Thomas Guignard
Impact in
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- Genomics and Rare Diseases
- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
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- Retinal Development and Disorders
- RNA modifications and cancer
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
Papers in
- Genetics 13
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 2
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- Cancer Genomics and Diagnostics 3
- Co-authors
- David Baux (3 shared papers)Charles Van Goethem (3 shared papers)Anne Bergougnoux (2 shared papers)Anne‐Françoise Roux (2 shared papers)Vincent Gâtinois (4 shared papers)François Juge (1 shared paper)Ana Boulanger (1 shared paper)Jean‐Maurice Dura (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Genetics in Medicine (2 papers)Journal of Molecular Diagnostics (2 papers)Nucleic Acids Research (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Thomas Guignard
18 papers receiving 432 citations
Peers
Comparison fields: 5 of 62
- Genetics 163
- Molecular Biology 225
- Genetics 30
- Ophthalmology 24
- Cellular and Molecular Neuroscience 51
Countries citing papers authored by Thomas Guignard
This map shows the geographic impact of Thomas Guignard'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 Guignard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Guignard more than expected).
Fields of papers citing papers by Thomas Guignard
This network shows the impact of papers produced by Thomas Guignard. 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 Guignard. The network helps show where Thomas Guignard may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Guignard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 70 | |
| 2 | 2019 | 68 | |
| 3 | 2010 | 67 | |
| 4 | 2021 | 48 | |
| 5 | 2017 | 25 | |
| 6 | 2017 | 23 | |
| 7 | 2018 | 22 | |
| 8 | 2023 | 22 | |
| 9 | 2018 | 16 | |
| 10 | 2010 | 13 | |
| 11 | 2023 | 12 | |
| 12 | 2019 | 12 | |
| 13 | 2019 | 11 | |
| 14 | 2022 | 9 | |
| 15 | 2018 | 7 | |
| 16 | 2022 | 6 | |
| 17 | Head-Related Transfer Function Customization by Frequency Scaling and Rotation Shift Based on a New Morphological Matching Method | 2008 | 2 |
| 18 | 2023 | 2 | |
| 19 | 2024 | 0 |
About Thomas Guignard
Thomas Guignard is a scholar working on Genetics, Cancer Research, Molecular Biology, Ophthalmology and Cell Biology, having authored 19 papers that have together received 435 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (4 papers), Cancer Genomics and Diagnostics (3 papers), Genomics and Phylogenetic Studies (3 papers), Retinal Development and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA and protein synthesis mechanisms (2 papers) and Retinal Diseases and Treatments (2 papers). The work is most often cited by research in Genetics (163 citations), Molecular Biology (225 citations), Genetics (30 citations), Ophthalmology (24 citations) and Cellular and Molecular Neuroscience (51 citations). Thomas Guignard has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include David Baux, Charles Van Goethem, Anne Bergougnoux, Anne‐Françoise Roux, Vincent Gâtinois, François Juge, Ana Boulanger, Jean‐Maurice Dura, Véronique Geoffroy and Sophie Scheidecker. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Journal of Molecular Diagnostics, Nucleic Acids Research and Human Molecular 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.