O Raoul
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 2
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- Epigenetics and DNA Methylation 2
- Co-authors
- M Poissonnier (3 shared papers)Delphine Allard (3 shared papers)M Prieur (8 shared papers)M O Rethoré (3 shared papers)J Lejeune (7 shared papers)J Couturier (2 shared papers)Valérie Cormier‐Daire (5 shared papers)Laurence Colleaux (4 shared papers)
- Journals
- Clinical Genetics (2 papers)Experimental Cell Research (2 papers)Journal of Medical Genetics (2 papers)Human Genetics (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
O Raoul
29 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 90
- Genetics 723
- Pediatrics, Perinatology and Child Health 269
- Cognitive Neuroscience 165
- Rheumatology 94
- Molecular Biology 464
Countries citing papers authored by O Raoul
This map shows the geographic impact of O Raoul'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 O Raoul with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites O Raoul more than expected).
Fields of papers citing papers by O Raoul
This network shows the impact of papers produced by O Raoul. 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 O Raoul. The network helps show where O Raoul may publish in the future.
Co-authors
The 25 scholars most cited alongside O Raoul, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 238 | |
| 2 | 1992 | 159 | |
| 3 | 1976 | 159 | |
| 4 | 1985 | 85 | |
| 5 | 2005 | 66 | |
| 6 | 1979 | 62 | |
| 7 | 1994 | 60 | |
| 8 | 2002 | 55 | |
| 9 | 2002 | 42 | |
| 10 | 1984 | 34 | |
| 11 | 2001 | 34 | |
| 12 | 2005 | 24 | |
| 13 | [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)]. | 1975 | 22 |
| 14 | [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)]. | 1976 | 21 |
| 15 | 1995 | 16 | |
| 16 | [Fragile site Xq27 and metabolism of monocarbons. Significant decrease of the frequency of chromosomal gaps by treatment in vitro and in vivo]. | 1981 | 7 |
| 17 | 2004 | 6 | |
| 18 | [Ring chromosome 14. I. A case report on homogeneous r(14)]. | 1984 | 6 |
| 19 | [X chromosome fragility and effects of trimethoprim]. | 1982 | 6 |
| 20 | [Ring-shaped chromosome 11 (46, XX, r11). A new case]. | 1981 | 6 |
About O Raoul
O Raoul is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Rheumatology, having authored 31 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (7 papers), Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (5 papers), Genomics and Rare Diseases (3 papers), Microtubule and mitosis dynamics (2 papers), Epigenetics and DNA Methylation (2 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (723 citations), Pediatrics, Perinatology and Child Health (269 citations), Cognitive Neuroscience (165 citations), Rheumatology (94 citations) and Molecular Biology (464 citations). O Raoul has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include M Poissonnier, Delphine Allard, M Prieur, M O Rethoré, J Lejeune, J Couturier, Valérie Cormier‐Daire, Laurence Colleaux, Damien Sanlaville and Stanislas Lyonnet. Their work appears in journals such as Clinical Genetics, Experimental Cell Research, Journal of Medical Genetics, Human Genetics 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.