M Prieur
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 5%
- Congenital heart defects research
- Epigenetics and DNA Methylation
Papers in
- Genetics 42
- Genomic variations and chromosomal abnormalities 35
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 7
- Genetic Syndromes and Imprinting 6
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- DNA Repair Mechanisms 8
- Congenital heart defects research 7
- Genomics and Chromatin Dynamics 5
- Co-authors
- Alain Aurias (15 shared papers)Bernard Dutrillaux (17 shared papers)JÉRÔME LEJEUNE (13 shared papers)CATHERINE TURLEAU (7 shared papers)Zoubida Chettouh (6 shared papers)F Ledeist (3 shared papers)E. Viégas-Pèquignot (5 shared papers)Jean‐Louis Blouin (5 shared papers)
- Journals
- Human Genetics (8 papers)Journal of Medical Genetics (6 papers)Clinical Genetics (5 papers)Chromosoma (2 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (2 papers)
- Partner nations
- FranceUnited KingdomLebanon
In The Last Decade
M Prieur
69 papers receiving 3.6k citations
M Prieur's Hit Papers
Peers
Comparison fields: 5 of 110
- Genetics 1.9k
- Molecular Biology 2.2k
- Pediatrics, Perinatology and Child Health 478
- Reproductive Medicine 145
- Public Health, Environmental and Occupational Health 479
Countries citing papers authored by M Prieur
This map shows the geographic impact of M Prieur'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 M Prieur with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Prieur more than expected).
Fields of papers citing papers by M Prieur
This network shows the impact of papers produced by M Prieur. 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 M Prieur. The network helps show where M Prieur may publish in the future.
Co-authors
The 25 scholars most cited alongside M Prieur, 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 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. Hit paper breakdown → | 1997 | 961 |
| 2 | 2006 | 253 | |
| 3 | 2007 | 247 | |
| 4 | 1993 | 245 | |
| 5 | 1989 | 226 | |
| 6 | 1999 | 215 | |
| 7 | 1978 | 136 | |
| 8 | 1986 | 101 | |
| 9 | 1974 | 82 | |
| 10 | Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region. | 1995 | 67 |
| 11 | 1985 | 65 | |
| 12 | 1986 | 63 | |
| 13 | 1994 | 61 | |
| 14 | 2002 | 61 | |
| 15 | 1994 | 59 | |
| 16 | 1993 | 56 | |
| 17 | 1988 | 53 | |
| 18 | 1997 | 52 | |
| 19 | Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases. | 1993 | 51 |
| 20 | [A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)]. | 1979 | 49 |
About M Prieur
M Prieur is a scholar working on Genetics, Molecular Biology, Genetics, Cancer Research and Public Health, Environmental and Occupational Health, having authored 69 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (35 papers), Genetics and Neurodevelopmental Disorders (9 papers), DNA Repair Mechanisms (8 papers), Genomics and Rare Diseases (7 papers), Chromosomal and Genetic Variations (7 papers), Congenital heart defects research (7 papers), Genetic Syndromes and Imprinting (6 papers) and Genomics and Chromatin Dynamics (5 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (2.2k citations), Pediatrics, Perinatology and Child Health (478 citations), Reproductive Medicine (145 citations) and Public Health, Environmental and Occupational Health (479 citations). M Prieur has collaborated with scholars based in France, United Kingdom and Lebanon. Frequent co-authors include Alain Aurias, Bernard Dutrillaux, JÉRÔME LEJEUNE, CATHERINE TURLEAU, Zoubida Chettouh, F Ledeist, E. Viégas-Pèquignot, Jean‐Louis Blouin, Marc Jeanpierre and Alain Fischer. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, Chromosoma and Mutation research. Fundamental and molecular mechanisms of mutagenesis.
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.