Thiébaut-Noël Willig
- Molecular Biology top 10%
- Genetics top 10%
- Hematology top 5%
- Oncology
- Genetics top 10%
- Co-authors
- Narla MohandasGil TcherniaNiklas DahlIrma DianzaniSarah E. BallDmitri TentlerPeter GustavssonBirgit Carlsson
- Topics
- RNA modifications and cancer (8 papers)Cancer-related gene regulation (8 papers)Epigenetics and DNA Methylation (5 papers)
- Cited by
- HematologyMolecular BiologyGenetics
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Thiébaut-Noël Willig
13 papers receiving 1.3k citations
Hit Papers
Peers
Comparison fields: 5 of 78
- Molecular Biology 1.0k
- Genetics 213
- Hematology 183
- Oncology 156
- Genetics 131
Countries citing papers authored by Thiébaut-Noël Willig
This map shows the geographic impact of Thiébaut-Noël Willig'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 Thiébaut-Noël Willig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thiébaut-Noël Willig more than expected).
Fields of papers citing papers by Thiébaut-Noël Willig
This network shows the impact of papers produced by Thiébaut-Noël Willig. 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 Thiébaut-Noël Willig. The network helps show where Thiébaut-Noël Willig may publish in the future.
Co-authorship network of co-authors of Thiébaut-Noël Willig
This figure shows the co-authorship network connecting the top 25 collaborators of Thiébaut-Noël Willig. A scholar is included among the top collaborators of Thiébaut-Noël Willig based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Thiébaut-Noël Willig. Thiébaut-Noël Willig is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 5 | |
| 3 | 3 | |
| 4 | 3 | |
| 5 | 0 | |
| 6 | 51 | |
| 7 | 78 | |
| 8 | 33 | |
| 9 | 98 | |
| 10 | 54 | |
| 11 | 129 | |
| 12 | Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression. | 157 |
| 13 | The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemiabreakdown → | 594 |
| 14 | 57 | |
| 15 | 31 |
About Thiébaut-Noël Willig
Thiébaut-Noël Willig is a scholar working on Pediatrics, Perinatology and Child Health, Psychiatry and Mental health and Radiological and Ultrasound Technology, having authored 15 papers that have together received 1.3k indexed citations. Recurring topics across this work include RNA modifications and cancer (8 papers), Cancer-related gene regulation (8 papers) and Epigenetics and DNA Methylation (5 papers). The work is most often cited by research in Hematology (183 citations), Molecular Biology (1.0k citations) and Genetics (131 citations). Thiébaut-Noël Willig has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Narla Mohandas, Gil Tchernia, Niklas Dahl, Irma Dianzani, Sarah E. Ball, Dmitri Tentler, Peter Gustavsson, Birgit Carlsson, Hans Matsson and Björn Andersson. Their work appears in journals such as Nature Genetics, Blood and The American Journal of Human Genetics.
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.