F Ballesta
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Trace Elements in Health
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Montserrat Milà (6 shared papers)Xavier Estivill (4 shared papers)Rafael Oliva (5 shared papers)H. Kruyer (2 shared papers)Judy Fantes (1 shared paper)Veronica van Heyningen (1 shared paper)Wendy A. Bickmore (1 shared paper)Ester Margarit (4 shared papers)
- Journals
- Human Genetics (3 papers)Neurology (2 papers)Pediatric Dermatology (1 paper)Journal of Medical Genetics (1 paper)Fetal Diagnosis and Therapy (1 paper)
- Partner nations
- SpainSwitzerlandUnited Kingdom
In The Last Decade
F Ballesta
27 papers receiving 518 citations
Peers
Comparison fields: 5 of 64
- Genetics 249
- Nutrition and Dietetics 74
- Hematology 52
- Pediatrics, Perinatology and Child Health 83
- Health, Toxicology and Mutagenesis 57
Countries citing papers authored by F Ballesta
This map shows the geographic impact of F Ballesta'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 Ballesta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Ballesta more than expected).
Fields of papers citing papers by F Ballesta
This network shows the impact of papers produced by F Ballesta. 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 Ballesta. The network helps show where F Ballesta may publish in the future.
Co-authors
The 25 scholars most cited alongside F Ballesta, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization. | 1992 | 89 |
| 2 | Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins. | 1994 | 79 |
| 3 | 2005 | 71 | |
| 4 | 1999 | 40 | |
| 5 | 1998 | 37 | |
| 6 | 1999 | 33 | |
| 7 | 1990 | 24 | |
| 8 | 1994 | 21 | |
| 9 | Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21. | 1999 | 21 |
| 10 | 1982 | 20 | |
| 11 | [Partial trisomy for the distal part of the short branch of chromosome 3]. | 1974 | 17 |
| 12 | 1996 | 14 | |
| 13 | 1997 | 14 | |
| 14 | 1999 | 14 | |
| 15 | [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome]. | 1999 | 13 |
| 16 | 1990 | 11 | |
| 17 | 1997 | 6 | |
| 18 | 1998 | 6 | |
| 19 | [Maternal translocation t (1; 8; 15) and trisomy 8 qter in her daughter. Genetic counseling]. | 1980 | 4 |
| 20 | 1998 | 3 |
About F Ballesta
F Ballesta is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Physiology and Surgery, having authored 28 papers that have together received 547 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Alzheimer's disease research and treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Metabolism and Genetic Disorders (2 papers), Chromosomal and Genetic Variations (2 papers), Trace Elements in Health (2 papers) and Sperm and Testicular Function (2 papers). The work is most often cited by research in Genetics (249 citations), Nutrition and Dietetics (74 citations), Hematology (52 citations), Pediatrics, Perinatology and Child Health (83 citations) and Health, Toxicology and Mutagenesis (57 citations). F Ballesta has collaborated with scholars based in Spain, Switzerland and United Kingdom. Frequent co-authors include Montserrat Milà, Xavier Estivill, Rafael Oliva, H. Kruyer, Judy Fantes, Veronica van Heyningen, Wendy A. Bickmore, Ester Margarit, Judy Fletcher and Isabel M. Hanson. Their work appears in journals such as Human Genetics, Neurology, Pediatric Dermatology, Journal of Medical Genetics and Fetal Diagnosis and Therapy.
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.