M O Rethoré
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 24
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 5
- Developmental Biology top 5%
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- Prenatal Screening and Diagnostics 14
- Rheumatology top 5%
- Folate and B Vitamins Research 6
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- Down syndrome and intellectual disability research 9
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- Chromosomal and Genetic Variations 8
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- Genomics and Chromatin Dynamics 4
- Co-authors
- J LejeuneClotilde MircherBernard DutrillauxB. DutrillauxAimé RavelCatherine LéonardDelphine AllardO Raoul
- Journals
- Experimental Cell Research (4 papers)Cytogenetic and Genome Research (3 papers)International Journal of Gynecological Cancer (2 papers)
- Partner nations
- FranceDenmarkUnited States
In The Last Decade
M O Rethoré
59 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 110
- Genetics 754
- Developmental Biology 45
- Pediatrics, Perinatology and Child Health 395
- Rheumatology 200
- Public Health, Environmental and Occupational Health 310
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-authorship network
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
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 22 | |
| 2 | 2017 | 5 | |
| 3 | 2014 | 3 | |
| 4 | 2014 | 2 | |
| 5 | 2013 | 24 | |
| 6 | 2009 | 164 | |
| 7 | 2006 | 8 | |
| 8 | 2004 | 11 | |
| 9 | 2004 | 11 | |
| 10 | 2004 | 44 | |
| 11 | 2002 | 14 | |
| 12 | 2001 | 24 | |
| 13 | 1995 | 7 | |
| 14 | 1993 | 20 | |
| 15 | 1989 | 27 | |
| 16 | Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation. | 1977 | 30 |
| 17 | A propos d'un cas de chromosome 9 en anneau. Indentification par dénaturation ménagée | 1974 | 8 |
| 18 | LA TRISOMIE 4p | 1974 | 16 |
| 19 | [Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. | 1973 | 25 |
| 20 | Maladie du cri du chat et sa réciproque. | 1965 | 17 |
About M O Rethoré
M O Rethoré is a scholar working on Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health, Anatomy and Rheumatology, having authored 62 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Prenatal Screening and Diagnostics (14 papers), Genetics and Neurodevelopmental Disorders (10 papers), Down syndrome and intellectual disability research (9 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 (754 citations), Developmental Biology (45 citations), Pediatrics, Perinatology and Child Health (395 citations), Rheumatology (200 citations) and Public Health, Environmental and Occupational Health (310 citations). M O Rethoré has collaborated with scholars based in France, Denmark and United States. Frequent co-authors include J Lejeune, Clotilde Mircher, Bernard Dutrillaux, B. Dutrillaux, Aimé Ravel, Catherine Léonard, Delphine Allard, O Raoul, M Poissonnier and André Mégarbané. Their work appears in journals such as Experimental Cell Research, Cytogenetic and Genome Research, International Journal of Gynecological Cancer, PLoS ONE and Journal of Intellectual Disability Research.
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.