Rethoré Mo
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Dermatoglyphics and Human Traits
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 52
- Genomic variations and chromosomal abnormalities 42
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Genomics and Rare Diseases 2
- Ocular Disorders and Treatments 2
- Genetics and Neurodevelopmental Disorders 2
- Craniofacial Disorders and Treatments 2
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- Down syndrome and intellectual disability research 5
- Co-authors
- JÉRÔME LEJEUNE (51 shared papers)Roland Berger (19 shared papers)Bernard Dutrillaux (13 shared papers)Jacques Lafourcade (14 shared papers)Jérôme Couturier (7 shared papers)M Prieur (7 shared papers)Sophie M. Carpentier (5 shared papers)H Jérôme (2 shared papers)
- Journals
- PubMed (55 papers)Annales de Génétique (1 paper)
- Partner nations
- France
In The Last Decade
Rethoré Mo
54 papers receiving 441 citations
Peers
Comparison fields: 5 of 37
- Genetics 443
- Developmental Biology 7
- Pediatrics, Perinatology and Child Health 35
- Public Health, Environmental and Occupational Health 50
- Urology 4
Countries citing papers authored by Rethoré Mo
This map shows the geographic impact of Rethoré Mo'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 Rethoré Mo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rethoré Mo more than expected).
Fields of papers citing papers by Rethoré Mo
This network shows the impact of papers produced by Rethoré Mo. 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 Rethoré Mo. The network helps show where Rethoré Mo may publish in the future.
Co-authors
The 25 scholars most cited alongside Rethoré Mo, 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 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME]. | 1964 | 47 |
| 2 | Endoréduplication sélective du bras long du chromosome 2 chez une femme et sa fille. | 1968 | 36 |
| 3 | [Chromosome 8 : complete trisomy and segmental trisomies]. | 1977 | 34 |
| 4 | [The Dr phenotype: a study of threee cases with a ring D chromosome]. | 1968 | 28 |
| 5 | [Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)]. | 1972 | 25 |
| 6 | [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)]. | 1975 | 24 |
| 7 | [Mosaic 14 trisomy in a female child with multiple abnormalities]. | 1975 | 24 |
| 8 | [Chimera 46,XX-69,XXY]. | 1967 | 20 |
| 9 | [Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)]. | 1976 | 17 |
| 10 | [A case of G-G translocation in tandem]. | 1965 | 15 |
| 11 | [The crying cat syndrome and its reciprocal]. | 1965 | 15 |
| 12 | [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)]. | 1967 | 14 |
| 13 | Un cas de translocation G G en tandem. | 1965 | 13 |
| 14 | [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation]. | 1972 | 12 |
| 15 | [Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]. | 1976 | 11 |
| 16 | [On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation]. | 1966 | 10 |
| 17 | [On three cases of C trisomy]. | 1969 | 10 |
| 18 | [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)]. | 1982 | 10 |
| 19 | [On a case of XXdc ovarian dysgenesis]. | 1966 | 8 |
| 20 | [A case of annular chromosome 9. Indentification by controlled denaturation]. | 1974 | 8 |
About Rethoré Mo
Rethoré Mo is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Radiology, Nuclear Medicine and Imaging, Pediatrics, Perinatology and Child Health and Pharmacy, having authored 58 papers that have together received 519 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (42 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Down syndrome and intellectual disability research (5 papers), Effects of Radiation Exposure (3 papers), Genomics and Rare Diseases (2 papers), Ocular Disorders and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (443 citations), Developmental Biology (7 citations), Pediatrics, Perinatology and Child Health (35 citations), Public Health, Environmental and Occupational Health (50 citations) and Urology (4 citations). Rethoré Mo has collaborated with scholars based in France. Frequent co-authors include JÉRÔME LEJEUNE, Roland Berger, Bernard Dutrillaux, Jacques Lafourcade, Jérôme Couturier, M Prieur, Sophie M. Carpentier, H Jérôme, O Raoul and Richard E. Berger. Their work appears in journals such as PubMed and Annales de Génétique.
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.