Intza Garin
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Surgery
- Nephrology top 10%
- Co-authors
- Guiomar Pérez de NanclaresLuís CastañoAgnès LinglartEduardo Fernández‐RebolloFrancesca Marta ElliGiovanna MantovaniArrate PeredaPablo Lapunzina
- Topics
- Genetic Syndromes and Imprinting (21 papers)Genomics and Rare Diseases (12 papers)Epigenetics and DNA Methylation (7 papers)
- Cited by
- GeneticsMolecular BiologyNephrology
- Journals
- SHILAP Revista de lepidopterologíaPLoS ONEEndocrine Reviews
- Partner nations
- SpainFranceUnited States
In The Last Decade
Intza Garin
31 papers receiving 609 citations
Peers
Comparison fields: 5 of 49
- Genetics 506
- Molecular Biology 476
- Pediatrics, Perinatology and Child Health 114
- Surgery 91
- Nephrology 43
Countries citing papers authored by Intza Garin
This map shows the geographic impact of Intza Garin'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 Intza Garin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Intza Garin more than expected).
Fields of papers citing papers by Intza Garin
This network shows the impact of papers produced by Intza Garin. 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 Intza Garin. The network helps show where Intza Garin may publish in the future.
Co-authorship network of co-authors of Intza Garin
This figure shows the co-authorship network connecting the top 25 collaborators of Intza Garin. A scholar is included among the top collaborators of Intza Garin 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 Intza Garin. Intza Garin 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 | 1 | |
| 3 | 1 | |
| 4 | 36 | |
| 5 | 1 | |
| 6 | 38 | |
| 7 | 18 | |
| 8 | 28 | |
| 9 | 32 | |
| 10 | 25 | |
| 11 | 31 | |
| 12 | 5 | |
| 13 | 18 | |
| 14 | 24 | |
| 15 | 10 | |
| 16 | 69 | |
| 17 | 23 | |
| 18 | 9 | |
| 19 | 24 | |
| 20 | 8 |
About Intza Garin
Intza Garin is a scholar working on Genetics, Nephrology and Molecular Biology, having authored 32 papers that have together received 638 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (21 papers), Genomics and Rare Diseases (12 papers) and Epigenetics and DNA Methylation (7 papers). The work is most often cited by research in Genetics (506 citations), Molecular Biology (476 citations) and Nephrology (43 citations). Intza Garin has collaborated with scholars based in Spain, France and United States. Frequent co-authors include Guiomar Pérez de Nanclares, Luís Castaño, Agnès Linglart, Eduardo Fernández‐Rebollo, Francesca Marta Elli, Giovanna Mantovani, Arrate Pereda, Pablo Lapunzina, Valeria Romanelli and Caroline Silve. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Endocrine Reviews.
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.