Emanuele Agolini
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
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- Cancer-related gene regulation
- Epigenetics and DNA Methylation
Papers in
-
- Hedgehog Signaling Pathway Studies 5
- Genetics 28
- Glioma Diagnosis and Treatment 10
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Kidney Cyst Diseases 5
- Connective tissue disorders research 5
- Co-authors
- Antonio Novelli (52 shared papers)Bruno Dallapiccola (12 shared papers)M. Cristina Digilio (14 shared papers)Francesco Brancati (5 shared papers)Angela Mastronuzzi (21 shared papers)Andrea Carai (17 shared papers)Antonella Cacchione (16 shared papers)Martina Rinelli (13 shared papers)
- Journals
- Clinical Genetics (7 papers)Frontiers in Oncology (6 papers)Genes (4 papers)European Journal of Human Genetics (3 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Emanuele Agolini
74 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 87
- Genetics 300
- Genetics 93
- Molecular Biology 430
- Neurology 86
- Immunology 107
Countries citing papers authored by Emanuele Agolini
This map shows the geographic impact of Emanuele Agolini'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 Emanuele Agolini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emanuele Agolini more than expected).
Fields of papers citing papers by Emanuele Agolini
This network shows the impact of papers produced by Emanuele Agolini. 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 Emanuele Agolini. The network helps show where Emanuele Agolini may publish in the future.
Co-authors
The 25 scholars most cited alongside Emanuele Agolini, 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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 173 | |
| 2 | 2010 | 93 | |
| 3 | 2020 | 84 | |
| 4 | 2021 | 43 | |
| 5 | 2018 | 36 | |
| 6 | 2017 | 33 | |
| 7 | 2014 | 28 | |
| 8 | 2012 | 25 | |
| 9 | 2019 | 25 | |
| 10 | 2020 | 24 | |
| 11 | 2021 | 23 | |
| 12 | 2019 | 22 | |
| 13 | 2020 | 20 | |
| 14 | 2020 | 20 | |
| 15 | 2021 | 18 | |
| 16 | 2019 | 17 | |
| 17 | 2022 | 16 | |
| 18 | 2018 | 16 | |
| 19 | 2022 | 15 | |
| 20 | 2020 | 13 |
About Emanuele Agolini
Emanuele Agolini is a scholar working on Molecular Biology, Genetics, Genetics, Neurology and Surgery, having authored 85 papers that have together received 1.0k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (10 papers), Genomics and Rare Diseases (8 papers), Neuroblastoma Research and Treatments (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genetic and Kidney Cyst Diseases (5 papers), Hedgehog Signaling Pathway Studies (5 papers) and Connective tissue disorders research (5 papers). The work is most often cited by research in Genetics (300 citations), Genetics (93 citations), Molecular Biology (430 citations), Neurology (86 citations) and Immunology (107 citations). Emanuele Agolini has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Antonio Novelli, Bruno Dallapiccola, M. Cristina Digilio, Francesco Brancati, Angela Mastronuzzi, Andrea Carai, Antonella Cacchione, Martina Rinelli, Emanuele Bellacchio and Franco Locatelli. Their work appears in journals such as Clinical Genetics, Frontiers in Oncology, Genes, European Journal of Human Genetics and The American Journal of 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.