635 total citations 63 papers, 561 citations indexed
About
Rethoré Mo is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology.
According to data from OpenAlex, Rethoré Mo has authored 63 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in Rethoré Mo's work include Genomic variations and chromosomal abnormalities (33 papers), Prenatal Screening and Diagnostics (12 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Rethoré Mo is often cited by papers focused on Genomic variations and chromosomal abnormalities (33 papers), Prenatal Screening and Diagnostics (12 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Rethoré Mo collaborates with scholars based in France. Rethoré Mo's co-authors include J Lejeune, J Lejeune, J Lafourcade, B. Dutrillaux, J Couturier, M Prieur, S. Carpentier, Ralph Berger, Roland Berger and Bernard Dutrillaux and has published in prestigious journals such as PubMed, Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and Annales de Génétique.
In The Last Decade
Rethoré Mo
58 papers
receiving
479 citations
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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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).
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-authorship network of co-authors of Rethoré Mo
This figure shows the co-authorship network connecting the top 25 collaborators of Rethoré Mo.
A scholar is included among the top collaborators of Rethoré Mo based on the total number of
citations received by their joint publications. Widths of edges
represent the number of papers authors have co-authored together.
Node borders
signify the number of papers an author published with Rethoré Mo. Rethoré Mo is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
20 of 20 papers shown
1.
Mo, Rethoré, et al.. (1994). [Metabolic anomalies in trisomy 21: a method for analyzing lymphocyte cultures].. PubMed. 178(8). 1521–32; discussion 1532.1 indexed citations
2.
Mo, Rethoré, J Lafourcade, J Couturier, et al.. (1982). [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)].. PubMed. 25(1). 36–42.10 indexed citations
3.
Schmelzeisen, Rainer, et al.. (1980). [Trisomy 10q24 leads to 10qter due to a familial translocation t(10;14)(q24;q32) (author's transl)].. PubMed. 23(3). 176–8.2 indexed citations
4.
Turleau, C, Rethoré Mo, Claudine Junien, J Lejeune, & de Grouchy J. (1979). [46,XX/46,XX,del (10) (p13)/47,XX,+r/47,XX,del (10) (p13), + r mosaicism and partial trisomy 10p phenotype (author's transl)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 22(3). 178–81.5 indexed citations
5.
Jc, Kaplan, et al.. (1978). [Trisomy 12p caused by malsegregation of a paternal translocation t(12;22) (p11;p11)].. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 21(4). 243–6.4 indexed citations
Mo, Rethoré, et al.. (1970). [Free 21 trisomy in mother and daughter].. PubMed. 13(1). 42–5.2 indexed citations
12.
Lejeune, J, et al.. (1970). [A case of 47XY, (?18q-)+].. PubMed. 13(1). 47–51.4 indexed citations
13.
Mo, Rethoré, et al.. (1970). [Ocular abnormalities of phenotype DR (ring D chromosome)].. PubMed. 203(8). 737–48.2 indexed citations
14.
Berger, Rudolphus, et al.. (1969). Un cas de syndrome 18q.. 17(3).4 indexed citations
15.
Lejeune, J, et al.. (1969). [A case of 18q-syndrome].. PubMed. 17(3). 423–8.4 indexed citations
16.
Dutrillaux, B., et al.. (1968). Endoréduplication sélective du bras long du chromosome 2 chez une femme et sa fille.. Comptes rendus hebdomadaires des séances de l Académie des sciences. 266(1).32 indexed citations
Berger, Roland, et al.. (1966). [On a case of an X chromosome in a ring].. PubMed. 9(2). 78–9.4 indexed citations
19.
Lejeune, J, et al.. (1965). Un cas de translocation G G en tandem.. Annales de Génétique. 8(1).13 indexed citations
20.
Lafourcade, J, et al.. (1965). [TRISOMY 18. 5 NEW CASES. REVIEW OF THE LITERATURE].. PubMed. 12. 24–35.5 indexed citations
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