László Bognár
Impact in
- Genetics top 0.05%
- Glioma Diagnosis and Treatment
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Cancer-related molecular mechanisms research
Papers in
- Co-authors
- Álmos Klekner (21 shared papers)Miklós Garami (11 shared papers)Péter Hauser (11 shared papers)Zoltán Hanzély (9 shared papers)Catherine Fischer (6 shared papers)Francis Turjman (6 shared papers)Nada Jabado (5 shared papers)George I. Jallo (2 shared papers)
In The Last Decade
László Bognár
98 papers receiving 8.9k citations
László Bognár's Hit Papers
Peers
Comparison fields: 5 of 111
- Genetics 5.5k
- Cancer Research 653
- Molecular Biology 2.1k
- Neurology 282
- Developmental Neuroscience 45
Countries citing papers authored by László Bognár
This map shows the geographic impact of László Bognár'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 László Bognár with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites László Bognár more than expected).
Fields of papers citing papers by László Bognár
This network shows the impact of papers produced by László Bognár. 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 László Bognár. The network helps show where László Bognár may publish in the future.
Co-authors
The 25 scholars most cited alongside László Bognár, 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 102 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Hit paper breakdown → | 2012 | 2087 |
| 2 | Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma Hit paper breakdown → | 2012 | 1522 |
| 3 | Subgroup-specific structural variation across 1,000 medulloblastoma genomes Hit paper breakdown → | 2012 | 735 |
| 4 | 2013 | 381 | |
| 5 | 2014 | 367 | |
| 6 | 2016 | 280 | |
| 7 | 2014 | 250 | |
| 8 | 2013 | 248 | |
| 9 | 2016 | 220 | |
| 10 | 2016 | 204 | |
| 11 | 2007 | 187 | |
| 12 | 2016 | 166 | |
| 13 | 2013 | 160 | |
| 14 | 2009 | 152 | |
| 15 | 2019 | 144 | |
| 16 | 2013 | 138 | |
| 17 | 2015 | 136 | |
| 18 | 2011 | 134 | |
| 19 | 2020 | 130 | |
| 20 | 2011 | 94 |
About László Bognár
László Bognár is a scholar working on Genetics, Neurology, Surgery, Epidemiology and Cellular and Molecular Neuroscience, having authored 102 papers that have together received 9.1k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (51 papers), Neurological disorders and treatments (7 papers), Meningioma and schwannoma management (6 papers), Intraoperative Neuromonitoring and Anesthetic Effects (5 papers), Cerebrospinal fluid and hydrocephalus (4 papers), Neuroscience and Music Perception (3 papers), Spinal Dysraphism and Malformations (3 papers) and Chromatin Remodeling and Cancer (2 papers). The work is most often cited by research in Genetics (5.5k citations), Cancer Research (653 citations), Molecular Biology (2.1k citations), Neurology (282 citations) and Developmental Neuroscience (45 citations). László Bognár has collaborated with scholars based in Hungary, Canada and Germany. Frequent co-authors include Álmos Klekner, Miklós Garami, Péter Hauser, Zoltán Hanzély, Catherine Fischer, Francis Turjman, Nada Jabado, George I. Jallo, Damien Faury and Tibor Hortobágyi. Their work appears in journals such as Acta Neurochirurgica, Pathology & Oncology Research, Journal of Clinical Oncology, Child s Nervous System and Acta Neuropathologica.
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.