Alexandra MacDonald
- Co-authors
- M.L. Martínez‐FernándezEva BermejoMaría Luisa Martínez‐FríasLaura RodríguezM. L. Martínez‐FríasSalvador Martı́nezJavier SuelaJ. Gonzalo Ocejo‐Vinyals
- Topics
- Congenital heart defects research (3 papers)Genomic variations and chromosomal abnormalities (3 papers)Congenital Ear and Nasal Anomalies (1 paper)
In The Last Decade
Alexandra MacDonald
7 papers receiving 45 citations
Peers
Comparison fields: 5 of 26
- Genetics 35
- Molecular Biology 17
- Pediatrics, Perinatology and Child Health 8
- Genetics 7
- Surgery 4
Countries citing papers authored by Alexandra MacDonald
This map shows the geographic impact of Alexandra MacDonald'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 Alexandra MacDonald with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandra MacDonald more than expected).
Fields of papers citing papers by Alexandra MacDonald
This network shows the impact of papers produced by Alexandra MacDonald. 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 Alexandra MacDonald. The network helps show where Alexandra MacDonald may publish in the future.
Co-authorship network of co-authors of Alexandra MacDonald
This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra MacDonald. A scholar is included among the top collaborators of Alexandra MacDonald 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 Alexandra MacDonald. Alexandra MacDonald is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 4 | |
| 3 | 6 | |
| 4 | 4 | |
| 5 | 12 | |
| 6 | Análisis de alteraciones cromosómicas estructurales y su distribución por cromosomas en la serie de recién nacidos con defectos congénitos del ECEMC / Analysis of the structural chromosomal anomalies and distribution by chromosomes in the ECEMC’s series of newborn infants with congenital defects | 1 |
| 7 | 15 |
About Alexandra MacDonald
Alexandra MacDonald is a scholar working on Speech and Hearing, Genetics and Genetics, having authored 7 papers that have together received 46 indexed citations. Recurring topics across this work include Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Congenital Ear and Nasal Anomalies (1 paper). The work is most often cited by research in Genetics (35 citations), Genetics (7 citations) and Pediatrics, Perinatology and Child Health (8 citations). Alexandra MacDonald has collaborated with scholars based in Spain and Portugal. Frequent co-authors include M.L. Martínez‐Fernández, Eva Bermejo, María Luisa Martínez‐Frías, Laura Rodríguez, M. L. Martínez‐Frías, Salvador Martı́nez, Javier Suela, J. Gonzalo Ocejo‐Vinyals, Isabel Llano‐Rivas and Rosa Arteaga. Their work appears in journals such as American Journal of Medical Genetics Part A.
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.