Elena Mansilla
- Genetics top 10%
- Pediatrics, Perinatology and Child Health top 5%
- Molecular Biology
- Plant Science
- Rheumatology
- Co-authors
- Gerardo SuárezM.L. Martínez‐FernándezPablo LapunzinaLuís FernándezJulián NevadoFe Amalia García‐SantiagoLaura RodríguezMaría Ángeles Mori
- Topics
- Genomic variations and chromosomal abnormalities (16 papers)Prenatal Screening and Diagnostics (13 papers)Chromosomal and Genetic Variations (7 papers)
- Journals
- SHILAP Revista de lepidopterologíaJournal of Medical GeneticsHuman Genetics
- Partner nations
- SpainGermanyUnited Kingdom
In The Last Decade
Elena Mansilla
27 papers receiving 440 citations
Peers
Comparison fields: 5 of 78
- Genetics 276
- Pediatrics, Perinatology and Child Health 191
- Molecular Biology 143
- Plant Science 66
- Rheumatology 55
Countries citing papers authored by Elena Mansilla
This map shows the geographic impact of Elena Mansilla'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 Elena Mansilla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elena Mansilla more than expected).
Fields of papers citing papers by Elena Mansilla
This network shows the impact of papers produced by Elena Mansilla. 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 Elena Mansilla. The network helps show where Elena Mansilla may publish in the future.
Co-authorship network of co-authors of Elena Mansilla
This figure shows the co-authorship network connecting the top 25 collaborators of Elena Mansilla. A scholar is included among the top collaborators of Elena Mansilla 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 Elena Mansilla. Elena Mansilla 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 | 0 | |
| 3 | 0 | |
| 4 | 2 | |
| 5 | 4 | |
| 6 | 8 | |
| 7 | 3 | |
| 8 | 5 | |
| 9 | 3 | |
| 10 | 27 | |
| 11 | 69 | |
| 12 | 1 | |
| 13 | 8 | |
| 14 | 7 | |
| 15 | 2 | |
| 16 | 23 | |
| 17 | 31 | |
| 18 | 63 | |
| 19 | ¿Es la especificación OHSAS 18001:1999 la solución? | 1 |
| 20 | 34 |
About Elena Mansilla
Elena Mansilla is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Marketing, having authored 31 papers that have together received 456 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (13 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (276 citations), Pediatrics, Perinatology and Child Health (191 citations) and Rheumatology (55 citations). Elena Mansilla has collaborated with scholars based in Spain, Germany and United Kingdom. Frequent co-authors include Gerardo Suárez, M.L. Martínez‐Fernández, Pablo Lapunzina, Luís Fernández, Julián Nevado, Fe Amalia García‐Santiago, Laura Rodríguez, María Ángeles Mori, María Torres and Elena Vallespín. Their work appears in journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Human Genetics.
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.