E. Eggermont
About
In The Last Decade
E. Eggermont
195 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 128
- Molecular Biology 983
- Surgery 676
- Pulmonary and Respiratory Medicine 598
- Pediatrics, Perinatology and Child Health 572
- Genetics 526
Countries citing papers authored by E. Eggermont
This map shows the geographic impact of E. Eggermont'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 E. Eggermont with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Eggermont more than expected).
Fields of papers citing papers by E. Eggermont
This network shows the impact of papers produced by E. Eggermont. 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 E. Eggermont. The network helps show where E. Eggermont may publish in the future.
Co-authorship network of co-authors of E. Eggermont
This figure shows the co-authorship network connecting the top 25 collaborators of E. Eggermont. A scholar is included among the top collaborators of E. Eggermont 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 E. Eggermont. E. Eggermont is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | Avis n° 49 du 20 avril 2009 relatif à l'utilisation du diagnostic génétique préimplantatoire (DPI) pour détecter les porteurs sains d'une mutation causant une affection héréditaire grave qui peut entraîner un risque élevé pour les descendants | 1 |
| 3 | 23 | |
| 4 | 10 | |
| 5 | Possible role of platelet activation in the pathogenesis of the transient neonatal hyperammonemia syndrome | 8 |
| 6 | 13 | |
| 7 | 7 | |
| 8 | 9 | |
| 9 | Iodine Intake of Breast-fed Versus Bottle-fed Healthy Newborns and Prematures | 3 |
| 10 | 4 | |
| 11 | 1 | |
| 12 | 2 | |
| 13 | HLA-DR expression and lymphocytic subsets in small bowel biopsies in coeliac disease and cow's milk intolerance | 3 |
| 14 | Leukodystrophy with increased csf and plasma gamma-aminobutyric acid and beta-alanine - gamma-aminobutyric acid transaminase deficiency | 4 |
| 15 | Congenital folate malabsorption with mental-retardation and cerebral calcifications | 3 |
| 16 | Plasma Androgens Before and Throughout Puberty | 1 |
| 17 | Complete trisomy 8 in a polymalformed newborn. | 1 |
| 18 | Transient hyperammonaemia in a preterm neonate. | 1 |
| 19 | Familial deficiency of granulocyte bactericidal capacity associated with growth retardation. | 3 |
| 20 | 30 |
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.