Francisco Galán
- Genetics
- Molecular Biology
- Public Health, Environmental and Occupational Health
- Infectious Diseases
- Pediatrics, Perinatology and Child Health
- Co-authors
- Jean LangBetzana ZambranoGustavo H. DayanJorge Luis PooRémi ForratBelén LledóRafael BernabéuJorge Ten
- Topics
- Prenatal Screening and Diagnostics (8 papers)Congenital heart defects research (4 papers)Genomic variations and chromosomal abnormalities (4 papers)
In The Last Decade
Francisco Galán
17 papers receiving 333 citations
Peers
Comparison fields: 5 of 53
- Genetics 139
- Molecular Biology 106
- Public Health, Environmental and Occupational Health 101
- Infectious Diseases 81
- Pediatrics, Perinatology and Child Health 63
Countries citing papers authored by Francisco Galán
This map shows the geographic impact of Francisco Galán'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 Francisco Galán with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francisco Galán more than expected).
Fields of papers citing papers by Francisco Galán
This network shows the impact of papers produced by Francisco Galán. 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 Francisco Galán. The network helps show where Francisco Galán may publish in the future.
Co-authorship network of co-authors of Francisco Galán
This figure shows the co-authorship network connecting the top 25 collaborators of Francisco Galán. A scholar is included among the top collaborators of Francisco Galán 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 Francisco Galán. Francisco Galán is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 11 | |
| 2 | 1 | |
| 3 | 20 | |
| 4 | 6 | |
| 5 | 92 | |
| 6 | 20 | |
| 7 | 18 | |
| 8 | 2 | |
| 9 | 62 | |
| 10 | 16 | |
| 11 | 36 | |
| 12 | PREIMPLANTATION GENETIC DIAGNOSIS | 1 |
| 13 | 25 | |
| 14 | 15 | |
| 15 | 14 | |
| 16 | Full trisomy 22 in a malformed newborn female. | 11 |
| 17 | 69,XXX karyotype in a malformed liveborn female. Maternal origin of triploidy. | 2 |
| 18 | Partial trisomy 13q22----qter. A new case. | 3 |
About Francisco Galán
Francisco Galán is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Sensory Systems, having authored 18 papers that have together received 355 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (8 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Developmental Biology (21 citations), Genetics (139 citations) and Infectious Diseases (81 citations). Francisco Galán has collaborated with scholars based in Spain, Mexico and France. Frequent co-authors include Jean Lang, Betzana Zambrano, Gustavo H. Dayan, Jorge Luis Poo, Rémi Forrat, Belén Lledó, Rafael Bernabéu, Jorge Ten, Luís A. Alcaraz and Alma Ortíz-Plata. Their work appears in journals such as Fertility and Sterility, Developmental Medicine & Child Neurology and Human Mutation.
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.