F. Prieto
Impact in
- Hematology top 10%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 3
-
- RNA and protein synthesis mechanisms 3
- Co-authors
- Lourdes Badı́a (13 shared papers)Francesc Palau (6 shared papers)Francisco Martı́nez (5 shared papers)José M. Millán (2 shared papers)Magdalena Beneyto (2 shared papers)Carmen Orellana (3 shared papers)Françesc Solé (1 shared paper)Carlos Besses (1 shared paper)
- Journals
- Human Genetics (7 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (1 paper)Cytogenetic and Genome Research (1 paper)Genetic Epidemiology (1 paper)
- Partner nations
- SpainGermanyUnited States
In The Last Decade
F. Prieto
30 papers receiving 313 citations
Peers
Comparison fields: 5 of 61
- Hematology 79
- Genetics 184
- Developmental Biology 9
- Pediatrics, Perinatology and Child Health 69
- Genetics 37
Countries citing papers authored by F. Prieto
This map shows the geographic impact of F. Prieto'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 F. Prieto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. Prieto more than expected).
Fields of papers citing papers by F. Prieto
This network shows the impact of papers produced by F. Prieto. 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 F. Prieto. The network helps show where F. Prieto may publish in the future.
Co-authors
The 25 scholars most cited alongside F. Prieto, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 52 | |
| 2 | 1993 | 36 | |
| 3 | 1980 | 29 | |
| 4 | 1995 | 25 | |
| 5 | 2001 | 24 | |
| 6 | 1978 | 24 | |
| 7 | 2003 | 22 | |
| 8 | 1987 | 19 | |
| 9 | 1998 | 15 | |
| 10 | 1981 | 14 | |
| 11 | [Twenty-six chromosomes hypodiploidy in acute lymphoblastic leukaemia (author's transl)]. | 1978 | 13 |
| 12 | 1980 | 12 | |
| 13 | 1996 | 11 | |
| 14 | 1989 | 10 | |
| 15 | El trabajo como fenomeno psicosocial | 1996 | 9 |
| 16 | 1995 | 8 | |
| 17 | [Down's syndrome and leukemia]. | 1986 | 8 |
| 18 | [Cytogenetics in the study of myelodysplastic syndromes]. | 1985 | 8 |
| 19 | [Chromosome abnormalities in refractory anaemia with partial myeloblastosis (author's transl)]. | 1976 | 6 |
| 20 | [Trisomy 21 by translocation (21q,21q) in two sibs of a mother with a supernumerary microchromosome (author's transl)]. | 1981 | 5 |
About F. Prieto
F. Prieto is a scholar working on Genetics, Molecular Biology, Plant Science, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health, having authored 31 papers that have together received 374 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers), Genetics and Neurodevelopmental Disorders (3 papers), Employment, Labor, and Gender Studies (3 papers), Genetic Neurodegenerative Diseases (3 papers), RNA and protein synthesis mechanisms (3 papers), Prenatal Screening and Diagnostics (3 papers) and Organizational Management and Innovation (2 papers). The work is most often cited by research in Hematology (79 citations), Genetics (184 citations), Developmental Biology (9 citations), Pediatrics, Perinatology and Child Health (69 citations) and Genetics (37 citations). F. Prieto has collaborated with scholars based in Spain, Germany and United States. Frequent co-authors include Lourdes Badı́a, Francesc Palau, Francisco Martı́nez, José M. Millán, Magdalena Beneyto, Carmen Orellana, Françesc Solé, Carlos Besses, M.R. Caballı́n and S Woessner. Their work appears in journals such as Human Genetics, Clinical Genetics, Journal of Medical Genetics, Cytogenetic and Genome Research and Genetic Epidemiology.
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.