714 total citations 50 papers, 576 citations indexed
About
J Lejeune is a scholar working on Genetics, Molecular Biology and Epidemiology.
According to data from OpenAlex, J Lejeune has authored 50 papers receiving a total of 576 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Epidemiology. Recurrent topics in J Lejeune's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Biochemical and Molecular Research (5 papers). J Lejeune is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Biochemical and Molecular Research (5 papers). J Lejeune collaborates with scholars based in France and United States. J Lejeune's co-authors include Rethoré Mo, B. Dutrillaux, R Charachon, H Jérôme, J Couturier, M Prieur, M O Rethoré, H.‐D. Rott, Holger Hoehn and Ralph Berger and has published in prestigious journals such as The Journal of Immunology, Human Genetics and Journal of Intellectual Disability Research.
In The Last Decade
J Lejeune
47 papers
receiving
501 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 J Lejeune'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 J Lejeune with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J Lejeune more than expected).
This network shows the impact of papers produced by J Lejeune. 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 J Lejeune. The network helps show where J Lejeune may publish in the future.
Co-authorship network of co-authors of J Lejeune
This figure shows the co-authorship network connecting the top 25 collaborators of J Lejeune.
A scholar is included among the top collaborators of J Lejeune 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 J Lejeune. J Lejeune is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Peeters, Marie, et al.. (1991). Metabolic anomalies in cri du chat syndrome (5p-) lymphocytes and de novo purine synthesis.. PubMed. 34(3-4). 219–25.2 indexed citations
6.
Lejeune, J, M O Rethoré, Mathilde Blois, & Marie Peeters. (1989). [Infantile psychosis, pseudo-Alzheimer syndrome, and trisomy 21. A trial of treatment with folinic acid: preliminary report].. PubMed. 44(2). 115–21.5 indexed citations
7.
Goutières, Françoise, et al.. (1988). [Familial Miller-Dieker syndrome and (15;17) chromosome translocation].. PubMed. 44(7). 501–4.6 indexed citations
8.
Mo, Rethoré, et al.. (1985). [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].. PubMed. 28(3). 149–53.3 indexed citations
9.
Lejeune, J, et al.. (1982). [X chromosome fragility and effects of trimethoprim].. PubMed. 25(3). 149–51.6 indexed citations
Aurias, Alain, et al.. (1976). [De novo trisomy 4p by 4p isochromosome].. PubMed. 19(2). 127–127.9 indexed citations
13.
Dutrillaux, B., et al.. (1973). An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques.. PubMed. 16(1). 11–6.30 indexed citations
14.
Forabosco, Antonino, et al.. (1973). [Infant with free trisomy 21 and maternal t(14q 22q) translocation].. PubMed. 16(1). 57–9.3 indexed citations
15.
Dutrillaux, Bernard, et al.. (1972). [Differentiation of X chromosomes by despiralization methods using 5-bromodeoxyuridine (BUDR) and controlled thermal denaturation].. PubMed. 15(4). 271–4.12 indexed citations
16.
Carpentier, S., Bernard Dutrillaux, & J Lejeune. (1972). [Effect of the ionic medium on controlled heat denaturation of human chromosomes].. PubMed. 15(3). 203–5.6 indexed citations
17.
Carpentier, S. & J Lejeune. (1970). Banque de cellules diploïdes humaines a caryotypes anormaux.. Annales de Génétique. 13(2).2 indexed citations
18.
Lejeune, J, et al.. (1965). Un cas de translocation G G en tandem.. Annales de Génétique. 8(1).13 indexed citations
19.
Lejeune, J, et al.. (1962). [Heterokaryotic monozygotism, normal twin and 21 trisomal twin].. PubMed. 254. 4404–6.5 indexed citations
20.
Jérôme, H, et al.. (1960). [Study of the urinary excretion of some tryptophan metabolites in mongoloid children].. PubMed. 251. 474–6.10 indexed citations
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