Martin Sill

19.6k citations
150 papers · 13.8k · 9 hit papers · h-index 49

Impact in

Papers in

    • Glioma Diagnosis and Treatment 87
    • Cancer Genomics and Diagnostics 25
    • MicroRNA in disease regulation 7

Martin Sill

146 papers receiving 13.6k citations

Martin Sill's Hit Papers

Sarcoma classification by DNA methylation profiling 2021 · 388 citations
3880+4+9Years since publication50010001.5k2.0k

Peers

Martin Sill
Comparison fields: 5 of 145
  • Genetics 7.7k
  • Cancer Research 2.6k
  • Neurology 2.5k
  • Molecular Biology 4.9k
  • Pulmonary and Respiratory Medicine 2.1k
Replace Ulrich Schüller with:
Ulrich Schüller Germany
Pascale Varlet France
Jens Schittenhelm Germany
Matthias A. Karajannis United States
David Reuß Germany
Daniel Schrimpf Germany
Marina Vladimirovna Ryzhova Russia
Kristian W. Pajtler Germany
Dominik Sturm Germany
Christian Koelsche Germany
Martin Sill relative to Ulrich Schüller Germany Ulrich Schüller's profile →
Citations per field
00.5×1.5×
Ulrich Schüller · 1×
Citations per year

Countries citing papers authored by Martin Sill

Since Specialization
Citations

This map shows the geographic impact of Martin Sill'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 Martin Sill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martin Sill more than expected).

Fields of papers citing papers by Martin Sill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin Sill. 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 Martin Sill. The network helps show where Martin Sill may publish in the future.

Co-authors

The 25 scholars most cited alongside Martin Sill, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Martin Sill Line = papers co-authored together Martin Sill links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 150 papers — load more, or switch the sort, to bring in the rest.

#Work
1
DNA methylation-based classification of central nervous system tumours
Hit paper breakdown →
20182183
2
Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma
Hit paper breakdown →
20121513
3
Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups
Hit paper breakdown →
2015899
4
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Hit paper breakdown →
2016716
5
DNA methylation-based classification and grading system for meningioma: a multicentre, retrospective analysis
Hit paper breakdown →
2017649
6
Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Hit paper breakdown →
2014485
7 2011433
8
Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience
Hit paper breakdown →
2018413
9
Sarcoma classification by DNA methylation profiling
Hit paper breakdown →
2021388
10 2016257
11 2018237
12 2016221
13 2018215
14 2019215
15 2020200
16 2017179
17
Integrated Molecular-Morphologic Meningioma Classification: A Multicenter Retrospective Analysis, Retrospectively and Prospectively Validated
Hit paper breakdown →
2021179
18 2014173
19 2016150
20 2010148

About Martin Sill

Martin Sill is a scholar working on Genetics, Cancer Research, Molecular Biology, Neurology and Pulmonary and Respiratory Medicine, having authored 150 papers that have together received 13.8k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (87 papers), Cancer Genomics and Diagnostics (25 papers), Epigenetics and DNA Methylation (23 papers), Chromatin Remodeling and Cancer (19 papers), Neuroblastoma Research and Treatments (13 papers), Sarcoma Diagnosis and Treatment (9 papers), Meningioma and schwannoma management (7 papers) and MicroRNA in disease regulation (7 papers). The work is most often cited by research in Genetics (7.7k citations), Cancer Research (2.6k citations), Neurology (2.5k citations), Molecular Biology (4.9k citations) and Pulmonary and Respiratory Medicine (2.1k citations). Martin Sill has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Stefan M. Pfister, David Jones, Andreas von Deimling, David Capper, Axel Benner, Wolfgang Wick, Martin Bendszus, Philipp Kickingereder, Antje Wick and David Bonekamp. Their work appears in journals such as Acta Neuropathologica, Neuro-Oncology, Acta Neuropathologica Communications, Nature Communications and Cancer Cell.

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.

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