Rethoré Mo
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 33
- Genetics and Neurodevelopmental Disorders 3
- Congenital Ear and Nasal Anomalies 3
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- Prenatal Screening and Diagnostics 12
- Co-authors
- J Lejeune (33 shared papers)J Lejeune (17 shared papers)J Lafourcade (13 shared papers)B. Dutrillaux (13 shared papers)J Couturier (8 shared papers)M Prieur (10 shared papers)S. Carpentier (5 shared papers)Roland Berger (7 shared papers)
- Journals
- PubMed (60 papers)Comptes rendus hebdomadaires des séances de l Académie des sciences (1 paper)Annales de Génétique (1 paper)
- Partner nations
- France
In The Last Decade
Rethoré Mo
58 papers receiving 480 citations
Peers
Comparison fields: 5 of 48
- Developmental Biology 51
- Genetics 453
- Pediatrics, Perinatology and Child Health 203
- Plant Science 147
- Genetics 34
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 63 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME]. | 1964 | 45 |
| 2 | [Chromosome 8 : complete trisomy and segmental trisomies]. | 1977 | 33 |
| 3 | Endoréduplication sélective du bras long du chromosome 2 chez une femme et sa fille. | 1968 | 32 |
| 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 | [Metabolism of monocarbons and trisomy 21: sensitivity to methotrexate]. | 1986 | 23 |
| 7 | [Mosaic 14 trisomy in a female child with multiple abnormalities]. | 1975 | 23 |
| 8 | [Partial 14q trisomy. I. Partial 14q trisomy by maternal translocation t(10;14) (p15.2;q22)]. | 1975 | 22 |
| 9 | [Trisomy 4p due to recombination aneusomy of an inversion 4 (p 14, q 35)]. | 1974 | 17 |
| 10 | [Chimera 46,XX-69,XXY]. | 1967 | 17 |
| 11 | [Partial trisomy of the long arm of the chromosme 11 by malsegregation of a maternal translocation t(11;22)(q23 1;q1 11)]. | 1976 | 16 |
| 12 | [The crying cat syndrome and its reciprocal]. | 1965 | 14 |
| 13 | Un cas de translocation G G en tandem. | 1965 | 13 |
| 14 | [Two cases of 18q- syndrome with mosaicism (46,XX / 46,XX, 18q-)]. | 1967 | 13 |
| 15 | [A case of G-G translocation in tandem]. | 1965 | 13 |
| 16 | [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation]. | 1972 | 12 |
| 17 | [Localization of the gene of the glyceraldehyde 3 phosphate dehydrogenase on the distal segment of the short arm of the chromosome 12]. | 1976 | 12 |
| 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 partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation]. | 1966 | 9 |
| 20 | [On three cases of C trisomy]. | 1969 | 8 |
About Rethoré Mo
Rethoré Mo is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Hematology, having authored 63 papers that have together received 561 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (33 papers), Prenatal Screening and Diagnostics (12 papers), Immunodeficiency and Autoimmune Disorders (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Blood groups and transfusion (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Biochemical and Molecular Research (3 papers) and Radiopharmaceutical Chemistry and Applications (3 papers). The work is most often cited by research in Developmental Biology (51 citations), Genetics (453 citations), Pediatrics, Perinatology and Child Health (203 citations), Plant Science (147 citations) and Genetics (34 citations). Rethoré Mo has collaborated with scholars based in France. Frequent co-authors include J Lejeune, J Lejeune, J Lafourcade, B. Dutrillaux, J Couturier, M Prieur, S. Carpentier, Roland Berger, Ralph Berger and Bernard Dutrillaux. Their work appears in journals such as PubMed, Comptes rendus hebdomadaires des séances de l Académie des sciences 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.