Éric Pasmant
Impact in
- Cancer Research top 1%
- Cancer-related molecular mechanisms research
- MicroRNA in disease regulation
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases
Papers in
-
- Chromatin Remodeling and Cancer 8
- RNA modifications and cancer 6
- Epigenetics and DNA Methylation 5
- Neurology 30
- Neurofibromatosis and Schwannoma Cases 28
- Neuroblastoma Research and Treatments 7
- Co-authors
- Michel Vidaud (33 shared papers)Ivan Bièche (18 shared papers)Dominique Vidaud (27 shared papers)Audrey Sabbagh (8 shared papers)Ingrid Laurendeau (5 shared papers)Delphine Héron (2 shared papers)P. Wolkenstein (17 shared papers)Béatrice Parfait (19 shared papers)
- Journals
- Journal of Medical Genetics (7 papers)European Journal of Human Genetics (4 papers)Human Mutation (4 papers)Cancer Research (3 papers)Clinical Epigenetics (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Éric Pasmant
78 papers receiving 3.7k citations
Éric Pasmant's Hit Papers
Peers
Comparison fields: 5 of 110
- Cancer Research 1.0k
- Neurology 966
- Molecular Biology 1.8k
- Rheumatology 248
- Pulmonary and Respiratory Medicine 484
Countries citing papers authored by Éric Pasmant
This map shows the geographic impact of Éric Pasmant'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 Éric Pasmant with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Éric Pasmant more than expected).
Fields of papers citing papers by Éric Pasmant
This network shows the impact of papers produced by Éric Pasmant. 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 Éric Pasmant. The network helps show where Éric Pasmant may publish in the future.
Co-authors
The 25 scholars most cited alongside Éric Pasmant, 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 84 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Characterization of a Germ-Line Deletion, Including the Entire INK4/ARF Locus, in a Melanoma-Neural System Tumor Family: Identification of ANRIL , an Antisense Noncoding RNA Whose Expression Coclusters with ARF Hit paper breakdown → | 2007 | 502 |
| 2 | 2010 | 351 | |
| 3 | 2014 | 333 | |
| 4 | 2020 | 284 | |
| 5 | 2007 | 173 | |
| 6 | 2015 | 124 | |
| 7 | 2013 | 118 | |
| 8 | 2012 | 108 | |
| 9 | 2019 | 105 | |
| 10 | 2009 | 100 | |
| 11 | 2012 | 92 | |
| 12 | 2011 | 90 | |
| 13 | 2016 | 84 | |
| 14 | 2014 | 78 | |
| 15 | 2016 | 76 | |
| 16 | 2014 | 75 | |
| 17 | 2012 | 69 | |
| 18 | 2009 | 65 | |
| 19 | 2015 | 55 | |
| 20 | 2018 | 52 |
About Éric Pasmant
Éric Pasmant is a scholar working on Molecular Biology, Neurology, Pulmonary and Respiratory Medicine, Oncology and Pathology and Forensic Medicine, having authored 84 papers that have together received 3.8k indexed citations. Recurring topics across this work include Neurofibromatosis and Schwannoma Cases (28 papers), Sarcoma Diagnosis and Treatment (14 papers), Chromatin Remodeling and Cancer (8 papers), Neuroblastoma Research and Treatments (7 papers), RNA modifications and cancer (6 papers), Epigenetics and DNA Methylation (5 papers), Soft tissue tumor case studies (5 papers) and Cancer-related molecular mechanisms research (5 papers). The work is most often cited by research in Cancer Research (1.0k citations), Neurology (966 citations), Molecular Biology (1.8k citations), Rheumatology (248 citations) and Pulmonary and Respiratory Medicine (484 citations). Éric Pasmant has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Michel Vidaud, Ivan Bièche, Dominique Vidaud, Audrey Sabbagh, Ingrid Laurendeau, Delphine Héron, P. Wolkenstein, Béatrice Parfait, Julien Masliah‐Planchon and Ingrid Laurendeau. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Human Mutation, Cancer Research and Clinical Epigenetics.
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.