Yline Capri
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
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- Protein Tyrosine Phosphatases
- RNA modifications and cancer
- Bone Metabolism and Diseases
Papers in
- Genetics 21
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Connective tissue disorders research 4
- Dermatological and Skeletal Disorders 3
- Genomics and Rare Diseases 3
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- RNA modifications and cancer 5
- Protein Tyrosine Phosphatases 5
- Co-authors
- Alain Verloès (13 shared papers)Anne‐Claude Tabet (6 shared papers)Clarisse Baumann (4 shared papers)Céline Dupont (6 shared papers)Azzedine Aboura (4 shared papers)Laurence Perrin (5 shared papers)Séverine Drunat (4 shared papers)Catherine Delanöe (2 shared papers)
- Journals
- Clinical Genetics (8 papers)European Journal of Medical Genetics (7 papers)Acta Neuropathologica Communications (1 paper)Pigment Cell & Melanoma Research (1 paper)Orphanet Journal of Rare Diseases (1 paper)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Yline Capri
29 papers receiving 349 citations
Peers
Comparison fields: 5 of 59
- Genetics 181
- Molecular Biology 222
- Immunology 62
- Pediatrics, Perinatology and Child Health 56
- Endocrinology, Diabetes and Metabolism 29
Countries citing papers authored by Yline Capri
This map shows the geographic impact of Yline Capri'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 Yline Capri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yline Capri more than expected).
Fields of papers citing papers by Yline Capri
This network shows the impact of papers produced by Yline Capri. 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 Yline Capri. The network helps show where Yline Capri may publish in the future.
Co-authors
The 25 scholars most cited alongside Yline Capri, 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 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 67 | |
| 2 | 2016 | 37 | |
| 3 | 2019 | 31 | |
| 4 | 2013 | 31 | |
| 5 | 2018 | 26 | |
| 6 | 2017 | 23 | |
| 7 | 2015 | 19 | |
| 8 | 2019 | 19 | |
| 9 | 2017 | 15 | |
| 10 | 2012 | 15 | |
| 11 | 2020 | 12 | |
| 12 | 2020 | 11 | |
| 13 | 2022 | 10 | |
| 14 | 2020 | 10 | |
| 15 | 2020 | 7 | |
| 16 | 2021 | 7 | |
| 17 | 2018 | 6 | |
| 18 | 2022 | 6 | |
| 19 | 2016 | 5 | |
| 20 | 2021 | 4 |
About Yline Capri
Yline Capri is a scholar working on Genetics, Molecular Biology, Cell Biology, Immunology and Genetics, having authored 33 papers that have together received 381 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), RNA modifications and cancer (5 papers), Protein Tyrosine Phosphatases (5 papers), Connective tissue disorders research (4 papers), Galectins and Cancer Biology (3 papers), Dermatological and Skeletal Disorders (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (181 citations), Molecular Biology (222 citations), Immunology (62 citations), Pediatrics, Perinatology and Child Health (56 citations) and Endocrinology, Diabetes and Metabolism (29 citations). Yline Capri has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Alain Verloès, Anne‐Claude Tabet, Clarisse Baumann, Céline Dupont, Azzedine Aboura, Laurence Perrin, Séverine Drunat, Catherine Delanöe, Stéphane Auvin and Essam Al Ageeli. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Acta Neuropathologica Communications, Pigment Cell & Melanoma Research and Orphanet Journal of Rare Diseases.
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.