ; Schlesner, Matthias ; Jones, David T. ; Loose, Matthew ; Sill, Martin ; Sahm, Felix
Rapid-CNS2: rapid comprehensive adaptive nanopore-sequencing of CNS tumors, a proof-of-concept study (2022)
Patel, Areeba ; Dogan, Helin ; Payne, Alexander ; Krause, Elena ; Sievers, Philipp ; Schoebe, Natalie ; Schrimpf, Daniel ; Blume, Christina ; Stichel, Damian ; Holmes, Nadine ; Euskirchen, Philipp ; Hench, Jürgen ; Frank, Stephan ; Rosenstiel-Goidts, Violaine ; Ratliff, Miriam ; Etminan, Nima ; Unterberg, Andreas ; Dieterich, Christoph ; Herold-Mende, Christel ; Pfister, Stefan M. ; Wick, Wolfgang ; Loose, Matthew ; von Deimling, Andreas ; Sill, Martin ; Jones, David T. W. ; Schlesner, Matthias ; Sahm, Felix
Prospective, multicenter validation of a platform for rapid molecular profiling of central nervous system tumors (2025)
Patel, Areeba ; Göbel, Kirsten ; Ille, Sebastian ; Hinz, Felix ; Schoebe, Natalie ; Bogumil, Henri ; Meyer, Jochen ; Brehm, Michelle ; Kardo, Helin ; Schrimpf, Daniel ; Lomakin, Artem ; Ritter, Michael ; Göller, Pauline ; Kerbs, Paul ; Pfeifer, Lisa ; Hamelmann, Stefan ; Blume, Christina ; Ippen, Franziska M. ; Berghaus, Natalie ; Euskirchen, Philipp ; Schweizer, Leonille ; Hultschig, Claus ; Van Roy, Nadine ; Van Dorpe, Jo ; Van der Meulen, Joni ; Loontiens, Siebe ; Dedeurwaerdere, Franceska ; Leske, Henning ; Halldórsson, Skarphéðinn ; Fox, Graeme ; Deacon, Simon ; Cahyani, Inswasti ; Holmes, Nadine ; Wibowo, Satrio ; Munro, Rory ; Martin, Dan ; Sharif, Abid ; Housley, Mark ; Goldspring, Robert ; Brandner, Sebastian ; Roy, Somak ; Hench, Jürgen ; Frank, Stephan ; Unterberg, Andreas ; Goidts, Violaine ; Jäger, Natalie ; Paine, Simon ; Smith, Stuart ; Herold-Mende, Christel ; Wick, Wolfgang ; Pfister, Stefan M. ; Vik-Mo, Einar O. ; von Deimling, Andreas ; Krieg, Sandro ; Jones, David T. W. ; Loose, Matthew ; Schlesner, Matthias ; Sill, Martin ; Sahm, Felix
Molecular data integration plays a central role in central nervous system (CNS) tumor diagnostics but currently used assays pose limitations due to technical complexity, equipment and reagent costs, as well as lengthy turnaround times. We previously reported the development of Rapid-CNS2, an adaptive-sampling-based nanopore sequencing workflow. Here we comprehensively validated and further developed Rapid-CNS2 for intraoperative use. It now offers real-time methylation classification and DNA copy number information within a 30-min intraoperative window, followed by comprehensive molecular profiling within 24 h, covering the complete spectrum of diagnostically and therapeutically relevant information for the respective entity. We validated Rapid-CNS2 in a multicenter setting on 301 archival and prospective samples including 18 samples sequenced intraoperatively. To broaden the utility of methylation-based CNS tumor classification, we developed MNP-Flex, a platform-agnostic methylation classifier encompassing 184 classes. MNP-Flex achieved 99.6% accuracy for methylation families and 99.2% accuracy for methylation classes with clinically applicable thresholds across a global validation cohort of more than 78,000 frozen and formalin-fixed paraffin-embedded samples spanning five different technologies. Integration of these tools has the potential to advance CNS tumor diagnostics by providing broad access to rapid, actionable molecular insights crucial for personalized treatment strategies.
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