J Lejeune
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Plant Science
- Public Health, Environmental and Occupational Health
- Topics
- Genomic variations and chromosomal abnormalities (11 papers)Genetics and Neurodevelopmental Disorders (6 papers)Biochemical and Molecular Research (5 papers)
- Partner nations
- FranceUnited States
In The Last Decade
J Lejeune
47 papers receiving 501 citations
Peers
Comparison fields: 5 of 80
- Genetics 328
- Molecular Biology 202
- Pediatrics, Perinatology and Child Health 163
- Plant Science 99
- Public Health, Environmental and Occupational Health 91
Countries citing papers authored by J Lejeune
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).
Fields of papers citing papers by J Lejeune
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.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 39 | |
| 3 | [Metabolic anomalies in trisomy 21: a method for analyzing lymphocyte cultures]. | 1 |
| 4 | 20 | |
| 5 | 10 | |
| 6 | 13 | |
| 7 | 6 | |
| 8 | [Familial Miller-Dieker syndrome and (15;17) chromosome translocation]. | 6 |
| 9 | [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)]. | 10 |
| 10 | 18 | |
| 11 | [X chromosome fragility and effects of trimethoprim]. | 6 |
| 12 | 4 | |
| 13 | [De novo trisomy 4p by 4p isochromosome]. | 9 |
| 14 | An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. | 30 |
| 15 | [Infant with free trisomy 21 and maternal t(14q 22q) translocation]. | 3 |
| 16 | [Effect of the ionic medium on controlled heat denaturation of human chromosomes]. | 6 |
| 17 | Banque de cellules diploïdes humaines a caryotypes anormaux. | 2 |
| 18 | [Exclusion of certain autosomal localizations of blood and serum group genes]. | 6 |
| 19 | Un cas de translocation G G en tandem. | 13 |
| 20 | [Heterokaryotic monozygotism, normal twin and 21 trisomal twin]. | 5 |
About J Lejeune
J Lejeune is a scholar working on Otorhinolaryngology, Genetics and Applied Microbiology and Biotechnology, having authored 50 papers that have together received 576 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Biochemical and Molecular Research (5 papers). The work is most often cited by research in Developmental Biology (29 citations), Genetics (328 citations) and Otorhinolaryngology (43 citations). J Lejeune has collaborated with scholars based in France and United States. Frequent co-authors include Rethoré Mo, B. Dutrillaux, R Charachon, H Jérôme, J Couturier, M Prieur, M O Rethoré, Holger Hoehn, Ralph Berger and H.‐D. Rott. Their work appears in journals such as The Journal of Immunology, Human Genetics 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.