Yline Capri
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- Protein Tyrosine Phosphatases
- RNA modifications and cancer
- Congenital heart defects research
- Epigenetics and DNA Methylation
- DNA Repair Mechanisms
Papers in
- Genetics 49
- Genetics and Neurodevelopmental Disorders 20
- Genomics and Rare Diseases 17
- Genomic variations and chromosomal abnormalities 15
- Connective tissue disorders research 7
- Neurogenetic and Muscular Disorders Research 4
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- Protein Tyrosine Phosphatases 11
- RNA modifications and cancer 9
- RNA Research and Splicing 4
- Co-authors
- Alain Verloès (15 shared papers)Anne‐Claude Tabet (6 shared papers)Clarisse Baumann (5 shared papers)Céline Dupont (6 shared papers)Azzedine Aboura (4 shared papers)Séverine Drunat (5 shared papers)Laurence Perrin (6 shared papers)Catherine Delanöe (2 shared papers)
- Journals
- Clinical Genetics (11 papers)European Journal of Human Genetics (10 papers)European Journal of Medical Genetics (9 papers)Journal of Medical Genetics (6 papers)Genetics in Medicine (5 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Yline Capri
86 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 90
- Genetics 897
- Molecular Biology 1000
- Genetics 116
- Immunology 178
- Pediatrics, Perinatology and Child Health 145
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 93 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 178 | |
| 2 | 2016 | 142 | |
| 3 | 2013 | 99 | |
| 4 | 2013 | 77 | |
| 5 | 2016 | 75 | |
| 6 | 2016 | 73 | |
| 7 | 2020 | 72 | |
| 8 | 2017 | 63 | |
| 9 | 2015 | 59 | |
| 10 | 2019 | 53 | |
| 11 | 2019 | 50 | |
| 12 | 2018 | 45 | |
| 13 | 2016 | 45 | |
| 14 | 2019 | 45 | |
| 15 | 2015 | 44 | |
| 16 | 2021 | 41 | |
| 17 | 2019 | 35 | |
| 18 | 2017 | 34 | |
| 19 | 2017 | 34 | |
| 20 | 2013 | 33 |
About Yline Capri
Yline Capri is a scholar working on Genetics, Molecular Biology, Genetics, Rheumatology and Developmental Neuroscience, having authored 93 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (20 papers), Genomics and Rare Diseases (17 papers), Genomic variations and chromosomal abnormalities (15 papers), Protein Tyrosine Phosphatases (11 papers), RNA modifications and cancer (9 papers), Connective tissue disorders research (7 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Genetics (897 citations), Molecular Biology (1000 citations), Genetics (116 citations), Immunology (178 citations) and Pediatrics, Perinatology and Child Health (145 citations). Yline Capri has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Alain Verloès, Anne‐Claude Tabet, Clarisse Baumann, Céline Dupont, Azzedine Aboura, Séverine Drunat, Laurence Perrin, Catherine Delanöe, Hélène Cavé and Stéphane Auvin. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Medical Genetics and Genetics in Medicine.
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.