J Lafourcade
About
In The Last Decade
J Lafourcade
47 papers receiving 602 citations
Peers
Comparison fields: 5 of 74
- Genetics 476
- Molecular Biology 216
- Pediatrics, Perinatology and Child Health 188
- Plant Science 174
- Developmental Biology 54
Countries citing papers authored by J Lafourcade
This map shows the geographic impact of J Lafourcade'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 Lafourcade with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J Lafourcade more than expected).
Fields of papers citing papers by J Lafourcade
This network shows the impact of papers produced by J Lafourcade. 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 Lafourcade. The network helps show where J Lafourcade may publish in the future.
Co-authorship network of co-authors of J Lafourcade
This figure shows the co-authorship network connecting the top 25 collaborators of J Lafourcade. A scholar is included among the top collaborators of J Lafourcade 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 Lafourcade. J Lafourcade is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | [Thalassodrepanocyte disease. Biological and genetic study of a case]. | 0 |
| 2 | Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness. | 18 |
| 3 | [CHROMOSOME ABNORMALITIES AND HUMAN DISEASES. CONTRIBUTION TO THE ANATOMICAL STUDY OF TRISOMY 13]. | 0 |
| 4 | [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 |
| 5 | [Larsen's syndrome. Clinical findings and inheritance (author's transl)]. | 1 |
| 6 | 18 | |
| 7 | [Free 21 trisomy in mother and daughter]. | 2 |
| 8 | [Systemic lupus erythematosus. Transmission of clinical manifestations and biological factors from the mother to the newborn]. | 1 |
| 9 | Acrodermatitis entéropathica. Action du régime pauvre en tryptophane. | 2 |
| 10 | Endoréduplication sélective du bras long du chromosome 2 chez une femme et sa fille. | 32 |
| 11 | [On a case of an X chromosome in a ring]. | 4 |
| 12 | Maladie du cri du chat et sa réciproque. | 17 |
| 13 | [TRISOMY 18. 5 NEW CASES. REVIEW OF THE LITERATURE]. | 5 |
| 14 | ABERRATIONS CHROMOSOMIQUES ET MALADIES HUMAINES. CONTRIBUTION 'A L''ETUDE ANATOMIQUE DE LA TRISOMIE 13. | 3 |
| 15 | [A FAMILIAL DISEASE PRESENTING IN CERTAIN SUBJECTS THE APPEARANCE OF EULENBURG'S PARAMYOTONIA AND RESEMBLING IN OTHERS HEREDITARY EPISODIC ADYNAMIA]. | 4 |
| 16 | [FAMILIAL 2 - 22 TRANSLOCATION; ASSOCIATION WITH A HAPLO-X TURNER'S SYNDROME]. | 4 |
| 17 | [Wilson's disease with preceding hepatic and hematological symptoms in a 10-year-old child]. | 1 |
| 18 | [Heterokaryotic monozygotism, normal twin and 21 trisomal twin]. | 5 |
| 19 | Hernie diaphragmatique congénitale de type embryonnaire (fente pleuro-péritonéale gauche): coïncidence chez deux cousins germains de cette malformation isolée. | 5 |
| 20 | Aberrations chromosomiques et maladies humaines; la polydysspondylle à 45 chromosomes. | 6 |
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.