Thomas Smol
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
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- Multiple Myeloma Research and Treatments
Papers in
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- RNA modifications and cancer 7
- Congenital heart defects research 4
- RNA Research and Splicing 3
- RNA and protein synthesis mechanisms 3
- Wnt/β-catenin signaling in development and cancer 2
- Genetics 12
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 5
- Co-authors
- Jamal Ghoumid (17 shared papers)Sylvie Manouvrier‐Hanu (7 shared papers)Florence Petit (8 shared papers)Clémence Vanlerberghe (6 shared papers)C. Thuillier (9 shared papers)Roseline Caumes (8 shared papers)Frédéric Frénois (5 shared papers)Catherine Roche‐Lestienne (3 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (4 papers)Genetics in Medicine (2 papers)The American Journal of Human Genetics (1 paper)Journal of Assisted Reproduction and Genetics (1 paper)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Thomas Smol
27 papers receiving 238 citations
Peers
Comparison fields: 5 of 56
- Genetics 31
- Hematology 30
- Genetics 54
- Molecular Biology 121
- Cell Biology 20
Countries citing papers authored by Thomas Smol
This map shows the geographic impact of Thomas Smol'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 Thomas Smol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Smol more than expected).
Fields of papers citing papers by Thomas Smol
This network shows the impact of papers produced by Thomas Smol. 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 Thomas Smol. The network helps show where Thomas Smol may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Smol, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 32 | |
| 2 | 2018 | 30 | |
| 3 | 2022 | 26 | |
| 4 | 2019 | 25 | |
| 5 | 2017 | 14 | |
| 6 | 2020 | 12 | |
| 7 | 2019 | 10 | |
| 8 | 2017 | 10 | |
| 9 | 2021 | 10 | |
| 10 | 2019 | 9 | |
| 11 | 2015 | 9 | |
| 12 | 2019 | 7 | |
| 13 | 2021 | 7 | |
| 14 | 2020 | 6 | |
| 15 | 2023 | 5 | |
| 16 | 2019 | 5 | |
| 17 | 2023 | 4 | |
| 18 | 2024 | 3 | |
| 19 | 2022 | 3 | |
| 20 | 2020 | 3 |
About Thomas Smol
Thomas Smol is a scholar working on Molecular Biology, Genetics, Public Health, Environmental and Occupational Health, Cell Biology and Genetics, having authored 34 papers that have together received 241 indexed citations. Recurring topics across this work include RNA modifications and cancer (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (5 papers), Congenital heart defects research (4 papers), RNA Research and Splicing (3 papers), RNA and protein synthesis mechanisms (3 papers), Cellular transport and secretion (2 papers) and Wnt/β-catenin signaling in development and cancer (2 papers). The work is most often cited by research in Genetics (31 citations), Hematology (30 citations), Genetics (54 citations), Molecular Biology (121 citations) and Cell Biology (20 citations). Thomas Smol has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Jamal Ghoumid, Sylvie Manouvrier‐Hanu, Florence Petit, Clémence Vanlerberghe, C. Thuillier, Roseline Caumes, Frédéric Frénois, Catherine Roche‐Lestienne, Agnès Daudignon and Anne Dieux‐Coëslier. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Genetics in Medicine, The American Journal of Human Genetics and Journal of Assisted Reproduction and 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.