Péter Hauser
Impact in
- Genetics top 0.05%
- Glioma Diagnosis and Treatment
- Cancer Research top 2%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 63
- Glioma Diagnosis and Treatment 63
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- Sarcoma Diagnosis and Treatment 11
- Co-authors
- Miklós Garami (29 shared papers)László Bognár (11 shared papers)Nada Jabado (5 shared papers)Damien Faury (4 shared papers)Zoltán Hanzély (6 shared papers)André Nantel (3 shared papers)Steffen Albrecht (3 shared papers)Takrima Haque (2 shared papers)
In The Last Decade
Péter Hauser
96 papers receiving 11k citations
Péter Hauser's Hit Papers
Peers
Comparison fields: 5 of 102
- Genetics 7.2k
- Cancer Research 908
- Molecular Biology 2.7k
- Developmental Neuroscience 64
- Oncology 400
Countries citing papers authored by Péter Hauser
This map shows the geographic impact of Péter Hauser'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 Péter Hauser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Péter Hauser more than expected).
Fields of papers citing papers by Péter Hauser
This network shows the impact of papers produced by Péter Hauser. 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 Péter Hauser. The network helps show where Péter Hauser may publish in the future.
Co-authors
The 25 scholars most cited alongside Péter Hauser, 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 104 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 | Intertumoral Heterogeneity within Medulloblastoma Subgroups Hit paper breakdown → | 2017 | 905 |
| 4 | Subgroup-specific structural variation across 1,000 medulloblastoma genomes Hit paper breakdown → | 2012 | 735 |
| 5 | Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma Hit paper breakdown → | 2014 | 520 |
| 6 | 2013 | 381 | |
| 7 | 2014 | 367 | |
| 8 | 2018 | 284 | |
| 9 | 2016 | 280 | |
| 10 | 2017 | 270 | |
| 11 | 2014 | 250 | |
| 12 | 2013 | 248 | |
| 13 | 2016 | 204 | |
| 14 | 2007 | 187 | |
| 15 | 2016 | 166 | |
| 16 | 2013 | 160 | |
| 17 | 2009 | 152 | |
| 18 | 2013 | 138 | |
| 19 | 2013 | 136 | |
| 20 | 2015 | 136 |
About Péter Hauser
Péter Hauser is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Public Health, Environmental and Occupational Health, Molecular Biology and Cancer Research, having authored 104 papers that have together received 11.2k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (63 papers), Sarcoma Diagnosis and Treatment (11 papers), Chromatin Remodeling and Cancer (11 papers), Palliative and Oncologic Care (6 papers), Acute Lymphoblastic Leukemia research (6 papers), Palliative Care and End-of-Life Issues (5 papers), Childhood Cancer Survivors' Quality of Life (3 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Genetics (7.2k citations), Cancer Research (908 citations), Molecular Biology (2.7k citations), Developmental Neuroscience (64 citations) and Oncology (400 citations). Péter Hauser has collaborated with scholars based in Hungary, Germany and Canada. Frequent co-authors include Miklós Garami, László Bognár, Nada Jabado, Damien Faury, Zoltán Hanzély, André Nantel, Steffen Albrecht, Takrima Haque, Rolando F. Del Maestro and Enrique López‐Aguilar. Their work appears in journals such as Acta Neuropathologica, Journal of Clinical Oncology, Nature, Neuro-Oncology and The Lancet Oncology.
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.