M O Rethoré
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Developmental Biology top 5%
Papers in
- Genetics 29
- Genomic variations and chromosomal abnormalities 23
- Genetics and Neurodevelopmental Disorders 9
- Genomics and Rare Diseases 5
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- Genomics and Chromatin Dynamics 4
- Co-authors
- J Lejeune (17 shared papers)Clotilde Mircher (10 shared papers)Bernard Dutrillaux (6 shared papers)Aimé Ravel (7 shared papers)B. Dutrillaux (5 shared papers)Catherine Léonard (2 shared papers)Franck Sturtz (3 shared papers)Delphine Allard (3 shared papers)
- Journals
- Experimental Cell Research (4 papers)International Journal of Gynecological Cancer (2 papers)British Journal of Haematology (1 paper)Biochemical and Biophysical Research Communications (1 paper)Journal of the Neurological Sciences (1 paper)
- Partner nations
- FranceUnited StatesDenmark
In The Last Decade
M O Rethoré
59 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 111
- Genetics 746
- Developmental Biology 47
- Pediatrics, Perinatology and Child Health 341
- Rheumatology 191
- Public Health, Environmental and Occupational Health 331
Countries citing papers authored by M O Rethoré
This map shows the geographic impact of M O Rethoré'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 O Rethoré with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M O Rethoré more than expected).
Fields of papers citing papers by M O Rethoré
This network shows the impact of papers produced by M O Rethoré. 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 O Rethoré. The network helps show where M O Rethoré may publish in the future.
Co-authors
The 25 scholars most cited alongside M O Rethoré, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 179 | |
| 2 | 1976 | 159 | |
| 3 | 1988 | 128 | |
| 4 | 1985 | 85 | |
| 5 | 2005 | 79 | |
| 6 | Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region. | 1995 | 66 |
| 7 | [4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity]. | 1970 | 63 |
| 8 | 2017 | 49 | |
| 9 | 2004 | 47 | |
| 10 | No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21. | 1992 | 43 |
| 11 | 1973 | 39 | |
| 12 | 2010 | 36 | |
| 13 | Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation. | 1977 | 30 |
| 14 | [Increase of the LDH-B activity in a boy with 12p trisomy by malsegregation of a maternal translocation t(12;14) (q12;p11)]. | 1975 | 30 |
| 15 | [Selective endoreduplication of the long arm of the 2 chromosome in a woman and her daughter]. | 1968 | 28 |
| 16 | 2013 | 26 | |
| 17 | 2001 | 25 | |
| 18 | [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. | 1973 | 25 |
| 19 | 1995 | 24 | |
| 20 | 2019 | 23 |
About M O Rethoré
M O Rethoré is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Plant Science, having authored 62 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Prenatal Screening and Diagnostics (12 papers), Genetics and Neurodevelopmental Disorders (9 papers), Down syndrome and intellectual disability research (8 papers), Chromosomal and Genetic Variations (8 papers), Folate and B Vitamins Research (6 papers), Genomics and Rare Diseases (5 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Genetics (746 citations), Developmental Biology (47 citations), Pediatrics, Perinatology and Child Health (341 citations), Rheumatology (191 citations) and Public Health, Environmental and Occupational Health (331 citations). M O Rethoré has collaborated with scholars based in France, United States and Denmark. Frequent co-authors include J Lejeune, Clotilde Mircher, Bernard Dutrillaux, Aimé Ravel, B. Dutrillaux, Catherine Léonard, Franck Sturtz, Delphine Allard, O Raoul and M Poissonnier. Their work appears in journals such as Experimental Cell Research, International Journal of Gynecological Cancer, British Journal of Haematology, Biochemical and Biophysical Research Communications and Journal of the Neurological Sciences.
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.