Lucia Grillo
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- PI3K/AKT/mTOR signaling in cancer
- Congenital heart defects research
- Epigenetics and DNA Methylation
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Congenital Ear and Nasal Anomalies 1
- Genomics and Rare Diseases 1
- Coagulation, Bradykinin, Polyphosphates, and Angioedema 1
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- Ubiquitin and proteasome pathways 1
- Co-authors
- Maria Bottitta (3 shared papers)Maurizio Elia (3 shared papers)Giuseppe Calabrese (2 shared papers)Corrado Romano (7 shared papers)Marco Fichera (8 shared papers)D Luciano (3 shared papers)Maria Esposito (1 shared paper)Daniela Benedetto (4 shared papers)
- Journals
- Molecular Cytogenetics (2 papers)European Journal of Medical Genetics (1 paper)Seizure (1 paper)Gene (1 paper)Human Genetics (1 paper)
- Partner nations
- Italy
In The Last Decade
Lucia Grillo
11 papers receiving 162 citations
Peers
Comparison fields: 5 of 40
- Genetics 106
- Molecular Biology 96
- Cognitive Neuroscience 24
- Pediatrics, Perinatology and Child Health 18
- Cellular and Molecular Neuroscience 11
Countries citing papers authored by Lucia Grillo
This map shows the geographic impact of Lucia Grillo'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 Lucia Grillo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucia Grillo more than expected).
Fields of papers citing papers by Lucia Grillo
This network shows the impact of papers produced by Lucia Grillo. 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 Lucia Grillo. The network helps show where Lucia Grillo may publish in the future.
Co-authors
The 25 scholars most cited alongside Lucia Grillo, 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 | 2014 | 43 | |
| 2 | 2012 | 38 | |
| 3 | 2010 | 33 | |
| 4 | 2013 | 19 | |
| 5 | 2013 | 15 | |
| 6 | 2019 | 11 | |
| 7 | 2014 | 10 | |
| 8 | 2008 | 10 | |
| 9 | 2014 | 4 | |
| 10 | 2015 | 3 | |
| 11 | 2016 | 1 |
About Lucia Grillo
Lucia Grillo is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 11 papers that have together received 187 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Congenital Ear and Nasal Anomalies (1 paper), Ubiquitin and proteasome pathways (1 paper), Genomics and Rare Diseases (1 paper), Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper), Folate and B Vitamins Research (1 paper) and Birth, Development, and Health (1 paper). The work is most often cited by research in Genetics (106 citations), Molecular Biology (96 citations), Cognitive Neuroscience (24 citations), Pediatrics, Perinatology and Child Health (18 citations) and Cellular and Molecular Neuroscience (11 citations). Lucia Grillo has collaborated with scholars based in Italy. Frequent co-authors include Maria Bottitta, Maurizio Elia, Giuseppe Calabrese, Corrado Romano, Marco Fichera, D Luciano, Maria Esposito, Daniela Benedetto, Marco Carotenuto and S Reitano. Their work appears in journals such as Molecular Cytogenetics, European Journal of Medical Genetics, Seizure, Gene and Human Genetics.
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.