Marc Remke
Impact in
- Genetics top 0.02%
- Glioma Diagnosis and Treatment
- Cancer Research top 0.2%
- Cancer Genomics and Diagnostics
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
Papers in
- Genetics 93
- Glioma Diagnosis and Treatment 93
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- Cancer-related molecular mechanisms research 17
- MicroRNA in disease regulation 15
- Cancer Genomics and Diagnostics 14
- Co-authors
- Michael D. Taylor (44 shared papers)Stefan M. Pfister (28 shared papers)Andrey Korshunov (24 shared papers)Paul A. Northcott (13 shared papers)Peter Lichter (13 shared papers)Marcel Kool (9 shared papers)Stefan Rutkowski (9 shared papers)Charles G. Eberhart (3 shared papers)
- Journals
- Acta Neuropathologica (25 papers)Neuro-Oncology (15 papers)Journal of Clinical Oncology (12 papers)Cancer Cell (11 papers)Nature Communications (7 papers)
- Partner nations
- GermanyCanadaUnited States
In The Last Decade
Marc Remke
207 papers receiving 20.8k citations
Marc Remke's Hit Papers
Peers
Comparison fields: 5 of 138
- Genetics 10.3k
- Cancer Research 4.4k
- Neurology 2.9k
- Molecular Biology 12.4k
- Oncology 2.2k
Countries citing papers authored by Marc Remke
This map shows the geographic impact of Marc Remke's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marc Remke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marc Remke more than expected).
Fields of papers citing papers by Marc Remke
This network shows the impact of papers produced by Marc Remke. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marc Remke. The network helps show where Marc Remke may publish in the future.
Co-authors
The 25 scholars most cited alongside Marc Remke, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 214 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Molecular subgroups of medulloblastoma: the current consensus Hit paper breakdown → | 2011 | 1484 |
| 2 | Intertumoral Heterogeneity within Medulloblastoma Subgroups Hit paper breakdown → | 2017 | 894 |
| 3 | Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas Hit paper breakdown → | 2012 | 808 |
| 4 | Subgroup-specific structural variation across 1,000 medulloblastoma genomes Hit paper breakdown → | 2012 | 731 |
| 5 | New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs Hit paper breakdown → | 2016 | 716 |
| 6 | Dissecting the genomic complexity underlying medulloblastoma Hit paper breakdown → | 2012 | 702 |
| 7 | Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations Hit paper breakdown → | 2012 | 688 |
| 8 | Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition Hit paper breakdown → | 2014 | 617 |
| 9 | Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma Hit paper breakdown → | 2014 | 515 |
| 10 | Risk stratification of childhood medulloblastoma in the molecular era: the current consensus Hit paper breakdown → | 2016 | 494 |
| 11 | Epigenomic alterations define lethal CIMP-positive ependymomas of infancy Hit paper breakdown → | 2014 | 485 |
| 12 | 2011 | 433 | |
| 13 | 2008 | 421 | |
| 14 | 2013 | 378 | |
| 15 | 2017 | 374 | |
| 16 | 2013 | 343 | |
| 17 | 2011 | 322 | |
| 18 | 2013 | 321 | |
| 19 | 2015 | 283 | |
| 20 | 2016 | 275 |
About Marc Remke
Marc Remke is a scholar working on Genetics, Cancer Research, Molecular Biology, Neurology and Cell Biology, having authored 214 papers that have together received 21.2k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (93 papers), Hedgehog Signaling Pathway Studies (43 papers), Chromatin Remodeling and Cancer (28 papers), Epigenetics and DNA Methylation (26 papers), Cancer-related molecular mechanisms research (17 papers), MicroRNA in disease regulation (15 papers), Cancer Genomics and Diagnostics (14 papers) and Neuroblastoma Research and Treatments (13 papers). The work is most often cited by research in Genetics (10.3k citations), Cancer Research (4.4k citations), Neurology (2.9k citations), Molecular Biology (12.4k citations) and Oncology (2.2k citations). Marc Remke has collaborated with scholars based in Germany, Canada and United States. Frequent co-authors include Michael D. Taylor, Stefan M. Pfister, Andrey Korshunov, Paul A. Northcott, Peter Lichter, Marcel Kool, Stefan Rutkowski, Charles G. Eberhart, Scott L. Pomeroy and Vijay Ramaswamy. Their work appears in journals such as Acta Neuropathologica, Neuro-Oncology, Journal of Clinical Oncology, Cancer Cell and Nature Communications.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.