R Turpin
About
In The Last Decade
R Turpin
28 papers receiving 1.1k citations
Hit Papers
Peers
Comparison fields: 5 of 117
- Genetics 703
- Molecular Biology 412
- Public Health, Environmental and Occupational Health 275
- Pediatrics, Perinatology and Child Health 258
- Plant Science 193
Countries citing papers authored by R Turpin
This map shows the geographic impact of R Turpin'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 R Turpin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R Turpin more than expected).
Fields of papers citing papers by R Turpin
This network shows the impact of papers produced by R Turpin. 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 R Turpin. The network helps show where R Turpin may publish in the future.
Co-authorship network of co-authors of R Turpin
This figure shows the co-authorship network connecting the top 25 collaborators of R Turpin. A scholar is included among the top collaborators of R Turpin 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 R Turpin. R Turpin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13]. | 0 |
| 2 | 3 | |
| 3 | [Systemic lupus erythematosus. Transmission of clinical manifestations and biological factors from the mother to the newborn]. | 1 |
| 4 | Human afflictions and chromosomal aberrations | 8 |
| 5 | Les chromosomes humains : caryotype normal et variations pathologiques | 9 |
| 6 | Les Chromosomes humains | 114 |
| 7 | [Wilson's disease with preceding hepatic and hematological symptoms in a 10-year-old child]. | 1 |
| 8 | [3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME]. | 119 |
| 9 | [Heterokaryotic monozygotism, normal twin and 21 trisomal twin]. | 5 |
| 10 | Somatic chromosomes in mongolism. | 6 |
| 11 | [Human diseases caused by chromosomal aberrations]. | 1 |
| 12 | [Chromosome aberrations and human diseases. XXY Klinefelter's syndrome from 46 chromosomes caused by T-T centromeric fusion]. | 17 |
| 13 | [Karyotype analysis in 3 cases of male pseudo-hermaphroditism]. | 3 |
| 14 | Aberrations chromosomiques et maladies humaines; la polydysspondylle à 45 chromosomes. | 6 |
| 15 | [Study of somatic chromosomes from 9 mongoloid children]. breakdown → | 621 |
| 16 | [Chromosome aberrations & human diseases; multiple spinal abnormalities with 45 chromosomes]. | 16 |
| 17 | 4 | |
| 18 | [Influence of the age of parents on the masculinity of living births]. | 6 |
| 19 | 1 | |
| 20 | L'hérédité des prédispositions morbides | 2 |
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.