Stella Lanni
Impact in
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- Genetic Neurodegenerative Diseases
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- Genetics and Neurodevelopmental Disorders
Papers in
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- Epigenetics and DNA Methylation 3
- DNA Repair Mechanisms 2
- RNA modifications and cancer 2
- Mitochondrial Function and Pathology 1
- Genetics 6
- Genetics and Neurodevelopmental Disorders 6
- Co-authors
- Christopher E. Pearson (3 shared papers)Giovanni Neri (4 shared papers)Elisabetta Tabolacci (4 shared papers)Fabrizio Ferrè (2 shared papers)Manuela Helmer‐Citterich (2 shared papers)Pietro Chiurazzi (3 shared papers)Mohiuddin Mohiuddin (2 shared papers)Jean‐Yves Masson (2 shared papers)
- Journals
- Epigenetics & Chromatin (1 paper)Human Genetics (1 paper)Journal of Huntington s Disease (1 paper)European Journal of Human Genetics (1 paper)PLoS Genetics (1 paper)
- Partner nations
- ItalyCanadaUnited States
In The Last Decade
Stella Lanni
7 papers receiving 175 citations
Peers
Comparison fields: 5 of 33
- Cellular and Molecular Neuroscience 71
- Genetics 80
- Molecular Biology 150
- Cognitive Neuroscience 29
- Aging 2
Countries citing papers authored by Stella Lanni
This map shows the geographic impact of Stella Lanni'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 Stella Lanni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stella Lanni more than expected).
Fields of papers citing papers by Stella Lanni
This network shows the impact of papers produced by Stella Lanni. 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 Stella Lanni. The network helps show where Stella Lanni may publish in the future.
Co-authors
The 25 scholars most cited alongside Stella Lanni, 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 | 2019 | 45 | |
| 2 | 2021 | 37 | |
| 3 | 2013 | 31 | |
| 4 | 2016 | 22 | |
| 5 | 2020 | 18 | |
| 6 | 2021 | 18 | |
| 7 | 2015 | 5 |
About Stella Lanni
Stella Lanni is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Cognitive Neuroscience, having authored 7 papers that have together received 176 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Epigenetics and DNA Methylation (3 papers), Genetic Neurodegenerative Diseases (3 papers), DNA Repair Mechanisms (2 papers), RNA modifications and cancer (2 papers), Child Development and Digital Technology (1 paper), Neurological disorders and treatments (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (71 citations), Genetics (80 citations), Molecular Biology (150 citations), Cognitive Neuroscience (29 citations) and Aging (2 citations). Stella Lanni has collaborated with scholars based in Italy, Canada and United States. Frequent co-authors include Christopher E. Pearson, Giovanni Neri, Elisabetta Tabolacci, Fabrizio Ferrè, Manuela Helmer‐Citterich, Pietro Chiurazzi, Mohiuddin Mohiuddin, Jean‐Yves Masson, Marie‐Christine Caron and Gagan B. Panigrahi. Their work appears in journals such as Epigenetics & Chromatin, Human Genetics, Journal of Huntington s Disease, European Journal of Human Genetics and PLoS 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.