Fernanda T. Bellucco
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- Genomic variations and chromosomal abnormalities 16
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 3
- Genetic Associations and Epidemiology 2
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- Congenital heart defects research 5
- Glycosylation and Glycoproteins Research 2
- Hedgehog Signaling Pathway Studies 2
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- Chromosomal and Genetic Variations 6
Fernanda T. Bellucco
24 papers receiving 209 citations
Peers
Comparison fields: 5 of 51
- Genetics 140
- Biological Psychiatry 6
- Pediatrics, Perinatology and Child Health 43
- Molecular Biology 107
- Plant Science 56
Countries citing papers authored by Fernanda T. Bellucco
This map shows the geographic impact of Fernanda T. Bellucco'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 Fernanda T. Bellucco with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fernanda T. Bellucco more than expected).
Fields of papers citing papers by Fernanda T. Bellucco
This network shows the impact of papers produced by Fernanda T. Bellucco. 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 Fernanda T. Bellucco. The network helps show where Fernanda T. Bellucco may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Fernanda T. Bellucco, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 1 | |
| 2 | 2022 | 1 | |
| 3 | 2022 | 50 | |
| 4 | 2021 | 1 | |
| 5 | 2021 | 4 | |
| 6 | 2020 | 2 | |
| 7 | 2019 | 6 | |
| 8 | 2019 | 3 | |
| 9 | 2019 | 8 | |
| 10 | 2018 | 3 | |
| 11 | 2014 | 12 | |
| 12 | 2013 | 20 | |
| 13 | 2012 | 26 | |
| 14 | 2012 | 16 | |
| 15 | 2010 | 4 | |
| 16 | 2010 | 3 | |
| 17 | 2010 | 16 | |
| 18 | 2010 | 9 | |
| 19 | 2010 | 6 | |
| 20 | 2008 | 24 |
About Fernanda T. Bellucco
Fernanda T. Bellucco is a scholar working on Genetics, Molecular Biology and Genetics, having authored 24 papers that have together received 233 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Genetics and Neurodevelopmental Disorders (6 papers), Chromosomal and Genetic Variations (6 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers), Glycosylation and Glycoproteins Research (2 papers), Genetic Associations and Epidemiology (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). The work is most often cited by research in Genetics (140 citations), Biological Psychiatry (6 citations) and Pediatrics, Perinatology and Child Health (43 citations). Fernanda T. Bellucco has collaborated with scholars based in Brazil, Canada and United States. Frequent co-authors include Maria Isabel Melaragno, Leslie Domenici Kulikowski, Síntia Belangero, Denise Maria Christofolini, Maria Betânia Pereira Toralles, Rodrigo A. Bressan, Marcos Santoro, Jair de Jesus Mari, Ary Gadelha and Marı́lia de Arruda Cardoso Smith.
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.