L Osvaldo
- Co-authors
- Harrison LattaEdward W. BlankJerry A. PetersonW. H. JohnstonJeremy D. JacksonMargery L. CookElizabeth SternM. R. Mickey
- Topics
- Chronic Kidney Disease and Diabetes (3 papers)Barrier Structure and Function Studies (2 papers)Cancer Genomics and Diagnostics (1 paper)
- Cited by
- NeurologyNephrologyCell Biology
- Journals
- NatureJournal of Ultrastructure ResearchPubMed
- Partner nations
- United StatesUnited Kingdom
In The Last Decade
L Osvaldo
9 papers receiving 204 citations
Peers
Comparison fields: 5 of 62
- Molecular Biology 111
- Neurology 52
- Pulmonary and Respiratory Medicine 41
- Cell Biology 40
- Physiology 39
Countries citing papers authored by L Osvaldo
This map shows the geographic impact of L Osvaldo'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 L Osvaldo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L Osvaldo more than expected).
Fields of papers citing papers by L Osvaldo
This network shows the impact of papers produced by L Osvaldo. 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 L Osvaldo. The network helps show where L Osvaldo may publish in the future.
Co-authorship network of co-authors of L Osvaldo
This figure shows the co-authorship network connecting the top 25 collaborators of L Osvaldo. A scholar is included among the top collaborators of L Osvaldo 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 L Osvaldo. L Osvaldo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Comparison of rates of phenotypic variability in surface antigen expression in normal and cancerous human breast epithelial cells. | 39 |
| 2 | Unilateral renovascular hypertension in rats. Measurements of medullary granules, juxtaglomerular granularity and cellularity, and areas of adrenal zones. | 4 |
| 3 | 14 | |
| 4 | 67 | |
| 5 | 49 | |
| 6 | REACTIONS OF KIDNEY CELLS DURING AUTOLYSIS: LIGHT MICROSCOPIC OBSERVATIONS. | 17 |
| 7 | 9 | |
| 8 | CHANGES IN RENAL CORTICAL TUBULES DURING AUTOLYSIS: ELECTRON MICROSCOPIC OBSERVATIONS. | 41 |
| 9 | CHANGES IN RENAL GLOMERULI DURING AUTOLYSIS: ELECTRON MICROSCOPIC OBSERVATIONS. | 15 |
About L Osvaldo
L Osvaldo is a scholar working on Nephrology, Neurology and Biotechnology, having authored 9 papers that have together received 255 indexed citations. Recurring topics across this work include Chronic Kidney Disease and Diabetes (3 papers), Barrier Structure and Function Studies (2 papers) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Neurology (52 citations), Nephrology (38 citations) and Cell Biology (40 citations). L Osvaldo has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Harrison Latta, Edward W. Blank, Jerry A. Peterson, W. H. Johnston, Jeremy D. Jackson, Margery L. Cook, Elizabeth Stern and M. R. Mickey. Their work appears in journals such as Nature, Journal of Ultrastructure Research and PubMed.
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.